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B Brais

Showing results (11-20 of 38) with videos related to

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Human Molecular Genetics|August 15, 2000
CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulationC Gaspar, M Jannatipour, P Dion, et al.
Human Molecular Genetics|April 1, 1996
The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13qZ Kibar, V M Der Kaloustian, B Brais, et al.
Clinical Genetics|September 7, 2005
Population history and its impact on medical genetics in QuebecA-M Laberge, J Michaud, A Richter, et al.
Neuromuscular Disorders : NMD|December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophyJ Mathieu, G Lapointe, A Brassard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian clusterM Tétreault, M Srour, J Allyson, et al.
Human Molecular Genetics|September 26, 2000
Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNAA Calado, F M Tomé, B Brais, et al.
Neuromuscular Disorders : NMD|February 8, 2005
(GCG)11 founder mutation in the PABPN1 gene of OPMD Uruguayan familiesM Rodríguez, C Camejo, B Bertoni, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
Neurology|November 14, 2007
A novel founder SCN4A mutation causes painful cold-induced myotonia in French-CanadiansE Rossignol, J Mathieu, I Thiffault, et al.
Cell Death & Disease|October 5, 2013
Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathwayA Abu-Baker, J Laganiere, R Gaudet, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|August 15, 2000
CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulationC Gaspar, M Jannatipour, P Dion, et al.
Human Molecular Genetics|April 1, 1996
The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13qZ Kibar, V M Der Kaloustian, B Brais, et al.
Clinical Genetics|September 7, 2005
Population history and its impact on medical genetics in QuebecA-M Laberge, J Michaud, A Richter, et al.
Neuromuscular Disorders : NMD|December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophyJ Mathieu, G Lapointe, A Brassard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian clusterM Tétreault, M Srour, J Allyson, et al.
Human Molecular Genetics|September 26, 2000
Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNAA Calado, F M Tomé, B Brais, et al.
Neuromuscular Disorders : NMD|February 8, 2005
(GCG)11 founder mutation in the PABPN1 gene of OPMD Uruguayan familiesM Rodríguez, C Camejo, B Bertoni, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
Neurology|November 14, 2007
A novel founder SCN4A mutation causes painful cold-induced myotonia in French-CanadiansE Rossignol, J Mathieu, I Thiffault, et al.
Cell Death & Disease|October 5, 2013
Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathwayA Abu-Baker, J Laganiere, R Gaudet, et al.
Pageof 4