Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis. - Wikidata - wikimedia - TriplyDB

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

http://www.wikidata.org/entity/Q43671971

about

Formation of soluble amyloid oligomers and amyloid fibrils by the multifunctional protein vitronectin A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration Complement factor H polymorphism in age-related macular degeneration Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD Potential of Induced Pluripotent Stem Cells (iPSCs) for Treating Age-Related Macular Degeneration (AMD)A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration The complement system and age-related macular degeneration.Macular degeneration: recent advances and therapeutic opportunities.Age-related macular degeneration--emerging pathogenetic and therapeutic concepts.Modeling how CD46 deficiency predisposes to atypical hemolytic uremic syndrome Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains.Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.Complement factor H: using atomic resolution structure to illuminate disease mechanisms.Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities.Systemic complement inhibition with eculizumab for geographic atrophy in age-related macular degeneration: the COMPLETE study Extracellular matrix nitration alters growth factor release and activates bioactive complement in human retinal pigment epithelial cells Evidence for an inflammatory process in age-related macular degeneration gains new support.Retinal basement membrane abnormalities and the retinopathy of Alport syndrome Age-related retinopathy in NRF2-deficient mice.Mitochondrial oxidative stress in the retinal pigment epithelium leads to localized retinal degeneration Multicenter prospective, randomized, double-masked, placebo-controlled study of Rheopheresis to treat nonexudative age-related macular degeneration: interim analysis.Age-related macular degeneration: genetic and environmental factors of disease Current concepts in C3 glomerulopathy.The significance of the complement system for the pathogenesis of age-related macular degeneration - current evidence and translation into clinical application Interaction of complement factor h and fibulin3 in age-related macular degeneration Exosomes from retinal astrocytes contain antiangiogenic components that inhibit laser-induced choroidal neovascularization.Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapy.Complement, age-related macular degeneration and a vision of the future Cell culture model that mimics drusen formation and triggers complement activation associated with age-related macular degeneration.Kidney function, albuminuria and age-related macular degeneration in NHANES III.Stem cells as tools for studying the genetics of inherited retinal degenerations.Genomic regulation of senescence and innate immunity signaling in the retinal pigment epithelium.Age-Related Macular Degeneration: A Disease of Systemic or Local Complement Dysregulation?Vision-threatening retinal abnormalities in chronic kidney disease stages 3 to 5.A local complement response by RPE causes early-stage macular degeneration.Complement Dysregulation and Disease: Insights from Contemporary Genetics.Reengineering Human Bruch's Membrane Increases Rod Outer Segment Phagocytosis by Human Retinal Pigment Epithelium.Anatomy and development of the macula: specialisation and the vulnerability to macular degeneration.The role of inflammation in the pathogenesis of age-related macular degeneration.

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P2860

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

http://www.wikidata.org/entity/Q43671971

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2001 nî lūn-bûn

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P2860

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration

Glomerulonephritis.

Fundus changes in mesangiocapillary glomerulonephritis type II: clinical and fluorescein angiographic findings.

Fundus changes in mesangiocapillary glomerulonephritis type II: vitreous fluorophotometry.

Subretinal neovascular membranes associated with chronic membranoproliferative glomerulonephritis type II.

Electrophysiology of type II mesangiocapillary glomerulonephritis with associated fundus abnormalities

An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group.

Goodpasture disease. Characterization of a single conformational epitope as the target of pathogenic autoantibodies.

Correlation between biochemical composition and fluorescein binding of deposits in Bruch's membrane.

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Pt 3

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