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J M Ervasti

Showing results (21-30 of 32) with videos related to

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Nature|May 24, 1990
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscleJ M Ervasti, K Ohlendieck, S D Kahl, et al.
Veterinary Pathology|March 1, 2014
Postanesthetic death in a cat with myopathyG Remmers, D W Hayden, M A Jaeger, et al.
The American Journal of Physiology|January 1, 1991
Ryanodine receptor in different malignant hyperthermia-susceptible porcine musclesJ M Ervasti, M A Strand, T P Hanson, et al.
Biochimica Et Biophysica Acta|November 17, 1989
An electron paramagnetic resonance study of skeletal muscle membrane fluidity in malignant hyperthermiaJ M Ervasti, J R Mickelson, S M Lewis, et al.
The American Journal of Physiology|July 1, 1994
Skeletal muscle junctional membrane protein content in pigs with different ryanodine receptor genotypesJ R Mickelson, J M Ervasti, L A Litterer, et al.
Biophysical Journal|March 22, 2001
Binding of dystrophin's tandem calponin homology domain to F-actin is modulated by actin's structureA Orlova, I N Rybakova, E Prochniewicz, et al.
Neuron|September 1, 1991
Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscleK Ohlendieck, J M Ervasti, K Matsumura, et al.
The Journal of Biological Chemistry|September 3, 1998
Differential heparin sensitivity of alpha-dystroglycan binding to laminins expressed in normal and dy/dy mouse skeletal muscleE L McDearmon, A L Burwell, A C Combs, et al.
FEBS Letters|August 22, 1994
Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophyJ M Ervasti, S L Roberds, R D Anderson, et al.
Nature|February 20, 1992
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixO Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Nature|May 24, 1990
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscleJ M Ervasti, K Ohlendieck, S D Kahl, et al.
Veterinary Pathology|March 1, 2014
Postanesthetic death in a cat with myopathyG Remmers, D W Hayden, M A Jaeger, et al.
The American Journal of Physiology|January 1, 1991
Ryanodine receptor in different malignant hyperthermia-susceptible porcine musclesJ M Ervasti, M A Strand, T P Hanson, et al.
Biochimica Et Biophysica Acta|November 17, 1989
An electron paramagnetic resonance study of skeletal muscle membrane fluidity in malignant hyperthermiaJ M Ervasti, J R Mickelson, S M Lewis, et al.
The American Journal of Physiology|July 1, 1994
Skeletal muscle junctional membrane protein content in pigs with different ryanodine receptor genotypesJ R Mickelson, J M Ervasti, L A Litterer, et al.
Biophysical Journal|March 22, 2001
Binding of dystrophin's tandem calponin homology domain to F-actin is modulated by actin's structureA Orlova, I N Rybakova, E Prochniewicz, et al.
Neuron|September 1, 1991
Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscleK Ohlendieck, J M Ervasti, K Matsumura, et al.
The Journal of Biological Chemistry|September 3, 1998
Differential heparin sensitivity of alpha-dystroglycan binding to laminins expressed in normal and dy/dy mouse skeletal muscleE L McDearmon, A L Burwell, A C Combs, et al.
FEBS Letters|August 22, 1994
Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophyJ M Ervasti, S L Roberds, R D Anderson, et al.
Nature|February 20, 1992
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixO Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, et al.
Pageof 4