These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
210 related articles for article (PubMed ID: 3980729)
21. Activation of branched-chain alpha-ketoacid dehydrogenase complex by alpha-chloroisocaproate in normal and enzyme-deficient fibroblasts. Toshima K; Kuroda Y; Yokota I; Naito E; Ito M; Watanabe T; Takeda E; Miyao M Clin Chim Acta; 1985 Apr; 147(2):103-8. PubMed ID: 3987057 [TBL] [Abstract][Full Text] [Related]
22. Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex. Tsuruta M; Mitsubuchi H; Mardy S; Miura Y; Hayashida Y; Kinugasa A; Ishitsu T; Matsuda I; Indo Y J Hum Genet; 1998; 43(2):91-100. PubMed ID: 9621512 [TBL] [Abstract][Full Text] [Related]
23. Maple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the disease. Nobukuni Y; Mitsubuchi H; Akaboshi I; Indo Y; Endo F; Yoshioka A; Matsuda I J Clin Invest; 1991 May; 87(5):1862-6. PubMed ID: 2022752 [TBL] [Abstract][Full Text] [Related]
24. Metabolism of branched-chain amino acids in fibroblasts from patients with maple syrup urine disease and other abnormalities of branched-chain ketoacid dehydrogenase activity. Yoshida I; Sweetman L; Nyhan WL Pediatr Res; 1986 Feb; 20(2):169-74. PubMed ID: 3080729 [TBL] [Abstract][Full Text] [Related]
25. Activities of branched-chain 2-oxo acid dehydrogenase and its components in skin fibroblasts from normal and classical-maple-syrup-urine-disease subjects. Chuang DT; Niu WL; Cox RP Biochem J; 1981 Oct; 200(1):59-67. PubMed ID: 6895847 [TBL] [Abstract][Full Text] [Related]
26. Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine disease. Indo Y; Kitano A; Endo F; Akaboshi I; Matsuda I J Clin Invest; 1987 Jul; 80(1):63-70. PubMed ID: 3597778 [TBL] [Abstract][Full Text] [Related]
28. Gene preference in maple syrup urine disease. Nellis MM; Danner DJ Am J Hum Genet; 2001 Jan; 68(1):232-7. PubMed ID: 11112664 [TBL] [Abstract][Full Text] [Related]
29. Altered phosphorylation state of branched-chain 2-oxo acid dehydrogenase in a branched-chain acyltransferase deficient human fibroblast cell line. Eisenstein RS; Hoganson G; Miller RH; Harper AE J Inherit Metab Dis; 1991; 14(1):37-44. PubMed ID: 1861457 [TBL] [Abstract][Full Text] [Related]
30. Maple syrup urine disease as a cause of spongiform encephalopathy in calves. Harper PA; Healy PJ; Dennis JA Vet Rec; 1986 Jul; 119(3):62-5. PubMed ID: 3529596 [TBL] [Abstract][Full Text] [Related]
31. Molecular phenotypes in cultured maple syrup urine disease cells. Complete E1 alpha cDNA sequence and mRNA and subunit contents of the human branched chain alpha-keto acid dehydrogenase complex. Fisher CW; Chuang JL; Griffin TA; Lau KS; Cox RP; Chuang DT J Biol Chem; 1989 Feb; 264(6):3448-53. PubMed ID: 2914958 [TBL] [Abstract][Full Text] [Related]
32. Expression and assembly of a functional E1 component (alpha 2 beta 2) of mammalian branched-chain alpha-ketoacid dehydrogenase complex in Escherichia coli. Davie JR; Wynn RM; Cox RP; Chuang DT J Biol Chem; 1992 Aug; 267(23):16601-6. PubMed ID: 1644840 [TBL] [Abstract][Full Text] [Related]
33. Detection of heterozygotes in maple-syrup-urine disease: measurements of branched-chain alpha-ketoacid dehydrogenase and its components in cell cultures. Chuang DT; Ku LS; Kerr DS; Cox RP Am J Hum Genet; 1982 May; 34(3):416-24. PubMed ID: 7081220 [TBL] [Abstract][Full Text] [Related]
34. Maple syrup urine disease in Poll Shorthorn calves. Healy PJ; Dennis JA; Harper PA; Graham R; Reuter RE Aust Vet J; 1992 Jun; 69(6):143-4. PubMed ID: 1642599 [No Abstract] [Full Text] [Related]
35. Molecular genetic characterization of maple syrup urine disease in European families. Peinemann F; Wendel U; Danner DJ Biochem Med Metab Biol; 1993 Dec; 50(3):338-45. PubMed ID: 8123297 [TBL] [Abstract][Full Text] [Related]
36. Natural osmolyte trimethylamine N-oxide corrects assembly defects of mutant branched-chain alpha-ketoacid decarboxylase in maple syrup urine disease. Song JL; Chuang DT J Biol Chem; 2001 Oct; 276(43):40241-6. PubMed ID: 11507102 [TBL] [Abstract][Full Text] [Related]
37. Enzyme assays with mutant cell lines of maple syrup urine disease. Chuang DT; Cox RP Methods Enzymol; 1988; 166():135-46. PubMed ID: 3071697 [No Abstract] [Full Text] [Related]