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Nicholas C P Cross

Showing results (91-100 of 221) with videos related to

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Genes, Chromosomes & Cancer|January 22, 2008
The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre-mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1Claire Hidalgo-Curtis, Andrew Chase, Milton Drachenberg, et al.
Annals of Hematology|January 23, 2016
Diagnostic challenges in the work up of hypereosinophilia: pitfalls in bone marrow core biopsy interpretationJuliana Schwaab, Mohamad Jawhar, Nicole Naumann, et al.
Blood|December 31, 2002
Imatinib therapy for hypereosinophilic syndrome and other eosinophilic disordersAnimesh Pardanani, Terra Reeder, Luis F Porrata, et al.
Haematologica|April 28, 2010
Transcription factor mutations in myelodysplastic/myeloproliferative neoplasmsThomas Ernst, Andrew Chase, Katerina Zoi, et al.
Leukemia|April 24, 2020
Mutational mechanisms of EZH2 inactivation in myeloid neoplasmsAndrew Chase, Joannah Score, Feng Lin, et al.
Human Molecular Genetics|May 25, 2002
The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRAE Joanna Baxter, Andreas Hochhaus, Pascual Bolufer, et al.
British Journal of Haematology|August 4, 2004
Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemiaJacqueline Boultwood, Andrea Pellagatti, Fiona Watkins, et al.
British Journal of Haematology|June 9, 2007
Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemiaClaire E Curtis, Francis H Grand, Pellegrino Musto, et al.
European Journal of Clinical Investigation|February 26, 2016
Impact of centralized evaluation of bone marrow histology in systemic mastocytosisMohamad Jawhar, Juliana Schwaab, Hans-Peter Horny, et al.
Molecular Biotechnology|April 17, 2007
Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin geneDavid J Bunyan, Alison C Skinner, Emma J Ashton, et al.
Pageof 23

Showing results (91-100 of 221) with videos related to

Sort By:
Pageof 23
Genes, Chromosomes & Cancer|January 22, 2008
The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre-mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1Claire Hidalgo-Curtis, Andrew Chase, Milton Drachenberg, et al.
Annals of Hematology|January 23, 2016
Diagnostic challenges in the work up of hypereosinophilia: pitfalls in bone marrow core biopsy interpretationJuliana Schwaab, Mohamad Jawhar, Nicole Naumann, et al.
Blood|December 31, 2002
Imatinib therapy for hypereosinophilic syndrome and other eosinophilic disordersAnimesh Pardanani, Terra Reeder, Luis F Porrata, et al.
Haematologica|April 28, 2010
Transcription factor mutations in myelodysplastic/myeloproliferative neoplasmsThomas Ernst, Andrew Chase, Katerina Zoi, et al.
Leukemia|April 24, 2020
Mutational mechanisms of EZH2 inactivation in myeloid neoplasmsAndrew Chase, Joannah Score, Feng Lin, et al.
Human Molecular Genetics|May 25, 2002
The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRAE Joanna Baxter, Andreas Hochhaus, Pascual Bolufer, et al.
British Journal of Haematology|August 4, 2004
Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemiaJacqueline Boultwood, Andrea Pellagatti, Fiona Watkins, et al.
British Journal of Haematology|June 9, 2007
Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemiaClaire E Curtis, Francis H Grand, Pellegrino Musto, et al.
European Journal of Clinical Investigation|February 26, 2016
Impact of centralized evaluation of bone marrow histology in systemic mastocytosisMohamad Jawhar, Juliana Schwaab, Hans-Peter Horny, et al.
Molecular Biotechnology|April 17, 2007
Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin geneDavid J Bunyan, Alison C Skinner, Emma J Ashton, et al.
Pageof 23