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David Vetrie

Showing results (21-30 of 34) with videos related to

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Science Translational Medicine|September 29, 2021
ULK1 inhibition promotes oxidative stress-induced differentiation and sensitizes leukemic stem cells to targeted therapyAngela Ianniciello, Martha M Zarou, Kevin M Rattigan, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Nature Communications|January 21, 2024
Activating p53 abolishes self-renewal of quiescent leukaemic stem cells in residual CML diseaseMary T Scott, Wei Liu, Rebecca Mitchell, et al.
Genome Research|September 12, 2006
Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sitesGeorge A Follows, Pawan Dhami, Berthold Göttgens, et al.
Molecular and Biochemical Parasitology|May 13, 2004
Expression profiling of the Leishmania life cycle: cDNA arrays identify developmentally regulated genes present but not annotated in the genomeRenata Almeida, Brian J Gilmartin, Sharon H McCann, et al.
Cancer Discovery|September 16, 2016
Epigenetic Reprogramming Sensitizes CML Stem Cells to Combined EZH2 and Tyrosine Kinase InhibitionMary T Scott, Koorosh Korfi, Peter Saffrey, et al.
Science (New York, N.Y.)|April 28, 2007
Requirement of bic/microRNA-155 for normal immune functionAntony Rodriguez, Elena Vigorito, Simon Clare, et al.
Plos One|September 3, 2010
Complex exon-intron marking by histone modifications is not determined solely by nucleosome distributionPawandeep Dhami, Peter Saffrey, Alexander W Bruce, et al.
Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Human Mutation|November 16, 2005
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2Patrick G Buckley, Kiran K Mantripragada, Teresita Díaz de Ståhl, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Science Translational Medicine|September 29, 2021
ULK1 inhibition promotes oxidative stress-induced differentiation and sensitizes leukemic stem cells to targeted therapyAngela Ianniciello, Martha M Zarou, Kevin M Rattigan, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Nature Communications|January 21, 2024
Activating p53 abolishes self-renewal of quiescent leukaemic stem cells in residual CML diseaseMary T Scott, Wei Liu, Rebecca Mitchell, et al.
Genome Research|September 12, 2006
Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sitesGeorge A Follows, Pawan Dhami, Berthold Göttgens, et al.
Molecular and Biochemical Parasitology|May 13, 2004
Expression profiling of the Leishmania life cycle: cDNA arrays identify developmentally regulated genes present but not annotated in the genomeRenata Almeida, Brian J Gilmartin, Sharon H McCann, et al.
Cancer Discovery|September 16, 2016
Epigenetic Reprogramming Sensitizes CML Stem Cells to Combined EZH2 and Tyrosine Kinase InhibitionMary T Scott, Koorosh Korfi, Peter Saffrey, et al.
Science (New York, N.Y.)|April 28, 2007
Requirement of bic/microRNA-155 for normal immune functionAntony Rodriguez, Elena Vigorito, Simon Clare, et al.
Plos One|September 3, 2010
Complex exon-intron marking by histone modifications is not determined solely by nucleosome distributionPawandeep Dhami, Peter Saffrey, Alexander W Bruce, et al.
Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Human Mutation|November 16, 2005
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2Patrick G Buckley, Kiran K Mantripragada, Teresita Díaz de Ståhl, et al.
Pageof 4