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 *

191 related articles for article (PubMed ID: 29170418)

  • 1. Gene Therapy Restores Mfrp and Corrects Axial Eye Length.
    Velez G; Tsang SH; Tsai YT; Hsu CW; Gore A; Abdelhakim AH; Mahajan M; Silverman RH; Sparrow JR; Bassuk AG; Mahajan VB
    Sci Rep; 2017 Nov; 7(1):16151. PubMed ID: 29170418
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene therapy in the rd6 mouse model of retinal degeneration.
    Dinculescu A; Min SH; Deng WT; Li Q; Hauswirth WW
    Adv Exp Med Biol; 2014; 801():711-8. PubMed ID: 24664762
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene therapy in patient-specific stem cell lines and a preclinical model of retinitis pigmentosa with membrane frizzled-related protein defects.
    Li Y; Wu WH; Hsu CW; Nguyen HV; Tsai YT; Chan L; Nagasaki T; Maumenee IH; Yannuzzi LA; Hoang QV; Hua H; Egli D; Tsang SH
    Mol Ther; 2014 Sep; 22(9):1688-97. PubMed ID: 24895994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human
    Chekuri A; Sahu B; Chavali VRM; Voronchikhina M; Soto-Hermida A; Suk JJ; Alapati AN; Bartsch DU; Ayala-Ramirez R; Zenteno JC; Dinculescu A; Jablonski MM; Borooah S; Ayyagari R
    Hum Gene Ther; 2019 May; 30(5):632-650. PubMed ID: 30499344
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 174delG mutation in mouse MFRP causes photoreceptor degeneration and RPE atrophy.
    Fogerty J; Besharse JC
    Invest Ophthalmol Vis Sci; 2011 Sep; 52(10):7256-66. PubMed ID: 21810984
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of Zebrafish Mfrp Causes Nanophthalmia, Hyperopia, and Accumulation of Subretinal Macrophages.
    Collery RF; Volberding PJ; Bostrom JR; Link BA; Besharse JC
    Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6805-6814. PubMed ID: 28002843
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis.
    Won J; Charette JR; Philip VM; Stearns TM; Zhang W; Naggert JK; Krebs MP; Nishina PM
    Exp Eye Res; 2014 Jan; 118():30-5. PubMed ID: 24200520
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spatial and temporal expression of MFRP and its interaction with CTRP5.
    Mandal MN; Vasireddy V; Jablonski MM; Wang X; Heckenlively JR; Hughes BA; Reddy GB; Ayyagari R
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5514-21. PubMed ID: 17122143
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6.
    Kameya S; Hawes NL; Chang B; Heckenlively JR; Naggert JK; Nishina PM
    Hum Mol Genet; 2002 Aug; 11(16):1879-86. PubMed ID: 12140190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept.
    Dinculescu A; Estreicher J; Zenteno JC; Aleman TS; Schwartz SB; Huang WC; Roman AJ; Sumaroka A; Li Q; Deng WT; Min SH; Chiodo VA; Neeley A; Liu X; Shu X; Matias-Florentino M; Buentello-Volante B; Boye SL; Cideciyan AV; Hauswirth WW; Jacobson SG
    Hum Gene Ther; 2012 Apr; 23(4):367-76. PubMed ID: 22142163
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation.
    Koli S; Labelle-Dumais C; Zhao Y; Paylakhi S; Nair KS
    PLoS Genet; 2021 Mar; 17(3):e1009458. PubMed ID: 33755662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic Interaction between
    Gogna N; Weatherly S; Zhao F; Collin GB; Pinkney J; Stone L; Naggert JK; Carter GW; Nishina PM
    Int J Mol Sci; 2022 Jan; 23(3):. PubMed ID: 35163536
    [No Abstract]   [Full Text] [Related]  

  • 13. Developmental basis of nanophthalmos: MFRP Is required for both prenatal ocular growth and postnatal emmetropization.
    Sundin OH; Dharmaraj S; Bhutto IA; Hasegawa T; McLeod DS; Merges CA; Silval ED; Maumenee IH; Lutty GA
    Ophthalmic Genet; 2008 Mar; 29(1):1-9. PubMed ID: 18363166
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ADIPOR1 is essential for vision and its RPE expression is lost in the Mfrp
    Sluch VM; Banks A; Li H; Crowley MA; Davis V; Xiang C; Yang J; Demirs JT; Vrouvlianis J; Leehy B; Hanks S; Hyman AM; Aranda J; Chang B; Bigelow CE; Rice DS
    Sci Rep; 2018 Sep; 8(1):14339. PubMed ID: 30254279
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.
    Garnai SJ; Brinkmeier ML; Emery B; Aleman TS; Pyle LC; Veleva-Rotse B; Sisk RA; Rozsa FW; Ozel AB; Li JZ; Moroi SE; Archer SM; Lin CM; Sheskey S; Wiinikka-Buesser L; Eadie J; Urquhart JE; Black GCM; Othman MI; Boehnke M; Sullivan SA; Skuta GL; Pawar HS; Katz AE; Huryn LA; Hufnagel RB; ; Camper SA; Richards JE; Prasov L
    PLoS Genet; 2019 May; 15(5):e1008130. PubMed ID: 31048900
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments.
    Won J; Smith RS; Peachey NS; Wu J; Hicks WL; Naggert JK; Nishina PM
    Vis Neurosci; 2008; 25(4):563-74. PubMed ID: 18764959
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia.
    Metlapally R; Li YJ; Tran-Viet KN; Bulusu A; White TR; Ellis J; Kao D; Young TL
    Mol Vis; 2008 Mar; 14():387-93. PubMed ID: 18334955
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ablation of mpeg+ Macrophages Exacerbates mfrp-Related Hyperopia.
    Brandt ZJ; Collery RF; Besharse JC; Link BA
    Invest Ophthalmol Vis Sci; 2021 Dec; 62(15):13. PubMed ID: 34913948
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of MFRP Mutations in Chinese Families with High Hyperopia.
    Xu Y; Guan L; Xiao X; Zhang J; Li S; Jiang H; Jia X; Yin Y; Guo X; Yang Z; Zhang Q
    Optom Vis Sci; 2016 Jan; 93(1):19-26. PubMed ID: 26583794
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.
    Sundin OH; Leppert GS; Silva ED; Yang JM; Dharmaraj S; Maumenee IH; Santos LC; Parsa CF; Traboulsi EI; Broman KW; Dibernardo C; Sunness JS; Toy J; Weinberg EM
    Proc Natl Acad Sci U S A; 2005 Jul; 102(27):9553-8. PubMed ID: 15976030
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.