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Results 1 - 10 of 75 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Acidosis, Lactic 31282308 Expanding the Phenotype: Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements and Lactic Acidosis, With or Without Seizures (NEMMLAS) due to WARS2 Biallelic Variants, Encoding Mitochondrial Tryptophanyl-tRNA Synthase. causal interaction
unassigned
4
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Acidosis, Lactic 31684799 Expanding the Phenotype: Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements and Lactic Acidosis, With or Without Seizures (NEMMLAS) Due to WARS2 Biallelic Variants, Encoding Mitochondrial Tryptophanyl-tRNA Synthase. causal interaction
unassigned
2
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Alzheimer Disease 16616781 Mapping and molecular characterization of novel monoclonal antibodies to conformational epitopes on NH2 and COOH termini of mammalian tryptophanyl-tRNA synthetase reveal link of the epitopes to aggregation and Alzheimer's disease. diagnostic usage
ongoing research
unassigned
3
3
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Alzheimer Disease 29973830 Synthetic Peptide Corresponding to The Amino-Terminal Region of the Human Tryptophanyl-Trna Synthetase, a Component Of Alzheimer'S Disease Special Congophlic Plaques Aggregates In Vitro to Form Amyloid-Like Fibrils. ongoing research
unassigned
2
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Ataxia 31282308 Expanding the Phenotype: Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements and Lactic Acidosis, With or Without Seizures (NEMMLAS) due to WARS2 Biallelic Variants, Encoding Mitochondrial Tryptophanyl-tRNA Synthase. causal interaction
unassigned
4
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Athetosis 28650581 Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. causal interaction
unassigned
4
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Brain Diseases 28905505 Biallelic variants in WARS2 encoding mitochondrial tryptophanyl-tRNA synthase in six individuals with mitochondrial encephalopathy. causal interaction
unassigned
3
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Breast Neoplasms 24098497 Concurrent Gene Signatures for Han Chinese Breast Cancers. diagnostic usage
ongoing research
unassigned
1
1
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Breast Neoplasms 33408886 Tryptophanyl-tRNA Synthetase Sensitizes Hormone Receptor-Positive Breast Cancer to Docetaxel-Based Chemotherapy. diagnostic usage
ongoing research
therapeutic application
unassigned
1
4
3
0
Show all pathways known for 6.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.2Carcinogenesis 10376788 Tryptamine-mediated stabilization of tryptophanyl-tRNA synthetase in human cervical carcinoma cell line. causal interaction
diagnostic usage
ongoing research
therapeutic application
2
1
4
3
Results 1 - 10 of 75 > >>