Rui-Ming Liu, Gang Liu. Exp Gerontol 2020
Times Cited: 16
Times Cited: 16
Times Cited
Times Co-cited
Similarity
Cellular senescence mediates fibrotic pulmonary disease.
Marissa J Schafer, Thomas A White, Koji Iijima, Andrew J Haak, Giovanni Ligresti, Elizabeth J Atkinson, Ann L Oberg, Jodie Birch, Hanna Salmonowicz, Yi Zhu,[...]. Nat Commun 2017
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Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study.
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Reversal of persistent fibrosis in aging by targeting Nox4-Nrf2 redox imbalance.
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An essential role for senescent cells in optimal wound healing through secretion of PDGF-AA.
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Metformin reverses established lung fibrosis in a bleomycin model.
Sunad Rangarajan, Nathaniel B Bone, Anna A Zmijewska, Shaoning Jiang, Dae Won Park, Karen Bernard, Morgan L Locy, Saranya Ravi, Jessy Deshane, Roslyn B Mannon,[...]. Nat Med 2018
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IPF lung fibroblasts have a senescent phenotype.
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Senotherapeutics: Targeting senescence in idiopathic pulmonary fibrosis.
Wolfgang Merkt, Marta Bueno, Ana L Mora, David Lagares. Semin Cell Dev Biol 2020
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Glycolytic Reprogramming in Myofibroblast Differentiation and Lung Fibrosis.
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Impaired Myofibroblast Dedifferentiation Contributes to Nonresolving Fibrosis in Aging.
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Mechanisms of Lung Fibrosis Resolution.
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Fibrotic extracellular matrix activates a profibrotic positive feedback loop.
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The matricellular protein CCN1 induces fibroblast senescence and restricts fibrosis in cutaneous wound healing.
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Senescence of activated stellate cells limits liver fibrosis.
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Mitochondrial dysfunction contributes to the senescent phenotype of IPF lung fibroblasts.
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Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor.
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The Achilles' heel of senescent cells: from transcriptome to senolytic drugs.
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A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
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Accelerated epithelial cell senescence in IPF and the inhibitory role of SIRT6 in TGF-β-induced senescence of human bronchial epithelial cells.
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Cellular senescence: from physiology to pathology.
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Senolytic drugs target alveolar epithelial cell function and attenuate experimental lung fibrosis ex vivo.
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Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases.
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Feedback amplification of fibrosis through matrix stiffening and COX-2 suppression.
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Mitochondria in the spotlight of aging and idiopathic pulmonary fibrosis.
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Circulating mitochondrial DAMPs cause inflammatory responses to injury.
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Metabolic reprogramming in the pathogenesis of chronic lung diseases, including BPD, COPD, and pulmonary fibrosis.
Haifeng Zhao, Phyllis A Dennery, Hongwei Yao. Am J Physiol Lung Cell Mol Physiol 2018
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BH3 mimetics as anti-fibrotic therapy: Unleashing the mitochondrial pathway of apoptosis in myofibroblasts.
Tobias Kuehl, David Lagares. Matrix Biol 2018
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Thyroid hormone inhibits lung fibrosis in mice by improving epithelial mitochondrial function.
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Telomere shortening in familial and sporadic pulmonary fibrosis.
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Inhibition of mechanosensitive signaling in myofibroblasts ameliorates experimental pulmonary fibrosis.
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mTORC1 activation decreases autophagy in aging and idiopathic pulmonary fibrosis and contributes to apoptosis resistance in IPF fibroblasts.
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Short telomere length in IPF lung associates with fibrotic lesions and predicts survival.
Reinier Snetselaar, Aernoud A van Batenburg, Matthijs F M van Oosterhout, Karin M Kazemier, Suzan M Roothaan, Ton Peeters, Joanne J van der Vis, Roel Goldschmeding, Jan C Grutters, Coline H M van Moorsel. PLoS One 2017
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Evasion of apoptosis by myofibroblasts: a hallmark of fibrotic diseases.
Boris Hinz, David Lagares. Nat Rev Rheumatol 2020
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Hexokinase 2 couples glycolysis with the profibrotic actions of TGF-β.
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Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis.
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Mitochondrial 8-oxoguanine DNA glycosylase mitigates alveolar epithelial cell PINK1 deficiency, mitochondrial DNA damage, apoptosis, and lung fibrosis.
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Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection.
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Essential Role for Premature Senescence of Myofibroblasts in Myocardial Fibrosis.
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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
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Animal models of fibrotic lung disease.
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Incidence and prevalence of idiopathic pulmonary fibrosis.
Ganesh Raghu, Derek Weycker, John Edelsberg, Williamson Z Bradford, Gerry Oster. Am J Respir Crit Care Med 2006
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Telomerase mutations in families with idiopathic pulmonary fibrosis.
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Targeted apoptosis of myofibroblasts with the BH3 mimetic ABT-263 reverses established fibrosis.
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Extracellular Matrix Cross-Linking Enhances Fibroblast Growth and Protects against Matrix Proteolysis in Lung Fibrosis.
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Mechanisms for the Resolution of Organ Fibrosis.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.