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 > MYOBASE > METHODOLOGIE > modélisation
modélisationSynonyme(s)modelling ;model building ;modelization modeling |
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Avancées dans l'amyotrophie spinale proximale liée à SMN1
Myoinfo (AFM-Téléthon), Lefebvre S, André C
Avancées de la recherche, Savoir & Comprendre, 2020, 52 p
Avancées dans les dystrophies musculaires d'Emery-Dreifuss
Myoinfo (AFM-Téléthon), Bonne G, Ben Yaou R
Avancées de la recherche, Savoir & Comprendre, 2020, 10 p
Avancées dans la myopathie facio-scapulo-humérale
Myoinfo (AFM-Téléthon), Dumonceaux J
Avancées de la recherche, Savoir & Comprendre, 2020, 19 p
Myopathy reversion in mice after restauration of mitochondrial complex I
Pereira CV, Peralta S, Arguello T, et al.
EMBO Molecular Medicine, 2020, 12, 2
Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism
Chivet M, Marchioretti C, Pirazzini M, et al.
Cells, 2020, 9, 2
Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine
Wasala NB, Chen SJ, Duan D
Expert opinion on drug discovery, 2020
Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1
Yin Q, Wang H, Li N, et al.
Cell Research, 2019
Cored in the act: the use of models to understand core myopathies
Fusto A, Moyle LA, Gilbert PM, et al.
Disease models & mechanisms, 2019, 12, 12
In vitro models of neuromuscular junctions and their potential for novel drug discovery and development
Vila OF, Qu Y, Vunjak-Novakovic G
Expert opinion on drug discovery, 2019
Drosophila SMN2 minigene reporter model identifies moxifloxacin as a candidate therapy for SMA
Konieczny P, Artero R
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019
Insights into wild type dynamin 2 and the consequences of DNM2 mutations from transgenic zebrafish
Zhao M, Smith L, Volpatti J, et al.
Human molecular genetics, 2019
McArdle Disease: New Insights into Its Underlying Molecular Mechanisms
Llavero F, Arrazola Sastre A, Luque Montoro M, et al.
International Journal of molecular sciences, 2019, 20, 23
Molecular Mechanisms and Therapeutics for SBMA/Kennedy's Disease
Arnold FJ, Merry DE
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2019
Development of a novel severe mouse model of spinal muscular atrophy with respiratory distress type 1: FVB-nmd
Shababi M, Smith CE, Kacher M, et al.
Biochemical and biophysical research communications, 2019
Improvement of motor conduction velocity in hereditary neuropathy of LAMA2-CMD dy(2J)/dy(2J) mouse model by glatiramer acetate
Rabie M, Yanay N, Fellig Y, et al.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2019, 130, 10
A gene-edited mouse model of Limb-Girdle muscular dystrophy 2C for testing exon skipping
Demonbreun AR, Wyatt EJ, Fallon KS, et al.
Disease models & mechanisms, 2019
Identification of 2,6-Disubstituted 3H-Imidazo[4,5-b]pyridines as Therapeutic Agents for Dysferlinopathies through Phenotypic Screening on Patient-Derived Induced Pluripotent Stem Cells
Takada H, Kaieda A, Tawada M, et al.
Journal of Medicinal Chemistry, 2019
In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse
Amoasii L, Li H, Zhang Y, et al.
Nature communications, 2019, 10, 1
At the heart of genetic disease: an interview with Elizabeth McNally
McNally E
Disease models & mechanisms, 2019, 13, 2
Immunophenotype of a Rat Model of Duchenne's Disease and Demonstration of Improved Muscle Strength After Anti-CD45RC Antibody Treatment
Ouisse LH, Remy S, Lafoux A, et al.
Frontiers in immunology, 2019, 10
Augmenting canonical Wnt signalling in therapeutically inert cells converts them into therapeutically potent exosome factories
Ibrahim AGE, Li C, Rogers R, et al.
Nature biomedical engineering, 2019, 3, 9, p 695
