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Items: 1 to 20 of 131

1.

Copy number variation in autoimmunity--importance hidden in complexity?

Olsson LM, Holmdahl R.

Eur J Immunol. 2012 Aug;42(8):1969-76. doi: 10.1002/eji.201242601. Review.

2.

Correlating multiallelic copy number polymorphisms with disease susceptibility.

Cantsilieris S, White SJ.

Hum Mutat. 2013 Jan;34(1):1-13. doi: 10.1002/humu.22172. Epub 2012 Aug 23. Review.

PMID:
22837109
3.

Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases.

Mamtani M, Anaya JM, He W, Ahuja SK.

Genes Immun. 2010 Mar;11(2):155-60. doi: 10.1038/gene.2009.71. Epub 2009 Sep 10.

PMID:
19741716
4.

Frequency distribution of autoimmunity associated FCGR3B gene copy number in Indian population.

Almal SH, Padh H.

Int J Immunogenet. 2015 Feb;42(1):26-30. doi: 10.1111/iji.12165. Epub 2014 Nov 27.

PMID:
25428402
5.

Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes.

McKinney C, Merriman TR.

Hum Mol Genet. 2012 May 15;21(10):2370-6. doi: 10.1093/hmg/dds039. Epub 2012 Feb 14.

PMID:
22337955
6.

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

Fanciulli M, Norsworthy PJ, Petretto E, Dong R, Harper L, Kamesh L, Heward JM, Gough SC, de Smith A, Blakemore AI, Froguel P, Owen CJ, Pearce SH, Teixeira L, Guillevin L, Graham DS, Pusey CD, Cook HT, Vyse TJ, Aitman TJ.

Nat Genet. 2007 Jun;39(6):721-3. Epub 2007 May 21.

7.

Association study of copy number variants in FCGR3A and FCGR3B gene with risk of ankylosing spondylitis in a Chinese population.

Wang L, Yang X, Cai G, Xin L, Xia Q, Zhang X, Li X, Wang M, Wang K, Xia G, Xu S, Xu J, Zou Y, Pan F.

Rheumatol Int. 2016 Mar;36(3):437-42. doi: 10.1007/s00296-015-3384-0. Epub 2015 Oct 22.

PMID:
26494566
8.

Association between FCGR3B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.

Lee YH, Bae SC, Seo YH, Kim JH, Choi SJ, Ji JD, Song GG.

Inflamm Res. 2015 Dec;64(12):983-91. doi: 10.1007/s00011-015-0882-1. Epub 2015 Sep 25. Review.

PMID:
26407570
9.

Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis.

McKinney C, Merriman ME, Chapman PT, Gow PJ, Harrison AA, Highton J, Jones PB, McLean L, O'Donnell JL, Pokorny V, Spellerberg M, Stamp LK, Willis J, Steer S, Merriman TR.

Ann Rheum Dis. 2008 Mar;67(3):409-13. Epub 2007 Jun 29.

PMID:
17604289
10.

What a difference copy number variation makes.

Kehrer-Sawatzki H.

Bioessays. 2007 Apr;29(4):311-3.

PMID:
17373652
11.

Clinical implications of copy number variations in autoimmune disorders.

Yim SH, Jung SH, Chung B, Chung YJ.

Korean J Intern Med. 2015 May;30(3):294-304. doi: 10.3904/kjim.2015.30.3.294. Epub 2015 Apr 29. Review.

12.

Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.

Marques RB, Thabet MM, White SJ, Houwing-Duistermaat JJ, Bakker AM, Hendriks GJ, Zhernakova A, Huizinga TW, van der Helm-van Mil AH, Toes RE.

PLoS One. 2010 Oct 5;5(10). pii: e13173. doi: 10.1371/journal.pone.0013173.

13.

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake.

Willcocks LC, Lyons PA, Clatworthy MR, Robinson JI, Yang W, Newland SA, Plagnol V, McGovern NN, Condliffe AM, Chilvers ER, Adu D, Jolly EC, Watts R, Lau YL, Morgan AW, Nash G, Smith KG.

J Exp Med. 2008 Jul 7;205(7):1573-82. doi: 10.1084/jem.20072413. Epub 2008 Jun 16.

14.

Copy number variation in the human genome and its implication in autoimmunity.

Schaschl H, Aitman TJ, Vyse TJ.

Clin Exp Immunol. 2009 Apr;156(1):12-6. doi: 10.1111/j.1365-2249.2008.03865.x. Epub 2009 Feb 11. Review.

15.

FCGR3B copy number variation is not associated with lupus nephritis in a Chinese population.

Lv J, Yang Y, Zhou X, Yu L, Li R, Hou P, Zhang H.

Lupus. 2010 Feb;19(2):158-61. doi: 10.1177/0961203309350319. Epub 2009 Nov 27.

PMID:
19946035
16.

Human gene copy number variation and infectious disease.

Hollox EJ, Hoh BP.

Hum Genet. 2014 Oct;133(10):1217-33. doi: 10.1007/s00439-014-1457-x. Epub 2014 Jun 5. Review.

PMID:
25110110
17.

[Analysis of the genetic variability of complement component C4 by real-time PCR].

Agnes S, Bernadett B, Dénes S, György F, Sasvári-Székely M, Zsolt R.

Neuropsychopharmacol Hung. 2007 Mar;9(1):5-10. Hungarian.

18.

Lower copy numbers of the chemokine CCL3L1 gene in patients with chronic hepatitis C.

Grünhage F, Nattermann J, Gressner OA, Wasmuth HE, Hellerbrand C, Sauerbruch T, Spengler U, Lammert F.

J Hepatol. 2010 Feb;52(2):153-9. doi: 10.1016/j.jhep.2009.11.001. Epub 2009 Nov 27.

PMID:
20044164
19.

Copy number variation of the gene NCF1 is associated with rheumatoid arthritis.

Olsson LM, Nerstedt A, Lindqvist AK, Johansson SC, Medstrand P, Olofsson P, Holmdahl R.

Antioxid Redox Signal. 2012 Jan 1;16(1):71-8. doi: 10.1089/ars.2011.4013. Epub 2011 Aug 23.

PMID:
21728841
20.

Novel association strategy with copy number variation for identifying new risk Loci of human diseases.

Chen X, Li X, Wang P, Liu Y, Zhang Z, Zhao G, Xu H, Zhu J, Qin X, Chen S, Hu L, Kong X.

PLoS One. 2010 Aug 20;5(8):e12185. doi: 10.1371/journal.pone.0012185.

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