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Capucine Picard

Showing results (141-150 of 400) with videos related to

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European Journal of Immunology|October 12, 2013
Human plasma cells express granzyme BWei Xu, Priya Narayanan, Ning Kang, et al.
The Journal of Allergy and Clinical Immunology|July 1, 2011
Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbsDespina Moshous, Isabelle Meyts, Sylvie Fraitag, et al.
Blood|October 17, 2014
IRAK-4 and MyD88 deficiencies impair IgM responses against T-independent bacterial antigensPaul J Maglione, Noa Simchoni, Samuel Black, et al.
Haematologica|January 11, 2020
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiencyChantal Lagresle-Peyrou, Aurélien Olichon, Hanem Sadek, et al.
The Journal of Experimental Medicine|September 19, 2012
Macrophages induce differentiation of plasma cells through CXCL10/IP-10Wei Xu, HyeMee Joo, Sandra Clayton, et al.
Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Plos One|September 7, 2012
Inherited MST1 deficiency underlies susceptibility to EV-HPV infectionsAmandine Crequer, Capucine Picard, Etienne Patin, et al.
Lancet (London, England)|December 14, 2004
Clinical features of dominant and recessive interferon gamma receptor 1 deficienciesSusan E Dorman, Capucine Picard, David Lammas, et al.
Clinical Immunology (Orlando, Fla.)|April 5, 2019
Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study resultsCaroline Thomas, Isabelle Durand-Zaleski, Jérôme Frenkiel, et al.
The Journal of Pediatrics|May 2, 2006
Autosomal recessive interleukin-1 receptor-associated kinase 4 deficiency in fourth-degree relativesMaría Cardenes, Horst von Bernuth, Ayoze García-Saavedra, et al.
Pageof 40

Showing results (141-150 of 400) with videos related to

Sort By:
Pageof 40
European Journal of Immunology|October 12, 2013
Human plasma cells express granzyme BWei Xu, Priya Narayanan, Ning Kang, et al.
The Journal of Allergy and Clinical Immunology|July 1, 2011
Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbsDespina Moshous, Isabelle Meyts, Sylvie Fraitag, et al.
Blood|October 17, 2014
IRAK-4 and MyD88 deficiencies impair IgM responses against T-independent bacterial antigensPaul J Maglione, Noa Simchoni, Samuel Black, et al.
Haematologica|January 11, 2020
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiencyChantal Lagresle-Peyrou, Aurélien Olichon, Hanem Sadek, et al.
The Journal of Experimental Medicine|September 19, 2012
Macrophages induce differentiation of plasma cells through CXCL10/IP-10Wei Xu, HyeMee Joo, Sandra Clayton, et al.
Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Plos One|September 7, 2012
Inherited MST1 deficiency underlies susceptibility to EV-HPV infectionsAmandine Crequer, Capucine Picard, Etienne Patin, et al.
Lancet (London, England)|December 14, 2004
Clinical features of dominant and recessive interferon gamma receptor 1 deficienciesSusan E Dorman, Capucine Picard, David Lammas, et al.
Clinical Immunology (Orlando, Fla.)|April 5, 2019
Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study resultsCaroline Thomas, Isabelle Durand-Zaleski, Jérôme Frenkiel, et al.
The Journal of Pediatrics|May 2, 2006
Autosomal recessive interleukin-1 receptor-associated kinase 4 deficiency in fourth-degree relativesMaría Cardenes, Horst von Bernuth, Ayoze García-Saavedra, et al.
Pageof 40