Détail du congrès:
Congrès: Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) (26-30 mai 2008)
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Documents disponibles provenant de ce congrès (565)
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Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Mericskay M ; Blanc J ; Tritsch E ; Moriez R ; Aubert P ; Neunlist M ; Feil R ; Li Z | 2008SRF regulates the expression of muscle genes and immediate early genes and plays a crucial role in the heart and the skeletal muscles. Here, we investigated the consequences of inactivating SRF in adult gastrointestinal smooth muscle cells (SMCs[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Desdouits M ; Huerre M ; Mouly V ; Rivière JP ; Butler-Browne GS ; Gessain A ; Ozden S ; Ceccaldi PE | 2008Background: HTLV-1 (Human T-Lymphotropic is a retrovirus that infects about 20 million people around the world and is the aetiological agent of two major diseases: Adult T Cell leukemia and Tropical Spastic Paraparesis; besides these diseases, i[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Monnet A ; Wary C ; Wuyam B ; Verges S ; Duteil S ; Carlier PG | 2008Introduction: NMR is a powerful tool to assess musculo-skeletal perfusion and metabolism non-invasively and with a high time resolution. Blood oxygen level dependent (BOLD) NMR imaging readily provides contrast which depends on oxygenation but a[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Sandona D ; Gastaldello S ; Franzoso S ; Fanin M ; Angelini C ; Vidal J ; Basse N ; Reboud-Ravaux M ; Betto R | 2008Sarcoglycanopathies are progressive muscle wasting disorders caused by genetic defects of four proteins, ?-, ?-, ?-, and ?-sarcoglycan, elements of a key transmembrane complex of striated muscle. The proper assembly of the sarcoglycan complex re[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Brigitte M ; Plonquet A ; Tajbakhsh S ; Chazaud B ; Alberts M ; Gherardi R ; Chrétien F | 2008Perimuscular connective tissue has been poorly investigated at the cellular level although several inflammatory myopathies may exhibit huge epimysial macrophage infiltration. We examined murine muscle connective tissue in steady state conditions[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Sarparanta J ; Vihola A ; Hackman P ; Richard I ; Udd B | 2008Tibial muscular dystrophy (TMD) is a dominant late onset distal myopathy caused by mutations in M-line titin. In the few homozygotes known, the same mutations lead to the different, more severe limb-girdle muscular dystrophy LGMD2J. Most of the [...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Le Guen L ; Notarnicola C ; de Santa Barbara P | 2008The gastrointestinal tract is a vital organ system present in all multicellular animals initially derived from a simple tubal structure. The morphology of the gut requires reciprocal signaling between the mesoderm and endoderm during development[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Di Giorgio F ; Carrasco M ; Siao MC ; Maniatis T ; Eggan K | 2008Here we report an in vitro model system to study the molecular and cellular mechanisms that underlie the neurodegenerative disease Amyotrophic Lateral Sclerosis (ALS). Embryonic stem (ES) cells derived from mice carrying transgenic alleles of t[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Mitchell KJ ; Sassoon D ; Marazzi G | 2008Non-satellite cells are known to possess myogenic potential and can participate in muscle regeneration, however, their precise position, origin and relationship to satellite cells remain unclear. During postnatal growth, PW1/Peg3, a gene co-expr[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Skuk D ; Paradis M ; Goulet M ; Tremblay J | 2008The main constraint of the therapeutic strategy of intramuscularly injecting myogenic cells is that the implanted cells fuse only with the myofibers reached by the injection trajectories. An intravascular delivery of myogenic cells may be obviou[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Fauré J ; Cacheux M ; Monnier N ; Brocard J ; Fourest-Lieuvin A ; Oddoux S ; Lunardi J ; Marty I | 2008Muscle contraction relies on efficient calcium release from sarcoplasmic reticulum (SR), performed by the ryanodine receptor (RyR1) upon cell stimulation. RyR1 is 5000 amino acids long, anchored in the membrane of SR, and coupled to the voltage-[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Skuk D ; Paradis M ; Goulet M ; Tremblay JP | 2008The main constraint of the therapeutic strategy of intramuscular myogenic-cell delivery is that the transplanted cells fuse only with the myofibers reached by the injection trajectories. This phenomenon is traditionally attributed to a “lack of [...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Rodriguez-Munoz R ; Mornet D ; Martinez-Rojas D | 2008?-Dystroglycan (?-DG) is a transmembrane protein that links the extracellular matrix with the cytoskeleton. This protein is a Dystrophin-associated protein (DAP) that has an important role in cell signaling, and cytoplasm and nuclear organizatio[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Stum M ; Bangratz M ; Bernard V ; Davoine CS ; Fontaine B ; Krejci E ; Nicole S | 2008Schwartz-Jampel syndrome (SJS) is a recessive disorder with neuromyotonia and chondrodysplasia that appear during childhood and slowly progress until adulthood. SJS results from hypomorphic mutations in the perlecan gene, a proteoglycan secreted[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Grifone R ; Jarry T ; Kelly RG | 2008Vertebrate craniofacial and trunk myogenesis are regulated by distinct genetic programs. Branchiomeric craniofacial muscles regulate jaw opening and closing, facial expression and laryngeal and pharyngeal function. These muscles correspond to th[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Faralli H ; Caubit X ; Coré N ; Fasano L | 2008Muscle growth and repair depend on Satellite Cells (SCs), myogenic stem cells located between the plasma membrane and the basal lamina of the myofiber. When muscles are damaged, SCs become activated, proliferate and differentiate to form multinu[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Laurent FX ; Marie J | 2008Myotonic dystrophy type 1 (DM1) is a multisystemic disorder caused by an expanded CTG repeat sequence in the 3’ untranslated region of the DMPK gene. One of the most typical features is the disruption of alternative splicing of several pre-mRNA [...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Roumes H ; Daury L ; Cottin P ; Brustis JJ | 2008Ubiquitous calpains (µ- and m-calpain) are proteases of which enzymatic and structural properties are well characterized. Their implication in the early stages of myogenesis and more particularly in the fusion and migration of myoblasts seems we[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Pinset C | 2008The general objective of cell therapy techniques is to replace population of deficient cells to restore the functions of damaged tissue due to disease or traumatism. Cell therapy technologies and methods have already beed developed for muscle di[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Gitiaux C ; Christov C ; Bassez G ; Dimitri D ; Authier FJ ; Gherardi R | 2008DM is considered as an humorally-mediated disease specifically targeting endomysial capillaries , but its pathophysiology remains uncertain. Recently, plamacytoid dendritic cells have been found in perimysium providing novel insights into immuno[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Khattar P ; Decostre V ; Catelain C ; Schwartz K ; Fiszman M ; Bonne G ; Vilquin JT | 2008Purpose: Islet-1+ cells are cardiogenic and angiogenic progenitors participating to heart formation. The first aim was to locate and quantify these cells in view of potential pre-clinical developments. The second aim was to compare their presenc[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Konig S ; Bader CR ; Bernheim L | 2008Our work is based on human primary myoblast cultures derived from single satellite cells. Human myoblasts are able to proliferate for several weeks in culture, and terminal differentiation into myotubes can be induced by serum withdrawal. In hum[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Beroud C ; Hamroun D ; Desmet FO ; Lalande M ; Tuffery-Giraud S ; Humbertclaude V ; Collod-Béroud G ; Claustres M | 2008The development of new genotype based therapeutic approaches has reinforced the interest about Locus Specific Databases (LSDB). This field is a crossroad of bioinformatics, genetics, clinics and research and many initiatives have been developed [...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Maisonobe T ; Suominen T ; Eymard B ; Udd B | 2008Laing early-onset distal myopathy (MPD1) is an autosomal dominant myopathy due to mutations within the slow skeletal muscle fibre myosin heavy chain, MYH7. We report the phenotype of a French family with four affected individuals on two generati[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Méjat A ; Decostre V ; Renou L ; Kesari A ; Stewart CL ; Bonne G ; Hoffman E ; Misteli T | 2008The LMNA gene encodes lamins A and C, two intermediate filament type proteins that are important determinants of interphase nuclear architecture as they play essential roles in maintaining the integrity of the nuclear envelope and chromatin stru[...]