Interaction between PHOX2B and CREBBP mediates synergistic activation: mechanistic implications of PHOX2B mutants (Q28308129)

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20 January 2020

title

Interaction between PHOX2B and CREBBP mediates synergistic activation: mechanistic implications of PHOX2B mutants (English)

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20 January 2020

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20 January 2020

Han-Tsang Wu

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20 January 2020

Yi-Ning Su

series ordinal

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20 January 2020

Chia-Cheng Hung

series ordinal

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20 January 2020

Kou-Juey Wu

series ordinal

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20 January 2020

language of work or name

English

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publication date

1 April 2009

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20 January 2020

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20 January 2020

volume

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20 January 2020

issue

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20 January 2020

page(s)

655-660

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A molecular pathogenesis for transcription factor associated poly-alanine tract expansions

20 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

The other trinucleotide repeat: polyalanine expansion disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Alanine tracts: the expanding story of human illness and trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Activation of phosphoinositide 3-kinase by the NBS1 DNA repair protein through a novel activation motif.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

c-Myc directly regulates the transcription of the NBS1 gene involved in DNA double-strand break repair

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

SUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Specification of neurotransmitter identity by Phox2 proteins in neural crest stem cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Molecular analysis of congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Molecular consequences of PHOX2B missense, frameshift and alanine expansion mutations leading to autonomic dysfunction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Polyalanine expansions might not result from unequal crossing-over

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Idiopathic congenital central hypoventilation syndrome: diagnosis and management. American Thoracic Society

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Coordinated regulation of iron-controlling genes, H-ferritin and IRP2, by c-MYC

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Paired-like homeodomain proteins, Phox2a and Phox2b, are responsible for noradrenergic cell-specific transcription of the dopamine beta-hydroxylase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20929

7 January 2021

Identifiers

DOI

10.1002/HUMU.20929

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19191321%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19191321%20AND%20SRC:MED&resulttype=core&format=json