Showing results (71-80 of 86) with videos related to
Sort By:
Pageof 9
The Journal of Allergy and Clinical Immunology|October 15, 2014
Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 bindingValentina Cetica, Yvonne Hackmann, Samantha Grieve, et al.Traffic (Copenhagen, Denmark)|February 11, 2005
Normal lytic granule secretion by cytotoxic T lymphocytes deficient in BLOC-1, -2 and -3 and myosins Va, VIIa and XVGiovanna Bossi, Sarah Booth, Richard Clark, et al.Frontiers in Immunology|December 28, 2020
Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector EngagementYuta Ohishi, Sandra Ammann, Vahid Ziaee, et al.Nature Communications|January 22, 2020
Distinctive phenotypes and functions of innate lymphoid cells in human decidua during early pregnancyOisín Huhn, Martin A Ivarsson, Lucy Gardner, et al.Journal of Medical Genetics|August 28, 2010
STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5Valentina Cetica, Alessandra Santoro, Kimberly C Gilmour, et al.The Journal of Allergy and Clinical Immunology|September 7, 2015
Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registryValentina Cetica, Elena Sieni, Daniela Pende, et al.Journal of Medical Genetics|January 21, 2011
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3Elena Sieni, Valentina Cetica, Alessandra Santoro, et al.Frontiers in Immunology|June 30, 2023
Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A)Nina Brauer, Yuto Maruta, Miriam Lisci, et al.Journal of Immunology (Baltimore, Md. : 1950)|January 8, 2010
Ca2+ release from the endoplasmic reticulum of NY-ESO-1-specific T cells is modulated by the affinity of TCR and by the use of the CD8 coreceptorJi-Li Chen, Anthony J Morgan, Guillaume Stewart-Jones, et al.The Journal of Allergy and Clinical Immunology|November 13, 2012
Reduced type I interferon production by dendritic cells and weakened antiviral immunity in patients with Wiskott-Aldrich syndrome protein deficiencyPhilipp A Lang, Namir Shaabani, Stephanie Borkens, et al.Pageof 9