Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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The cell biology of vision

P2860

Q35005573-C248C3CE-8172-4FC2-89B3-2EC8FA2B9107

P2860

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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http://www.wikidata.org/entity/Q36717097

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2006 nî lūn-bûn

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2006年の論文

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2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

2006年论文

@zh

2006年论文

@zh-cn

name

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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type

Item

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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P1476

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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P2093

Muna I Naash

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Xi-Qin Ding

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P2860

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression.

Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects.

Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.

The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa.

Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa

The C terminus of peripherin/rds participates in rod outer segment targeting and alignment of disk incisures.

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene

Heterologous expression of photoreceptor peripherin/rds and Rom-1 in COS-1 cells: assembly, interactions, and localization of multisubunit complexes.

P304

141-146

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scholarly article

P356

10.1007/0-387-32442-9_21

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English

P478

572

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2006-01-01T00:00:00Z

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6553238

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17249567

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2793174

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Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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P2860

P2860

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932