Title : β-Catenin is required for Ron receptor-induced mammary tumorigenesis.

Pub. Date : 2011 Aug 25

PMID : 21423209






6 Functional Relationships(s)
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1 beta-Catenin has also been shown to be regulated through tyrosine phosphorylation by the receptor tyrosine kinases Met, Fer and Fyn. Tyrosine catenin beta 1 Homo sapiens
2 Our data also demonstrate that activation of Ron, through ligand binding by hepatocyte growth factor-like protein (HGFL), induces the tyrosine phosphorylation of beta-catenin, primarily on tyrosine residues Tyr 654 and Tyr 670. Tyrosine catenin beta 1 Homo sapiens
3 Our data also demonstrate that activation of Ron, through ligand binding by hepatocyte growth factor-like protein (HGFL), induces the tyrosine phosphorylation of beta-catenin, primarily on tyrosine residues Tyr 654 and Tyr 670. Tyrosine catenin beta 1 Homo sapiens
4 Our data also demonstrate that activation of Ron, through ligand binding by hepatocyte growth factor-like protein (HGFL), induces the tyrosine phosphorylation of beta-catenin, primarily on tyrosine residues Tyr 654 and Tyr 670. Tyrosine catenin beta 1 Homo sapiens
5 Our data also demonstrate that activation of Ron, through ligand binding by hepatocyte growth factor-like protein (HGFL), induces the tyrosine phosphorylation of beta-catenin, primarily on tyrosine residues Tyr 654 and Tyr 670. Tyrosine catenin beta 1 Homo sapiens
6 In addition, HGFL-mediated Ron activation induces both beta-catenin nuclear localization and transcriptional activity, with Tyr 654 and Tyr 670 residues of beta-catenin being critical for these processes. Tyrosine catenin beta 1 Homo sapiens