The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cells (Q24542332)

8

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Roberto Ravazzolo

7

object named as

Roberto Ravazzolo

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author name string

Silvia Borghini

1

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Tiziana Bachetti

2

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Monica Fava

3

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Marco Di Duca

4

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Francesca Cargnin

PHOX2B regulates its own expression by a transcriptional auto-regulatory mechanism

5

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language of work or name

English

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publication date

15 April 2006

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published in

Biochemical Journal

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volume

395

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issue

2

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page(s)

355-61

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cites work

1 reference

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

24 March 2017

1 reference

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A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions

24 March 2017

1 reference

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

24 March 2017

1 reference

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The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

24 March 2017

1 reference

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The Tlx-2 homeobox gene is a downstream target of BMP signalling and is required for mouse mesoderm development

24 March 2017

1 reference

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A novel pathogenesis of megacolon in Ncx/Hox11L.1 deficient mice

24 March 2017

1 reference

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Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis

24 March 2017

1 reference

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MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data

24 March 2017

1 reference

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Mechanisms and perspectives on differentiation of autonomic neurons

7 April 2017

1 reference

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Intestinal neuronal dysplasia

27 September 2017

1 reference

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Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox11L1-/- mice

27 September 2017

1 reference

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An enhancer element for expression of the Ncx (Enx, Hox11L1) gene in neural crest-derived cells

27 September 2017

1 reference

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Noradrenergic-specific transcription of the dopamine beta-hydroxylase gene requires synergy of multiple cis-acting elements including at least two Phox2a-binding sites.

27 September 2017

1 reference

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Development expression of Hox11 and specification of splenic cell fate.

27 September 2017

1 reference

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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

27 September 2017

1 reference

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

30 May 2018

1 reference

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

30 May 2018

1 reference

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Acetylcholine-related bowel dysmotility in homozygous mutant NCX/HOX11L.1-deficient (NCX-/-) mice-evidence that acetylcholine is implicated in causing intestinal neuronal dysplasia

29 November 2018

1 reference

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Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1422762

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1422762

Enx (Hox11L1)-deficient mice develop myenteric neuronal hyperplasia and megacolon.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1422762

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

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16402914

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16402914