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Items: 1 to 20 of 48

1.

Autoimmune diseases and 8.1 ancestral haplotype: An update.

Gambino CM, Aiello A, Accardi G, Caruso C, Candore G.

HLA. 2018 Jun 6. doi: 10.1111/tan.13305. [Epub ahead of print] Review.

PMID:
29877054
2.

Risk factors and disease mechanisms in myositis.

Miller FW, Lamb JA, Schmidt J, Nagaraju K.

Nat Rev Rheumatol. 2018 Apr 20;14(5):255-268. doi: 10.1038/nrrheum.2018.48. Review.

PMID:
29674613
3.

New developments in genetics of myositis.

Rothwell S, Lamb JA, Chinoy H.

Curr Opin Rheumatol. 2016 Nov;28(6):651-6. doi: 10.1097/BOR.0000000000000328. Review.

PMID:
27466937
4.

The PTPN22 gene is associated with idiopathic inflammatory myopathy.

Maundrell A, Lester S, Rischmueller M, Hill C, Cleland LG, Blumbergs P, Wiese M, Limaye V.

Muscle Nerve. 2017 Feb;55(2):270-273. doi: 10.1002/mus.25222. Epub 2016 Nov 10.

PMID:
27312665
5.

Inheritance of the 8.1 ancestral haplotype in recurrent pregnancy loss.

Kolte AM, Nielsen HS, Steffensen R, Crespi B, Christiansen OB.

Evol Med Public Health. 2015 Dec 16;2015(1):325-31. doi: 10.1093/emph/eov031. Print 2015.

6.

A conserved linkage group on chromosome 6, the 8.1 ancestral haplotype, is a predisposing factor of chronic rhinosinusitis associated with nasal polyposis in aspirin-sensitive Hungarians.

Szabó K, Polyánka H, Kiricsi Á, Révész M, Vóna I, Szabó Z, Bella Z, Kadocsa E, Kemény L, Széll M, Hirschberg A.

Hum Immunol. 2015 Nov;76(11):858-62. doi: 10.1016/j.humimm.2015.09.048. Epub 2015 Oct 9.

PMID:
26433033
7.

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.

Rothwell S, Cooper RG, Lundberg IE, Miller FW, Gregersen PK, Bowes J, Vencovsky J, Danko K, Limaye V, Selva-O'Callaghan A, Hanna MG, Machado PM, Pachman LM, Reed AM, Rider LG, Cobb J, Platt H, Molberg Ø, Benveniste O, Mathiesen P, Radstake T, Doria A, De Bleecker J, De Paepe B, Maurer B, Ollier WE, Padyukov L, O'Hanlon TP, Lee A, Amos CI, Gieger C, Meitinger T, Winkelmann J, Wedderburn LR, Chinoy H, Lamb JA; Myositis Genetics Consortium.

Ann Rheum Dis. 2016 Aug;75(8):1558-66. doi: 10.1136/annrheumdis-2015-208119. Epub 2015 Sep 11.

8.

Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.

Miller FW, Chen W, O'Hanlon TP, Cooper RG, Vencovsky J, Rider LG, Danko K, Wedderburn LR, Lundberg IE, Pachman LM, Reed AM, Ytterberg SR, Padyukov L, Selva-O'Callaghan A, Radstake TR, Isenberg DA, Chinoy H, Ollier WE, Scheet P, Peng B, Lee A, Byun J, Lamb JA, Gregersen PK, Amos CI; Myositis Genetics Consortium.

Genes Immun. 2015 Oct;16(7):470-80. doi: 10.1038/gene.2015.28. Epub 2015 Aug 20.

9.

The Influence of the Autoimmunity-Associated Ancestral HLA Haplotype AH8.1 on the Human Gut Microbiota: A Cross-Sectional Study.

Hov JR, Zhong H, Qin B, Anmarkrud JA, Holm K, Franke A, Lie BA, Karlsen TH.

PLoS One. 2015 Jul 24;10(7):e0133804. doi: 10.1371/journal.pone.0133804. eCollection 2015.

10.

Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis.

Scott AP, Laing NG, Mastaglia F, Dalakas M, Needham M, Allcock RJ.

J Neuroimmunol. 2012 Sep 15;250(1-2):66-70. doi: 10.1016/j.jneuroim.2012.04.021. Epub 2012 Jun 23.

PMID:
22732452
11.

Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.

Scott AP, Laing NG, Mastaglia F, Needham M, Walter MC, Dalakas MC, Allcock RJ.

J Neuroimmunol. 2011 Jun;235(1-2):77-83. doi: 10.1016/j.jneuroim.2011.02.011. Epub 2011 May 2.

PMID:
21543121
12.

Juvenile dermatomyositis: advances in pathogenesis, evaluation, and treatment.

Huber AM.

Paediatr Drugs. 2009;11(6):361-74. doi: 10.2165/11310550-000000000-00000. Review.

PMID:
19877722
13.

An update on the immunogenetics of idiopathic inflammatory myopathies: major histocompatibility complex and beyond.

Chinoy H, Lamb JA, Ollier WE, Cooper RG.

Curr Opin Rheumatol. 2009 Nov;21(6):588-93. doi: 10.1097/BOR.0b013e3283315a22. Review.

PMID:
19730377
14.

HLA-DPB1 associations differ between DRB1*03 positive anti-Jo-1 and anti-PM-Scl antibody positive idiopathic inflammatory myopathy.

Chinoy H, Payne D, Poulton KV, Fertig N, Betteridge Z, Gunawardena H, Davidson JE, Oddis CV, McHugh NJ, Wedderburn LR, Ollier WE, Cooper RG; UK Adult Onset Myositis Immunogenetic Collaboration & UK Juvenile Dermatomyositis Research Group.

Rheumatology (Oxford). 2009 Oct;48(10):1213-7. doi: 10.1093/rheumatology/kep248. Epub 2009 Aug 18.

PMID:
19690132
15.

Role of human leukocyte antigen, killer-cell immunoglobulin-like receptors, and cytokine gene polymorphisms in leptospirosis.

Fialho RN, Martins L, Pinheiro JP, Bettencourt BF, Couto AR, Santos MR, Peixoto MJ, Garrett F, Leal J, Tomás AM, Bruges-Armas J.

Hum Immunol. 2009 Nov;70(11):915-20. doi: 10.1016/j.humimm.2009.08.007. Epub 2009 Aug 13.

PMID:
19683555
16.

Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population.

Blaskó B, Bánlaki Z, Gyapay G, Pozsonyi E, Sasvári-Székely M, Rajczy K, Füst G, Szilágyi A.

Mol Immunol. 2009 Aug;46(13):2623-9. doi: 10.1016/j.molimm.2009.04.033. Epub 2009 Jun 7.

PMID:
19505723
17.

Efficacy of adalimumab in the treatment of generalized granuloma annulare in monozygotic twins carrying the 8.1 ancestral haplotype.

Knoell KA.

Arch Dermatol. 2009 May;145(5):610-1. doi: 10.1001/archdermatol.2009.92. No abstract available.

PMID:
19451522
18.

Relationship of polymorphisms located in tumor necrosis factor region and HLA loci among Croatians.

Stingl K, Grubic Z, Car H, Zunec R.

Am J Hum Biol. 2009 Mar-Apr;21(2):220-3. doi: 10.1002/ajhb.20853.

PMID:
19107922
19.
20.

Epistasis between the MHC and the RCA alpha block in primary Sjögren syndrome.

Lester S, McLure C, Williamson J, Bardy P, Rischmueller M, Dawkins RL.

Ann Rheum Dis. 2008 Jun;67(6):849-54. Epub 2007 Sep 18.

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