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Alice Y Chan

Showing results (11-20 of 32) with videos related to

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The Journal of Experimental Medicine|March 20, 2025
Dominant interfering CARD11 variants disrupt JNK signaling to promote GATA3 expression in T cellsBradly M Bauman, Jeffrey R Stinson, Melissa A Kallarakal, et al.
The Journal of Experimental Medicine|June 11, 2021
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell toleranceJeremy T Warshauer, Julia A Belk, Alice Y Chan, et al.
ERJ Open Research|July 7, 2018
Analysis of pulmonary features and treatment approaches in the COPA syndromeJessica L Tsui, Oscar A Estrada, Zimu Deng, et al.
Communications Biology|February 23, 2019
A large CRISPR-induced bystander mutation causes immune dysregulationDimitre R Simeonov, Alexander J Brandt, Alice Y Chan, et al.
Journal of Human Immunity|February 2, 2026
Complete and partial forms of X-linked MCTS1 deficiency in patients with mycobacterial diseaseQinhua Zhou, Ivan Bagarić, Fabian Komma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 17, 2025
The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2Vanessa C Jacovas, Michelle Zelnick, Shannon McNulty, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in <i>ADA</i> , <i>DCLRE1C</i> , <i>IL2RG</i> , <i>IL7R</i> , <i>JAK3</i> , <i>RAG1</i> , and <i>RAG2</i>Vanessa C Jacovas, Michelle Zelnick, Shannon McNulty, et al.
The Journal of Allergy and Clinical Immunology|October 1, 2019
Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & ImmunologyIvan K Chinn, Alice Y Chan, Karin Chen, et al.
Clinical Immunology (Orlando, Fla.)|December 19, 2025
Clinical spectrum of Wiskott-Aldrich syndrome carriers: Self-reported survey of 193 carriersShanmuganathan Chandrakasan, Adrianna Westbrook, Linda M Griffith, et al.
Journal of Clinical Immunology|October 29, 2024
Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the EBMT Inborn Errors Working PartyHelena Buso, Etai Adam, Peter D Arkwright, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
The Journal of Experimental Medicine|March 20, 2025
Dominant interfering CARD11 variants disrupt JNK signaling to promote GATA3 expression in T cellsBradly M Bauman, Jeffrey R Stinson, Melissa A Kallarakal, et al.
The Journal of Experimental Medicine|June 11, 2021
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell toleranceJeremy T Warshauer, Julia A Belk, Alice Y Chan, et al.
ERJ Open Research|July 7, 2018
Analysis of pulmonary features and treatment approaches in the COPA syndromeJessica L Tsui, Oscar A Estrada, Zimu Deng, et al.
Communications Biology|February 23, 2019
A large CRISPR-induced bystander mutation causes immune dysregulationDimitre R Simeonov, Alexander J Brandt, Alice Y Chan, et al.
Journal of Human Immunity|February 2, 2026
Complete and partial forms of X-linked MCTS1 deficiency in patients with mycobacterial diseaseQinhua Zhou, Ivan Bagarić, Fabian Komma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 17, 2025
The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2Vanessa C Jacovas, Michelle Zelnick, Shannon McNulty, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in <i>ADA</i> , <i>DCLRE1C</i> , <i>IL2RG</i> , <i>IL7R</i> , <i>JAK3</i> , <i>RAG1</i> , and <i>RAG2</i>Vanessa C Jacovas, Michelle Zelnick, Shannon McNulty, et al.
The Journal of Allergy and Clinical Immunology|October 1, 2019
Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & ImmunologyIvan K Chinn, Alice Y Chan, Karin Chen, et al.
Clinical Immunology (Orlando, Fla.)|December 19, 2025
Clinical spectrum of Wiskott-Aldrich syndrome carriers: Self-reported survey of 193 carriersShanmuganathan Chandrakasan, Adrianna Westbrook, Linda M Griffith, et al.
Journal of Clinical Immunology|October 29, 2024
Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the EBMT Inborn Errors Working PartyHelena Buso, Etai Adam, Peter D Arkwright, et al.
Pageof 4