Pages that link to "Q24315746"
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The following pages link to Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies (Q24315746):
Displaying 50 items.
- Retinal outer segment membrane protein 1 (Q21134395) (← links)
- Isolation of a ubiquitin-like (UBL5) gene from a screen identifying highly expressed and conserved iris genes (Q24290760) (← links)
- Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina (Q24306695) (← links)
- SFA-1, a novel cellular gene induced by human T-cell leukemia virus type 1, is a member of the transmembrane 4 superfamily (Q24310639) (← links)
- Negative regulation of ciliary length by ciliary male germ cell-associated kinase (Mak) is required for retinal photoreceptor survival (Q24314850) (← links)
- Human retina-specific amine oxidase (RAO): cDNA cloning, tissue expression, and chromosomal mapping (Q24316466) (← links)
- NAG-2, a novel transmembrane-4 superfamily (TM4SF) protein that complexes with integrins and other TM4SF proteins (Q24324473) (← links)
- Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome (Q24652543) (← links)
- The L6 membrane proteins--a new four-transmembrane superfamily (Q24672051) (← links)
- Uroplakins Ia and Ib, two major differentiation products of bladder epithelium, belong to a family of four transmembrane domain (4TM) proteins (Q24673396) (← links)
- Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM (Q24679722) (← links)
- The role of primary cilia in the development and disease of the retina (Q26822720) (← links)
- Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR (Q28117716) (← links)
- The cGMP-gated channel and related glutamic acid-rich proteins interact with peripherin-2 at the rim region of rod photoreceptor disc membranes (Q28201043) (← links)
- Photoreceptor renewal: a role for peripherin/rds (Q28218313) (← links)
- Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11 (Q28243149) (← links)
- Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene (Q28268699) (← links)
- Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy (Q28268707) (← links)
- Folding and subunit assembly of photoreceptor peripherin/rds is mediated by determinants within the extracellular/intradiskal EC2 domain: implications for heterogeneous molecular pathologies (Q28350970) (← links)
- Molecular cloning of a novel membrane glycoprotein, pal, specifically expressed in photoreceptor cells of the retina and containing leucine-rich repeat (Q28579759) (← links)
- Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1 (Q28588396) (← links)
- Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation (Q28589610) (← links)
- RP1 is required for the correct stacking of outer segment discs (Q28589750) (← links)
- The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein (Q28591131) (← links)
- Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degeneration (Q28592002) (← links)
- A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice (Q28594074) (← links)
- Structural and functional relationships between photoreceptor tetraspanins and other superfamily members (Q28742243) (← links)
- The proteome of the mouse photoreceptor sensory cilium complex (Q29619586) (← links)
- Expression and characterization of peripherin/rds-rom-1 complexes and mutants implicated in retinal degenerative diseases. (Q30326779) (← links)
- Molecular characterization of the skate peripherin/rds gene: relationship to its orthologues and paralogues (Q31143155) (← links)
- Glutamic acid-rich proteins of rod photoreceptors are natively unfolded (Q33226936) (← links)
- Retinitis pigmentosa: defined from a molecular point of view (Q33534644) (← links)
- Complex disorders in ophthalmology (Q33572052) (← links)
- Role of the second intradiscal loop of peripherin/rds in homo and hetero associations (Q33662611) (← links)
- Peripherin-2 and Rom-1 have opposing effects on rod outer segment targeting of retinitis pigmentosa-linked peripherin-2 mutants. (Q33725907) (← links)
- Rhodopsin trafficking and its role in retinal dystrophies. (Q33798214) (← links)
- Disulfide-mediated oligomerization of Peripherin/Rds and Rom-1 in photoreceptor disk membranes. Implications for photoreceptor outer segment morphogenesis and degeneration (Q33890711) (← links)
- Lipid metabolism in vertebrate retinal rod outer segments (Q33944604) (← links)
- Harnessing the power of forward genetics--analysis of neuronal diversity and patterning in the zebrafish retina (Q34080485) (← links)
- Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS (Q34341141) (← links)
- Cloning of the cDNA for a novel photoreceptor protein (Q34372883) (← links)
- Impact of signaling microcompartment geometry on GPCR dynamics in live retinal photoreceptors (Q34379117) (← links)
- The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse (Q34463210) (← links)
- The complexities of ocular genetics (Q34592303) (← links)
- Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations (Q34667367) (← links)
- Therapeutic challenges to retinitis pigmentosa: from neuroprotection to gene therapy. (Q35092187) (← links)
- Late-onset autosomal dominant macular dystrophy with choroidal neovascularization and nonexudative maculopathy associated with mutation in the RDS gene (Q35185818) (← links)
- Electrophysiological analysis of visual function in mutant mice. (Q35195026) (← links)
- Light regulates the ciliary protein transport and outer segment disc renewal of mammalian photoreceptors (Q35218045) (← links)
- SNAREs Interact with Retinal Degeneration Slow and Rod Outer Segment Membrane Protein-1 during Conventional and Unconventional Outer Segment Targeting (Q35788032) (← links)