(Q35606654)

9 August 2017

title

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus (English)

1 reference

9 August 2017

Samira Saee-Rad

1 reference

9 August 2017

Hassan Hashemi

1 reference

9 August 2017

Mohammad Miraftab

1 reference

9 August 2017

Mohammad Reza Noori-Daloii

1 reference

9 August 2017

Morteza Hashemzadeh Chaleshtori

1 reference

9 August 2017

Reza Raoofian

1 reference

9 August 2017

Fatemeh Jafari

1 reference

9 August 2017

Wayne Greene

1 reference

9 August 2017

Ghasem Fakhraie

1 reference

9 August 2017

Farhad Rezvan

1 reference

9 August 2017

Mansour Heidari

1 reference

9 August 2017

publication date

30 November 2011

1 reference

9 August 2017

1 reference

9 August 2017

1 reference

9 August 2017

page(s)

3128-3136

1 reference

Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

VSX1 gene analysis in keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

12 July 2018

Keratoconus: a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

A novel VSX1 mutation identified in an individual with keratoconus in India

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

SOD1 haplotypes in familial keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Identification of novel p53 target genes by cDNA AFLP in glioblastoma cells.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

SOD1: a candidate gene for keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

No VSX1 gene mutations associated with keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

MONGOLISM (DOWN'S SYNDROME) AND KERATOCONUS.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Does ethnic origin influence the incidence or severity of keratoconus?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Genetic epidemiological study of keratoconus: evidence for major gene determination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Mutational screening of VSX1 in keratoconus patients from the European population.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Identification of a new locus for isolated familial keratoconus at 2p24.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Keratokonus: Epidemiologie, Risikofaktoren und Diagnostik

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3235532

Fine mapping of the keratoconus with cataract locus on chromosome 15q and candidate gene analysis

7 December 2018

1 reference

12 December 2020

A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families

1 reference

12 December 2020

The genetics of keratoconus

1 reference

12 December 2020

Detection of specific collagen types in normal and keratoconus corneas

1 reference

12 December 2020

Linkage of posterior polymorphous corneal dystrophy to 20q11

1 reference

12 December 2020

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

1 reference

12 December 2020

Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asian and white patients

1 reference

12 December 2020

Identifiers

PMC publication ID

3235532

1 reference

9 August 2017

1 reference