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Capucine Picard

Showing results (331-340 of 400) with videos related to

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Blood|April 4, 2019
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genesJérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Science (New York, N.Y.)|April 13, 2013
Ribosomal protein SA haploinsufficiency in humans with isolated congenital aspleniaAlexandre Bolze, Nizar Mahlaoui, Minji Byun, et al.
Blood|June 11, 2011
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative studyDaniele Moratto, Silvia Giliani, Carmem Bonfim, et al.
Nature Communications|July 29, 2015
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndromePeter E Thijssen, Yuya Ito, Giacomo Grillo, et al.
The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.
The Journal of Experimental Medicine|November 13, 2013
Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cellsElissa K Deenick, Danielle T Avery, Anna Chan, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 25, 2014
Invasive pneumococcal disease in children can reveal a primary immunodeficiencyJean Gaschignard, Corinne Levy, Maya Chrabieh, et al.
Cell|February 25, 2017
Human Adaptive Immunity Rescues an Inborn Error of Innate ImmunityLaura Israel, Ying Wang, Katarzyna Bulek, et al.
JAMA|April 22, 2015
Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndromeSalima Hacein-Bey Abina, H Bobby Gaspar, Johanna Blondeau, et al.
Pageof 40

Showing results (331-340 of 400) with videos related to

Sort By:
Pageof 40
Blood|April 4, 2019
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genesJérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Science (New York, N.Y.)|April 13, 2013
Ribosomal protein SA haploinsufficiency in humans with isolated congenital aspleniaAlexandre Bolze, Nizar Mahlaoui, Minji Byun, et al.
Blood|June 11, 2011
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative studyDaniele Moratto, Silvia Giliani, Carmem Bonfim, et al.
Nature Communications|July 29, 2015
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndromePeter E Thijssen, Yuya Ito, Giacomo Grillo, et al.
The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.
The Journal of Experimental Medicine|November 13, 2013
Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cellsElissa K Deenick, Danielle T Avery, Anna Chan, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 25, 2014
Invasive pneumococcal disease in children can reveal a primary immunodeficiencyJean Gaschignard, Corinne Levy, Maya Chrabieh, et al.
Cell|February 25, 2017
Human Adaptive Immunity Rescues an Inborn Error of Innate ImmunityLaura Israel, Ying Wang, Katarzyna Bulek, et al.
JAMA|April 22, 2015
Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndromeSalima Hacein-Bey Abina, H Bobby Gaspar, Johanna Blondeau, et al.
Pageof 40