Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice. (Q40238247)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20424327%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice (English)

1 reference

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1 February 2020

1 reference

1 reference

9

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1 February 2020

author name string

Helen A Thomason

1

1 reference

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1 February 2020

Huiqing Zhou

2

1 reference

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1 February 2020

Evelyn N Kouwenhoven

3

1 reference

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1 February 2020

Gian-Paolo Dotto

4

1 reference

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1 February 2020

Gaia Restivo

5

1 reference

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1 February 2020

Bach-Cuc Nguyen

6

1 reference

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1 February 2020

Hayley Little

7

1 reference

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1 February 2020

Michael J Dixon

8

1 reference

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1 February 2020

Jill Dixon

10

1 reference

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1 February 2020

language of work or name

English

0 references

publication date

26 April 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20424327%20AND%20SRC:MED&resulttype=core&format=json

Journal of Clinical Investigation

1 February 2020

published in

1 reference

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1 February 2020

volume

120

1 reference

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1 February 2020

issue

5

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1 February 2020

page(s)

1561-1569

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A regulatory feedback loop involving p63 and IRF6 links the pathogenesis of 2 genetically different human ectodermal dysplasias

1 February 2020

cites work

1 reference

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An active role of the DeltaN isoform of p63 in regulating basal keratin genes K5 and K14 and directing epidermal cell fate

22 September 2017

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Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence.

22 September 2017

1 reference

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The alpha/beta carboxy-terminal domains of p63 are required for skin and limb development. New insights from the Brdm2 mouse which is not a complete p63 knockout but expresses p63 gamma-like proteins

22 September 2017

1 reference

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Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

22 September 2017

1 reference

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ChIP-seq accurately predicts tissue-specific activity of enhancers

22 September 2017

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The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models

22 September 2017

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Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

22 September 2017

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Genome-wide profiling of PPARgamma:RXR and RNA polymerase II occupancy reveals temporal activation of distinct metabolic pathways and changes in RXR dimer composition during adipogenesis

22 September 2017

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Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

22 September 2017

1 reference

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Model-based analysis of ChIP-Seq (MACS)

22 September 2017

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Characterization of genome-wide p53-binding sites upon stress response.

22 September 2017

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TFAP2A mutations result in branchio-oculo-facial syndrome

22 September 2017

1 reference

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A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes.

22 September 2017

1 reference

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Interferon regulatory factor 6 promotes cell cycle arrest and is regulated by the proteasome in a cell cycle-dependent manner

22 September 2017

1 reference

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Mouse genetic models of cleft lip with or without cleft palate

22 September 2017

1 reference

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Identification of novel functional TBP-binding sites and general factor repertoires

22 September 2017

1 reference

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Relationships between p63 binding, DNA sequence, transcription activity, and biological function in human cells

22 September 2017

1 reference

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Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch

22 September 2017

1 reference

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Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

22 September 2017

1 reference

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Molecular control of secondary palate development

22 September 2017

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Cross-regulation between Notch and p63 in keratinocyte commitment to differentiation

22 September 2017

1 reference

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p63 regulates multiple signalling pathways required for ectodermal organogenesis and differentiation

22 September 2017

1 reference

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The p53-family members p63 and p73 inhibit insulin-like growth factor-I receptor gene expression in colon cancer cells

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

p63 deficiency activates a program of cellular senescence and leads to accelerated aging

22 September 2017

1 reference

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p63-specific activation of the BPAG-1e promoter

22 September 2017

1 reference

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IGFBP-3 is a direct target of transcriptional regulation by DeltaNp63alpha in squamous epithelium

22 September 2017

1 reference

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In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

22 September 2017

1 reference

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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

22 September 2017

1 reference

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MSX1 and TGFB3 contribute to clefting in South America

22 September 2017

1 reference

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The Delta Np63 alpha phosphoprotein binds the p21 and 14-3-3 sigma promoters in vivo and has transcriptional repressor activity that is reduced by Hay-Wells syndrome-derived mutations

22 September 2017

1 reference

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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

22 September 2017

1 reference

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Complex transcriptional effects of p63 isoforms: identification of novel activation and repression domains

22 September 2017

1 reference

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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

22 September 2017

1 reference

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A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

22 September 2017

1 reference

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Gene/environment causes of cleft lip and/or palate

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

22 September 2017

1 reference

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Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

A new mathematical model for relative quantification in real-time RT-PCR

22 September 2017

1 reference

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IRF family of transcription factors as regulators of host defense

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

22 September 2017

1 reference

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p63 is a p53 homologue required for limb and epidermal morphogenesis

22 September 2017

1 reference

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p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Keratins (Kl6 and Kl7) as markers of keratinocyte hyperproliferation in psoriasis in vivo and in vitro

22 September 2017

1 reference

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Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Facial clefting in Tp63 deficient mice results from altered Bmp4, Fgf8 and Shh signaling.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Etiology of facial clefts: prospective evaluation of 428 patients.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Developmental aspects of secondary palate formation

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Perp is a p63-regulated gene essential for epithelial integrity.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Death is the major fate of medial edge epithelial cells and the cause of basal lamina degradation during palatogenesis

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Differential regulation of transcription and induction of programmed cell death by human p53-family members p63 and p73.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Zebrafish DeltaNp63 is a direct target of Bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

A dominant-negative form of p63 is required for epidermal proliferation in zebrafish.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860913

Differentiation of cultured palatal shelves from alligator, chick, and mouse embryos

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20424327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/20424327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI40266

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20424327%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20424327%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

PubMed publication ID

20424327

1 reference