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 > MYOBASE > ORGANISMES VIVANTS > Eucaryotes > Animaux > Arthropodes > Insectes > drosophile
drosophileSynonyme(s)drosophilae ;Drosophila melanogaster ;Drosophilidae ;mouche du vinaigre ;fruit fly drosophila |
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Straightjacket/alpha2delta3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1
Auxerre-Plantie E, Nakamori M, Renaud Y, et al.
eLife, 2019, 8
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
Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy
Bervoets S, Wei N, Erfurth ML, et al.
Nature communications, 2019, 10, 1
Mitochondrial impairment activates the Wallerian pathway through depletion of NMNAT2 leading to SARM1-dependent axon degeneration
Loreto A, Hill CS, Hewitt VL, et al.
Neurobiology of disease, 2019, 134
Increased Muscleblind levels by chloroquine treatment improve myotonic dystrophy type 1 phenotypes in in vitro and in vivo models
Bargiela A, Sabater-Arcis M, Espinosa-Espinosa J, et al.
Proceedings of the national Academy of sciences of the United States of America, 2019
Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway
Suda K, Muraoka Y, Ortega-Yanez A, et al.
Experimental cell research, 2019
Type IV Collagen Is Essential for Proper Function of Integrin-Mediated Adhesion in Drosophila Muscle Fibers
Kiss AA, Somlyai-Popovics N, Kiss M, et al.
International Journal of molecular sciences, 2019, 20, 20
Blocking p62/SQSTM1-dependent SMN degradation ameliorates spinal muscular atrophy disease phenotypes
Rodriguez-Muela N, Parkhitko A, Grass T, et al.
The Journal of clinical investigation, 2018
Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development
Martinez Carrera LA, Gabriel E, Donohoe C, et al.
Human molecular genetics, 2018
Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy
Chakraborty M, Sellier C, Ney M, et al.
Disease models & mechanisms, 2018, 11, 4
Bruno-3 regulates sarcomere component expression and contributes to muscle phenotypes of myotonic dystrophy type 1
Picchio L, Legagneux V, Deschamps S, et al.
Disease models & mechanisms, 2018, 11, 5
La recherche animale : une étape sur le chemin du médicament : Le dossier 01
VLM. Vaincre les myopathies, 2017, 182, p .20-21
La recherche in vivo à l'origine d'avancées médicales majeures : Le dossier 03
Dupuy-Maury F
VLM. Vaincre les myopathies, 2017, 182, p. 24-25
Criblage de molécules : En quête de traitements... : Le dossier 01
Dupuy-Maury F
VLM. Vaincre les myopathies, 2017, 181, p.19-23
Réseau DMOP : en route vers des traitements
Dupuy-Maury F
VLM. Vaincre les myopathies, 2017, 180, p. 14-15
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy
Manole A, Jaunmuktane Z, Hargreaves I, et al.
Brain : a journal of neurology, 2017, 140, 11, p 2820
Myology 2016 : 5th International Congress of Myology ; Posters n° 104 to 156 - Dystrophinopathies (Duchenne, Becker, others)
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 72-97
Myology 2016 : 5th International Congress of Myology ; Posters n° 256 to 274 - Miscellaneous
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 146-156
Myology 2016 : 5th International Congress of Myology ; Posters n° 27 to 49 - Animal models
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 37-47
A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy
Bott LC, Badders NM, Chen KL, et al.
Human molecular genetics, 2016, 25, 10, p 1979
In Vitro and In Vivo Modeling of Spinal and Bulbar Muscular Atrophy
Pennuto M, Basso M
Journal of molecular neuroscience, 2016, 58, 3, p 365
Utilisation d'un modèle de drosophile de la Dystrophie Myotonique de Type 1 pour l'identification de marqueurs moléculaires responsables des symptômes musculaires et cardiaques
Plantié E
Thèse de Doctorat, 2016, 332 p
Colloque Jeunes Chercheurs : Actes de colloque 12 Juin 2015 Paris
Collectif
AFM-TELETHON, 2015, 97 p
A fly model for the CCUG-repeat expansion of myotonic dystrophy type 2 reveals a novel interaction with MBNL1
Yu Z, Goodman LD, Shieh SY, et al.
Human molecular genetics, 2015, 24, 4, p 954
