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Sven Kracker

Showing results (21-30 of 66) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 26, 2005
Nibrin functions in Ig class-switch recombinationSven Kracker, Yvonne Bergmann, Ilja Demuth, et al.
Journal of Human Immunity|January 30, 2026
A heterozygous USB1 variant linked to immunodeficiencyAlice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 18, 2012
Human MSH6 deficiency is associated with impaired antibody maturationPauline Gardès, Monique Forveille, Marie-Alexandra Alyanakian, et al.
Journal of Biomedical Informatics|July 30, 2017
Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stackNicolas Garcelon, Antoine Neuraz, Vincent Benoit, et al.
The Journal of Clinical Investigation|April 2, 2015
A human immunodeficiency caused by mutations in the PIK3R1 geneMarie-Céline Deau, Lucie Heurtier, Pierre Frange, et al.
Clinical Immunology (Orlando, Fla.)|June 9, 2026
Corrigendum to "Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registry" [Clinical Immunology 283 (2025) 110632]Maria Elena Maccari, Sven Kracker, Anita Chandra, et al.
Clinical Immunology (Orlando, Fla.)|November 2, 2025
Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registryMaria Elena Maccari, Sven Kracker, Anita Chandra, et al.
The Journal of Clinical Investigation|August 19, 2014
A human immunodeficiency caused by mutations in the PIK3R1 geneMarie-Céline Deau, Lucie Heurtier, Pierre Frange, et al.
Molecular Therapy. Methods & Clinical Development|December 28, 2023
Rescuing the cytolytic function of APDS1 patient T cells via TALEN-mediated PIK3CD gene correctionLucie Poggi, Loïc Chentout, Sabrina Lizot, et al.
Frontiers in Immunology|November 15, 2021
UnAIDed Class Switching in Activated B-Cells Reveals Intrinsic Features of a Self-Cleaving IgH LocusIman Dalloul, Brice Laffleur, Zeinab Dalloul, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|January 26, 2005
Nibrin functions in Ig class-switch recombinationSven Kracker, Yvonne Bergmann, Ilja Demuth, et al.
Journal of Human Immunity|January 30, 2026
A heterozygous USB1 variant linked to immunodeficiencyAlice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 18, 2012
Human MSH6 deficiency is associated with impaired antibody maturationPauline Gardès, Monique Forveille, Marie-Alexandra Alyanakian, et al.
Journal of Biomedical Informatics|July 30, 2017
Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stackNicolas Garcelon, Antoine Neuraz, Vincent Benoit, et al.
The Journal of Clinical Investigation|April 2, 2015
A human immunodeficiency caused by mutations in the PIK3R1 geneMarie-Céline Deau, Lucie Heurtier, Pierre Frange, et al.
Clinical Immunology (Orlando, Fla.)|June 9, 2026
Corrigendum to "Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registry" [Clinical Immunology 283 (2025) 110632]Maria Elena Maccari, Sven Kracker, Anita Chandra, et al.
Clinical Immunology (Orlando, Fla.)|November 2, 2025
Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registryMaria Elena Maccari, Sven Kracker, Anita Chandra, et al.
The Journal of Clinical Investigation|August 19, 2014
A human immunodeficiency caused by mutations in the PIK3R1 geneMarie-Céline Deau, Lucie Heurtier, Pierre Frange, et al.
Molecular Therapy. Methods & Clinical Development|December 28, 2023
Rescuing the cytolytic function of APDS1 patient T cells via TALEN-mediated PIK3CD gene correctionLucie Poggi, Loïc Chentout, Sabrina Lizot, et al.
Frontiers in Immunology|November 15, 2021
UnAIDed Class Switching in Activated B-Cells Reveals Intrinsic Features of a Self-Cleaving IgH LocusIman Dalloul, Brice Laffleur, Zeinab Dalloul, et al.
Pageof 7