Myopia research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Myopia treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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7743 Abstracts
Research
Further pharmacological and genetic evidence for the efficacy of PlGF inhibition in cancer and eye disease.
Van de Veire Sara, Stalmans Ingeborg, Heindryckx Femke, Oura Hajimu, Tijeras-Raballand Annemilaï ...
Cell Vol 141(1)
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Date 02 Apr 2010
Research
Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease.
Chou Christopher M, Nelson Christine, Tarlé Susan A, Pribila Jonathan T, Bardakjian Tanya ...
Cell Vol 161(3)
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Date 23 Apr 2015
Research
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.
Olschwang S, Tiret A, Laurent-Puig P, Muleris M, Parc R ...
Cell Vol 75(5)
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Date 03 Dec 1993
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Date 23 Apr 2015
Research
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.
Solouki Abbas M, Verhoeven Virginie J M, van Duijn Cornelia M, Verkerk Annemieke J M H, Ikram M Kamran ...
Nature genetics Vol 42(10)
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Date 01 Oct 2010
Research
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.
Hysi Pirro G, Young Terri L, Mackey David A, Andrew Toby, Fernández-Medarde Alberto ...
Nature genetics Vol 42(10)
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Date 01 Oct 2010
Research
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts Heleen H, Doherty Dan, van Beersum Sylvia E C, Parisi Melissa A, Letteboer Stef J F ...
Nature genetics Vol 39(7)
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Date 01 Jul 2007
Research
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Bech-Hansen N T, Naylor M J, Maybaum T A, Pearce W G, Koop B ...
Nature genetics Vol 19(3)
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Date 01 Jul 1998
Research
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.
Chen Z Y, Battinelli E M, Fielder A, Bundey S, Sims K ...
Nature genetics Vol 5(2)
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Date 01 Oct 1993
Research
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
Pusch C M, Zeitz C, Brandau O, Pesch K, Achatz H ...
Nature genetics Vol 26(3)
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Date 01 Nov 2000
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