Molecular links among the causative genes for ocular malformation: Otx2 and Sox2 coregulate Rax expression (Q36535426)

14 August 2017

Molecular links among the causative genes for ocular malformation: Otx2 and Sox2 coregulate Rax expression (English)

1 reference

14 August 2017

Keisuke Hitachi

3

0 references

Makoto Asashima

object named as

Makoto Asashima

6

0 references

author name string

Hiroki Danno

1

1 reference

14 August 2017

Tatsuo Michiue

2

1 reference

14 August 2017

Akira Yukita

4

1 reference

14 August 2017

Shoichi Ishiura

5

1 reference

14 August 2017

language of work or name

English

0 references

publication date

2 April 2008

1 reference

14 August 2017

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

14 August 2017

105

1 reference

14 August 2017

14

1 reference

14 August 2017

5408-5413

1 reference

Molecular mechanisms of optic vesicle development: complexities, ambiguities and controversies

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Elevating the levels of Sox2 in embryonal carcinoma cells and embryonic stem cells inhibits the expression of Sox2:Oct-3/4 target genes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

SOX2 is a dose-dependent regulator of retinal neural progenitor competence

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Heterozygous mutations of OTX2 cause severe ocular malformations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

VISTA: computational tools for comparative genomics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Xrx1 controls proliferation and neurogenesis in Xenopus anterior neural plate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Crystal structure of a POU/HMG/DNA ternary complex suggests differential assembly of Oct4 and Sox2 on two enhancers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

OTX2 activates the molecular network underlying retina pigment epithelium differentiation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Mutations in SOX2 cause anophthalmia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Xenopus tropicalis transgenic lines and their use in the study of embryonic induction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Immunoprecipitation techniques for the analysis of transcription factor complexes.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Pax6 and SOX2 form a co-DNA-binding partner complex that regulates initiation of lens development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

The role of Otx2 in organizing the anterior patterning in mouse

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

EMBOSS: the European Molecular Biology Open Software Suite

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Both PCE-1/RX and OTX/CRX interactions are necessary for photoreceptor-specific gene expression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Drosophila Goosecoid requires a conserved heptapeptide for repression of paired-class homeoprotein activators.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Sequential roles for Otx2 in visceral endoderm and neuroectoderm for forebrain and midbrain induction and specification.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

The Rx homeobox gene is essential for vertebrate eye development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Homeodomain-DNA recognition

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

From fly head to mammalian forebrain: the story of otd and Otx.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

Nucleosome regulator Xhmgb3 is required for cell proliferation of the eye and brain as a downstream target of Xenopus rax/Rx1.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2291098

SOX2 anophthalmia syndrome.

28 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

Targeted expression of the dominant-negative FGFR4a in the eye using Xrx1A regulatory sequences interferes with normal retinal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

FusionDB: a database for in-depth analysis of prokaryotic gene fusion events

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

Involvement of Pax6 and Otx2 in the forebrain-specific regulation of the vertebrate homeobox gene ANF/Hesx1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

Functional analysis of chicken Sox2 enhancers highlights an array of diverse regulatory elements that are conserved in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

XIdax, an inhibitor of the canonical Wnt pathway, is required for anterior neural structure formation in Xenopus

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

Recurrence ofSOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0710954105

The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18385377

12 December 2020

inferred from PubMed ID database lookup

PAX6 and SOX2-dependent regulation of the Sox2 enhancer N-3 involved in embryonic visual system development

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18385377

12 December 2020

inferred from PubMed ID database lookup

Requirement of Sox2-mediated signaling for differentiation of early Xenopus neuroectoderm

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18385377

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.0710954105

1 reference

14 August 2017

0 references

1 reference

14 August 2017

1 reference