These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 11115851)

  • 21. Constitutive Activation of Guanylate Cyclase by the G86R GCAP1 Variant Is Due to "Locking" Cation-π Interactions that Impair the Activator-to-Inhibitor Structural Transition.
    Abbas S; Marino V; Bielefeld L; Koch KW; Dell'Orco D
    Int J Mol Sci; 2020 Jan; 21(3):. PubMed ID: 31979372
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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).
    Peshenko IV; Moiseyev GP; Olshevskaya EV; Dizhoor AM
    Biochemistry; 2004 Nov; 43(43):13796-804. PubMed ID: 15504042
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.
    Newbold RJ; Deery EC; Walker CE; Wilkie SE; Srinivasan N; Hunt DM; Bhattacharya SS; Warren MJ
    Hum Mol Genet; 2001 Jan; 10(1):47-54. PubMed ID: 11136713
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Variants at codon 838 in the
    Sun Z; Wu S; Zhu T; Li H; Wei X; Du H; Sui R
    Ophthalmic Genet; 2020 Dec; 41(6):548-555. PubMed ID: 32811265
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autosomal dominant cone-rod dystrophy with R838H and R838C mutations in the GUCY2D gene in Japanese patients.
    Ito S; Nakamura M; Ohnishi Y; Miyake Y
    Jpn J Ophthalmol; 2004; 48(3):228-35. PubMed ID: 15175914
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Transgenic zebrafish expressing mutant human RETGC-1 exhibit aberrant cone and rod morphology.
    Collery RF; Cederlund ML; Kennedy BN
    Exp Eye Res; 2013 Mar; 108():120-8. PubMed ID: 23328348
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D.
    Sharon D; Wimberg H; Kinarty Y; Koch KW
    Prog Retin Eye Res; 2018 Mar; 63():69-91. PubMed ID: 29061346
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neuronal Calcium Sensor GCAP1 Encoded by
    Abbas S; Marino V; Weisschuh N; Kieninger S; Solaki M; Dell'Orco D; Koch KW
    ACS Chem Neurosci; 2020 May; 11(10):1458-1470. PubMed ID: 32298085
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Novel
    Biasi A; Marino V; Dal Cortivo G; Maltese PE; Modarelli AM; Bertelli M; Colombo L; Dell'Orco D
    Int J Mol Sci; 2021 Oct; 22(19):. PubMed ID: 34639157
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A).
    Jiang L; Katz BJ; Yang Z; Zhao Y; Faulkner N; Hu J; Baird J; Baehr W; Creel DJ; Zhang K
    Mol Vis; 2005 Feb; 11():143-51. PubMed ID: 15735604
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
    Van Ghelue M; Eriksen HL; Ponjavic V; Fagerheim T; Andréasson S; Forsman-Semb K; Sandgren O; Holmgren G; Tranebjaerg L
    Ophthalmic Genet; 2000 Dec; 21(4):197-209. PubMed ID: 11135490
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Guanylate cyclase activating proteins, guanylate cyclase and disease.
    Newbold RJ; Deery EC; Payne AM; Wilkie SE; Hunt DM; Warren MJ
    Adv Exp Med Biol; 2002; 514():411-38. PubMed ID: 12596936
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of functional regions of guanylate cyclase-activating protein 1 (GCAP1) using GCAP1/GCIP chimeras.
    Li N; Sokal I; Bronson JD; Palczewski K; Baehr W
    Biol Chem; 2001 Aug; 382(8):1179-88. PubMed ID: 11592399
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa.
    Avesani A; Bielefeld L; Weisschuh N; Marino V; Mazzola P; Stingl K; Haack TB; Koch KW; Dell'Orco D
    Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328663
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD).
    Sokal I; Dupps WJ; Grassi MA; Brown J; Affatigato LM; Roychowdhury N; Yang L; Filipek S; Palczewski K; Stone EM; Baehr W
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1124-32. PubMed ID: 15790869
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Structural insights for activation of retinal guanylate cyclase by GCAP1.
    Lim S; Peshenko IV; Dizhoor AM; Ames JB
    PLoS One; 2013; 8(11):e81822. PubMed ID: 24236217
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Structure of Guanylyl Cyclase Activator Protein 1 (GCAP1) Mutant V77E in a Ca2+-free/Mg2+-bound Activator State.
    Lim S; Peshenko IV; Olshevskaya EV; Dizhoor AM; Ames JB
    J Biol Chem; 2016 Feb; 291(9):4429-41. PubMed ID: 26703466
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransduction.
    Dell'Orco D; Sulmann S; Zägel P; Marino V; Koch KW
    Cell Mol Life Sci; 2014 Oct; 71(19):3829-40. PubMed ID: 24566882
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
    Kitiratschky VB; Wilke R; Renner AB; Kellner U; Vadalà M; Birch DG; Wissinger B; Zrenner E; Kohl S
    Invest Ophthalmol Vis Sci; 2008 Nov; 49(11):5015-23. PubMed ID: 18487367
    [TBL] [Abstract][Full Text] [Related]  

  • 40. GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy.
    Sokal I; Li N; Surgucheva I; Warren MJ; Payne AM; Bhattacharya SS; Baehr W; Palczewski K
    Mol Cell; 1998 Jul; 2(1):129-33. PubMed ID: 9702199
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.