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Idan Cohen

Showing results (41-50 of 72) with videos related to

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Journal of Immunotoxicology|December 17, 2009
Effects of IL-1 molecules on growth patterns of 3-MCA-induced cell lines: an interplay between immunogenicity and invasive potentialElena Voronov, Eli Reich, Shahar Dotan, et al.
Frontiers in Immunology|July 13, 2013
Unique Versus Redundant Functions of IL-1α and IL-1β in the Tumor MicroenvironmentElena Voronov, Shahar Dotan, Yakov Krelin, et al.
European Journal of Human Genetics : EJHG|July 18, 2013
Autosomal recessive Adams-Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferaseIdan Cohen, Eldad Silberstein, Yonatan Perez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Differential release of chromatin-bound IL-1alpha discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammationIdan Cohen, Peleg Rider, Yaron Carmi, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndromeNoam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, et al.
Clinical Genetics|October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan JewsMarina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
Frontiers in Immunology|August 11, 2025
Cannabidiol polarizes human neutrophils toward a cancer-promoting phenotypeMona Khoury, Yuxiang Hong, Dayana Blokon-Kogan, et al.
International Immunology|February 26, 2010
IL-1-induced inflammation promotes development of leishmaniasis in susceptible BALB/c miceElena Voronov, Shahar Dotan, Lubov Gayvoronsky, et al.
European Journal of Human Genetics : EJHG|March 3, 2024
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and miceNoam Hadar, Omri Porgador, Idan Cohen, et al.
American Journal of Human Genetics|April 24, 2012
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2CHila Romi, Idan Cohen, Daniella Landau, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Journal of Immunotoxicology|December 17, 2009
Effects of IL-1 molecules on growth patterns of 3-MCA-induced cell lines: an interplay between immunogenicity and invasive potentialElena Voronov, Eli Reich, Shahar Dotan, et al.
Frontiers in Immunology|July 13, 2013
Unique Versus Redundant Functions of IL-1α and IL-1β in the Tumor MicroenvironmentElena Voronov, Shahar Dotan, Yakov Krelin, et al.
European Journal of Human Genetics : EJHG|July 18, 2013
Autosomal recessive Adams-Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferaseIdan Cohen, Eldad Silberstein, Yonatan Perez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Differential release of chromatin-bound IL-1alpha discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammationIdan Cohen, Peleg Rider, Yaron Carmi, et al.
European Journal of Human Genetics : EJHG|January 4, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndromeNoam Hadar, Ruth Schreiber, Marina Eskin-Schwartz, et al.
Clinical Genetics|October 10, 2023
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan JewsMarina Eskin-Schwartz, Vadim Dolgin, Elena Didkovsky, et al.
Frontiers in Immunology|August 11, 2025
Cannabidiol polarizes human neutrophils toward a cancer-promoting phenotypeMona Khoury, Yuxiang Hong, Dayana Blokon-Kogan, et al.
International Immunology|February 26, 2010
IL-1-induced inflammation promotes development of leishmaniasis in susceptible BALB/c miceElena Voronov, Shahar Dotan, Lubov Gayvoronsky, et al.
European Journal of Human Genetics : EJHG|March 3, 2024
Heterozygous THBS2 pathogenic variant causes Ehlers-Danlos syndrome with prominent vascular features in humans and miceNoam Hadar, Omri Porgador, Idan Cohen, et al.
American Journal of Human Genetics|April 24, 2012
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2CHila Romi, Idan Cohen, Daniella Landau, et al.
Pageof 8