176 related articles for article (PubMed ID: 10754342)
1. Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families.
Vorechovský I; Cullen M; Carrington M; Hammarström L; Webster AD
J Immunol; 2000 Apr; 164(8):4408-16. PubMed ID: 10754342
[TBL] [Abstract][Full Text] [Related]
2. Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency.
Kralovicova J; Hammarström L; Plebani A; Webster AD; Vorechovsky I
J Immunol; 2003 Mar; 170(5):2765-75. PubMed ID: 12594308
[TBL] [Abstract][Full Text] [Related]
3. Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.
Vorechovský I; Webster AD; Plebani A; Hammarström L
Am J Hum Genet; 1999 Apr; 64(4):1096-109. PubMed ID: 10090895
[TBL] [Abstract][Full Text] [Related]
4. MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes.
De la Concha EG; Fernandez-Arquero M; Gual L; Vigil P; Martinez A; Urcelay E; Ferreira A; Garcia-Rodriguez MC; Fontan G
J Immunol; 2002 Oct; 169(8):4637-43. PubMed ID: 12370403
[TBL] [Abstract][Full Text] [Related]
5. Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes.
Schroeder HW; Zhu ZB; March RE; Campbell RD; Berney SM; Nedospasov SA; Turetskaya RL; Atkinson TP; Go RC; Cooper MD; Volanakis JE
Mol Med; 1998 Feb; 4(2):72-86. PubMed ID: 9508785
[TBL] [Abstract][Full Text] [Related]
6. A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families.
Vorechovský I; Blennow E; Nordenskjöld M; Webster AD; Hammarström L
J Immunol; 1999 Aug; 163(4):2236-42. PubMed ID: 10438966
[TBL] [Abstract][Full Text] [Related]
7. Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.
Schäffer AA; Pfannstiel J; Webster AD; Plebani A; Hammarström L; Grimbacher B
Hum Genet; 2006 Feb; 118(6):725-9. PubMed ID: 16328471
[TBL] [Abstract][Full Text] [Related]
8. Family and linkage study of selective IgA deficiency and common variable immunodeficiency.
Vorechovský I; Zetterquist H; Paganelli R; Koskinen S; Webster AD; Björkander J; Smith CI; Hammarström L
Clin Immunol Immunopathol; 1995 Nov; 77(2):185-92. PubMed ID: 7586726
[TBL] [Abstract][Full Text] [Related]
9. HLA class II homozygosity confers susceptibility to common variable immunodeficiency (CVID).
De La Concha EG; Fernandez-Arquero M; Martinez A; Vidal F; Vigil P; Conejero L; Garcia-Rodriguez MC; Fontan G
Clin Exp Immunol; 1999 Jun; 116(3):516-20. PubMed ID: 10361244
[TBL] [Abstract][Full Text] [Related]
10. Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
Finck A; Van der Meer JW; Schäffer AA; Pfannstiel J; Fieschi C; Plebani A; Webster AD; Hammarström L; Grimbacher B
Eur J Hum Genet; 2006 Jul; 14(7):867-75. PubMed ID: 16639407
[TBL] [Abstract][Full Text] [Related]
11. Age-related changes in serum immunoglobulins in patients with familial IgA deficiency and common variable immunodeficiency (CVID).
Johnson ML; Keeton LG; Zhu ZB; Volanakis JE; Cooper MD; Schroeder HW
Clin Exp Immunol; 1997 Jun; 108(3):477-83. PubMed ID: 9182895
[TBL] [Abstract][Full Text] [Related]
12. Major histocompatibility complex haplotypes in Spanish immunoglobulin A deficiency patients: a comparative fine mapping microsatellite study.
Gual L; Martínez A; Fernández-Arquero M; García-Rodríguez MC; Ferreira A; Fontán G; de la Concha EG; Urcelay E
Tissue Antigens; 2004 Dec; 64(6):671-7. PubMed ID: 15546340
[TBL] [Abstract][Full Text] [Related]
13. MSH5 is not a genetic predisposing factor for immunoglobulin A deficiency but marks the HLA-DRB1*0102 subgroup carrying susceptibility.
Pozo ND; Medrano LM; Cénit MC; Fernández-Arquero M; Ferreira A; García-Rodríguez MC; de la Concha EG; Urcelay E; Núñez C
Hum Immunol; 2010 Sep; 71(9):861-4. PubMed ID: 20542071
[TBL] [Abstract][Full Text] [Related]
14. Shared HLA class II-associated genetic susceptibility and resistance, related to the HLA-DQB1 gene, in IgA deficiency and common variable immunodeficiency.
Olerup O; Smith CI; Björkander J; Hammarström L
Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10653-7. PubMed ID: 1438261
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21.
Herr M; Dudbridge F; Zavattari P; Cucca F; Guja C; March R; Campbell RD; Barnett AH; Bain SC; Todd JA; Koeleman BP
Hum Mol Genet; 2000 May; 9(9):1291-301. PubMed ID: 10814711
[TBL] [Abstract][Full Text] [Related]
16. Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency.
Abolhassani H; Lim CK; Aghamohammadi A; Hammarström L
Front Immunol; 2020; 11():14. PubMed ID: 32038658
[TBL] [Abstract][Full Text] [Related]
17. The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.
Haimila K; Einarsdottir E; de Kauwe A; Koskinen LL; Pan-Hammarström Q; Kaartinen T; Kurppa K; Ziberna F; Not T; Vatta S; Ventura A; Korponay-Szabo IR; Adány R; Pocsai Z; Széles G; Dukes E; Kaukinen K; Mäki M; Koskinen S; Partanen J; Hammarström L; Saavalainen P
Genes Immun; 2009 Mar; 10(2):151-61. PubMed ID: 19020530
[TBL] [Abstract][Full Text] [Related]
18. Central MHC genes affect IgA levels in the human: reciprocal effects in IgA deficiency and IgA nephropathy.
Matthews VB; Witt CS; French MA; Machulla HK; De la Concha EG; Cheong KY; Vigil P; Hollingsworth PN; Warr KJ; Christiansen FT; Price P
Hum Immunol; 2002 May; 63(5):424-33. PubMed ID: 11975987
[TBL] [Abstract][Full Text] [Related]
19. IgA deficiency: what is new?
Wang N; Hammarström L
Curr Opin Allergy Clin Immunol; 2012 Dec; 12(6):602-8. PubMed ID: 23026772
[TBL] [Abstract][Full Text] [Related]
20. Genetic and immunologic analysis of a family containing five patients with common-variable immune deficiency or selective IgA deficiency.
Ashman RF; Schaffer FM; Kemp JD; Yokoyama WM; Zhu ZB; Cooper MD; Volanakis JE
J Clin Immunol; 1992 Nov; 12(6):406-14. PubMed ID: 1363103
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
