(Q52037698)

20 April 2018

title

Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment development. (English)

1 reference

20 April 2018

author

Philip Gage

series ordinal

2

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20 April 2018

author name string

Amanda L Evans

series ordinal

1

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20 April 2018

publication date

3 October 2005

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20 April 2018

published in

Human Molecular Genetics

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20 April 2018

volume

14

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20 April 2018

issue

22

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20 April 2018

page(s)

3347-3359

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20 April 2018

Risk of glaucoma in ocular hypertension with and without pseudoexfoliation

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21 January 2018

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21 January 2018

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21 January 2018

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Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

21 January 2018

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Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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NG2 proteoglycan is expressed exclusively by mural cells during vascular morphogenesis

21 January 2018

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Characterization of smooth muscle cell and pericyte differentiation in the rat retina in vivo.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Hedgehog signalling maintains the optic stalk-retinal interface through the regulation of Vax gene activity

21 January 2018

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Eye development: a view from the retina pigmented epithelium

21 January 2018

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Retinal pigmented epithelium determination requires the redundant activities of Pax2 and Pax6

21 January 2018

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Role of Mitf in differentiation and transdifferentiation of chicken pigmented epithelial cell

21 January 2018

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Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently.

21 January 2018

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OTX2 regulates expression of DOPAchrome tautomerase in human retinal pigment epithelium

21 January 2018

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Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma

21 January 2018

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Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts

21 January 2018

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A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

21 January 2018

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Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein

21 January 2018

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Recombinant angiopoietin-1 restores higher-order architecture of growing blood vessels in mice in the absence of mural cells.

21 January 2018

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The two PDGF receptors maintain conserved signaling in vivo despite divergent embryological functions

21 January 2018

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Bmp7 regulates branching morphogenesis of the lacrimal gland by promoting mesenchymal proliferation and condensation.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Stabilization of the retinal vascular network by reciprocal feedback between blood vessels and astrocytes.

21 January 2018

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Retinal vessel diameters and incident open-angle glaucoma and optic disc changes: the Rotterdam study

21 January 2018

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Retinal vessel diameter and open-angle glaucoma: the Blue Mountains Eye Study

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Mutations in SOX2 cause anophthalmia

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Heterozygous mutations of OTX2 cause severe ocular malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

The Rx homeobox gene is essential for vertebrate eye development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Six6 (Optx2) is a novel murine Six3-related homeobox gene that demarcates the presumptive pituitary/hypothalamic axis and the ventral optic stalk

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Coordinate expression of Fgf8, Otx2, Bmp4, and Shh in the rostral prosencephalon during development of the telencephalic and optic vesicles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

Role of the Lens in the Morphogenesis of the Iris and Cornea

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI365

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI365

1 reference

20 April 2018

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20 April 2018