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Seminars in Immunology|September 26, 2006
Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical featuresOrchidée Filipe-Santos, Jacinta Bustamante, Ariane Chapgier, et al.
Cell|October 1, 2013
Hira-dependent histone H3.3 deposition facilitates PRC2 recruitment at developmental loci in ES cellsLaura A Banaszynski, Duancheng Wen, Scott Dewell, et al.
Journal of Medical Genetics|February 13, 2007
A novel X-linked recessive form of Mendelian susceptibility to mycobaterial diseaseJacinta Bustamante, Capucine Picard, Claire Fieschi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 5, 2006
T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cellsFrancesc Miro, Cinzia Nobile, Nicolas Blanchard, et al.
The Journal of Clinical Investigation|May 14, 2009
A partial form of recessive STAT1 deficiency in humansAriane Chapgier, Xiao-Fei Kong, Stéphanie Boisson-Dupuis, et al.
The Journal of Experimental Medicine|July 16, 2008
Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylationGuillaume Vogt, Jacinta Bustamante, Ariane Chapgier, et al.
European Journal of Pediatrics|August 11, 2005
Inherited disorders of the IL-12-IFN-gamma axis in patients with disseminated BCG infectionDavood Mansouri, Parisa Adimi, Mehdi Mirsaeidi, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiencyCarolina Prando, Stéphanie Boisson-Dupuis, Audrey V Grant, et al.
European Journal of Immunology|September 24, 2004
Bacillus Calmette Guerin triggers the IL-12/IFN-gamma axis by an IRAK-4- and NEMO-dependent, non-cognate interaction between monocytes, NK, and T lymphocytesJacqueline Feinberg, Claire Fieschi, Rainer Doffinger, et al.
Human Molecular Genetics|November 3, 2009
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codonXiao-Fei Kong, Guillaume Vogt, Ariane Chapgier, et al.
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