Human Genome Epidemiology Literature Finder
|
Records 1 - 14 (of 14 Records) |
| Query Trace: Insulin Resistance and LMNA[original query] |
|---|
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Clinical usefulness of multigene screening with phenotype-driven bioinformatics analysis for the diagnosis of patients with monogenic diabetes or severe insulin resistance. Diabetes research and clinical practice 2020 9 169 108461. Hosoe Jun, Miya Fuyuki, Kadowaki Hiroko, Fujiwara Toyofumi, Suzuki Ken, Kato Takashi, Waki Hironori, Sasako Takayoshi, Aizu Katsuya, Yamamura Natsumi, Sasaki Fusako, Kurano Makoto, Hara Kazuo, Tanaka Masaki, Ishiura Hiroyuki, Tsuji Shoji, Honda Kenjiro, Yoshimura Jun, Morishita Shinichi, Matsuzawa Fumiko, Aikawa Sei-Ichi, Boroevich Keith A, Nangaku Masaomi, Okada Yukinori, Tsunoda Tatsuhiko, Shojima Nobuhiro, Yamauchi Toshimasa, Kadowaki Takas |
| Rare variation in LMNA underlies polycystic ovary syndrome (PCOS) pathogenesis in two independent cohorts. The Journal of clinical endocrinology and metabolism 2024 11 . Rosemary Bauer, Chloe Parker, Lidija K Gorsic, M Geoffrey Hayes, Allen R Kunselman, Richard S Legro, Corrine K Welt, Margrit Urban |
- Page last reviewed:Feb 1, 2024
- Content source: