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Chi A Ma

Showing results (11-20 of 26) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 16, 2013
Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAKHong-Ying Wang, Chi A Ma, Yongge Zhao, et al.
Human Mutation|April 17, 2008
A novel mutation in NFKBIA/IKBA results in a degradation-resistant N-truncated protein and is associated with ectodermal dysplasia with immunodeficiencyEduardo Lopez-Granados, Jeffrey E Keenan, Matthew C Kinney, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 24, 2026
Oral lichenoid lesions in CTLA-4 haploinsufficiency: Targeting IFN-γ-driven mucosal immunopathologyChen Wang, Laurie Brenchley, Teresa Greenwell-Wild, et al.
Journal of Clinical Immunology|May 1, 2019
Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor RepertoireShirly Frizinsky, Erez Rechavi, Ortal Barel, et al.
The Journal of Experimental Medicine|July 16, 2017
PD-L1 up-regulation restrains Th17 cell differentiation in <i>STAT3</i> loss- and <i>STAT1</i> gain-of-function patientsYuan Zhang, Chi A Ma, Monica G Lawrence, et al.
Blood|December 14, 2016
Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrheaChi A Ma, Liqiang Xi, Brian Cauff, et al.
Clinical Immunology (Orlando, Fla.)|March 31, 2012
CD40 agonist antibody mediated improvement of chronic Cryptosporidium infection in patients with X-linked hyper IgM syndromeXiying Fan, Bhaskar Upadhyaya, Liming Wu, et al.
The Journal of Allergy and Clinical Immunology|September 25, 2018
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisAlon Peled, Ofer Sarig, Guangping Sun, et al.
The Journal of Pediatrics|February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta SyndromeAdam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
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.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2013
Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAKHong-Ying Wang, Chi A Ma, Yongge Zhao, et al.
Human Mutation|April 17, 2008
A novel mutation in NFKBIA/IKBA results in a degradation-resistant N-truncated protein and is associated with ectodermal dysplasia with immunodeficiencyEduardo Lopez-Granados, Jeffrey E Keenan, Matthew C Kinney, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 24, 2026
Oral lichenoid lesions in CTLA-4 haploinsufficiency: Targeting IFN-γ-driven mucosal immunopathologyChen Wang, Laurie Brenchley, Teresa Greenwell-Wild, et al.
Journal of Clinical Immunology|May 1, 2019
Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor RepertoireShirly Frizinsky, Erez Rechavi, Ortal Barel, et al.
The Journal of Experimental Medicine|July 16, 2017
PD-L1 up-regulation restrains Th17 cell differentiation in <i>STAT3</i> loss- and <i>STAT1</i> gain-of-function patientsYuan Zhang, Chi A Ma, Monica G Lawrence, et al.
Blood|December 14, 2016
Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrheaChi A Ma, Liqiang Xi, Brian Cauff, et al.
Clinical Immunology (Orlando, Fla.)|March 31, 2012
CD40 agonist antibody mediated improvement of chronic Cryptosporidium infection in patients with X-linked hyper IgM syndromeXiying Fan, Bhaskar Upadhyaya, Liming Wu, et al.
The Journal of Allergy and Clinical Immunology|September 25, 2018
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisAlon Peled, Ofer Sarig, Guangping Sun, et al.
The Journal of Pediatrics|February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta SyndromeAdam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
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.
Pageof 3