189 results on '"Lainé, Jeanne"'
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2. Correction: Activated dendritic cells modulate proliferation and differentiation of human myoblasts
3. The actin-spectrin submembrane scaffold restricts endocytosis along proximal axons
4. Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation
5. Ultrastructural and dynamic studies of the endosomal compartment in Down syndrome
6. MBNL‐dependent impaired development within the neuromuscular system in myotonic dystrophy type 1
7. Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
8. Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation
9. MBNL dependent-impaired development connectivity within neuromuscular circuits in Myotonic Dystrophy type
10. Physiological and ultrastructural features of human induced pluripotent and embryonic stem cell-derived skeletal myocytes in vitro
11. Activated dendritic cells modulate proliferation and differentiation of human myoblasts
12. MBNL-dependent impaired development connectivity within neuromuscular circuits in myotonic dystrophy type 1
13. In-depth analysis of the secretome identifies three major independent secretory pathways in differentiating human myoblasts
14. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
15. The α2-subunit of the AP2 clathrin adaptor as a new causal gene in an atypical myopathy with granulofilamentous inclusions
16. Two novel COLVI long chains in zebrafish that are essential for muscle development
17. The actin-spectrin submembrane scaffold restricts endocytosis along proximal axons.
18. N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy
19. Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion
20. Muscle cells of sporadic ALS patients secrete neurotoxic vesicles
21. Additional file 2 of Ultrastructural and dynamic studies of the endosomal compartment in Down syndrome
22. Additional file 1 of Ultrastructural and dynamic studies of the endosomal compartment in Down syndrome
23. Development of the excitation-contraction coupling machinery and its relation to myofibrillogenesis in human iPSC-derived skeletal myocytes
24. Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity
25. Atrophy, Fibrosis, and Increased PAX7-Positive Cells in Pharyngeal Muscles of Oculopharyngeal Muscular Dystrophy Patients
26. A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice
27. Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques
28. Differential physiological role of BIN1 isoforms in skeletal muscle development, function and regeneration
29. A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice
30. Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes
31. The type 1 cannabinoid receptor is highly expressed in embryonic cortical projection neurons and negatively regulates neurite growth in vitro
32. Cellular and subcellular morphological localization of normal prion protein in rodent cerebellum
33. Author response: Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes
34. Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle
35. Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy
36. Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques.
37. Guanabenz treatment improves Oculopharyngeal muscular dystrophy phenotype
38. Mechanosensitive clathrin platforms anchor desmin intermediate filaments in skeletal muscle
39. A simple shortcut for observing unroofed cells by either TEM or SEM
40. Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle
41. Abnormal splicing switch of DMD’s penultimate exon compromises muscle fibre maintenance in myotonic dystrophy
42. Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1
43. N‐ WASP is required for Amphiphysin‐2/ BIN 1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy
44. Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization
45. Cellular micro-environments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors
46. Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts
47. Mutations in Lamin A/C Gene Causes Mechanosensing Defects in Human Myoblasts
48. Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations
49. Characterization of Membrane-shed Microvesicles from Cytokine-stimulated β-Cells Using Proteomics Strategies
50. Neurotransmitter Release at the Thalamocortical Synapse Instructs Barrel Formation But Not Axon Patterning in the Somatosensory Cortex
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