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Cited by in F6Publishing
For: Antunes D, Chowdhury A, Aich A, Saladi S, Harpaz N, Stahl M, Schuldiner M, Herrmann JM, Rehling P, Rapaport D. Overexpression of branched-chain amino acid aminotransferases rescues the growth defects of cells lacking the Barth syndrome-related gene TAZ1. J Mol Med (Berl) 2019;97:269-79. [PMID: 30604168 DOI: 10.1007/s00109-018-1728-4] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
Number Citing Articles
1 Toyokawa Y, Koonthongkaew J, Takagi H. An overview of branched-chain amino acid aminotransferases: functional differences between mitochondrial and cytosolic isozymes in yeast and human. Appl Microbiol Biotechnol 2021;105:8059-72. [PMID: 34622336 DOI: 10.1007/s00253-021-11612-4] [Reference Citation Analysis]
2 Ji J, Greenberg ML. Cardiolipin function in the yeast S. cerevisiae and the lessons learned for Barth syndrome. J Inherit Metab Dis 2021. [PMID: 34626131 DOI: 10.1002/jimd.12447] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Finsterer J. Barth syndrome: mechanisms and management. Appl Clin Genet 2019;12:95-106. [PMID: 31239752 DOI: 10.2147/TACG.S171481] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 4.3] [Reference Citation Analysis]