OPN1MW

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Opsin 1, senzitivan na srednje talasne dužine
Identifikatori
SimboliOPN1MW; CBBM; CBD; GCP
Vanjski IDOMIM303800 HomoloGene88332 GeneCards: OPN1MW Gene
Ortolozi
VrstaČovekMiš
Entrez2652n/a
Ensembln/an/a
UniProtn/an/a
RefSeq (mRNA)NM_000513n/a
RefSeq (protein)NP_000504n/a
Lokacija (UCSC)n/an/a
PubMed pretraga[1]n/a

OPN1MW, zeleno-senzitivni opsin, je protein koji je kod ljudi kodiran OPN1MW genom.[1]

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Literatura[uredi - уреди | uredi kôd]

Dodatna literatura[uredi - уреди | uredi kôd]

  • Applebury ML, Hargrave PA (1987). „Molecular biology of the visual pigments.”. Vision Res. 26 (12): 1881–95. DOI:10.1016/0042-6989(86)90115-X. PMID 3303660. 
  • Winderickx J, Sanocki E, Lindsey DT, et al. (1993). „Defective colour vision associated with a missense mutation in the human green visual pigment gene.”. Nat. Genet. 1 (4): 251–6. DOI:10.1038/ng0792-251. PMID 1302020. 
  • Neitz J, Neitz M, Jacobs GH (1990). „Analysis of fusion gene and encoded photopigment of colour-blind humans.”. Nature 342 (6250): 679–82. DOI:10.1038/342679a0. PMID 2574415. 
  • Nathans J, Thomas D, Hogness DS (1986). „Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.”. Science 232 (4747): 193–202. DOI:10.1126/science.2937147. PMID 2937147. 
  • Li ZY, Kljavin IJ, Milam AH (1995). „Rod photoreceptor neurite sprouting in retinitis pigmentosa.”. J. Neurosci. 15 (8): 5429–38. PMID 7643192. 
  • Ladekjaer-Mikkelsen AS, Rosenberg T, Jørgensen AL (1996). „A new mechanism in blue cone monochromatism.”. Hum. Genet. 98 (4): 403–8. DOI:10.1007/s004390050229. PMID 8792812. 
  • Ferreira PA, Nakayama TA, Pak WL, Travis GH (1996). „Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.”. Nature 383 (6601): 637–40. DOI:10.1038/383637a0. PMID 8857542. 
  • Vissers PM, Bovee-Geurts PH, Portier MD, et al. (1998). „Large-scale production and purification of the human green cone pigment: characterization of late photo-intermediates.”. Biochem. J.. 330 (Pt 3): 1201–8. PMC 1219262. PMID 9494086. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1219262/. 
  • Bernstein SL, Wong P (1998). „Regional expression of disease-related genes in human and monkey retina.”. Mol. Vis. 4: 24. PMID 9815288. 
  • Hayashi T, Motulsky AG, Deeb SS (1999). „Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.”. Nat. Genet. 22 (1): 90–3. DOI:10.1038/8798. PMID 10319869. 
  • Ueyama H, Kuwayama S, Imai H, et al. (2002). „Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies.”. Biochem. Biophys. Res. Commun. 294 (2): 205–9. DOI:10.1016/S0006-291X(02)00458-8. PMID 12051694. 
  • Zhu X, Brown B, Li A, et al. (2003). „GRK1-dependent phosphorylation of S and M opsins and their binding to cone arrestin during cone phototransduction in the mouse retina.”. J. Neurosci. 23 (14): 6152–60. PMID 12853434. 
  • Bonilha VL, Hollyfield JG, Grover S, Fishman GA (2005). „Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.”. Ophthalmic Genet. 26 (2): 69–76. DOI:10.1080/13816810590968041. PMID 16020309. 

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