Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis (Q24302555)

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English	Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis	scientific article

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Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis (English)

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Forkhead box C1

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GOA release 2020-03-11

positive regulation of transcription by RNA polymerase II

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GOA release 2020-03-11

Axenfeld-Rieger syndrome

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based on heuristic

inferred from title

6

object named as

Philip J Gage

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4

object named as

Tim Footz

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author name string

Fred B Berry

1

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Matthew A Lines

2

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J Martin Oas

3

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D Alan Underhill

5

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Michael A Walter

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language of work or name

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publication date

15 March 2006

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Human Molecular Genetics

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15

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6

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905-19

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Axenfeld-Rieger syndrome in the age of molecular genetics

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Molecular genetics of Axenfeld-Rieger malformations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Evidence that Rieger syndrome maps to 4q25 or 4q27

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Rieger's anomaly and glaucoma associated with partial trisomy 16q. Case report.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Differential regulation of gene expression by PITX2 isoforms

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Identification of a dominant negative homeodomain mutation in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Forkhead transcription factors: key players in development and metabolism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Fox's in development and disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Mouse Otlx2/RIEG expression in the odontogenic epithelium precedes tooth initiation and requires mesenchyme-derived signals for its maintenance.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Joint regulation of the MAP1B promoter by HNF3beta/Foxa2 and Engrailed is the result of a highly conserved mechanism for direct interaction of homeoproteins and Fox transcription factors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

PITX genes are required for cell survival and Lhx3 activation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

Retinoic acid-dependent eye morphogenesis is orchestrated by neural crest cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL008

21 January 2018

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