Dokal I - Search Results

1

Sbarrato T, Horvilleur E, Pöyry T, Hill K, Chaplin LC, Spriggs RV, Stoneley M, Wilson L, Jayne S, Vulliamy T, Beck D, Dokal I, Dyer MJ, Yeomans AM, Packham G, Bushell M, Wagner SD, Willis AE. Sbarrato T, et al. Among authors: dokal i. Cell Death Dis. 2016 Jun 2;7(6):e2249. doi: 10.1038/cddis.2016.148. Cell Death Dis. 2016. PMID: 27253413 Free PMC article.

2

Fine mapping of the dyskeratosis congenita locus in Xq28.

Knight SW, Vulliamy T, Forni GL, Oscier D, Mason PJ, Dokal I. Knight SW, et al. Among authors: dokal i. J Med Genet. 1996 Dec;33(12):993-5. doi: 10.1136/jmg.33.12.993. J Med Genet. 1996. PMID: 9004129 Free PMC article.

3

Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.

Vulliamy TJ, Knight SW, Dokal I, Mason PJ. Vulliamy TJ, et al. Among authors: dokal i. Blood. 1997 Sep 15;90(6):2213-6. Blood. 1997. PMID: 9310472 Free article.

4

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.

Heiss NS, Knight SW, Vulliamy TJ, Klauck SM, Wiemann S, Mason PJ, Poustka A, Dokal I. Heiss NS, et al. Among authors: dokal i. Nat Genet. 1998 May;19(1):32-8. doi: 10.1038/ng0598-32. Nat Genet. 1998. PMID: 9590285

5

1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis.

Knight SW, Vulliamy TJ, Heiss NS, Matthijs G, Devriendt K, Connor JM, D'Urso M, Poustka A, Mason PJ, Dokal I. Knight SW, et al. Among authors: dokal i. J Med Genet. 1998 Dec;35(12):993-6. doi: 10.1136/jmg.35.12.993. J Med Genet. 1998. PMID: 9863595 Free PMC article.

6

Dyskeratosis Congenita (DC) Registry: identification of new features of DC.

Knight S, Vulliamy T, Copplestone A, Gluckman E, Mason P, Dokal I. Knight S, et al. Among authors: dokal i. Br J Haematol. 1998 Dec;103(4):990-6. doi: 10.1046/j.1365-2141.1998.01103.x. Br J Haematol. 1998. PMID: 9886310 Free article.

7

X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.

Knight SW, Heiss NS, Vulliamy TJ, Greschner S, Stavrides G, Pai GS, Lestringant G, Varma N, Mason PJ, Dokal I, Poustka A. Knight SW, et al. Among authors: dokal i. Am J Hum Genet. 1999 Jul;65(1):50-8. doi: 10.1086/302446. Am J Hum Genet. 1999. PMID: 10364516 Free PMC article.

8

Dyskeratosis congenita caused by a 3' deletion: germline and somatic mosaicism in a female carrier.

Vulliamy TJ, Knight SW, Heiss NS, Smith OP, Poustka A, Dokal I, Mason PJ. Vulliamy TJ, et al. Among authors: dokal i. Blood. 1999 Aug 15;94(4):1254-60. Blood. 1999. PMID: 10438713 Free article.

9

Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformation.

McCloy M, Almeida A, Daly P, Vulliamy T, Roberts IA, Dokal I. McCloy M, et al. Among authors: dokal i. Br J Haematol. 2001 Feb;112(2):427-9. doi: 10.1046/j.1365-2141.2001.02585.x. Br J Haematol. 2001. PMID: 11167843 Free article.

10

Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita.

Vulliamy TJ, Knight SW, Mason PJ, Dokal I. Vulliamy TJ, et al. Among authors: dokal i. Blood Cells Mol Dis. 2001 Mar-Apr;27(2):353-7. doi: 10.1006/bcmd.2001.0389. Blood Cells Mol Dis. 2001. PMID: 11259155

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