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Alexandra F Freeman

Showing results (91-100 of 268) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 19, 2014
STAT3 interrupts ATR-Chk1 signaling to allow oncovirus-mediated cell proliferationSiva Koganti, Joyce Hui-Yuen, Shane McAllister, et al.
Arthritis and Rheumatism|December 14, 2011
Brief report: genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne)Andrew P Demidowich, Alexandra F Freeman, Douglas B Kuhns, et al.
Pediatrics|April 18, 2007
Brain abnormalities in patients with hyperimmunoglobulin E syndromeAlexandra F Freeman, Christina J Collura-Burke, Nicholas J Patronas, et al.
Journal of Virology|August 23, 2013
Signal transducer and activator of transcription 3 limits Epstein-Barr virus lytic activation in B lymphocytesErik R Hill, Siva Koganti, Jizu Zhi, et al.
Frontiers in Pediatrics|March 16, 2017
DOCK 8 Deficiency, EBV+ Lymphomatoid Granulomatosis, and Intrafamilial Variation in PresentationVictoria R Dimitriades, Vincent Devlin, Stefania Pittaluga, et al.
Transfusion|February 2, 2021
Daratumumab for delayed RBC engraftment following major ABO mismatched haploidentical bone marrow transplantationBonnie Yates, Eoghan Molloy, Alina Dulau-Florea, et al.
Archives of Dermatology|September 21, 2011
Cutaneous manifestations of DOCK8 deficiency syndromeEmily Y Chu, Alexandra F Freeman, Huie Jing, et al.
Pathogens (Basel, Switzerland)|June 8, 2017
Molecular Typing of Staphylococcus aureus Isolated from Patients with Autosomal Dominant Hyper IgE SyndromeInka Sastalla, Kelli W Williams, Erik D Anderson, et al.
Journal of Clinical Immunology|June 17, 2015
IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotypeAmy P Hsu, Stefania Pittaluga, Bianca Martinez, et al.
Annals of the American Thoracic Society|September 9, 2016
Mediastinal and Disseminated Mycobacterium kansasii Disease in GATA2 DeficiencyJana P Lovell, Christa S Zerbe, Kenneth N Olivier, et al.
Pageof 27

Showing results (91-100 of 268) with videos related to

Sort By:
Pageof 27
Proceedings of the National Academy of Sciences of the United States of America|March 19, 2014
STAT3 interrupts ATR-Chk1 signaling to allow oncovirus-mediated cell proliferationSiva Koganti, Joyce Hui-Yuen, Shane McAllister, et al.
Arthritis and Rheumatism|December 14, 2011
Brief report: genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne)Andrew P Demidowich, Alexandra F Freeman, Douglas B Kuhns, et al.
Pediatrics|April 18, 2007
Brain abnormalities in patients with hyperimmunoglobulin E syndromeAlexandra F Freeman, Christina J Collura-Burke, Nicholas J Patronas, et al.
Journal of Virology|August 23, 2013
Signal transducer and activator of transcription 3 limits Epstein-Barr virus lytic activation in B lymphocytesErik R Hill, Siva Koganti, Jizu Zhi, et al.
Frontiers in Pediatrics|March 16, 2017
DOCK 8 Deficiency, EBV+ Lymphomatoid Granulomatosis, and Intrafamilial Variation in PresentationVictoria R Dimitriades, Vincent Devlin, Stefania Pittaluga, et al.
Transfusion|February 2, 2021
Daratumumab for delayed RBC engraftment following major ABO mismatched haploidentical bone marrow transplantationBonnie Yates, Eoghan Molloy, Alina Dulau-Florea, et al.
Archives of Dermatology|September 21, 2011
Cutaneous manifestations of DOCK8 deficiency syndromeEmily Y Chu, Alexandra F Freeman, Huie Jing, et al.
Pathogens (Basel, Switzerland)|June 8, 2017
Molecular Typing of Staphylococcus aureus Isolated from Patients with Autosomal Dominant Hyper IgE SyndromeInka Sastalla, Kelli W Williams, Erik D Anderson, et al.
Journal of Clinical Immunology|June 17, 2015
IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotypeAmy P Hsu, Stefania Pittaluga, Bianca Martinez, et al.
Annals of the American Thoracic Society|September 9, 2016
Mediastinal and Disseminated Mycobacterium kansasii Disease in GATA2 DeficiencyJana P Lovell, Christa S Zerbe, Kenneth N Olivier, et al.
Pageof 27