Functional variants of the HMGA1 gene and type 2 diabetes mellitus

Autor: Chiefari E, Tanyolaç S, Paonessa F, Pullinger CR, Capula C, Iiritano S, Mazza T, Forlin M, Fusco A, Durlach V, Durlach A, Malloy MJ, Kane JP, Heiner SW, Filocamo M, Foti DP, Goldfine ID, Brunetti A.

Publikováno v: Journal of the American Medical Association
Journal of the American Medical Association, American Medical Association (AMA), 2011, 305 (9), pp.903-912
305 (2011).
info:cnr-pdr/source/autori:Chiefari E, Tanyolaç S, Paonessa F, Pullinger CR, Capula C, Iiritano S, Mazza T, Forlin M, Fusco A, Durlach V, Durlach A, Malloy MJ, Kane JP, Heiner SW, Filocamo M, Foti DP, Goldfine ID, Brunetti A./titolo:Functional variants of the HMGA1 gene and type 2 diabetes mellitus./doi:/rivista:/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume:305

CONTEXT: High-mobility group A1 (HMGA1) protein is a key regulator of insulin receptor (INSR) gene expression. We previously identified a functional HMGA1 gene variant in 2 insulin-resistant patients with decreased INSR expression and type 2 diabetes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::64641ecd363b6dee1f33f147be02fa30
https://hal.archives-ouvertes.fr/hal-00573386

Genetic variants of the ENPP1/PC-1 gene are associated with hypertriglyceridemia in male subjects.

Autor: Tanyolaç S; Diabetes Center and Department of Medicine, University of California, San Francisco, California 94115, USA., Bremer AA, Hodoglugil U, Movsesyan I, Pullinger CR, Heiner SW, Malloy MJ, Kane JP, Goldfine ID

Publikováno v: Metabolic syndrome and related disorders [Metab Syndr Relat Disord] 2009 Dec; Vol. 7 (6), pp. 543-8.