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LncGPR107 drives the self-renewal of liver tumor initiating cells and liver tumorigenesis through GPR107-dependent manner.

Guanqun Huang | Hui Jiang | Ye Lin | Wuzheng Xia | Yuanwei Luo | Yanpeng Wu | Weilong Cai | Xinke Zhou | Xianhan Jiang
Journal of experimental & clinical cancer research : CR | 2018

With self-renewal and differentiation properties, liver tumor initiating cells (TICs) are the reasons for tumor initiation, metastasis and drug resistance. G protein coupled receptors (GPCR) are critical modulators in many physiological and pathological processes. While, their roles in liver TICs are unknown.

Pubmed ID: 29925408

Research resources used in this publication

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Antibodies used in this publication

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Associated grants

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This is a list of tools and resources that we have found mentioned in this publication.


DAVID (tool)

RRID:SCR_001881

Bioinformatics resource system including web server and web service for functional annotation and enrichment analyses of gene lists. Consists of comprehensive knowledgebase and set of functional analysis tools. Includes gene centered database integrating heterogeneous gene annotation resources to facilitate high throughput gene functional analysis.

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Bioconductor (tool)

RRID:SCR_006442

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RRID:SCR_008984

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RRID:SCR_018934

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BALB/cAnNCrl (tool)

RRID:MGI:2683685

laboratory mouse with name BALB/cAnNCrl from MGI.

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BALB/cAnNCrl (tool)

RRID:MGI:2683685

laboratory mouse with name BALB/cAnNCrl from MGI.

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