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Emily M Mace

Showing results (131-140 of 138) with videos related to

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Nature Communications|July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Nature Genetics|April 21, 2015
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritisLevi B Watkin, Birthe Jessen, Wojciech Wiszniewski, et al.
Blood Cancer Discovery|March 5, 2022
Identification and Targeting of the Developmental Blockade in Extranodal Natural Killer/T-cell LymphomaBethany L Mundy-Bosse, Christoph Weigel, Yue-Zhong Wu, et al.
Science (New York, N.Y.)|July 11, 2020
HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory diseaseSarah A Cook, William A Comrie, M Cecilia Poli, 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.
Cancer Cell|September 13, 2022
NKG2A and HLA-E define an alternative immune checkpoint axis in bladder cancerBérengère Salomé, John P Sfakianos, Daniel Ranti, et al.
The Journal of Experimental Medicine|October 12, 2019
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 functionMichael T Lam, Simona Coppola, Oliver H F Krumbach, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2016
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disordersAsbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
Pageof 14

Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Nature Communications|July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Nature Genetics|April 21, 2015
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritisLevi B Watkin, Birthe Jessen, Wojciech Wiszniewski, et al.
Blood Cancer Discovery|March 5, 2022
Identification and Targeting of the Developmental Blockade in Extranodal Natural Killer/T-cell LymphomaBethany L Mundy-Bosse, Christoph Weigel, Yue-Zhong Wu, et al.
Science (New York, N.Y.)|July 11, 2020
HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory diseaseSarah A Cook, William A Comrie, M Cecilia Poli, 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.
Cancer Cell|September 13, 2022
NKG2A and HLA-E define an alternative immune checkpoint axis in bladder cancerBérengère Salomé, John P Sfakianos, Daniel Ranti, et al.
The Journal of Experimental Medicine|October 12, 2019
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 functionMichael T Lam, Simona Coppola, Oliver H F Krumbach, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2016
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disordersAsbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
Pageof 14