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Journal of Immunology (Baltimore, Md. : 1950)|August 17, 2011
Functional gap junctions accumulate at the immunological synapse and contribute to T cell activationAriadna Mendoza-Naranjo, Gerben Bouma, Cristián Pereda, et al.European Journal of Immunology|August 11, 2015
B-cell intrinsic TLR7 signals promote depletion of the marginal zone in a murine model of Wiskott-Aldrich syndromeNikita S Kolhatkar, Nicole E Scharping, Jenna M Sullivan, et al.Journal of Virology|June 15, 2012
Safer, silencing-resistant lentiviral vectors: optimization of the ubiquitous chromatin-opening element through elimination of aberrant splicingSean Knight, Fang Zhang, Uta Mueller-Kuller, et al.Immunity|June 16, 2007
Transcellular diapedesis is initiated by invasive podosomesChristopher V Carman, Peter T Sage, Tracey E Sciuto, et al.Molecular Genetics & Genomic Medicine|February 19, 2020
The co-occurrence of Wilson disease and X-linked agammaglobulinemia in one family highlights the promising diagnostic potential of proteolytic analysisSheri A Poskanzer, Jenny Thies, Christopher J Collins, et al.Frontiers in Immunology|November 17, 2018
Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) SyndromeEleonora Gambineri, Sara Ciullini Mannurita, David Hagin, et al.Nature Immunology|September 6, 2003
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombinationKohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.Blood|July 31, 2004
Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlationYinzhu Jin, Cinzia Mazza, Jacinda R Christie, et al.Frontiers in Immunology|December 20, 2018
Rapid Multiplexed Proteomic Screening for Primary Immunodeficiency Disorders From Dried Blood SpotsChristopher J Collins, Irene J Chang, Sunhee Jung, et al.Human Gene Therapy. Clinical Development|October 22, 2013
Phase I study protocol for ex-vivo lentiviral gene therapy for the inherited skin disease, Netherton SyndromeWei-Li Di, Jemima E Mellerio, Catina Bernadis, et al.Pageof 51