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Amy P Hsu

Showing results (81-90 of 150) with videos related to

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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 mosaicismAmy 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 sequencingAmy 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 trajectoriesKirby 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 infectionsSvetlana O Sharapova, Emma Haapaniemi, Inga S Sakovich, et al.
Journal of Clinical Immunology|April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndromeAlexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Haematologica|January 15, 2026
GATA2 at 14: genotype-phenotype correlationsAmy 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 CoccidiomycosisDaniel 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 cellsMoonjung 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 analysisDouglas B Kuhns, Amy P Hsu, David Sun, et al.
Pageof 15

Showing results (81-90 of 150) with videos related to

Sort By:
Pageof 15
The Journal of Allergy and Clinical Immunology|April 30, 2013
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicismAmy 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 sequencingAmy 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 trajectoriesKirby 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 infectionsSvetlana O Sharapova, Emma Haapaniemi, Inga S Sakovich, et al.
Journal of Clinical Immunology|April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndromeAlexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Haematologica|January 15, 2026
GATA2 at 14: genotype-phenotype correlationsAmy 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 CoccidiomycosisDaniel 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 cellsMoonjung 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 analysisDouglas B Kuhns, Amy P Hsu, David Sun, et al.
Pageof 15