Molloy G - Search Results

1

Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia.

Raghavan M, Smith LL, Lillington DM, Chaplin T, Kakkas I, Molloy G, Chelala C, Cazier JB, Cavenagh JD, Fitzgibbon J, Lister TA, Young BD. Raghavan M, et al. Among authors: molloy g. Blood. 2008 Aug 1;112(3):814-21. doi: 10.1182/blood-2008-01-132431. Epub 2008 May 19. Blood. 2008. PMID: 18490517 Free article.

2

Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia.

Gupta M, Raghavan M, Gale RE, Chelala C, Allen C, Molloy G, Chaplin T, Linch DC, Cazier JB, Young BD. Gupta M, et al. Among authors: molloy g. Genes Chromosomes Cancer. 2008 Sep;47(9):729-39. doi: 10.1002/gcc.20573. Genes Chromosomes Cancer. 2008. PMID: 18506749

3

Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis.

Purdie KJ, Lambert SR, Teh MT, Chaplin T, Molloy G, Raghavan M, Kelsell DP, Leigh IM, Harwood CA, Proby CM, Young BD. Purdie KJ, et al. Among authors: molloy g. Genes Chromosomes Cancer. 2007 Jul;46(7):661-9. doi: 10.1002/gcc.20447. Genes Chromosomes Cancer. 2007. PMID: 17420988 Free PMC article.

4

Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemia.

Dixon-McIver A, East P, Mein CA, Cazier JB, Molloy G, Chaplin T, Andrew Lister T, Young BD, Debernardi S. Dixon-McIver A, et al. Among authors: molloy g. PLoS One. 2008 May 14;3(5):e2141. doi: 10.1371/journal.pone.0002141. PLoS One. 2008. PMID: 18478077 Free PMC article.

5

Mitotic recombination in haematological malignancy.

Raghavan M, Gupta M, Molloy G, Chaplin T, Young BD. Raghavan M, et al. Among authors: molloy g. Adv Enzyme Regul. 2010;50(1):96-103. doi: 10.1016/j.advenzreg.2009.10.030. Epub 2009 Nov 4. Adv Enzyme Regul. 2010. PMID: 19895835 Review. No abstract available.

6

Genome wide analysis of acute myeloid leukemia reveal leukemia specific methylome and subtype specific hypomethylation of repeats.

Saied MH, Marzec J, Khalid S, Smith P, Down TA, Rakyan VK, Molloy G, Raghavan M, Debernardi S, Young BD. Saied MH, et al. Among authors: molloy g. PLoS One. 2012;7(3):e33213. doi: 10.1371/journal.pone.0033213. Epub 2012 Mar 29. PLoS One. 2012. PMID: 22479372 Free PMC article.

7

MicroRNA miR-181a correlates with morphological sub-class of acute myeloid leukaemia and the expression of its target genes in global genome-wide analysis.

Debernardi S, Skoulakis S, Molloy G, Chaplin T, Dixon-McIver A, Young BD. Debernardi S, et al. Among authors: molloy g. Leukemia. 2007 May;21(5):912-6. doi: 10.1038/sj.leu.2404605. Epub 2007 Mar 1. Leukemia. 2007. PMID: 17330104

8

Rapid high-resolution karyotyping with precise identification of chromosome breakpoints.

Mao X, James SY, Yáñez-Muñoz RJ, Chaplin T, Molloy G, Oliver RT, Young BD, Lu YJ. Mao X, et al. Among authors: molloy g. Genes Chromosomes Cancer. 2007 Jul;46(7):675-83. doi: 10.1002/gcc.20452. Genes Chromosomes Cancer. 2007. PMID: 17431877

9

Trisomy 8 Acute Myeloid Leukemia Analysis Reveals New Insights of DNA Methylome with Identification of HHEX as Potential Diagnostic Marker.

Saied MH, Marzec J, Khalid S, Smith P, Molloy G, Young BD. Saied MH, et al. Among authors: molloy g. Biomark Cancer. 2015 Jan 29;7:1-6. doi: 10.4137/BIC.S19614. eCollection 2015. Biomark Cancer. 2015. PMID: 25674022 Free PMC article.

10

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.

Paulsson K, An Q, Moorman AV, Parker H, Molloy G, Davies T, Griffiths M, Ross FM, Irving J, Harrison CJ, Young BD, Strefford JC. Paulsson K, et al. Among authors: molloy g. Br J Haematol. 2009 Mar;144(6):838-47. doi: 10.1111/j.1365-2141.2008.07523.x. Epub 2008 Dec 19. Br J Haematol. 2009. PMID: 19120349 Free article.

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