Levinsky R - Search Results

1

The molecular basis of X-linked immunodeficiency disease.

Kinnon C, Levinsky R. Kinnon C, et al. Among authors: levinsky r. J Inherit Metab Dis. 1992;15(4):674-82. doi: 10.1007/BF01799623. J Inherit Metab Dis. 1992. PMID: 1528025 Review.

2

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: levinsky rj. Hum Genet. 1995 Oct;96(4):427-32. doi: 10.1007/BF00191801. Hum Genet. 1995. PMID: 7557965

3

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: levinsky rj. 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.

4

X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox.

Porter CD, Parkar MH, Levinsky RJ, Collins MK, Kinnon C. Porter CD, et al. Among authors: levinsky rj. Blood. 1993 Oct 1;82(7):2196-202. Blood. 1993. PMID: 8400270 Free article.

5

Efficient retroviral transduction of human bone marrow progenitor and long-term culture-initiating cells: partial reconstitution of cells from patients with X-linked chronic granulomatous disease by gp91-phox expression.

Porter CD, Parkar MH, Collins MK, Levinsky RJ, Kinnon C. Porter CD, et al. Among authors: levinsky rj. Blood. 1996 May 1;87(9):3722-30. Blood. 1996. PMID: 8611697 Free article.

6

RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determination.

Pelham A, O'Reilly MA, Malcolm S, Levinsky RJ, Kinnon C. Pelham A, et al. Among authors: levinsky rj. Blood. 1990 Aug 15;76(4):820-4. Blood. 1990. PMID: 1974472 Free article.

7

An additional NsiI RFLP at the X-linked chronic granulomatous disease (CYBB) locus.

Pelham A, Malcolm S, Levinsky RJ, Kinnon C. Pelham A, et al. Among authors: levinsky rj. Nucleic Acids Res. 1990 Dec 11;18(23):7199. doi: 10.1093/nar/18.23.7199. Nucleic Acids Res. 1990. PMID: 1979867 Free PMC article. No abstract available.

8

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector.

Gaspar HB, Parsley KL, Howe S, King D, Gilmour KC, Sinclair J, Brouns G, Schmidt M, Von Kalle C, Barington T, Jakobsen MA, Christensen HO, Al Ghonaium A, White HN, Smith JL, Levinsky RJ, Ali RR, Kinnon C, Thrasher AJ. Gaspar HB, et al. Among authors: levinsky rj. Lancet. 2004 Dec 18-31;364(9452):2181-7. doi: 10.1016/S0140-6736(04)17590-9. Lancet. 2004. PMID: 15610804

9

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. Among authors: levinsky r. Immunodeficiency. 1995;5(3):179-85. Immunodeficiency. 1995. PMID: 7749437 No abstract available.

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: levinsky r. 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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