Wilson DB - Search Results

1

Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome.

Field JJ, Mason PJ, An P, Kasai Y, McLellan M, Jaeger S, Barnes YJ, King AA, Bessler M, Wilson DB. Field JJ, et al. Among authors: wilson db. J Pediatr Hematol Oncol. 2006 Jul;28(7):450-3. doi: 10.1097/01.mph.0000212952.58597.84. J Pediatr Hematol Oncol. 2006. PMID: 16825992

2

Human telomerase RNA mutations and bone marrow failure.

Wilson DB, Ivanovich J, Whelan A, Goodfellow PJ, Bessler M. Wilson DB, et al. Lancet. 2003 Jun 7;361(9373):1993-4. doi: 10.1016/S0140-6736(03)13575-1. Lancet. 2003. PMID: 12801777 No abstract available.

3

Dyskeratosis congenita and telomerase.

Bessler M, Wilson DB, Mason PJ. Bessler M, et al. Among authors: wilson db. Curr Opin Pediatr. 2004 Feb;16(1):23-8. doi: 10.1097/00008480-200402000-00006. Curr Opin Pediatr. 2004. PMID: 14758110 Review.

4

Dyskeratosis congenita -- a disease of dysfunctional telomere maintenance.

Mason PJ, Wilson DB, Bessler M. Mason PJ, et al. Among authors: wilson db. Curr Mol Med. 2005 Mar;5(2):159-70. doi: 10.2174/1566524053586581. Curr Mol Med. 2005. PMID: 15974869 Review.

5

A four base pair insertion in exon 1 of the RPS19 gene is a common polymorphism in African-Americans.

Huang Q, Robledo S, Wilson DB, Bessler M, Mason PJ. Huang Q, et al. Among authors: wilson db. Br J Haematol. 2006 Dec;135(5):745-6. doi: 10.1111/j.1365-2141.2006.06368.x. Br J Haematol. 2006. PMID: 17107358 Free article. No abstract available.

6

Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production.

Idol RA, Robledo S, Du HY, Crimmins DL, Wilson DB, Ladenson JH, Bessler M, Mason PJ. Idol RA, et al. Among authors: wilson db. Blood Cells Mol Dis. 2007 Jul-Aug;39(1):35-43. doi: 10.1016/j.bcmd.2007.02.001. Epub 2007 Mar 21. Blood Cells Mol Dis. 2007. PMID: 17376718

7

Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome.

Du HY, Idol R, Robledo S, Ivanovich J, An P, Londono-Vallejo A, Wilson DB, Mason PJ, Bessler M. Du HY, et al. Among authors: wilson db. Aging Cell. 2007 Oct;6(5):689-97. doi: 10.1111/j.1474-9726.2007.00324.x. Aging Cell. 2007. PMID: 17875000 Free PMC article.

8

Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene.

Du HY, Pumbo E, Manley P, Field JJ, Bayliss SJ, Wilson DB, Mason PJ, Bessler M. Du HY, et al. Among authors: wilson db. Blood. 2008 Feb 1;111(3):1128-30. doi: 10.1182/blood-2007-10-120907. Epub 2007 Nov 27. Blood. 2008. PMID: 18042801 Free PMC article.

9

TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.

Du HY, Pumbo E, Ivanovich J, An P, Maziarz RT, Reiss UM, Chirnomas D, Shimamura A, Vlachos A, Lipton JM, Goyal RK, Goldman F, Wilson DB, Mason PJ, Bessler M. Du HY, et al. Among authors: wilson db. Blood. 2009 Jan 8;113(2):309-16. doi: 10.1182/blood-2008-07-166421. Epub 2008 Oct 17. Blood. 2009. PMID: 18931339 Free PMC article.

10

TINF2 mutations in children with severe aplastic anemia.

Du HY, Mason PJ, Bessler M, Wilson DB. Du HY, et al. Among authors: wilson db. Pediatr Blood Cancer. 2009 May;52(5):687. doi: 10.1002/pbc.21903. Pediatr Blood Cancer. 2009. PMID: 19090550 Free PMC article. No abstract available.

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