A 129-kb Deletion on Chromosome 12 Confers Substantial Protection Against Rheumatoid Arthritis, Implicating the GeneSLC2A3-Reference-Cited by-同舟云学术

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A 129-kb Deletion on Chromosome 12 Confers Substantial Protection Against Rheumatoid Arthritis, Implicating the GeneSLC2A3

Published:2013-12-02 Issue:2 Volume:35 Page:248-256
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Veal Colin D.¹,Reekie Katherine E.¹,Lorentzen Johnny C.²,Gregersen Peter K.³,Padyukov Leonid⁴,Brookes Anthony J.¹

Affiliation:

1. Department of Genetics; University of Leicester; Leicester UK

2. Institute of Environmental Medicine; Unit of Work Environment Toxicology; Karolinska Institute Stockholm Sweden

3. Robert S. Boas Center for Genomics and Human Genetics; Feinstein Institute for Medical Research; New York

4. Rheumatology Unit; Department of Medicine, Karolinska University Hosiptals; Solna Karolinska Institute Stockholm Sweden

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference54 articles.

1. Pannus invasion and cartilage degradation in rheumatoid arthritis: involvement of MMP-3 and interleukin-1beta;Ainola;Clin Exp Rheumatol,2005

2. Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease;Aldhous;Hum Mol Genet,2010

3. Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats;Armour;Nucleic Acids Res,2007

4. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis;Arnett;Arthritis Rheum,1988

5. Interleukin-1 in combination with oncostatin M up-regulates multiple genes in chondrocytes: implications for cartilage destruction and repair;Barksby;Arthritis Rheum,2006

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1. Identification and experimental validation of ferroptosis-related gene SLC2A3 is involved in rheumatoid arthritis;European Journal of Pharmacology;2023-03

2. A 1.1 Mb duplication CNV on chromosome 17 contributes to skeletal muscle development in Boer goats;Zoological Research;2023

3. SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population;Journal of Clinical Laboratory Analysis;2022-04-25

4. Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation;The Cleft Palate-Craniofacial Journal;2021-11-17

5. Adult glut3 homozygous null mice survive to demonstrate neural excitability and altered neurobehavioral responses reminiscent of neurodevelopmental disorders;Experimental Neurology;2021-04

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