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Georgia Campbell

Explore the profile of Georgia Campbell including associated specialties, affiliations and a list of published articles. Areas
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Articles 7
Citations 98
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Recent Articles
1.
Na T, Sander V, Davidson A, Lin R, Hermant Y, Hardie Boys M, et al.
Angew Chem Int Ed Engl . 2024 Jun; 63(39):e202407764. PMID: 38932510
Lipopeptides are an important class of biomolecules for drug development. Compared with conventional acylation, a chemoselective lipidation strategy offers a more efficient strategy for late-stage structural derivatisation of a peptide...
2.
Palpal-Latoc D, Horsfall A, Cameron A, Campbell G, Ferguson S, Cook G, et al.
J Nat Prod . 2024 Feb; 87(4):764-773. PMID: 38423998
The brevicidines represent a novel class of nonribosomal antimicrobial peptides that possess remarkable potency and selectivity toward highly problematic and resistant Gram-negative pathogenic bacteria. A recently discovered member of the...
3.
Todd Rose F, Darnell R, Morris S, Rose O, Paxie O, Campbell G, et al.
Mol Microbiol . 2023 Jul; 120(3):408-424. PMID: 37475106
Antimicrobial tolerance is the ability of a microbial population to survive, but not proliferate, during antimicrobial exposure. Significantly, it has been shown to precede the development of bona fide antimicrobial...
4.
Berger N, Cooley D, Graham M, Harrison C, Campbell G, Best R
Int J Environ Res Public Health . 2021 Nov; 18(22). PMID: 34831820
Background: We describe the requirements and physiological changes when running 10 consecutive marathons in 10 days at the same consistent pace by a female ultra-endurance athlete. Methods: Sharon Gayter (SG)...
5.
Campbell G, Krishnan K, Deschauer M, Taylor R, Turnbull D
Hum Mol Genet . 2014 Apr; 23(17):4612-20. PMID: 24740879
Large-scale mitochondrial DNA (mtDNA) deletions are an important cause of mitochondrial disease, while somatic mtDNA deletions cause focal respiratory chain deficiency associated with ageing and neurodegenerative disorders. As mtDNA deletions...
6.
Grady J, Campbell G, Ratnaike T, Blakely E, Falkous G, Nesbitt V, et al.
Brain . 2013 Nov; 137(Pt 2):323-34. PMID: 24277717
Single, large-scale deletions of mitochondrial DNA are a common cause of mitochondrial disease and cause a broad phenotypic spectrum ranging from mild myopathy to devastating multi-system syndromes such as Kearns-Sayre...
7.
Spendiff S, Reza M, Murphy J, Gorman G, Blakely E, Taylor R, et al.
Hum Mol Genet . 2013 Jul; 22(23):4739-47. PMID: 23847047
Progressive myopathy is a major clinical feature of patients with mitochondrial DNA (mtDNA) disease. There is limited treatment available for these patients although exercise and other approaches to activate muscle...