Pages that link to "Q40896642"
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The following pages link to Retinitis pigmentosa. The Friedenwald Lecture (Q40896642):
Displaying 50 items.
- Genes associated with retinitis pigmentosa and allied diseases are frequently mutated in the general population (Q21560782) (← links)
- The Whole Nucleotide Sequence and Chromosomal Localization of the Gene for Human Metabotropic Glutamate Receptor Subtype 6 (Q24316397) (← links)
- Long-term safety and efficacy of human-induced pluripotent stem cell (iPS) grafts in a preclinical model of retinitis pigmentosa (Q24600170) (← links)
- Long-term visual prognoses in patients with retinitis pigmentosa: the Ludwig von Sallmann lecture (Q24628682) (← links)
- Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy (Q24646440) (← links)
- Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa (Q24655474) (← links)
- Novel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family (Q24674843) (← links)
- Retinal Cell Degeneration in Animal Models (Q26771160) (← links)
- Constitutively active rhodopsin and retinal disease (Q27023938) (← links)
- The role of mislocalized phototransduction in photoreceptor cell death of retinitis pigmentosa (Q27308102) (← links)
- Rhodopsin mutant P23H destabilizes rod photoreceptor disk membranes (Q27310120) (← links)
- The Diversity of Spine Synapses in Animals (Q28077465) (← links)
- A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p (Q28274400) (← links)
- Ocular pulse amplitude is reduced in patients with advanced retinitis pigmentosa (Q28365758) (← links)
- Immunocytochemical evidence of Tulp1-dependent outer segment protein transport pathways in photoreceptor cells (Q28513878) (← links)
- The effects of IRE1, ATF6, and PERK signaling on adRP-linked rhodopsins (Q28820980) (← links)
- Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects (Q28975783) (← links)
- Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa (Q29147466) (← links)
- Differential light-induced responses in sectorial inherited retinal degeneration. (Q30368295) (← links)
- Structure and function in rhodopsin: Mass spectrometric identification of the abnormal intradiscal disulfide bond in misfolded retinitis pigmentosa mutants (Q30988298) (← links)
- Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population (Q33239006) (← links)
- XIAP protection of photoreceptors in animal models of retinitis pigmentosa (Q33279531) (← links)
- Non-invasive stem cell therapy in a rat model for retinal degeneration and vascular pathology (Q33532634) (← links)
- Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations (Q33584461) (← links)
- Engineering retina from human retinal progenitors (cell lines). (Q33606405) (← links)
- A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa (Q33661285) (← links)
- Physical Activity and Quality of Life in Retinitis Pigmentosa (Q33741324) (← links)
- Microincision vitrectomy surgery in vitreomacular traction syndrome of retinitis pigmentosa patients (Q33804090) (← links)
- Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice (Q33825000) (← links)
- Extended wearing trial of Trifield lens device for 'tunnel vision' (Q33839216) (← links)
- Identification of core amino acids stabilizing rhodopsin (Q33904229) (← links)
- Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods (Q33944067) (← links)
- Calpain and PARP activation during photoreceptor cell death in P23H and S334ter rhodopsin mutant rats (Q33963936) (← links)
- Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. (Q34050979) (← links)
- A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family (Q34081528) (← links)
- Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis (Q34085940) (← links)
- Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. (Q34086505) (← links)
- Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa (Q34088214) (← links)
- A 350 bp region of the proximal promoter of Rds drives cell-type specific gene expression (Q34119861) (← links)
- Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration (Q34135509) (← links)
- Defective lipid transport and biosynthesis in recessive and dominant Stargardt macular degeneration (Q34157723) (← links)
- Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa (Q34277608) (← links)
- Clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin A (Q34330189) (← links)
- Effect of brain-derived neurotrophic factor on c-jun expression in the rd mouse retina (Q34330756) (← links)
- Genetic analysis of Chinese families reveals a novel truncation allele of the retinitis pigmentosa GTPase regulator gene (Q34390529) (← links)
- A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family (Q34429120) (← links)
- Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration (Q34535642) (← links)
- A comparison of progressive loss of the ellipsoid zone (EZ) band in autosomal dominant and x-linked retinitis pigmentosa (Q34547027) (← links)
- Retinal diseases linked with photoreceptor guanylate cyclase (Q34599860) (← links)
- shRNA knockdown of guanylate cyclase 2e or cyclic nucleotide gated channel alpha 1 increases photoreceptor survival in a cGMP phosphodiesterase mouse model of retinitis pigmentosa (Q34768118) (← links)