TTC8 gene

Known as: TETRATRICOPEPTIDE REPEAT DOMAIN-CONTAINING PROTEIN 8, BBS8, TTC8 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2009-2015
012320092015

Papers overview

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2016
2016
Ciliary genes FAM161A and TTC8 have been implicated in retinal degeneration (RD) in humans and in dogs. The identification of… (More)
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2015
2015
Nonsyndromic retinitis pigmentosa (RP) is genetically highly heterogeneous, with >100 disease genes identified. However… (More)
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2015
2015
Bardet-Biedl Syndrome (BBS) is a rare, autosomal-recessive ciliopathy characterized by obesity, rod-cone dystrophy, postaxial… (More)
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2015
2015
In this study, we elucidated the architectures of two multisubunit complexes, the BBSome and exocyst, through a novel application… (More)
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2013
2013
Generalized progressive retinal atrophy (PRA) is a group of inherited eye diseases characterised by progressive retinal… (More)
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2009
2009
Bardet Biedl syndrome is a genetically heterogeneous ciliopathy with fourteen genes currently identified. To date, mutations in… (More)
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