about
Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy.Personalized ophthalmology.MiR-204 is responsible for inherited retinal dystrophy associated with ocular colobomaA role for repressive complexes and H3K9 di-methylation in PRDM5-associated brittle cornea syndrome.Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome.Brittle cornea syndrome: recognition, molecular diagnosis and managementZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.Predicting mortality using two renal function estimation methods in hospitalised stroke patients.Identification of a Novel Locus for Autosomal Dominant Primary Open Angle Glaucoma on 4q35.1-q35.2Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genesUnintended consequences and MRSA screening policy
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Louise Porter
@ast
Louise Porter
@en
Louise Porter
@es
Louise Porter
@nl
Louise Porter
@sl
type
label
Louise Porter
@ast
Louise Porter
@en
Louise Porter
@es
Louise Porter
@nl
Louise Porter
@sl
prefLabel
Louise Porter
@ast
Louise Porter
@en
Louise Porter
@es
Louise Porter
@nl
Louise Porter
@sl
P106
P21
P31
P496
0000-0002-7406-0319