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

Susan Lin

Showing results (91-100 of 99) with videos related to

Pageof 10
Sort By:
You have reached the last page of results.This site can display upto 99 results.
Frontiers in Immunology|July 12, 2021
Optimizing a Multi-Component Intranasal <i>Entamoeba Histolytica</i> Vaccine Formulation Using a Design of Experiments StrategyMayuresh M Abhyankar, Mark T Orr, Robert Kinsey, et al.
Blood|July 5, 2022
Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancyMehul Sharma, Maggie P Fu, Henry Y Lu, et al.
Science Signaling|July 9, 2024
An antibody that inhibits TGF-β1 release from latent extracellular matrix complexes attenuates the progression of renal fibrosisJustin W Jackson, Frederick C Streich, Ajai Pal, et al.
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Journal of Medical Genetics|June 14, 2023
Dominant negative variants in <i>IKZF2</i> cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delayArezoo Mohajeri, Maryam Vaseghi-Shanjani, Jill A Rosenfeld, et al.
Nature Communications|January 20, 2021
A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brainAnoushka Joglekar, Andrey Prjibelski, Ahmed Mahfouz, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
Frontiers in Immunology|July 12, 2021
Optimizing a Multi-Component Intranasal <i>Entamoeba Histolytica</i> Vaccine Formulation Using a Design of Experiments StrategyMayuresh M Abhyankar, Mark T Orr, Robert Kinsey, et al.
Blood|July 5, 2022
Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancyMehul Sharma, Maggie P Fu, Henry Y Lu, et al.
Science Signaling|July 9, 2024
An antibody that inhibits TGF-β1 release from latent extracellular matrix complexes attenuates the progression of renal fibrosisJustin W Jackson, Frederick C Streich, Ajai Pal, et al.
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Journal of Medical Genetics|June 14, 2023
Dominant negative variants in <i>IKZF2</i> cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delayArezoo Mohajeri, Maryam Vaseghi-Shanjani, Jill A Rosenfeld, et al.
Nature Communications|January 20, 2021
A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brainAnoushka Joglekar, Andrey Prjibelski, Ahmed Mahfouz, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 10