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Genomics
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May 1, 1994
Detection of three nonsense mutations and one missense mutation in the interleukin-2 receptor gamma chain gene in SCIDX1 that differently affect the mRNA processing
S Markiewicz, A Subtil, A Dautry-Varsat, et al.
Immunology Today
|
May 29, 2000
Perforin: more than just an effector molecule
S E Stepp, P A Mathew, M Bennett, et al.
Human Mutation
|
January 1, 1996
Novel nonsense mutation in the hypoxanthine guanine phosphoribosyltransferase gene and nonrandom X-inactivation causing Lesch-Nyhan syndrome in a female patient
B Aral, G de Saint Basile, S Al-Garawi, et al.
Genomics
|
July 1, 1997
Localization of the Rab escort protein-2 (REP2) and inositol 1,4,5-trisphosphate 3-kinase (ITPKB) genes to mouse chromosome 1 by in situ hybridization and precision of the syntenic regions between mouse and human 1q42-q44
F J Barrat, D Depetris, S Certain, et al.
Prostaglandins, Leukotrienes, and Medicine
|
March 1, 1986
Regulation of prostaglandin E2 and plasminogen activator by various immunomodulators in human monocytes
F Homo-Delarche, G de Saint-Basile, F Le Deist, et al.
European Journal of Immunology
|
February 1, 1994
Interleukin-2 (IL-2) receptor gamma chain mutations in X-linked severe combined immunodeficiency disease result in the loss of high-affinity IL-2 receptor binding
J P DiSanto, A Dautry-Varsat, S Certain, et al.
Advances in Experimental Medicine and Biology
|
January 5, 2002
Gene therapy of severe combined immunodeficiencies
A Fischer, S Hacein-Bey, F Le Deist, et al.
Immunodeficiency
|
January 1, 1993
Control of human B cell tumor growth in SCID mice by monoclonal anti-B cell antibodies
A Durandy, N Brousse, F Rozenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 27, 1994
Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells
J P DiSanto, F Rieux-Laucat, A Dautry-Varsat, et al.
Journal of the Neurological Sciences
|
July 22, 2014
Motor neuronopathy in Chediak-Higashi syndrome
S Mathis, P Cintas, G de Saint-Basile, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 106) with videos related to
Sort By:
Page
of 11
Genomics
|
May 1, 1994
Detection of three nonsense mutations and one missense mutation in the interleukin-2 receptor gamma chain gene in SCIDX1 that differently affect the mRNA processing
S Markiewicz, A Subtil, A Dautry-Varsat, et al.
Immunology Today
|
May 29, 2000
Perforin: more than just an effector molecule
S E Stepp, P A Mathew, M Bennett, et al.
Human Mutation
|
January 1, 1996
Novel nonsense mutation in the hypoxanthine guanine phosphoribosyltransferase gene and nonrandom X-inactivation causing Lesch-Nyhan syndrome in a female patient
B Aral, G de Saint Basile, S Al-Garawi, et al.
Genomics
|
July 1, 1997
Localization of the Rab escort protein-2 (REP2) and inositol 1,4,5-trisphosphate 3-kinase (ITPKB) genes to mouse chromosome 1 by in situ hybridization and precision of the syntenic regions between mouse and human 1q42-q44
F J Barrat, D Depetris, S Certain, et al.
Prostaglandins, Leukotrienes, and Medicine
|
March 1, 1986
Regulation of prostaglandin E2 and plasminogen activator by various immunomodulators in human monocytes
F Homo-Delarche, G de Saint-Basile, F Le Deist, et al.
European Journal of Immunology
|
February 1, 1994
Interleukin-2 (IL-2) receptor gamma chain mutations in X-linked severe combined immunodeficiency disease result in the loss of high-affinity IL-2 receptor binding
J P DiSanto, A Dautry-Varsat, S Certain, et al.
Advances in Experimental Medicine and Biology
|
January 5, 2002
Gene therapy of severe combined immunodeficiencies
A Fischer, S Hacein-Bey, F Le Deist, et al.
Immunodeficiency
|
January 1, 1993
Control of human B cell tumor growth in SCID mice by monoclonal anti-B cell antibodies
A Durandy, N Brousse, F Rozenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 27, 1994
Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells
J P DiSanto, F Rieux-Laucat, A Dautry-Varsat, et al.
Journal of the Neurological Sciences
|
July 22, 2014
Motor neuronopathy in Chediak-Higashi syndrome
S Mathis, P Cintas, G de Saint-Basile, et al.
Page
of 11