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The Journal of Allergy and Clinical Immunology
|
March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder
Michael D Keller, Rahul Pandey, Dong Li, et al.
Frontiers in Pediatrics
|
August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
Alejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
JCI Insight
|
November 8, 2022
Partial loss-of-function mutations in GINS4 lead to NK cell deficiency with neutropenia
Matilde I Conte, M Cecilia Poli, Angelo Taglialatela, et al.
Genes & Development
|
August 4, 2010
miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta
Duonan Yu, Camila O dos Santos, Guowei Zhao, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
June 11, 2005
Practice parameter for the diagnosis and management of primary immunodeficiency
Francisco A Bonilla, I Leonard Bernstein, David A Khan, et al.
Cell Reports
|
January 15, 2025
The Golgi complex governs natural killer cell lytic granule positioning to promote directionality in cytotoxicity
Luis A Pedroza, Frederique van den Haak, Alexander Frumovitz, et al.
Pediatrics
|
August 2, 2023
Justice, Equity, Diversity, and Inclusion in the Pediatric Faculty Research Workforce: Call to Action
Danielle E Soranno, Tamara D Simon, Samudragupta Bora, et al.
The Journal of Allergy and Clinical Immunology
|
April 19, 2011
Genome-wide association identifies diverse causes of common variable immunodeficiency
Jordan S Orange, Joseph T Glessner, Elena Resnick, et al.
Scientific Reports
|
November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
Beate Hagl, Benedikt D Spielberger, Silvia Thoene, et al.
The Journal of Allergy and Clinical Immunology
|
March 28, 2016
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism
Petra Netter, Sanny K Chan, Pinaki P Banerjee, et al.
Page
of 36
Search research articles
Search
Showing results (251-260 of 357) with videos related to
Sort By:
Page
of 36
The Journal of Allergy and Clinical Immunology
|
March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder
Michael D Keller, Rahul Pandey, Dong Li, et al.
Frontiers in Pediatrics
|
August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
Alejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
JCI Insight
|
November 8, 2022
Partial loss-of-function mutations in GINS4 lead to NK cell deficiency with neutropenia
Matilde I Conte, M Cecilia Poli, Angelo Taglialatela, et al.
Genes & Development
|
August 4, 2010
miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta
Duonan Yu, Camila O dos Santos, Guowei Zhao, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
June 11, 2005
Practice parameter for the diagnosis and management of primary immunodeficiency
Francisco A Bonilla, I Leonard Bernstein, David A Khan, et al.
Cell Reports
|
January 15, 2025
The Golgi complex governs natural killer cell lytic granule positioning to promote directionality in cytotoxicity
Luis A Pedroza, Frederique van den Haak, Alexander Frumovitz, et al.
Pediatrics
|
August 2, 2023
Justice, Equity, Diversity, and Inclusion in the Pediatric Faculty Research Workforce: Call to Action
Danielle E Soranno, Tamara D Simon, Samudragupta Bora, et al.
The Journal of Allergy and Clinical Immunology
|
April 19, 2011
Genome-wide association identifies diverse causes of common variable immunodeficiency
Jordan S Orange, Joseph T Glessner, Elena Resnick, et al.
Scientific Reports
|
November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
Beate Hagl, Benedikt D Spielberger, Silvia Thoene, et al.
The Journal of Allergy and Clinical Immunology
|
March 28, 2016
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism
Petra Netter, Sanny K Chan, Pinaki P Banerjee, et al.
Page
of 36