Geniposide accelerates proteasome degradation of Txnip to inhibit insulin secretion in pancreatic β-cells. (Q51246114)

2 April 2018

title

Geniposide accelerates proteasome degradation of Txnip to inhibit insulin secretion in pancreatic β-cells. (English)

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2 April 2018

author name string

C Y Liu

1

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2 April 2018

Y N Hao

2

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2 April 2018

F Yin

3

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2 April 2018

Y L Zhang

4

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2 April 2018

J H Liu

5

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2 April 2018

publication date

20 December 2016

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2 April 2018

Journal of Endocrinological Investigation

published in

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2 April 2018

volume

40

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2 April 2018

issue

5

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2 April 2018

page(s)

505-512

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2 April 2018

https://scigraph.springernature.com/pub.10.1007/s40618-016-0591-9

exact match

0 references

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Cyclic AMP signaling stimulates proteasome degradation of thioredoxin interacting protein (TxNIP) in pancreatic beta-cells

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Glucagon-like peptide 1 receptor plays a critical role in geniposide-regulated insulin secretion in INS-1 cells

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Geniposide regulates glucose-stimulated insulin secretion possibly through controlling glucose metabolism in INS-1 cells

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Geniposide, a novel agonist for GLP-1 receptor, prevents PC12 cells from oxidative damage via MAP kinase pathway.

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Geniposide Suppresses Hepatic Glucose Production via AMPK in HepG2 Cells.

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Transcription factor Ets1 regulates expression of thioredoxin-interacting protein and inhibits insulin secretion in pancreatic β-cells

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TXNIP Links Redox Circuitry to Glucose Control

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Oxidative stress and diabetes mellitus

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Role of superoxide as a signaling molecule.

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Beta-cells in type 2 diabetes: a loss of function and mass

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10.1007/S40618-016-0591-9

Identifiers

DOI

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2 April 2018

PubMed ID

28000177

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2 April 2018