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PAX6 does not regulate Nfia and Nfib expression during neocortical development.
scientific article published on 29 May 2015
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PMC publication ID
4448127
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
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15 February 2020
title
PAX6 does not regulate Nfia and Nfib expression during neocortical development
(English)
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Europe PubMed Central
PMC publication ID
4448127
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
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15 February 2020
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Jens Bunt
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1
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Europe PubMed Central
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4448127
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15 February 2020
Jonathan W C Lim
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2
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Europe PubMed Central
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4448127
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
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15 February 2020
Linda Richards
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5
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4448127
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15 February 2020
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Lu Zhao
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3
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15 February 2020
Sharon Mason
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15 February 2020
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29 May 2015
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15 February 2020
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Scientific Reports
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15 February 2020
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15 February 2020
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15 February 2020
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29 May 2015
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Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome
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Multiple non-cell-autonomous defects underlie neocortical callosal dysgenesis in Nfib-deficient mice
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The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis
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The transcription factor Nfix is essential for normal brain development
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Loss- and gain-of-function analyses reveal targets of Pax6 in the developing mouse telencephalon.
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Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum
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Pax6 controls radial glia differentiation in the cerebral cortex
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Forebrain patterning defects in Small eye mutant mice.
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27 July 2018
Pax-6, a murine paired box gene, is expressed in the developing CNS
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Mouse small eye results from mutations in a paired-like homeobox-containing gene
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Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature
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25 September 2018
The BAF complex interacts with Pax6 in adult neural progenitors to establish a neurogenic cross-regulatory transcriptional network.
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PubMed Central
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25 September 2018
Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia
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25 September 2018
Cellular retinaldehyde-binding protein (CRALBP) is a direct downstream target of transcription factor Pax6.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
NFIA controls telencephalic progenitor cell differentiation through repression of the Notch effector Hes1.
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25 September 2018
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
Specific glial populations regulate hippocampal morphogenesis.
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25 September 2018
Nuclear factor I gene expression in the developing forebrain.
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PubMed Central
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25 September 2018
Tlx and Pax6 co-operate genetically to establish the pallio-subpallial boundary in the embryonic mouse telencephalon
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
Pax6 is required for the normal development of the forebrain axonal connections.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
Novel ENU-induced eye mutations in the mouse: models for human eye disease
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PubMed Central
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25 September 2018
Pax6 is required to regulate the cell cycle and the rate of progression from symmetrical to asymmetrical division in mammalian cortical progenitors.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448127
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25 September 2018
Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2.
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25 September 2018
Roles of Pax-genes in developing and adult brain as suggested by expression patterns.
1 reference
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25 September 2018
Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia
1 reference
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https://pubmed.ncbi.nlm.nih.gov/26021864
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12 December 2020
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The effect of dose fractionation on the frequency of ethylnitrosourea-induced dominant cataract and recessive specific locus mutations in germ cells of the mouse
1 reference
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https://pubmed.ncbi.nlm.nih.gov/26021864
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12 December 2020
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Lens morphogenesis is dependent on Pax6-mediated inhibition of the canonical Wnt/beta-catenin signaling in the lens surface ectoderm
1 reference
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https://pubmed.ncbi.nlm.nih.gov/26021864
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12 December 2020
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Identifiers
DOI
10.1038/SREP10668
1 reference
stated in
Europe PubMed Central
PMC publication ID
4448127
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 February 2020
PMC publication ID
4448127
1 reference
stated in
Europe PubMed Central
PMC publication ID
4448127
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 February 2020
PubMed publication ID
26021864
1 reference
stated in
Europe PubMed Central
PMC publication ID
4448127
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021864%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 February 2020
ResearchGate publication ID
277406651
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