Zobrazeno 1 - 10
of 156
pro vyhledávání: '"RICHARD J. PIERCY"'
Publikováno v:
Royal Society Open Science, Vol 11, Iss 7 (2024)
Objective assessment of activity via accelerometry can provide valuable insights into dog health and welfare. Common activity metrics involve using acceleration cut-points to group data into intensity categories and reporting the time spent in each c
Externí odkaz:
https://doaj.org/article/d7252d61b0b243fe93a50c736ca9c486
Autor:
Victoria Lindsay-McGee, Enrique Sanchez-Molano, Georgios Banos, Emily L. Clark, Richard J. Piercy, Androniki Psifidi
Publikováno v:
Genetics Selection Evolution, Vol 55, Iss 1, Pp 1-22 (2023)
Abstract Background The Connemara pony (CP) is an Irish breed that has experienced varied selection by breeders over the last fifty years, with objectives ranging from the traditional hardy pony to an agile athlete. We compared these ponies with well
Externí odkaz:
https://doaj.org/article/c1b34160251a4d01ae1aee80ca61dad3
Autor:
Brigida Boccanegra, Roberta Lenti, Paola Mantuano, Elena Conte, Lisamaura Tulimiero, Richard J. Piercy, Ornella Cappellari, John C. W. Hildyard, Annamaria De Luca
Publikováno v:
PLoS ONE, Vol 19, Iss 11 (2024)
Externí odkaz:
https://doaj.org/article/e95513fd18bc46e2bd35eb1f304f8290
Publikováno v:
PLoS ONE, Vol 19, Iss 8 (2024)
Externí odkaz:
https://doaj.org/article/3da12d066abe4d8793ec7340bf3dbe84
Autor:
Dominique O. Riddell, John C. W. Hildyard, Rachel C. M. Harron, Frances Taylor-Brown, Joe N. Kornegay, Dominic J. Wells, Richard J. Piercy
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 12 (2023)
Externí odkaz:
https://doaj.org/article/c387e8a46e8b41748d428582fea41666
Publikováno v:
BMC Neuroscience, Vol 24, Iss 1, Pp 1-9 (2023)
Abstract Background Duchenne muscular dystrophy is a X-linked disease characterized by severe and progressive muscle weakness, alongside cognitive impairment and a range of neurobehavioral disorders secondary to brain dystrophin deficiency. Duchenne
Externí odkaz:
https://doaj.org/article/bdd23c13a17242c4a39958f3f01d775d
Publikováno v:
Wellcome Open Research, Vol 6 (2023)
Background: In addition to progressive, debilitating muscle degeneration, ~50% of patients with Duchenne muscular dystrophy (DMD) have associated cognitive and behavioural disorders secondary to deficiency of dystrophin protein in the brain. The brai
Externí odkaz:
https://doaj.org/article/62bd459e6dca438687855c58b9f1ef7f
Autor:
Dominique O. Riddell, John C. W. Hildyard, Rachel C. M. Harron, Natasha L. Hornby, Dominic J. Wells, Richard J. Piercy
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 12 (2022)
Externí odkaz:
https://doaj.org/article/eaebdf03e3144dd0bd2358adbcfa3fff
Autor:
Claire Massey, Emma M.A. Foster, Dominic J. Wells, Frances Taylor-Brown, Richard J. Piercy, Dominique O. Riddell, John C.W. Hildyard, Faye Rawson, Rachel C.M. Harron
Publikováno v:
Wellcome Open Research, Vol 7 (2022)
Background: Animal models of Duchenne muscular dystrophy (DMD) are essential to study disease progression and assess efficacy of therapeutic intervention, however dystrophic mice fail to display a clinically relevant phenotype, limiting translational
Externí odkaz:
https://doaj.org/article/532c4fb87eb64f77ac0d251978adbb7f
Publikováno v:
Wellcome Open Research, Vol 6 (2022)
Background: Progression through mammalian embryogenesis involves many interacting cell types and multiple differentiating cell lineages. Quantitative polymerase chain reaction (qPCR) analysis of gene expression in the developing embryo is a valuable
Externí odkaz:
https://doaj.org/article/c7cd96f87dd54967b014f00527ce30d7