122 related articles for article (PubMed ID: 30574758)
1. Contributions of VSX1 gene to keratoconus.
Kalasidou G; Frydas I; Kozei A; Syrmakesi P; Loukovitis E; Sfakianakis K; Balidis M; Zachariadis Z; Tranos P; Kozeis N; Anogeianakis G
J Biol Regul Homeost Agents; 2018; 32(6):1515-1518. PubMed ID: 30574758
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Visual System Homeobox 1 (VSX1) Gene Analysis in Keratoconus: Design of Specific Primers and DNA Amplification Protocols for Accurate Molecular Characterization.
Ng JB; Poh RY; Lee KR; Subrayan V; Deva JP; Lau AY; Tan JA
Clin Lab; 2016 Sep; 62(9):1731-1737. PubMed ID: 28164597
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. VSX1 gene analysis in keratoconus.
Tanwar M; Kumar M; Nayak B; Pathak D; Sharma N; Titiyal JS; Dada R
Mol Vis; 2010 Nov; 16():2395-401. PubMed ID: 21139977
[TBL] [Abstract][Full Text] [Related]
14. A new perspective on the genetics of keratoconus: why have we not been more successful?
Valgaeren H; Koppen C; Van Camp G
Ophthalmic Genet; 2018 Apr; 39(2):158-174. PubMed ID: 29111844
[TBL] [Abstract][Full Text] [Related]
15. A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India.
Chakravarty M; Ponnam SPG; Bardoloi N; Kumar S; Saikia P
Eur J Ophthalmol; 2022 May; 32(3):1361-1369. PubMed ID: 35296157
[TBL] [Abstract][Full Text] [Related]
16. Novel visual system homeobox 1 gene mutations in Turkish patients with keratoconus.
Bardak H; Gunay M; Yildiz E; Bardak Y; Gunay B; Ozbas H; Bagci O
Genet Mol Res; 2016 Nov; 15(4):. PubMed ID: 27819732
[TBL] [Abstract][Full Text] [Related]
17. Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant.
Vincent AL; Jordan C; Sheck L; Niederer R; Patel DV; McGhee CN
Mol Vis; 2013; 19():852-60. PubMed ID: 23592923
[TBL] [Abstract][Full Text] [Related]
18. VSX1 gene variants are associated with keratoconus in unrelated Korean patients.
Mok JW; Baek SJ; Joo CK
J Hum Genet; 2008; 53(9):842-849. PubMed ID: 18626569
[TBL] [Abstract][Full Text] [Related]
19. Molecular analysis of the VSX1 gene in familial keratoconus.
Liskova P; Ebenezer ND; Hysi PG; Gwilliam R; El-Ashry MF; Moodaley LC; Hau S; Twa M; Tuft SJ; Bhatacharya SS
Mol Vis; 2007 Oct; 13():1887-91. PubMed ID: 17960127
[TBL] [Abstract][Full Text] [Related]
20. Analysis of the VSX1 gene in sporadic keratoconus patients from China.
Guan T; Wang X; Zheng LB; Wu HJ; Yao YF
BMC Ophthalmol; 2017 Sep; 17(1):173. PubMed ID: 28950846
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
