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A Dautigny

Showing results (41-50 of 54) with videos related to

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Human Molecular Genetics|December 1, 1993
The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23D Pham-Dinh, Y Fourbil, F Blanquet, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipidD Pham-Dinh, J L Popot, O Boespflug-Tanguy, et al.
Human Mutation|January 1, 1996
Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein PoF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Human Genetics|December 1, 1994
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 geneE Nelis, V Timmerman, P De Jonghe, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 11, 1998
Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en PlaquesD Rodriguez, B Della Gaspera, B Zalc, et al.
Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.
Immunogenetics|January 1, 1995
Physical mapping of the human and mouse MOG gene at the distal end of the MHC class Ib regionD Pham-Dinh, E P Jones, G Pitiot, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complexD Pham-Dinh, M G Mattei, J L Nussbaum, et al.
Acta Neuropathologica|May 20, 1999
Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two casesD Rodriguez, A Gelot, B della Gaspera, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|December 1, 1993
The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23D Pham-Dinh, Y Fourbil, F Blanquet, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipidD Pham-Dinh, J L Popot, O Boespflug-Tanguy, et al.
Human Mutation|January 1, 1996
Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein PoF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Human Genetics|December 1, 1994
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 geneE Nelis, V Timmerman, P De Jonghe, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 11, 1998
Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en PlaquesD Rodriguez, B Della Gaspera, B Zalc, et al.
Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.
Immunogenetics|January 1, 1995
Physical mapping of the human and mouse MOG gene at the distal end of the MHC class Ib regionD Pham-Dinh, E P Jones, G Pitiot, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complexD Pham-Dinh, M G Mattei, J L Nussbaum, et al.
Acta Neuropathologica|May 20, 1999
Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two casesD Rodriguez, A Gelot, B della Gaspera, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Pageof 6