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Diabetes|April 1, 1988
Reversible impairment of glucose-induced insulin secretion in SHR/N-cp rats. Genetic model of type II diabetesN R Voyles, A M Powell, K I Timmers, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|May 1, 1987
Tissue somatostatin levels in three models of genetic obesity in ratsN R Voyles, S J Bhathena, B Kennedy, et al.
Genomics|July 1, 1993
Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectivelyC Collins, C Duff, A M Duncan, et al.
Obesity Research|March 1, 1997
The rat corpulent (cp) mutation maps to the same interval on (Pgm1-Glut1) rat chromosome 5 as the fatty (fa) mutationE B Kahle, K G Butz, S C Chua, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|October 1, 1989
Effect of dietary carbohydrates on insulin and glucagon receptors in a new model of noninsulin-dependent diabetes-SHR/N-corpulent ratS J Bhathena, B W Kennedy, J Jones, et al.
Archives of Neurology|July 13, 2000
Creatine therapy in myophosphorylase deficiency (McArdle disease): a placebo-controlled crossover trialM Vorgerd, T Grehl, M Jager, et al.
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|June 9, 1998
[Regional distribution of predisposition to maligant hyperthermia in Germany: tate in 1997]E Hartung, M Anetseder, D Olthoff, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
The European Respiratory Journal|November 18, 2008
Extracorporeal pumpless interventional lung assist in clinical practice: determinants of efficacyT Müller, M Lubnow, A Philipp, et al.
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