McElwaine S - Search Results

1

Functional copy number changes in Sézary syndrome: toward an integrated molecular cytogenetic map III.

Mao X, McElwaine S. Mao X, et al. Among authors: mcelwaine s. Cancer Genet Cytogenet. 2008 Sep;185(2):86-94. doi: 10.1016/j.cancergencyto.2008.05.006. Cancer Genet Cytogenet. 2008. PMID: 18722877

2

Gene expression changes in a zebrafish model of drug dependency suggest conservation of neuro-adaptation pathways.

Kily LJ, Cowe YC, Hussain O, Patel S, McElwaine S, Cotter FE, Brennan CH. Kily LJ, et al. Among authors: mcelwaine s. J Exp Biol. 2008 May;211(Pt 10):1623-34. doi: 10.1242/jeb.014399. J Exp Biol. 2008. PMID: 18456890

3

Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker.

McElwaine S, Mulligan C, Groet J, Spinelli M, Rinaldi A, Denyer G, Mensah A, Cavani S, Baldo C, Dagna-Bricarelli F, Hann I, Basso G, Cotter FE, Nizetic D. McElwaine S, et al. Br J Haematol. 2004 Jun;125(6):729-42. doi: 10.1111/j.1365-2141.2004.04982.x. Br J Haematol. 2004. PMID: 15180862 Free article.

4

Tissue-specific effects of wild-type and mutant connexin 31: a role in neurite outgrowth.

Unsworth HC, Aasen T, McElwaine S, Kelsell DP. Unsworth HC, et al. Among authors: mcelwaine s. Hum Mol Genet. 2007 Jan 15;16(2):165-72. doi: 10.1093/hmg/ddl452. Epub 2006 Dec 1. Hum Mol Genet. 2007. PMID: 17142249

5

Loss-of-function JAK3 mutations in TMD and AMKL of Down syndrome.

De Vita S, Mulligan C, McElwaine S, Dagna-Bricarelli F, Spinelli M, Basso G, Nizetic D, Groet J. De Vita S, et al. Among authors: mcelwaine s. Br J Haematol. 2007 May;137(4):337-41. doi: 10.1111/j.1365-2141.2007.06574.x. Br J Haematol. 2007. PMID: 17456055 Free article.

6

Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder.

Groet J, McElwaine S, Spinelli M, Rinaldi A, Burtscher I, Mulligan C, Mensah A, Cavani S, Dagna-Bricarelli F, Basso G, Cotter FE, Nizetic D. Groet J, et al. Among authors: mcelwaine s. Lancet. 2003 May 10;361(9369):1617-20. doi: 10.1016/S0140-6736(03)13266-7. Lancet. 2003. PMID: 12747884

7

Trinucleotide repeat dynamic mutation identifying susceptibility in familial and sporadic chronic lymphocytic leukaemia.

Auer RL, Dighiero G, Goldin LR, Syndercombe-Court D, Jones C, McElwaine S, Newland AC, Fegan CD, Caporaso N, Cotter FE. Auer RL, et al. Among authors: mcelwaine s. Br J Haematol. 2007 Jan;136(1):73-9. doi: 10.1111/j.1365-2141.2006.06388.x. Epub 2006 Nov 20. Br J Haematol. 2007. PMID: 17116127 Free article.

8

Identification of a potential role for POU2AF1 and BTG4 in the deletion of 11q23 in chronic lymphocytic leukemia.

Auer RL, Starczynski J, McElwaine S, Bertoni F, Newland AC, Fegan CD, Cotter FE. Auer RL, et al. Among authors: mcelwaine s. Genes Chromosomes Cancer. 2005 May;43(1):1-10. doi: 10.1002/gcc.20159. Genes Chromosomes Cancer. 2005. PMID: 15672409

9

Independent clones at separable stages of differentiation, bearing different GATA1 mutations, in the same TMD patient with Down syndrome.

Groet J, Mulligan C, Spinelli M, Serra A, McElwaine S, Cotter FE, Dagna-Bricarelli F, Saglio G, Basso G, Nizetic D. Groet J, et al. Among authors: mcelwaine s. Blood. 2005 Sep 1;106(5):1887-8. doi: 10.1182/blood-2005-03-1071. Blood. 2005. PMID: 16113234 Free article. No abstract available.

10

Role of DNA methylation in the suppression of Apaf-1 protein in human leukaemia.

Fu WN, Bertoni F, Kelsey SM, McElwaine SM, Cotter FE, Newland AC, Jia L. Fu WN, et al. Oncogene. 2003 Jan 23;22(3):451-5. doi: 10.1038/sj.onc.1206147. Oncogene. 2003. PMID: 12545166

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