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pro vyhledávání: '"Marie Pierre Chevron"'
Autor:
Marie-Pierre Chevron
Publikováno v:
Perspectives in Science, Vol 2, Iss 1, Pp 46-54 (2014)
Developing meaningful learning is not only difficult to achieve but also time consuming, because it requires a large number of different skills to develop and master. Many studies have shown that organizing knowledge in concept maps helps teachers an
Autor:
Marie Pierre Chevron, Doris Martin, Richard P. Tucker, Beatrix P. Rubin, Ronelle J. Hall, Ruth Chiquet-Ehrismann
Publikováno v:
Developmental Dynamics. 220:27-39
Teneurin-2 is a member of a novel family of transmembrane proteins characterized to date in fish, birds, mammals, and Drosophila (e.g., the pair-rule gene product Ten-m). We have shown that teneurin-2 is expressed by neurons in the developing avian v
Autor:
Bernard Calas, Francis Poulat, Philippe Berta, Catherine Gozé, Xavier Rebillard, Marie Pierre Chevron, Ned J.C. Lamb, Franck Girard
Publikováno v:
The Journal of Cell Biology
We have studied the expression of the human SRY protein (termed p27SRY) in two different cell lines by using specific antibodies. Confocal microscopy enabled us to localize p27SRY precisely in the nucleus in a discrete punctuate pattern. Furthermore,
Publikováno v:
Neuromuscular Disorders. 2:47-50
Becker muscular dystrophy (BMD) often results from in-frame mutations of the dystrophin gene, leading to the production of an altered-sized protein. We examined the expression of dystrophin in a BMD patient and in his asymptomatic mother by Western b
Publikováno v:
Neuromuscular disorders : NMD. 4(5-6)
Dystrophin, the product of the DMD gene, is present in all muscle types in normal individuals. Its function has yet to be elucidated, but its absence or the presence of a truncated version of the protein is responsible for the appearance of Duchenne
Autor:
Mireille Claustres, Bernard Echenne, Patricia Martinez, Sylvie Tuffery, Marie-Pierre Jozelon, Marie-Pierre Chevron, Jacques Demaille
Publikováno v:
Human genetics. 88(2)
We studied 38 unrelated patients from southern France with Duchenne (DMD) or Becker (BMD) muscular dystrophy for intragenic deletions of the DMD/BMD gene. We used both multiplex amplification of selected exons and cDNA probes. Of the 26 (68%) unrelat
Publikováno v:
New England Journal of Medicine. 331:1162-1163
To the Editor: Utrophin is an autosomally inherited protein encoded by chromosome 6 that is homologous to dystrophin and localized in normal adult muscle exclusively at neuromuscular junctions.1 No clinical disorder is recognized that relates to alte