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30. Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency. Saunders ME; Sherwood WG; Duthie M; Surh L; Gravel RA Am J Hum Genet; 1982 Jul; 34(4):590-601. PubMed ID: 7102675 [TBL] [Abstract][Full Text] [Related]
31. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism. Baumgartner ER; Suormala T Int J Vitam Nutr Res; 1997; 67(5):377-84. PubMed ID: 9350481 [TBL] [Abstract][Full Text] [Related]
32. Reduced half-life of holocarboxylase synthetase from patients with severe multiple carboxylase deficiency. Bailey LM; Ivanov RA; Jitrapakdee S; Wilson CJ; Wallace JC; Polyak SW Hum Mutat; 2008 Jun; 29(6):E47-57. PubMed ID: 18429047 [TBL] [Abstract][Full Text] [Related]
33. Holocarboxylase synthetase deficiency: 9-year follow-up of a patient on chronic biotin therapy and a review of the literature. Michalski AJ; Berry GT; Segal S J Inherit Metab Dis; 1989; 12(3):312-6. PubMed ID: 2515372 [TBL] [Abstract][Full Text] [Related]
34. Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample. Suormala T; Wick H; Bonjour JP; Baumgartner ER Clin Chim Acta; 1985 Jan; 145(2):151-62. PubMed ID: 3918814 [TBL] [Abstract][Full Text] [Related]
35. Holocarboxylase synthetase is an obligate participant in biotin-mediated regulation of its own expression and of biotin-dependent carboxylases mRNA levels in human cells. Solórzano-Vargas RS; Pacheco-Alvarez D; León-Del-Río A Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5325-30. PubMed ID: 11959985 [TBL] [Abstract][Full Text] [Related]