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The Journal of Allergy and Clinical Immunology
|
January 3, 2017
Update on the use of immunoglobulin in human disease: A review of evidence
Elena E Perez, Jordan S Orange, Francisco Bonilla, et al.
The Journal of Clinical Investigation
|
June 5, 2002
Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations
Jordan S Orange, Scott R Brodeur, Ashish Jain, et al.
The Journal of Allergy and Clinical Immunology
|
April 4, 2006
Use of intravenous immunoglobulin in human disease: a review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology
Jordan S Orange, Elham M Hossny, Catherine R Weiler, et al.
Scientific Reports
|
August 2, 2016
IL-2 in the tumor microenvironment is necessary for Wiskott-Aldrich syndrome protein deficient NK cells to respond to tumors in vivo
Joanna S Kritikou, Carin I M Dahlberg, Marisa A P Baptista, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
September 15, 2019
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantation
Caitlin M Burk, Kara E Coffey, Emily M Mace, et al.
The New England Journal of Medicine
|
November 12, 2010
Stem-cell gene therapy for the Wiskott-Aldrich syndrome
Kaan Boztug, Manfred Schmidt, Adrian Schwarzer, et al.
Journal of Clinical Immunology
|
June 7, 2018
The International Alliance of Primary Immune Deficiency Societies
Andrew R Gennery, Roshini S Abraham, Troy R Torgerson, et al.
Blood
|
February 1, 2013
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset
Emily M Mace, Amy P Hsu, Linda Monaco-Shawver, et al.
Pediatric Research
|
January 20, 2021
Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19
Catherine S Forster, Suong T Nguyen, Weston T Powell, et al.
American Journal of Human Genetics
|
July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles
Zeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Page
of 36
Search research articles
Search
Showing results (261-270 of 357) with videos related to
Sort By:
Page
of 36
The Journal of Allergy and Clinical Immunology
|
January 3, 2017
Update on the use of immunoglobulin in human disease: A review of evidence
Elena E Perez, Jordan S Orange, Francisco Bonilla, et al.
The Journal of Clinical Investigation
|
June 5, 2002
Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations
Jordan S Orange, Scott R Brodeur, Ashish Jain, et al.
The Journal of Allergy and Clinical Immunology
|
April 4, 2006
Use of intravenous immunoglobulin in human disease: a review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology
Jordan S Orange, Elham M Hossny, Catherine R Weiler, et al.
Scientific Reports
|
August 2, 2016
IL-2 in the tumor microenvironment is necessary for Wiskott-Aldrich syndrome protein deficient NK cells to respond to tumors in vivo
Joanna S Kritikou, Carin I M Dahlberg, Marisa A P Baptista, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
September 15, 2019
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantation
Caitlin M Burk, Kara E Coffey, Emily M Mace, et al.
The New England Journal of Medicine
|
November 12, 2010
Stem-cell gene therapy for the Wiskott-Aldrich syndrome
Kaan Boztug, Manfred Schmidt, Adrian Schwarzer, et al.
Journal of Clinical Immunology
|
June 7, 2018
The International Alliance of Primary Immune Deficiency Societies
Andrew R Gennery, Roshini S Abraham, Troy R Torgerson, et al.
Blood
|
February 1, 2013
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset
Emily M Mace, Amy P Hsu, Linda Monaco-Shawver, et al.
Pediatric Research
|
January 20, 2021
Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19
Catherine S Forster, Suong T Nguyen, Weston T Powell, et al.
American Journal of Human Genetics
|
July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles
Zeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Page
of 36