Biological influence of Hakai in cancer: a 10-year review - sprookjes - yvandenbroek - TriplyDB

Biological influence of Hakai in cancer: a 10-year review

Biological influence of Hakai in cancer: a 10-year review

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Identification of factors required for m6 A mRNA methylation in Arabidopsis reveals a role for the conserved E3 ubiquitin ligase HAKAI.Role of the microtubule-targeting drug vinflunine on cell-cell adhesions in bladder epithelial tumour cells.miR-203 regulates cell proliferation through its influence on Hakai expression.Proliferation of colorectal cancer is promoted by two signaling transduction expression patterns: ErbB2/ErbB3/AKT and MET/ErbB3/MAPK Posttranscriptional regulation by RNA-binding proteins during epithelial-to-mesenchymal transition.E-cadherin dysfunction in gastric cancer--cellular consequences, clinical applications and open questions.Cell regulation by phosphotyrosine-targeted ubiquitin ligases.High selectivity imaging of nitroreductase using a near-infrared fluorescence probe in hypoxic tumor.The role of ubiquitination and deubiquitination in the regulation of cell junctions.Btbd7 is essential for region-specific epithelial cell dynamics and branching morphogenesis in vivo.Upregulation of CBLL1 in rat brain cortex after lipopolysaccharide treated.Basolateral CD147 Induces Hepatocyte Polarity Loss by E-cadherin Ubiquitination and Degradation in Hepatocellular Carcinoma Progress.Hakai overexpression effectively induces tumour progression and metastasis in vivo.

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Biological influence of Hakai in cancer: a 10-year review

http://www.wikidata.org/entity/Q24622900

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2012 nî lūn-bûn

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2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Biological influence of Hakai in cancer: a 10-year review

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Cancer and Metastasis Reviews

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Biological influence of Hakai in cancer: a 10-year review

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Angélica Figueroa

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Guillermo Alonso

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Luis A Aparicio

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Manuel Valladares

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Moisés Blanco

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P2860

The Hallmarks of Cancer

The interaction of Src and RACK1 is enhanced by activation of protein kinase C and tyrosine phosphorylation of RACK1

The neuronal repellent Slit inhibits leukocyte chemotaxis induced by chemotactic factors

The corepressor mSin3a interacts with the proline-rich domain of p53 and protects p53 from proteasome-mediated degradation

Hakai, a c-Cbl-like protein, ubiquitinates and induces endocytosis of the E-cadherin complex

Structure of a novel phosphotyrosine-binding domain in Hakai that targets E-cadherin

Dynamic and static interactions between p120 catenin and E-cadherin regulate the stability of cell-cell adhesion

Rack1 promotes epithelial cell-cell adhesion by regulating E-cadherin endocytosis

RACK1, a receptor for activated C kinase and a homolog of the beta subunit of G proteins, inhibits activity of src tyrosine kinases and growth of NIH 3T3 cells

A novel pro-apoptotic function of RACK1: suppression of Src activity in the intrinsic and Akt pathways

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