about
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1FA Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)Missense variations in the fibulin 5 gene and age-related macular degenerationOxidative stress and the regulation of complement activation in human glaucomaRetinal synthesis and deposition of complement components induced by ocular hypertension.Intraocular pressure measurement in mice: a comparison between Goldmann and rebound tonometry.Neuroglobin and cytoglobin distribution in the anterior eye segment: a comparative immunohistochemical study.The genetics of age-related macular degeneration.Hemoglobin expression and regulation in glaucoma: insights into retinal ganglion cell oxygenation.Genetic dependence of central corneal thickness among inbred strains of mice.Transplantation of BDNF-secreting mesenchymal stem cells provides neuroprotection in chronically hypertensive rat eyesGenomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.Induction of trabecular meshwork cells from induced pluripotent stem cellsRetinal neurodegeneration may precede microvascular changes characteristic of diabetic retinopathy in diabetes mellitus.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociMicroarray analysis of iris gene expression in mice with mutations influencing pigmentation.Lipofuscin in human glaucomatous optic nerves.Removal of potentially confounding phenotypes from a Siamese-derived feline glaucoma breeding colony.Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma.Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds.Proteomics Analysis of Molecular Risk Factors in the Ocular Hypertensive Human RetinaAdoptive transfer of immune cells from glaucomatous mice provokes retinal ganglion cell loss in recipients.Retinal ganglion cell death in glaucoma: mechanisms and neuroprotective strategies.Lack of immunoglobulins does not prevent C1q binding to RGC and does not alter the progression of experimental glaucoma.The genetic mechanisms of primary angle closure glaucoma.Cryopreserved Mesenchymal Stromal Cells Maintain Potency in a Retinal Ischemia/Reperfusion Injury Model: Toward an off-the-shelf TherapyTransplantation of iPSC-derived TM cells rescues glaucoma phenotypes in vivo.Autosomal recessive retinitis pigmentosa due to ABCA4 mutations: clinical, pathologic, and molecular characterization.Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound.Novel drug delivery systems for glaucoma.Immune phenomena in glaucoma and conformational disorders: why is the second eye not involved?Elevated membrane attack complex in human choroid with high risk complement factor H genotypes.Sustained Delivery of Timolol Maleate for Over 90 Days by Subconjunctival Injection.MMP19 expression in the human optic nerve.Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly.The Ability of Nitric Oxide to Lower Intraocular Pressure Is Dependent on Guanylyl Cyclase.Correction: A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus).Neuroinflammation in advanced canine glaucoma.Disruption of the complement cascade delays retinal ganglion cell death following retinal ischemia-reperfusion.Organization of the human IMPG2 gene and its evaluation as a candidate gene in age-related macular degeneration and other retinal degenerative disorders.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Markus H Kuehn
@ast
Markus H Kuehn
@en
Markus H Kuehn
@es
Markus H Kuehn
@nl
Markus H Kuehn
@sl
type
label
Markus H Kuehn
@ast
Markus H Kuehn
@en
Markus H Kuehn
@es
Markus H Kuehn
@nl
Markus H Kuehn
@sl
prefLabel
Markus H Kuehn
@ast
Markus H Kuehn
@en
Markus H Kuehn
@es
Markus H Kuehn
@nl
Markus H Kuehn
@sl
P106
P21
P31
P496
0000-0003-3940-198X