HuGE Literature Finder
Records 1-12
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Genotype of the LMNA 1908C>T variant is associated with generalized obesity in Asian Indians in North India.
Clinical endocrinology 2011 Nov 75 (5): 642-9. Sharma Mukti, Misra Anoop, Vikram Naval, Suryaprakash Bhatt, Chhabra Shivani, Garg Neha, Pandey Ravindra Mohan, Upadhyay Ashish Datt, Luthra Kalpa |
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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 |
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LMNA rs4641 and the muscle lamin A and C isoforms in twins--metabolic implications and transcriptional regulation.
The Journal of clinical endocrinology and metabolism 2010 Aug 95 (8): 3884-92. Wegner L, Anthonsen S, Bork-Jensen J, Dalgaard L, Hansen T, Pedersen O, Poulsen P, Vaag |
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LMNA gene mutation search in Polish patients: new features of the heterozygous Arg482Gln mutation phenotype.
Endocrine 2009 Dec 36 (3): 518-23. Klupa Tomasz, Szopa Magdalena, Skupien Jan, Wojtyczek Katarzyna, Cyganek Katarzyna, Kowalska Irina, Malecki Maciej |
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The role of genetic variation in the lamin a/c gene in the etiology of polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2009 Jul 94 (7): 2665-9. Urbanek Margrit, Nampiaparampil Geetha, D'Souza Janine, Sefton Elizabeth, Ackerman Christine, Legro Richard S, Dunaif Andr |
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Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.
Diabetes 2007 Mar 56 (3): 879-83. Owen Katharine R, Groves Christopher J, Hanson Robert L, Knowler William C, Shuldiner Alan R, Elbein Steven C, Mitchell Braxton D, Froguel Philippe, Ng Maggie C Y, Chan Juliana C, Jia Weiping, Deloukas Panos, Hitman Graham A, Walker Mark, Frayling Timothy M, Hattersley Andrew T, Zeggini Eleftheria, McCarthy Mark |
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Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies.
Diabetes 2007 Mar 56 (3): 884-9. Mesa José L, Loos Ruth J F, Franks Paul W, Ong Ken K, Luan Jian'an, O'Rahilly Stephen, Wareham Nicholas J, Barroso In |
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Aging syndrome genes and premature coronary artery disease.
BMC medical genetics 2005 Oct 6 (): 38. Low Adrian F, O'Donnell Christopher J, Kathiresan Sekar, Everett Brendan, Chae Claudia U, Shaw Stanley Y, Ellinor Patrick T, MacRae Calum |
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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 |
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An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese.
Metabolism: clinical and experimental 2002 Aug 51 (8): 1017-21. Murase Yuko, Yagi Kunimasa, Katsuda Yuko, Asano Akimichi, Koizumi Junji, Mabuchi Hiros |
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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 |
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Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.
Molecular genetics and metabolism 2001 Mar 72 (3): 231-8. Weyer C, Wolford J K, Hanson R L, Foley J E, Tataranni P A, Bogardus C, Pratley R |
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- Page last updated:Sep 23, 2021
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