Zobrazeno 1 - 10
of 31
pro vyhledávání: '"D J Danner"'
Autor:
Frank Peinemann, D. J. Danner
Publikováno v:
Journal of Inherited Metabolic Disease. 17:3-15
The clinical, molecular genetic and other biochemical aspects of branched-chain α-ketoacid dehydrogenase defects are reviewed.
Autor:
W J Herring, David T. Chuang, D J Danner, Kim S. Lau, Jacinta L. Chuang, Rody P. Cox, M McKean
Publikováno v:
Journal of Biological Chemistry. 267:24090-24096
We have determined the structural organization of the dihydrolipoyl transacylase (E2) gene of the human branched chain alpha-keto acid dehydrogenase complex. The single copy E2 gene spans approximately 68 kilobases of genomic DNA. The complete coding
Akademický článek
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Autor:
D J, Danner
Publikováno v:
Methods in enzymology. 324
Autor:
C B, Doering, D J, Danner
Publikováno v:
Methods in enzymology. 324
Publikováno v:
Developments in biological standardization. 99
Publikováno v:
Journal of cellular biochemistry. 61(1)
Constitutive expression of nuclear genes encoding mitochondrial proteins raises the question of whether these proteins are present in similar amounts in mitochondria of different tissues. We report that amounts of a single multienzyme complex can var
Autor:
D. J. Danner, M. C. McKean
Publikováno v:
Alpha-Keto Acid Dehydrogenase Complexes ISBN: 9783034898539
Our understanding of inborn errors of metabolism began with Sir Archibald Garrod’s description of alcaptonuria and the fact that this disorder tended to “run in families”(Garrod, 1908, 1923). By the 1950s, this understanding extended to knowing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f54d7cb0eb59456247181cce4fb7256d
https://doi.org/10.1007/978-3-0348-8981-0_19
https://doi.org/10.1007/978-3-0348-8981-0_19
Autor:
P S, Leung, D T, Chuang, R M, Wynn, S, Cha, D J, Danner, A, Ansari, R L, Coppel, M E, Gershwin
Publikováno v:
Hepatology (Baltimore, Md.). 22(2)
Primary biliary cirrhosis (PBC) is an autoimmune disease of liver associated with a unique serologic response to mitochondrial autoantigens. Many of the autoantigens recognized by autoantibodies in PBC are members of the 2-oxo-acid dehydrogenase comp
Autor:
A A, Ansari, N, Neckelmann, F, Villinger, P, Leung, D J, Danner, S S, Brar, S, Zhao, M B, Gravanis, A, Mayne, M E, Gershwin
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 153(10)
Sera from 29 of 48 patients with idiopathic dilated cardiomyopathy (IDCM) and six of six patients with dilated cardiomyopathy (DCM) secondary to suspected viral myocarditis were shown to react with the branched chain alpha-ketoacid dehydrogenase (BCK