نتایج جستجو برای: htra1

تعداد نتایج: 528  

Journal: :Molecular & Cellular Proteomics : MCP 2009
Jiayin Gu Gayle J. T. Pauer Xiuzhen Yue Umadevi Narendra Gwen M. Sturgill James Bena Xiaorong Gu Neal S. Peachey Robert G. Salomon Stephanie A. Hagstrom John W. Crabb

Age-related macular degeneration (AMD) is a progressive disease and major cause of severe visual loss. Toward the discovery of tools for early identification of AMD susceptibility, we evaluated the combined predictive capability of proteomic and genomic AMD biomarkers. We quantified plasma carboxyethylpyrrole (CEP) oxidative protein modifications and CEP autoantibodies by ELISA in 916 AMD and 4...

Journal: :Investigative ophthalmology & visual science 2009
Gareth J McKay Giuliana Silvestri Christopher C Patterson Ruth E Hogg Usha Chakravarthy Anne E Hughes

PURPOSE Polymorphic variation in genes involved in regulation of the complement system has been implicated as a major cause of genetic risk, in addition to the LOC387715/HTRA1 locus and other environmental influences. Previous studies have identified polymorphisms in the complement component 2 (CC2) and factor B (CFB) genes, as potential functional variants associated with AMD, in particular CF...

Journal: :Investigative ophthalmology & visual science 2011
Barbara Kloeckener-Gruissem Daniel Barthelmes Stephan Labs Christian Schindler Malaika Kurz-Levin Stephan Michels Johannes Fleischhauer Wolfgang Berger Florian Sutter Moreno Menghini

PURPOSE Neovascular age-related macular degeneration (AMD) resulting in decreased central vision severely impairs affected individuals. Current standard treatment is an intravitreal anti-VEGF therapy (ranibizumab), but responses to treatment show large variability. Genetic factors that influence AMD and that affect the outcome of ranibizumab treatment were sought within a sample of Swiss patien...

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