Cassandra Terry
Overview
Explore the profile of Cassandra Terry including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
17
Citations
415
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Haxhiraj M, White K, Terry C
Int J Mol Sci
. 2024 Jul;
25(13).
PMID: 39000103
The number of people diagnosed with type 2 diabetes is on the increase worldwide. Of growing concern, the prevalence of type 2 diabetes in children and youths is increasing rapidly...
2.
Hassan S, White K, Terry C
Biosci Rep
. 2022 Apr;
42(5).
PMID: 35475576
There are over 40 identified human disorders that involve certain proteins folding incorrectly, accumulating in the body causing damage to cells and organs and causing disease. Type 2 Diabetes Mellitus...
3.
Sevcuka A, White K, Terry C
Life (Basel)
. 2022 Apr;
12(4).
PMID: 35455074
Cases of Type 2 Diabetes Mellitus (T2DM) are increasing at an alarming rate due to the rise in obesity, sedentary lifestyles, glucose-rich diets and other factors. Numerous studies have increasingly...
4.
Benilova I, Reilly M, Terry C, Wenborn A, Schmidt C, Marinho A, et al.
Proc Natl Acad Sci U S A
. 2020 Sep;
117(38):23815-23822.
PMID: 32900920
Prions are infectious agents which cause rapidly lethal neurodegenerative diseases in humans and animals following long, clinically silent incubation periods. They are composed of multichain assemblies of misfolded cellular prion...
5.
Terry C, Wadsworth J
Front Mol Neurosci
. 2019 Jul;
12:169.
PMID: 31338021
Prions are lethal pathogens, which cause fatal neurodegenerative diseases in mammals. They are unique infectious agents and are composed of self-propagating multi-chain assemblies of misfolded host-encoded prion protein (PrP). Understanding...
6.
Terry C, Harniman R, Sells J, Wenborn A, Joiner S, Saibil H, et al.
Sci Rep
. 2019 Jan;
9(1):376.
PMID: 30675000
Seeded polymerisation of proteins forming amyloid fibres and their spread in tissues has been implicated in the pathogenesis of multiple neurodegenerative diseases: so called "prion-like" mechanisms. While ex vivo mammalian...
7.
Sarell C, Quarterman E, Yip D, Terry C, Nicoll A, Wadsworth J, et al.
Open Biol
. 2017 Nov;
7(11).
PMID: 29142106
Mammalian prions cause lethal neurodegenerative diseases such as Creutzfeldt-Jakob disease (CJD) and consist of multi-chain assemblies of misfolded cellular prion protein (PrP). Ligands that bind to PrP can inhibit prion...
8.
Terry C, Jiang S, Radford D, Wan Q, Tzokov S, Moir A, et al.
Mol Microbiol
. 2017 Feb;
104(4):539-552.
PMID: 28214340
Bacteria of the genera Bacillus and Clostridium form highly resistant spores, which in the case of some pathogens act as the infectious agents. An exosporium forms the outermost layer of...
9.
Terry C, Wenborn A, Gros N, Sells J, Joiner S, Hosszu L, et al.
Open Biol
. 2016 Jun;
6(5).
PMID: 27249641
Mammalian prions are hypothesized to be fibrillar or amyloid forms of prion protein (PrP), but structures observed to date have not been definitively correlated with infectivity and the three-dimensional structure...
10.
Wenborn A, Terry C, Gros N, Joiner S, DCastro L, Panico S, et al.
Sci Rep
. 2015 May;
5:10062.
PMID: 25950908
Mammalian prions exist as multiple strains which produce characteristic and highly reproducible phenotypes in defined hosts. How this strain diversity is encoded by a protein-only agent remains one of the...