Conjunctivitis research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Conjunctivitis 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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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 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
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
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.
Hoffman H M, Mueller J L, Broide D H, Wanderer A A, Kolodner R D
Nature genetics Vol 29(3)
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Date 01 Nov 2001
Research
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.
Delous Marion, Baala Lekbir, Salomon Rémi, Laclef Christine, Vierkotten Jeanette ...
Nature genetics Vol 39(7)
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Date 01 Jul 2007
Research
Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
Yamamoto H, Simon A, Eriksson U, Harris E, Berson E L ...
Nature genetics Vol 22(2)
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Date 01 Jun 1999
Research
Biochemical defects in ABCR protein variants associated with human retinopathies.
Sun H, Smallwood P M, Nathans J
Nature genetics Vol 26(2)
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Date 01 Oct 2000
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