(Q35956918)

English

Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development

scholarly article

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scholarly article

1 reference

Europe PubMed Central

11 August 2017

Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development (English)

1 reference

Europe PubMed Central

11 August 2017

Julie A Siegenthaler

2

object named as

Julie A Siegenthaler

1 reference

Europe PubMed Central

11 August 2017

author name string

Konstantinos Zarbalis

1

1 reference

Europe PubMed Central

11 August 2017

Youngshik Choe

3

1 reference

Europe PubMed Central

11 August 2017

Scott R May

4

1 reference

Europe PubMed Central

11 August 2017

Andrew S Peterson

5

1 reference

Europe PubMed Central

11 August 2017

Samuel J Pleasure

6

1 reference

Europe PubMed Central

11 August 2017

language of work or name

0 references

publication date

21 August 2007

1 reference

Europe PubMed Central

11 August 2017

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

1 reference

Europe PubMed Central

11 August 2017

104

1 reference

Europe PubMed Central

11 August 2017

14002-14007

1 reference

Europe PubMed Central

11 August 2017

35

1 reference

Europe PubMed Central

11 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1955817/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Cortical dysplasia: neuropathological aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Regulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascade

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

The forkhead genes, Foxc1 and Foxc2, regulate paraxial versus intermediate mesoderm cell fate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Cell migration in the forebrain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Smooth, rough and upside-down neocortical development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Differential expression of multiple fork head related genes during gastrulation and axial pattern formation in the mouse embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

2 October 2017

Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

27 July 2018

Developmental morphology of the subarachnoid space and contiguous structures in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

27 July 2018

Foxc1 integrates Fgf and Bmp signalling independently of twist or noggin during calvarial bone development.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Schizophrenia in an adult with 6p25 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Tissue origins and interactions in the mammalian skull vault

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Meningeal cells organize the superficial glia limitans of the cerebellum and produce components of both the interstitial matrix and the basement membrane.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

The mechanism of drainage of the cerebrospinal fluid.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Beyond laminar fate: toward a molecular classification of cortical projection/pyramidal neurons

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

Breaches of the pial basement membrane and disappearance of the glia limitans during development underlie the cortical lamination defect in the mouse model of muscle-eye-brain disease.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0702618104

21 January 2018

A critical function of the pial basement membrane in cortical histogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

24 September 2018

Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955817

24 September 2018

Neovascularization and the appearance of morphological characteristics of the blood-brain barrier in the embryonic mouse central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/17715063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression domains of murine ephrin-A5 in the pituitary and hypothalamus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17715063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/17715063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0702618104

1 reference

Europe PubMed Central

11 August 2017

2007PNAS..10414002Z

0 references

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

ResearchGate publication ID

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