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pro vyhledávání: '"Hildyard J"'
Background: The dystrophin gene has multiple isoforms: full-length dystrophin (dp427) is principally known for its expression in skeletal and cardiac muscle, but is also expressed in the brain, and several internal promoters give rise to shorter, N-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::3c4216936e432e6aaf6d713e85a76f95
Autor:
Morin A; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France., Stantzou A; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France., Petrova ON; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France., Hildyard J; Department of Clinical Science and Services, Comparative Neuromuscular Diseases Laboratory, Royal Veterinary College, London NW1 0TU, United Kingdom., Tensorer T; SQY Therapeutics, 78180 Montigny-le-Bretonneux, France., Matouk M; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France., Petkova MV; NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, 10117 Berlin, Germany.; Department of Neuropediatrics, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, 10117 Berlin, Germany.; Berlin Institute of Health, 10117 Berlin, Germany., Richard I; Généthon, Integrare Unité Mixte de Recherche (UMR)_S951, Université Evry, Université Paris-Saclay, Inserm, 91002 Evry, France., Manoliu T; Plate-forme Imagerie et Cytométrie, Unité Mixte de Service Analyse Moléculaire, Modélisation et Imagerie de la Maladie Cancéreuse (UMS AMMICa), Gustave Roussy Cancer Campus, Université Paris-Saclay, 94805 Villejuif, France., Goyenvalle A; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France.; Laboratoire International Associé dédié aux Biothérapies Appliquées aux Handicaps Neuromusculaires (LIA BAHN), Centre scientifique de Monaco, 98000 Monaco., Falcone S; UM76, INSERM U974, Centre de Recherche en Myologie, Institut de Myologie, Sorbonne Université, 75013 Paris, France., Schuelke M; NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, 10117 Berlin, Germany.; Department of Neuropediatrics, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, 10117 Berlin, Germany.; Berlin Institute of Health, 10117 Berlin, Germany., Laplace-Builhé C; Plate-forme Imagerie et Cytométrie, Unité Mixte de Service Analyse Moléculaire, Modélisation et Imagerie de la Maladie Cancéreuse (UMS AMMICa), Gustave Roussy Cancer Campus, Université Paris-Saclay, 94805 Villejuif, France., Piercy RJ; Department of Clinical Science and Services, Comparative Neuromuscular Diseases Laboratory, Royal Veterinary College, London NW1 0TU, United Kingdom., Garcia L; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France.; Laboratoire International Associé dédié aux Biothérapies Appliquées aux Handicaps Neuromusculaires (LIA BAHN), Centre scientifique de Monaco, 98000 Monaco., Amthor H; Evolution of Neuromuscular Diseases - Innovative Concepts and Practice (END-ICAP) U1179, Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines, Inserm, 78000 Versailles, France.; Laboratoire International Associé dédié aux Biothérapies Appliquées aux Handicaps Neuromusculaires (LIA BAHN), Centre scientifique de Monaco, 98000 Monaco.; Centre de Références des Maladies Neuromusculaires, Service de Pédiatrie, Université Paris-Saclay, APHP,Raymond Poincaré Hospital, 92380 Garches, France.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2023 Jan 10; Vol. 120 (2), pp. e2206324120. Date of Electronic Publication: 2023 Jan 03.
Publikováno v:
PLoS One
The mdx mouse is the most widely-used animal model of the human disease Duchenne muscular dystrophy, and quantitative PCR analysis of gene expression in the muscles of this animal plays a key role in the study of pathogenesis and disease progression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::94897ea7e9b77a77de9d47feaa223c58
https://researchonline.rvc.ac.uk/id/eprint/11913/1/11913.pdf
https://researchonline.rvc.ac.uk/id/eprint/11913/1/11913.pdf
Autor:
Hildyard, J. C. W.1, Lacey, E.1, Booler, H.1, Hopkinson, M.1, Wells, D. J.1, Brown, S. C.1 scbrown@rvc.ac.uk
Publikováno v:
PLoS ONE. 7/28/2016, Vol. 11 Issue 7, p1-20. 20p.
Autor:
Amoasii, L, Hildyard, J C W, Li, H, Sanchez-Ortiz, E, Mireault, A, Caballero, D, Harron, R, Stathopoulou, T-R, Massey, C A, Shelton, J M, Bassel-Duby, R, Piercy, R J, Olson, E N
Publikováno v:
SCIENCE
Mutations in the gene encoding dystrophin, a protein that maintains muscle integrity and function, cause Duchenne muscular dystrophy (DMD). The deltaE50-MD dog model of DMD harbors a mutation corresponding to a mutational “hotspot” in the human D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::f88f6b2d59111b0f2edc2b71741bff17
https://researchonline.rvc.ac.uk/id/eprint/11792/1/11792.pdf
https://researchonline.rvc.ac.uk/id/eprint/11792/1/11792.pdf
Publikováno v:
Frontiers in Molecular Biosciences
Highly pathogenic avian influenza (HPAI) H5N1 virus has been circulating in Vietnam since 2003, while outbreaks of HPAI H5N6 virus are more recent, having only been reported since 2014. Although the spatial distribution of H5N1 outbreaks and risk fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::a2bca82700b2e93081cabf508a4d0ad6
https://researchonline.rvc.ac.uk/id/eprint/11227/1/11227.pdf
https://researchonline.rvc.ac.uk/id/eprint/11227/1/11227.pdf
Autor:
Hildyard, J C W, Wells, D J
Publikováno v:
PLoS Currents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::6840a059bd5d61a96c76df09b3dff8e2
https://researchonline.rvc.ac.uk/id/eprint/10404/1/10404.pdf
https://researchonline.rvc.ac.uk/id/eprint/10404/1/10404.pdf
Autor:
Berciano, María T.1,2,3 (AUTHOR) berciant@unican.es, Gatius, Alaó4 (AUTHOR) alao.gatius@udl.cat, Puente-Bedia, Alba5 (AUTHOR) alba.puente@unican.es, Rufino-Gómez, Alexis6 (AUTHOR) alu0101313382@ull.edu.es, Tarabal, Olga4 (AUTHOR) olga.tarabal@udl.cat, Rodríguez-Rey, José C.1,2 (AUTHOR) rodriguj@unican.es, Calderó, Jordi4 (AUTHOR) jordi.caldero@udl.cat, Lafarga, Miguel2,3,7 (AUTHOR), Tapia, Olga6 (AUTHOR) otapiama@ull.edu.es
Publikováno v:
International Journal of Molecular Sciences. Nov2024, Vol. 25 Issue 22, p12415. 32p.
Autor:
Davenport, Mackenzie L.1,2,3,4 (AUTHOR) davenport.m@ufl.edu, Fong, Amaya1,2,3 (AUTHOR), Albury, Kaela N.1,2,3 (AUTHOR), Henley-Beasley, C. Spencer4,5 (AUTHOR), Barton, Elisabeth R.4,5 (AUTHOR), Maden, Malcolm3,6 (AUTHOR), Swanson, Maurice S.1,2,3,4 (AUTHOR) mswanson@ufl.edu
Publikováno v:
Skeletal Muscle. 10/29/2024, Vol. 14 Issue 1, p1-13. 13p.
Publikováno v:
In Neuromuscular Disorders October 2019 29 Supplement 1:S161-S161