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Nigel F Clarke

Showing results (21-30 of 67) with videos related to

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Neuromuscular Disorders : NMD|June 18, 2010
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3Leigh B Waddell, Michaela Kreissl, Andrew Kornberg, 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.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
Skeletal Muscle|May 8, 2015
Effect of levosimendan on the contractility of muscle fibers from nemaline myopathy patients with mutations in the nebulin geneJosine M de Winter, Barbara Joureau, Vasco Sequeira, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
The Journal of Biological Chemistry|August 21, 2014
Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissuesKei-ichiro Inamori, Tobias Willer, Yuji Hara, et al.
Annals of Neurology|December 21, 2005
SEPN1: associated with congenital fiber-type disproportion and insulin resistanceNigel F Clarke, Warren Kidson, Susana Quijano-Roy, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, 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.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|June 18, 2010
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3Leigh B Waddell, Michaela Kreissl, Andrew Kornberg, 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.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
Skeletal Muscle|May 8, 2015
Effect of levosimendan on the contractility of muscle fibers from nemaline myopathy patients with mutations in the nebulin geneJosine M de Winter, Barbara Joureau, Vasco Sequeira, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
The Journal of Biological Chemistry|August 21, 2014
Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissuesKei-ichiro Inamori, Tobias Willer, Yuji Hara, et al.
Annals of Neurology|December 21, 2005
SEPN1: associated with congenital fiber-type disproportion and insulin resistanceNigel F Clarke, Warren Kidson, Susana Quijano-Roy, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, 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.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Pageof 7