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equal amounts of isozyme L and M
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ras-transformed
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PFKFB4 is overexpressed in human cancers
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isozyme variant F-PFK2
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Q75IQ9
expression less detectable in
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expression analysis in
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uPFK-2
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placenta-type isozyme is expressed in Kupffer cells of the liver
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PFKFB3 is overexpressed in human cancers
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ras-transformed
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gland
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PFKFB4 is overexpressed in human cancers
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expression analysis in
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Q75IQ9
low expression
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Q75IQ9
low expression in
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uPFK-2
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uPFK-2, tPFK-2
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PFKFB4 is overexpressed in human cancers
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40 human astrocytic gliomas and 20 non-neoplastic brain tissue specimens, different malignity grades, expression analysis in
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low and high malignancy grades according to histological criteria, expression analysis in
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cortex
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isozyme U-PFK2
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under hypoxia, expression analysis of alternative splice variants in
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brain-specific PFK2 isozyme
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primary
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primary
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expression pattern of isozyme encoding pfk1, pfkfb1, pfkfb2, pfkfb3, and pfkfb4 genes in Xenopus laevis embryos. Gene pfkfb transcripts expression is overlapping at blastula and gastrula stages and from neurulation to tadpole stages, they display tissue-specific, complementary and dynamic developmental expression patterns. At the tailbud stage, pfkfb1 is mainly expressed in the somites and in the head. At tadpole stage 26, pfkfb1 is expressed in the somites, in the spinal cord, in the notochord and in the head, and at tadpole stage 40, pfkfb1 is expressed in head mesenchyme, the somites, the spinal cord, the pronephros and the dorsal fin
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expression pattern of isozyme encoding pfk1, pfkfb1, pfkfb2, pfkfb3, and pfkfb4 genes in Xenopus laevis embryos. Gene pfkfb transcripts expression is overlapping at blastula and gastrula stages and from neurulation to tadpole stages, they display tissue-specific, complementary and dynamic developmental expression patterns. At the tailbud stage, Pfkfb2 is not detected above background. At tadpole stage 26, pfkfb2 was expressed in the ectoderm, the neural tube and the pronephros, with a low expression in the lateral somite, and at tadpole stage 40, pfkfb2 is expressed in head mesenchyme, neural tube, pronephros and at low levels in the somites
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expression pattern of isozyme encoding pfk1, pfkfb1, pfkfb2, pfkfb3, and pfkfb4 genes in Xenopus laevis embryos. Gene pfkfb transcripts expression is overlapping at blastula and gastrula stages and from neurulation to tadpole stages, they display tissue-specific, complementary and dynamic developmental expression patterns. At the tailbud stage, pfkfb4 is expressed in the cement gland, in the spinal cord, in the somites and in the ventral blood island. At tadpole stage 26, pfkfb4 is detected in the somites and in the cement gland, and at tadpole stage 40, Pfkfb4 is expressed in the somites, the spinal cord, the notochord, the dorsal fin and the head of the embryo
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expression pattern of isozyme encoding pfk1, pfkfb1, pfkfb2, pfkfb3, and pfkfb4 genes in Xenopus laevis embryos.Gene pfkfb transcripts expression is overlapping at blastula and gastrula stages and from neurulation to tadpole stages, they display tissue-specific, complementary and dynamic developmental expression patterns. At the tailbud stage, pfkfb3 is mainly found in the spinal cord and at lower level in the notochord and in the somites. At tadpole stage 26, pfkfb3 is found in the somites and at lower levels in the spinal cord and in the notochord, and at tadpole stage 40, Pfkfb3 is expressed in the spinal cord, the notochord and the dorsal fin, and at a low level in the somites
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PFKFB3 is overexpressed in human cancers
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PFKFB4 is overexpressed in human cancers
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two isozymic forms
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2 isozymes: result of alternative splitting of the same primary transcript
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heart isozyme PFKFB2
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long isozyme variants H1-PFK2, H2-PFK2, and H4-PFK2, and short isozyme variant H3-PFK2
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transgenic mice, expressed in
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heart PFK-2 isozyme
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heart isozyme PFKFB2
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heart isozyme PFKFB2
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PFKFB3 is overexpressed in human cancers
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primary culture
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coordinate roles for glucokinase and PFK2 in the elevated hepatic glycolysis in fa/fa rats
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primary culture, treated and untreated with adenoviral vector to overexpress wild-type PFK-2 and mutant PKF2-M lacking Ser-32 phosphorylation site
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resembles muscle enzyme
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expressed at high abundance in both hypothalami and clonal hypothalamic neurons. In response to re-feeding, isoform PFKFB3 mRNA levels are increased by 10fold in mouse hypothalami
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engineered to overexpress PFKFB3, inhibitor studies on recombinant PFKFB3 activity in
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Q75IQ9
mRNA expressed in, metabolite analysis in
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Q75IQ9
mRNA primarily expressed in, metabolite analysis in
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PFKFB3 is constitutively expressed
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constitutively expressed in
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transgenic line of Mus musculus
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isozyme variant L-PFK2
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94932, 94935, 94948, 640281, 640282, 640283, 640284, 640285, 640286, 640287, 640288, 640289, 640290, 640291, 640292, 640295, 640297, 640298, 640300, 640302, 640305, 640306, 640307, 640324, 640325, 640330, 640336, 640339, 661569 brenda
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liver isozyme
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binding of glucokinase to 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase promotes a coordinated upregulation of glucose phosphorylation and glycolysis in the liver. The interaction may also serve as a metabolic signal transduction pathway for the glucose sensor, glucokinase, in the liver
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liver isozyme
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sterol regulatory element binding protein-1a binds to a sterol regulatory element box and transcriptionally activates Sparus aurata liver PFKFB1
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PFKFB4 is overexpressed in human cancers
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under hypoxia, expression analysis of alternative splice variants in
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overexpression of isozyme PFKFB4. PFKFB4 expression correlates with hypoxia in human lung adenocarcinoma xenografts
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PFKFB4 is overexpressed in human cancers
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isozyme variant M-PFK2
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expressed at high abundance in both hypothalami and clonal hypothalamic neurons
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isozyme iPFK2
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isozyme iPFK2
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PFKFB3 is overexpressed in human cancers
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increased expression of PFKFB4 in multiple solid tumor types including breast, colon, and prostate
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PFKFB4 is overexpressed in human cancers
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isozyme U-PFK2
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isozyme variant T-PFK2
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under hypoxia, expression analysis of alternative splice variants in
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additional information
enzyme PFKFB3 is highly expressed and activated in human cancer cells
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additional information
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enzyme PFKFB3 is highly expressed and activated in human cancer cells
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additional information
isozyme PFKFB3 variants are ubiquitously expressed, the variant I-PFK2 is inducible
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additional information
isozyme PFKFB3 variants are ubiquitously expressed, the variant I-PFK2 is inducible
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additional information
isozyme PFKFB3 variants are ubiquitously expressed, the variant I-PFK2 is inducible
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additional information
isozyme PFKFB3 variants are ubiquitously expressed, the variant I-PFK2 is inducible
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additional information
isozyme PFKFB4 tissue expression analysis, overview
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additional information
PFKFB3 is overexpressed in human cancers
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additional information
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PFKFB3 is overexpressed in human cancers
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additional information
PFKFB4 expression is induced in breast, colon, lung, gastric and pancreatic cancer cell lines
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additional information
PFKFB4 expression is induced in breast, colon, lung, gastric and pancreatic cancer cell lines
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additional information
PFKFB4 expression is induced in breast, colon, lung, gastric and pancreatic cancer cell lines
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additional information
PFKFB4 expression is induced in breast, colon, lung, gastric and pancreatic cancer cell lines
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additional information
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tissue distribution, in extrahepatic tissue only 10% or less of activity in liver
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additional information
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POROS-HQ column chromatography followed by Western blot analysis of extracts from various rat tissues show that proteins of placenta-type isozyme are expressed in placenta, brain, testis, liver, spleen, heart and lung, but not in kidney and skeletal muscle
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additional information
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Pfkfb enzymes are overexpressed in different cancer cell lines, like melanoma, prostate, pancreatic and gastric cancer cells and mammary gland malignant cells
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additional information
Pfkfb enzymes are overexpressed in different cancer cell lines, like melanoma, prostate, pancreatic and gastric cancer cells and mammary gland malignant cells
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additional information
Pfkfb enzymes are overexpressed in different cancer cell lines, like melanoma, prostate, pancreatic and gastric cancer cells and mammary gland malignant cells
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