Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Sinadinos A"'
Autor:
Phillip M. Brailey, Lauren Evans, Juan Carlos López-Rodríguez, Anthony Sinadinos, Victoria Tyrrel, Gavin Kelly, Valerie O’Donnell, Peter Ghazal, Susan John, Patricia Barral
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-15 (2022)
Modulation of metabolic pathways is linked to regulation of immune cells including macrophages. Here the authors identify a role for CD1d in the metabolic rewiring of macrophages, which alters responsiveness to innate stimuli.
Externí odkaz:
https://doaj.org/article/7fbedabfbd094fb7873e3dad81a05d67
Autor:
Christopher Sinadinos
Publikováno v:
Journal of Innovation Management, Vol 10, Iss 1, Pp I-X (2022)
A reciprocal relationship has been documented between registering formal intellectual property rights (IPR), obtaining public grants, and undertaking publicly subsidised R&D innovation projects. Focusing on SMEs as key beneficiaries of such grants, t
Externí odkaz:
https://doaj.org/article/e8a85a5e15c042ddae42d7a329de97c7
Publikováno v:
In Journal of Biomechanics 3 October 2016 49(14):3444-3451
Akademický článek
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Autor:
Kate Kenny, Alan J. Mighell, Susan Parekh, F. Soldani, F. Lafferty, H. Al Siyabi, J. Monteiro, A. Sinadinos, Richard Balmer
Publikováno v:
European Archives of Paediatric Dentistry. 22:929-936
The burden of dental care in Amelogenesis Imperfecta (AI) has not been well described. This condition results in weak, discoloured and often sensitive teeth. Specialist paediatric care is available for AI patients in the UK, but treatment protocols a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1d9bb1404f62da4019115e45aeb3576
https://doi.org/10.1007/s40368-021-00638-x
https://doi.org/10.1007/s40368-021-00638-x
Autor:
C. Sinadinos, T. Burbidge-King, D. Soh, L.M. Thompson, J.L. Marsh, A. Wyttenbach, A.K. Mudher
Publikováno v:
Neurobiology of Disease, Vol 34, Iss 2, Pp 389-395 (2009)
Huntington's Disease is a neurodegenerative condition caused by a polyglutamine expansion in the huntingtin (Htt) protein, which aggregates and also causes neuronal dysfunction. Pathogenic N-terminal htt fragments perturb axonal transport in vitro. T
Externí odkaz:
https://doaj.org/article/b0b7fbafeb864876a72e10fd1bc707f0
Autor:
Anthony Sinadinos, Christopher N J Young, Rasha Al-Khalidi, Anna Teti, Paweł Kalinski, Shafini Mohamad, Léonore Floriot, Tiphaine Henry, Gianluca Tozzi, Taiwen Jiang, Olivier Wurtz, Alexis Lefebvre, Mikhail Shugay, Jie Tong, David Vaudry, Stephen Arkle, Jean-Claude doRego, Dariusz C Górecki
Publikováno v:
PLoS Medicine, Vol 12, Iss 10, p e1001888 (2015)
BackgroundDuchenne muscular dystrophy (DMD) is the most common inherited muscle disease, leading to severe disability and death in young men. Death is caused by the progressive degeneration of striated muscles aggravated by sterile inflammation. The
Externí odkaz:
https://doaj.org/article/2382264224b74bba97356135e450e25b
Autor:
U. Griesenbach, E. Alton, C. Boyd, M. Chan, J. Davies, D. Gill, S. Hyde, G. McLachlan, C. Meng, A. Sergijenko, A. Sinadinos
Publikováno v:
Journal of Cystic Fibrosis. 21:S341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbb7f5a69f3a155071be53a82a331f11
https://doi.org/10.1016/s1569-1993(22)01306-6
https://doi.org/10.1016/s1569-1993(22)01306-6
Publikováno v:
Journal of Cystic Fibrosis. 20:S249-S250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::871cbb386d4b4f9f0307b7eb5cdc5f91
https://doi.org/10.1016/s1569-1993(21)01952-4
https://doi.org/10.1016/s1569-1993(21)01952-4