Linda A Terry
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Explore the profile of Linda A Terry including associated specialties, affiliations and a list of published articles.
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20
Citations
391
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Recent Articles
1.
Spiropoulos J, Lockey R, Beck K, Vickery C, Holder T, Thorne L, et al.
Transbound Emerg Dis
. 2019 May;
66(5):1993-2001.
PMID: 31111687
Prions are highly resistant to the decontamination procedures normally used to inactivate conventional pathogens. This is a challenging problem not only in the medical and veterinary fields for minimizing the...
2.
Corda E, Thorne L, Beck K, Lockey R, Green R, Vickery C, et al.
Acta Neuropathol Commun
. 2015 Apr;
3:21.
PMID: 25853789
Introduction: Scrapie and bovine spongiform encephalopathy (BSE) are transmissible spongiform encephalopathies (TSEs) which naturally affect small and large ruminants respectively. However, small ruminants, which are susceptible to BSE under experimental...
3.
Konold T, Moore S, Bellworthy S, Terry L, Thorne L, Ramsay A, et al.
BMC Vet Res
. 2013 May;
9:99.
PMID: 23651710
Background: Evidence for scrapie transmission from VRQ/VRQ ewes to lambs via milk was first reported in 2008 but in that study there were concerns that lateral transmission may have contributed...
4.
Beck K, Thorne L, Lockey R, Vickery C, Terry L, Bujdoso R, et al.
PLoS One
. 2013 Mar;
8(3):e57851.
PMID: 23472112
According to traditional murine bioassay methodology, prions must be serially passaged within a new host before a stable phenotype, and therefore a strain, can be assigned. Prions often transmit with...
5.
Beck K, Vickery C, Lockey R, Holder T, Thorne L, Terry L, et al.
Vet Res
. 2012 Nov;
43:77.
PMID: 23116457
Mouse bioassay can be readily employed for strain typing of naturally occurring transmissible spongiform encephalopathy cases. Classical scrapie strains have been characterised historically based on the established methodology of assessing...
6.
Bannach O, Birkmann E, Reinartz E, Jaeger K, Langeveld J, Rohwer R, et al.
PLoS One
. 2012 May;
7(5):e36620.
PMID: 22567169
Prion diseases are transmissible neurodegenerative diseases affecting humans and animals. The agent of the disease is the prion consisting mainly, if not solely, of a misfolded and aggregated isoform of...
7.
Spiropoulos J, Lockey R, Sallis R, Terry L, Thorne L, Holder T, et al.
Emerg Infect Dis
. 2011 Dec;
17(12):2253-61.
PMID: 22172149
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases that include variant Creutzfeldt-Jakob disease in humans, scrapie in small ruminants, and bovine spongiform encephalopathy (BSE) in cattle. Scrapie is not considered a...
8.
Gough K, Baker C, Rees H, Terry L, Spiropoulos J, Thorne L, et al.
J Virol
. 2011 Oct;
86(1):566-71.
PMID: 22013047
Preclinical sheep with the highly scrapie-susceptible VRQ/VRQ PRNP genotype secrete prions from the oral cavity. In order to further understand the significance of orally available prions, buccal swabs were taken...
9.
Taema M, Maddison B, Thorne L, Bishop K, Owen J, Hunter N, et al.
Mol Biotechnol
. 2011 Oct;
51(3):233-9.
PMID: 21987099
Whilst ovine BSE displays distinct pathological characteristics to ovine CH1641-like scrapie upon passage in rodents, they have very similar molecular phenotypes. As such, the in vitro differentiation of these strains...
10.
Beck K, Sallis R, Lockey R, Vickery C, Beringue V, Laude H, et al.
Brain Pathol
. 2011 Sep;
22(3):265-79.
PMID: 21919992
Two cases of unusual transmissible spongiform encephalopathy (TSE) were diagnosed on the same farm in ARQ/ARQ PrP sheep showing attributes of both bovine spongiform encephalopathy (BSE) and scrapie. These cases,...