Vorechovsky I - Search Results

1

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. Eur J Hum Genet. 2001 Aug;9(8):590-8. doi: 10.1038/sj.ejhg.5200688. Eur J Hum Genet. 2001. PMID: 11528504

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

DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemia.

Vorechovský I, Vihinen M, de Saint Basile G, Honsová S, Hammarström L, Müller S, Nilsson L, Fischer A, Smith CI. Vorechovský I, et al. Hum Mol Genet. 1995 Jan;4(1):51-8. doi: 10.1093/hmg/4.1.51. Hum Mol Genet. 1995. PMID: 7711734

6

Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.

Vihinen M, Vetrie D, Maniar HS, Ochs HD, Zhu Q, Vorechovský I, Webster AD, Notarangelo LD, Nilsson L, Sowadski JM, et al. Vihinen M, et al. Among authors: vorechovsky i. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12803-7. doi: 10.1073/pnas.91.26.12803. Proc Natl Acad Sci U S A. 1994. PMID: 7809124 Free PMC article.

7

An intragenic TaqI RFLP at the PAX5 locus.

Vorechovský I, Kozmík Z, Hammarström L, Smith CI, Busslinger M. Vorechovský I, et al. Hum Mol Genet. 1994 Apr;3(4):681. doi: 10.1093/hmg/3.4.681-a. Hum Mol Genet. 1994. PMID: 7915168 No abstract available.

8

SSCP/SacI polymorphism in the PAX5 gene.

Vorechovský I, Kurzbauer R, Kozmík Z, Hammarström L, Smith CI, Busslinger M. Vorechovský I, et al. Hum Mol Genet. 1994 May;3(5):839. doi: 10.1093/hmg/3.5.839. Hum Mol Genet. 1994. PMID: 7915933 No abstract available.

9

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.

10

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

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