检索结果 - Brian H. Robinson
- Showing 1 - 19 results of 19
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
-
10
-
11
-
12
-
13
-
14
Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts... 由 Michael F. Marusich, Brian H. Robinson, Jan‐Willem Taanman, Soo Jin Kim, Robynn V. Schillace, Jordan L. Smith, Roderick Capaldi
出版 1997Artigo -
15
Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes 由 Jessie M. Cameron, Alexandre Janer, Valeriy Levandovskiy, Nevena MacKay, Tracey A. Rouault, Wing-Hang Tong, Isla Ogilvie, Eric A. Shoubridge, Brian H. Robinson
出版 2011Artigo -
16
Mutations in the X-linked pyruvate dehydrogenase (E1) ? subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency 由 Willy Lissens, Linda De Meırleır, Sara Seneca, Inge Liebaers, Garry K. Brown, Ruth M. Brown, Michinori Ito, Etsuo Naito, Yasuhiro Kuroda, Douglas S. Kerr, Isaiah D. Wexler, Mulchand S. Patel, Brian H. Robinson, Agnieszka Seyda
出版 2000Revisão -
17
Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky Encephalopathy 由 Karen M. Vernau, Jonathan A. Runstadler, Emily Brown, Jessie M. Cameron, Heather J. Huson, Robert Higgins, Cameron Ackerley, Beverly K. Sturges, Peter J. Dickinson, Birgit Puschner, Cecilia Giulivi, G. Diane Shelton, Brian H. Robinson, Salvatore DiMauro, Andrew W. Bollen, Danika L. Bannasch
出版 2013Artigo -
18
Inhibition of Mitochondrial Translation as a Therapeutic Strategy for Human Acute Myeloid Leukemia 由 Marko Škrtić, Shrivani Sriskanthadevan, Bozhena Jhas, Marinella Gebbia, Xiaoming Wang, Zezhou Wang, Rose Hurren, Yulia Jitkova, Marcela Gronda, Neil MacLean, Courteney K. Lai, Yanina Eberhard, Justyna Bartoszko, Paul A. Spagnuolo, Angela C. Rutledge, Alessandro Datti, Troy Ketela, Jason Moffat, Brian H. Robinson, Jessie Cameron, Jeffery L. Wrana, Connie J. Eaves, Mark D. Minden, Jean Wang, John E. Dick, R. Keith Humphries, Corey Nislow, Guri Giaever, Aaron D. Schimmer
出版 2011Artigo -
19
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5 由 Peter R. Baker, Marisa W. Friederich, Michael A. Swanson, Tamim H. Shaikh, Kaustuv Bhattacharya, Gunter Scharer, Joseph K. Aicher, Geralyn Creadon‐Swindell, Elizabeth A. Geiger, Kenneth N. Maclean, Wang‐Tso Lee, Charu Deshpande, Mary-Louise Freckmann, Ling-Yu Shih, Melissa Wasserstein, Malene Bøgehus Rasmussen, Allan M. Lund, Peter Procopis, Jessie M. Cameron, Brian H. Robinson, Garry K. Brown, Ruth M. Brown, Alison G. Compton, Carol L. Dieckmann, Renata Collard, Curtis R. Coughlin, Elaine Spector, Michael F. Wempe, Johan L.K. Van Hove
出版 2013Artigo
相关主题
Biology
Biochemistry
Gene
Mitochondrion
Genetics
Medicine
Enzyme
Internal medicine
Molecular biology
Chemistry
Mutation
Cytochrome c oxidase
Endocrinology
Mitochondrial DNA
Exon
Lactic acidosis
Phenotype
Respiratory chain
Cell biology
Computer science
DNA
Frameshift mutation
Leigh disease
Library science
Missense mutation
Mitochondrial respiratory chain
Oxidase test
ATP synthase
Acidosis
Adipose tissue