Capsule Opacification research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Capsule Opacification 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 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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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
Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice.
Gong X, Li E, Klier G, Huang Q, Wu Y ...
Cell Vol 91(6)
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Date 12 Dec 1997
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
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Transgenic mice expressing a hemopoietic growth factor gene (GM-CSF) develop accumulations of macrophages, blindness, and a fatal syndrome of tissue d...
Lang R A, Metcalf D, Cuthbertson R A, Lyons I, Stanley E ...
Cell Vol 51(4)
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Date 20 Nov 1987
Research
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
Zara Federico, Biancheri Roberta, Bruno Claudio, Bordo Laura, Assereto Stefania ...
Nature genetics Vol 38(10)
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Date 01 Oct 2006
Research
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy.
Klesert T R, Cho D H, Clark J I, Maylie J, Adelman J ...
Nature genetics Vol 25(1)
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Date 01 May 2000
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Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.
Bu Lei, Jin Yiping, Shi Yuefeng, Chu Renyuan, Ban Airong ...
Nature genetics Vol 31(3)
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Date 01 Jul 2002
Research
Mutations in the founder of the MIP gene family underlie cataract development in the mouse.
Shiels A, Bassnett S
Nature genetics Vol 12(2)
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Date 01 Feb 1996
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