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Miranda D Grounds

Showing results (81-90 of 121) with videos related to

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Disease Models & Mechanisms|April 1, 2020
Mouse models for muscular dystrophies: an overviewMaaike van Putten, Erin M Lloyd, Jessica C de Greef, et al.
Journal of Cell Science|February 25, 2010
A growth stimulus is needed for IGF-1 to induce skeletal muscle hypertrophy in vivoThea Shavlakadze, Jinfen Chai, Kirsten Maley, et al.
BMC Genomics|January 8, 2017
MicroRNA expression patterns in post-natal mouse skeletal muscle developmentSéverine Lamon, Evelyn Zacharewicz, Lauren C Butchart, et al.
Transplantation|June 30, 2004
Innate inflammatory cells are not responsible for early death of donor myoblasts after myoblast transfer therapyLeanne M Sammels, Erika Bosio, Clayton T Fragall, et al.
Differentiation; Research in Biological Diversity|August 19, 2007
Analysis of the callipyge phenotype through skeletal muscle development; association of Dlk1 with muscle precursor cellsJason D White, Tony Vuocolo, Matthew McDonagh, et al.
The American Journal of Pathology|April 2, 2014
Lipid accumulation in dysferlin-deficient musclesMiranda D Grounds, Jessica R Terrill, Hannah G Radley-Crabb, et al.
Journal of Biomedical Optics|March 5, 2008
Three-dimensional optical coherence tomography of whole-muscle autografts as a precursor to morphological assessment of muscular dystrophy in miceBlake R Klyen, Julian J Armstrong, Steven G Adie, et al.
Plos One|June 2, 2015
Interactions between Skeletal Muscle Myoblasts and their Extracellular Matrix Revealed by a Serum Free Culture SystemVishal Chaturvedi, Danielle E Dye, Beverley F Kinnear, et al.
The FEBS Journal|January 22, 2013
Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathiesJessica R Terrill, Hannah G Radley-Crabb, Tomohito Iwasaki, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 31, 2013
Quantitative assessment of muscle damage in the mdx mouse model of Duchenne muscular dystrophy using polarization-sensitive optical coherence tomographyXiaojie Yang, Lixin Chin, Blake R Klyen, et al.
Pageof 13

Showing results (81-90 of 121) with videos related to

Sort By:
Pageof 13
Disease Models & Mechanisms|April 1, 2020
Mouse models for muscular dystrophies: an overviewMaaike van Putten, Erin M Lloyd, Jessica C de Greef, et al.
Journal of Cell Science|February 25, 2010
A growth stimulus is needed for IGF-1 to induce skeletal muscle hypertrophy in vivoThea Shavlakadze, Jinfen Chai, Kirsten Maley, et al.
BMC Genomics|January 8, 2017
MicroRNA expression patterns in post-natal mouse skeletal muscle developmentSéverine Lamon, Evelyn Zacharewicz, Lauren C Butchart, et al.
Transplantation|June 30, 2004
Innate inflammatory cells are not responsible for early death of donor myoblasts after myoblast transfer therapyLeanne M Sammels, Erika Bosio, Clayton T Fragall, et al.
Differentiation; Research in Biological Diversity|August 19, 2007
Analysis of the callipyge phenotype through skeletal muscle development; association of Dlk1 with muscle precursor cellsJason D White, Tony Vuocolo, Matthew McDonagh, et al.
The American Journal of Pathology|April 2, 2014
Lipid accumulation in dysferlin-deficient musclesMiranda D Grounds, Jessica R Terrill, Hannah G Radley-Crabb, et al.
Journal of Biomedical Optics|March 5, 2008
Three-dimensional optical coherence tomography of whole-muscle autografts as a precursor to morphological assessment of muscular dystrophy in miceBlake R Klyen, Julian J Armstrong, Steven G Adie, et al.
Plos One|June 2, 2015
Interactions between Skeletal Muscle Myoblasts and their Extracellular Matrix Revealed by a Serum Free Culture SystemVishal Chaturvedi, Danielle E Dye, Beverley F Kinnear, et al.
The FEBS Journal|January 22, 2013
Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathiesJessica R Terrill, Hannah G Radley-Crabb, Tomohito Iwasaki, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 31, 2013
Quantitative assessment of muscle damage in the mdx mouse model of Duchenne muscular dystrophy using polarization-sensitive optical coherence tomographyXiaojie Yang, Lixin Chin, Blake R Klyen, et al.
Pageof 13