(Q54739039)

English

Extremely rare cause of congenital diarrhea: enteric anendocrinosis.

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Extremely rare cause of congenital diarrhea: enteric anendocrinosis. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

0 references

congenital diarrhea

1 reference

based on heuristic

inferred from title

object named as

Ersin Sayar

1

0 references

object named as

Sarah E Flanagan

5

0 references

author name string

Ali Islek

2

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Aygen Yilmaz

3

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Mustafa Akcam

4

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Reha Artan

6

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

publication date

1 October 2013

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Pediatrics International

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

55

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

5

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

661-663

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

Mutant neurogenin-3 in congenital malabsorptive diarrhea

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Permanent Neonatal Diabetes and Enteric Anendocrinosis Associated With Biallelic Mutations in NEUROG3.

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Neurogenin3 is differentially required for endocrine cell fate specification in the intestinal and gastric epithelium

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Requirement of Math1 for secretory cell lineage commitment in the mouse intestine

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Gastrointestinal stem cells. II. Intestinal stem cells

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

On the origin of the beta cell

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Neurogenin 3-expressing progenitor cells in the gastrointestinal tract differentiate into both endocrine and non-endocrine cell types

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Notch signals control the fate of immature progenitor cells in the intestine

1 reference

https://api.crossref.org/works/10.1111%2FPED.12169

21 January 2018

Identifiers

10.1111/PED.12169

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/24134759

ResearchGate publication ID

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