Disease on EC 2.7.2.3 - phosphoglycerate kinase
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6-phosphofructokinase deficiency
Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.
ACTH-Secreting Pituitary Adenoma
Clonal origins of adrenocorticotropin-secreting pituitary tissue in Cushing's disease.
Acute Kidney Injury
Familial phosphoglycerate kinase deficiency associated with rhabdomyolysis and acute renal failure: abnormality in mRNA splicing?
Adenocarcinoma
Overexpression and elevated serum levels of phosphoglycerate kinase 1 in pancreatic ductal adenocarcinoma.
Adenoma
Lentiviral vectors efficiently transduce human gonadotroph and somatotroph adenomas in vitro. Targeted expression of transgene by pituitary hormone promoters.
adenylate kinase deficiency
Red cell enzymopathies as a model of inborn errors of metabolism.
Alzheimer Disease
Increased phosphoglycerate kinase in the brains of patients with Down's syndrome but not with Alzheimer's disease.
Anemia
Long-term and stable correction of uremic anemia by intramuscular injection of plasmids containing hypoxia-regulated system of Epo expression.
Anemia
Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy.
Anemia
Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.
Anemia, Aplastic
Clonal hematopoiesis as defined by polymorphic X-linked loci occurs infrequently in aplastic anemia.
Anemia, Hemolytic
A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemia.
Anemia, Hemolytic
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: Molecular and functional characterization.
Anemia, Hemolytic
A novel missense mutation (1060G --> C) in the phosphoglycerate kinase gene in a Japanese boy with chronic haemolytic anaemia, developmental delay and rhabdomyolysis.
Anemia, Hemolytic
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population.
Anemia, Hemolytic
A phosphoglycerate kinase mutant (PGK Herlev; D285V) in a Danish patient with isolated chronic hemolytic anemia: mechanism of mutation and structure-function relationships.
Anemia, Hemolytic
A phosphoglycerate kinase variant, PGK Uppsala, associated with hemolytic anemia.
Anemia, Hemolytic
Altered expression of PGK1 in a family with phosphoglycerate kinase deficiency.
Anemia, Hemolytic
Characterization of a phosphoglycerate kinase deficiency variants not associated with hemolytic anemia.
Anemia, Hemolytic
Characterization of a phosphoglycerate kinase variant associated with hemolytic anemia.
Anemia, Hemolytic
Deficiencies of glycolytic enzymes as a possible cause of hemolytic anemia.
Anemia, Hemolytic
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
Anemia, Hemolytic
Enzymatic and metabolic characterization of the phosphoglycerate kinase deficiency associated with chronic hemolytic anemia caused by the PGK-Barcelona mutation.
Anemia, Hemolytic
Erythrocyte phosphoglycerate kinase deficiency: enzymatic and oxygen binding studies.
Anemia, Hemolytic
Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia.
Anemia, Hemolytic
Human erythrocyte phosphoglycerate kinase deficiency: presence in a deficient patient of a stable variant with lowered catalytic activity.
Anemia, Hemolytic
Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes: PGK Créteil and PGK Amiens.
Anemia, Hemolytic
Molecular abnormality of phosphoglycerate kinase-Uppsala associated with chronic nonspherocytic hemolytic anemia.
Anemia, Hemolytic
Molecular defect of a phosphoglycerate kinase variant (PGK-Matsue) associated with hemolytic anemia: Leu----Pro substitution caused by T/A----C/G transition in exon 3.
Anemia, Hemolytic
Molecular defect of a phosphoglycerate kinase variant associated with haemolytic anaemia and neurological disorders in a large kindred.
Anemia, Hemolytic
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency.
Anemia, Hemolytic
Monoclonal anti-double-stranded DNA antibodies cross-react with phosphoglycerate kinase 1 and inhibit the expression and production of IL-2 in activated Jurkat T cell line.
Anemia, Hemolytic
Normal mRNA content in a phosphoglycerate kinase variant with severe enzyme deficiency.
Anemia, Hemolytic
Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.
Anemia, Hemolytic
Parkinsonism in PGK1 deficiency implicates the glycolytic pathway in nigrostriatal dysfunction.
Anemia, Hemolytic
Phosphoglycerate kinase (PKG) deficiency hereditary nonspherocytic hemolytic anemia: report of a case found in a Japanese family.
Anemia, Hemolytic
Phosphoglycerate kinase abnormalities: functional, structural and genomic aspects.
Anemia, Hemolytic
Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy.
Anemia, Hemolytic
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.
Anemia, Hemolytic
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzyme.
Anemia, Hemolytic
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.
Anemia, Hemolytic
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
Anemia, Hemolytic
Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.
Anemia, Hemolytic
Slowly progressive leukodystrophy in an adolescent male with phosphoglycerate kinase deficiency.
Anemia, Hemolytic
Structural and functional properties of mutant Arg203Pro from yeast phosphoglycerate kinase, as a model of phosphoglycerate kinase-Uppsala.
Anemia, Hemolytic
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Anemia, Hemolytic
Therapeutic Benefit of Blood Transfusion in a Patient With Novel PGK1 Mutation (c.461T>C [p.L154P]).
Anemia, Hemolytic
Tissue levels of glycolytic enzymes in phosphoglycerate kinase deficiency.
Anemia, Hemolytic
Two new phosphoglycerate kinase mutations associated with chronic haemolytic anaemia and neurological dysfunction in two patients from Spain.
Anemia, Hemolytic
Use of cultured lymphoblastoid cells for the study of abnormal enzymes: molecular abnormality of a phosphoglycerate kinase variant associated with hemolytic anemia.
Anemia, Hemolytic, Congenital
Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome.
Anemia, Hemolytic, Congenital
Hereditary hemolytic anemia: association with phosphoglycerate kinase deficiency in erythrocytes and leukocytes.
Anemia, Hemolytic, Congenital
Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
Anemia, Hemolytic, Congenital
[Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes]
Anemia, Hemolytic, Congenital Nonspherocytic
Molecular defect of a phosphoglycerate kinase variant (PGK-Matsue) associated with hemolytic anemia: Leu----Pro substitution caused by T/A----C/G transition in exon 3.
Anemia, Hemolytic, Congenital Nonspherocytic
Normal mRNA content in a phosphoglycerate kinase variant with severe enzyme deficiency.
Anemia, Sideroblastic
Linkage analysis of a large pedigree with hereditary sideroblastic anaemia.
Anemia, Sideroblastic
X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.
Arthritis
Overexpression of CXC chemokine ligand 14 exacerbates collagen-induced arthritis.
Asthenozoospermia
Characteristics of testis-specific phosphoglycerate kinase 2 and its association with human sperm quality.
Astrocytoma
Over-expression of cofilin-1 and phosphoglycerate kinase 1 in astrocytomas involved in pathogenesis of radioresistance.
Ataxia
X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.
Bacteremia
Comparative Exoproteomics and Host Inflammatory Response in Staphylococcus aureus Skin and Soft Tissue Infections, Bacteremia, and Subclinical Colonization.
Bone Diseases, Metabolic
A proteomic study of protein variation between osteopenic and age-matched control bone tissue.
Bone Resorption
Perturbations in bone formation and resorption in insulin-like growth factor binding protein-3 transgenic mice.
Brain Neoplasms
[Enzymes in cerebrospinal fluid (HK, TIM, GAPDH, PGK, enolase, PK, LDH, GPT, ChE) in normal samples, in brain neoplasms and other neurologic diseases]
Breast Neoplasms
Clonal analysis of benign and malignant human breast tumors by means of polymerase chain reaction.
Breast Neoplasms
Discrimination between multicentric and multifocal carcinomas of the breast through clonal analysis.
Breast Neoplasms
Phosphoglycerate kinase-1 is a predictor of poor survival and a novel prognostic biomarker of chemoresistance to paclitaxel treatment in breast cancer.
Breast Neoplasms
Proteomic study reveals that proteins involved in metabolic and detoxification pathways are highly expressed in HER-2/neu-positive breast cancer.
Candidiasis
Proteomics-based identification of novel Candida albicans antigens for diagnosis of systemic candidiasis in patients with underlying hematological malignancies.
Candidiasis
Synthetic glycopeptide vaccines combining beta-mannan and peptide epitopes induce protection against candidiasis.
carboxypeptidase t deficiency
[Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes]
Carcinogenesis
A spring loaded release mechanism regulates domain movement and catalysis in phosphoglycerate kinase.
Carcinogenesis
Coordinate up-regulation of hypoxia inducible factor (HIF)-1alpha and HIF-1 target genes during multi-stage epidermal carcinogenesis and wound healing.
Carcinogenesis
Intraclonal conversion from papilloma to carcinoma in the skin of Pgk-1a/Pgk-1b mice treated by a complete carcinogenesis process or by an initiation-promotion regimen.
Carcinogenesis
Long noncoding RNA MSC-AS1 promotes hepatocellular carcinoma oncogenesis via inducing the expression of phosphoglycerate kinase 1.
Carcinogenesis
pH-dependent relationship between thermodynamic and kinetic stability in the denaturation of human phosphoglycerate kinase 1.
Carcinogenesis
Phosphoglycerate kinase: structural aspects and functions, with special emphasis on the enzyme from Kinetoplastea.
Carcinogenesis
Sequential studies of skin tumorigenesis in PGK mosaic mice: the effect of repeated exposure to a carcinogen on regressed mouse skin papillomas.
Carcinogenesis
Sequential studies of skin tumorigenesis in phosphoglycerate kinase mosaic mice: effect of resumption of promotion on regressed papillomas.
Carcinogenesis
Studies of skin tumorigenesis in PGK mosaic mice: many promoter-independent papillomas and carcinomas do not develop from pre-existing promoter-dependent papillomas.
Carcinogenesis
X-linked allozymes of phosphoglycerate kinase as tools in experimental carcinogenesis in the mouse.
Carcinoma
Clonal origin of skin and bone tumors produced by repeated beta-irradiation in mosaic cell mice.
Carcinoma
Discrimination between multicentric and multifocal carcinomas of the breast through clonal analysis.
Carcinoma
Effect of hypoxia on the expression of phosphoglycerate kinase and antitumor activity of troxacitabine and gemcitabine in non-small cell lung carcinoma.
Carcinoma
Intraclonal conversion from papilloma to carcinoma in the skin of Pgk-1a/Pgk-1b mice treated by a complete carcinogenesis process or by an initiation-promotion regimen.
Carcinoma
Lentivirus vectors incorporating the immunoglobulin heavy chain enhancer and matrix attachment regions provide position-independent expression in B lymphocytes.
Carcinoma
Mapping of DNA alkylation sites induced by adozelesin and bizelesin in human cells by ligation-mediated polymerase chain reaction.
Carcinoma
Nucleotide-binding domain of phosphoglycerate kinase 1 reduces tumor growth by suppressing COX-2 expression.
Carcinoma
Phosphoglycerate kinase 1-overexpressing lung cancer cells reduce cyclooxygenase 2 expression and promote anti-tumor immunity in vivo.
Carcinoma
Purification and characterization of 3-phosphoglycerate kinase from Ehrlich ascites carcinoma cells.
Carcinoma
Regulation of urokinase receptor expression by phosphoglycerate kinase is independent of its catalytic activity.
Carcinoma
Short tandem repeat polymorphism linkage to the androgen receptor gene in prostate carcinoma.
Carcinoma
Studies of skin tumorigenesis in PGK mosaic mice: many promoter-independent papillomas and carcinomas do not develop from pre-existing promoter-dependent papillomas.
Carcinoma
Test of recurrence after experimental radiation therapy of chemically induced autochthonous tumors in mosaic mice.
Carcinoma
The phosphoglycerate kinase 1 variants found in carcinoma cells display different catalytic activity and conformational stability compared to the native enzyme.
Carcinoma, Adenosquamous
Colliding primary lung cancers of adenosquamous carcinoma and large cell neuroendocrine carcinoma.
Carcinoma, Ehrlich Tumor
Direct effect of basic fibroblast growth factor on gene transcription in a cell-free system.
Carcinoma, Embryonal
Comparative analysis of retroviral vector expression in mouse embryonal carcinoma cells.
Carcinoma, Embryonal
DNA methylation of two X chromosome genes in female somatic and embryonal carcinoma cells.
Carcinoma, Embryonal
Enhanced transgene expression in embryonal carcinoma stem cells: transcription through introns and exons increases gene copy numbers and forestalls silencing.
Carcinoma, Embryonal
Intragenic regions of the murine Pgk-1 locus enhance integration of transfected DNAs into genomes of embryonal carcinoma cells.
Carcinoma, Hepatocellular
Antrodia cinnamomea Inhibits Migration in Human Hepatocellular Carcinoma Cells: The Role of ERp57 and PGK-1.
Carcinoma, Hepatocellular
Clonality in hepatocellular carcinoma: analysis of methylation pattern of polymorphic X-chromosome-linked phosphoglycerate kinase gene in females.
Carcinoma, Hepatocellular
Development of a gene therapy strategy to target hepatocellular carcinoma based inhibition of protein phosphatase 2A using the ?-fetoprotein promoter enhancer and pgk promoter: an in vitro and in vivo study.
Carcinoma, Hepatocellular
Downregulation of long non-protein coding RNA MVIH impairs glioblastoma cell proliferation and invasion through an miR-302a-dependent mechanism.
Carcinoma, Hepatocellular
Gene therapy for hepatocellular carcinoma based on tumour-selective suicide gene expression using the alpha-fetoprotein (AFP) enhancer and a housekeeping gene promoter.
Carcinoma, Hepatocellular
Induction of phosphoglycerate kinase 1 gene expression by hypoxia. Roles of Arnt and HIF1alpha.
Carcinoma, Hepatocellular
Inhibition of Non-flux-Controlling Enzymes Deters Cancer Glycolysis by Accumulation of Regulatory Metabolites of Controlling Steps.
Carcinoma, Hepatocellular
Long noncoding RNA MSC-AS1 promotes hepatocellular carcinoma oncogenesis via inducing the expression of phosphoglycerate kinase 1.
Carcinoma, Hepatocellular
MicroRNA-450b-3p inhibits cell growth by targeting phosphoglycerate kinase 1 in hepatocellular carcinoma.
Carcinoma, Hepatocellular
Subchromosomal localization and order of GLA, PGK1, HPRT, and G6PD loci on the X chromosome of the American mink (Mustela vison).
Carcinoma, Hepatocellular
[Influence of phosphoglycerate kinase 1 on metastasis and invasion of hepatoma cells and prognosis of liver cancer].
Carcinoma, Hepatocellular
[The distribution of 4 genes (alpha GAL, PGK-1, HPRT and G6PD) on the X chromosome of the American mink (Mustela vison)]
Carcinoma, Intraductal, Noninfiltrating
Clonal analysis of predominantly intraductal carcinoma and precancerous lesions of the breast by means of polymerase chain reaction.
Carcinoma, Lewis Lung
Nucleotide-binding domain of phosphoglycerate kinase 1 reduces tumor growth by suppressing COX-2 expression.
Carcinoma, Lewis Lung
Phosphoglycerate kinase 1-overexpressing lung cancer cells reduce cyclooxygenase 2 expression and promote anti-tumor immunity in vivo.
Carcinoma, Neuroendocrine
Colliding primary lung cancers of adenosquamous carcinoma and large cell neuroendocrine carcinoma.
Carcinoma, Non-Small-Cell Lung
Effect of hypoxia on the expression of phosphoglycerate kinase and antitumor activity of troxacitabine and gemcitabine in non-small cell lung carcinoma.
Carcinoma, Pancreatic Ductal
Enhanced levels of annexins in pancreatic carcinoma cells of Syrian hamsters and their intrapancreatic allografts.
Carcinoma, Squamous Cell
Clonal origin of skin and bone tumors produced by repeated beta-irradiation in mosaic cell mice.
Carcinoma, Squamous Cell
Coordinate up-regulation of hypoxia inducible factor (HIF)-1alpha and HIF-1 target genes during multi-stage epidermal carcinogenesis and wound healing.
Cholesteatoma
Pathogenesis of Middle Ear Cholesteatoma. A New Model of Experimentally Induced Cholesteatoma in Mongolian Gerbils.
Choroideremia
22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125-DXS95 in human Xq12-q21.31.
Choroideremia
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.
Clonorchiasis
Molecular cloning and immunological characterization of phosphoglycerate kinase from Clonorchis sinensis.
Coronary Artery Disease
Optimisation of methods for quantifying plasma mRNA levels from genes responsible for coronary artery plaque development and destabilization.
Cysts
Analysis of clonality in human endometriotic cysts based on evaluation of X chromosome inactivation in archival formalin-fixed, paraffin-embedded tissue.
Deafness
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.
Dehydration
Phosphoglycerate kinase 1 expression responds to freezing, anoxia, and dehydration stresses in the freeze tolerant wood frog, Rana sylvatica.
Diabetes Mellitus, Type 1
Red cell phosphoglycerate kinase in insulin-dependent diabetes mellitus.
Down Syndrome
Increased phosphoglycerate kinase in the brains of patients with Down's syndrome but not with Alzheimer's disease.
Dystonia Musculorum Deformans
22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125-DXS95 in human Xq12-q21.31.
Endometrial Neoplasms
[Expression of phosphoglycerate kinase 1 in endometrial carcinoma and its association with patients' outcome].
Endometriosis
Analysis of clonality in human endometriotic cysts based on evaluation of X chromosome inactivation in archival formalin-fixed, paraffin-embedded tissue.
Fibrosarcoma
Evidence concerning the clonal nature of chemically induced tumors: phosphoglycerate kinase-1 isozyme patterns in chemically induced fibrosarcomas.
Fibrosarcoma
Evidence for single-cell origin of 3-methylcholanthrene-induced fibrosarcomas in mice with cellular mosaicism.
Fibrosarcoma
Phosphoglycerate kinase acts in tumour angiogenesis as a disulphide reductase.
fructose-bisphosphate aldolase deficiency
Red cell enzymopathies as a model of inborn errors of metabolism.
fructose-bisphosphate aldolase deficiency
Tarui disease and distal glycogenoses: clinical and genetic update.
Gallbladder Neoplasms
Down-Regulated Phosphoglycerate Kinase 1 Expression Is Associated With Poor Prognosis in Patients With Gallbladder Cancer.
Gallbladder Neoplasms
Long non-coding RNA GBCDRlnc1 induces chemoresistance of gallbladder cancer cells by activating autophagy.
Genetic Diseases, Inborn
A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report.
Genetic Diseases, Inborn
Structural and energetic basis of protein kinetic destabilization in human phosphoglycerate kinase 1 deficiency.
Glioblastoma
Hypoxia-induced acetylation of PAK1 enhances autophagy and promotes brain tumorigenesis via phosphorylating ATG5.
Glioma
Cofilin-1 and phosphoglycerate kinase 1 as promising indicators for glioma radiosensibility and prognosis.
Glioma
Hypoxia-induced acetylation of PAK1 enhances autophagy and promotes brain tumorigenesis via phosphorylating ATG5.
Glioma
The Neurogenic Compound P7C3 Regulates the Aerobic Glycolysis by Targeting Phosphoglycerate Kinase 1 in Glioma.
Glucose Intolerance
Glucose intolerance in aging male IGFBP-3 transgenic mice: differential effects of human IGFBP-3 and its mutant IGFBP-3 devoid of IGF binding ability.
glucose-6-phosphate isomerase deficiency
Enzymatic diagnosis in non-spherocytic hemolytic anemia.
Glycogen Storage Disease
Tarui disease and distal glycogenoses: clinical and genetic update.
Growth Hormone-Secreting Pituitary Adenoma
Lentiviral vectors efficiently transduce human gonadotroph and somatotroph adenomas in vitro. Targeted expression of transgene by pituitary hormone promoters.
Heart Arrest
Selection of reference genes for quantitative real-time PCR in a rat asphyxial cardiac arrest model.
Hematologic Neoplasms
Clonal determination by the fragile X (FMR1) and phosphoglycerate kinase (PGK) genes in hematological malignancies.
Hepatitis
Human CMV immediate-early enhancer: a useful tool to enhance cell-type-specific expression from lentiviral vectors.
Herpes Simplex
Comparative analysis of retroviral vector expression in mouse embryonal carcinoma cells.
Herpes Simplex
Gene therapy for hepatocellular carcinoma based on tumour-selective suicide gene expression using the alpha-fetoprotein (AFP) enhancer and a housekeeping gene promoter.
Herpes Simplex
Type and position of promoter elements in retroviral vectors have substantial effects on the expression level of an enhanced green fluorescent protein reporter gene.
Histiocytosis
Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease.
Hyperparathyroidism
Clonal analysis of nodular parathyroid hyperplasia in renal hyperparathyroidism.
Hyperparathyroidism, Secondary
PDGFB-based stem cell gene therapy increases bone strength in the mouse.
Hypospadias
A hemizygous short tandem repeat polymorphism 3' to the human phosphoglycerate kinase gene.
Hypospadias
Short tandem repeat polymorphism linkage to the androgen receptor gene in prostate carcinoma.
Incontinentia Pigmenti
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.
Infections
A hypothetical model of crossing Bombyx mori nucleopolyhedrovirus through its host midgut physical barrier.
Infections
Analysis of the serologic response to systemic Candida albicans infection in a murine model.
Infections
Chloroplast phosphoglycerate kinase is involved in the targeting of Bamboo mosaic virus to chloroplasts in Nicotiana benthamiana plants.
Infections
Construction of a lentiviral T/A vector for direct analysis of PCR-amplified promoters.
Infections
Efficient transduction of monocyte- and CD34+-derived Langerhans cells with lentiviral vectors in the absence of phenotypic and functional maturation.
Infections
Elongation factor 1 (EF1alpha) promoter in a lentiviral backbone improves expression of the CD20 suicide gene in primary T lymphocytes allowing efficient rituximab-mediated lysis.
Infections
HIF1A and NFAT5 coordinate Na+-boosted antibacterial defense via enhanced autophagy and autolysosomal targeting.
Infections
Immune response to Schistosoma mansoni phosphoglycerate kinase during natural and experimental infection: identification of a schistosome-specific B-cell epitope.
Infections
Immune responses in rats and sheep induced by a DNA vaccine containing the phosphoglycerate kinase gene of Fasciola hepatica and liver fluke infection.
Infections
Linear correlation between average fluorescence intensity of green fluorescent protein and the multiplicity of infection of recombinant adenovirus.
Infections
Lymphocyte responses of rats vaccinated with cDNA encoding a phosphoglycerate kinase of Fasciola hepatica (FhPGK) and F. hepatica infection.
Infections
Microarray analysis of rat immune responses to liver fluke infection following vaccination with Fasciola hepatica phosphoglycerate kinase.
Infections
Murine Retroviral but not Human Cellular Promoters Induce In Vivo Erythroid-specific Deregulation that can be Partially Prevented by Insulators.
Infertility
Electrophoresis of phosphoglycerate kinase-2 to determine testicular damage induced by ethylene glycol monomethyl ether and sterility associated with chromosomal abnormality.
Intellectual Disability
A Drosophila temperature-sensitive seizure mutant in phosphoglycerate kinase disrupts ATP generation and alters synaptic function.
Intellectual Disability
Altered expression of PGK1 in a family with phosphoglycerate kinase deficiency.
Intellectual Disability
Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes: PGK Créteil and PGK Amiens.
Intellectual Disability
Intronic mutation in the PGK1 gene may cause recurrent myoglobinuria by aberrant splicing.
Intellectual Disability
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.
Intellectual Disability
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.
Intellectual Disability
Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.
Intellectual Disability
Recurrent myoglobinuria in a child with mental retardation: phosphoglycerate kinase deficiency.
l-lactate dehydrogenase deficiency
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.
Leiomyoma
Clonal determination of uterine leiomyomas by analyzing differential inactivation of the X-chromosome-linked phosphoglycerokinase gene.
Leiomyoma
Compensatory alterations in energy homeostasis characterized in uterine tumors from hereditary leiomyomatosis and renal cell cancer.
Leiomyoma
[X-chromosome inactivation patterns of different tumor nodules in multiple leiomyomas of uterus]
Leiomyosarcoma
[X-chromosome inactivation patterns of different tumor nodules in multiple leiomyomas of uterus]
Leukemia
Clonal nature of mink cell focus-inducing virus-induced AKR leukemia: studies with X-chromosome inactivation cellular mosaicism.
Leukemia
Clonal nature of spontaneous AKR leukemia: studies utilizing the X-linked enzyme phosphoglycerate kinase.
Leukemia
Correction of ornithine-delta-aminotransferase deficiency in a Chinese hamster ovary cell line mediated by retrovirus gene transfer.
Leukemia
Enhanced inhibition of human immunodeficiency virus type 1 replication by novel lentiviral vectors expressing human immunodeficiency virus type 1 envelope antisense RNA.
Leukemia
Expression of human glucocerebrosidase in murine macrophages: identification of efficient retroviral vectors.
Leukemia
Functional analysis of various promoters in lentiviral vectors at different stages of in vitro differentiation of mouse embryonic stem cells.
Leukemia
Increase in nitrosourea resistance in mammalian cells by retrovirally mediated gene transfer of bacterial O6-alkylguanine-DNA alkyltransferase.
Leukemia
Prolonged survival of mice with myeloid leukemia by subcutaneous injection of recombinant human G-CSF.
Leukemia
Retrovirus-mediated gene expression in hematopoietic cells correlates inversely with growth factor stimulation.
Leukemia
The detection of normal hidden stem cells during the development of leukemia: assays with PGK isozyme.
Leukemia
[Exploration of the variance in exogenous gene expression driven by the different promoters in leukemia cells].
Leukemia, Erythroblastic, Acute
The silencer of mouse Pgk-2 consists of two discrete DNA elements that individually have no effect.
Leukemia, Myeloid
A new cell line of murine myeloid leukemia with A-type phosphoglycerate kinase as marker isoenzyme.
Leukemia, Myeloid
Clonal origin of radiation-induced myeloid leukemia in mice with cellular mosaicism.
Leukemia, Myeloid
Prolonged survival of mice with myeloid leukemia by subcutaneous injection of recombinant human G-CSF.
Leukemia, Myeloid, Acute
Clonal analysis in acute myeloid leukemia by polymerase chain reaction.
Leukocytosis
Spontaneous loss of Ph chromosome with maintenance of clonal hemopoiesis in an untreated patient with myeloproliferative disease and a long survival.
Liver Neoplasms
[Influence of phosphoglycerate kinase 1 on metastasis and invasion of hepatoma cells and prognosis of liver cancer].
Lung Neoplasms
Colliding primary lung cancers of adenosquamous carcinoma and large cell neuroendocrine carcinoma.
Lung Neoplasms
Metabolic protein phosphoglycerate kinase 1 confers lung cancer migration by directly binding HIV Tat specific factor 1.
Lung Neoplasms
Phosphoglycerate kinase 1-overexpressing lung cancer cells reduce cyclooxygenase 2 expression and promote anti-tumor immunity in vivo.
Lymphoma
Identification of genuine primary pulmonary NK cell lymphoma via clinicopathologic observation and clonality assay.
Lymphoma
Single cell origin of radiation-induced thymic lymphoma in mice with cellular mosaicism.
Lymphoma
[Detection of cyclin D1 mRNA by reverse transcription-polymerase chain reaction in paraffin-embedded tissues and its diagnostic significance for mantle cell lymphoma]
Lymphoma, Mantle-Cell
[Detection of cyclin D1 mRNA by reverse transcription-polymerase chain reaction in paraffin-embedded tissues and its diagnostic significance for mantle cell lymphoma]
Lymphoproliferative Disorders
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.
Malaria
Glycolytic pathway of the human malaria parasite Plasmodium falciparum: primary sequence analysis of the gene encoding 3-phosphoglycerate kinase and chromosomal mapping studies.
Malaria
Plasmodium falciparum: identification and purification of the phosphoglycerate kinase of the malaria parasite.
Malaria
The use of enzymopathic human red cells in the study of malarial parasite glucose metabolism.
Malaria, Falciparum
The use of enzymopathic human red cells in the study of malarial parasite glucose metabolism.
Melanoma
[Silencing of PKG1 expression enhances the efficacy of vemurafenib against melanoma cell].
Menkes Kinky Hair Syndrome
Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice.
Menkes Kinky Hair Syndrome
Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1.
Mental Retardation, X-Linked
22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125-DXS95 in human Xq12-q21.31.
Mental Retardation, X-Linked
X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.
Migraine Disorders
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Mouth Neoplasms
5-Methoxytryptophan-dependent inhibition of oral squamous cell carcinoma metastasis.
Movement Disorders
Exposure to Phosphoglycerate Kinase 1 Activators and Incidence of Parkinson's Disease.
Multiple Endocrine Neoplasia
Clonal emergence in uremic parathyroid hyperplasia is not related to MEN1 gene abnormality.
Multiple Endocrine Neoplasia Type 1
Clonal emergence in uremic parathyroid hyperplasia is not related to MEN1 gene abnormality.
Muscular Diseases
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
Muscular Diseases
Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes: PGK Créteil and PGK Amiens.
Muscular Diseases
Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiency.
Muscular Diseases
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency.
Muscular Diseases
Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.
Muscular Diseases
Parkinsonism in PGK1 deficiency implicates the glycolytic pathway in nigrostriatal dysfunction.
Muscular Diseases
Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy.
Muscular Diseases
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzyme.
Muscular Diseases
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.
Muscular Diseases
Slowly progressive leukodystrophy in an adolescent male with phosphoglycerate kinase deficiency.
Muscular Diseases
Therapeutic Benefit of Blood Transfusion in a Patient With Novel PGK1 Mutation (c.461T>C [p.L154P]).
Muscular Dystrophy, Duchenne
Comparison of the physical and recombination maps of the mouse X chromosome.
Myalgia
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.
Myalgia
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)
Myelodysplastic Syndromes
Clonal analysis of myelodysplastic syndromes: evidence of multipotent stem cell origin.
Myelodysplastic Syndromes
Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene.
Myelodysplastic Syndromes
Clonality in myelodysplastic syndromes: demonstration of pluripotent stem cell origin using X-linked restriction fragment length polymorphisms.
Myelodysplastic Syndromes
Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction.
Myelodysplastic Syndromes
Detection of monoclonal hematopoiesis using restriction fragment length polymorphism (RFLP) of phosphoglycerokinase (PGK) gene in a patient with hypoplastic myelodysplastic syndrome (MDS).
Myelodysplastic Syndromes
In vivo effects of granulocyte-macrophage colony-stimulating factor and interleukin-3 on clonal and non-clonal cell populations in patients with clonal hematopoietic disorders.
Myeloproliferative Disorders
Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms.
Myeloproliferative Disorders
Clonal analysis of transient myeloproliferative disorder in Down's syndrome.
Myeloproliferative Disorders
Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: demonstration of heterogeneity in lineage involvement.
Myeloproliferative Disorders
Myeloproliferative disorders: usefulness of X-linked probes in diagnosis.
Myoglobinuria
A single amino acid substitution (157 Gly----Val) in a phosphoglycerate kinase variant (PGK Shizuoka) associated with chronic hemolysis and myoglobinuria.
Myoglobinuria
Intronic mutation in the PGK1 gene may cause recurrent myoglobinuria by aberrant splicing.
Myoglobinuria
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzyme.
Myoglobinuria
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)
Myoglobinuria
Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.
Myoglobinuria
Recurrent myoglobinuria in a child with mental retardation: phosphoglycerate kinase deficiency.
Myoglobinuria
Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant.
Myoglobinuria
[1H and 31P magnetic resonance spectroscopy study of a case of phosphoglycerate kinase deficiency]
Myoglobinuria
[Myoglobinuria due to enzyme abnormalities in glycolytic pathway--especially lactate dehydrogenase M subunit deficiency]
Myoglobinuria
[Phosphoglycerate kinase deficiency with recurrent myoglobinuria: morphological and biochemical analysis]
Neoplasm Metastasis
5-Methoxytryptophan-dependent inhibition of oral squamous cell carcinoma metastasis.
Neoplasm Metastasis
Evidence by cellular mosaicism for monoclonal metastasis of spontaneous mouse mammary tumors.
Neoplasm Metastasis
FLNA and PGK1 are Two Potential Markers for Progression in Hepatocellular Carcinoma.
Neoplasm Metastasis
Phosphoglycerate kinase 1 promoting tumor progression and metastasis in gastric cancer - detected in a tumor mouse model using positron emission tomography/magnetic resonance imaging.
Neoplasm Metastasis
shRNA-mediated inhibition of PhosphoGlycerate Kinase 1 (PGK1) enhances cytotoxicity of intraperitoneal chemotherapy in peritoneal metastasis of gastric origin.
Neoplasm Metastasis
[Influence of phosphoglycerate kinase 1 on metastasis and invasion of hepatoma cells and prognosis of liver cancer].
Neoplasms
A novel clonality assay for the mouse: application to hepatocellular carcinomas induced with diethylnitrosamine.
Neoplasms
Analysis of clonality in archival tissues by polymerase chain reaction amplification of PGK-1.
Neoplasms
Antrodia cinnamomea Inhibits Migration in Human Hepatocellular Carcinoma Cells: The Role of ERp57 and PGK-1.
Neoplasms
Blood level of phosphoglycerate kinase does not correlate with presence or extent of tumor.
Neoplasms
Characterization of phosphoglycerate kinase-1 expression of stromal cells derived from tumor microenvironment in prostate cancer progression.
Neoplasms
Clonal analysis of human gynecologic cancers by means of the polymerase chain reaction.
Neoplasms
Clonal emergence in uremic parathyroid hyperplasia is not related to MEN1 gene abnormality.
Neoplasms
Clonal nature of mink cell focus-inducing virus-induced AKR leukemia: studies with X-chromosome inactivation cellular mosaicism.
Neoplasms
Clonal nature of spontaneous AKR leukemia: studies utilizing the X-linked enzyme phosphoglycerate kinase.
Neoplasms
Clonal origin of epithelial ovarian carcinoma: analysis by loss of heterozygosity, p53 mutation, and X-chromosome inactivation.
Neoplasms
Clonal origin of skin and bone tumors produced by repeated beta-irradiation in mosaic cell mice.
Neoplasms
Clonal origin of spontaneous multiple mammary tumors in mice with cellular mosaicism.
Neoplasms
Clonality in hepatocellular carcinoma: analysis of methylation pattern of polymorphic X-chromosome-linked phosphoglycerate kinase gene in females.
Neoplasms
Combinatorial regulation of neuroblastoma tumor progression by N-Myc and hypoxia inducible factor (HIF)-1{alpha}.
Neoplasms
Development of cartilage-like tissue from androgen-dependent Shionogi carcinoma 115 in androgen-depleted hosts.
Neoplasms
Direct effect of basic fibroblast growth factor on gene transcription in a cell-free system.
Neoplasms
Dose response of monoclonal tumor induction with 3-methylcholanthrene in mosaic mice.
Neoplasms
Downregulation of long non-protein coding RNA MVIH impairs glioblastoma cell proliferation and invasion through an miR-302a-dependent mechanism.
Neoplasms
Effect of hypoxia on the expression of phosphoglycerate kinase and antitumor activity of troxacitabine and gemcitabine in non-small cell lung carcinoma.
Neoplasms
Enzyme activities at the surface of intact Ehrlich tumor cells with albumin in the isotonic assay medium.
Neoplasms
Epigenetic deregulation of miR-29a and miR-1256 by isoflavone contributes to the inhibition of prostate cancer cell growth and invasion.
Neoplasms
Evidence by cellular mosaicism for monoclonal metastasis of spontaneous mouse mammary tumors.
Neoplasms
Evidence concerning the clonal nature of chemically induced tumors: phosphoglycerate kinase-1 isozyme patterns in chemically induced fibrosarcomas.
Neoplasms
Evidence for single-cell origin of 3-methylcholanthrene-induced fibrosarcomas in mice with cellular mosaicism.
Neoplasms
FOXO3A-induced LINC00926 suppresses breast tumor growth and metastasis through inhibition of PGK1-mediated Warburg effect.
Neoplasms
Gene therapy for hepatocellular carcinoma based on tumour-selective suicide gene expression using the alpha-fetoprotein (AFP) enhancer and a housekeeping gene promoter.
Neoplasms
Hypoxia-induced acetylation of PAK1 enhances autophagy and promotes brain tumorigenesis via phosphorylating ATG5.
Neoplasms
Identification of a novel non-ATP-competitive protein kinase inhibitor of PGK1 from marine nature products.
Neoplasms
In situ identification of host derived infiltrating cells in chemically induced fibrosarcomas of interspecific chimeric mice.
Neoplasms
In vivo targeting of tumor endothelial cells by systemic delivery of lentiviral vectors.
Neoplasms
Influence of dose of initiator on two-stage skin carcinogenesis in BALB/c mice with cellular mosaicism.
Neoplasms
Insulin-like growth factor (IGF) binding protein-3 attenuates prostate tumor growth by IGF-dependent and IGF-independent mechanisms.
Neoplasms
Intraclonal conversion from papilloma to carcinoma in the skin of Pgk-1a/Pgk-1b mice treated by a complete carcinogenesis process or by an initiation-promotion regimen.
Neoplasms
Lentiviral vector design for optimal TCR gene expression in the transduction of PBL and TIL.
Neoplasms
Macrophage-Associated PGK1 Phosphorylation Promotes Aerobic Glycolysis and Tumorigenesis.
Neoplasms
MicroRNA-16-1-3p Represses Breast Tumor Growth and Metastasis by Inhibiting PGK1-Mediated Warburg Effect.
Neoplasms
Multicellular origin of fibrosarcomas in mice induced by the chemical carcinogen 3-methylcholanthrene.
Neoplasms
Nucleotide-binding domain of phosphoglycerate kinase 1 reduces tumor growth by suppressing COX-2 expression.
Neoplasms
Perturbation of phosphoglycerate kinase 1 (PGK1) only marginally affects glycolysis in cancer cells.
Neoplasms
PGK1 as predictor of CXCR4 expression, bone marrow metastases and survival in neuroblastoma.
Neoplasms
pH-dependent relationship between thermodynamic and kinetic stability in the denaturation of human phosphoglycerate kinase 1.
Neoplasms
Phosphoglycerate kinase 1 (PGK1) in cancer: A promising target for diagnosis and therapy.
Neoplasms
Phosphoglycerate kinase 1 promoting tumor progression and metastasis in gastric cancer - detected in a tumor mouse model using positron emission tomography/magnetic resonance imaging.
Neoplasms
Phosphoglycerate kinase 1-overexpressing lung cancer cells reduce cyclooxygenase 2 expression and promote anti-tumor immunity in vivo.
Neoplasms
Phosphoglycerate kinase-1 is a predictor of poor survival and a novel prognostic biomarker of chemoresistance to paclitaxel treatment in breast cancer.
Neoplasms
Polyclonal origin of parathyroid tumors is common and is associated with multiple gland disease in primary hyperparathyroidism.
Neoplasms
Protein alterations in infiltrating ductal carcinomas of the breast as detected by nonequilibrium pH gradient electrophoresis and mass spectrometry.
Neoplasms
Recent progress in breast cancer research at Osaka Medical Center for Cancer and Cardiovascular Diseases.
Neoplasms
Secretion of phosphoglycerate kinase from tumour cells is controlled by oxygen-sensing hydroxylases.
Neoplasms
Single-cell origin of bladder cancer induced by N-butyl-N-(4-hydroxybutyl) nitrosamine in mice with cellular mosaicism.
Neoplasms
Solitary polyclonal autonomous thyroid nodule: a rare cause of childhood hyperthyroidism.
Neoplasms
Somatic mutations detected by mini- and microsatellite DNA markers reveal clonal intratumor heterogeneity in gastrointestinal cancers.
Neoplasms
Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour.
Neoplasms
Stable Lyonization of X-linked pgk-1 gene during aging in normal tissues and tumors of mice carrying Searle's translocation.
Neoplasms
Targeted expression of SV40 large tumour antigen (TAg) induces a transient enhancement of spermatocyte proliferation and apoptosis.
Neoplasms
Test of recurrence after experimental radiation therapy of chemically induced autochthonous tumors in mosaic mice.
Neoplasms
The effect of CELLFOODTM on radiotherapy or combined chemoradiotherapy: preclinical evidence.
Neoplasms
The identification of auto-antibodies in pancreatic cancer patient sera using a naturally fractionated Panc-1 cell line.
Neoplasms
The identification of phosphoglycerate kinase-1 and histone H4 autoantibodies in pancreatic cancer patient serum using a natural protein microarray.
Neoplasms
The phosphoglycerate kinase 1 variants found in carcinoma cells display different catalytic activity and conformational stability compared to the native enzyme.
Neoplasms
Therapeutic targeting of circ-CUX1/EWSR1/MAZ axis inhibits glycolysis and neuroblastoma progression.
Neoplasms
Two proliferation-related proteins, TYMS and PGK1, could be new cytotoxic T lymphocyte-directed tumor-associated antigens of HLA-A2+ colon cancer.
Neoplasms
Urokinase receptor expression involves tyrosine phosphorylation of phosphoglycerate kinase.
Neoplasms
Use of the PSA enhancer core element to modulate the expression of prostate- and non-prostate-specific basal promoters in a lentiviral vector context.
Neoplasms
X-chromosomal inactivation analysis of uterine leiomyomas reveals a common clonal origin of different tumor nodules in some multiple leiomyomas.
Neoplasms
X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females.
Neoplasms
[Detection of FUS-CHOP fusion gene in paraffin-embedded tissues and its clinicopathologic significance for myxoid/round cell liposarcomas]
Nervous System Diseases
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
Nervous System Diseases
Molecular defect of a phosphoglycerate kinase variant associated with haemolytic anaemia and neurological disorders in a large kindred.
Nervous System Diseases
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
Neuroblastoma
Combinatorial regulation of neuroblastoma tumor progression by N-Myc and hypoxia inducible factor (HIF)-1{alpha}.
Neurodegenerative Diseases
Differential transport and local translation of cytoskeletal, injury-response, and neurodegeneration protein mRNAs in axons.
Neurofibroma
The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.
Neuromuscular Diseases
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
Neuromuscular Manifestations
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
Osteoarthritis
A proteomic study of protein variation between osteopenic and age-matched control bone tissue.
Osteosarcoma
Clonal origin of skin and bone tumors produced by repeated beta-irradiation in mosaic cell mice.
Ovarian Neoplasms
Down-regulation of Ras-related protein Rab 5C-dependent endocytosis and glycolysis in cisplatin-resistant ovarian cancer cell lines.
Pancreatic Neoplasms
The identification of phosphoglycerate kinase-1 and histone H4 autoantibodies in pancreatic cancer patient serum using a natural protein microarray.
Pancreatitis, Chronic
The identification of phosphoglycerate kinase-1 and histone H4 autoantibodies in pancreatic cancer patient serum using a natural protein microarray.
Papilloma
Clonal analysis of solitary intraductal papilloma of the breast by means of polymerase chain reaction.
Papilloma
Influence of dose of initiator on two-stage skin carcinogenesis in BALB/c mice with cellular mosaicism.
Papilloma
Intraclonal conversion from papilloma to carcinoma in the skin of Pgk-1a/Pgk-1b mice treated by a complete carcinogenesis process or by an initiation-promotion regimen.
Papilloma
Sequential studies of skin tumorigenesis in PGK mosaic mice: the effect of repeated exposure to a carcinogen on regressed mouse skin papillomas.
Papilloma
Sequential studies of skin tumorigenesis in phosphoglycerate kinase mosaic mice: effect of resumption of promotion on regressed papillomas.
Papilloma
Studies of skin tumorigenesis in PGK mosaic mice: many promoter-independent papillomas and carcinomas do not develop from pre-existing promoter-dependent papillomas.
Papilloma, Intraductal
Clonal analysis of solitary intraductal papilloma of the breast by means of polymerase chain reaction.
Parathyroid Neoplasms
Clonal analysis of parathyroid adenomas by means of the polymerase chain reaction.
Parkinson Disease
Exposure to Phosphoglycerate Kinase 1 Activators and Incidence of Parkinson's Disease.
Parkinsonian Disorders
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
Parkinsonian Disorders
Levodopa Responsive Parkinsonism in Two Patients With Phosphoglycerate Kinase Deficiency.
Parkinsonian Disorders
Novel Drosophila model for parkinsonism by targeting phosphoglycerate kinase.
Peritoneal Neoplasms
PGK1 a potential marker for peritoneal dissemination in gastric cancer.
Peritoneal Neoplasms
Phosphoglycerate kinase 1 a promoting enzyme for peritoneal dissemination in gastric cancer.
phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency
[Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies]
phosphoglycerate kinase deficiency
1,3-Diphosphoglycerate in phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
A Drosophila temperature-sensitive seizure mutant in phosphoglycerate kinase disrupts ATP generation and alters synaptic function.
phosphoglycerate kinase deficiency
A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report.
phosphoglycerate kinase deficiency
A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemia.
phosphoglycerate kinase deficiency
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: Molecular and functional characterization.
phosphoglycerate kinase deficiency
A novel missense mutation (837T-->C) in the phosphoglycerate kinase gene of a patient with a myopathic form of phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
A phosphoglycerate kinase variant, PGK Uppsala, associated with hemolytic anemia.
phosphoglycerate kinase deficiency
A splice junction mutation in a new myopathic variant of phosphoglycerate kinase deficiency (PGK North Carolina).
phosphoglycerate kinase deficiency
Altered expression of PGK1 in a family with phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Calmodulin binds to and inhibits the activity of phosphoglycerate kinase.
phosphoglycerate kinase deficiency
Characterization of a phosphoglycerate kinase deficiency variants not associated with hemolytic anemia.
phosphoglycerate kinase deficiency
Deficiencies of glycolytic enzymes as a possible cause of hemolytic anemia.
phosphoglycerate kinase deficiency
Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?
phosphoglycerate kinase deficiency
Enzymatic and metabolic characterization of the phosphoglycerate kinase deficiency associated with chronic hemolytic anemia caused by the PGK-Barcelona mutation.
phosphoglycerate kinase deficiency
Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease.
phosphoglycerate kinase deficiency
Erythrocyte phosphoglycerate kinase deficiency: enzymatic and oxygen binding studies.
phosphoglycerate kinase deficiency
Evidence of the decreased muscle enzyme activity in erythrocyte phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Familial phosphoglycerate kinase deficiency associated with rhabdomyolysis and acute renal failure: abnormality in mRNA splicing?
phosphoglycerate kinase deficiency
Genome-wide identification of pseudogenes capable of disease-causing gene conversion.
phosphoglycerate kinase deficiency
Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.
phosphoglycerate kinase deficiency
Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia.
phosphoglycerate kinase deficiency
Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome.
phosphoglycerate kinase deficiency
Hereditary hemolytic anemia: association with phosphoglycerate kinase deficiency in erythrocytes and leukocytes.
phosphoglycerate kinase deficiency
Human erythrocyte phosphoglycerate kinase deficiency: presence in a deficient patient of a stable variant with lowered catalytic activity.
phosphoglycerate kinase deficiency
Immunochemical studies on phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Insights into human phosphoglycerate kinase 1 deficiency as a conformational disease from biochemical, biophysical, and in vitro expression analyses.
phosphoglycerate kinase deficiency
Lack of effect of increased 2,3-diphosphoglycerate on flux through the oxidative pathway in phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Levodopa Responsive Parkinsonism in Two Patients With Phosphoglycerate Kinase Deficiency.
phosphoglycerate kinase deficiency
Mitochondrial changes in muscle phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency.
phosphoglycerate kinase deficiency
Molecular insights on pathogenic effects of mutations causing phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Monoclonal anti-double-stranded DNA antibodies cross-react with phosphoglycerate kinase 1 and inhibit the expression and production of IL-2 in activated Jurkat T cell line.
phosphoglycerate kinase deficiency
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations.
phosphoglycerate kinase deficiency
Myopathy and parkinsonism in phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Neutrophil function in congenital phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.
phosphoglycerate kinase deficiency
Parkinsonism in PGK1 deficiency implicates the glycolytic pathway in nigrostriatal dysfunction.
phosphoglycerate kinase deficiency
PAS domain-containing phosphoglycerate kinase deficiency in Leishmania major results in increased autophagosome formation and cell death.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzyme.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: A nationwide multicenter retrospective study.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuria.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: an adult myopathic form with a novel mutation.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)
phosphoglycerate kinase deficiency
Phosphoglycerate kinase deficiency: biochemical studies on hair follicles.
phosphoglycerate kinase deficiency
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
phosphoglycerate kinase deficiency
Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Recurrent myoglobinuria in a child with mental retardation: phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Red cell enzymopathies as a model of inborn errors of metabolism.
phosphoglycerate kinase deficiency
Red cell glycolysis in a case of 3-phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.
phosphoglycerate kinase deficiency
Slowly progressive leukodystrophy in an adolescent male with phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
Structural and energetic basis of protein kinetic destabilization in human phosphoglycerate kinase 1 deficiency.
phosphoglycerate kinase deficiency
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
phosphoglycerate kinase deficiency
Therapeutic Benefit of Blood Transfusion in a Patient With Novel PGK1 Mutation (c.461T>C [p.L154P]).
phosphoglycerate kinase deficiency
Tissue levels of glycolytic enzymes in phosphoglycerate kinase deficiency.
phosphoglycerate kinase deficiency
X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.
phosphoglycerate kinase deficiency
[1H and 31P magnetic resonance spectroscopy study of a case of phosphoglycerate kinase deficiency]
phosphoglycerate kinase deficiency
[A modification of the fluorescent stain method for identifying a deficit of erythrocyte phosphoglycerate kinase in mass screening]
phosphoglycerate kinase deficiency
[Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies]
phosphoglycerate kinase deficiency
[Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes]
phosphoglycerate kinase deficiency
[Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes]
phosphoglycerate kinase deficiency
[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature]
phosphoglycerate kinase deficiency
[Phosphoglycerate kinase deficiency with recurrent myoglobinuria: morphological and biochemical analysis]
phosphoglycerate kinase deficiency
[Studies on erythrocye and leukocyte phosphoglycerate kinase deficiency with neurologic disease (author's transl)]
Phyllodes Tumor
Recent progress in breast cancer research at Osaka Medical Center for Cancer and Cardiovascular Diseases.
Pituitary ACTH Hypersecretion
Clonal origins of adrenocorticotropin-secreting pituitary tissue in Cushing's disease.
Polycythemia
The application of X-chromosome gene probes to the diagnosis of myeloproliferative disease.
Polycythemia Vera
Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction.
Prostatic Neoplasms
A hemizygous short tandem repeat polymorphism 3' to the human phosphoglycerate kinase gene.
Prostatic Neoplasms
Characterization of phosphoglycerate kinase-1 expression of stromal cells derived from tumor microenvironment in prostate cancer progression.
Prostatitis
X Chromosomal short tandem repeat polymorphisms near the phosphoglycerate kinase gene in men with chronic prostatitis.
Pulmonary Emphysema
Overexpression of placenta growth factor contributes to the pathogenesis of pulmonary emphysema.
Pulmonary Sclerosing Hemangioma
Determination of clonal status of pulmonary sclerosing hemangioma with X-chromosome inactivation mosaicism and polymorphism of phosphoglycerate kinase and androgen receptor genes.
Pulmonary Sclerosing Hemangioma
Gene expression and clonality analysis of the androgen receptor and phosphoglycerate kinase genes in polygonal cells and cuboidal cells in so-called pulmonary sclerosing hemangioma.
Pulmonary Sclerosing Hemangioma
[Study of androgen receptor and phosphoglycerate kinase gene polymorphism in major cellular components of the so-called pulmonary sclerosing hemangioma]
Retinal Degeneration
Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina.
Retinal Dystrophies
A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report.
Retinal Dystrophies
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Retinitis Pigmentosa
Genome-wide identification of pseudogenes capable of disease-causing gene conversion.
Retinitis Pigmentosa
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)
Rhabdomyolysis
A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemia.
Rhabdomyolysis
A novel missense mutation (1060G --> C) in the phosphoglycerate kinase gene in a Japanese boy with chronic haemolytic anaemia, developmental delay and rhabdomyolysis.
Rhabdomyolysis
Familial phosphoglycerate kinase deficiency associated with rhabdomyolysis and acute renal failure: abnormality in mRNA splicing?
Rhabdomyolysis
Parkinsonism in PGK1 deficiency implicates the glycolytic pathway in nigrostriatal dysfunction.
Rhabdomyolysis
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.
Rhabdomyolysis
Phosphoglycerate kinase San Francisco: a new variant associated with hemolytic anemia but not with neuromuscular manifestations.
Rhabdomyolysis
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Sarcoma
Expression of human glucocerebrosidase in murine macrophages: identification of efficient retroviral vectors.
Sarcoma
Optimal promoter usage for lentiviral vector-mediated transduction of cultured central nervous system cells.
Sarcoma
Sheep gene mapping: additional DNA markers included (CASB, CASK, LALBA, IGF-1 and AMH).
Sarcoma
Test of recurrence after experimental radiation therapy of chemically induced autochthonous tumors in mosaic mice.
Sarcoma, Avian
Efficient marking of neural stem cell-derived neurons with a modified murine embryonic stem cell virus, MESV2.
Sarcoma, Avian
Expression of bacterial cysteine biosynthesis genes in transgenic mice and sheep: toward a new in vivo amino acid biosynthesis pathway and improved wool growth.
Sarcoma, Avian
Impact of Different Promoters on Episomal Vectors Harbouring Characteristic Motifs of Matrix Attachment Regions.
Sarcoma, Avian
Increase in nitrosourea resistance in mammalian cells by retrovirally mediated gene transfer of bacterial O6-alkylguanine-DNA alkyltransferase.
Schistosomiasis
Cloning, expression and enzymatic characterization of 3-phosphoglycerate kinase from Schistosoma japonicum.
Schistosomiasis
Immune response to Schistosoma mansoni phosphoglycerate kinase during natural and experimental infection: identification of a schistosome-specific B-cell epitope.
Seizures
A Drosophila temperature-sensitive seizure mutant in phosphoglycerate kinase disrupts ATP generation and alters synaptic function.
Seizures
Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.
Seizures
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Spinal Cord Injuries
Cell adhesion molecule l1-transfected embryonic stem cells with enhanced survival support regrowth of corticospinal tract axons in mice after spinal cord injury.
Spinal Dysraphism
A human autosomal phosphoglycerate kinase locus maps near the HLA cluster.
Starvation
Phosphate Starvation Inducible ;Bypasses' of Adenylate and Phosphate Dependent Glycolytic Enzymes in Brassica nigra Suspension Cells.
Stomach Neoplasms
Induction of tumor stem cell differentiation-novel strategy to overcome therapy resistance in gastric cancer.
Stomach Neoplasms
Metabolic alteration--Overcoming therapy resistance in gastric cancer via PGK-1 inhibition in a combined therapy with standard chemotherapeutics.
Stomach Neoplasms
Phosphoglycerate kinase 1 a promoting enzyme for peritoneal dissemination in gastric cancer.
Stomach Neoplasms
Phosphoglycerate kinase 1 promoting tumor progression and metastasis in gastric cancer - detected in a tumor mouse model using positron emission tomography/magnetic resonance imaging.
Teratocarcinoma
Genetic activity of X chromosomes in pluripotent female teratocarcinoma cells and their differentiated progeny.
Thrombocythemia, Essential
In vivo effects of granulocyte-macrophage colony-stimulating factor and interleukin-3 on clonal and non-clonal cell populations in patients with clonal hematopoietic disorders.
Thrombosis
Pneumococcal phosphoglycerate kinase interacts with plasminogen and its tissue activator.
Thymoma
Clonal nature of mink cell focus-inducing virus-induced AKR leukemia: studies with X-chromosome inactivation cellular mosaicism.
Thymoma
Clonal nature of spontaneous AKR leukemia: studies utilizing the X-linked enzyme phosphoglycerate kinase.
Trypanosomiasis, African
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine.
Urinary Bladder Neoplasms
Single-cell origin of bladder cancer induced by N-butyl-N-(4-hydroxybutyl) nitrosamine in mice with cellular mosaicism.
Urogenital Abnormalities
Short tandem repeat polymorphism linkage to the androgen receptor gene in prostate carcinoma.
Urogenital Diseases
A hemizygous short tandem repeat polymorphism 3' to the human phosphoglycerate kinase gene.
Vesicular Stomatitis
Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells.
Vesicular Stomatitis
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro.
Vesicular Stomatitis
Retinal cell type expression specificity of HIV-1-derived gene transfer vectors upon subretinal injection in the adult rat: influence of pseudotyping and promoter.
X-Linked Combined Immunodeficiency Diseases
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.
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