[cite web | title = Entrez Gene: GUCA1A guanylate cyclase activator 1A (retina)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2978| accessdate = ] ] PBB_Summary
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References
Further reading
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citations =
*cite journal | author=Subbaraya I, Ruiz CC, Helekar BS, "et al." |title=Molecular characterization of human and mouse photoreceptor guanylate cyclase-activating protein (GCAP) and chromosomal localization of the human gene. |journal=J. Biol. Chem. |volume=269 |issue= 49 |pages= 31080–9 |year= 1995 |pmid= 7983048 |doi=
*cite journal | author=Surguchov A, Bronson JD, Banerjee P, "et al." |title=The human GCAP1 and GCAP2 genes are arranged in a tail-to-tail array on the short arm of chromosome 6 (p21.1). |journal=Genomics |volume=39 |issue= 3 |pages= 312–22 |year= 1997 |pmid= 9119368 |doi= 10.1006/geno.1996.4513
*cite journal | author=Payne AM, Downes SM, Bessant DA, "et al." |title=A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1. |journal=Hum. Mol. Genet. |volume=7 |issue= 2 |pages= 273–7 |year= 1998 |pmid= 9425234 |doi=
*cite journal | author=Dizhoor AM, Boikov SG, Olshevskaya EV |title=Constitutive activation of photoreceptor guanylate cyclase by Y99C mutant of GCAP-1. Possible role in causing human autosomal dominant cone degeneration. |journal=J. Biol. Chem. |volume=273 |issue= 28 |pages= 17311–4 |year= 1998 |pmid= 9651312 |doi=
*cite journal | author=Sokal I, Li N, Surgucheva I, "et al." |title=GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy. |journal=Mol. Cell |volume=2 |issue= 1 |pages= 129–33 |year= 1998 |pmid= 9702199 |doi=
*cite journal | author=Sokal I, Li N, Verlinde CL, "et al." |title=Ca(2+)-binding proteins in the retina: from discovery to etiology of human disease(1). |journal=Biochim. Biophys. Acta |volume=1498 |issue= 2-3 |pages= 233–51 |year= 2001 |pmid= 11108966 |doi=
*cite journal | author=Downes SM, Holder GE, Fitzke FW, "et al." |title=Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. |journal=Arch. Ophthalmol. |volume=119 |issue= 1 |pages= 96–105 |year= 2001 |pmid= 11146732 |doi=
*cite journal | author=Wilkie SE, Li Y, Deery EC, "et al." |title=Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy. |journal=Am. J. Hum. Genet. |volume=69 |issue= 3 |pages= 471–80 |year= 2001 |pmid= 11484154 |doi=
*cite journal | author=Hwang JY, Koch KW |title=Calcium- and myristoyl-dependent properties of guanylate cyclase-activating protein-1 and protein-2. |journal=Biochemistry |volume=41 |issue= 43 |pages= 13021–8 |year= 2002 |pmid= 12390029 |doi=
*cite journal | author=Hwang JY, Koch KW |title=The myristoylation of the neuronal Ca2+ -sensors guanylate cyclase-activating protein 1 and 2. |journal=Biochim. Biophys. Acta |volume=1600 |issue= 1-2 |pages= 111–7 |year= 2002 |pmid= 12445466 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Pennesi ME, Howes KA, Baehr W, Wu SM |title=Guanylate cyclase-activating protein (GCAP) 1 rescues cone recovery kinetics in GCAP1/GCAP2 knockout mice. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue= 11 |pages= 6783–8 |year= 2003 |pmid= 12732716 |doi= 10.1073/pnas.1130102100
*cite journal | author=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Peshenko IV, Moiseyev GP, Olshevskaya EV, Dizhoor AM |title=Factors that determine Ca2+ sensitivity of photoreceptor guanylyl cyclase. Kinetic analysis of the interaction between the Ca2+-bound and the Ca2+-free guanylyl cyclase activating proteins (GCAPs) and recombinant photoreceptor guanylyl cyclase 1 (RetGC-1). |journal=Biochemistry |volume=43 |issue= 43 |pages= 13796–804 |year= 2004 |pmid= 15504042 |doi= 10.1021/bi048943m
*cite journal | author=Nishiguchi KM, Sokal I, Yang L, "et al." |title=A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degeneration. |journal=Invest. Ophthalmol. Vis. Sci. |volume=45 |issue= 11 |pages= 3863–70 |year= 2004 |pmid= 15505030 |doi= 10.1167/iovs.04-0590
*cite journal | author=Jiang L, Katz BJ, Yang Z, "et al." |title=Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A). |journal=Mol. Vis. |volume=11 |issue= |pages= 143–51 |year= 2005 |pmid= 15735604 |doi=
*cite journal | author=Sokal I, Dupps WJ, Grassi MA, "et al." |title=A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD). |journal=Invest. Ophthalmol. Vis. Sci. |volume=46 |issue= 4 |pages= 1124–32 |year= 2005 |pmid= 15790869 |doi= 10.1167/iovs.04-1431
*cite journal | author=Michaelides M, Wilkie SE, Jenkins S, "et al." |title=Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy. |journal=Ophthalmology |volume=112 |issue= 8 |pages= 1442–7 |year= 2005 |pmid= 15953638 |doi= 10.1016/j.ophtha.2005.02.024
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