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PMID:25540073

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Citation

Nizard, P, Ezan, F, Bonnier, D, Le Meur, N, Langouët, S, Baffet, G, Arlot-Bonnemains, Y and Théret, N (2014) Integrative analysis of high-throughput RNAi screen data identifies the FER and CRKL tyrosine kinases as new regulators of the mitogenic ERK-dependent pathways in transformed cells. BMC Genomics 15:1169

Abstract

Cell proliferation is a hallmark of cancer and depends on complex signaling networks that are chiefly supported by protein kinase activities. Therapeutic strategies have been used to target specific kinases but new methods are required to identify combined targets and improve treatment. Here, we propose a small interfering RNA genetic screen and an integrative approach to identify kinase networks involved in the proliferation of cancer cells.

Links

PubMed PMC4367906 Online version:[1]

Keywords


Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

HUMAN:FER

GO:0008284: positive regulation of cell proliferation

ECO:0000315:

P

Fig. 7 Decrease in proliferation index due to RNAi knockout of FER

complete
CACAO 10817

HUMAN:FER

involved_in

GO:0008284: positive regulation of cell population proliferation

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

HUMAN:CRKL

GO:0008284: positive regulation of cell proliferation

ECO:0000315:

P

Fig. 7 Decrease in proliferation index due to RNAi knockout of CRKL

complete
CACAO 10816

HUMAN:CRKL

involved_in

GO:0008284: positive regulation of cell population proliferation

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

Notes

See also

References

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