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Raz Somech

Showing results (111-120 of 200) with videos related to

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Immunologic Research|January 10, 2022
B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemiaOri Toker, Arnon Broides, Atar Lev, et al.
American Journal of Medical Genetics. Part A|September 27, 2025
A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss-of-Function of DMRT2Jonathan Rips, Hagar Mor-Shaked, Oded Shamriz, et al.
The Journal of Allergy and Clinical Immunology|September 22, 2009
Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cellsRaz Somech, Amos J Simon, Atar Lev, et al.
Science Translational Medicine|February 27, 2015
Timely and spatially regulated maturation of B and T cell repertoire during human fetal developmentErez Rechavi, Atar Lev, Yu Nee Lee, et al.
Frontiers in Pediatrics|May 14, 2025
Case Report: Clinical manifestations of uncommon monogenic disorders: revisiting activated phosphoinositide 3-kinase delta syndrome 2Oded Shamriz, Amarilla Mandola, Amos J Simon, et al.
Pediatric Research|July 10, 2019
Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)Rona Merdler-Rabinowicz, Anna Grinberg, Jeffrey M Jacobson, 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.
Nature Communications|October 27, 2023
CRISPR-Cas9 engineering of the RAG2 locus via complete coding sequence replacement for therapeutic applicationsDaniel Allen, Orli Knop, Bryan Itkowitz, et al.
Journal of Clinical Immunology|February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Journal of Pediatric Hematology/Oncology|February 8, 2013
Impact of conditioning on outcome of hematopoietic stem cell transplantation for wiskott-Aldrich syndromePolina Stepensky, Aviva Krauss, Gal Goldstein, et al.
Pageof 20

Showing results (111-120 of 200) with videos related to

Sort By:
Pageof 20
Immunologic Research|January 10, 2022
B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemiaOri Toker, Arnon Broides, Atar Lev, et al.
American Journal of Medical Genetics. Part A|September 27, 2025
A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss-of-Function of DMRT2Jonathan Rips, Hagar Mor-Shaked, Oded Shamriz, et al.
The Journal of Allergy and Clinical Immunology|September 22, 2009
Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cellsRaz Somech, Amos J Simon, Atar Lev, et al.
Science Translational Medicine|February 27, 2015
Timely and spatially regulated maturation of B and T cell repertoire during human fetal developmentErez Rechavi, Atar Lev, Yu Nee Lee, et al.
Frontiers in Pediatrics|May 14, 2025
Case Report: Clinical manifestations of uncommon monogenic disorders: revisiting activated phosphoinositide 3-kinase delta syndrome 2Oded Shamriz, Amarilla Mandola, Amos J Simon, et al.
Pediatric Research|July 10, 2019
Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)Rona Merdler-Rabinowicz, Anna Grinberg, Jeffrey M Jacobson, 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.
Nature Communications|October 27, 2023
CRISPR-Cas9 engineering of the RAG2 locus via complete coding sequence replacement for therapeutic applicationsDaniel Allen, Orli Knop, Bryan Itkowitz, et al.
Journal of Clinical Immunology|February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Journal of Pediatric Hematology/Oncology|February 8, 2013
Impact of conditioning on outcome of hematopoietic stem cell transplantation for wiskott-Aldrich syndromePolina Stepensky, Aviva Krauss, Gal Goldstein, et al.
Pageof 20