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C Sparrow

Showing results (91-100 of 104) with videos related to

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Neuromuscular Disorders : NMD|August 19, 2003
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.
Neuromuscular Disorders : NMD|May 11, 2010
Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin geneSarah E Haigh, Sheetal S Salvi, Maria Sevdali, et al.
Oncology|January 1, 1995
Treatment of non-small cell lung cancer with ifosfamide (IFO)+ 4'-epiadriamycin (EPI)+platinum vs. IFO+EPI: a GETLAC Study. Grupo de Estudio y Tratamiento Latinoamericano del Cáncer StudyN Brocato, M F Bruno, C E Araujo, et al.
Invertebrate Neuroscience : IN|April 30, 2008
Neuromuscular control of a single twitch muscle in wild type and mutant Drosophila, measured with an ergometerJennifer Harvey, Holly Brunger, C Adam Middleton, et al.
Neurosurgery|July 20, 2012
The SILVER (Silver Impregnated Line Versus EVD Randomized trial): a double-blind, prospective, randomized, controlled trial of an intervention to reduce the rate of external ventricular drain infectionNicole Chwee Har Keong, Diederik Olivier Bulters, Hugh K Richards, et al.
Biochimica Et Biophysica Acta|July 21, 2000
A target for cholesterol absorption inhibitors in the enterocyte brush border membraneP A Detmers, S Patel, M Hernandez, et al.
Neuromuscular Disorders : NMD|July 13, 2010
Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutationWerner Stenzel, Stefan Prokop, Wolfram Kress, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Molecular Biology and Evolution|September 2, 2003
Molecular evolutionary convergence of the flight muscle protein arthrin in Diptera and hemipteraStephan Schmitz, Christoph J Schankin, Heino Prinz, et al.
Annals of Neurology|October 7, 2004
Actin mutations are one cause of congenital fibre type disproportionNigel G Laing, Nigel F Clarke, Danielle E Dye, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Neuromuscular Disorders : NMD|August 19, 2003
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.
Neuromuscular Disorders : NMD|May 11, 2010
Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin geneSarah E Haigh, Sheetal S Salvi, Maria Sevdali, et al.
Oncology|January 1, 1995
Treatment of non-small cell lung cancer with ifosfamide (IFO)+ 4'-epiadriamycin (EPI)+platinum vs. IFO+EPI: a GETLAC Study. Grupo de Estudio y Tratamiento Latinoamericano del Cáncer StudyN Brocato, M F Bruno, C E Araujo, et al.
Invertebrate Neuroscience : IN|April 30, 2008
Neuromuscular control of a single twitch muscle in wild type and mutant Drosophila, measured with an ergometerJennifer Harvey, Holly Brunger, C Adam Middleton, et al.
Neurosurgery|July 20, 2012
The SILVER (Silver Impregnated Line Versus EVD Randomized trial): a double-blind, prospective, randomized, controlled trial of an intervention to reduce the rate of external ventricular drain infectionNicole Chwee Har Keong, Diederik Olivier Bulters, Hugh K Richards, et al.
Biochimica Et Biophysica Acta|July 21, 2000
A target for cholesterol absorption inhibitors in the enterocyte brush border membraneP A Detmers, S Patel, M Hernandez, et al.
Neuromuscular Disorders : NMD|July 13, 2010
Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutationWerner Stenzel, Stefan Prokop, Wolfram Kress, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Molecular Biology and Evolution|September 2, 2003
Molecular evolutionary convergence of the flight muscle protein arthrin in Diptera and hemipteraStephan Schmitz, Christoph J Schankin, Heino Prinz, et al.
Annals of Neurology|October 7, 2004
Actin mutations are one cause of congenital fibre type disproportionNigel G Laing, Nigel F Clarke, Danielle E Dye, et al.
Pageof 11