Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. (Q48087598)

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scientific article published on 21 May 2006

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English	Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.	scientific article published on 21 May 2006

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

title

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

main subject

neonatal diabetes mellitus

1 reference

based on heuristic

inferred from title

author

Valérie Senée

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Claude Chelala

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Pascal Boileau

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Cécile Julier

series ordinal

13

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Pierre Bougnères

series ordinal

11

object named as

Pierre Bougnères

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Douglas R. Cavener

series ordinal

10

object named as

Douglas R Cavener

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

author name string

Sabine Duchatelet

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Daorong Feng

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Hervé Blanc

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Jack-Christophe Cossec

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Céline Charon

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Marc Nicolino

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

Doris Taha

series ordinal

12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

language of work or name

English

0 references

publication date

21 May 2006

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

published in

Nature Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

volume

38

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

issue

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

page(s)

682-687

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

cites work

GLIS3, a novel member of the GLIS subfamily of Kruppel-like zinc finger proteins with repressor and activation functions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1802

retrieved

21 January 2018

Primary structure and functional characterization of a high-affinity glutamate transporter

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21 January 2018

Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

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

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Mutations in PTF1A cause pancreatic and cerebellar agenesis

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

1 reference

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Primary congenital glaucoma in a patient with trisomy 2q (q33----qter) and monosomy 9p(p24----pter). Case report

1 reference

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter

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Crossref

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Genetics of congenital hypothyroidism

1 reference

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https://api.crossref.org/works/10.1038%2FNG1802

retrieved

21 January 2018

Identification of Glis1, a novel Gli-related, Kruppel-like zinc finger protein containing transactivation and repressor functions

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Characterization of Glis2, a novel gene encoding a Gli-related, Krüppel-like transcription factor with transactivation and repressor functions. Roles in kidney development and neurogenesis

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

Lack of TCF2/vHNF1 in mice leads to pancreas agenesis

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https://api.crossref.org/works/10.1038%2FNG1802

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21 January 2018

The sonic hedgehog-patched-gli pathway in human development and disease

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21 January 2018

The hedgehog signalling pathway in the gastrointestinal tract: implications for development, homeostasis, and disease

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21 January 2018

Hedgehog signaling in pancreas development

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21 January 2018

Automated identification of single nucleotide polymorphisms from sequencing data

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21 January 2018

Transgenic mice with green fluorescent protein-labeled pancreatic beta -cells.

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21 January 2018

Neonatal diabetes mellitus, congenital hypothyroidism, hepatic fibrosis, polycystic kidneys, and congenital glaucoma: a new autosomal recessive syndrome?

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1802

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital glaucoma in a child with partial 1q duplication and 9p deletion

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1802

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG1802

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

PubMed publication ID

16715098

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16715098

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16715098%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 January 2020

 

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