Kinnon C - Search Results

1

Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis.

Bradley LA, Sweatman AK, Lovering RC, Jones AM, Morgan G, Levinsky RJ, Kinnon C. Bradley LA, et al. Among authors: kinnon c. Hum Mol Genet. 1994 Jan;3(1):79-83. doi: 10.1093/hmg/3.1.79. Hum Mol Genet. 1994. PMID: 8162056

2

Identification of CpG islands around the DXS178 locus in the region of the X-linked agammaglobulinaemia gene locus in Xq22.

O'Reilly MA, Alterman LA, Malcolm S, Levinsky RJ, Kinnon C. O'Reilly MA, et al. Among authors: kinnon c. Hum Genet. 1992 Nov;90(3):275-8. doi: 10.1007/BF00220078. Hum Genet. 1992. PMID: 1487242

3

Gene therapy for cancer.

Kinnon C, Levinsky RJ. Kinnon C, et al. Eur J Cancer. 1990;26(5):638-40. doi: 10.1016/0277-5379(90)90096-c. Eur J Cancer. 1990. PMID: 2169279 Review. No abstract available.

4

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.

Clark PA, Lester T, Genet S, Jones AM, Hendriks R, Levinsky RJ, Kinnon C. Clark PA, et al. Among authors: kinnon c. Hum Genet. 1995 Oct;96(4):427-32. doi: 10.1007/BF00191801. Hum Genet. 1995. PMID: 7557965

5

Mutation analysis in Bruton's tyrosine kinase, the X-linked agammaglobulinaemia gene, including identification of an insertional hotspot.

Gaspar HB, Bradley LA, Katz F, Lovering RC, Roifman CM, Morgan G, Levinsky RJ, Kinnon C. Gaspar HB, et al. Among authors: kinnon c. Hum Mol Genet. 1995 Apr;4(4):755-7. doi: 10.1093/hmg/4.4.755. Hum Mol Genet. 1995. PMID: 7633429 No abstract available.

6

The protein defective in X-linked agammaglobulinemia, Bruton's tyrosine kinase, shows increased autophosphorylation activity in vitro when isolated from cells in which the B cell receptor has been cross-linked.

Hinshelwood S, Lovering RC, Genevier HC, Levinsky RJ, Kinnon C. Hinshelwood S, et al. Among authors: kinnon c. Eur J Immunol. 1995 Apr;25(4):1113-6. doi: 10.1002/eji.1830250439. Eur J Immunol. 1995. PMID: 7737282

7

Physical and genetic approaches to the isolation of the gene for X-linked agammaglobulinemia.

Kinnon C, Lovering R, O'Reilly MA, Sweatman A, Bradley L, Parkar M, Alterman L, Levinsky R. Kinnon C, et al. Immunodeficiency. 1995;5(3):179-85. Immunodeficiency. 1995. PMID: 7749437 No abstract available.

8

Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

Lester T, de Alwis M, Clark PA, Jones AM, Katz F, Levinsky RJ, Kinnon C. Lester T, et al. Among authors: kinnon c. J Med Genet. 1994 Sep;31(9):717-20. doi: 10.1136/jmg.31.9.717. J Med Genet. 1994. PMID: 7815443 Free PMC article.

9

Physical mapping in the region of the Bruton's tyrosine kinase and alpha-galactosidase A gene loci in proximal Xq22.

Sweatman AK, Bradley LA, Lovering RC, O'Reilly MA, Levinsky RJ, Kinnon C. Sweatman AK, et al. Among authors: kinnon c. Hum Genet. 1994 Dec;94(6):624-8. doi: 10.1007/BF00206955. Hum Genet. 1994. PMID: 7989038

10

A new restriction fragment length polymorphism at the DXS101 locus allows carrier detection in a family with X linked agammaglobulinaemia.

Sweatman A, Lovering R, Middleton-Price H, Jones A, Morgan G, Levinsky R, Kinnon C. Sweatman A, et al. Among authors: kinnon c. J Med Genet. 1993 Jun;30(6):512-4. doi: 10.1136/jmg.30.6.512. J Med Genet. 1993. PMID: 8100857 Free PMC article.

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