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Anne Durandy

Showing results (31-40 of 104) with videos related to

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Human Immunology|October 23, 2012
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old maleSvetlana O Sharapova, Alexandr Migas, Irina Guryanova, et al.
Clinical Immunology (Orlando, Fla.)|May 17, 2005
Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2Kohsuke Imai, Yi Zhu, Patrick Revy, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2014
Analysis of somatic hypermutations in the IgM switch region in human B cellsKatsuyuki Horiuchi, Kohsuke Imai, Kanako Mitsui-Sekinaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 8, 2005
Defined blocks in terminal plasma cell differentiation of common variable immunodeficiency patientsNadine Taubenheim, Marcus von Hornung, Anne Durandy, et al.
The Journal of Experimental Medicine|August 20, 2003
Retinoids regulate survival and antigen presentation by immature dendritic cellsFrédéric Geissmann, Patrick Revy, Nicole Brousse, et al.
The Journal of Experimental Medicine|October 1, 2008
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombinationSophie Péron, Ayse Metin, Pauline Gardès, et al.
Journal of Immunoassay & Immunochemistry|February 27, 2014
Class switch recombination process in ataxia telangiectasia patients with elevated serum levels of IgMPayam Mohammadinejad, Hassan Abolhassani, Asghar Aghamohammadi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 19, 2010
Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal-Hreidarsson syndromeFabien Touzot, Isabelle Callebaut, Jean Soulier, et al.
The Journal of Experimental Medicine|June 22, 2005
B cells from hyper-IgM patients carrying UNG mutations lack ability to remove uracil from ssDNA and have elevated genomic uracilBodil Kavli, Sonja Andersen, Marit Otterlei, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 28, 2021
Known and potential molecules associated with altered B cell development leading to predominantly antibody deficienciesParisa Amirifar, Reza Yazdani, Gholamreza Azizi, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Human Immunology|October 23, 2012
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old maleSvetlana O Sharapova, Alexandr Migas, Irina Guryanova, et al.
Clinical Immunology (Orlando, Fla.)|May 17, 2005
Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2Kohsuke Imai, Yi Zhu, Patrick Revy, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2014
Analysis of somatic hypermutations in the IgM switch region in human B cellsKatsuyuki Horiuchi, Kohsuke Imai, Kanako Mitsui-Sekinaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 8, 2005
Defined blocks in terminal plasma cell differentiation of common variable immunodeficiency patientsNadine Taubenheim, Marcus von Hornung, Anne Durandy, et al.
The Journal of Experimental Medicine|August 20, 2003
Retinoids regulate survival and antigen presentation by immature dendritic cellsFrédéric Geissmann, Patrick Revy, Nicole Brousse, et al.
The Journal of Experimental Medicine|October 1, 2008
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombinationSophie Péron, Ayse Metin, Pauline Gardès, et al.
Journal of Immunoassay & Immunochemistry|February 27, 2014
Class switch recombination process in ataxia telangiectasia patients with elevated serum levels of IgMPayam Mohammadinejad, Hassan Abolhassani, Asghar Aghamohammadi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 19, 2010
Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal-Hreidarsson syndromeFabien Touzot, Isabelle Callebaut, Jean Soulier, et al.
The Journal of Experimental Medicine|June 22, 2005
B cells from hyper-IgM patients carrying UNG mutations lack ability to remove uracil from ssDNA and have elevated genomic uracilBodil Kavli, Sonja Andersen, Marit Otterlei, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 28, 2021
Known and potential molecules associated with altered B cell development leading to predominantly antibody deficienciesParisa Amirifar, Reza Yazdani, Gholamreza Azizi, et al.
Pageof 11