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Bryan D Young

Showing results (51-60 of 84) with videos related to

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Human Molecular Genetics|December 3, 2003
Replication timing of the human genomeKathryn Woodfine, Heike Fiegler, David M Beare, et al.
American Journal of Cancer Research|October 14, 2011
Chromosome rearrangement associated inactivation of tumour suppressor genes in prostate cancerXueying Mao, Lara K Boyd, Rafael J Yáñez-Muñoz, et al.
Blood|October 20, 2005
AML engraftment in the NOD/SCID assay reflects the outcome of AML: implications for our understanding of the heterogeneity of AMLDaniel J Pearce, David Taussig, Kazem Zibara, et al.
British Journal of Haematology|July 26, 2002
JH probe real-time quantitative polymerase chain reaction assay for Bcl-2/IgH rearrangementsMichael J Jenner, Karin E Summers, Andrew J Norton, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|January 11, 2003
Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemiaChristopher D Dalley, Michael J Neat, Nicola J Foot, 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.
Cancer Research|October 6, 2005
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic eventMuy-Teck Teh, Diana Blaydon, Tracy Chaplin, et al.
Journal of Cutaneous Pathology|May 23, 2008
A genomic and expression study of AP-1 in primary cutaneous T-cell lymphoma: evidence for dysregulated expression of JUNB and JUND in MF and SSXin Mao, Guy Orchard, Tracey J Mitchell, et al.
Genes, Chromosomes & Cancer|September 23, 2008
Integration of genomic and gene expression data of childhood ALL without known aberrations identifies subgroups with specific genetic hallmarksSilvia Bungaro, Marta Campo Dell'Orto, Andrea Zangrando, 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 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|December 3, 2003
Replication timing of the human genomeKathryn Woodfine, Heike Fiegler, David M Beare, et al.
American Journal of Cancer Research|October 14, 2011
Chromosome rearrangement associated inactivation of tumour suppressor genes in prostate cancerXueying Mao, Lara K Boyd, Rafael J Yáñez-Muñoz, et al.
Blood|October 20, 2005
AML engraftment in the NOD/SCID assay reflects the outcome of AML: implications for our understanding of the heterogeneity of AMLDaniel J Pearce, David Taussig, Kazem Zibara, et al.
British Journal of Haematology|July 26, 2002
JH probe real-time quantitative polymerase chain reaction assay for Bcl-2/IgH rearrangementsMichael J Jenner, Karin E Summers, Andrew J Norton, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|January 11, 2003
Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemiaChristopher D Dalley, Michael J Neat, Nicola J Foot, 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.
Cancer Research|October 6, 2005
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic eventMuy-Teck Teh, Diana Blaydon, Tracy Chaplin, et al.
Journal of Cutaneous Pathology|May 23, 2008
A genomic and expression study of AP-1 in primary cutaneous T-cell lymphoma: evidence for dysregulated expression of JUNB and JUND in MF and SSXin Mao, Guy Orchard, Tracey J Mitchell, et al.
Genes, Chromosomes & Cancer|September 23, 2008
Integration of genomic and gene expression data of childhood ALL without known aberrations identifies subgroups with specific genetic hallmarksSilvia Bungaro, Marta Campo Dell'Orto, Andrea Zangrando, 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 9