David A Parry
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Explore the profile of David A Parry including associated specialties, affiliations and a list of published articles.
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63
Citations
2734
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Recent Articles
1.
Martin C, Sarlos K, Logan C, Thakur R, Parry D, Bizard A, et al.
Am J Hum Genet
. 2024 May;
111(5):996.
PMID: 38701747
No abstract available.
2.
Dodd D, Mechaussier S, Yeyati P, McPhie F, Anderson J, Khoo C, et al.
Science
. 2024 Apr;
384(6694):eadf5489.
PMID: 38662826
Tubulin, one of the most abundant cytoskeletal building blocks, has numerous isotypes in metazoans encoded by different conserved genes. Whether these distinct isotypes form cell type- and context-specific microtubule structures...
3.
Vandersteen A, Weerakkody R, Parry D, Kanonidou C, Toddie-Moore D, Vandrovcova J, et al.
J Med Genet
. 2023 Oct;
61(3):232-238.
PMID: 37813462
Background: The Ehlers-Danlos syndromes (EDS) are heritable disorders of connective tissue (HDCT), reclassified in the 2017 nosology into 13 subtypes. The genetic basis for hypermobile Ehlers-Danlos syndrome (hEDS) remains unknown....
4.
Ollerton M, Folkvord J, La Mantia A, Parry D, Meditz A, McCarter M, et al.
Front Immunol
. 2022 Nov;
13:878273.
PMID: 36420277
Follicular helper CD4 T cells (TFH) are highly permissive to HIV and major foci of virus expression in both untreated and treated infection. Follicular regulatory CD4 T cells (TFR) limit...
5.
Panagiotou E, Fernandez-Fuentes N, Farraj L, McKibbin M, Elcioglu N, Jafri H, et al.
Mol Vis
. 2022 Jun;
28:57-69.
PMID: 35693420
Purpose: To investigate the molecular basis of recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia in two consanguineous families. Methods: Conventional autozygosity mapping was...
6.
Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germline
Reijns M, Parry D, Williams T, Nadeu F, Hindshaw R, Rios Szwed D, et al.
Nature
. 2022 May;
605(7910):E7.
PMID: 35504971
No abstract available.
7.
Reijns M, Parry D, Williams T, Nadeu F, Hindshaw R, Rios Szwed D, et al.
Nature
. 2022 Feb;
602(7898):623-631.
PMID: 35140396
The mutational landscape is shaped by many processes. Genic regions are vulnerable to mutation but are preferentially protected by transcription-coupled repair. In microorganisms, transcription has been demonstrated to be mutagenic;...
8.
Beetham H, Griffith B, Murina O, Loftus A, Parry D, Temps C, et al.
Cancer Res
. 2021 Dec;
82(4):632-647.
PMID: 34921014
Significance: A CRISPR-Cas9 screen reveals that loss of integrin-linked kinase synergizes with SRC inhibition, providing a new opportunity for enhancing the clinical effectiveness of SRC inhibitors in breast cancer.
9.
Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
Duker A, Kinderman D, Jordan C, Niiler T, Baker-Smith C, Thompson L, et al.
Orphanet J Rare Dis
. 2021 May;
16(1):231.
PMID: 34016138
Background: Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features,...
10.
Reijns M, Thompson L, Carlos Acosta J, Black H, Sanchez-Luque F, Diamond A, et al.
PLoS Biol
. 2020 Dec;
18(12):e3001030.
PMID: 33320856
With the ongoing COVID-19 (Coronavirus Disease 2019) pandemic, caused by the novel coronavirus SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2), there is a need for sensitive, specific, and affordable diagnostic...