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Dolev Rahat

Showing results (1-10 of 8) with videos related to

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Scientific Reports|August 31, 2018
Schlafen2 mutation in mice causes an osteopetrotic phenotype due to a decrease in the number of osteoclast progenitorsIbrahim Omar, Gali Guterman-Ram, Dolev Rahat, et al.
Current Neurology and Neuroscience Reports|August 24, 2019
MYORG Mutations: a Major Cause of Recessive Primary Familial Brain CalcificationMax Bauer, Dolev Rahat, Elad Zisman, et al.
Neurogenetics|April 3, 2021
Multi-system neurological disorder associated with a CRYAB variantMenachem Sadeh, Dolev Rahat, Vardiella Meiner, et al.
Annals of Clinical and Translational Neurology|January 19, 2019
<i>MYORG</i> is associated with recessive primary familial brain calcificationDavid Arkadir, Alexander Lossos, Dolev Rahat, et al.
Genome Research|February 6, 2019
Mapping global and local coevolution across 600 species to identify novel homologous recombination repair genesDana Sherill-Rofe, Dolev Rahat, Steven Findlay, et al.
NAR Cancer|April 11, 2022
Multi-omics data integration analysis identifies the spliceosome as a key regulator of DNA double-strand break repairDana Sherill-Rofe, Oded Raban, Steven Findlay, et al.
Molecular Cell|November 8, 2018
UV-Protection Timer Controls Linkage between Stress and Pigmentation Skin Protection SystemsHagar Malcov-Brog, Ayelet Alpert, Tamar Golan, et al.
The EMBO Journal|August 30, 2018
SHLD2/FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choiceSteven Findlay, John Heath, Vincent M Luo, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Scientific Reports|August 31, 2018
Schlafen2 mutation in mice causes an osteopetrotic phenotype due to a decrease in the number of osteoclast progenitorsIbrahim Omar, Gali Guterman-Ram, Dolev Rahat, et al.
Current Neurology and Neuroscience Reports|August 24, 2019
MYORG Mutations: a Major Cause of Recessive Primary Familial Brain CalcificationMax Bauer, Dolev Rahat, Elad Zisman, et al.
Neurogenetics|April 3, 2021
Multi-system neurological disorder associated with a CRYAB variantMenachem Sadeh, Dolev Rahat, Vardiella Meiner, et al.
Annals of Clinical and Translational Neurology|January 19, 2019
<i>MYORG</i> is associated with recessive primary familial brain calcificationDavid Arkadir, Alexander Lossos, Dolev Rahat, et al.
Genome Research|February 6, 2019
Mapping global and local coevolution across 600 species to identify novel homologous recombination repair genesDana Sherill-Rofe, Dolev Rahat, Steven Findlay, et al.
NAR Cancer|April 11, 2022
Multi-omics data integration analysis identifies the spliceosome as a key regulator of DNA double-strand break repairDana Sherill-Rofe, Oded Raban, Steven Findlay, et al.
Molecular Cell|November 8, 2018
UV-Protection Timer Controls Linkage between Stress and Pigmentation Skin Protection SystemsHagar Malcov-Brog, Ayelet Alpert, Tamar Golan, et al.
The EMBO Journal|August 30, 2018
SHLD2/FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choiceSteven Findlay, John Heath, Vincent M Luo, et al.
Pageof 1