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Nature
|
February 11, 1993
CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM
J P DiSanto, J Y Bonnefoy, J F Gauchat, et al.
Immunodeficiency
|
January 1, 1993
IgH repertoire and Ig-related gene expression in X-linked agammaglobulinemia
C Schiff, M Milili, F Le Deist, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
August 5, 2000
[Gene therapy of severe combined immunodeficiencies]
M Cavazzana-Calvo, S Hacein-Bey, G de Saint-Basile, et al.
Immunity
|
August 4, 2001
Gene therapy for human severe combined immunodeficiencies
A Fischer, S Hacein-Bey, F Le Deist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 5, 2016
Familial haemophagocytosis lymphohisticytosis type 3: A case report
F Kamoun, M Hsairi, V Grandin, et al.
The Journal of Clinical Investigation
|
March 1, 1992
Genetic study of a new X-linked recessive immunodeficiency syndrome
G de Saint-Basile, F Le Deist, M Caniglia, et al.
The Journal of Clinical Investigation
|
September 1, 1992
Control of human B cell tumor growth in severe combined immunodeficiency mice by monoclonal anti-B cell antibodies
A Durandy, N Brousse, F Rozenberg, et al.
The Journal of Clinical Investigation
|
April 1, 1993
Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire
M Milili, F Le Deist, G de Saint-Basile, et al.
Immunology Letters
|
June 1, 1997
A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case
E Meffre, F LeDeist, G de Saint-Basile, et al.
Human Molecular Genetics
|
December 1, 1995
Improved oligonucleotide primer set for molecular diagnosis of X-linked agammaglobulinaemia: predominance of amino acid substitutions in the catalytic domain of Bruton's tyrosine kinase
I Vorechovský, L Luo, G de Saint Basile, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 106) with videos related to
Sort By:
Page
of 11
Nature
|
February 11, 1993
CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM
J P DiSanto, J Y Bonnefoy, J F Gauchat, et al.
Immunodeficiency
|
January 1, 1993
IgH repertoire and Ig-related gene expression in X-linked agammaglobulinemia
C Schiff, M Milili, F Le Deist, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
August 5, 2000
[Gene therapy of severe combined immunodeficiencies]
M Cavazzana-Calvo, S Hacein-Bey, G de Saint-Basile, et al.
Immunity
|
August 4, 2001
Gene therapy for human severe combined immunodeficiencies
A Fischer, S Hacein-Bey, F Le Deist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 5, 2016
Familial haemophagocytosis lymphohisticytosis type 3: A case report
F Kamoun, M Hsairi, V Grandin, et al.
The Journal of Clinical Investigation
|
March 1, 1992
Genetic study of a new X-linked recessive immunodeficiency syndrome
G de Saint-Basile, F Le Deist, M Caniglia, et al.
The Journal of Clinical Investigation
|
September 1, 1992
Control of human B cell tumor growth in severe combined immunodeficiency mice by monoclonal anti-B cell antibodies
A Durandy, N Brousse, F Rozenberg, et al.
The Journal of Clinical Investigation
|
April 1, 1993
Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire
M Milili, F Le Deist, G de Saint-Basile, et al.
Immunology Letters
|
June 1, 1997
A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case
E Meffre, F LeDeist, G de Saint-Basile, et al.
Human Molecular Genetics
|
December 1, 1995
Improved oligonucleotide primer set for molecular diagnosis of X-linked agammaglobulinaemia: predominance of amino acid substitutions in the catalytic domain of Bruton's tyrosine kinase
I Vorechovský, L Luo, G de Saint Basile, et al.
Page
of 11