Retinitis pigmentosa: defined from a molecular point of view.
about
Autosomal dominant retinitis pigmentosa mutations in inosine 5'-monophosphate dehydrogenase type I disrupt nucleic acid bindingRetinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from IndiaNovel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese familyHearing loss: a common disorder caused by many rare alleles.Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus conesFunctional annotation of the human retinal pigment epithelium transcriptomeA nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.Saturation of the human phenomeSpectrum of rhodopsin gene mutations in Chinese patients with retinitis pigmentosa.Gene therapy and retinitis pigmentosa: advances and future challenges.Diagnostic challenges in retinitis pigmentosa: genotypic multiplicity and phenotypic variability.Bcl-xL overexpression blocks bax-mediated mitochondrial contact site formation and apoptosis in rod photoreceptors of lead-exposed mice.A profile of transcriptomic changes in the rd10 mouse model of retinitis pigmentosa.The comparative protective effects of ganoderma spores lipid and fish oil on N-methyl-N-nitrosourea-induced photoreceptor cell lesion in rats.Spectrum of rhodopsin mutations in Korean patients with retinitis pigmentosa.Therapeutic challenges to retinitis pigmentosa: from neuroprotection to gene therapy.AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa.A proper protocol for isolation of retinal pigment epithelium from rabbit eyes.General pathophysiology in retinal degeneration.A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosaUltra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases.Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptorsGenetics of Hearing Loss: SyndromicCircadian rhythm dysfunction in glaucoma: A hypothesis.Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Two-Step Reactivation of Dormant Cones in Retinitis PigmentosaNimodipine inhibits N-methyl-N-nitrosourea-induced retinal photoreceptor apoptosis in vivo.Functional implications of tetraspanin proteins in cancer biology.Nimodipine rescues N-methyl-N-nitrosourea-induced retinal degeneration in ratsDonepezil delays photoreceptor apoptosis induced by N-methyl-N-nitrosourea in micePhotoreceptor disc shedding in the living human eye.Molecular characterization of retinitis pigmentosa in Saudi Arabia.The natural retinoprotectant chrysophanol attenuated photoreceptor cell apoptosis in an N-methyl-N-nitrosourea-induced mouse model of retinal degenaration.Light-emitting-diode induced retinal damage and its wavelength dependency in vivo.Retinal pigment epithelium differentiation of stem cells: current status and challenges.Physiology of circadian entrainment.Endothelin-1 role in human eye: a review.Autosomal dominant retinitis pigmentosa secondary to pre-mRNA splicing-factor gene PRPF31 (RP11): review of disease mechanism and report of a family with a novel 3-base pair insertion.The value of clinical electrophysiology in the assessment of the eye and visual system in the era of advanced imaging.Primary visual cortical remapping in patients with inherited peripheral retinal degeneration.
P2860
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P2860
Retinitis pigmentosa: defined from a molecular point of view.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Retinitis pigmentosa: defined from a molecular point of view.
@ast
Retinitis pigmentosa: defined from a molecular point of view.
@en
Retinitis pigmentosa: defined from a molecular point of view.
@nl
type
label
Retinitis pigmentosa: defined from a molecular point of view.
@ast
Retinitis pigmentosa: defined from a molecular point of view.
@en
Retinitis pigmentosa: defined from a molecular point of view.
@nl
prefLabel
Retinitis pigmentosa: defined from a molecular point of view.
@ast
Retinitis pigmentosa: defined from a molecular point of view.
@en
Retinitis pigmentosa: defined from a molecular point of view.
@nl
P2093
P1476
Retinitis pigmentosa: defined from a molecular point of view.
@en
P2093
Bleeker-Wagemakers EM
Westerveld A
de Jong PT
van Soest S
P304
P356
10.1016/S0039-6257(98)00046-0
P577
1999-01-01T00:00:00Z