HuGE Literature Finder
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| C1824T mutation in the LMNA gene has no association with senile cataract. Neurobiology of aging 2012 Jul 33 (7): 1487.e15-9. Sadikov Tamilla, Simon Amos J, Avraham-Lubin Bat-Chen R, Dratviman-Storobinsky Olga, Cohen Yoram, Goldenberg-Cohen Nit |
| Human longevity and common variations in the LMNA gene: a meta-analysis. Aging cell 2012 Jun 11 (3): 475-81. Conneely Karen N, Capell Brian C, Erdos Michael R, Sebastiani Paola, Solovieff Nadia, Swift Amy J, Baldwin Clinton T, Budagov Temuri, Barzilai Nir, Atzmon Gil, Puca Annibale A, Perls Thomas T, Geesaman Bard J, Boehnke Michael, Collins Francis |
| Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study. Journal of molecular medicine (Berlin, Germany) 2010 Feb 88 (2): 193-201. Fontaine-Bisson Benedicte, Alessi Marie-Christine, Saut Noemie, Fumeron Frederic, Marre Michel, Dutour Anne, Badens Catherine, Levy Nicolas, Tichet Jean, Juhan-Vague Irene, Trégouët David-Alexandre, Balkau Beverly, Morange Pierre-Emmanu |
| 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 |
| Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation. The American journal of cardiology 2009 May 103 (10): 1426-8. Brauch Katharine M, Chen Lin Y, Olson Timothy |
| 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 |
| 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 |
| 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 |
| Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes. Clinical endocrinology 2005 Sep 63 (3): 317-22. Liang H, Murase Y, Katuta Y, Asano A, Kobayashi J, Mabuchi H |
| 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 |
| 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 |
| 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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