Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Lipodystrophy 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 |
| 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 |
| Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites. Diabetes 2007 Mar 56 (3): 694-8. Wegner Lise, Andersen Gitte, Sparsø Thomas, Grarup Niels, Glümer Charlotte, Borch-Johnsen Knut, Jørgensen Torben, Hansen Torben, Pedersen Ol |
| 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 |
| 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 |
| 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 |
| Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlation. Diabetes & metabolism 2018 Oct . Kwapich M, Lacroix D, Espiard S, Ninni S, Brigadeau F, Kouakam C, Degroote P, Laurent J M, Tiffreau V, Jannin A, Humbert L, Ben Hamou A, Tard C, Ben Yaou R, Lamblin N, Klug D, Richard P, Vigouroux C, Bonne G, Vantyghem M C, |
| Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort. Diabetes 2019 12 69 (2): 249-258. Gonzaga-Jauregui Claudia, Ge Wenzhen, Staples Jeffrey, Van Hout Cristopher, Yadav Ashish, Colonie Ryan, Leader Joseph B, Kirchner H Lester, Murray Michael F, Reid Jeffrey G, Carey David J, Overton John D, Shuldiner Alan R, Gottesman Omri, Gao Steve, Gromada Jesper, Baras Aris, Altarejos Judith, |
| Homozygous LMNA p.R582H pathogenic variant reveals increasing effect on the severity of fat loss in lipodystrophy. Clinical diabetes and endocrinology 2020 7 6 13. Soyaltin Utku Erdem, Simsir Ilgin Yildirim, Akinci Baris, Altay Canan, Adiyaman Suleyman Cem, Lee Kristen, Onay Huseyin, Oral Elif Ariog |
| Cardiac phenotype in familial partial lipodystrophy. Clinical endocrinology 2021 1 94 (6): 1043-1053. Eldin Abdelwahab Jalal, Akinci Baris, da Rocha Andre Monteiro, Meral Rasimcan, Simsir Ilgin Yildirim, Adiyaman Suleyman Cem, Ozpelit Ebru, Bhave Nicole, Gen Ramazan, Yurekli Banu, Ozdemir Kutbay Nilufer, Siklar Zeynep, Neidert Adam H, Hench Rita, Tayeh Marwan K, Innis Jeffrey W, Jalife Jose, Oral Hakan, Oral Elif |
| Familial Partial Lipodystrophy: Clinical Features, Genetics and Treatment in a Greek Referral Center. International journal of molecular sciences 2023 8 24 (15): . Aikaterini Kountouri, Emmanouil Korakas, Eirini Maratou, Ignatios Ikonomidis, Konstantinos Balampanis, Stavros Liatis, Nikolaos Tentolouris, Panagiotis Toulas, Foteini Kousathana, Christophoros Giatzakis, George D Dimitriadis, Vaia Lambadia |
| The Clinical Characteristics and Potential Molecular Mechanism of LMNA Mutation-Related Lipodystrophy. Advanced biology 2023 6 e2200301. Cheng Xiao, Jieying Liu, Chunru Yang, Xiaojun Zhai, Peng Liu, Xinhua Xiao, Miao |
| A cohort analysis of familial partial lipodystrophy from two Mediterranean countries. Diabetes, obesity & metabolism 2024 8 . Antía Fernández-Pombo, Ilgin Yildirim Simsir, Sofía Sánchez-Iglesias, Samim Ozen, Ana I Castro, Tahir Atik, Lourdes Loidi, Huseyin Onay, Teresa Prado-Moraña, Cem Adiyaman, Everardo Josué Díaz-López, Canan Altay, Maria José Ginzo-Villamayor, Baris Akinci, David Araújo-Vil |
- Page last reviewed:Feb 1, 2024
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