Webster AD - Search Results

1

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

Salzer U, Chapel HM, Webster AD, Pan-Hammarström Q, Schmitt-Graeff A, Schlesier M, Peter HH, Rockstroh JK, Schneider P, Schäffer AA, Hammarström L, Grimbacher B. Salzer U, et al. Among authors: webster ad. Nat Genet. 2005 Aug;37(8):820-8. doi: 10.1038/ng1600. Epub 2005 Jul 10. Nat Genet. 2005. PMID: 16007087

2

Improved oligonucleotide primer set for molecular diagnosis of X-linked agammaglobulinaemia: predominance of amino acid substitutions in the catalytic domain of Bruton's tyrosine kinase.

Vorechovský I, Luo L, de Saint Basile G, Hammarström L, Webster AD, Smith CI. Vorechovský I, et al. Among authors: webster ad. Hum Mol Genet. 1995 Dec;4(12):2403-5. doi: 10.1093/hmg/4.12.2403. Hum Mol Genet. 1995. PMID: 8634718 No abstract available.

3

Mapping genes underlying complex disorders: progress on IgA deficiency and common variable immunodeficiency.

Vorechovsky I, Webster AD, Hammarstrom L. Vorechovsky I, et al. Among authors: webster ad. Adv Exp Med Biol. 2001;495:183-90. doi: 10.1007/978-1-4615-0685-0_25. Adv Exp Med Biol. 2001. PMID: 11774565 Review. No abstract available.

4

Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia.

Vorechovský I, Luo L, Dyer MJ, Catovsky D, Amlot PL, Yaxley JC, Foroni L, Hammarström L, Webster AD, Yuille MA. Vorechovský I, et al. Among authors: webster ad. Nat Genet. 1997 Sep;17(1):96-9. doi: 10.1038/ng0997-96. Nat Genet. 1997. PMID: 9288106

5

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. Vorechovský I, et al. Among authors: webster ad. J Immunol. 2000 Apr 15;164(8):4408-16. doi: 10.4049/jimmunol.164.8.4408. J Immunol. 2000. PMID: 10754342

6

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. Vorechovský I, et al. Among authors: webster ad. Clin Immunol Immunopathol. 1995 Nov;77(2):185-92. doi: 10.1006/clin.1995.1142. Clin Immunol Immunopathol. 1995. PMID: 7586726

7

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. Vorechovský I, et al. Among authors: webster ad. Am J Hum Genet. 1999 Apr;64(4):1096-109. doi: 10.1086/302326. Am J Hum Genet. 1999. PMID: 10090895 Free PMC article.

8

ATM mutations in cancer families.

Vorechovský I, Luo L, Lindblom A, Negrini M, Webster AD, Croce CM, Hammarström L. Vorechovský I, et al. Among authors: webster ad. Cancer Res. 1996 Sep 15;56(18):4130-3. Cancer Res. 1996. PMID: 8797579

9

Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA).

Jin H, Webster AD, Vihinen M, Sideras P, Vorechovsky I, Hammarstróm L, Bernatowska-Matuszkiewicz E, Smith CI, Bobrow M, Vetrie D. Jin H, et al. Among authors: webster ad. Hum Mol Genet. 1995 Apr;4(4):693-700. doi: 10.1093/hmg/4.4.693. Hum Mol Genet. 1995. PMID: 7633420

10

Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region.

Vorechovsky I, Kralovicova J, Laycock MD, Webster AD, Marsh SG, Madrigal A, Hammarström L. Vorechovsky I, et al. Among authors: webster ad. Eur J Hum Genet. 2001 Aug;9(8):590-8. doi: 10.1038/sj.ejhg.5200688. Eur J Hum Genet. 2001. PMID: 11528504

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