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Showing results (181-190 of 200) with videos related to

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The Journal of Experimental Medicine|November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsAtar Lev, Yu Nee Lee, Guangping Sun, et al.
Cell Death & Disease|January 12, 2026
Mutations in VPS18 lead to a neutrophil maturation defect associated with disturbed vesicle homeostasisJincheng Gao, Almke Bader, Monika I Linder, et al.
The Journal of Allergy and Clinical Immunology|May 5, 2019
Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indicesStephen R Daley, Hui-Fern Koay, Kerry Dobbs, et al.
The Journal of Pediatrics|September 24, 2020
Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology DisordersRyan W Himes, Eric H Chiou, Karen Queliza, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
Frontiers in Immunology|September 28, 2017
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio EradicationAsghar Aghamohammadi, Hassan Abolhassani, Necil Kutukculer, et al.
The Journal of Clinical Investigation|September 22, 2020
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiencyPaul Bastard, Jeremy Manry, Jie Chen, et al.
Gastroenterology|September 30, 2018
Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 DeficiencyAnna S Lehle, Henner F Farin, Benjamin Marquardt, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 20

Showing results (181-190 of 200) with videos related to

Sort By:
Pageof 20
The Journal of Experimental Medicine|November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsAtar Lev, Yu Nee Lee, Guangping Sun, et al.
Cell Death & Disease|January 12, 2026
Mutations in VPS18 lead to a neutrophil maturation defect associated with disturbed vesicle homeostasisJincheng Gao, Almke Bader, Monika I Linder, et al.
The Journal of Allergy and Clinical Immunology|May 5, 2019
Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indicesStephen R Daley, Hui-Fern Koay, Kerry Dobbs, et al.
The Journal of Pediatrics|September 24, 2020
Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology DisordersRyan W Himes, Eric H Chiou, Karen Queliza, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
Frontiers in Immunology|September 28, 2017
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio EradicationAsghar Aghamohammadi, Hassan Abolhassani, Necil Kutukculer, et al.
The Journal of Clinical Investigation|September 22, 2020
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiencyPaul Bastard, Jeremy Manry, Jie Chen, et al.
Gastroenterology|September 30, 2018
Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 DeficiencyAnna S Lehle, Henner F Farin, Benjamin Marquardt, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 20