Vorechovsky I - Search Results

1

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. Kralovicova J, et al. Among authors: vorechovsky i. J Immunol. 2003 Mar 1;170(5):2765-75. doi: 10.4049/jimmunol.170.5.2765. J Immunol. 2003. PMID: 12594308

2

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. Clin Immunol Immunopathol. 1995 Nov;77(2):185-92. doi: 10.1006/clin.1995.1142. Clin Immunol Immunopathol. 1995. PMID: 7586726

3

The PAX5 gene: a linkage and mutation analysis in candidate human primary immunodeficiencies.

Vorechovský I, Koskinen S, Paganelli R, Smith CI, Busslinger M, Hammarström L. Vorechovský I, et al. Immunogenetics. 1995;42(2):149-52. doi: 10.1007/BF00178590. Immunogenetics. 1995. PMID: 7607706 No abstract available.

4

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: vorechovsky i. Hum Mol Genet. 1995 Apr;4(4):693-700. doi: 10.1093/hmg/4.4.693. Hum Mol Genet. 1995. PMID: 7633420

5

X-linked agammaglobulinemia and other immunoglobulin deficiencies.

Smith CI, Islam KB, Vorechovský I, Olerup O, Wallin E, Rabbani H, Baskin B, Hammarström L. Smith CI, et al. Among authors: vorechovsky i. Immunol Rev. 1994 Apr;138:159-83. doi: 10.1111/j.1600-065x.1994.tb00851.x. Immunol Rev. 1994. PMID: 8070814 Review. No abstract available.

6

Molecular diagnosis of X-linked agammaglobulinaemia.

Vorechovsky I, Zhou JN, Vetrie D, Bentley D, Björkander J, Hammarström L, Smith CI. Vorechovsky I, et al. Lancet. 1993 May 1;341(8853):1153. doi: 10.1016/0140-6736(93)93172-w. Lancet. 1993. PMID: 8097835 No abstract available.

7

Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.

Vorechovský I, Holland J, Sideras P, Dunham I, Hammarström L, Smith CI, Bentley DR, Vetrie D. Vorechovský I, et al. Immunodeficiency. 1993;4(1-4):221-4. Immunodeficiency. 1993. PMID: 8167705

8

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.

Vetrie D, Vorechovský I, Sideras P, Holland J, Davies A, Flinter F, Hammarström L, Kinnon C, Levinsky R, Bobrow M, et al. Vetrie D, et al. Among authors: vorechovsky i. Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0. Nature. 1993. PMID: 8380905

9

Genetics of IgA deficiency.

Truedsson L, Baskin B, Pan Q, Rabbani H, Vorĕchovský I, Smith CI, Hammarström L. Truedsson L, et al. Among authors: vorechovsky i. APMIS. 1995 Dec;103(12):833-42. doi: 10.1111/j.1699-0463.1995.tb01442.x. APMIS. 1995. PMID: 8562023 Review.

10

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. 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.

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