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 *

176 related articles for article (PubMed ID: 23833072)

  • 1. Mutational analysis of MIR184 in sporadic keratoconus and myopia.
    Lechner J; Bae HA; Guduric-Fuchs J; Rice A; Govindarajan G; Siddiqui S; Abi Farraj L; Yip SP; Yap M; Das M; Souzeau E; Coster D; Mills RA; Lindsay R; Phillips T; Mitchell P; Ali M; Inglehearn CF; Sundaresan P; Craig JE; Simpson DA; Burdon KP; Willoughby CE
    Invest Ophthalmol Vis Sci; 2013 Aug; 54(8):5266-72. PubMed ID: 23833072
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia.
    Abu-Amero KK; Helwa I; Al-Muammar A; Strickland S; Hauser MA; Allingham RR; Liu Y
    Biomed Res Int; 2015; 2015():604508. PubMed ID: 26380287
    [TBL] [Abstract][Full Text] [Related]  

  • 3. C.57 C > T Mutation in MIR 184 is Responsible for Congenital Cataracts and Corneal Abnormalities in a Five-generation Family from Galicia, Spain.
    Bykhovskaya Y; Caiado Canedo AL; Wright KW; Rabinowitz YS
    Ophthalmic Genet; 2015; 36(3):244-7. PubMed ID: 24138095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutational Analysis of Pre-miR-184 and hsa-mir-568 in Greek Patients With Sporadic Keratoconus.
    Moschos MM; Droutsas K; Sioziou A; Dettoraki M; Gazouli M
    Cornea; 2016 May; 35(5):631-3. PubMed ID: 26845316
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
    Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
    Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Independent origin of c.57 C > T mutation in MIR184 associated with inherited corneal and lens abnormalities.
    Bykhovskaya Y; Seldin MF; Liu Y; Ransom M; Li X; Rabinowitz YS
    Ophthalmic Genet; 2015 Mar; 36(1):95-7. PubMed ID: 25373792
    [No Abstract]   [Full Text] [Related]  

  • 7. Mutation altering the miR-184 seed region causes familial keratoconus with cataract.
    Hughes AE; Bradley DT; Campbell M; Lechner J; Dash DP; Simpson DA; Willoughby CE
    Am J Hum Genet; 2011 Nov; 89(5):628-33. PubMed ID: 21996275
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
    Iliff BW; Riazuddin SA; Gottsch JD
    Invest Ophthalmol Vis Sci; 2012 Jan; 53(1):348-53. PubMed ID: 22131394
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.
    Du X; Chen P; Sun D
    Graefes Arch Clin Exp Ophthalmol; 2017 Sep; 255(9):1779-1786. PubMed ID: 28567551
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of seven novel
    Yu X; Chen B; Zhang X; Shentu X
    Mol Vis; 2017; 23():296-305. PubMed ID: 28484309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Are miRNAs Dynamic Biomarkers in Keratoconus? A Review of the Literature.
    Stunf Pukl S
    Genes (Basel); 2022 Mar; 13(4):. PubMed ID: 35456395
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ophthalmic findings in patients with arterial tortuosity syndrome and carriers: A case series.
    Hardin JS; Zarate YA; Callewaert B; Phillips PH; Warner DB
    Ophthalmic Genet; 2018; 39(1):29-34. PubMed ID: 28726533
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.
    Jiang D; Li J; Xiao X; Li S; Jia X; Sun W; Guo X; Zhang Q
    Invest Ophthalmol Vis Sci; 2014 Dec; 56(1):339-45. PubMed ID: 25525168
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for MIR184 Mutations in Iranian Patients with Keratoconus.
    Farzadfard A; Nassiri N; Moghadam TN; Paylakhi SH; Elahi E
    J Ophthalmic Vis Res; 2016; 11(1):3-7. PubMed ID: 27195078
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus.
    Davidson AE; Borasio E; Liskova P; Khan AO; Hassan H; Cheetham ME; Plagnol V; Alkuraya FS; Tuft SJ; Hardcastle AJ
    Invest Ophthalmol Vis Sci; 2015 Jan; 56(1):578-86. PubMed ID: 25564447
    [TBL] [Abstract][Full Text] [Related]  

  • 16. VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.
    Bisceglia L; Ciaschetti M; De Bonis P; Campo PA; Pizzicoli C; Scala C; Grifa M; Ciavarella P; Delle Noci N; Vaira F; Macaluso C; Zelante L
    Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):39-45. PubMed ID: 15623752
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Documenting the corneal phenotype associated with the MIR184 c.57C>T mutation.
    Iliff BW; Riazuddin SA; Gottsch JD
    Am J Hum Genet; 2012 May; 90(5):934; author reply 934-5. PubMed ID: 22560093
    [No Abstract]   [Full Text] [Related]  

  • 18. TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.
    Bykhovskaya Y; Fardaei M; Khaled ML; Nejabat M; Salouti R; Dastsooz H; Liu Y; Inaloo S; Rabinowitz YS
    Invest Ophthalmol Vis Sci; 2017 Dec; 58(14):6462-6469. PubMed ID: 29261847
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNA-Seq analysis and comparison of corneal epithelium in keratoconus and myopia patients.
    You J; Corley SM; Wen L; Hodge C; Höllhumer R; Madigan MC; Wilkins MR; Sutton G
    Sci Rep; 2018 Jan; 8(1):389. PubMed ID: 29321650
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcriptome-wide Investigation of mRNA/circRNA in miR-184 and Its r.57c > u Mutant Type Treatment of Human Lens Epithelial Cells.
    Luo Y; Liu S; Yao K
    Mol Ther Nucleic Acids; 2017 Jun; 7():71-80. PubMed ID: 28624226
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.