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The Journal of Allergy and Clinical Immunology
|
February 14, 2013
Blood CD4+CD45RO+CXCR5+ T cells are decreased but partially functional in signal transducer and activator of transcription 3 deficiency
Fabienne Mazerolles, Capucine Picard, Sven Kracker, et al.
Journal of Clinical Immunology
|
July 31, 2023
A Case Report of Folliculin-Interacting Protein 1 Deficiency
Nidia Moreno-Corona, Alice Valagussa, Romane Thouenon, et al.
Frontiers in Pediatrics
|
July 12, 2021
Activated PI3Kinase Delta Syndrome-A Multifaceted Disease
Romane Thouenon, Nidia Moreno-Corona, Lucie Poggi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 19, 2016
Mouse model for acute Epstein-Barr virus infection
Tristan Wirtz, Timm Weber, Sven Kracker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 8, 2010
Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair
Sven Kracker, Kohsuke Imai, Pauline Gardès, et al.
The Journal of Experimental Medicine
|
February 11, 2009
Pol zeta ablation in B cells impairs the germinal center reaction, class switch recombination, DNA break repair, and genome stability
Dominik Schenten, Sven Kracker, Gloria Esposito, et al.
The Journal of Experimental Medicine
|
May 23, 2012
DNA polymerase ζ generates tandem mutations in immunoglobulin variable regions
Huseyin Saribasak, Robert W Maul, Zheng Cao, et al.
Annals of the Rheumatic Diseases
|
June 3, 2018
Comment on: 'Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors' by Giannelou <i>et al</i>: mutations in <i>TRNT1</i> result in a constitutive activation of type I interferon signalling
Marie-Louise Frémond, Isabelle Melki, Sven Kracker, et al.
The Journal of Allergy and Clinical Immunology
|
March 4, 2024
Loss-of-phosphorylation of IKZF1 results in gain-of-function associated with immune dysregulation
Akihiro Hoshino, Benoît Heid Picard, Sophia Polychronopoulou, et al.
The Journal of Pediatrics
|
May 20, 2020
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine Deaminase Deficiency: Unraveling an Inherited Immunodeficiency after 50 Years
Jehane Fadlallah, Loic Chentout, Bertrand Boisson, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 66) with videos related to
Sort By:
Page
of 7
The Journal of Allergy and Clinical Immunology
|
February 14, 2013
Blood CD4+CD45RO+CXCR5+ T cells are decreased but partially functional in signal transducer and activator of transcription 3 deficiency
Fabienne Mazerolles, Capucine Picard, Sven Kracker, et al.
Journal of Clinical Immunology
|
July 31, 2023
A Case Report of Folliculin-Interacting Protein 1 Deficiency
Nidia Moreno-Corona, Alice Valagussa, Romane Thouenon, et al.
Frontiers in Pediatrics
|
July 12, 2021
Activated PI3Kinase Delta Syndrome-A Multifaceted Disease
Romane Thouenon, Nidia Moreno-Corona, Lucie Poggi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 19, 2016
Mouse model for acute Epstein-Barr virus infection
Tristan Wirtz, Timm Weber, Sven Kracker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 8, 2010
Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair
Sven Kracker, Kohsuke Imai, Pauline Gardès, et al.
The Journal of Experimental Medicine
|
February 11, 2009
Pol zeta ablation in B cells impairs the germinal center reaction, class switch recombination, DNA break repair, and genome stability
Dominik Schenten, Sven Kracker, Gloria Esposito, et al.
The Journal of Experimental Medicine
|
May 23, 2012
DNA polymerase ζ generates tandem mutations in immunoglobulin variable regions
Huseyin Saribasak, Robert W Maul, Zheng Cao, et al.
Annals of the Rheumatic Diseases
|
June 3, 2018
Comment on: 'Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors' by Giannelou <i>et al</i>: mutations in <i>TRNT1</i> result in a constitutive activation of type I interferon signalling
Marie-Louise Frémond, Isabelle Melki, Sven Kracker, et al.
The Journal of Allergy and Clinical Immunology
|
March 4, 2024
Loss-of-phosphorylation of IKZF1 results in gain-of-function associated with immune dysregulation
Akihiro Hoshino, Benoît Heid Picard, Sophia Polychronopoulou, et al.
The Journal of Pediatrics
|
May 20, 2020
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine Deaminase Deficiency: Unraveling an Inherited Immunodeficiency after 50 Years
Jehane Fadlallah, Loic Chentout, Bertrand Boisson, et al.
Page
of 7