Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 95

1.

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. 2013 Oct 7. [Epub ahead of print]

PMID:
24099280
[PubMed - as supplied by publisher]
2.

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. doi: 10.1097/ICO.0b013e31815a50e7.

PMID:
18216574
[PubMed - indexed for MEDLINE]
3.

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. Epub 2011 Nov 30.

PMID:
22171159
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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. doi: 10.1159/000353297. Epub 2013 Oct 1.

PMID:
24107477
[PubMed - indexed for MEDLINE]
5.

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 Aug 1:1-3. [Epub ahead of print]

PMID:
25083577
[PubMed - as supplied by publisher]
6.

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. doi: 10.1097/ICO.0b013e3181aebf7a.

PMID:
20023586
[PubMed - indexed for MEDLINE]
7.

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. Epub 2011 Sep 24.

PMID:
21976959
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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. doi: 10.1080/13816810802008242.

PMID:
18484309
[PubMed - indexed for MEDLINE]
9.

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 4;13:1887-91.

PMID:
17960127
[PubMed - indexed for MEDLINE]
Free Article
10.

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.

PMID:
15623752
[PubMed - indexed for MEDLINE]
Free Article
11.

VSX1 gene and keratoconus: genetic analysis in Korean patients.

Jeoung JW, Kim MK, Park SS, Kim SY, Ko HS, Wee WR, Lee JH.

Cornea. 2012 Jul;31(7):746-50. doi: 10.1097/ICO.0b013e3181e16dd0.

PMID:
22531431
[PubMed - indexed for MEDLINE]
12.

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 18;6:103. doi: 10.1186/1756-0500-6-103.

PMID:
23506487
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
20664914
[PubMed - indexed for MEDLINE]
Free Article
14.

VSX1 gene analysis in keratoconus.

Tanwar M, Kumar M, Nayak B, Pathak D, Sharma N, Titiyal JS, Dada R.

Mol Vis. 2010 Nov 16;16:2395-401.

PMID:
21139977
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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 Apr 11;19:852-60. Print 2013.

PMID:
23592923
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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.

PMID:
16799019
[PubMed - indexed for MEDLINE]
Free Article
17.

SOD1: a candidate gene for keratoconus.

Udar N, Atilano SR, Brown DJ, Holguin B, Small K, Nesburn AB, Kenney MC.

Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3345-51.

PMID:
16877401
[PubMed - indexed for MEDLINE]
Free Article
18.

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. 2014 Jun 18:1-7. [Epub ahead of print]

PMID:
24940934
[PubMed - as supplied by publisher]
19.

VSX1 gene variants are associated with keratoconus in unrelated Korean patients.

Mok JW, Baek SJ, Joo CK.

J Hum Genet. 2008;53(9):842-9. doi: 10.1007/s10038-008-0319-6. Epub 2008 Jul 15.

PMID:
18626569
[PubMed - indexed for MEDLINE]
20.

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

Gajecka M, Radhakrishna U, Winters D, Nath SK, Rydzanicz M, Ratnamala U, Ewing K, Molinari A, Pitarque JA, Lee K, Leal SM, Bejjani BA.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1531-9. doi: 10.1167/iovs.08-2173. Epub 2008 Nov 14.

PMID:
19011015
[PubMed - indexed for MEDLINE]
Free Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk