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Sandra T Cooper

Showing results (21-30 of 97) with videos related to

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Neuromuscular Disorders : NMD|February 17, 2007
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesisSandra T Cooper, Eddy Kizana, Jonathon D Yates, et al.
Journal of Molecular and Cellular Cardiology|May 12, 2004
Expression of aquaporin 1 in human cardiac and skeletal muscleCarol G Au, Sandra T Cooper, Harriet P Lo, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Annals of Neurology|November 25, 2004
An alphaTropomyosin mutation alters dimer preference in nemaline myopathyMark A Corbett, P Anthony Akkari, Ana Domazetovska, et al.
Brain : a Journal of Neurology|October 12, 2007
Mechanisms underlying intranuclear rod formationAna Domazetovska, Biljana Ilkovski, Sandra T Cooper, et al.
Acta Neuropathologica Communications|December 3, 2016
Dopamine-2 receptor extracellular N-terminus regulates receptor surface availability and is the target of human pathogenic antibodies from children with movement and psychiatric disordersNese Sinmaz, Fiona Tea, Deepti Pilli, et al.
Science Advances|March 13, 2024
Lmod2 is necessary for effective skeletal muscle contractionTania M Larrinaga, Gerrie P Farman, Rachel M Mayfield, et al.
Human Molecular Genetics|June 17, 2004
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoformsBiljana Ilkovski, Kristen J Nowak, Ana Domazetovska, et al.
Acta Neuropathologica|April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patientsCarol G Au, Tanya L Butler, Jonathan R Egan, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Neuromuscular Disorders : NMD|February 17, 2007
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesisSandra T Cooper, Eddy Kizana, Jonathon D Yates, et al.
Journal of Molecular and Cellular Cardiology|May 12, 2004
Expression of aquaporin 1 in human cardiac and skeletal muscleCarol G Au, Sandra T Cooper, Harriet P Lo, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Annals of Neurology|November 25, 2004
An alphaTropomyosin mutation alters dimer preference in nemaline myopathyMark A Corbett, P Anthony Akkari, Ana Domazetovska, et al.
Brain : a Journal of Neurology|October 12, 2007
Mechanisms underlying intranuclear rod formationAna Domazetovska, Biljana Ilkovski, Sandra T Cooper, et al.
Acta Neuropathologica Communications|December 3, 2016
Dopamine-2 receptor extracellular N-terminus regulates receptor surface availability and is the target of human pathogenic antibodies from children with movement and psychiatric disordersNese Sinmaz, Fiona Tea, Deepti Pilli, et al.
Science Advances|March 13, 2024
Lmod2 is necessary for effective skeletal muscle contractionTania M Larrinaga, Gerrie P Farman, Rachel M Mayfield, et al.
Human Molecular Genetics|June 17, 2004
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoformsBiljana Ilkovski, Kristen J Nowak, Ana Domazetovska, et al.
Acta Neuropathologica|April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patientsCarol G Au, Tanya L Butler, Jonathan R Egan, et al.
Pageof 10