C. Gineste

发表

Multimodal MRI and 31P-MRS Investigations of the ACTA1(Asp286Gly) Mouse Model of Nemaline Myopathy Provide Evidence of Impaired In Vivo Muscle Function, Altered Muscle Structure and Disturbed Energy Metabolism

P. Cozzone, G. Duhamel, Y. le Fur, 2013, PloS one.

Disruption of the microphysiological niche alters matrix deposition and causes loss of mitochondrial Ca2+ control in skeletal muscle fibers

H. Westerblad, Sabine U. Vorrink, V. Lauschke, 2022, bioRxiv.

Cytoskeleton-extracellular matrix interaction is required to maintain mitochondrial Ca2+ control in mouse skeletal muscle fibres

H. Westerblad, Sabine U. Vorrink, V. Lauschke, 2021 .

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy

E. Hardeman, P. Cozzone, C. Ottenheijm, 2014, PloS one.

L-tyrosine supplementation is not therapeutic for skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy

Augustin C. Ogier, R. Bryson-Richardson, N. Laing, 2017, bioRxiv.

Angio‐adaptation in unloaded skeletal muscle: new insights into an early and muscle type‐specific dynamic process

E. Roudier, D. Desplanches, O. Birot, 2010, The Journal of physiology.

Cyclosporin A delays the terminal disease stage in Tfam KO mice without improving mitochondrial energy production

Augustin C. Ogier, H. Westerblad, J. Gondin, 2022, bioRxiv.

Enzymatically dissociated muscle fibers display rapid dedifferentiation and impaired mitochondrial calcium control

H. Westerblad, Sabine U. Vorrink, V. Lauschke, 2022, iScience.

L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy

Augustin C. Ogier, R. Bryson-Richardson, N. Laing, 2018, Scientific Reports.

Therapeutic approaches in different congenital myopathies.

J. Laporte, C. Gineste, 2022, Current opinion in pharmacology.

Acute and chronic tirasemtiv treatment improves in vivo and in vitro muscle performance in actin-based nemaline myopathy mice

C. Ottenheijm, A. Beggs, L. Brocca, 2021, Human molecular genetics.

Cyclophilin D, a target for counteracting skeletal muscle dysfunction in mitochondrial myopathy.

H. Westerblad, D. Andersson, A. Cheng, 2015, Human molecular genetics.

Angiomotin p80/p130 ratio: a new indicator of exercise‐induced angiogenic activity in skeletal muscles from obese and non‐obese rats?

E. Roudier, J. Lavoie, S. Décary, 2009, The Journal of physiology.

In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype

M. Jubeau, N. Gretz, P. Cozzone, 2013, Neuromuscular Disorders.

Combined MRI and 31P-MRS Investigations of the ACTA1(H40Y) Mouse Model of Nemaline Myopathy Show Impaired Muscle Function and Altered Energy Metabolism

E. Hardeman, P. Cozzone, Y. le Fur, 2013, PloS one.

Impaired aerobic capacity and premature fatigue preceding muscle weakness in the skeletal muscle Tfam-knockout mouse model

Augustin C. Ogier, H. Westerblad, J. Rieusset, 2021, Disease models & mechanisms.

In vivo characterization of skeletal muscle function in nebulin‐deficient mice

Augustin C. Ogier, H. Granzier, M. Bernard, 2019, Muscle & nerve.

Striated muscle angio-adaptation requires changes in Vasohibin-1 expression pattern.

E. Roudier, D. Desplanches, S. Décary, 2010, Biochemical and biophysical research communications.

In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype

M. Jubeau, N. Gretz, P. Cozzone, 2013, Neuromuscular Disorders.

Tirasemtiv enhances submaximal muscle tension in an Acta1:p.Asp286Gly mouse model of nemaline myopathy.

L. Brocca, D. Hwee, R. Bottinelli, 2024, The Journal of general physiology.