Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N - Wikidata - wikimedia - TriplyDB

Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N

Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N

http://www.wikidata.org/entity/Q37359842

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Constitutively active rhodopsin and retinal disease Fundus autofluorescence, optical coherence tomography, and electroretinogram findings in choroidal sclerosis Fundus autofluorescence and optical coherence tomography of congenital grouped albinotic spots Early structural anomalies observed by high-resolution imaging in two related cases of autosomal-dominant retinitis pigmentosa The role of fundus autofluorescence in late-onset retinitis pigmentosa (LORP) diagnosis Mice with a D190N mutation in the gene encoding rhodopsin: a model for human autosomal-dominant retinitis pigmentosa Microarray-based mutation detection and phenotypic characterization in Korean patients with retinitis pigmentosa.Thermal stability of rhodopsin and progression of retinitis pigmentosa: comparison of S186W and D190N rhodopsin mutants.Next-generation sequencing revealed a novel mutation in the gene encoding the beta subunit of rod phosphodiesterase."In situ" observation of the role of chloride ion binding to monkey green sensitive visual pigment by ATR-FTIR spectroscopy.An experimental comparison of human and bovine rhodopsin provides insight into the molecular basis of retinal disease.Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis Pigmentosa.

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P2860

Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N

http://www.wikidata.org/entity/Q37359842

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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name

Phenotype-genotype correlation ...... igmentosa caused by RHO, D190N

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Phenotype-genotype correlation ...... gmentosa caused by RHO, D190N.

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type

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Phenotype-genotype correlation ...... igmentosa caused by RHO, D190N

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Phenotype-genotype correlation ...... gmentosa caused by RHO, D190N.

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Phenotype-genotype correlation ...... igmentosa caused by RHO, D190N

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Phenotype-genotype correlation ...... gmentosa caused by RHO, D190N.

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Phenotype-genotype correlation ...... igmentosa caused by RHO, D190N

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Chai Lin Chou

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Chyuan-Sheng Lin

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Neeco Palmer

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Stephen H Tsang

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P2860

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

Long-term visual prognoses in patients with retinitis pigmentosa: the Ludwig von Sallmann lecture

Safety and efficacy of gene transfer for Leber's congenital amaurosis

Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions

Effect of gene therapy on visual function in Leber's congenital amaurosis

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families

Light, Ca2+, and photoreceptor death: new evidence for the equivalent-light hypothesis from arrestin knockout mice.

GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase.

Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.

Retinal counterion switch in the photoactivation of the G protein-coupled receptor rhodopsin

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11

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