Expression of superoxide dismutase in whole lens prevents cataract formationLocalization and H2O2-specific induction of PRDX3 in the eye lensExpression and immunolocalization of plasma membrane calcium ATPase isoforms in human corneal epitheliumIntegrin beta1-mediated signaling is involved in transforming growth factor-beta2-promoted migration in human lens epithelial cellsThe regulatory subunit of PDE6 interacts with PACSIN in photoreceptorsStem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneasTargeted inhibition of p57 and p15 blocks transforming growth factor beta-inhibited proliferation of primary cultured human limbal epithelial cellsNatriuretic peptide system in the human retinaMolecular characterization and functional analysis of phagocytosis by human embryonic stem cell-derived RPE cells using a novel human retinal assayA nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese familyOverexpression of CERKL, a gene responsible for retinitis pigmentosa in humans, protects cells from apoptosis induced by oxidative stressCrystallin gene mutations in Indian families with inherited pediatric cataractA mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani familyHomozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaIntraocular and serum cytokine profiles in patients with intermediate uveitisHorizontal gaze palsy with progressive scoliosis: three novel ROBO3 mutations and descriptions of the phenotypes of four patientsMapracorat, a novel selective glucocorticoid receptor agonist, inhibits hyperosmolar-induced cytokine release and MAPK pathways in human corneal epithelial cellsInterleukin-17 production and T helper 17 cells in peripheral blood mononuclear cells in response to ocular lysate in patients with birdshot chorioretinopathyIdentification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridiaIdentification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese populationExploring the retinal connectomeMicroRNA expression in human retinal pigment epithelial (ARPE-19) cells: increased expression of microRNA-9 by N-(4-hydroxyphenyl)retinamideRetinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the beta-subunit of transducin with digenic diseaseIdentification of Notch-1 expression in the limbal basal epitheliumMass spectrometry-based proteomic analyses of contact lens depositionA novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophyFive novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmusBOL-303242-X, a novel selective glucocorticoid receptor agonist, with full anti-inflammatory properties in human ocular cellsA novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese familyMarked reduction of alcohol dehydrogenase in keratoconus corneal fibroblastsCone-rod dystrophy and a frameshift mutation in the PROM1 geneGenetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative geneHuman embryonic and neuronal stem cell markers in retinoblastomaIdentification of three novel NHS mutations in families with Nance-Horan syndromeVariations in the WDR36 gene in German patients with normal tension glaucomaMutational screening of 10 genes in Chinese patients with microphthalmia and/or colobomaCommon MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopiaChordin-like 1, a bone morphogenetic protein-4 antagonist, is upregulated by hypoxia in human retinal pericytes and plays a role in regulating angiogenesis
P1433
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P1433
description
czasopismo okulistyczne
@pl
journal
@en
revista científica
@es
revue scientifique
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rivista scientifica
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vědecký časopis
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wetenschappelijk tijdschrift van Emory-universiteit
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wissenschaftliche Fachzeitschrift
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مجلة
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वैज्ञानिक पत्रिका
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name
Molecular Vision
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Molecular Vision
@da
Molecular Vision
@en
Molecular Vision
@es
Molecular Vision
@fi
Molecular Vision
@fr
Molecular Vision
@it
Molecular Vision
@nb
Molecular Vision
@nl
Molecular Vision
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type
label
Molecular Vision
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Molecular Vision
@da
Molecular Vision
@en
Molecular Vision
@es
Molecular Vision
@fi
Molecular Vision
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Molecular Vision
@it
Molecular Vision
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Molecular Vision
@nl
Molecular Vision
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altLabel
Mol Vis
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Mol Vis
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prefLabel
Molecular Vision
@ast
Molecular Vision
@da
Molecular Vision
@en
Molecular Vision
@es
Molecular Vision
@fi
Molecular Vision
@fr
Molecular Vision
@it
Molecular Vision
@nb
Molecular Vision
@nl
Molecular Vision
@nn
P31
P243
P4616
P101
P1055
P1058
P1156
P1159
P1160
P123
P1277
P1476
Molecular Vision
@en