Characterization of copy number variants for CCL3L1 gene in rheumatoid arthritis for French trio families and Tunisian cases and controls-Reference-Cited by-同舟云学术

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Characterization of copy number variants for CCL3L1 gene in rheumatoid arthritis for French trio families and Tunisian cases and controls

Published:2016-01-04 Issue:8 Volume:35 Page:1917-1922
ISSN:0770-3198
Container-title:Clinical Rheumatology
language:en
Short-container-title:Clin Rheumatol

Author:

Ben Kilani Mohamed Sahbi,Achour Yosser,Perea Javier,Cornelis François,Bardin Thomas,Chaudru Valérie,Maalej Abdellatif,Petit-Teixeira Elisabeth

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Rheumatology

Link

http://link.springer.com/content/pdf/10.1007/s10067-015-3156-y.pdf

Reference23 articles.

1. Charo IF, Ransohoff RM (2006) The many roles of chemokines and chemokine receptors in inflammation. N Engl J Med 6:610–621

2. Iwamoto T, Okamoto H, Toyama Y, Momohara S (2008) Molecular aspects of rheumatoid arthritis: chemokines in the joints of patients. FEBS J 18:4448–4455

3. Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, Catano G et al (2005) The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 5714:1434–1440

4. Carpenter D, Farnert A, Rooth I, Armour JA, Shaw MA (2012) CCL3L1 copy number and susceptibility to malaria. Infect Genet Evol 5:1147–1154

5. Stastny P (1976) Mixed lymphocyte cultures in rheumatoid arthritis. J Clin Invest 57:1148

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1. Chemokines and chemokine receptors as promising targets in rheumatoid arthritis;Frontiers in Immunology;2023-02-13

2. Association of Fc Gamma Receptor 3B Gene Copy Number Variation with Rheumatoid Arthritis Susceptibility;Genes;2022-11-29

3. An Update Evolving View of Copy Number Variations in Autoimmune Diseases;Frontiers in Genetics;2022-01-20

4. Development and Evaluation of a Droplet Digital PCR Assay for 8p23 β-Defensin Cluster Copy Number Determination;Molecular Diagnosis & Therapy;2021-07-29

5. Accurate diagnosis and heterogeneity analysis of a 17q12 deletion syndrome family with adulthood diabetes onset and complex clinical phenotypes;Endocrine;2021-03-20

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