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Ramon Y Birnbaum

Showing results (11-20 of 28) with videos related to

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Journal of Medical Genetics|November 8, 2015
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCNYonatan Perez, Rotem Kadir, Michael Volodarsky, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesisShai Adar-Levor, Dikla Nachmias, Shani T Gal-Oz, et al.
BMC Medical Genetics|December 22, 2011
Association analysis identifies ZNF750 regulatory variants in psoriasisRamon Y Birnbaum, Genki Hayashi, Idan Cohen, et al.
Plos Genetics|October 30, 2018
Unraveling the transcriptional regulation of TWIST1 in limb developmentNaama Hirsch, Reut Eshel, Reut Bar Yaacov, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
Human Molecular Genetics|February 8, 2020
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristicsEva D'haene, Reut Bar-Yaacov, Inbar Bariah, et al.
Human Molecular Genetics|November 17, 2018
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristicsEva D'haene, Reut Bar-Yaacov, Inbar Bariah, et al.
Plos Genetics|October 24, 2014
Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulationRamon Y Birnbaum, Rupali P Patwardhan, Mee J Kim, et al.
Stem Cell Reports|July 21, 2015
Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem CellsShira Yanovsky-Dagan, Michal Avitzour, Gheona Altarescu, et al.
Plos Genetics|March 24, 2016
ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain SizeRotem Kadir, Tamar Harel, Barak Markus, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|November 8, 2015
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCNYonatan Perez, Rotem Kadir, Michael Volodarsky, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesisShai Adar-Levor, Dikla Nachmias, Shani T Gal-Oz, et al.
BMC Medical Genetics|December 22, 2011
Association analysis identifies ZNF750 regulatory variants in psoriasisRamon Y Birnbaum, Genki Hayashi, Idan Cohen, et al.
Plos Genetics|October 30, 2018
Unraveling the transcriptional regulation of TWIST1 in limb developmentNaama Hirsch, Reut Eshel, Reut Bar Yaacov, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
Human Molecular Genetics|February 8, 2020
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristicsEva D'haene, Reut Bar-Yaacov, Inbar Bariah, et al.
Human Molecular Genetics|November 17, 2018
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristicsEva D'haene, Reut Bar-Yaacov, Inbar Bariah, et al.
Plos Genetics|October 24, 2014
Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulationRamon Y Birnbaum, Rupali P Patwardhan, Mee J Kim, et al.
Stem Cell Reports|July 21, 2015
Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem CellsShira Yanovsky-Dagan, Michal Avitzour, Gheona Altarescu, et al.
Plos Genetics|March 24, 2016
ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain SizeRotem Kadir, Tamar Harel, Barak Markus, et al.
Pageof 3