Possible involvement of LKB1-AMPK signaling in non-homologous end joining. - Wikidata - wikimedia - TriplyDB

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

http://www.wikidata.org/entity/Q39166811

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A mouse model uncovers LKB1 as an UVB-induced DNA damage sensor mediating CDKN1A (p21WAF1/CIP1) degradation AMPKα1 deficiency promotes cellular proliferation and DNA damage via p21 reduction in mouse embryonic fibroblasts.LKB1 preserves genome integrity by stimulating BRCA1 expression.LKB1 reduces ROS-mediated cell damage via activation of p38.Loss of Liver Kinase B1 (LKB1) in Beta Cells Enhances Glucose-stimulated Insulin Secretion Despite Profound Mitochondrial Defects.Regulation of triple-negative breast cancer cell metastasis by the tumor-suppressor liver kinase B1.Clinical Relevance of Liver Kinase B1(LKB1) Protein and Gene Expression in Breast Cancer Targeting the LKB1 tumor suppressor.LKB1 is a DNA damage response protein that regulates cellular sensitivity to PARP inhibitors.Effect of β-catenin silencing in overcoming radioresistance of head and neck cancer cells by antagonizing the effects of AMPK on Ku70/Ku80.The mTOR-S6K pathway links growth signalling to DNA damage response by targeting RNF168.

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Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

http://www.wikidata.org/entity/Q39166811

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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name

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@en

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@nl

type

label

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@en

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@nl

prefLabel

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@en

Possible involvement of LKB1-AMPK signaling in non-homologous end joining.

@nl

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P2860

Interplay between human DNA repair proteins at a unique double-strand break in vivo

RAD6-Mediated transcription-coupled H2B ubiquitylation directly stimulates H3K4 methylation in human cells

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites.

Distinct roles for SWR1 and INO80 chromatin remodeling complexes at chromosomal double-strand breaks.

The yeast chromatin remodeler RSC complex facilitates end joining repair of DNA double-strand breaks

Activation of yeast Snf1 and mammalian AMP-activated protein kinase by upstream kinases.

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

Chromosomal stability and the DNA double-stranded break connection

LKB1 associates with Brg1 and is necessary for Brg1-induced growth arrest

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1640-1648

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