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      Pathogenesis of systemic sclerosis: recent insights of molecular and cellular mechanisms and therapeutic opportunities

      1 , 2 , 3
      Journal of Scleroderma and Related Disorders
      SAGE Publications

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          Fibrotic disease and the T(H)1/T(H)2 paradigm.

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            The Hippo pathway effectors TAZ and YAP in development, homeostasis and disease.

            Studies over the past 20 years have defined the Hippo signaling pathway as a major regulator of tissue growth and organ size. Diverse roles for the Hippo pathway have emerged, the majority of which in vertebrates are determined by the transcriptional regulators TAZ and YAP (TAZ/YAP). Key processes regulated by TAZ/YAP include the control of cell proliferation, apoptosis, movement and fate. Accurate control of the levels and localization of these factors is thus essential for early developmental events, as well as for tissue homeostasis, repair and regeneration. Recent studies have revealed that TAZ/YAP activity is regulated by mechanical and cytoskeletal cues as well as by various extracellular factors. Here, I provide an overview of these and other regulatory mechanisms and outline important developmental processes controlled by TAZ and YAP.
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              An updated overview on Wnt signaling pathways: a prelude for more.

              Growth factor signaling is required for cellular differentiation, tissue morphogenesis, and tissue homeostasis. Misregulation of intracellular signal transduction can lead to developmental defects during embryogenesis or particular diseases in the adult. One family of growth factors important for these aspects is given by the Wnt proteins. In particular, Wnts have important functions in stem cell biology, cardiac development and differentiation, angiogenesis, cardiac hypertrophy, cardiac failure, and aging. Knowledge of growth factor signaling during differentiation will allow for improvement of targeted differentiation of embryonic or adult stem cells toward functional cardiomyocytes or for understanding the basis of diseases. Our major aim here is to provide a state of the art review summarizing our present knowledge of the intracellular Wnt-mediated signaling network. In particular, we provide evidence that the subdivision into canonical and noncanonical Wnt signaling pathways solely based on the identity of Wnt ligands or Frizzled receptors is not appropriate anymore. We thereby deliver a solid base for further upcoming articles of a review series focusing on the role of Wnt proteins on different aspects of cardiovascular development and dysfunction.
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                Author and article information

                Journal
                Journal of Scleroderma and Related Disorders
                Journal of Scleroderma and Related Disorders
                SAGE Publications
                2397-1983
                2397-1991
                March 02 2018
                September 2017
                March 02 2018
                September 2017
                : 2
                : 3
                : 137-152
                Affiliations
                [1 ] Northwestern Scleroderma Program, Northwestern University, Chicago, IL - USA
                [2 ] Arthritis Center, Boston University, Boston, MA - USA
                [3 ] Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo - Japan
                Article
                10.5301/jsrd.5000249
                8f973102-6097-43f3-86ea-3dee4f8663bc
                © 2017

                http://journals.sagepub.com/page/policies/text-and-data-mining-license

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