Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus. (Q33680682)

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English	Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.	scientific article

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13 February 2020

Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus (English)

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Simon J van Heeringen

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Martijn A Huynen

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Joris A Veltman

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Miguel Manzanares

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José Luis Gómez-Skarmeta

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Hendrik Gerard Stunnenberg

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Evelyn N Kouwenhoven

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M Eva Alonso

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19 August 2010

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Creative Commons Attribution 4.0 International

19 August 2010

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Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

p63 is a p53 homologue required for limb and epidermal morphogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Crystal structure of a p53 tumor suppressor-DNA complex: understanding tumorigenic mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Cloning and characterization of two members of the vertebrate Dlx gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

A contiguous gene deletion syndrome at 7q21-q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

DNA binding activities of three murine Jun proteins: stimulation by Fos.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

POSSUM: the microcomputer laser-videodisk syndrome information system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Ectro-amelia syndrome associated with an interstitial deletion of 7q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

Epidermal growth factor and the multiplication of cultured human epidermal keratinocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924305

21 June 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanisms.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

p63 consensus DNA-binding site: identification, analysis and application into a p63MH algorithm.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Molecular clock and gene function.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

The Mouse Genome Database genotypes::phenotypes

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Deletion mapping of split hand/split foot malformation with hearing impairment: a case report

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

1994 ASHG presidential address. Who are we? Where are we going? Anticipating the 21st century

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

A higher-order background model improves the detection of promoter regulatory elements by Gibbs sampling.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Odd-skipped genes encode repressors that control kidney development.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

meis1 regulates cyclin D1 and c-myc expression, and controls the proliferation of the multipotent cells in the early developing zebrafish eye.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

Zebrafish enhancer detection (ZED) vector: A new tool to facilitate transgenesis and the functional analysis ofcis-regulatory regions in zebrafish

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001065

21 January 2018

[Interstitial deletion of the long arm of chromosome 7 and its clinical correlations]

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ectrodactyly and proximal/intermediate interstitial deletion 7q

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenome connections

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the complex 7q21.3 rearrangement in a patient with bilateral split-foot malformation and hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern of p63 mutations and their phenotypes--update

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1001065

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20808887%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20808887%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20808887%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

ResearchGate publication ID

0 references

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