Dysgenesis of enteroendocrine cells in Aristaless-Related Homeobox polyalanine expansion mutations (Q35019818)

5 August 2017

title

Dysgenesis of enteroendocrine cells in Aristaless-Related Homeobox polyalanine expansion mutations (English)

1 reference

5 August 2017

Natalie A Terry

1

1 reference

5 August 2017

Randall A Lee

2

1 reference

5 August 2017

Erik R Walp

3

1 reference

5 August 2017

Klaus H Kaestner

4

1 reference

5 August 2017

Catherine Lee May

5

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 February 2015

1 reference

Journal of Pediatric Gastroenterology and Nutrition

5 August 2017

published in

1 reference

5 August 2017

volume

60

1 reference

5 August 2017

issue

2

1 reference

5 August 2017

page(s)

192-199

1 reference

The inactivation of Arx in pancreatic α-cells triggers their neogenesis and conversion into functional β-like cells

5 August 2017

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8 July 2018

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The homeodomain-containing transcription factors Arx and Pax4 control enteroendocrine subtype specification in mice

8 July 2018

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Arx is required for normal enteroendocrine cell development in mice and humans

8 July 2018

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8 July 2018

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Enteroendocrine cells: neglected players in gastrointestinal disorders?

8 July 2018

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Loss of enteroendocrine cells in mice alters lipid absorption and glucose homeostasis and impairs postnatal survival

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

8 July 2018

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Opposing actions of Arx and Pax4 in endocrine pancreas development

8 July 2018

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

8 July 2018

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8 July 2018

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Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

8 July 2018

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Disruption of PC1/3 expression in mice causes dwarfism and multiple neuroendocrine peptide processing defects

8 July 2018

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8 July 2018

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Neurogenin 3 is essential for the proper specification of gastric enteroendocrine cells and the maintenance of gastric epithelial cell identity

8 July 2018

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

8 July 2018

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X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings

8 July 2018

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neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas

8 July 2018

1 reference

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X-linked lissencephaly with absent corpus callosum and ambiguous genitalia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4308495

Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation

8 July 2018

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Loss of enteroendocrine cells in autoimmune-polyendocrine-candidiasis-ectodermal-dystrophy (APECED) syndrome with gastrointestinal dysfunction

25 October 2018

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Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice

25 October 2018

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A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption

25 October 2018

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Effect of sequential erythromycin and octreotide on antroduodenal manometry

25 October 2018

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Proprotein convertases (PC1/PC3 and PC2) in normal and neoplastic human tissues: their use as markers of neuroendocrine differentiation

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25171319

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Malabsorption due to cholecystokinin deficiency in a patient with autoimmune polyglandular syndrome type I

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25171319

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/MPG.0000000000000542

1 reference

5 August 2017

1 reference

5 August 2017

1 reference