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

Henry Y Lu

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
Cold Spring Harbor Molecular Case Studies|June 14, 2020
Clinical IRAK4 deficiency caused by homozygosity for the novel <i>IRAK4</i> (c.1049delG, p.Gly350Glufs*15) variantAlicia Jia, Elliot James, Henry Y Lu, et al.
Frontiers in Immunology|November 1, 2021
MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory ResponsivenessShan-Yu Fung, Henry Y Lu, Mehul Sharma, et al.
The Journal of Allergy and Clinical Immunology|August 24, 2021
Inborn errors of immunity manifesting as atopic disordersMaryam Vaseghi-Shanjani, Kelsey L Smith, Rahnuma J Sara, et al.
Frontiers in Immunology|December 10, 2021
A Novel Germline Heterozygous <i>BCL11B</i> Variant Causing Severe Atopic Disease and Immune DysregulationHenry Y Lu, Robert Sertori, Alejandra V Contreras, et al.
BMC Pediatrics|January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case reportGeraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
Nature Cancer|February 5, 2022
Mutational landscape influences immunotherapy outcomes among patients with non-small-cell lung cancer with human leukocyte antigen supertype B44Amy L Cummings, Jaklin Gukasyan, Henry Y Lu, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiencyHenry Y Lu, Mehul Sharma, Ashish A Sharma, et al.
Cell Stem Cell|November 12, 2024
Regulated GATA1 expression as a universal gene therapy for Diamond-Blackfan anemiaRichard A Voit, Xiaotian Liao, Alexis Caulier, 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.
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.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Cold Spring Harbor Molecular Case Studies|June 14, 2020
Clinical IRAK4 deficiency caused by homozygosity for the novel <i>IRAK4</i> (c.1049delG, p.Gly350Glufs*15) variantAlicia Jia, Elliot James, Henry Y Lu, et al.
Frontiers in Immunology|November 1, 2021
MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory ResponsivenessShan-Yu Fung, Henry Y Lu, Mehul Sharma, et al.
The Journal of Allergy and Clinical Immunology|August 24, 2021
Inborn errors of immunity manifesting as atopic disordersMaryam Vaseghi-Shanjani, Kelsey L Smith, Rahnuma J Sara, et al.
Frontiers in Immunology|December 10, 2021
A Novel Germline Heterozygous <i>BCL11B</i> Variant Causing Severe Atopic Disease and Immune DysregulationHenry Y Lu, Robert Sertori, Alejandra V Contreras, et al.
BMC Pediatrics|January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case reportGeraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
Nature Cancer|February 5, 2022
Mutational landscape influences immunotherapy outcomes among patients with non-small-cell lung cancer with human leukocyte antigen supertype B44Amy L Cummings, Jaklin Gukasyan, Henry Y Lu, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiencyHenry Y Lu, Mehul Sharma, Ashish A Sharma, et al.
Cell Stem Cell|November 12, 2024
Regulated GATA1 expression as a universal gene therapy for Diamond-Blackfan anemiaRichard A Voit, Xiaotian Liao, Alexis Caulier, 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.
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.
Pageof 3