Conor M Ramsden
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Explore the profile of Conor M Ramsden including associated specialties, affiliations and a list of published articles.
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13
Citations
768
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Recent Articles
1.
Zihni C, Georgiadis A, Ramsden C, Sanchez-Heras E, Haas A, Nommiste B, et al.
J Cell Biol
. 2022 Sep;
221(11).
PMID: 36121394
Phagocytosis requires actin dynamics, but whether actomyosin contractility plays a role in this morphodynamic process is unclear. Here, we show that in the retinal pigment epithelium (RPE), particle binding to...
2.
Anguita R, Brennan N, Ramsden C, Mehat M, Keegan D, Cahill R, et al.
Eur J Ophthalmol
. 2021 Aug;
32(4):2445-2451.
PMID: 34392739
Objective: To assess the patterns of patient generated aerosol in the context of ophthalmic surgery and ophthalmic examinations. To inform medical teams regarding potential hazards and suggest mitigating measures. Methods:...
3.
Ramsden C, Ozturk M, Mehat M, Brennan N, Wickham L
Eye (Lond)
. 2021 Aug;
36(7):1510-1511.
PMID: 34363048
No abstract available.
4.
Eastlake K, Wang W, Jayaram H, Murray-Dunning C, Carr A, Ramsden C, et al.
Stem Cells Transl Med
. 2019 May;
8(8):775-784.
PMID: 31037833
Glaucoma is one of the leading causes of blindness, and there is an ongoing need for new therapies. Recent studies indicate that cell transplantation using Müller glia may be beneficial,...
5.
da Cruz L, Fynes K, Georgiadis O, Kerby J, Luo Y, Ahmado A, et al.
Nat Biotechnol
. 2018 Mar;
36(4):328-337.
PMID: 29553577
Age-related macular degeneration (AMD) remains a major cause of blindness, with dysfunction and loss of retinal pigment epithelium (RPE) central to disease progression. We engineered an RPE patch comprising a...
6.
Ramsden C, Nommiste B, R Lane A, Carr A, Powner M, Smart M, et al.
Sci Rep
. 2017 Mar;
7(1):51.
PMID: 28246391
Inherited retinal dystrophies are an important cause of blindness, for which currently there are no effective treatments. In order to study this heterogeneous group of diseases, adequate disease models are...
7.
Carter D, Smart M, Letton W, Ramsden C, Nommiste B, Chen L, et al.
Sci Rep
. 2016 Sep;
6:33792.
PMID: 27653836
Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a rare, early-onset retinal dystrophy characterised by distinct bands of circumferential pigmentary degeneration in the peripheral retina and developmental eye defects. ADVIRC is caused by...
8.
Parfitt D, Lane A, Ramsden C, Carr A, Munro P, Jovanovic K, et al.
Cell Stem Cell
. 2016 May;
18(6):769-781.
PMID: 27151457
Leber congenital amaurosis (LCA) is an inherited retinal dystrophy that causes childhood blindness. Photoreceptors are especially sensitive to an intronic mutation in the cilia-related gene CEP290, which causes missplicing and...
9.
Ramsden C, da Cruz L, Coffey P
Invest Ophthalmol Vis Sci
. 2016 Apr;
57(5):ORSFb1-3.
PMID: 27116659
No abstract available.
10.
Yvon C, Ramsden C, Lane A, Powner M, da Cruz L, Coffey P, et al.
Comput Struct Biotechnol J
. 2015 Jun;
13:382-9.
PMID: 26106463
Retinal degeneration arises from the loss of photoreceptors or retinal pigment epithelium (RPE). It is one of the leading causes of irreversible blindness worldwide with limited effective treatment options. Generation...