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Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.
Mahtani MM, Widén E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. Mahtani MM, et al. Among authors: widen e. Nat Genet. 1996 Sep;14(1):90-4. doi: 10.1038/ng0996-90. Nat Genet. 1996. PMID: 8782826
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.
Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström M, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen MR, Groop L. Lehto M, et al. Among authors: widen e. J Clin Invest. 1997 Feb 15;99(4):582-91. doi: 10.1172/JCI119199. J Clin Invest. 1997. PMID: 9045858 Free PMC article.
Insulin resistance in type 2 (non-insulin-dependent) diabetic patients and their relatives is not associated with a defect in the expression of the insulin-responsive glucose transporter (GLUT-4) gene in human skeletal muscle.
Eriksson J, Koranyi L, Bourey R, Schalin-Jäntti C, Widén E, Mueckler M, Permutt AM, Groop LC. Eriksson J, et al. Among authors: widen e. Diabetologia. 1992 Feb;35(2):143-7. doi: 10.1007/BF00402546. Diabetologia. 1992. PMID: 1547918
313 results