(Q33775747)

29 July 2017

title

GATA6 haploinsufficiency causes pancreatic agenesis in humans (English)

1 reference

29 July 2017

0 references

Ildem Akerman

5

0 references

Richard Caswell

Richard Caswell

6

0 references

Jorge Ferrer

Jorge Ferrer

8

0 references

Hana Lango Allen

Hana Lango Allen

1

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Sarah Flanagan

Sarah E Flanagan

2

0 references

Sian Ellard

Sian Ellard

10

0 references

Andrew Tym Hattersley

9

Andrew T Hattersley

1 reference

29 July 2017

3

Charles Shaw-Smith

1 reference

International Pancreatic Agenesis Consortium

29 July 2017

7

International Pancreatic Agenesis Consortium

1 reference

29 July 2017

Elisa De Franco

4

1 reference

29 July 2017

language of work or name

English

0 references

publication date

11 December 2011

1 reference

29 July 2017

1 reference

29 July 2017

volume

44

1 reference

29 July 2017

issue

1

1 reference

29 July 2017

page(s)

20-22

1 reference

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

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Identification of GATA6 sequence variants in patients with congenital heart defects.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

In vivo reprogramming of adult pancreatic exocrine cells to beta-cells

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Development of the mammalian liver and ventral pancreas is dependent on GATA4.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Gata6 is an important regulator of mouse pancreas development

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Mutations in PTF1A cause pancreatic and cerebellar agenesis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Transcriptional networks controlling pancreatic development and beta cell function.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

GATA6 regulates HNF4 and is required for differentiation of visceral endoderm in the mouse embryo

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4062962

Neonatal diabetes mellitus with pancreatic agenesis in an infant with homozygous IPF-1 Pro63fsX60 mutation.

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.1035

Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delay.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.1035

A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.1035

21 January 2018

Identifiers

DOI

10.1038/NG.1035

1 reference

29 July 2017

1 reference

29 July 2017

1 reference