J H Hollis|L R Draper|F Samson - JoVE Visualize

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European Journal of Pediatrics|July 1, 1994

Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.

American Journal of Human Genetics|July 1, 1995

Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.

Journal of Medical Genetics|December 1, 1994

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, et al.

American Journal of Human Genetics|August 1, 1992

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.

Cardiovascular Research|August 6, 1999

Decreased type VI adenylyl cyclase mRNA concentration and Mg(2+)-dependent adenylyl cyclase activities and unchanged type V adenylyl cyclase mRNA concentration and Mn(2+)-dependent adenylyl cyclase activities in the left ventricle of rats with myocardial infarction and longstanding heart failureI Espinasse, V Iourgenko, C Richer, et al.

Neuroscience|March 21, 2007

Identification of an immune-responsive mesolimbocortical serotonergic system: potential role in regulation of emotional behaviorC A Lowry, J H Hollis, A de Vries, et al.

Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Nature Genetics|March 31, 2000

Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2S C Coste, R A Kesterson, K A Heldwein, et al.

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Showing results (71-80 of 78) with videos related to

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You have reached the last page of results.This site can display upto 78 results.

European Journal of Pediatrics|July 1, 1994

Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.

American Journal of Human Genetics|July 1, 1995

Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.

Journal of Medical Genetics|December 1, 1994

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, et al.

American Journal of Human Genetics|August 1, 1992

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.

Cardiovascular Research|August 6, 1999

Decreased type VI adenylyl cyclase mRNA concentration and Mg(2+)-dependent adenylyl cyclase activities and unchanged type V adenylyl cyclase mRNA concentration and Mn(2+)-dependent adenylyl cyclase activities in the left ventricle of rats with myocardial infarction and longstanding heart failureI Espinasse, V Iourgenko, C Richer, et al.

Neuroscience|March 21, 2007

Identification of an immune-responsive mesolimbocortical serotonergic system: potential role in regulation of emotional behaviorC A Lowry, J H Hollis, A de Vries, et al.

Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Nature Genetics|March 31, 2000

Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2S C Coste, R A Kesterson, K A Heldwein, et al.

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