Results 251 to 260 of about 17,667 (261)

Proton Abstraction Reaction, Steady-State Kinetics, and Oxidation−Reduction Potential of Human Glutaryl-CoA Dehydrogenase

, 2000
Timothy M. Dwyer, K. Sudhindra Rao, Stephen I. Goodman, Frank E. Frerman   +3 more
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Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans

Molecular Genetics and Metabolism, 2010
Surita Meldau
exaly  

The pleiotropic effects of the hydroxy-methyl-glutaryl-CoA reductase inhibitors in rheumatologic disorders: a comprehensive review

Rheumatology International, 2012
Christos G Mihos, Orlando Santana
exaly  

Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

Human Genetics, 2011
J. Martí‐Massó, J. Ruiz‐Martinez, Vladimir Makarov, A. L. Munain, A. Gorostidi, A. Bergareche, Seungtai Yoon, J. Buxbaum, C. Paisán-Ruiz   +8 more
semanticscholar   +1 more source

Disruption of brain redox homeostasis in glutaryl-CoA dehydrogenase deficient mice treated with high dietary lysine supplementation

Molecular Genetics and Metabolism, 2013
Bianca Seminotti, Alexandre Umpierrez Amaral, Guilhian Leipnitz   +2 more
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Glutaryl-CoA Dehydrogenase Deficiency

2009
David J. Timson, Richard J. Reece, James B. Thoden, Hazel M. Holden, Andrea L. Utz, Beverly M. K. Biller, Eugen-Matthias Strehle, Markus Böhm, Thomas A. Luger, Alexander K. C. Leung, Andrew L. Wong, Markus G. Donner, Dieter Häussinger, Nirmal S. Mann, Marcus Schmitt, Alexander K. C. Leung, William Lane M. Robson, Andrew L. Wong, Manisha Balwani, Ainu Prakash-Cheng*, Robert J. Desnick, Holger Lerche, Ingrid E. Scheffer, Samuel F. Berkovic, Brigitte M. Lobnig, Peter L. M. Jansen, Siegfried Waldegger, Florian Lang, Hugo ten Cate, Hagen Thieme, Michael Weller, Bärbel Schütte, Ronnie Fass, Hideki Kato, Masaomi Nangaku, Hideki Kato, Masaomi Nangaku, Anthony Chang, Pradeep V. Kadambi, Jessy J. Alexander, Pierre Ronco, Hanna Debiec, Christian Hugo, Brigitte M. Lobnig, Brigitte M. Lobnig, John-John B. Schnog, Victor E. A. Gerdes, Jean Francis, David S. Geller, Knut Brockmann, Dong Wang, Darryl C. Vivo, Stefan Kölker, Stefan Kölker, Elardus Erasmus, Lodewyk J. Mienie, John Vissing, Arnold Reuser, Catherine E. Correia, David A. Weinstein, Joseph I. Wolfsdorf, Yoon S. Shin, Reinout P. Hesselink, Maarten R. Drost, Anton J. M. Wagenmakers, Ger J. Vusse, Stefan Kiechl, Jonas Denecke, Ute Schepers, Thomas Kolter, Konrad Sandhoff, Dianna C. Martin, Barbara L. Triggs-Raine, Seda Sancak, Ralf Paschke, Dorin-Bogdan Borza, Sonja Ständer, Heiko Traupe, Michael A. Becker, Hanneke M. Straaten, Leo F. Verdonck, Hugo Ten Cate, Martin Mempel, Dietrich Abeck, Ismat Ghanem, Samer El Hage, Johannes G. Bode, Thomas A. Fleisher, Steven M. Holland, Bennett Myers, David Herrmann, Zaki Kraiem, Yaron Tomer, Terry F. Davies, James G. White, Sylvia Stöckler-Ipsiroglu, Guido Stoll, Klaus V. Toyka, Valéria Lamounier-Zepter, Klaus Ruether   +99 more
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Crystal Structures of Human Glutaryl-CoA Dehydrogenase with and without an Alternate Substrate: Structural Bases of Dehydrogenation and Decarboxylation Reactions^,

, 2004
Zhuji Fu, Ming Wang, Rosemary Paschke, K. Sudhindra Rao, Frank E. Frerman, Jung‐Ja P. Kim   +5 more
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Reduction of lysine intake while avoiding malnutrition—Major goals and major problems in dietary treatment of glutaryl‐CoA dehydrogenase deficiency

, 2004
Edith Müller, Stefan Kölker
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Pork and human cDNAs encoding glutaryl-CoA dehydrogenase.

, 1992
Goodman Si, Kratz Le, Frerman Fe
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[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)].

, 1991
Trefz Fk, Hoffmann Gf, Ertan Mayatepek, Uta Lichter‐Konecki, Jutta Weisser, Anne Otten, U. Wendel, D. Rating, Bremer Hj   +8 more
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