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C C Chiang

Showing results (81-90 of 114) with videos related to

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Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
The Journal of Allergy and Clinical Immunology. in Practice|May 25, 2021
A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary ImmunodeficiencyVijaya Knight, Jennifer R Heimall, Hey Chong, et al.
Blood|February 18, 2017
Adaptive NK cells can persist in patients with <i>GATA2</i> mutation depleted of stem and progenitor cellsHeinrich Schlums, Moonjung Jung, Hongya Han, et al.
The Journal of Allergy and Clinical Immunology|May 6, 2018
Screening for Wiskott-Aldrich syndrome by flow cytometrySamuel C C Chiang, Sue M Vergamini, Ammar Husami, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
Blood|September 21, 2011
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13DMarie Meeths, Samuel C C Chiang, Stephanie M Wood, et al.
Annals of Hematology|November 23, 2024
Clinical spectrum of primary hemophagocytic lymphohistiocytosis: experience of reference centers in Central and Southeast AnatoliaŞefika Akyol, Ebru Yılmaz, Hüseyin Tokgöz, et al.
Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Pageof 12

Showing results (81-90 of 114) with videos related to

Sort By:
Pageof 12
Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
The Journal of Allergy and Clinical Immunology. in Practice|May 25, 2021
A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary ImmunodeficiencyVijaya Knight, Jennifer R Heimall, Hey Chong, et al.
Blood|February 18, 2017
Adaptive NK cells can persist in patients with <i>GATA2</i> mutation depleted of stem and progenitor cellsHeinrich Schlums, Moonjung Jung, Hongya Han, et al.
The Journal of Allergy and Clinical Immunology|May 6, 2018
Screening for Wiskott-Aldrich syndrome by flow cytometrySamuel C C Chiang, Sue M Vergamini, Ammar Husami, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
Blood|February 17, 2017
Gain-of-function <i>SAMD9L</i> mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.
Blood|September 21, 2011
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13DMarie Meeths, Samuel C C Chiang, Stephanie M Wood, et al.
Annals of Hematology|November 23, 2024
Clinical spectrum of primary hemophagocytic lymphohistiocytosis: experience of reference centers in Central and Southeast AnatoliaŞefika Akyol, Ebru Yılmaz, Hüseyin Tokgöz, et al.
Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Pageof 12