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Hagar Mor-Shaked

Showing results (1-10 of 52) with videos related to

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Frontiers in Molecular Neuroscience|February 23, 2018
Reevaluation of <i>FMR1</i> Hypermethylation Timing in Fragile X SyndromeHagar Mor-Shaked, Rachel Eiges
Genes|October 1, 2016
Modeling Fragile X Syndrome Using Human Pluripotent Stem CellsHagar Mor-Shaked, Rachel Eiges
World Journal of Stem Cells|July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cellsShira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
Frontiers in Immunology|August 30, 2021
The Clinical Aspect of Adaptor Molecules in T Cell Signaling: Lessons Learnt From Inborn Errors of ImmunityYael Dinur-Schejter, Irina Zaidman, Hagar Mor-Shaked, et al.
European Journal of Medical Genetics|September 2, 2023
Prenatal diagnosis of lanosterol synthase deficiency: Fetal ultrasound findings as a window on family geneticsSigal Matza Porges, Hagar Mor-Shaked, Avraham Shaag, et al.
American Journal of Medical Genetics. Part A|September 11, 2019
Homozygous variants in MAPRE2 and CDON in individual with skin folds, growth delay, retinal coloboma, and pyloric stenosisLina Berkun, Mordechai Slae, Hagar Mor-Shaked, et al.
American Journal of Medical Genetics. Part A|October 7, 2020
De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic featuresJonathan Rips, Hagar Mor-Shaked, Serkan Erdin, et al.
European Journal of Human Genetics : EJHG|November 23, 2020
Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected childHagar Mor-Shaked, Jonathan Rips, Shiri Gershon Naamat, et al.
Plos One|May 27, 2021
Characterization of a L136P mutation in Formin-like 2 (FMNL2) from a patient with chronic inflammatory bowel diseaseRaphael Trefzer, Orly Elpeleg, Tatyana Gabrusskaya, et al.
Bone|October 8, 2021
Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosisEhud Even-Or, Gali Schiesel, Natalia Simanovsky, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Molecular Neuroscience|February 23, 2018
Reevaluation of <i>FMR1</i> Hypermethylation Timing in Fragile X SyndromeHagar Mor-Shaked, Rachel Eiges
Genes|October 1, 2016
Modeling Fragile X Syndrome Using Human Pluripotent Stem CellsHagar Mor-Shaked, Rachel Eiges
World Journal of Stem Cells|July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cellsShira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
Frontiers in Immunology|August 30, 2021
The Clinical Aspect of Adaptor Molecules in T Cell Signaling: Lessons Learnt From Inborn Errors of ImmunityYael Dinur-Schejter, Irina Zaidman, Hagar Mor-Shaked, et al.
European Journal of Medical Genetics|September 2, 2023
Prenatal diagnosis of lanosterol synthase deficiency: Fetal ultrasound findings as a window on family geneticsSigal Matza Porges, Hagar Mor-Shaked, Avraham Shaag, et al.
American Journal of Medical Genetics. Part A|September 11, 2019
Homozygous variants in MAPRE2 and CDON in individual with skin folds, growth delay, retinal coloboma, and pyloric stenosisLina Berkun, Mordechai Slae, Hagar Mor-Shaked, et al.
American Journal of Medical Genetics. Part A|October 7, 2020
De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic featuresJonathan Rips, Hagar Mor-Shaked, Serkan Erdin, et al.
European Journal of Human Genetics : EJHG|November 23, 2020
Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected childHagar Mor-Shaked, Jonathan Rips, Shiri Gershon Naamat, et al.
Plos One|May 27, 2021
Characterization of a L136P mutation in Formin-like 2 (FMNL2) from a patient with chronic inflammatory bowel diseaseRaphael Trefzer, Orly Elpeleg, Tatyana Gabrusskaya, et al.
Bone|October 8, 2021
Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosisEhud Even-Or, Gali Schiesel, Natalia Simanovsky, et al.
Pageof 6