Chiang Samuel CC
Cited by
Cited by
Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector function
H Schlums, F Cichocki, B Tesi, J Theorell, V Beziat, TD Holmes, H Han, ...
Immunity 42 (3), 443-456, 2015
CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin
S Cheuk, H Schlums, IG Sérézal, E Martini, SC Chiang, N Marquardt, ...
Immunity 46 (2), 287-300, 2017
A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes
YT Bryceson, D Pende, A Maul-Pavicic, KC Gilmour, H Ufheil, T Vraetz, ...
Blood 119 (12), 2754-2763, 2012
Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3
EM Haapaniemi, M Kaustio, HLM Rajala, AJ van Adrichem, L Kainulainen, ...
Blood 125 (4), 639-648, 2015
Molecular mechanisms of natural killer cell activation
YT Bryceson, SCC Chiang, S Darmanin, C Fauriat, H Schlums, J Theorell, ...
Journal of innate immunity 3 (3), 216-226, 2011
ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis
A Maul-Pavicic, SCC Chiang, A Rensing-Ehl, B Jessen, C Fauriat, ...
Proceedings of the National Academy of Sciences 108 (8), 3324-3329, 2011
Surface CD107a/LAMP-1 protects natural killer cells from degranulation-associated damage
A Cohnen, SC Chiang, A Stojanovic, H Schmidt, M Claus, P Saftig, ...
Blood 122 (8), 1411-1418, 2013
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms
B Tesi, J Davidsson, M Voss, E Rahikkala, TD Holmes, SCC Chiang, ...
Blood 129 (16), 2266-2279, 2017
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine …
SCC Chiang, J Theorell, M Entesarian, M Meeths, M Mastafa, W Al-Herz, ...
Blood 121 (8), 1345-1356, 2013
Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2
M Meeths, M Entesarian, W Al-Herz, SCC Chiang, SM Wood, W Al-Ateeqi, ...
Blood 116 (15), 2635-2643, 2010
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT
M Kvarnung, D Nilsson, A Lindstrand, GC Korenke, SCC Chiang, ...
Journal of medical genetics 50 (8), 521-528, 2013
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D
M Meeths, SCC Chiang, SM Wood, M Entesarian, H Schlums, B Bang, ...
Blood 118 (22), 5783-5793, 2011
Different NK cell–activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity
SM Wood, M Meeths, SCC Chiang, AG Bechensteen, JJ Boelens, ...
Blood 114 (19), 4117-4127, 2009
Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiency
B Tesi, E Sieni, C Neves, F Romano, V Cetica, AI Cordeiro, S Chiang, ...
Journal of Allergy and Clinical Immunology 135 (6), 1638-1641. e5, 2015
Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells
H Schlums, M Jung, H Han, J Theorell, V Bigley, SCC Chiang, DSJ Allan, ...
Blood 129 (14), 1927-1939, 2017
Chediak-Higashi syndrome: Lysosomal trafficking regulator domains regulate exocytosis of lytic granules but not cytokine secretion by natural killer cells
A Gil-Krzewska, SM Wood, Y Murakami, V Nguyen, SCC Chiang, ...
Journal of Allergy and Clinical Immunology 137 (4), 1165-1177, 2016
Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity
M Meeths, SCC Chiang, A Löfstedt, ML Müller, B Tesi, JI Henter, ...
Experimental cell research 325 (1), 10-17, 2014
Successful hematopoietic stem cell transplantation in a patient with LPS-responsive beige-like anchor (LRBA) gene mutation
B Tesi, P Priftakis, F Lindgren, SCC Chiang, N Kartalis, A Löfstedt, ...
Journal of clinical immunology 36 (5), 480-489, 2016
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
B Tesi, K Lagerstedt-Robinson, SCC Chiang, EB Bdira, M Abboud, ...
Genome medicine 7 (1), 130, 2015
A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease
T Patiroglu, HH Akar, K Gilmour, E Unal, MA Ozdemir, S Bibi, S Burns, ...
Clinical immunology (Orlando, Fla.) 159 (1), 58-62, 2015
The system can't perform the operation now. Try again later.
Articles 1–20