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N Soussi-Yanicostas

Showing results (1-10 of 15) with videos related to

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Developmental Biology|October 1, 1991
Transcription of the embryonic myosin light chain gene is restricted to type II muscle fibers in human adult masseterN Soussi-Yanicostas, G S Butler-Browne
Human Molecular Genetics|May 1, 1993
Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genomeN Soussi-Yanicostas, R G Whalen, C Petit
FEBS Letters|March 25, 1991
Biphasic expression of slow myosin light chains and slow tropomyosin isoforms during the development of the human quadriceps muscleC Laurent-Winter, N Soussi-Yanicostas, G S Butler-Browne
Nucleic Acids Research|April 11, 1991
The human embryonic myosin alkali light chain gene: use of alternative promoters and 3' non-coding regionsM Rotter, K Zimmerman, A Poustka, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Kallmann syndromeJ P Hardelin, N Soussi-Yanicostas, O Ardouin, et al.
Development (Cambridge, England)|February 1, 1990
Transition of myosin isozymes during development of human masseter muscle. Persistence of developmental isoforms during postnatal stageN Soussi-Yanicostas, J P Barbet, C Laurent-Winter, et al.
Journal of Cell Science|September 10, 1998
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific mannerN Soussi-Yanicostas, C Faivre-Sarrailh, J P Hardelin, et al.
Journal of the Neurological Sciences|May 1, 1992
Evolution of muscle specific proteins in Werdnig-Hoffman's diseaseN Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Journal of the Neurological Sciences|May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophyC B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Muscle & Nerve|April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophyC Ben Hamida, N Soussi-Yanicostas, G S Butler-Browne, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Developmental Biology|October 1, 1991
Transcription of the embryonic myosin light chain gene is restricted to type II muscle fibers in human adult masseterN Soussi-Yanicostas, G S Butler-Browne
Human Molecular Genetics|May 1, 1993
Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genomeN Soussi-Yanicostas, R G Whalen, C Petit
FEBS Letters|March 25, 1991
Biphasic expression of slow myosin light chains and slow tropomyosin isoforms during the development of the human quadriceps muscleC Laurent-Winter, N Soussi-Yanicostas, G S Butler-Browne
Nucleic Acids Research|April 11, 1991
The human embryonic myosin alkali light chain gene: use of alternative promoters and 3' non-coding regionsM Rotter, K Zimmerman, A Poustka, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Kallmann syndromeJ P Hardelin, N Soussi-Yanicostas, O Ardouin, et al.
Development (Cambridge, England)|February 1, 1990
Transition of myosin isozymes during development of human masseter muscle. Persistence of developmental isoforms during postnatal stageN Soussi-Yanicostas, J P Barbet, C Laurent-Winter, et al.
Journal of Cell Science|September 10, 1998
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific mannerN Soussi-Yanicostas, C Faivre-Sarrailh, J P Hardelin, et al.
Journal of the Neurological Sciences|May 1, 1992
Evolution of muscle specific proteins in Werdnig-Hoffman's diseaseN Soussi-Yanicostas, C Ben Hamida, K Bejaoui, et al.
Journal of the Neurological Sciences|May 1, 1994
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophyC B Hamida, N Soussi-Yanicostas, K Bejaoui, et al.
Muscle & Nerve|April 1, 1994
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophyC Ben Hamida, N Soussi-Yanicostas, G S Butler-Browne, et al.
Pageof 2