Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Sarah E. Lloyd"'
Autor:
Samutr Assavachin, Sarah E. Lloyd, Benjamin A. Nail, Renato V. Gonçalves, Justin R. Mulcahy, Frank E. Osterloh
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Chromium-doped SrTiO3 nanocrystals of perovskite structure type and 45 nm (±15 nm) edge lengths were obtained by hydrothermal synthesis in water from titanium oxide, strontium hydroxide, and chromium(III) nitrate. According to XPS, the majority of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b4b7b5a34c0c942bab6bdeb0f2b2f4f
https://doi.org/10.1039/d0ma00463d
https://doi.org/10.1039/d0ma00463d
Autor:
Shaheen Akhtar, Julia Grizenkova, Adam Wenborn, Holger Hummerich, Mar Fernandez de Marco, Sebastian Brandner, John Collinge, Sarah E Lloyd
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54454 (2013)
Prion infections, causing neurodegenerative conditions such as Creutzfeldt-Jakob disease and kuru in humans, scrapie in sheep and BSE in cattle are characterised by prolonged and variable incubation periods that are faithfully reproduced in mouse mod
Externí odkaz:
https://doaj.org/article/1a15c0560d754a2f9ecdcc3f35af4c69
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28741 (2011)
Prion disease incubation time in mice is determined by many factors including PrP expression level, Prnp alleles, genetic background, prion strain and route of inoculation. Sex differences have been described in age of onset for vCJD and in disease d
Externí odkaz:
https://doaj.org/article/7fbb5d71e7e543c197a15459798ef18a
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e15019 (2010)
In neurodegenerative conditions such as Alzheimer's and prion disease it has been shown that host genetic background can have a significant effect on susceptibility. Indeed, human genome-wide association studies (GWAS) have implicated several candida
Externí odkaz:
https://doaj.org/article/5d0e84103e4345ccba2d7b9c0cbd2cca
Autor:
Sarah E Lloyd, Emma G Maytham, Hirva Pota, Julia Grizenkova, Eleni Molou, James Uphill, Holger Hummerich, Jerome Whitfield, Michael P Alpers, Simon Mead, John Collinge
Publikováno v:
PLoS Genetics, Vol 5, Iss 2, p e1000383 (2009)
Prion diseases are fatal transmissible neurodegenerative disorders, which include Scrapie, Bovine Spongiform Encephalopathy (BSE), Creutzfeldt-Jakob Disease (CJD), and kuru. They are characterised by a prolonged clinically silent incubation period, v
Externí odkaz:
https://doaj.org/article/ea236d7807b243039970fe21131ee691
Publikováno v:
Annual review of genetics. 53
Mammalian prion diseases are a group of neurodegenerative conditions caused by infection of the central nervous system with proteinaceous agents called prions, including sporadic, variant, and iatrogenic Creutzfeldt-Jakob disease; kuru; inherited pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e30524d1657080a09f4111889363c8fa
https://pubmed.ncbi.nlm.nih.gov/31537104
https://pubmed.ncbi.nlm.nih.gov/31537104
Publikováno v:
Journal of Rural Studies. 42:133-143
Scholars of rural studies have investigated a range of places and subcultures to identify varieties of rural masculinity—both new and old—and to understand how they shape social relations (e.g., Bell, 2004; Campbell, 2000; Hennen, 2008). Yet a si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06b5a25ac4a308804db7d3c4198dd127
https://doi.org/10.1016/j.jrurstud.2015.10.001
https://doi.org/10.1016/j.jrurstud.2015.10.001
Autor:
Sarah E. Lloyd, Jill Lindsey Harrison
Publikováno v:
Social Problems. 60:281-301
While sociologists have shown how employers contribute to occupational segregation along lines of race, gender, and nativity,little attentionhas been paidtounpackingwhyemployersengagein thosepractices. We takeonthis gap through a case study of hired
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ffa75a885382777334b2e4b9adaa0bb
https://doi.org/10.1525/sp.2013.60.3.281
https://doi.org/10.1525/sp.2013.60.3.281
Autor:
Simon E. Fisher, Steven J. Scheinman, Blanche Schwappach, Sarah E. Lloyd, Alessandra Bolino, Paul Goodyer, Marcella Devoto, Simon H. S. Pearce, Thomas J. Jentsch, Brian Harding, Ian W. Craig, Oliver Wrong, S.P.A. Rigden, Rajesh V. Thakker, Klaus Steinmeyer
Kidney stones (nephrolithiasis), which affect 12% of males and 5% of females in the western world, are familial in 45% of patients and are most commonly associated with hypercalciuria. Three disorders of hypercalciuric nephrolithiasis (Dent's disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cd7524fba670237804848ff75108d38
https://ora.ox.ac.uk/objects/uuid:53c7ff7c-6cb3-4204-be2a-db9f34918a36
https://ora.ox.ac.uk/objects/uuid:53c7ff7c-6cb3-4204-be2a-db9f34918a36
We describe a familial syndrome in two brothers who were investigated after the casual discovery of tubular proteinuria in their 1st month of life. During a follow-up of 20 and 11 years, respectively, the two children grew well and were asymptomatic,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f725f47aae853ddf66a7d5228392063
https://ora.ox.ac.uk/objects/uuid:806e38d8-a2b3-4b2d-9bba-947b5184cf75
https://ora.ox.ac.uk/objects/uuid:806e38d8-a2b3-4b2d-9bba-947b5184cf75