Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Guiraud, S"'
Autor:
Guiraud, S, Squire, S, Edwards, B, Chen, H, Burns, D, Shah, N, Babbs, A, Davies, S, Wynne, G, Russell, A, Elsey, D, Wilson, F, Tinsley, J, Davies, K
Publikováno v:
Human Molecular Genetics
Duchenne muscular dystrophy (DMD) is a lethal, X-linked muscle-wasting disease caused by lack of the cytoskeletal protein dystrophin. There is currently no cure for DMD although various promising approaches are progressing through human clinical tria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a3ca9c8e5740eab159c0814c5169a782
https://doi.org/10.1093/hmg/ddv154
https://doi.org/10.1093/hmg/ddv154
Autor:
Kennedy, T, Guiraud, S, Edwards, B, Squire, S, Moir, L, Babbs, A, Odom, G, Golebiowski, D, Schneider, J, Chamberlain, J, Davies, K
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 11, Iss, Pp 92-105 (2018)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Duchenne muscular dystrophy (DMD) is an X-linked muscle-wasting disease caused by mutations in the dystrophin gene. DMD boys are wheelchair-bound around 12 years and generally survive into their twenties. There is currently no effective treatment exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::44bd1d1080097b0519008ce810c59578
https://ora.ox.ac.uk/objects/uuid:870cd85e-faa0-432f-a83a-90e989c5bce5
https://ora.ox.ac.uk/objects/uuid:870cd85e-faa0-432f-a83a-90e989c5bce5
Autor:
Fairclough, RJ, Guiraud, S, Squire, SE, Babbs, A, Edward, B, Shah, N, Bracchi, A, Wilson, FX, Horne, G, Robinson, N, Araujo, N, Hewings, DS, Vuorinen, A, Davies, SG, Wynne, GM, Russell, AJ, Tinsley, J, Davies, KE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4d121565d69d865eb99f94f26a3d56ad
https://ora.ox.ac.uk/objects/uuid:10531575-8f57-4738-9198-5184a03dfa44
https://ora.ox.ac.uk/objects/uuid:10531575-8f57-4738-9198-5184a03dfa44
Autor:
Guiraud, S., Aartsma-Rus, A., Vieira, N.M., Davies, K.E., Ommen, G.J.B. van, Kunkel, L.M., Chakravarti, A., Green, E.
Publikováno v:
Annual Review of Genomics and Human Genetics, 16, 281
Current molecular genomic approaches to human genetic disorders have led to an explosion in the identification of the genes and their encoded proteins responsible for these disorders. The identification of the gene altered by mutations in Duchenne an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38c968ec9b8f118a7b18a1d6a9e71d89
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Publikováno v:
Experimental Physiology
New Findings What is the topic of this review? This review highlights recent progress in genetically based therapies targeting the primary defect of Duchenne muscular dystrophy. What advances does it highlight? Over the last two decades, considerable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fb083d25b2bba66303416aba542a58df
https://pubmed.ncbi.nlm.nih.gov/26140505
https://pubmed.ncbi.nlm.nih.gov/26140505
Akademický článek
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Autor:
Wynne, G., Vuorinen, A., Emer, E., Conole, D., Chatzopoulou, M., Davies, S., Russell, A., Guiraud, S., Squire, S., Berg, A., Edwards, B., Hemming, S., Kennedy, T., Moir, L., Davies, K., Harriman, S., Tinsley, J., Wilson, F.
Publikováno v:
In Neuromuscular Disorders October 2017 27 Supplement 2:S189-S189
Publikováno v:
In Neuromuscular Disorders October 2017 27 Supplement 2:S167-S167
Publikováno v:
In Neuromuscular Disorders October 2017 27 Supplement 2:S166-S166
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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