Doug Turnbull
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Explore the profile of Doug Turnbull including associated specialties, affiliations and a list of published articles.
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25
Citations
839
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Recent Articles
1.
Faitg J, Davey T, Laws R, Lawless C, Tuppen H, Fitton E, et al.
Commun Biol
. 2025 Jan;
8(1):24.
PMID: 39789156
Mitochondria play a crucial role in maintaining cellular health. It is interesting that the shape of mitochondria can vary depending on the type of cell, mitochondrial function, and other cellular...
2.
Vincent A, Chen C, Gomes T, Di Leo V, Laalo T, Pabis K, et al.
Biochim Biophys Acta Mol Basis Dis
. 2024 Mar;
1870(5):167131.
PMID: 38521420
Mitochondrial DNA (mtDNA) deletions which clonally expand in skeletal muscle of patients with mtDNA maintenance disorders, impair mitochondrial oxidative phosphorylation dysfunction. Previously we have shown that these mtDNA deletions arise...
3.
Bourke J, Ng Y, Tynan M, Bates M, Mohiddin S, Turnbull D, et al.
Open Heart
. 2022 Apr;
9(1).
PMID: 35393351
Aims: To define the prevalence of non-sustained tachyarrhythmias and bradyarrhythmias in patients with the m.3243A>G mitochondrial genotype and a previously defined, profile, associated with 'high sudden-death risk'. Methods And Results:...
4.
Yu X, Arden C, Berlinguer-Palmini R, Chen C, Bradshaw C, Smith A, et al.
Mol Metab
. 2022 Apr;
60:101489.
PMID: 35390502
Objective: There is strong evidence that mitochondrial DNA mutations and mitochondrial dysfunction play a role in diabetes pathogenesis. The homozygous knock-in mtDNA mutator mouse is a model of premature aging...
5.
Feeney C, Gorman G, Stefanetti R, McFarland R, Turnbull D, Harding C, et al.
Neurourol Urodyn
. 2020 Sep;
39(8):2253-2263.
PMID: 32969525
Aims: Mitochondrial diseases present with a spectrum of clinical features, usually with multiorgan involvement and are often characterized by a loss of smooth muscle function. Hence, we hypothesized that mitochondrial...
6.
Hatton C, Reeve A, Lax N, Blain A, Ng Y, El-Agnaf O, et al.
Acta Neuropathol Commun
. 2020 Jul;
8(1):103.
PMID: 32646480
Neurons of the nucleus basalis of Meynert (nbM) are vulnerable to Lewy body formation and neuronal loss, which is thought to underlie cognitive dysfunction in Lewy body dementia (LBD). There...
7.
Christie K, Robertson L, Conway C, Blighe K, DeDionisio L, Chao-Shern C, et al.
Mol Ther
. 2020 May;
28(8):1846-1857.
PMID: 32416058
CRISPR-Cas9 provides a tool to treat autosomal dominant disease by non-homologous end joining (NHEJ) gene disruption of the mutant allele. In order to discriminate between wild-type and mutant alleles, Streptococcus...
8.
Herbert M, Turnbull D
Nat Rev Mol Cell Biol
. 2018 Jan;
19(2):71-72.
PMID: 29358685
Mitochondrial DNA is maternally inherited, and pathogenic mutations cause a range of life-limiting conditions. Recent studies indicate that transmission of pathogenic mutations may be prevented by reproductive technologies designed to...
9.
Herbert M, Turnbull D
N Engl J Med
. 2016 Dec;
376(2):171-173.
PMID: 28030773
No abstract available.
10.
Cadete V, Deschenes S, Cuillerier A, Brisebois F, Sugiura A, Vincent A, et al.
J Physiol
. 2016 Jun;
594(18):5343-62.
PMID: 27311616
Key Points: Mitochondrial-derived vesicle (MDV) formation occurs under baseline conditions and is rapidly upregulated in response to stress-inducing conditions in H9c2 cardiac myoblasts. In mice formation of MDVs occurs readily...