Bench A - Search Results

1

Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions.

Aziz A, Baxter EJ, Edwards C, Cheong CY, Ito M, Bench A, Kelley R, Silber Y, Beer PA, Chng K, Renfree MB, McEwen K, Gray D, Nangalia J, Mufti GJ, Hellstrom-Lindberg E, Kiladjian JJ, McMullin MF, Campbell PJ, Ferguson-Smith AC, Green AR. Aziz A, et al. Among authors: bench a. J Clin Invest. 2013 May;123(5):2169-82. doi: 10.1172/JCI66113. Epub 2013 Apr 1. J Clin Invest. 2013. PMID: 23543057 Free PMC article.

2

Double jeopardy from a single translocation: deletions of the derivative chromosome 9 in chronic myeloid leukemia.

Huntly BJ, Bench A, Green AR. Huntly BJ, et al. Among authors: bench a. Blood. 2003 Aug 15;102(4):1160-8. doi: 10.1182/blood-2003-01-0123. Epub 2003 May 1. Blood. 2003. PMID: 12730117 Free article. Review.

3

Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies.

Li J, Bench AJ, Vassiliou GS, Fourouclas N, Ferguson-Smith AC, Green AR. Li J, et al. Proc Natl Acad Sci U S A. 2004 May 11;101(19):7341-6. doi: 10.1073/pnas.0308195101. Epub 2004 Apr 30. Proc Natl Acad Sci U S A. 2004. PMID: 15123827 Free PMC article.

4

L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting.

Li J, Bench AJ, Piltz S, Vassiliou G, Baxter EJ, Ferguson-Smith AC, Green AR. Li J, et al. Genomics. 2005 Oct;86(4):489-94. doi: 10.1016/j.ygeno.2005.06.012. Genomics. 2005. PMID: 16081246

5

Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia.

Fourouclas N, Campbell PJ, Bench AJ, Swanton S, Baxter EJ, Huntly BJ, Green AR. Fourouclas N, et al. Haematologica. 2006 Jul;91(7):952-5. Haematologica. 2006. PMID: 16818283

6

Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation.

Campbell PJ, Baxter EJ, Beer PA, Scott LM, Bench AJ, Huntly BJ, Erber WN, Kusec R, Larsen TS, Giraudier S, Le Bousse-Kerdilès MC, Griesshammer M, Reilly JT, Cheung BY, Harrison CN, Green AR. Campbell PJ, et al. Among authors: bench aj. Blood. 2006 Nov 15;108(10):3548-55. doi: 10.1182/blood-2005-12-013748. Epub 2006 Jul 27. Blood. 2006. PMID: 16873677 Free article.

7

Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies.

Bench AJ, Li J, Huntly BJ, Delabesse E, Fourouclas N, Hunt AR, Deloukas P, Green AR. Bench AJ, et al. Br J Haematol. 2004 Dec;127(5):509-18. doi: 10.1111/j.1365-2141.2004.05278.x. Br J Haematol. 2004. PMID: 15566354 Free article.

8

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.

Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, Vassiliou GS, Bench AJ, Boyd EM, Curtin N, Scott MA, Erber WN, Green AR; Cancer Genome Project. Baxter EJ, et al. Among authors: bench aj. Lancet. 2005 Mar 19-25;365(9464):1054-61. doi: 10.1016/S0140-6736(05)71142-9. Lancet. 2005. PMID: 15781101

9

Methods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders.

Campbell PJ, Scott LM, Baxter EJ, Bench AJ, Green AR, Erber WN. Campbell PJ, et al. Methods Mol Med. 2006;125:253-64. doi: 10.1385/1-59745-017-0:253. Methods Mol Med. 2006. PMID: 16502590

10

Clonal diversity in the myeloproliferative neoplasms: independent origins of genetically distinct clones.

Beer PA, Jones AV, Bench AJ, Goday-Fernandez A, Boyd EM, Vaghela KJ, Erber WN, Odeh B, Wright C, McMullin MF, Cullis J, Huntly BJ, Harrison CN, Cross NC, Green AR. Beer PA, et al. Among authors: bench aj. Br J Haematol. 2009 Mar;144(6):904-8. doi: 10.1111/j.1365-2141.2008.07560.x. Epub 2009 Jan 16. Br J Haematol. 2009. PMID: 19170680 Free article.

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