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A Ma

Showing results (261-270 of 270) with videos related to

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Molecular Cell|February 13, 2001
The combined functions of proapoptotic Bcl-2 family members bak and bax are essential for normal development of multiple tissuesT Lindsten, A J Ross, A King, 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.
The Journal of Experimental Medicine|March 15, 2017
Correction: ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humansJ J Lyons, Y Liu, C A Ma, et al.
The Journal of Experimental Medicine|January 28, 2017
ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humansJ J Lyons, Y Liu, C A Ma, et al.
The Journal of Experimental Medicine|June 26, 2019
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responsesSarah Spencer, Sevgi Köstel Bal, William Egner, et al.
Nature Genetics|October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics|June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
The New England Journal of Medicine|May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory SyndromeHratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood|November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsJoshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Pageof 27

Showing results (261-270 of 270) with videos related to

Sort By:
Pageof 27
You have reached the last page of results.This site can display upto 270 results.
Molecular Cell|February 13, 2001
The combined functions of proapoptotic Bcl-2 family members bak and bax are essential for normal development of multiple tissuesT Lindsten, A J Ross, A King, 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.
The Journal of Experimental Medicine|March 15, 2017
Correction: ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humansJ J Lyons, Y Liu, C A Ma, et al.
The Journal of Experimental Medicine|January 28, 2017
ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humansJ J Lyons, Y Liu, C A Ma, et al.
The Journal of Experimental Medicine|June 26, 2019
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responsesSarah Spencer, Sevgi Köstel Bal, William Egner, et al.
Nature Genetics|October 28, 2017
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
Nature Genetics|June 20, 2017
Germline hypomorphic CARD11 mutations in severe atopic diseaseChi A Ma, Jeffrey R Stinson, Yuan Zhang, et al.
The New England Journal of Medicine|May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory SyndromeHratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood|November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsJoshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Pageof 27