(Q24671057)

English

FoxA2, Nkx2.2, and PDX-1 regulate islet beta-cell-specific mafA expression through conserved sequences located between base pairs -8118 and -7750 upstream from the transcription start site

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scholarly article

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FoxA2, Nkx2.2, and PDX-1 regulate islet beta-cell-specific mafA expression through conserved sequences located between base pairs -8118 and -7750 upstream from the transcription start site (English)

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6

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Jonathan Schisler

7

object named as

Jonathan C Schisler

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Christopher B Newgard

8

object named as

Christopher B Newgard

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author name string

Jeffrey C Raum

1

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Kevin Gerrish

2

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Isabella Artner

3

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Eva Henderson

4

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Min Guo

5

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Roland Stein

9

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language of work or name

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publication date

August 2006

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Molecular and Cellular Biology

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26

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15

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5735-43

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1 reference

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The MafA transcription factor appears to be responsible for tissue-specific expression of insulin

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7 April 2017

MafA is a glucose-regulated and pancreatic beta-cell-specific transcriptional activator for the insulin gene

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7 April 2017

Conserved sequences in a tissue-specific regulatory region of the pdx-1 gene mediate transcription in Pancreatic beta cells: role for hepatocyte nuclear factor 3 beta and Pax6

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Identification of beta-cell-specific insulin gene transcription factor RIPE3b1 as mammalian MafA.

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PAX6 mutation as a genetic factor common to aniridia and glucose intolerance

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Members of the large Maf transcription family regulate insulin gene transcription in islet beta cells

1 reference

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Mice lacking the homeodomain transcription factor Nkx2.2 have diabetes due to arrested differentiation of pancreatic beta cells

1 reference

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7 April 2017

The Nkx6.1 homeodomain transcription factor suppresses glucagon expression and regulates glucose-stimulated insulin secretion in islet beta cells

1 reference

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Conserved transcriptional regulatory domains of the pdx-1 gene

1 reference

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Mouse MafA, homologue of zebrafish somite Maf 1, contributes to the specific transcriptional activity through the insulin promoter

1 reference

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Rat endocrine pancreatic development in relation to two homeobox gene products (Pdx-1 and Nkx 6.1)

1 reference

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1 reference

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1 reference

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1 reference

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FoxO1 protects against pancreatic beta cell failure through NeuroD and MafA induction

1 reference

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Interactions between areas I and II direct pdx-1 expression specifically to islet cell types of the mature and developing pancreas

1 reference

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1 reference

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beta-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the beta-cell phenotype and maturity onset diabetes

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequences within the 5'-flanking region of the S14 gene confer responsiveness to glucose in primary hepatocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16847327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XIHbox 8, an endoderm-specific Xenopus homeodomain protein, is closely related to a mammalian insulin gene transcription factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/16847327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16847327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early-onset type-II diabetes mellitus (MODY4) linked to IPF1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16847327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16847327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.00249-06

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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