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The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestationA Wedell, A Thilén, E M Ritzén, et al.Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Regulation of human insulin receptor RNA splicing in vivoS Norgren, J Zierath, A Wedell, et al.Diabetes|May 1, 1993
Differences in the ratio of RNA encoding two isoforms of the insulin receptor between control and NIDDM patients. The RNA variant without Exon 11 predominates in both groupsS Norgren, J Zierath, D Galuska, et al.Human Genetics|August 1, 1991
DNA haplotype analysis suggests linkage disequilibrium in the human insulin receptor geneM Sten-Linder, M Olsson, L Iselius, et al.Journal of Magnetic Resonance (San Diego, Calif. : 1997)|June 1, 2000
Determination of molecular geometry by high-order multiple-quantum evolution in solid-state NMRM Edén, A Brinkmann, H Luthman, et al.Journal of Neuroimmunology|October 5, 2001
Polygenic control of autoimmune peripheral nerve inflammation in ratI Dahlman, E Wallström, H Jiao, et al.Genomics|March 1, 1990
The gene for insulin-like growth factor-binding protein-1 is localized to human chromosomal region 7p14-p12J Ekstrand, E Ehrenborg, I Stern, et al.Diabetes|December 1, 1994
Glucose potentiation of arginine-induced insulin secretion is impaired in subjects with a glucokinase Glu256Lys mutationA Wajngot, M Alvarsson, A Glaser, et al.Human Molecular Genetics|June 5, 2002
Susceptibility loci for atopic dermatitis on chromosomes 3, 13, 15, 17 and 18 in a Swedish populationM Bradley, C Söderhäll, H Luthman, et al.European Journal of Endocrinology|June 13, 1998
Effect of growth hormone treatment on insulin action in adipocytes from children with Prader-Willi syndromeA Kamel, S Norgren, A C Lindgren, et al.Pageof 9