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The Journal of Biological Chemistry
|
December 2, 2010
Reverse engineering gene network identifies new dysferlin-interacting proteins
Mafalda Cacciottolo, Vincenzo Belcastro, Steve Laval, et al.
Plos One
|
February 26, 2013
Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy
Alison Blain, Elizabeth Greally, Steve Laval, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 17, 2007
From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis
Lars Klinge, Steve Laval, Sharon Keers, et al.
Genesis (New York, N.Y. : 2000)
|
April 5, 2014
Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects
Terence Gordon Smith, Steve Laval, Fangli Chen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
January 18, 2013
Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy
Elizabeth Greally, Benjamin J Davison, Alison Blain, et al.
European Journal of Heart Failure
|
August 3, 2010
Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy
Ralf Bauer, Alison Blain, Elizabeth Greally, et al.
Plos Currents
|
June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis
Elizabeth Harris, Steve Laval, Judith Hudson, et al.
Stem Cells and Development
|
June 22, 2013
Exon skipping and gene transfer restore dystrophin expression in hiPSC-cardiomyocytes harbouring DMD mutations
Emily Dick, Spandan Kalra, David Anderson, et al.
Muscle & Nerve
|
January 19, 2010
Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle
Lars Klinge, John Harris, Caroline Sewry, et al.
Human Molecular Genetics
|
December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb
Ramakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
The Journal of Biological Chemistry
|
December 2, 2010
Reverse engineering gene network identifies new dysferlin-interacting proteins
Mafalda Cacciottolo, Vincenzo Belcastro, Steve Laval, et al.
Plos One
|
February 26, 2013
Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy
Alison Blain, Elizabeth Greally, Steve Laval, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 17, 2007
From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis
Lars Klinge, Steve Laval, Sharon Keers, et al.
Genesis (New York, N.Y. : 2000)
|
April 5, 2014
Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects
Terence Gordon Smith, Steve Laval, Fangli Chen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
January 18, 2013
Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy
Elizabeth Greally, Benjamin J Davison, Alison Blain, et al.
European Journal of Heart Failure
|
August 3, 2010
Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy
Ralf Bauer, Alison Blain, Elizabeth Greally, et al.
Plos Currents
|
June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis
Elizabeth Harris, Steve Laval, Judith Hudson, et al.
Stem Cells and Development
|
June 22, 2013
Exon skipping and gene transfer restore dystrophin expression in hiPSC-cardiomyocytes harbouring DMD mutations
Emily Dick, Spandan Kalra, David Anderson, et al.
Muscle & Nerve
|
January 19, 2010
Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle
Lars Klinge, John Harris, Caroline Sewry, et al.
Human Molecular Genetics
|
December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb
Ramakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
Page
of 2