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Kubo A(2001)The transcription factor Acta Ophthalmol Scand 79 497-undefined
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Kitahara K(undefined) functions in retinal progenitors to suppress cone cell generation undefined undefined undefined-undefined
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Audo I(undefined)Nuclear receptor undefined undefined undefined-undefined
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Michaelides M(undefined) gene mutations distort human retinal laminar architecture and cause an unusual degeneration undefined undefined undefined-undefined
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Robson AG(undefined)Shared mutations in undefined undefined undefined-undefined
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Hawlina M(undefined) in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration undefined undefined undefined-undefined
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Vaclavik V(undefined)The photoreceptor cell-specific nuclear receptor gene ( undefined undefined undefined-undefined
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Sandbach JM(undefined)) accounts for retinitis pigmentosa in the crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition undefined undefined undefined-undefined
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Pachydaki SI(undefined)Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa undefined undefined undefined-undefined