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F Fougerousse

Showing results (21-30 of 37) with videos related to

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Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Cell and Tissue Research|June 19, 2008
Genetic inactivation of acetylcholinesterase causes functional and structural impairment of mouse soleus musclesA Vignaud, F Fougerousse, E Mouisel, et al.
Advances in Experimental Medicine and Biology|September 15, 2000
Molecular tools for the study of titin's differential expressionT Centner, F Fougerousse, A Freiburg, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Circulation Research|July 1, 1992
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French familiesK Schwartz, J Beckmann, C Dufour, et al.
Nature|March 12, 1992
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitusP Froguel, M Vaxillaire, F Sun, et al.
Gene Therapy|March 3, 2007
AAV-mediated delivery of a mutated myostatin propeptide ameliorates calpain 3 but not alpha-sarcoglycan deficiencyM Bartoli, J Poupiot, A Vulin, et al.
Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Science (New York, N.Y.)|September 5, 1997
Dynamic molecular combing: stretching the whole human genome for high-resolution studiesX Michalet, R Ekong, F Fougerousse, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Cell and Tissue Research|June 19, 2008
Genetic inactivation of acetylcholinesterase causes functional and structural impairment of mouse soleus musclesA Vignaud, F Fougerousse, E Mouisel, et al.
Advances in Experimental Medicine and Biology|September 15, 2000
Molecular tools for the study of titin's differential expressionT Centner, F Fougerousse, A Freiburg, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Circulation Research|July 1, 1992
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French familiesK Schwartz, J Beckmann, C Dufour, et al.
Nature|March 12, 1992
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitusP Froguel, M Vaxillaire, F Sun, et al.
Gene Therapy|March 3, 2007
AAV-mediated delivery of a mutated myostatin propeptide ameliorates calpain 3 but not alpha-sarcoglycan deficiencyM Bartoli, J Poupiot, A Vulin, et al.
Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Science (New York, N.Y.)|September 5, 1997
Dynamic molecular combing: stretching the whole human genome for high-resolution studiesX Michalet, R Ekong, F Fougerousse, et al.
Pageof 4