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Journal Articles

Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

Blood (2024) 144 (8): 873–887.

https://doi.org/10.1182/blood.2024024499

Published: 2024

Includes: Supplemental data

Journal Articles

Quercetin ameliorates XIAP deficiency–associated hyperinflammation

Samuel C. C. Chiang, Erika Owsley, Neelam Panchal, Vijaya Chaturvedi, Catherine E. Terrell, Michael B. Jordan, Parinda A. Mehta, Stella M. Davies, Nagako Akeno, Claire Booth, Rebecca A. Marsh

Blood (2022) 140 (7): 706–715.

https://doi.org/10.1182/blood.2021014335

Published: 2022

Includes: Supplemental data

Journal Articles

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Blood (2017) 129 (16): 2266–2279.

https://doi.org/10.1182/blood-2016-10-743302

Published: 2017

Includes: Supplemental data

Journal Articles

Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells

Blood (2017) 129 (14): 1927–1939.

https://doi.org/10.1182/blood-2016-08-734236

Published: 2017

Includes: Supplemental data

Journal Articles

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Blood (2013) 121 (8): 1345–1356.

https://doi.org/10.1182/blood-2012-07-442558

Published: 2013

Includes: Supplemental data

Journal Articles

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D

Blood (2011) 118 (22): 5783–5793.

https://doi.org/10.1182/blood-2011-07-369090

Published: 2011

Includes: Supplemental data

Journal Articles

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2

Marie Meeths, Miriam Entesarian, Waleed Al-Herz, Samuel C. C. Chiang, Stephanie M. Wood, Wafa Al-Ateeqi, Francisco Almazan, Jaap J. Boelens, Henrik Hasle, Marianne Ifversen, Bendik Lund, J. Merlijn van den Berg, Britt Gustafsson, Hans Hjelmqvist, Magnus Nordenskjöld, Yenan T. Bryceson, Jan-Inge Henter

Blood (2010) 116 (15): 2635–2643.

https://doi.org/10.1182/blood-2010-05-282541

Published: 2010

Journal Articles

Different NK cell–activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity

Stephanie M. Wood, Marie Meeths, Samuel C. C. Chiang, Anne Grete Bechensteen, Jaap J. Boelens, Carsten Heilmann, Hisanori Horiuchi, Steen Rosthøj, Olga Rutynowska, Jacek Winiarski, Jennifer L. Stow, Magnus Nordenskjöld, Jan-Inge Henter, Hans-Gustaf Ljunggren, Yenan T. Bryceson

Blood (2009) 114 (19): 4117–4127.

https://doi.org/10.1182/blood-2009-06-225359

Published: 2009

NARROW

Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

Quercetin ameliorates XIAP deficiency–associated hyperinflammation

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2

Different NK cell–activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity

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American Society of Hematology

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ASH Publications

American Society of Hematology

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