(Q28941244)

14 March 2017

title

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation (English)

1 reference

14 March 2017

0 references

1 reference

GOA release 2020-03-11

8

William B. Dobyns

1 reference

14 March 2017

9

Kathleen J. Millen

1 reference

14 March 2017

3

Louanne Hudgins

1 reference

14 March 2017

Kimberly A. Aldinger

1

1 reference

14 March 2017

Ordan J. Lehmann

2

1 reference

14 March 2017

Victor V. Chizhikov

4

1 reference

14 March 2017

Alexander G. Bassuk

5

1 reference

14 March 2017

Lesley C. Ades

6

1 reference

14 March 2017

Ian D. Krantz

7

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14 March 2017

language of work or name

English

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publication date

1 September 2009

1 reference

14 March 2017

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14 March 2017

volume

41

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14 March 2017

issue

9

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14 March 2017

page(s)

1037–1042

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Cerebellar development and disease

14 March 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

A novel role for the choroid plexus in BMP-mediated inhibition of differentiation of cerebellar neural progenitors

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Impaired B-lymphopoiesis, myelopoiesis, and derailed cerebellar neuron migration in CXCR4- and SDF-1-deficient mice

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Forkhead transcription factors regulate expression of the chemokine receptor CXCR4 in endothelial cells and CXCL12-induced cell migration

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

The dual specificity JKAP specifically activates the c-Jun N-terminal kinase pathway

23 March 2017

1 reference

Identification and characterization of a paralog of human cell cycle checkpoint gene HUS1

22 April 2017

1 reference

Control of roof plate formation by Lmx1a in the developing spinal cord

22 April 2017

1 reference

Neuronal patterning by BMPs: a requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord

22 April 2017

1 reference

Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex

22 April 2017

1 reference

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Foxc transcription factors directly regulate Dll4 and Hey2 expression by interacting with the VEGF-Notch signaling pathways in endothelial cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Identification of Tgf beta1i4 as a downstream target of Foxc1.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Transcription factors in glutamatergic neurogenesis: conserved programs in neocortex, cerebellum, and adult hippocampus

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Human malformations of the midbrain and hindbrain: review and proposed classification scheme

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Fox's in development and disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Analysis and classification of cerebellar malformations.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Math1 is essential for genesis of cerebellar granule neurons

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2843139

Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.

3 June 2018

1 reference

Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals.

21 January 2018

1 reference

Terminal deletion of 6p results in a recognizable phenotype.

21 January 2018

1 reference

The roof plate regulates cerebellar cell-type specification and proliferation

21 January 2018

1 reference

21 January 2018

1 reference

Generation of cerebellar granule neurons in vivo by transplantation of BMP-treated neural progenitor cells

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic analyses demonstrate that bone morphogenetic protein signaling is required for embryonic cerebellar development.

21 January 2018

1 reference

Effect of local environment on molecular conduction: isolated molecule versus self-assembled monolayer

21 January 2018

1 reference

Control of roof plate development and signaling by Lmx1b in the caudal vertebrate CNS.

21 January 2018

1 reference

Forkhead transcription factor Foxf2 (LUN)-deficient mice exhibit abnormal development of secondary palate.

21 January 2018

1 reference

Sequential actions of BMP receptors control neural precursor cell production and fate

21 January 2018

1 reference

Differences in the embryonic expression patterns of mouse Foxf1 and -2 match their distinct mutant phenotypes

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/19668217

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mouse brain organization revealed through direct genome-scale TF expression analysis

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Requirement for the transcription factor LSIRF/IRF4 for mature B and T lymphocyte function

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.422

1 reference

Dimensions Publication ID

1030356828

0 references

1 reference

1 reference

1 reference