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Nitzan Kol

Showing results (11-20 of 36) with videos related to

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Non-Coding RNA|April 17, 2018
Promoter-Associated RNAs Regulate HSPC152 Gene Expression in Malignant MelanomaHamutal Bonen, Nitzan Kol, Noam Shomron, et al.
Plos One|February 25, 2021
Transcriptomic profiling and genomic mutational analysis of Human coronavirus (HCoV)-229E -infected human cellsNehemya Friedman, Jasmine Jacob-Hirsch, Yaron Drori, et al.
BMC Genomics|August 28, 2016
G23D: Online tool for mapping and visualization of genomic variants on 3D protein structuresOz Solomon, Vered Kunik, Amos Simon, et al.
Muscle & Nerve|December 15, 2019
Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathyLior Greenbaum, Ortal Barel, Vera Nikitin, et al.
European Journal of Medical Genetics|July 15, 2018
Diaphanospondylodysostosis: Refining the prenatal diagnosis of a rare skeletal disorderLior Greenbaum, Yinon Gilboa, Annick Raas-Rothschild, et al.
Journal of Clinical Immunology|October 14, 2016
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF)Erez Rechavi, Atar Lev, Eran Eyal, et al.
Molecular Genetics & Genomic Medicine|April 26, 2019
BRPF1-associated intellectual disability, ptosis, and facial dysmorphism in a multiplex familyNaomi Pode-Shakked, Ortal Barel, Ben Pode-Shakked, et al.
Nature Communications|December 11, 2021
Dynamic regulation of N<sup>6</sup>,2'-O-dimethyladenosine (m<sup>6</sup>Am) in obesityMoshe Shay Ben-Haim, Yishay Pinto, Sharon Moshitch-Moshkovitz, et al.
Clinical Immunology (Orlando, Fla.)|March 6, 2020
Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous communityAmos J Simon, Adi Cohen Golan, Atar Lev, et al.
Frontiers in Immunology|December 5, 2022
RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing featuresMutaz Sultan, Mohammad Adawi, Nitzan Kol, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Non-Coding RNA|April 17, 2018
Promoter-Associated RNAs Regulate HSPC152 Gene Expression in Malignant MelanomaHamutal Bonen, Nitzan Kol, Noam Shomron, et al.
Plos One|February 25, 2021
Transcriptomic profiling and genomic mutational analysis of Human coronavirus (HCoV)-229E -infected human cellsNehemya Friedman, Jasmine Jacob-Hirsch, Yaron Drori, et al.
BMC Genomics|August 28, 2016
G23D: Online tool for mapping and visualization of genomic variants on 3D protein structuresOz Solomon, Vered Kunik, Amos Simon, et al.
Muscle & Nerve|December 15, 2019
Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathyLior Greenbaum, Ortal Barel, Vera Nikitin, et al.
European Journal of Medical Genetics|July 15, 2018
Diaphanospondylodysostosis: Refining the prenatal diagnosis of a rare skeletal disorderLior Greenbaum, Yinon Gilboa, Annick Raas-Rothschild, et al.
Journal of Clinical Immunology|October 14, 2016
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF)Erez Rechavi, Atar Lev, Eran Eyal, et al.
Molecular Genetics & Genomic Medicine|April 26, 2019
BRPF1-associated intellectual disability, ptosis, and facial dysmorphism in a multiplex familyNaomi Pode-Shakked, Ortal Barel, Ben Pode-Shakked, et al.
Nature Communications|December 11, 2021
Dynamic regulation of N<sup>6</sup>,2'-O-dimethyladenosine (m<sup>6</sup>Am) in obesityMoshe Shay Ben-Haim, Yishay Pinto, Sharon Moshitch-Moshkovitz, et al.
Clinical Immunology (Orlando, Fla.)|March 6, 2020
Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous communityAmos J Simon, Adi Cohen Golan, Atar Lev, et al.
Frontiers in Immunology|December 5, 2022
RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing featuresMutaz Sultan, Mohammad Adawi, Nitzan Kol, et al.
Pageof 4