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F RAPPAPORT

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

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Pediatric Blood & Cancer|September 22, 2021
KMT2A-MAML2 rearrangement emerged and regressed during neuroblastoma therapy without leukemia after 12.8-year follow-upCarolyn A Felix, Diana J Slater, James W Davenport, et al.
Human Mutation|December 2, 2010
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndromeTracy Busse, John M Graham, Gerald Feldman, et al.
Discovery Medicine|January 1, 2013
Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genomeMarni J Falk, Eric A Pierce, Mark Consugar, et al.
BMC Bioinformatics|February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnosticsXiaowu Gai, Juan C Perin, Kevin Murphy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 20, 2007
De novo identification of MIZ-1 (ZBTB17) encoding a MYC-interacting zinc-finger protein as a new favorable neuroblastoma geneNaohiko Ikegaki, Takahiro Gotoh, Bing Kung, et al.
Stem Cells and Development|March 14, 2007
Identification of cord blood-derived mesenchymal stem/stromal cell populations with distinct growth kinetics, differentiation potentials, and gene expression profilesVladimir Markov, Kenro Kusumi, Mahlet G Tadesse, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2000
Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genesM D Megonigal, E F Rappaport, R B Wilson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2001
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocationB D Lovett, L Lo Nigro, E F Rappaport, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 4, 2002
Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions of MLL translocations and identify complex translocation of MLL, AF-4, and CDK6Leslie J Raffini, Diana J Slater, Eric F Rappaport, et al.
Developmental Biology|March 17, 2007
Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell modelDilusha A William, Biagio Saitta, Joshua D Gibson, et al.
Pageof 9

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

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Pageof 9
Pediatric Blood & Cancer|September 22, 2021
KMT2A-MAML2 rearrangement emerged and regressed during neuroblastoma therapy without leukemia after 12.8-year follow-upCarolyn A Felix, Diana J Slater, James W Davenport, et al.
Human Mutation|December 2, 2010
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndromeTracy Busse, John M Graham, Gerald Feldman, et al.
Discovery Medicine|January 1, 2013
Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genomeMarni J Falk, Eric A Pierce, Mark Consugar, et al.
BMC Bioinformatics|February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnosticsXiaowu Gai, Juan C Perin, Kevin Murphy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 20, 2007
De novo identification of MIZ-1 (ZBTB17) encoding a MYC-interacting zinc-finger protein as a new favorable neuroblastoma geneNaohiko Ikegaki, Takahiro Gotoh, Bing Kung, et al.
Stem Cells and Development|March 14, 2007
Identification of cord blood-derived mesenchymal stem/stromal cell populations with distinct growth kinetics, differentiation potentials, and gene expression profilesVladimir Markov, Kenro Kusumi, Mahlet G Tadesse, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2000
Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genesM D Megonigal, E F Rappaport, R B Wilson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2001
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocationB D Lovett, L Lo Nigro, E F Rappaport, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 4, 2002
Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions of MLL translocations and identify complex translocation of MLL, AF-4, and CDK6Leslie J Raffini, Diana J Slater, Eric F Rappaport, et al.
Developmental Biology|March 17, 2007
Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell modelDilusha A William, Biagio Saitta, Joshua D Gibson, et al.
Pageof 9