Smith CI - Search Results

1

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

Vihinen M, Brandau O, Brandén LJ, Kwan SP, Lappalainen I, Lester T, Noordzij JG, Ochs HD, Ollila J, Pienaar SM, Riikonen P, Saha BK, Smith CI. Vihinen M, et al. Among authors: smith ci. Nucleic Acids Res. 1998 Jan 1;26(1):242-7. doi: 10.1093/nar/26.1.242. Nucleic Acids Res. 1998. PMID: 9399844 Free PMC article.

2

Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA).

Zhu Q, Zhang M, Rawlings DJ, Vihinen M, Hagemann T, Saffran DC, Kwan SP, Nilsson L, Smith CI, Witte ON, Chen SH, Ochs HD. Zhu Q, et al. Among authors: smith ci. J Exp Med. 1994 Aug 1;180(2):461-70. doi: 10.1084/jem.180.2.461. J Exp Med. 1994. PMID: 7519238 Free PMC article.

3

Structural basis of SH2 domain mutations in X-linked agammaglobulinemia.

Vihinen M, Nilsson L, Smith CI. Vihinen M, et al. Among authors: smith ci. Biochem Biophys Res Commun. 1994 Dec 15;205(2):1270-7. doi: 10.1006/bbrc.1994.2802. Biochem Biophys Res Commun. 1994. PMID: 7528500

4

Structural basis for X-linked agammaglobulinemia (XLA): mutations at interacting Btk residues R562, W563, and A582.

Maniar HS, Vihinen M, Webster AD, Nilsson L, Smith CI. Maniar HS, et al. Among authors: smith ci. Clin Immunol Immunopathol. 1995 Sep;76(3 Pt 2):S198-202. doi: 10.1016/s0090-1229(95)90216-3. Clin Immunol Immunopathol. 1995. PMID: 7554468

5

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

6

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. Among authors: smith ci. Hum Mol Genet. 1995 Jan;4(1):51-8. doi: 10.1093/hmg/4.1.51. Hum Mol Genet. 1995. PMID: 7711734

7

Structural basis for pleckstrin homology domain mutations in X-linked agammaglobulinemia.

Vihinen M, Zvelebil MJ, Zhu Q, Brooimans RA, Ochs HD, Zegers BJ, Nilsson L, Waterfield MD, Smith CI. Vihinen M, et al. Among authors: smith ci. Biochemistry. 1995 Feb 7;34(5):1475-81. doi: 10.1021/bi00005a002. Biochemistry. 1995. PMID: 7849006

8

Tec homology (TH) adjacent to the PH domain.

Vihinen M, Nilsson L, Smith CI. Vihinen M, et al. Among authors: smith ci. FEBS Lett. 1994 Aug 22;350(2-3):263-5. doi: 10.1016/0014-5793(94)00783-7. FEBS Lett. 1994. PMID: 8070576 Free article.

9

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: smith ci. 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.

10

X-linked agammaglobulinemia (XLA): a genetic tyrosine kinase (Btk) disease.

Mattsson PT, Vihinen M, Smith CI. Mattsson PT, et al. Among authors: smith ci. Bioessays. 1996 Oct;18(10):825-34. doi: 10.1002/bies.950181009. Bioessays. 1996. PMID: 8885720 Review.

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