Human GLI3 intragenic conserved non-coding sequences are tissue-specific enhancers (Q33281754)

25 July 2017

title

Human GLI3 intragenic conserved non-coding sequences are tissue-specific enhancers (English)

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25 July 2017

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25 July 2017

Sajid Malik

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Amir Ali Abbasi

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25 July 2017

Zissis Paparidis

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25 July 2017

Debbie K Goode

series ordinal

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25 July 2017

Heather Callaway

series ordinal

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25 July 2017

Karl-Heinz Grzeschik

series ordinal

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25 July 2017

language of work or name

English

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publication date

11 April 2007

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25 July 2017

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25 July 2017

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25 July 2017

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25 July 2017

page(s)

e366

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Creative Commons Attribution 4.0 International

25 July 2017

start time

11 April 2007

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April 2022 Public Data File from Crossref

copyrighted

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cites work

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Shuffling of cis-regulatory elements is a pervasive feature of the vertebrate lineage

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New technologies, new findings, and new concepts in the study of vertebrate cis-regulatory sequences

21 June 2018

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21 June 2018

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Gli function is essential for motor neuron induction in zebrafish

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21 June 2018

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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations

21 June 2018

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Highly conserved non-coding sequences are associated with vertebrate development

21 June 2018

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Zebrafish Gli3 functions as both an activator and a repressor in Hedgehog signaling

21 June 2018

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Gli2 and Gli3 have redundant and context-dependent function in skeletal muscle formation.

21 June 2018

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21 June 2018

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Spatial pattern of sonic hedgehog signaling through Gli genes during cerebellum development

21 June 2018

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Sonic hedgehog-patched Gli signaling in the developing rat prostate gland: lobe-specific suppression by neonatal estrogens reduces ductal growth and branching

21 June 2018

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21 June 2018

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rVISTA 2.0: evolutionary analysis of transcription factor binding sites

21 June 2018

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Comparative genomics at the vertebrate extremes

21 June 2018

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Ultraconserved Elements in the Human Genome

21 June 2018

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Interplays of Gli2 and Gli3 and their requirement in mediating Shh-dependent sclerotome induction

21 June 2018

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The emergent design of the neural tube: prepattern, SHH morphogen and GLI code

21 June 2018

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21 June 2018

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A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly

21 June 2018

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21 June 2018

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Parsing the prosencephalon

21 June 2018

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Dorsal-ventral patterning of the spinal cord requires Gli3 transcriptional repressor activity

21 June 2018

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A direct requirement for Hedgehog signaling for normal specification of all ventral progenitor domains in the presumptive mammalian spinal cord

21 June 2018

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Gli2, but not Gli1, is required for initial Shh signaling and ectopic activation of the Shh pathway

21 June 2018

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Pallister-Hall syndrome phenotype in mice mutant for Gli3

21 June 2018

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Gli1 can rescue the in vivo function of Gli2

21 June 2018

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VISTA : visualizing global DNA sequence alignments of arbitrary length

21 June 2018

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Gli2 functions in FGF signaling during antero-posterior patterning

21 June 2018

1 reference

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DNA binding sites: representation and discovery

21 June 2018

1 reference

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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Intronic enhancers control expression of zebrafish sonic hedgehog in floor plate and notochord.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Diminished Sonic hedgehog signaling and lack of floor plate differentiation in Gli2 mutant mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Mutation in GLI3 in postaxial polydactyly type A

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1838922

Point Mutations in Human GLI3 Cause Greig Syndrome

28 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Computational screening of conserved genomic DNA in search of functional noncoding elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Highly conserved regulatory elements around the SHH gene may contribute to the maintenance of conserved synteny across human chromosome 7q36.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000366

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt)

21 January 2018

1 reference

12 December 2020

Conservation of RET regulatory function from human to zebrafish without sequence similarity

1 reference

12 December 2020

Molecular linkage of the morphogenetic mutation add and the zinc finger gene Gli3

1 reference

12 December 2020

The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3

1 reference

12 December 2020

Pallister-Hall syndrome

1 reference

12 December 2020

Techniques in neural development

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0000366

Identifiers

DOI

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25 July 2017

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25 July 2017

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