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3. Simplified in vitro engineering of neuromuscular junctions between rat embryonic motoneurons and immortalized human skeletal muscle cells

4. A functional human motor unit platform engineered from human embryonic stem cells and immortalized skeletal myoblasts

7. HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies

11. Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy

14. Project Administration by Indian Federal R & D Agencies.

17. Myogenic cell transplantation in genetic and acquired diseases of skeletal muscle

20. Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.

22. Investigating the behaviour of small businesses: an empirical case for ethnography

24. The enactment of envy within organizations: Insights from a New Zealand Academic Department

25. FSHD / OPMD / MYOTONIC DYSTROPHY

27. Managing innovation in an emerging sector: the case of marine-based nutraceuticals

28. On the study of settings marked by severe superior-subordinate conflict

33. Clones of human satellite cells can express in vitro both fast and slow myosin heavy chains

38. miR-542 promotes mitochondrial dysfunction and SMAD activity and is raised in ICU Acquired Weakness

39. Exploring Women's Career Development: Implications for Theory and Practice

41. Public versus private-sector research and development: a comparative analysis of two Indian R and D project groups

42. Change induced by economic reforms in state-owned enterprises and industries: insights from qualitative case study research

43. Gene therapy for oculopharyngeal muscular dystrophy

46. PABPN1 gene therapy for oculopharyngeal muscular dystrophy

47. Survival and Failure of Small Businesses Arising Through Government Privatization: Insights from Two New Zealand Firms

48. Mitochondrial microARN profiling in Duchenne muscular dystrophy, Limb girdle muscular dystrophy and collagene VI related myopathies

49. CRISPR/Cas9-Induced (CTGCAG)n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing

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