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Cynthia Fernández-Lainez, Carmen Aláez-Verson, Isabel Ibarra-González, Sergio Enríquez-Flores, Karol Carrillo-Sanchez, Leonardo Flores-Lagunes, Sara Guillén-López, Leticia Belmont-Martínez, Marcela Vela-Amieva

Clinica chimica acta; international journal of clinical chemistry 2018;483():33-38

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Regulation of branched-chain amino acid catabolism: nutritional and hormonal regulation of activity and expression of the branched-chain alpha-keto acid dehydrogenase kinase.

M Obayashi, T Murakami, R A Harris, Y Shimomura

Current opinion in clinical nutrition and metabolic care 2002;4(5):419-23

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Structural basis of the dysfunctioning of human 2-oxo acid dehydrogenase complexes.

A F Hengeveld, A de Kok

Current medicinal chemistry 2002;9(4):499-520

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Prospective study of changes in the metabolomic profiles of men during their first three months of androgen deprivation therapy for prostate cancer.

Edward D Karoly, Philip J Saylor, Matthew R Smith

Clinical cancer research : an official journal of the American Association for Cancer Research 2012;18(13):3677-85

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Results for ""3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)""[mesh_terms]

The Critical Role of the Branched Chain Amino Acids (BCAAs) Catabolism-Regulating Enzymes, Branched-Chain Aminotransferase (BCAT) and Branched-Chain α-Keto Acid Dehydrogenase (BCKD), in Human Pathophysiology.

Activation of α-keto acid-dependent dioxygenases: application of an {FeNO}7/{FeO2}8 methodology for characterizing the initial steps of O2 activation.

Lipoamide dehydrogenase (LADH) deficiency: medical perspectives of the structural and functional characterization of LADH and its pathogenic variants.

2-Oxo acid dehydrogenase complexes in redox regulation.

Protein requirements for endurance athletes.

Research experimental design for the construction and identification of the pGEX-BCKD-E4A recombinant point-mutant plasmid.

Markers associated with inborn errors of metabolism of branched-chain amino acids and their relevance to upper levels of intake in healthy people: an implication from clinical and molecular investigations on maple syrup urine disease.

The complex fate of alpha-ketoacids.

Folding kinetics of the lipoic acid-bearing domain of human mitochondrial branched chain alpha-ketoacid dehydrogenase complex.

Neonatal maple syrup urine disease in China: two novel mutations in the BCKDHB gene and literature review.

Substrate channelling in 2-oxo acid dehydrogenase multienzyme complexes.

In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing.

Regulation of branched-chain amino acid catabolism: nutritional and hormonal regulation of activity and expression of the branched-chain alpha-keto acid dehydrogenase kinase.

Structural basis of the dysfunctioning of human 2-oxo acid dehydrogenase complexes.

Prospective study of changes in the metabolomic profiles of men during their first three months of androgen deprivation therapy for prostate cancer.

Results for

""3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)""[mesh_terms]