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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: munnelly k. Nat Genet. 1996 Sep;14(1):90-4. doi: 10.1038/ng0996-90. Nat Genet. 1996. PMID: 8782826
Novel mutations and a mutational hotspot in the MODY3 gene.
Glucksmann MA, Lehto M, Tayber O, Scotti S, Berkemeier L, Pulido JC, Wu Y, Nir WJ, Fang L, Markel P, Munnelly KD, Goranson J, Orho M, Young BM, Whitacre JL, McMenimen C, Wantman M, Tuomi T, Warram J, Forsblom CM, Carlsson M, Rosenzweig J, Kennedy G, Duyk GM, Thomas JD, et al. Glucksmann MA, et al. Among authors: munnelly kd. Diabetes. 1997 Jun;46(6):1081-6. doi: 10.2337/diab.46.6.1081. Diabetes. 1997. PMID: 9166684
miRNA profiling on high-throughput OpenArray™ system.
Grigorenko EV, Ortenberg E, Hurley J, Bond A, Munnelly K. Grigorenko EV, et al. Among authors: munnelly k. Methods Mol Biol. 2011;676:101-10. doi: 10.1007/978-1-60761-863-8_8. Methods Mol Biol. 2011. PMID: 20931393
17 results