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10.1186/s40880-017-0193-8 http://scihub22266oqcxt.onion/10.1186/s40880-017-0193-8 C5345190!5345190!28279208     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 251.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Chin+J+Cancer 2017 ; 36 (ä): ä Nephropedia Template TP {{tp|p=28279208|t=2017. Corepressor metastasis-associated protein 3 modulates epithelial-to-mesenchymal transition and metastasis |pdf=|usr=}}{{28279208}} gab.com Text Corepressor metastasis-associated protein 3 modulates epithelial-to-mesenchymal transition and metastasis JO: Chin J Cancer http://www.kidney.de/pget.php?&tw=1&pmid=28279208 #FOAvip Worldwide, metastasis is the leading cause of more than 90% of cancer-related deaths. Currently, no specific therapies effectively impede metastasis. Metastatic processes are controlled by complex regulatory networks and transcriptional hierarchy. Corepressor metastasis-associated protein 3 (MTA3) has been confirmed as a novel component of nucleosome remodeling and histone deacetylation (NuRD). Increasing evidence supports the theory that, in the recruitment of transcription factors, coregulators function as master regulators rather than passive passengers. As a master regulator, MTA3 governs the target selection for NuRD and functions as a transcriptional repressor. MTA3 dysregulation is associated with tumor progression, invasion, and metastasis in various cancers. MTA3 is also a key regulator of E-cadherin expression and epithelial-to-mesenchymal transition. Elucidating the functions of MTA3 might help to find additional therapeutic approaches for targeting components of NuRD. Twit Text FOAVip Corepressor metastasis-associated protein 3 modulates epithelial-to-mesenchymal transition and metastasis ????Chin J Cancer http://www.kidney.de/pget.php?&tw=1&pmid=28279208 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28279208 #FOAvip English Wikipedia <ref>{{Cite pmid|28279208}}</ref> Corepressor metastasis-associated protein 3 modulates epithelial-to-mesenchymal transition and metastasis #MMPMID28279208 Du L; Ning Z; Zhang H; Liu F Chin J Cancer 2017[]; 36 (ä): ä PMID28279208show ga Worldwide, metastasis is the leading cause of more than 90% of cancer-related deaths. Currently, no specific therapies effectively impede metastasis. Metastatic processes are controlled by complex regulatory networks and transcriptional hierarchy. Corepressor metastasis-associated protein 3 (MTA3) has been confirmed as a novel component of nucleosome remodeling and histone deacetylation (NuRD). Increasing evidence supports the theory that, in the recruitment of transcription factors, coregulators function as master regulators rather than passive passengers. As a master regulator, MTA3 governs the target selection for NuRD and functions as a transcriptional repressor. MTA3 dysregulation is associated with tumor progression, invasion, and metastasis in various cancers. MTA3 is also a key regulator of E-cadherin expression and epithelial-to-mesenchymal transition. Elucidating the functions of MTA3 might help to find additional therapeutic approaches for targeting components of NuRD. äCorepressor metastasis-associated protein 3 modulates epithelial-to-me(epmc).pdf DeepDyve Pubget Overpricing