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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
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
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Publikováno v:
In Neuromuscular Disorders October 2019 29 Supplement 1:S161-S161
Publikováno v:
In Neuromuscular Disorders October 2019 29 Supplement 1:S161-S162
Publikováno v:
In Neuromuscular Disorders October 2019 29 Supplement 1:S161-S161