146 related articles for article (PubMed ID: 1356100)
1. Involvement of both HLA and Ig heavy chain haplotypes in human IgA deficiency.
Olsson PG; Hammarström L; Cox DW; Smith CI
Immunogenetics; 1992; 36(6):389-95. PubMed ID: 1356100
[TBL] [Abstract][Full Text] [Related]
2. Detection of IgA heavy chain constant region genes in IgA deficient donors: evidence against gene deletions.
Hammarström L; Carlsson B; Smith CI; Wallin J; Wieslander L
Clin Exp Immunol; 1985 Jun; 60(3):661-4. PubMed ID: 2990782
[TBL] [Abstract][Full Text] [Related]
3. The complete map of the Ig heavy chain constant gene region reveals evidence for seven IgG isotypes and for IgD in the horse.
Wagner B; Miller DC; Lear TL; Antczak DF
J Immunol; 2004 Sep; 173(5):3230-42. PubMed ID: 15322185
[TBL] [Abstract][Full Text] [Related]
4. The genetics of IgG4 deficiency: role of the immunoglobulin heavy chain constant region and HLA loci.
Gallina R; Bottaro A; Boccazzi C; DeLange G; Danese P; Mazzola G; Amoroso A; DeMarchi M; Carbonara AO
Eur J Immunol; 1992 Jan; 22(1):227-33. PubMed ID: 1346112
[TBL] [Abstract][Full Text] [Related]
5. Restriction fragment haplotypes in the human immunoglobulin IGHG locus and their correlation with the Gm polymorphism.
Ghanem N; Dugoujon JM; Bensmana M; Huck S; Lefranc MP; Lefranc G
Eur J Immunol; 1988 Jul; 18(7):1067-72. PubMed ID: 2900148
[TBL] [Abstract][Full Text] [Related]
6. Molecular analysis of the IGHA and MHC class III region genes in one family with IgA and C4 deficiencies.
Keyeux G; Lefranc MP; Chevailler A; Lefranc G
Exp Clin Immunogenet; 1990; 7(3):170-80. PubMed ID: 1974449
[TBL] [Abstract][Full Text] [Related]
7. Two siblings with deficiency of IgA1, IgG2, IgG4 and IgE due to deletion of immunoglobulin heavy chain constant region genes.
Plebani A; Carbonara AO; Bottaro A; Gallina R; Boccazzi C; Crispino P; Ruggeri L; Soresina A; Meini A; Duina M
Year Immunol; 1993; 7():231-5. PubMed ID: 8372508
[No Abstract] [Full Text] [Related]
8. C4 polymorphism and major histocompatibility complex haplotypes in IgA deficiency: association with C4A null haplotypes.
Bućin D; Truedsson L; Hammarström L; Smith CI; Sjöholm AG
Exp Clin Immunogenet; 1991; 8(4):233-41. PubMed ID: 1817567
[TBL] [Abstract][Full Text] [Related]
9. HLA-A, B, Cw and DRB1, DRB3/4/5, DQB1, DPB1 frequencies in German immunoglobulin A-deficient individuals.
MacHulla HK; Schönermarck U; Schaaf A; Müller LP; Kloss C; Krüger J; Kunze G; Schönermarck G; Langner J
Scand J Immunol; 2000 Aug; 52(2):207-11. PubMed ID: 10931389
[TBL] [Abstract][Full Text] [Related]
10. Recurrent extended HLA haplotypes in children with selective IgA deficiency.
Cuccia-Belvedere M; Monafo V; Martinetti M; Plebani A; De Paoli F; Burgio GR
Tissue Antigens; 1989 Aug; 34(2):127-32. PubMed ID: 2609322
[TBL] [Abstract][Full Text] [Related]
11. IgA2 allotypes determined by restriction fragment length polymorphism in IgA deficiency. Re-expression of the silent A2m(2) allotype in the children of IgA-deficient patients.
Hammarström L; de Lange GG; Smith CI
J Immunogenet; 1987; 14(4-5):197-201. PubMed ID: 2900854
[TBL] [Abstract][Full Text] [Related]
12. Ig H chain variable and C region genes in common variable immunodeficiency. Characterization of two new deletion haplotypes.
Olsson PG; Hofker MH; Walter MA; Smith S; Hammarström L; Smith CI; Cox DW
J Immunol; 1991 Oct; 147(8):2540-6. PubMed ID: 1655893
[TBL] [Abstract][Full Text] [Related]
13. Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes.
Schaffer FM; Palermos J; Zhu ZB; Barger BO; Cooper MD; Volanakis JE
Proc Natl Acad Sci U S A; 1989 Oct; 86(20):8015-9. PubMed ID: 2573059
[TBL] [Abstract][Full Text] [Related]
14. Family studies of IgA deficiency.
Wilton AN; Cobain TJ; Dawkins RL
Immunogenetics; 1985; 21(4):333-42. PubMed ID: 3997207
[TBL] [Abstract][Full Text] [Related]
15. Relation of mesangial IgA glomerulonephritis to polymorphism of immunoglobulin heavy chain switch region.
Demaine AG; Rambausek M; Knight JF; Williams DG; Welsh KI; Ritz E
J Clin Invest; 1988 Feb; 81(2):611-4. PubMed ID: 2892861
[TBL] [Abstract][Full Text] [Related]
16. Genetic aspects of immunoglobulin A deficiency.
Cunningham-Rundles C
Adv Hum Genet; 1990; 19():235-66. PubMed ID: 2193490
[TBL] [Abstract][Full Text] [Related]
17. Alternative G1m, G2m and G3m allotypes of IGHG genes correlate with atopic and nonatopic pathways of immune regulation in children with bronchial asthma.
Oxelius VA; Carlsson AM; Aurivillius M
Int Arch Allergy Immunol; 1998 Mar; 115(3):215-9. PubMed ID: 9531163
[TBL] [Abstract][Full Text] [Related]
18. Structure of the genomic sequence comprising the immunoglobulin heavy constant (IGHC) genes from Sus scrofa.
Eguchi-Ogawa T; Toki D; Wertz N; Butler JE; Uenishi H
Mol Immunol; 2012 Oct; 52(3-4):97-107. PubMed ID: 22673207
[TBL] [Abstract][Full Text] [Related]
19. Immunoglobulin constant heavy G subclass chain genes in asthma and allergy.
Oxelius VA
Immunol Res; 2008; 40(2):179-91. PubMed ID: 18213529
[TBL] [Abstract][Full Text] [Related]
20. Major histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency.
Volanakis JE; Zhu ZB; Schaffer FM; Macon KJ; Palermos J; Barger BO; Go R; Campbell RD; Schroeder HW; Cooper MD
J Clin Invest; 1992 Jun; 89(6):1914-22. PubMed ID: 1351062
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
