Pages that link to "Q24680469"
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The following pages link to Autosomal recessive retinitis pigmentosa and E150K mutation in the opsin gene (Q24680469):
Displaying 16 items.
- Rab26 modulates the cell surface transport of α2-adrenergic receptors from the Golgi (Q24302003) (← links)
- Rab8 interacts with distinct motifs in alpha2B- and beta2-adrenergic receptors and differentially modulates their transport (Q33924469) (← links)
- Chaperoning G protein-coupled receptors: from cell biology to therapeutics (Q33927508) (← links)
- Electrostatic compensation restores trafficking of the autosomal recessive retinitis pigmentosa E150K opsin mutant to the plasma membrane (Q34121624) (← links)
- Regulation of G protein-coupled receptor export trafficking. (Q35827970) (← links)
- Anterograde Trafficking of Nascent α2B-Adrenergic Receptor: Structural Basis, Roles of Small GTPases (Q35875489) (← links)
- Regulation of post-Golgi traffic of G protein-coupled receptors (Q36701400) (← links)
- A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa (Q37454102) (← links)
- Inherent instability of the retinitis pigmentosa P23H mutant opsin (Q37691592) (← links)
- Transcriptional expression of cis-acting and trans-acting splicing mutations cause autosomal dominant retinitis pigmentosa. (Q39992013) (← links)
- Mouse models of human ocular disease for translational research (Q41577738) (← links)
- Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization. (Q42438771) (← links)
- Transcriptome profiling of NIH3T3 cell lines expressing opsin and the P23H opsin mutant identifies candidate drugs for the treatment of retinitis pigmentosa (Q42774910) (← links)
- Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2 -ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia (Q43041172) (← links)
- A novel rhodopsin-like gene expressed in zebrafish retina (Q47073474) (← links)
- Comparison of the retinitis pigmentosa mutations in rhodopsin with a functional map of the C5a receptor (Q80235057) (← links)