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Obstetrics and Gynecology|January 1, 1996
Repair of transversely incised abdominal wall fascia in a rabbit modelG L Maxwell, A P Soisson, P C Brittain, et al.
Behavior Genetics|October 3, 2009
Hybrid mice as genetic models of high alcohol consumptionY A Blednov, A R Ozburn, D Walker, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|May 18, 1999
Preoperative prediction of graft patency for infrapopliteal arterial bypass using pulse-generated runoffR A Harris, P Kumar, J Collin, et al.
The American Journal of Clinical Nutrition|July 17, 1998
A molecular model of human branched-chain amino acid metabolismA Suryawan, J W Hawes, R A Harris, et al.
The Journal of Biological Chemistry|December 15, 1993
Primary structure of pyruvate dehydrogenase kinase establishes a new family of eukaryotic protein kinasesK M Popov, N Y Kedishvili, Y Zhao, et al.
European Journal of Immunology|December 22, 1999
Visualization of inhibitory Ly49 receptor specificity with soluble major histocompatibility complex class I tetramersJ Michaëlsson, A Achour, M Salcedo, et al.
Journal of Biomedical Materials Research. Part A|December 25, 2008
In vitro biocompatibility of hydroxyapatite-reinforced polymeric composites manufactured by selective laser sinteringY Zhang, L Hao, M M Savalani, et al.
Molecular Genetics and Metabolism|October 27, 1998
Methylmalonic semialdehyde dehydrogenase deficiency: psychomotor delay and methylmalonic aciduria without metabolic decompensationC R Roe, E Struys, R M Kok, et al.
The Journal of Biological Chemistry|September 25, 1992
CoA-dependent methylmalonate-semialdehyde dehydrogenase, a unique member of the aldehyde dehydrogenase superfamily. cDNA cloning, evolutionary relationships, and tissue distributionN Y Kedishvili, K M Popov, P M Rougraff, et al.
Annals of the New York Academy of Sciences|January 1, 1989
cDNA cloning of the E1 alpha subunit of the branched-chain alpha-keto acid dehydrogenase and elucidation of a molecular basis for maple syrup urine diseaseB Zhang, M J Kuntz, G W Goodwin, et al.
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