نتایج جستجو برای: ژن slc30a8

تعداد نتایج: 15995  

2015
H Skärstrand E Krupinska T J K Haataja F Vaziri-Sani J O Lagerstedt Å Lernmark

Variant-specific zinc transporter 8 autoantibodies (ZnT8A) against either arginine (R) or tryptophan (W) at amino acid (aa) position 325 of the zinc transporter 8 (ZnT8) has been identified in type 1 diabetes (T1D) patients. Reciprocal cross-over tests revealed differences in half-maximal binding to indicate variable affinity of patient ZnT8 autoantibodies. Insufficient recombinant ZnT8 variant...

Journal: :European journal of endocrinology 2016
Natalia I Faccinetti Luciano L Guerra Alberto Penas Steinhardt Ruben F Iacono Gustavo D Frechtel Liliana Trifone Edgardo Poskus Aldana Trabucchi Silvina N Valdez

OBJECTIVE In order to gain further knowledge of the structure of zinc transporter 8 (ZnT8) epitopes, we studied the role of the amino acid at position 325 in the antigen and its dimeric conformation for autoantibodies to ZnT8 (ZnT8A) recognition. METHODS For this purpose, several ZnT8 C-terminal domain variants were designed: monomer carrying Arg325 or Trp325, homo-dimers ZnT8-Arg-Arg325 and ...

2015
Kommoju Uma Jyothi Battini Mohan Reddy

Fifteen SNPs from nine different genes were genotyped on 1379 individuals, 758 T2DM patients and 621 controls, from the city of Hyderabad, India, using Sequenom Massarray platform. These data were analyzed to examine the role of gene-gene and gene-environment interactions in the manifestation of T2DM. The multivariate analysis suggests that TCF7L2, CDKAL1, IGF2BP2, HHEX and PPARG genes are sign...

2017
Eirini Marouli Stavroula Kanoni Vasiliki Mamakou Sophie Hackinger Lorraine Southam Bram Prins Angela Rentari Maria Dimitriou Eleni Zengini Fragiskos Gonidakis Genovefa Kolovou Vassilis Kontaxakis Loukianos Rallidis Nikolaos Tentolouris Anastasia Thanopoulou Klea Lamnissou George Dedoussis Eleftheria Zeggini Panagiotis Deloukas

Recent genome-wide association studies have identified several single nucleotide polymorphisms (SNPs) associated with glucose levels. We tested the hypothesis here whether the cumulative effect of glucose raising SNPs, assessed via a score, is associated with glucose levels. A total of 1,434 participants of Greek descent from the THISEAS study and 1,160 participants form the GOMAP study were in...

Journal: :Diabetes research and clinical practice 2012
M Ekelund N Shaat P Almgren E Anderberg M Landin-Olsson V Lyssenko L Groop K Berntorp

AIMS To examine whether genetic variants that predispose individuals to type 2 diabetes (T2D) could predict the development of diabetes after gestational diabetes mellitus (GDM). METHODS 13 SNPs (FTO rs8050136, CDKAL1 rs7754840 and rs7756992, CDKN2A/2B rs10811661, HHEX rs1111875, IGF2BP2 rs1470579 and rs4402960, SLC30A8 rs13266634, TCF7L2 rs7903146, PPARG rs1801282, GCK rs1799884, HNF1A rs116...

2016
Rafael Ríos-Tamayo Carmen Belén Lupiañez Daniele Campa Thomas Hielscher Niels Weinhold Joaquin Martínez-López Andrés Jerez Stefano Landi Krzysztof Jamroziak Charles Dumontet Marzena Wątek Fabienne Lesueur Rui Manuel Reis Herlander Marques Artur Jurczyszyn Ulla Vogel Gabriele Buda Ramón García-Sanz Enrico Orciuolo Mario Petrini Annette J Vangsted Federica Gemignani Asta Försti Hartmut Goldschmidt Kari Hemminki Federico Canzian Manuel Jurado Juan Sainz

Diabetogenic single nucleotide polymorphisms (SNPs) have recently been associated with multiple myeloma (MM) risk but their impact on overall survival (OS) of MM patients has not been analysed yet. In order to investigate the impact of 58 GWAS-identified variants for type 2 diabetes (T2D) on OS of patients with MM, we analysed genotyping data of 936 MM patients collected by the International Mu...

Journal: :Diabetes 2015
Jonathan M Locke Gerald Hysenaj Andrew R Wood Michael N Weedon Lorna W Harries

Genome-wide association studies (GWAS) have identified variation at >65 genomic loci associated with susceptibility to type 2 diabetes, but little progress has been made in elucidating the molecular mechanisms behind most of these associations. Using samples heterozygous for transcribed single nucleotide polymorphisms (SNPs), allelic expression profiling is a powerful technique for identifying ...

Journal: :Diabetes 2008
Kirstine Juhl Suparna A. Sarkar Randall Wong Jan Jensen John C. Hutton

OBJECTIVE To document the transcriptome of the pancreatic islet during the early and late development of the mouse pancreas and highlight the qualitative and quantitative features of gene expression that contribute to the specification, growth, and differentiation of the major endocrine cell types. A further objective was to identify endocrine cell biomarkers, targets of diabetic autoimmunity, ...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2010
Sonali Pechlivanis André Scherag Thomas W Mühleisen Stefan Möhlenkamp Bernhard Horsthemke Tanja Boes Martina Bröcker-Preuss Klaus Mann Raimund Erbel Karl-Heinz Jöckel Markus M Nöthen Susanne Moebus

OBJECTIVE To examine the association between genomewide association study-based diabetes mellitus-related single-nucleotide polymorphisms (SNPs) and coronary artery calcification (CAC), a valid risk factor for coronary heart disease, in a large, unselected, population-based cohort. METHODS AND RESULTS We genotyped 11 validated genomewide association study-based diabetes SNPs in 4459 participa...

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