BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 20664914)

  • 1. Genetics and clinical characteristics of keratoconus.
    Stabuc-Silih M; Strazisar M; Ravnik-Glavac M; Hawlina M; Glavac D
    Acta Dermatovenerol Alp Pannonica Adriat; 2010; 19(2):3-10. PubMed ID: 20664914
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.
    Stabuc-Silih M; Strazisar M; Hawlina M; Glavac D
    Cornea; 2010 Feb; 29(2):172-6. PubMed ID: 20023586
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus.
    Stabuc-Silih M; Ravnik-Glavac M; Glavac D; Hawlina M; Strazisar M
    Mol Vis; 2009 Dec; 15():2848-60. PubMed ID: 20029656
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphism analysis of COL4A3 and COL4A4 genes in Greek patients with keratoconus.
    Kokolakis NS; Gazouli M; Chatziralli IP; Koutsandrea C; Gatzioufas Z; Peponis VG; Droutsas KD; Kalogeropoulos C; Anagnou N; Miltsakakis D; Moschos MM
    Ophthalmic Genet; 2014 Dec; 35(4):226-8. PubMed ID: 25083577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus.
    Moschos MM; Kokolakis N; Gazouli M; Chatziralli IP; Droutsas D; Anagnou NP; Ladas ID
    Ophthalmic Genet; 2015; 36(3):213-7. PubMed ID: 24099280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absence of significant genetic alterations in the
    Lopes AG; de Almeida GC; Miola MP; Teixeira RM; Pires FCBL; Miani RA; de Mattos LC; Brandão CC; Castiglioni L
    Ophthalmic Genet; 2022 Feb; 43(1):73-79. PubMed ID: 34802378
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Correlation between the COL4A3, MMP-9, and TIMP-1 polymorphisms and risk of keratoconus.
    Saravani R; Yari D; Saravani S; Hasanian-Langroudi F
    Jpn J Ophthalmol; 2017 May; 61(3):218-222. PubMed ID: 28197741
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.
    De Bonis P; Laborante A; Pizzicoli C; Stallone R; Barbano R; Longo C; Mazzilli E; Zelante L; Bisceglia L
    Mol Vis; 2011; 17():2482-94. PubMed ID: 21976959
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No VSX1 gene mutations associated with keratoconus.
    Aldave AJ; Yellore VS; Salem AK; Yoo GL; Rayner SA; Yang H; Tang GY; Piconell Y; Rabinowitz YS
    Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):2820-2. PubMed ID: 16799019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.
    Saee-Rad S; Hashemi H; Miraftab M; Noori-Daloii MR; Chaleshtori MH; Raoofian R; Jafari F; Greene W; Fakhraie G; Rezvan F; Heidari M
    Mol Vis; 2011; 17():3128-36. PubMed ID: 22171159
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The D144E substitution in the VSX1 gene: a non-pathogenic variant or a disease causing mutation?
    Eran P; Almogit A; David Z; Wolf HR; Hana G; Yaniv B; Elon P; Isaac A
    Ophthalmic Genet; 2008 Jun; 29(2):53-9. PubMed ID: 18484309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.
    Dehkordi FA; Rashki A; Bagheri N; Chaleshtori MH; Memarzadeh E; Salehi A; Ghatreh H; Zandi F; Yazdanpanahi N; Tabatabaiefar MA; Chaleshtori MH
    Acta Cytol; 2013; 57(6):646-51. PubMed ID: 24107477
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India.
    Shetty R; Nuijts RM; Nanaiah SG; Anandula VR; Ghosh A; Jayadev C; Pahuja N; Kumaramanickavel G; Nallathambi J
    BMC Med Genet; 2015 May; 16():33. PubMed ID: 25963163
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.
    Karolak JA; Polakowski P; Szaflik J; Szaflik JP; Gajecka M
    Ophthalmic Genet; 2016; 37(1):37-43. PubMed ID: 24940934
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of possible relationship between COL4A4 gene polymorphisms and risk of keratoconus.
    Saravani R; Hasanian-Langroudi F; Validad MH; Yari D; Bahari G; Faramarzi M; Khateri M; Bahadoram S
    Cornea; 2015 Mar; 34(3):318-22. PubMed ID: 25651396
    [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. Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
    Verma A; Das M; Srinivasan M; Prajna NV; Sundaresan P
    BMC Res Notes; 2013 Mar; 6():103. PubMed ID: 23506487
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Common single nucleotide polymorphisms and keratoconus in the Han Chinese population.
    Wang Y; Jin T; Zhang X; Wei W; Cui Y; Geng T; Liu Q; Gao J; Liu M; Chen C; Zhang C; Zhu X
    Ophthalmic Genet; 2013 Sep; 34(3):160-6. PubMed ID: 23289806
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus.
    Tang YG; Picornell Y; Su X; Li X; Yang H; Rabinowitz YS
    Cornea; 2008 Feb; 27(2):189-92. PubMed ID: 18216574
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of the SOD1 Gene in Keratoconus Patients from Saudi Arabia.
    Al-Muammar AM; Kalantan H; Azad TA; Sultan T; Abu-Amero KK
    Ophthalmic Genet; 2015; 36(4):373-5. PubMed ID: 24547927
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.