BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

333 related articles for article (PubMed ID: 33257550)

  • 1. Inverse correlation between fatty acid transport protein 4 and vision in Leber congenital amaurosis associated with RPE65 mutation.
    Li S; Gordon WC; Bazan NG; Jin M
    Proc Natl Acad Sci U S A; 2020 Dec; 117(50):32114-32123. PubMed ID: 33257550
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pharmacological Amelioration of Cone Survival and Vision in a Mouse Model for Leber Congenital Amaurosis.
    Li S; Samardzija M; Yang Z; Grimm C; Jin M
    J Neurosci; 2016 May; 36(21):5808-19. PubMed ID: 27225770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ablation of fatty acid transport protein-4 enhances cone survival, M-cone vision, and synthesis of cone-tropic 9-
    Li S; Jin M
    J Neurosci; 2024 May; ():. PubMed ID: 38811164
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intraperitoneal chromophore injections delay early-onset and rapid retinal cone degeneration in a mouse model of Leber congenital amaurosis.
    Dai X; Jin X; Ye Q; Huang H; Duo L; Lu C; Bao J; Chen H
    Exp Eye Res; 2021 Nov; 212():108776. PubMed ID: 34582935
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fatty acid transport protein 4 (FATP4) prevents light-induced degeneration of cone and rod photoreceptors by inhibiting RPE65 isomerase.
    Li S; Lee J; Zhou Y; Gordon WC; Hill JM; Bazan NG; Miner JH; Jin M
    J Neurosci; 2013 Feb; 33(7):3178-89. PubMed ID: 23407971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis.
    Li X; Li W; Dai X; Kong F; Zheng Q; Zhou X; Lü F; Chang B; Rohrer B; Hauswirth WW; Qu J; Pang JJ
    Invest Ophthalmol Vis Sci; 2011 Jan; 52(1):7-15. PubMed ID: 21169527
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Protection of cone photoreceptor M-opsin degradation with 9-cis-β-carotene-rich alga Dunaliella bardawil in Rpe65(-/-) mouse retinal explant culture.
    Ozaki T; Nakazawa M; Kudo T; Hirano S; Suzuki K; Ishiguro S
    Curr Eye Res; 2014 Dec; 39(12):1221-31. PubMed ID: 25006880
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathophysilogical mechanism and treatment strategies for Leber congenital amaurosis.
    Fu Y; Zhang T
    Adv Exp Med Biol; 2014; 801():791-6. PubMed ID: 24664772
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Light prevents exogenous 11-cis retinal from maintaining cone photoreceptors in chromophore-deficient mice.
    Fan J; Crouch RK; Kono M
    Invest Ophthalmol Vis Sci; 2011 Apr; 52(5):2412-6. PubMed ID: 21228385
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ciliary neurotrophic factor (CNTF) protects retinal cone and rod photoreceptors by suppressing excessive formation of the visual pigments.
    Li S; Sato K; Gordon WC; Sendtner M; Bazan NG; Jin M
    J Biol Chem; 2018 Sep; 293(39):15256-15268. PubMed ID: 30115683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trafficking of membrane-associated proteins to cone photoreceptor outer segments requires the chromophore 11-cis-retinal.
    Zhang H; Fan J; Li S; Karan S; Rohrer B; Palczewski K; Frederick JM; Crouch RK; Baehr W
    J Neurosci; 2008 Apr; 28(15):4008-14. PubMed ID: 18400900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
    Zhang T; Zhang N; Baehr W; Fu Y
    Proc Natl Acad Sci U S A; 2011 May; 108(21):8879-84. PubMed ID: 21555576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impacts of deletion and ichthyosis prematurity syndrome-associated mutations in fatty acid transport protein 4 on the function of RPE65.
    Li S; Green JF; Jin M
    FEBS Lett; 2020 Feb; 594(3):540-552. PubMed ID: 31595490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration.
    Hamann S; Schorderet DF; Cottet S
    PLoS One; 2009 Aug; 4(8):e6616. PubMed ID: 19672311
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mouse model of human RPE65 P25L hypomorph resembles wild type under normal light rearing but is fully resistant to acute light damage.
    Li Y; Yu S; Duncan T; Li Y; Liu P; Gene E; Cortes-Pena Y; Qian H; Dong L; Redmond TM
    Hum Mol Genet; 2015 Aug; 24(15):4417-28. PubMed ID: 25972377
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis.
    Bemelmans AP; Kostic C; Crippa SV; Hauswirth WW; Lem J; Munier FL; Seeliger MW; Wenzel A; Arsenijevic Y
    PLoS Med; 2006 Oct; 3(10):e347. PubMed ID: 17032058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis.
    Fan J; Rohrer B; Frederick JM; Baehr W; Crouch RK
    Invest Ophthalmol Vis Sci; 2008 Jun; 49(6):2384-9. PubMed ID: 18296659
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of M-Opsin Prevents M Cone Degeneration in a Mouse Model of Leber Congenital Amaurosis.
    Xu H; Enemchukwu N; Zhong X; Zhang O; Fu Y
    Am J Pathol; 2020 May; 190(5):1059-1067. PubMed ID: 32084365
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Altered expression of retinal molecular markers in the canine RPE65 model of Leber congenital amaurosis.
    Hernández M; Pearce-Kelling SE; Rodriguez FD; Aguirre GD; Vecino E
    Invest Ophthalmol Vis Sci; 2010 Dec; 51(12):6793-802. PubMed ID: 20671290
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement.
    Cideciyan AV; Jacobson SG; Beltran WA; Sumaroka A; Swider M; Iwabe S; Roman AJ; Olivares MB; Schwartz SB; Komáromy AM; Hauswirth WW; Aguirre GD
    Proc Natl Acad Sci U S A; 2013 Feb; 110(6):E517-25. PubMed ID: 23341635
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.