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Literature DB >> 9238511

IgA deficiency.

P D Burrows¹, M D Cooper.

Abstract

Entities: Disease

Mesh：

Substances：
Immunoglobulin A

Year: 1997 PMID： 9238511

Source DB: PubMed Journal: Adv Immunol ISSN： 0065-2776 Impact factor: 3.543

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Cited

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39 in total

Review 1. Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID).

Authors: L Hammarström; I Vorechovsky; D Webster
Journal: Clin Exp Immunol Date: 2000-05 Impact factor: 4.330

Review 2. Genetics of IgA deficiency and common variable immunodeficiency.

Authors: H W Schroeder
Journal: Clin Rev Allergy Immunol Date: 2000-10 Impact factor: 8.667

3. Molecular analysis of B-cell differentiation in selective or partial IgA deficiency.

Authors: T Asano; H Kaneko; T Terada; Y Kasahara; T Fukao; K Kasahara; N Kondo
Journal: Clin Exp Immunol Date: 2004-05 Impact factor: 4.330

4. Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

Authors: Ricardo C Ferreira; Qiang Pan-Hammarström; Robert R Graham; Vesela Gateva; Gumersindo Fontán; Annette T Lee; Ward Ortmann; Elena Urcelay; Miguel Fernández-Arquero; Concepción Núñez; Gudmundur Jorgensen; Björn R Ludviksson; Sinikka Koskinen; Katri Haimila; Hilary F Clark; Lars Klareskog; Peter K Gregersen; Timothy W Behrens; Lennart Hammarström
Journal: Nat Genet Date: 2010-08-08 Impact factor: 38.330

5. Increased apoptosis of CD20+ IgA + B cells is the basis for IgA deficiency: the molecular mechanism for correction in vitro by IL-10 and CD40L.

Authors: Zaheed Husain; Nichol Holodick; Caitlin Day; Irma Szymanski; Chester A Alper
Journal: J Clin Immunol Date: 2006-04-26 Impact factor: 8.317

6. IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype.

Authors: Javad Mohammadi; Ryan Ramanujam; Sara Jarefors; Nima Rezaei; Asghar Aghamohammadi; Peter K Gregersen; Lennart Hammarström
Journal: J Clin Immunol Date: 2009-10-16 Impact factor: 8.317

IgA deficiency.

Review 1. Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID).

Review 2. Genetics of IgA deficiency and common variable immunodeficiency.

3. Molecular analysis of B-cell differentiation in selective or partial IgA deficiency.

4. Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

5. Increased apoptosis of CD20+ IgA + B cells is the basis for IgA deficiency: the molecular mechanism for correction in vitro by IL-10 and CD40L.

6. IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype.

7. IL-10 and IL-4 co-operate to normalize in vitro IgA production in IgA-deficient (IgAD) patients.

8. Immunoglobulin subclasses and HLA alleles in immunoglobulin A deficiency.

9. Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity.

10. [Adult-onset primary immunodeficiencies].