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Literature DB >> 8070814

X-linked agammaglobulinemia and other immunoglobulin deficiencies.

C I Smith¹, K B Islam, I Vorechovský, O Olerup, E Wallin, H Rabbani, B Baskin, L Hammarström.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1994 PMID： 8070814 DOI： 10.1111/j.1600-065x.1994.tb00851.x

Source DB: PubMed Journal: Immunol Rev ISSN： 0105-2896 Impact factor: 12.988

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21 in total

1. Solution structure of the human BTK SH3 domain complexed with a proline-rich peptide from p120cbl.

Authors: S R Tzeng; Y C Lou; M T Pai; M L Jain; J W Cheng
Journal: J Biomol NMR Date: 2000-04 Impact factor: 2.835

2. Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.

Authors: Alejandro A Schäffer; Jessica Pfannstiel; A David B Webster; Alessandro Plebani; Lennart Hammarström; Bodo Grimbacher
Journal: Hum Genet Date: 2005-11-22 Impact factor: 4.132

Review 3. X-linked agammaglobulinemia: lack of mature B lineage cells caused by mutations in the Btk kinase.

Authors: C I Smith; C M Bäckesjö; A Berglöf; L J Brandén; T Islam; P T Mattsson; A J Mohamed; S Müller; B Nore; M Vihinen
Journal: Springer Semin Immunopathol Date: 1998

Review 4. Immunity, infection, and nasal disease.

Authors: S H Yoshida; M E Gershwin
Journal: Clin Rev Allergy Immunol Date: 1998 Spring-Summer Impact factor: 8.667

5. A novel Tth111I restriction fragment length polymorphism (RFLP) allows tracing of X-chromosome inactivation in the (Xid) heterozygote.

Authors: V Shanmugam; V M Chapman; K W Sell; B K Saha
Journal: Biochem Genet Date: 1996-02 Impact factor: 1.890

X-linked agammaglobulinemia and other immunoglobulin deficiencies.

1. Solution structure of the human BTK SH3 domain complexed with a proline-rich peptide from p120cbl.

2. Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.

Review 3. X-linked agammaglobulinemia: lack of mature B lineage cells caused by mutations in the Btk kinase.

Review 4. Immunity, infection, and nasal disease.

5. A novel Tth111I restriction fragment length polymorphism (RFLP) allows tracing of X-chromosome inactivation in the (Xid) heterozygote.

6. BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

7. Stability and peptide binding specificity of Btk SH2 domain: molecular basis for X-linked agammaglobulinemia.

8. Conformation of full-length Bruton tyrosine kinase (Btk) from synchrotron X-ray solution scattering.

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

10. Clinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients.