Common and Distinctive Functions of the Hippo Effectors Taz and Yap in Skeletal Muscle Stem Cell Function
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D. Matallanas | A. von Kriegsheim | A. García-Muñoz | H. Wackerhage | P. Zammit | N. Vargesson | E. Collie-Duguid | Abdalla D. Mohamed | H. P. Ortuste Quiroga | Congshan Sun | A. Tremblay | V. De Mello | Abdullah Al Bloshi
[1] K. Guan,et al. Characterization of Hippo Pathway Components by Gene Inactivation. , 2016, Molecular cell.
[2] J. Shipley,et al. The Hippo effector TAZ (WWTR1) transforms myoblasts and TAZ abundance is associated with reduced survival in embryonal rhabdomyosarcoma , 2016, The Journal of pathology.
[3] Bin Zhao,et al. Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer , 2015, Cell.
[4] José A. Dianes,et al. 2016 update of the PRIDE database and its related tools , 2015, Nucleic Acids Res..
[5] Bart O Williams,et al. Wnt signaling in bone and muscle. , 2015, Bone.
[6] G. G. Galli,et al. YAP Drives Growth by Controlling Transcriptional Pause Release from Dynamic Enhancers. , 2015, Molecular cell.
[7] K. Guan,et al. YAP and TAZ: a nexus for Hippo signaling and beyond. , 2015, Trends in cell biology.
[8] Young Chul Kim,et al. Alternative Wnt Signaling Activates YAP/TAZ , 2015, Cell.
[9] Antonio Rosato,et al. Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth , 2015, Nature Cell Biology.
[10] T. Hornberger,et al. Yes‐Associated Protein is up‐regulated by mechanical overload and is sufficient to induce skeletal muscle hypertrophy , 2015, FEBS letters.
[11] S. Bicciato,et al. Aerobic glycolysis tunes YAP/TAZ transcriptional activity , 2015, The EMBO journal.
[12] Randy L. Johnson,et al. Transcriptional co-repressor function of the hippo pathway transducers YAP and TAZ. , 2015, Cell reports.
[13] W. Heo,et al. Actin remodelling factors control ciliogenesis by regulating YAP/TAZ activity and vesicle trafficking , 2015, Nature Communications.
[14] K. Guan,et al. Cellular energy stress induces AMPK-mediated regulation of YAP and the Hippo pathway , 2015, Nature Cell Biology.
[15] Randy L. Johnson,et al. AMPK modulates Hippo pathway activity to regulate energy homeostasis , 2015, Nature Cell Biology.
[16] K. Harvey,et al. The Hippo pathway effector YAP is a critical regulator of skeletal muscle fibre size , 2015, Nature Communications.
[17] E. Nishida,et al. Dual role of YAP and TAZ in renewal of the intestinal epithelium , 2014, Nature Cell Biology.
[18] J. Asara,et al. Energy stress regulates hippo-YAP signaling involving AMPK-mediated regulation of angiomotin-like 1 protein. , 2014, Cell reports.
[19] M. Jeong,et al. Novel TAZ modulators enhance myogenic differentiation and muscle regeneration , 2014, British journal of pharmacology.
[20] M. Delorenzi,et al. The Hippo transducer YAP1 transforms activated satellite cells and is a potent effector of embryonal rhabdomyosarcoma formation. , 2014, Cancer cell.
[21] Marius Sudol,et al. The Hippo signal transduction network in skeletal and cardiac muscle , 2014, Science Signaling.
[22] E. Olson,et al. Myomaker is essential for muscle regeneration , 2014, Genes & development.
[23] Giuseppe Basso,et al. YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response , 2014, Cell.
[24] I. Kim,et al. Selenoprotein W enhances skeletal muscle differentiation by inhibiting TAZ binding to 14-3-3 protein. , 2014, Biochimica et biophysica acta.
[25] W. Kolch,et al. On-Beads Digestion in Conjunction with Data-Dependent Mass Spectrometry: A Shortcut to Quantitative and Dynamic Interaction Proteomics , 2014, Biology.
[26] Yu Xin Wang,et al. Wnt7a stimulates myogenic stem cell motility and engraftment resulting in improved muscle strength , 2014, The Journal of cell biology.
[27] Han-Sung Jung,et al. YAP and TAZ regulate skin wound healing. , 2014, The Journal of investigative dermatology.
[28] C. Marcelle,et al. ErbB3 binding protein-1 (Ebp1) controls proliferation and myogenic differentiation of muscle stem cells. , 2014, Developmental biology.
[29] W. Hahn,et al. Genomic insights into WNT/β-catenin signaling. , 2014, Trends in pharmacological sciences.
[30] Lin Feng,et al. Defining the Protein–Protein Interaction Network of the Human Hippo Pathway* , 2013, Molecular & Cellular Proteomics.
[31] C. Wells,et al. LKB1 tumor suppressor regulates AMP kinase/mTOR-independent cell growth and proliferation via the phosphorylation of Yap , 2013, Oncogene.
[32] F. Dilworth,et al. Six1 Regulates MyoD Expression in Adult Muscle Progenitor Cells , 2013, PloS one.
[33] Robert B. White,et al. The Hippo pathway member Yap plays a key role in influencing fate decisions in muscle satellite cells , 2013, Development.
[34] A. M. Carroll,et al. Constitutive Expression of Yes-Associated Protein (Yap) in Adult Skeletal Muscle Fibres Induces Muscle Atrophy and Myopathy , 2013, PloS one.
[35] P. Saftig,et al. Cellular Mechanotransduction Relies on Tension-Induced and Chaperone-Assisted Autophagy , 2013, Current Biology.
[36] M. Rudnicki,et al. Wnt signaling in myogenesis. , 2012, Trends in cell biology.
[37] F. Camargo,et al. Hippo signaling in mammalian stem cells. , 2012, Seminars in cell & developmental biology.
[38] Xiang-Dong Fu,et al. Regulation of the Hippo-YAP Pathway by G-Protein-Coupled Receptor Signaling , 2012, Cell.
[39] Peter S. Zammit,et al. Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage , 2012, Development.
[40] B. Cinar,et al. Threonine-120 Phosphorylation Regulated by Phosphoinositide-3-Kinase/Akt and Mammalian Target of Rapamycin Pathway Signaling Limits the Antitumor Activity of Mammalian Sterile 20-Like Kinase 1* , 2012, The Journal of Biological Chemistry.
[41] K. Guan,et al. Organ Size Control by Hippo and TOR Pathways , 2012, Current Biology.
[42] John McAnally,et al. Regulation of Insulin-Like Growth Factor Signaling by Yap Governs Cardiomyocyte Proliferation and Embryonic Heart Size , 2011, Science Signaling.
[43] T. Ye,et al. Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation , 2011, Cell Death and Differentiation.
[44] Nicola Elvassore,et al. Role of YAP/TAZ in mechanotransduction , 2011, Nature.
[45] O. Kirak,et al. Yap1 Acts Downstream of α-Catenin to Control Epidermal Proliferation , 2011, Cell.
[46] J. Morgan,et al. BMP signalling permits population expansion by preventing premature myogenic differentiation in muscle satellite cells , 2011, Cell Death and Differentiation.
[47] Janet Rossant,et al. The Crumbs complex couples cell density sensing to Hippo-dependent control of the TGF-β-SMAD pathway. , 2010, Developmental cell.
[48] A. Maitra,et al. The Hippo signaling pathway restricts the oncogenic potential of an intestinal regeneration program. , 2010, Genes & development.
[49] Michael B Yaffe,et al. TAZ as a novel enhancer of MyoD‐mediated myogenic differentiation , 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[50] K. Reid,et al. Yap is a novel regulator of C2C12 myogenesis. , 2010, Biochemical and biophysical research communications.
[51] A. Cumano,et al. An adult tissue-specific stem cell in its niche: a gene profiling analysis of in vivo quiescent and activated muscle satellite cells. , 2010, Stem cell research.
[52] S. Schiaffino,et al. Regeneration of mammalian skeletal muscle. Basic mechanisms and clinical implications. , 2010, Current pharmaceutical design.
[53] M. Hoch,et al. Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance , 2010, Current Biology.
[54] Satoshi Kaneko,et al. Phosphoinositide 3-Kinase/Akt Inhibits MST1-Mediated Pro-apoptotic Signaling through Phosphorylation of Threonine 120* , 2009, The Journal of Biological Chemistry.
[55] G. Pavlath,et al. MOR23 promotes muscle regeneration and regulates cell adhesion and migration. , 2009, Developmental cell.
[56] Sho Fujisawa,et al. Nuclear CDKs Drive Smad Transcriptional Activation and Turnover in BMP and TGF-β Pathways , 2009, Cell.
[57] Bernard Perbal,et al. The CCN family of proteins: structure–function relationships , 2008, Trends in biochemical sciences.
[58] C. Moorwood,et al. Syncoilin, an intermediate filament-like protein linked to the dystrophin associated protein complex in skeletal muscle , 2008, Cellular and Molecular Life Sciences.
[59] R. Jaenisch,et al. YAP1 Increases Organ Size and Expands Undifferentiated Progenitor Cells , 2007, Current Biology.
[60] P. Yelick,et al. The pro‐apoptotic kinase Mst1 and its caspase cleavage products are direct inhibitors of Akt1 , 2007, The EMBO journal.
[61] Y. Sunada,et al. Involvement of Wnt4 signaling during myogenic proliferation and differentiation of skeletal muscle , 2007, Developmental dynamics : an official publication of the American Association of Anatomists.
[62] M. Yaffe,et al. TAZ Promotes PC2 Degradation through a SCFβ-Trcp E3 Ligase Complex , 2007, Molecular and Cellular Biology.
[63] Susan S. Brown,et al. FHL3 binds MyoD and negatively regulates myotube formation , 2007, Journal of Cell Science.
[64] K. Harvey,et al. The Salvador–Warts–Hippo pathway — an emerging tumour-suppressor network , 2007, Nature Reviews Cancer.
[65] H. Ko,et al. Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1 , 2007, Proceedings of the National Academy of Sciences.
[66] Yosuke Nagata,et al. Pax7 and myogenic progression in skeletal muscle satellite cells , 2006, Journal of Cell Science.
[67] T. Magnuson,et al. Defects in Yolk Sac Vasculogenesis, Chorioallantoic Fusion, and Embryonic Axis Elongation in Mice with Targeted Disruption of Yap65 , 2006, Molecular and Cellular Biology.
[68] E. Olson,et al. A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[69] Thomas Benjamin,et al. TAZ, a Transcriptional Modulator of Mesenchymal Stem Cell Differentiation , 2005, Science.
[70] D. Garry,et al. Myogenic progenitor cells express filamin C in developing and regenerating skeletal muscle. , 2005, Stem cells and development.
[71] 김태완,et al. GFP(Green Fluorescent Protein)가 발현되는 형질전환 닭의 생산 , 2003 .
[72] J. Barral,et al. Two mammalian UNC-45 isoforms are related to distinct cytoskeletal and muscle-specific functions , 2002, Journal of Cell Science.
[73] M. Yaffe,et al. TAZ: a novel transcriptional co‐activator regulated by interactions with 14‐3‐3 and PDZ domain proteins , 2000, The EMBO journal.
[74] K. Ikeda,et al. Six family genes—structure and function as transcription factors and their roles in development , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.
[75] P. Bork,et al. Characterization of the Mammalian YAP (Yes-associated Protein) Gene and Its Role in Defining a Novel Protein Module, the WW Domain (*) , 1995, The Journal of Biological Chemistry.
[76] M. Nicolet,et al. N-cadherin and N-CAM in myoblast fusion: compared localisation and effect of blockade by peptides and antibodies. , 1992, Journal of cell science.
[77] J. Mar,et al. A conserved CATTCCT motif is required for skeletal muscle-specific activity of the cardiac troponin T gene promoter. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[78] K. Goto,et al. Isolation, Cryosection and Immunostaining of Skeletal Muscle. , 2016, Methods in molecular biology.
[79] L. Lum,et al. Wnt Signaling , 2016, Methods in Molecular Biology.
[80] P. Zammit,et al. Isolation, culture and immunostaining of skeletal muscle fibres to study myogenic progression in satellite cells. , 2014, Methods in molecular biology.
[81] M. Yaffe,et al. TAZ Promotes PC 2 Degradation through a SCF-Trcp E 3 Ligase Complex † , 2007 .