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The Journal of Allergy and Clinical Immunology
|
April 30, 2013
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism
Amy P Hsu, Kathryn J Sowerwine, Monica G Lawrence, et al.
Frontiers in Immunology
|
September 11, 2025
Reliable genetic diagnosis of <i>NCF1</i> (p47<sup>phox</sup>)-deficient chronic granulomatous disease using high-throughput sequencing
Amy P Hsu, Eric Karlins, Justin Lack, et al.
The Journal of Experimental Medicine
|
August 1, 2020
Constructing and deconstructing GATA2-regulated cell fate programs to establish developmental trajectories
Kirby D Johnson, Daniel J Conn, Evgenia Shishkova, et al.
Clinical Immunology (Orlando, Fla.)
|
May 10, 2019
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections
Svetlana O Sharapova, Emma Haapaniemi, Inga S Sakovich, et al.
Journal of Clinical Immunology
|
April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome
Alexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Haematologica
|
January 15, 2026
GATA2 at 14: genotype-phenotype correlations
Amy P Hsu, Subrata Paul, Jennifer L Kwan, et al.
Blood
|
September 19, 2007
Reversion mutations in patients with leukocyte adhesion deficiency type-1 (LAD-1)
Gulbu Uzel, Emilia Tng, Sergio D Rosenzweig, et al.
Immunohorizons
|
February 12, 2022
Mouse Model of a Human STAT4 Point Mutation That Predisposes to Disseminated Coccidiomycosis
Daniel A Powell, Amy P Hsu, Lisa F Shubitz, et al.
Blood Advances
|
December 13, 2018
GATA2 deficiency and human hematopoietic development modeled using induced pluripotent stem cells
Moonjung Jung, Stefan Cordes, Jizhong Zou, et al.
Blood Advances
|
January 18, 2019
<i>NCF1</i> (p47<sup>phox</sup>)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis
Douglas B Kuhns, Amy P Hsu, David Sun, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 150) with videos related to
Sort By:
Page
of 15
The Journal of Allergy and Clinical Immunology
|
April 30, 2013
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism
Amy P Hsu, Kathryn J Sowerwine, Monica G Lawrence, et al.
Frontiers in Immunology
|
September 11, 2025
Reliable genetic diagnosis of <i>NCF1</i> (p47<sup>phox</sup>)-deficient chronic granulomatous disease using high-throughput sequencing
Amy P Hsu, Eric Karlins, Justin Lack, et al.
The Journal of Experimental Medicine
|
August 1, 2020
Constructing and deconstructing GATA2-regulated cell fate programs to establish developmental trajectories
Kirby D Johnson, Daniel J Conn, Evgenia Shishkova, et al.
Clinical Immunology (Orlando, Fla.)
|
May 10, 2019
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections
Svetlana O Sharapova, Emma Haapaniemi, Inga S Sakovich, et al.
Journal of Clinical Immunology
|
April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome
Alexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Haematologica
|
January 15, 2026
GATA2 at 14: genotype-phenotype correlations
Amy P Hsu, Subrata Paul, Jennifer L Kwan, et al.
Blood
|
September 19, 2007
Reversion mutations in patients with leukocyte adhesion deficiency type-1 (LAD-1)
Gulbu Uzel, Emilia Tng, Sergio D Rosenzweig, et al.
Immunohorizons
|
February 12, 2022
Mouse Model of a Human STAT4 Point Mutation That Predisposes to Disseminated Coccidiomycosis
Daniel A Powell, Amy P Hsu, Lisa F Shubitz, et al.
Blood Advances
|
December 13, 2018
GATA2 deficiency and human hematopoietic development modeled using induced pluripotent stem cells
Moonjung Jung, Stefan Cordes, Jizhong Zou, et al.
Blood Advances
|
January 18, 2019
<i>NCF1</i> (p47<sup>phox</sup>)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis
Douglas B Kuhns, Amy P Hsu, David Sun, et al.
Page
of 15