Search research articles
Contact Us
Filters
Showing results (71-80 of 104) with videos related to
Page
of 11
Sort By:
Plos Genetics
|
June 15, 2019
Locus suicide recombination actively occurs on the functionally rearranged IgH allele in B-cells from inflamed human lymphoid tissues
Iman Dalloul, François Boyer, Zeinab Dalloul, et al.
The Journal of Experimental Medicine
|
December 12, 2012
Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")
Jana Pachlopnik Schmid, Roxane Lemoine, Nadine Nehme, et al.
The Journal of Allergy and Clinical Immunology
|
October 15, 2014
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex
Sven Kracker, Michela Di Virgilio, Jeremy Schwartzentruber, et al.
Immunity
|
November 8, 2015
Activation-Induced Cytidine Deaminase Expression in Human B Cell Precursors Is Essential for Central B Cell Tolerance
Tineke Cantaert, Jean-Nicolas Schickel, Jason M Bannock, et al.
Blood
|
March 5, 2020
Topoisomerase 2β mutation impairs early B-cell development
Olivier Papapietro, Anita Chandra, Davide Eletto, et al.
Clinical Immunology (Orlando, Fla.)
|
February 14, 2004
Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency
Pierre Quartier, Jacinta Bustamante, Ozden Sanal, et al.
Human Mutation
|
November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutations
Houda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
The Journal of Allergy and Clinical Immunology
|
May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patients
Anne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
The Journal of Clinical Investigation
|
December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiency
Amine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Haematologica
|
April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)
Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 104) with videos related to
Sort By:
Page
of 11
Plos Genetics
|
June 15, 2019
Locus suicide recombination actively occurs on the functionally rearranged IgH allele in B-cells from inflamed human lymphoid tissues
Iman Dalloul, François Boyer, Zeinab Dalloul, et al.
The Journal of Experimental Medicine
|
December 12, 2012
Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")
Jana Pachlopnik Schmid, Roxane Lemoine, Nadine Nehme, et al.
The Journal of Allergy and Clinical Immunology
|
October 15, 2014
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex
Sven Kracker, Michela Di Virgilio, Jeremy Schwartzentruber, et al.
Immunity
|
November 8, 2015
Activation-Induced Cytidine Deaminase Expression in Human B Cell Precursors Is Essential for Central B Cell Tolerance
Tineke Cantaert, Jean-Nicolas Schickel, Jason M Bannock, et al.
Blood
|
March 5, 2020
Topoisomerase 2β mutation impairs early B-cell development
Olivier Papapietro, Anita Chandra, Davide Eletto, et al.
Clinical Immunology (Orlando, Fla.)
|
February 14, 2004
Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency
Pierre Quartier, Jacinta Bustamante, Ozden Sanal, et al.
Human Mutation
|
November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutations
Houda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
The Journal of Allergy and Clinical Immunology
|
May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patients
Anne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
The Journal of Clinical Investigation
|
December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiency
Amine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Haematologica
|
April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)
Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Page
of 11