User profiles for Stéphane Blot
 | Stéphane BlotU955 - IMRB, Inserm, Ecole Nationale Vétérinaire d'Alfort, UPEC, Maisons-Alfort, F-94700 … Verified email at vet-alfort.fr Cited by 4475 |
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy
…, J Le Duff, JY Deschamps, I Barthelemy, S Blot… - Nature …, 2017 - nature.com
Duchenne muscular dystrophy (DMD) is an incurable X-linked muscle-wasting disease
caused by mutations in the dystrophin gene. Gene therapy using highly functional …
caused by mutations in the dystrophin gene. Gene therapy using highly functional …
Muscle function recovery in golden retriever muscular dystrophy after AAV1-U7 exon skipping
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder resulting from lesions
of the gene encoding dystrophin. These usually consist of large genomic deletions, the …
of the gene encoding dystrophin. These usually consist of large genomic deletions, the …
Tissue Doppler imaging detects early asymptomatic myocardial abnormalities in a dog model of Duchenne's cardiomyopathy
…, H Thibault, F Lallemand, C Thuillez, S Blot… - European heart …, 2004 - academic.oup.com
Aims Early diagnosis of Duchenne's dilated cardiomyopathy remains a challenge for
conventional echocardiography. We sought to determine whether tissue Doppler imaging (TDI) …
conventional echocardiography. We sought to determine whether tissue Doppler imaging (TDI) …
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis
…, JJ Panthier, G Aubin-Houzelstein, S Blot… - Proceedings of the …, 2010 - pnas.org
Neuronal ceroid lipofuscinoses (NCLs) represent the most common group of inherited
progressive encephalopathies in children. They are characterized by progressive loss of vision, …
progressive encephalopathies in children. They are characterized by progressive loss of vision, …
[HTML][HTML] Serum profiling identifies novel muscle miRNA and cardiomyopathy-related miRNA biomarkers in Golden Retriever muscular dystrophy dogs and Duchenne …
Duchenne muscular dystrophy (DMD) is a fatal, X-linked neuromuscular disease that affects
1 boy in 3500 to 5000 boys. The golden retriever muscular dystrophy dog is the best …
1 boy in 3500 to 5000 boys. The golden retriever muscular dystrophy dog is the best …
Prevalence of neurological disorders in French bulldog: a retrospective study of 343 cases (2002–2016)
V Mayousse, L Desquilbet, A Jeandel, S Blot - BMC veterinary research, 2017 - Springer
Background French Bulldog (FB) has significantly gained in popularity over the last few years,
and seems to be frequently affected by various neurological conditions. The purpose of …
and seems to be frequently affected by various neurological conditions. The purpose of …
Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy
Myostatin regulates skeletal muscle size via the activin receptor IIB (ActRIIB). However, its
effect on muscle energy metabolism and energy-dependent muscle function remains largely …
effect on muscle energy metabolism and energy-dependent muscle function remains largely …
Premature proliferative arrest of cricopharyngeal myoblasts in oculo-pharyngeal muscular dystrophy: therapeutic perspectives of autologous myoblast transplantation
Cultures of myoblasts isolated from cricopharyngeal muscles from patients with oculopharyngeal
muscular dystrophy (OPMD) have been performed to study the effect of the expanded (…
muscular dystrophy (OPMD) have been performed to study the effect of the expanded (…
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs
Human centronuclear and myotubular myopathies belong to a genetically heterogeneous
nosological group with clinical variability ranging from fatal disorder to mild weakness. The …
nosological group with clinical variability ranging from fatal disorder to mild weakness. The …
Human galectin 3 binding protein interacts with recombinant adeno-associated virus type 6
Recombinant adeno-associated viruses (rAAVs) hold enormous potential for human gene
therapy. Despite the well-established safety and efficacy of rAAVs for in vivo gene transfer, …
therapy. Despite the well-established safety and efficacy of rAAVs for in vivo gene transfer, …