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Sharon Zeligson

Showing results (11-20 of 37) with videos related to

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Plos One|August 1, 2015
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) RepairInbal Gazy, David A Zeevi, Paul Renbaum, et al.
Journal of Medical Genetics|March 10, 2022
Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcomeHagit Daum, Reeval Segel, Vardiella Meiner, et al.
Molecular Genetics and Genomics : MGG|April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangementsRachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Plos One|October 17, 2015
Establishment of Homozygote Mutant Human Embryonic Stem Cells by ParthenogenesisSilvina Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, et al.
Scientific Reports|October 21, 2023
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testingDaniel Backenroth, Gheona Altarescu, Fouad Zahdeh, et al.
Cancer Journal (Sudbury, Mass.)|October 9, 2007
Mechanisms operative in the antitumor activity of temozolomide in glioblastoma multiformeTamar Fisher, Gil Galanti, Gad Lavie, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.
Plos One|January 26, 2013
Snord 3A: a molecular marker and modulator of prion disease progressionEran Cohen, Dana Avrahami, Kati Frid, et al.
Journal of Medical Genetics|June 14, 2015
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stressAriella Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, et al.
Molecular Immunology|April 7, 2006
Identification of IRF-8 and IRF-1 target genes in activated macrophagesNatalie Dror, Michal Alter-Koltunoff, Aviva Azriel, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Plos One|August 1, 2015
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) RepairInbal Gazy, David A Zeevi, Paul Renbaum, et al.
Journal of Medical Genetics|March 10, 2022
Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcomeHagit Daum, Reeval Segel, Vardiella Meiner, et al.
Molecular Genetics and Genomics : MGG|April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangementsRachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Plos One|October 17, 2015
Establishment of Homozygote Mutant Human Embryonic Stem Cells by ParthenogenesisSilvina Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, et al.
Scientific Reports|October 21, 2023
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testingDaniel Backenroth, Gheona Altarescu, Fouad Zahdeh, et al.
Cancer Journal (Sudbury, Mass.)|October 9, 2007
Mechanisms operative in the antitumor activity of temozolomide in glioblastoma multiformeTamar Fisher, Gil Galanti, Gad Lavie, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.
Plos One|January 26, 2013
Snord 3A: a molecular marker and modulator of prion disease progressionEran Cohen, Dana Avrahami, Kati Frid, et al.
Journal of Medical Genetics|June 14, 2015
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stressAriella Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, et al.
Molecular Immunology|April 7, 2006
Identification of IRF-8 and IRF-1 target genes in activated macrophagesNatalie Dror, Michal Alter-Koltunoff, Aviva Azriel, et al.
Pageof 4