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Blood
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December 17, 2011
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
Nadine T Nehme, Jana Pachlopnik Schmid, Franck Debeurme, et al.
Nucleic Acids Research
|
April 16, 2008
DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transfer
Gary P Wang, Alexandrine Garrigue, Angela Ciuffi, et al.
The Journal of Experimental Medicine
|
May 9, 2007
A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair
Sophie Péron, Qiang Pan-Hammarström, Kohsuke Imai, et al.
Pediatrics
|
May 3, 2003
Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients
Sophie Dupuis-Girod, Jacques Medioni, Elie Haddad, et al.
Pediatrics
|
March 22, 2006
Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients
Marie Ouachée-Chardin, Caroline Elie, Geneviève de Saint Basile, et al.
The Journal of Allergy and Clinical Immunology
|
October 6, 2014
CD45RA depletion in HLA-mismatched allogeneic hematopoietic stem cell transplantation for primary combined immunodeficiency: A preliminary study
Fabien Touzot, Bénédicte Neven, Liliane Dal-Cortivo, et al.
The Journal of Cell Biology
|
November 5, 2016
Kinesin-1 controls mast cell degranulation and anaphylaxis through PI3K-dependent recruitment to the granular Slp3/Rab27b complex
Isabelle Munoz, Luca Danelli, Julien Claver, et al.
Hemasphere
|
April 3, 2023
CTP Synthase 1 Is a Novel Therapeutic Target in Lymphoma
Hélène Asnagli, Norbert Minet, Christina Pfeiffer, et al.
British Journal of Haematology
|
September 5, 2024
Long-term assessment of haematological recovery following somatic genetic rescue in a MYSM1-deficient patient: Implications for in vivo gene therapy
Sophie de Tocqueville, Emmanuel Martin, Quentin Riller, et al.
Pediatrics
|
January 26, 2011
Occurrence of aortic aneurysms in 5 cases of Wiskott-Aldrich syndrome
Isabelle Pellier, Sophie Dupuis Girod, Didier Loisel, et al.
Page
of 50
Search research articles
Search
Showing results (251-260 of 493) with videos related to
Sort By:
Page
of 50
Blood
|
December 17, 2011
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
Nadine T Nehme, Jana Pachlopnik Schmid, Franck Debeurme, et al.
Nucleic Acids Research
|
April 16, 2008
DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transfer
Gary P Wang, Alexandrine Garrigue, Angela Ciuffi, et al.
The Journal of Experimental Medicine
|
May 9, 2007
A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair
Sophie Péron, Qiang Pan-Hammarström, Kohsuke Imai, et al.
Pediatrics
|
May 3, 2003
Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients
Sophie Dupuis-Girod, Jacques Medioni, Elie Haddad, et al.
Pediatrics
|
March 22, 2006
Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients
Marie Ouachée-Chardin, Caroline Elie, Geneviève de Saint Basile, et al.
The Journal of Allergy and Clinical Immunology
|
October 6, 2014
CD45RA depletion in HLA-mismatched allogeneic hematopoietic stem cell transplantation for primary combined immunodeficiency: A preliminary study
Fabien Touzot, Bénédicte Neven, Liliane Dal-Cortivo, et al.
The Journal of Cell Biology
|
November 5, 2016
Kinesin-1 controls mast cell degranulation and anaphylaxis through PI3K-dependent recruitment to the granular Slp3/Rab27b complex
Isabelle Munoz, Luca Danelli, Julien Claver, et al.
Hemasphere
|
April 3, 2023
CTP Synthase 1 Is a Novel Therapeutic Target in Lymphoma
Hélène Asnagli, Norbert Minet, Christina Pfeiffer, et al.
British Journal of Haematology
|
September 5, 2024
Long-term assessment of haematological recovery following somatic genetic rescue in a MYSM1-deficient patient: Implications for in vivo gene therapy
Sophie de Tocqueville, Emmanuel Martin, Quentin Riller, et al.
Pediatrics
|
January 26, 2011
Occurrence of aortic aneurysms in 5 cases of Wiskott-Aldrich syndrome
Isabelle Pellier, Sophie Dupuis Girod, Didier Loisel, et al.
Page
of 50