Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Diabetes Mellitus and LMNA[original query] |
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| Analysis of the lamin A/C gene as a candidate for type II diabetes susceptibility in Pima Indians. Diabetologia 2001 Jun 44 (6): 779-82. Wolford J K, Hanson R L, Bogardus C, Prochazka |
| Variation in the lamin A/C gene: associations with metabolic syndrome. Arteriosclerosis, thrombosis, and vascular biology 2004 Sep 24 (9): 1708-13. Steinle Nanette I, Kazlauskaite Rasa, Imumorin Ikhide G, Hsueh Wen-Chi, Pollin Toni I, O'Connell Jeffrey R, Mitchell Braxton D, Shuldiner Alan |
| Characterisation of non-obese diabetic patients with marked insulin resistance identifies a novel familial partial lipodystrophy-associated PPAR? mutation (Y151C). Diabetologia 2011 Jul 54 (7): 1639-44. Visser M E, Kropman E, Kranendonk M E, Koppen A, Hamers N, Stroes E S, Kalkhoven E, Monajemi |
| A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation. The Journal of clinical endocrinology and metabolism 2017 12 103 (3): 1005-1014. Hussain Iram, Patni Nivedita, Ueda Masako, Sorkina Ekaterina, Valerio Cynthia M, Cochran Elaine, Brown Rebecca J, Peeden Joseph, Tikhonovich Yulia, Tiulpakov Anatoly, Stender Sarah R S, Klouda Elisabeth, Tayeh Marwan K, Innis Jeffrey W, Meyer Anders, Lal Priti, Godoy-Matos Amelio F, Teles Milena G, Adams-Huet Beverley, Rader Daniel J, Hegele Robert A, Oral Elif A, Garg Abhiman |
| Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register. Diabetologia 2022 11 66 (3): 438-449. Harsunen Minna, Kettunen Jarno L T, Härkönen Taina, Dwivedi Om, Lehtovirta Mikko, Vähäsalo Paula, Veijola Riitta, Ilonen Jorma, Miettinen Päivi J, Knip Mikael, Tuomi Tiinamai |
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