(Q38381588)

2 September 2017

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title

Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies (English)

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2 September 2017

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Giuseppe Castaldo

2

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Roberto Berni Canani

object named as

Roberto Berni Canani

1

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author name string

Rosa Bacchetta

3

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2 September 2017

Martín G Martín

4

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2 September 2017

Olivier Goulet

5

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2 September 2017

language of work or name

English

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publication date

17 March 2015

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Nature Reviews Gastroenterology & Hepatology

2 September 2017

published in

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2 September 2017

volume

12

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2 September 2017

issue

5

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2 September 2017

page(s)

293-302

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Recent progress in congenital diarrheal disorders

2 September 2017

cites work

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Transcriptional regulatory factor X6 (Rfx6) increases gastric inhibitory polypeptide (GIP) expression in enteroendocrine K-cells and is involved in GIP hypersecretion in high fat diet-induced obesity.

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRGASTRO.2015.44

Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRGASTRO.2015.44

Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRGASTRO.2015.44

Human myosin-Vc is a novel class V myosin expressed in epithelial cells

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25782092

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Nucleotide sequence of the Na+/H+ exchanger-8 in patients with congenital sodium diarrhea.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25782092

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25782092

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRGASTRO.2015.44

1 reference

2 September 2017

1 reference