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Gael Molloy

Showing results (1-10 of 8) with videos related to

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Biomarkers in Cancer|February 13, 2015
Trisomy 8 Acute Myeloid Leukemia Analysis Reveals New Insights of DNA Methylome with Identification of HHEX as Potential Diagnostic MarkerMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
Genes, Chromosomes & Cancer|April 14, 2007
Rapid high-resolution karyotyping with precise identification of chromosome breakpointsXueying Mao, Sharon Y James, Rafael J Yáñez-Muñoz, et al.
Plos One|May 15, 2008
Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemiaAmanda Dixon-McIver, Phil East, Charles A Mein, et al.
Genes, Chromosomes & Cancer|May 29, 2008
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemiaManu Gupta, Manoj Raghavan, Rosemary E Gale, et al.
Plos One|April 6, 2012
Genome wide analysis of acute myeloid leukemia reveal leukemia specific methylome and subtype specific hypomethylation of repeatsMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
British Journal of Haematology|January 6, 2009
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemiaKajsa Paulsson, Qian An, Anthony V Moorman, et al.
Genes, Chromosomes & Cancer|April 11, 2007
Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysisKarin J Purdie, Sally R Lambert, Muy-Teck Teh, et al.
Blood|May 21, 2008
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemiaManoj Raghavan, Lan-Lan Smith, Debra M Lillington, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Biomarkers in Cancer|February 13, 2015
Trisomy 8 Acute Myeloid Leukemia Analysis Reveals New Insights of DNA Methylome with Identification of HHEX as Potential Diagnostic MarkerMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
Genes, Chromosomes & Cancer|April 14, 2007
Rapid high-resolution karyotyping with precise identification of chromosome breakpointsXueying Mao, Sharon Y James, Rafael J Yáñez-Muñoz, et al.
Plos One|May 15, 2008
Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemiaAmanda Dixon-McIver, Phil East, Charles A Mein, et al.
Genes, Chromosomes & Cancer|May 29, 2008
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemiaManu Gupta, Manoj Raghavan, Rosemary E Gale, et al.
Plos One|April 6, 2012
Genome wide analysis of acute myeloid leukemia reveal leukemia specific methylome and subtype specific hypomethylation of repeatsMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
British Journal of Haematology|January 6, 2009
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemiaKajsa Paulsson, Qian An, Anthony V Moorman, et al.
Genes, Chromosomes & Cancer|April 11, 2007
Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysisKarin J Purdie, Sally R Lambert, Muy-Teck Teh, et al.
Blood|May 21, 2008
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemiaManoj Raghavan, Lan-Lan Smith, Debra M Lillington, et al.
Pageof 1