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Anne Durandy

Showing results (41-50 of 104) with videos related to

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The Journal of Pediatrics|May 20, 2020
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine Deaminase Deficiency: Unraveling an Inherited Immunodeficiency after 50 YearsJehane Fadlallah, Loic Chentout, Bertrand Boisson, et al.
Clinical Immunology (Orlando, Fla.)|December 4, 2020
Class Switch Recombination Defects: impact on B cell maturation and antibody responsesEllen D Renner, Carolin E Krätz, Jordan S Orange, et al.
Human Mutation|March 12, 2011
A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP)Véronique Pons, Corinne Rolland, Michel Nauze, et al.
The Journal of Pediatrics|April 18, 2006
A novel form of non-X-linked hyperigm associated with growth and pubertal disturbances and with lymphoma developmentViviana Moschese, Jiri Lintzman, Francesco Callea, 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.
DNA Repair|April 24, 2012
The UNG2 Arg88Cys variant abrogates RPA-mediated recruitment of UNG2 to single-stranded DNAKathrin Torseth, Berit Doseth, Lars Hagen, 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.
The Journal of Clinical Investigation|November 17, 2004
Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3Geneviève de Saint Basile, Frédéric Geissmann, Elisabeth Flori, 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.
Nucleic Acids Research|October 14, 2004
Repair of U/G and U/A in DNA by UNG2-associated repair complexes takes place predominantly by short-patch repair both in proliferating and growth-arrested cellsMansour Akbari, Marit Otterlei, Javier Peña-Diaz, et al.
Pageof 11

Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
The Journal of Pediatrics|May 20, 2020
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine Deaminase Deficiency: Unraveling an Inherited Immunodeficiency after 50 YearsJehane Fadlallah, Loic Chentout, Bertrand Boisson, et al.
Clinical Immunology (Orlando, Fla.)|December 4, 2020
Class Switch Recombination Defects: impact on B cell maturation and antibody responsesEllen D Renner, Carolin E Krätz, Jordan S Orange, et al.
Human Mutation|March 12, 2011
A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP)Véronique Pons, Corinne Rolland, Michel Nauze, et al.
The Journal of Pediatrics|April 18, 2006
A novel form of non-X-linked hyperigm associated with growth and pubertal disturbances and with lymphoma developmentViviana Moschese, Jiri Lintzman, Francesco Callea, 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.
DNA Repair|April 24, 2012
The UNG2 Arg88Cys variant abrogates RPA-mediated recruitment of UNG2 to single-stranded DNAKathrin Torseth, Berit Doseth, Lars Hagen, 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.
The Journal of Clinical Investigation|November 17, 2004
Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3Geneviève de Saint Basile, Frédéric Geissmann, Elisabeth Flori, 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.
Nucleic Acids Research|October 14, 2004
Repair of U/G and U/A in DNA by UNG2-associated repair complexes takes place predominantly by short-patch repair both in proliferating and growth-arrested cellsMansour Akbari, Marit Otterlei, Javier Peña-Diaz, et al.
Pageof 11