Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Roifman

Showing results (181-190 of 225) with videos related to

Pageof 23
Sort By:
Journal of Immunological Methods|February 28, 1994
High level functional engraftment of severe combined immunodeficient mice with human peripheral blood lymphocytes following pretreatment with radiation and anti-asialo GM1B Shpitz, C A Chambers, A B Singhal, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 5, 2021
DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patientsOri Scott, Harjit Dadi, Linda Vong, et al.
Neurobiology of Disease|April 24, 2012
Cerebellar abnormalities in purine nucleoside phosphorylase deficient miceAlireza Mansouri, Weixian Min, Christina J Cole, et al.
Nature|February 15, 1996
Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitorN Meydan, T Grunberger, H Dadi, et al.
Clinical Immunology (Orlando, Fla.)|December 9, 2019
Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapyEyal Grunebaum, Brenda Reid, Ahmed Naqvi, et al.
The Journal of Allergy and Clinical Immunology|November 29, 2019
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiencyAmit Nahum, Nigel Sharfe, Arnon Broides, et al.
The Journal of Allergy and Clinical Immunology|August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)Harjit Dadi, Tyler A Jones, Daniele Merico, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Journal of Autoimmunity|November 19, 2022
NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunityNigel Sharfe, Ilan Dalal, Zahra Naghdi, et al.
Pageof 23

Showing results (181-190 of 225) with videos related to

Sort By:
Pageof 23
Journal of Immunological Methods|February 28, 1994
High level functional engraftment of severe combined immunodeficient mice with human peripheral blood lymphocytes following pretreatment with radiation and anti-asialo GM1B Shpitz, C A Chambers, A B Singhal, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 5, 2021
DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patientsOri Scott, Harjit Dadi, Linda Vong, et al.
Neurobiology of Disease|April 24, 2012
Cerebellar abnormalities in purine nucleoside phosphorylase deficient miceAlireza Mansouri, Weixian Min, Christina J Cole, et al.
Nature|February 15, 1996
Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitorN Meydan, T Grunberger, H Dadi, et al.
Clinical Immunology (Orlando, Fla.)|December 9, 2019
Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapyEyal Grunebaum, Brenda Reid, Ahmed Naqvi, et al.
The Journal of Allergy and Clinical Immunology|November 29, 2019
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiencyAmit Nahum, Nigel Sharfe, Arnon Broides, et al.
The Journal of Allergy and Clinical Immunology|August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)Harjit Dadi, Tyler A Jones, Daniele Merico, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Journal of Autoimmunity|November 19, 2022
NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunityNigel Sharfe, Ilan Dalal, Zahra Naghdi, et al.
Pageof 23