Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus (Q24304627)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus	scientific article

Statements

instance of

scholarly article

0 references

title

Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus (English)

0 references

main subject

type 2 diabetes

0 references

Transcription factor AP-2 beta

1 reference

stated in

GOA release 2020-03-11

regulation of insulin secretion

1 reference

stated in

GOA release 2020-03-11

Transcription factor AP-2 beta

1 reference

stated in

GOA release 2020-03-11

author

Naoyuki Kamatani

series ordinal

24

0 references

Masafumi Matsuda

object named as

Masafumi Matsuda

series ordinal

10

0 references

Mark McCarthy

object named as

Mark I McCarthy

series ordinal

25

0 references

Andrew Tym Hattersley

series ordinal

17

object named as

Andrew T Hattersley

0 references

author name string

Shiro Maeda

series ordinal

1

0 references

Shuichi Tsukada

series ordinal

2

0 references

Akio Kanazawa

series ordinal

3

0 references

Akihiro Sekine

series ordinal

4

0 references

Tatsuhiko Tsunoda

series ordinal

5

0 references

Daisuke Koya

series ordinal

6

0 references

Hiroshi Maegawa

series ordinal

7

0 references

Atsunori Kashiwagi

series ordinal

8

0 references

Tetsuya Babazono

series ordinal

9

0 references

Yasushi Tanaka

series ordinal

11

0 references

Tomoaki Fujioka

series ordinal

12

0 references

Hiroshi Hirose

series ordinal

13

0 references

Takashi Eguchi

series ordinal

14

0 references

Yoichi Ohno

series ordinal

15

0 references

Christopher J Groves

series ordinal

16

0 references

Graham A Hitman

series ordinal

18

0 references

Mark Walker

series ordinal

19

0 references

Kohei Kaku

series ordinal

20

0 references

Yasuhiko Iwamoto

series ordinal

21

0 references

Ryuzo Kawamori

series ordinal

22

0 references

Ryuichi Kikkawa

series ordinal

23

0 references

Yusuke Nakamura

series ordinal

26

0 references

language of work or name

English

0 references

publication date

2005

0 references

published in

Journal of Human Genetics

0 references

volume

50

0 references

issue

6

0 references

page(s)

283-92

0 references

cites work

Adipogenesis and obesity: rounding out the big picture

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global and societal implications of the diabetes epidemic

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural organization and chromosomal assignment of the human obese gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

JSNP: a database of common gene variations in the Japanese population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic structure and mutations in adipose-specific gene, adiponectin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New perspectives into the molecular pathogenesis and treatment of type 2 diabetes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanism of metabolic syndrome X: contribution of adipocytokines adipocyte-derived bioactive substances

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibilit

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping of essential hypertension single-nucleotide polymorphisms by a homogeneous PCR method with universal energy transfer primers.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type 2 diabetes: when insulin secretion fails to compensate for insulin resistance

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and characterization of a second AP-2 transcription factor: AP-2 beta

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-throughput SNP typing system for genome-wide association studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution haplotype structure in the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial sequencing and analysis of the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an AP-2 element in the -323 to -285 region of the TNF-alpha gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The insulin gene VNTR, type 2 diabetes and birth weight

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15940393

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guilt by association

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10038-005-0253-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mersenne twister: a 623-dimensionally equidistributed uniform pseudo-random number generator

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10038-005-0253-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1007/S10038-005-0253-9

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2088542

Dimensions Publication ID

1002663826

0 references

OpenCitations bibliographic resource ID

2088542

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2088542

PubMed publication ID

15940393

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2088542

ResearchGate publication ID

7802741

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24304627&oldid=2176795774"