Nuclear hormone receptor

NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)

Genetics / Transcription / Humans / Mutation / Mice / Retinitis pigmentosa / Animals / Expression / Differential Diagnosis / Transcription Factor / Clinical Sciences / Genotype / Orphan Nuclear Receptors / Syndrome / Nuclear hormone receptor / Retinitis pigmentosa / Animals / Expression / Differential Diagnosis / Transcription Factor / Clinical Sciences / Genotype / Orphan Nuclear Receptors / Syndrome / Nuclear hormone receptor

PPARγ3 mRNA: a distinct PPARγ mRNA subtype transcribed from an independent promoter

Nuclear Receptor / Adipose tissue / Peroxisome proliferator-activated receptor / mRna expression levels / Prostaglandin E2 / Nuclear hormone receptor / Biochemistry and cell biology / Nuclear hormone receptor / Biochemistry and cell biology

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