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Items: 1 to 20 of 135

1.

Copy number variants in the sheep genome detected using multiple approaches.

Jenkins GM, Goddard ME, Black MA, Brauning R, Auvray B, Dodds KG, Kijas JW, Cockett N, McEwan JC.

BMC Genomics. 2016 Jun 8;17(1):441. doi: 10.1186/s12864-016-2754-7.

2.

Neutrophil MiRNA-128-3p is Decreased During Active Phase of Granulo-matosis with Polyangiitis.

Surmiak M, Hubalewska-Mazgaj M, Wawrzycka-Adamczyk K, Musiał J, Sanak M.

Curr Genomics. 2015 Oct;16(5):359-65. doi: 10.2174/1389202916666150707160434.

3.

Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.

Bentham J, Morris DL, Cunninghame Graham DS, Pinder CL, Tombleson P, Behrens TW, Martín J, Fairfax BP, Knight JC, Chen L, Replogle J, Syvänen AC, Rönnblom L, Graham RR, Wither JE, Rioux JD, Alarcón-Riquelme ME, Vyse TJ.

Nat Genet. 2015 Dec;47(12):1457-64. doi: 10.1038/ng.3434. Epub 2015 Oct 26.

4.

Copy number variation-based genome wide association study reveals additional variants contributing to meat quality in Swine.

Wang L, Xu L, Liu X, Zhang T, Li N, Hay el H, Zhang Y, Yan H, Zhao K, Liu GE, Zhang L, Wang L.

Sci Rep. 2015 Aug 3;5:12535. doi: 10.1038/srep12535.

5.

Complex and multi-allelic copy number variation in human disease.

Usher CL, McCarroll SA.

Brief Funct Genomics. 2015 Sep;14(5):329-38. doi: 10.1093/bfgp/elv028. Epub 2015 Jul 9. Review.

6.

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.

7.

Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes.

Franke L, el Bannoudi H, Jansen DT, Kok K, Trynka G, Diogo D, Swertz M, Fransen K, Knevel R, Gutierrez-Achury J, Ärlestig L, Greenberg JD, Kremer J, Pappas DA, Kanterakis A, Weersma RK, van der Helm-van Mil AH, Guryev V, Rantapää-Dahlqvist S, Gregersen PK, Plenge RM, Wijmenga C, Huizinga TW, Ioan-Facsinay A, Toes RE, Zhernakova A.

Eur J Hum Genet. 2016 Feb;24(2):263-70. doi: 10.1038/ejhg.2015.95. Epub 2015 May 13.

PMID:
25966632
8.

Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes.

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy M, Suresh RV, Manjegowda DS, Ramachandra NB.

PLoS One. 2015 Apr 24;10(4):e0121846. doi: 10.1371/journal.pone.0121846. eCollection 2015.

9.

Allele-specific copy-number discovery from whole-genome and whole-exome sequencing.

Wang W, Wang W, Sun W, Crowley JJ, Szatkiewicz JP.

Nucleic Acids Res. 2015 Aug 18;43(14):e90. doi: 10.1093/nar/gkv319. Epub 2015 Apr 16.

10.

Immunomodulation by IVIg and the Role of Fc-Gamma Receptors: Classic Mechanisms of Action after all?

Nagelkerke SQ, Kuijpers TW.

Front Immunol. 2015 Jan 21;5:674. doi: 10.3389/fimmu.2014.00674. eCollection 2014. Review.

11.

A comparison of assays for accurate copy number measurement of the low-affinity Fc gamma receptor genes FCGR3A and FCGR3B.

Haridan US, Mokhtar U, Machado LR, Abdul Aziz AT, Shueb RH, Zaid M, Sim B, Mustafa M, Nik Yusof NK, Lee CK, Abu Bakar S, AbuBakar S, Hollox EJ, Boon Peng H.

PLoS One. 2015 Jan 16;10(1):e0116791. doi: 10.1371/journal.pone.0116791. eCollection 2015.

12.

Genetic Susceptibility to ANCA-Associated Vasculitis: State of the Art.

Bonatti F, Reina M, Neri TM, Martorana D.

Front Immunol. 2014 Nov 17;5:577. doi: 10.3389/fimmu.2014.00577. eCollection 2014. Review.

13.

Copy number variation of the Lipoprotein(a) (LPA) gene is associated with coronary artery disease in a southern Han Chinese population.

Wu Z, Sheng H, Chen Y, Tang J, Liu Y, Chen Q, Lu L, Jin W.

Int J Clin Exp Med. 2014 Oct 15;7(10):3669-77. eCollection 2014.

14.

Genome-wide association study of copy number variations (CNVs) with opioid dependence.

Li D, Zhao H, Kranzler HR, Li MD, Jensen KP, Zayats T, Farrer LA, Gelernter J.

Neuropsychopharmacology. 2015 Mar;40(4):1016-26. doi: 10.1038/npp.2014.290. Epub 2014 Sep 27.

15.

Genome-wide scan identifies a copy number variable region at 3p21.1 that influences the TLR9 expression levels in IgA nephropathy patients.

Sallustio F, Cox SN, Serino G, Curci C, Pesce F, De Palma G, Papagianni A, Kirmizis D, Falchi M, Schena FP; European IgAN Consortium.

Eur J Hum Genet. 2015 Jul;23(7):940-8. doi: 10.1038/ejhg.2014.208. Epub 2014 Oct 8.

PMID:
25293716
16.

Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.

Chen JY, Wang CM, Chang SW, Cheng CH, Wu YJ, Lin JC, Yang B, Ho HH, Wu J.

Arthritis Rheumatol. 2014 Nov;66(11):3113-21. doi: 10.1002/art.38813.

17.

Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma.

Campbell CD, Mohajeri K, Malig M, Hormozdiari F, Nelson B, Du G, Patterson KM, Eng C, Torgerson DG, Hu D, Herman C, Chong JX, Ko A, O'Roak BJ, Krumm N, Vives L, Lee C, Roth LA, Rodriguez-Cintron W, Rodriguez-Santana J, Brigino-Buenaventura E, Davis A, Meade K, LeNoir MA, Thyne S, Jackson DJ, Gern JE, Lemanske RF Jr, Shendure J, Abney M, Burchard EG, Ober C, Eichler EE.

PLoS One. 2014 Aug 12;9(8):e104396. doi: 10.1371/journal.pone.0104396. eCollection 2014.

18.

Human FcR polymorphism and disease.

Li X, Gibson AW, Kimberly RP.

Curr Top Microbiol Immunol. 2014;382:275-302. doi: 10.1007/978-3-319-07911-0_13. Review.

19.

Contribution of Human FcγRs to Disease with Evidence from Human Polymorphisms and Transgenic Animal Studies.

Gillis C, Gouel-Chéron A, Jönsson F, Bruhns P.

Front Immunol. 2014 May 30;5:254. doi: 10.3389/fimmu.2014.00254. eCollection 2014. Review.

20.

A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes.

Zanda M, Onengut-Gumuscu S, Walker N, Shtir C, Gallo D, Wallace C, Smyth D, Todd JA, Hurles ME, Plagnol V, Rich SS.

PLoS Genet. 2014 May 29;10(5):e1004367. doi: 10.1371/journal.pgen.1004367. eCollection 2014.

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