about
Review and expert opinion in age related macular degeneration. Focus on the pathophysiology, angiogenesis and pharmacological and clinical dataSpectral-domain optical coherence tomography of the rodent eye: highlighting layers of the outer retina using signal averaging and comparison with histologyInducible nitric oxide synthase mediates the change from retinal to vitreal neovascularization in ischemic retinopathyProangiogenic effects of protease-activated receptor 2 are tumor necrosis factor-alpha and consecutively Tie2 dependentCD36 deficiency leads to choroidal involution via COX2 down-regulation in rodentsCX3CR1-dependent subretinal microglia cell accumulation is associated with cardinal features of age-related macular degeneration.Netrin-4 inhibits angiogenesis via binding to neogenin and recruitment of Unc5B.Adaptive optics imaging of geographic atrophy.MFGE8 does not influence chorio-retinal homeostasis or choroidal neovascularization in vivo.Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindnessNeonatal hyperglycemia inhibits angiogenesis and induces inflammation and neuronal degeneration in the retinaApolipoprotein E promotes subretinal mononuclear phagocyte survival and chronic inflammation in age-related macular degenerationVEGFR-1: a safe target for prophylaxis of retinopathy of prematurity?Experimental Branch Retinal Vein Occlusion Induces Upstream Pericyte Loss and Vascular Destabilization.Intraocular pressure reduction and neuroprotection conferred by bone marrow-derived mesenchymal stem cells in an animal model of glaucoma.Gut microbiota influences pathological angiogenesis in obesity-driven choroidal neovascularization.A regulatory domain is required for Foxn4 activity during retinogenesis.Trans-arachidonic acids generated during nitrative stress induce a thrombospondin-1-dependent microvascular degenerationSubretinal mononuclear phagocytes induce cone segment loss via IL-1β.Deficiency in the metabolite receptor SUCNR1 (GPR91) leads to outer retinal lesions.CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice.Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction.Activated monocytes resist elimination by retinal pigment epithelium and downregulate their OTX2 expression via TNF-α.Understanding ischemic retinopathies: emerging concepts from oxygen-induced retinopathy.CCL2/CCR2 and CX3CL1/CX3CR1 chemokine axes and their possible involvement in age-related macular degenerationComplement factor H and related proteins in age-related macular degeneration.Thrombospondin-1 and Pathogenesis of Age-Related Macular Degeneration.Comprehensive analysis of mouse retinal mononuclear phagocytes.The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.Complement Factor H Inhibits CD47-Mediated Resolution of Inflammation.Dystrophin Dp71 gene deletion induces retinal vascular inflammation and capillary degeneration.Altered astrocyte morphology and vascular development in dystrophin-Dp71-null mice.On phagocytes and macular degeneration.Upregulation of P2RX7 in Cx3cr1-Deficient Mononuclear Phagocytes Leads to Increased Interleukin-1β Secretion and Photoreceptor Neurodegeneration.Lebecetin, a C-type lectin, inhibits choroidal and retinal neovascularization.Ptf1a/Rbpj complex inhibits ganglion cell fate and drives the specification of all horizontal cell subtypes in the chick retina.APOE Isoforms Control Pathogenic Subretinal Inflammation in Age-Related Macular Degeneration.Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.Protection of Glial Müller Cells by Dexamethasone in a Mouse Model of Surgically Induced Blood-Retinal Barrier Breakdown.Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndrome.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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ricercatore
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հետազոտող
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name
Florian Sennlaub
@ast
Florian Sennlaub
@en
Florian Sennlaub
@es
Florian Sennlaub
@nl
Florian Sennlaub
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type
label
Florian Sennlaub
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Florian Sennlaub
@en
Florian Sennlaub
@es
Florian Sennlaub
@nl
Florian Sennlaub
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prefLabel
Florian Sennlaub
@ast
Florian Sennlaub
@en
Florian Sennlaub
@es
Florian Sennlaub
@nl
Florian Sennlaub
@sl
P214
P1053
F-2756-2017
P106
P1153
6603045217
P21
P213
0000 0003 5682 5987
P214
P31
P3829
P496
0000-0003-4412-1341
P735
P7859
viaf-193120822