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Keywords: TGF-β
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Cell migration
J Cell Sci (2023) 136 (1): jcs259275.
Published: 5 January 2023
... the cleft increased speed. As the cells slow down, they orient both migration and protrusions towards the nascent cleft, while cells in the adjacent branches orient towards the elongating tips. We next tested the hypothesis that TGF-β signaling controls mammary branching by regulating cell migration. We...
Includes: Supplementary data
Journal Articles
J Cell Sci (2019) 132 (16): jcs231399.
Published: 22 August 2019
..., our study indicated that MKL1 promoted the migration and invasion of PTC cells. MKL1 interacted with and recruited Smad3 to the promoter of MMP2 to activate MMP2 transcription upon treatment with TGF-β. Moreover, there was significant correlation between expression of TGF-β, MKL1 and MMP2 in our...
Includes: Supplementary data
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J Cell Sci (2018) 131 (8): jcs213959.
Published: 13 April 2018
...-of-function mutations in FLNB cause two groups of skeletal disorders that can be attributed to either the loss of repressive function on TGF-β signaling or a disruption in mechanosensory properties, respectively. In this Review, we highlight a unique family of vertebrate-specific short-lived filamin-binding...
Includes: Supplementary data
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Journal Articles
J Cell Sci (2016) 129 (15): 2925–2936.
Published: 1 August 2016
.... It is debated whether epithelial–mesenchymal transition (EMT) affects tubular cells, which under high-glucose conditions overproduce transforming growth factor-β (TGF-β), a fibrogenic cytokine involved in interstitial fibrosis development. Our study investigated the involvement of non-receptor tyrosine kinase...
Includes: Supplementary data
Journal Articles
J Cell Sci (2015) 128 (6): 1083–1089.
Published: 15 March 2015
.... TGF-β and hypoxia, two cues that initiate injury-induced fibrosis, caused human kidney cells to develop a mesenchymal phenotype, including increased fibronectin expression and secretion. However, upon hypoxia, assembled extracellular fibronectin fibrils were mostly absent, whereas treatment with TGF-β...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (3): 599–608.
Published: 1 February 2014
... −/− mice, during late stages, the mutant muscle exhibits necrotic fibers, calcium deposits and fibrosis. TGF-β expression, as well as levels of phosphorylated Smad2 and Smad3, are sustained in the mutant tissue and treatment with decorin, which blocks TGF-β signaling, improves the histopathology of Sharp-1...
Journal Articles
J Cell Sci (2014) 127 (1): 40–49.
Published: 1 January 2014
... this are poorly understood. Ski is a negative regulator of TGF-β–Smad signaling in myofibroblasts, and might redirect the myofibroblast phenotype back to fibroblasts. Meox2 could alter TGF-β-mediated cellular processes and is repressed by Zeb2. Here, we investigated whether Ski diminishes the myofibroblast...
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J Cell Sci (2008) 121 (7): 1036–1045.
Published: 1 April 2008
... at the level of DNA binding and transcriptional activation. * Author for correspondence (e-mail: [email protected] ) 10 1 2008 © The Company of Biologists Limited 2008 2008 Lung EMT TGF-β JNK SMAD Mouse Epithelial-to-mesenchymal transition (EMT) has emerged...
Includes: Supplementary data
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J Cell Sci (2005) 118 (16): 3573–3584.
Published: 15 August 2005
...Aristidis Moustakas; Carl-Henrik Heldin During the past 10 years, it has been firmly established that Smad pathways are central mediators of signals from the receptors for transforming growth factor β (TGF-β) superfamily members to the nucleus. However, growing biochemical and developmental...
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Journal Articles