Found: 18
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Dimerization Drives Proper Folding of Human Alanine:Glyoxylate Aminotransferase But Is Dispensable for Peroxisomal Targeting.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 4, p. 273, doi. 10.3390/jpm11040273
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- Publication type:
- Article
Metastatic Breast Cancer Cells Enter Into Dormant State and Express Cancer Stem Cells Phenotype Under Chronic Hypoxia.
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- Journal of Cellular Biochemistry, 2017, v. 118, n. 10, p. 3237, doi. 10.1002/jcb.25972
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- Article
Biochemical properties and oxalate‐degrading activity of oxalate decarboxylase from bacillus subtilis at neutral pH.
- Published in:
- IUBMB Life, 2019, v. 71, n. 7, p. 917, doi. 10.1002/iub.2027
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- Publication type:
- Article
Evolutionary Divergent Suppressor Mutations in Conformational Diseases.
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- Genes, 2018, v. 9, n. 7, p. 352, doi. 10.3390/genes9070352
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- Publication type:
- Article
Mutant p53 blocks SESN1/AMPK/PGC-1α/UCP2 axis increasing mitochondrial O<sub>2-</sub>· production in cancer cells.
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- 2018
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- Publication type:
- journal article
Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications.
- Published in:
- Proteins, 2014, v. 82, n. 1, p. 171, doi. 10.1002/prot.24447
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- Publication type:
- Article
Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications.
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- Proteins, 2013, v. 81, n. 8, p. 1457, doi. 10.1002/prot.24300
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- Publication type:
- Article
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5500, doi. 10.1093/hmg/ddv276
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- Publication type:
- Article
S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.
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- Human Molecular Genetics, 2014, v. 23, n. 22, p. 5998, doi. 10.1093/hmg/ddu329
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- Publication type:
- Article
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine.
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- Human Molecular Genetics, 2013, v. 22, n. 8, p. 1615, doi. 10.1093/hmg/ddt011
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- Publication type:
- Article
TAT-Mediated Delivery of Human Alanine:Glyoxylate Aminotransferase in a Cellular Model of Primary Hyperoxaluria Type I.
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- International Journal of Peptide Research & Therapeutics, 2013, v. 19, n. 2, p. 175, doi. 10.1007/s10989-012-9333-9
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- Publication type:
- Article
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B<sub>6</sub>.
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- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 2, p. 263, doi. 10.1007/s10545-017-0105-8
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- Publication type:
- Article
Molecular basis of primary hyperoxaluria: clues to innovative treatments.
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- Urolithiasis, 2019, v. 47, n. 1, p. 67, doi. 10.1007/s00240-018-1089-z
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- Publication type:
- Article
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition.
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- Molecular Oncology, 2016, v. 10, n. 7, p. 1008, doi. 10.1016/j.molonc.2016.04.001
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- Publication type:
- Article
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH.
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- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/161456
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- Publication type:
- Article
A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2.
- Published in:
- Scientific Reports, 2016, p. 35277, doi. 10.1038/srep35277
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- Publication type:
- Article
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 1, p. 1, doi. 10.1093/hmg/ddy323
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- Publication type:
- Article
A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptors.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 24, p. 4204, doi. 10.1093/hmg/ddy311
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- Publication type:
- Article