USP29 enhances chemotherapy-induced stemness in non-small cell lung cancer via stabilizing Snail1 in response to oxidative stress

The deubiquitinating gene Usp29 is dispensable for fertility in male mice

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Breaking the chains: deubiquitylating enzyme specificity begets function

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Comparing and contrasting predictive biomarkers for immunotherapy and targeted therapy of NSCLC

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USP26 promotes esophageal squamous cell carcinoma metastasis through stabilizing Snail

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USP1 links platinum resistance to cancer cell dissemination by regulating Snail stability

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The exon 19-deleted EGFR undergoes ubiquitylation-mediated endocytic degradation via dynamin activity-dependent and -independent mechanisms

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OTUB1 promotes esophageal squamous cell carcinoma metastasis through modulating Snail stability

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Oxidative stress-elicited YY1 potentiates antioxidative response via enhancement of NRF2-driven transcriptional activity: A potential neuronal defensive mechanism against ischemia/reperfusion cerebral injury

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TGFβ-Activated USP27X Deubiquitinase Regulates Cell Migration and Chemoresistance via Stabilization of Snail1

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Chemotherapy elicits pro-metastatic extracellular vesicles in breast cancer models

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Stress-inducible geneAtf3in the noncancer host cells contributes to chemotherapy-exacerbated breast cancer metastasis

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Neoadjuvant chemotherapy induces breast cancer metastasis through a TMEM-mediated mechanism

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Dub3 inhibition suppresses breast cancer invasion and metastasis by promoting Snail1 degradation

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CDK4/6-dependent activation of DUB3 regulates cancer metastasis through SNAIL1

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YY1’s role in the Peg3 imprinted domain

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Neratinib induces ErbB2 ubiquitylation and endocytic degradation via HSP90 dissociation in breast cancer cells

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EMT: 2016

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Balancing efficacy of and host immune responses to cancer therapy: the yin and yang effects

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F-box proteins: Keeping the epithelial-to-mesenchymal transition (EMT) in check

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Global, regional, and national age–sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013

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PKD1 Phosphorylation-Dependent Degradation of SNAIL by SCF-FBXO11 Regulates Epithelial-Mesenchymal Transition and Metastasis

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Emerging Potential of Therapeutic Targeting of Ubiquitin-Specific Proteases in the Treatment of Cancer

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USP29 controls the stability of checkpoint adaptor Claspin by deubiquitination

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Regulation of the protein stability of EMT transcription factors

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Nuclear ubiquitination by FBXL5 modulates Snail1 DNA binding and stability

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Deubiquitylases From Genes to Organism

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Online Survival Analysis Software to Assess the Prognostic Value of Biomarkers Using Transcriptomic Data in Non-Small-Cell Lung Cancer

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Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal

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Cellular functions of the DUBs

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Systematic survey of deubiquitinase localization identifies USP21 as a regulator of centrosome- and microtubule-associated functions

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The cBio Cancer Genomics Portal: An Open Platform for Exploring Multidimensional Cancer Genomics Data: Figure 1.

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JTV1 co-activates FBP to induce USP29 transcription and stabilize p53 in response to oxidative stress

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Defining the Human Deubiquitinating Enzyme Interaction Landscape

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Epithelial-Mesenchymal Transitions in Development and Disease

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The Hypoxia-controlled FBXL14 Ubiquitin Ligase Targets SNAIL1 for Proteasome Degradation

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Breaking the chains: structure and function of the deubiquitinases

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The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells

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Epithelial-Mesenchymal Transition: At the Crossroads of Development and Tumor Metastasis

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Mechanisms of Disease: epithelial–mesenchymal transition—does cellular plasticity fuel neoplastic progression?

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