Vorechovsky I - Search Results

1

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

2

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

3

Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia.

Lovering RC, Sweatman A, Genet SA, Middleton-Price HR, Vetrie D, Vorechovsky I, Bentley D, Fontan G, Español T, Morgan G, et al. Lovering RC, et al. Among authors: vorechovsky i. Hum Genet. 1994 Jul;94(1):77-9. doi: 10.1007/BF02272846. Hum Genet. 1994. PMID: 8034298

4

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

5

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.

6

Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia.

Vorechovský I, Luo L, Hertz JM, Frøland SS, Klemola T, Fiorini M, Quinti I, Paganelli R, Ozsahin H, Hammarström L, Webster AD, Smith CI. Vorechovský I, et al. Hum Mutat. 1997;9(5):418-25. doi: 10.1002/(SICI)1098-1004(1997)9:5<418::AID-HUMU7>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9143921

7

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.

8

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.

9

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.

Thomas JD, Sideras P, Smith CI, Vorechovský I, Chapman V, Paul WE. Thomas JD, et al. Among authors: vorechovsky i. Science. 1993 Jul 16;261(5119):355-8. doi: 10.1126/science.8332900. Science. 1993. PMID: 8332900

10

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

Vihinen M, Iwata T, Kinnon C, Kwan SP, Ochs HD, Vorechovský I, Smith CI. Vihinen M, et al. Among authors: vorechovsky i. Nucleic Acids Res. 1996 Jan 1;24(1):160-5. doi: 10.1093/nar/24.1.160. Nucleic Acids Res. 1996. PMID: 8594569 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

129 results

Search Page