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Items: 1 to 20 of 78


G protein-coupled receptor 56 regulates matrix production and motility of lung fibroblasts.

Yang J, Wang Z, Leng D, Dai H, Wang J, Liang J, Jiang D, Wang C.

Exp Biol Med (Maywood). 2014 Jun;239(6):686-96.


Cartilage oligomeric matrix protein in idiopathic pulmonary fibrosis.

Vuga LJ, Milosevic J, Pandit K, Ben-Yehudah A, Chu Y, Richards T, Sciurba J, Myerburg M, Zhang Y, Parwani AV, Gibson KF, Kaminski N.

PLoS One. 2013 Dec 20;8(12):e83120. doi: 10.1371/journal.pone.0083120.


miR-21 mediates fibrogenic activation of pulmonary fibroblasts and lung fibrosis.

Liu G, Friggeri A, Yang Y, Milosevic J, Ding Q, Thannickal VJ, Kaminski N, Abraham E.

J Exp Med. 2010 Aug 2;207(8):1589-97. doi: 10.1084/jem.20100035.


Transcription factor GATA-6 is expressed in quiescent myofibroblasts in idiopathic pulmonary fibrosis.

Leppäranta O, Pulkkinen V, Koli K, Vähätalo R, Salmenkivi K, Kinnula VL, Heikinheimo M, Myllärniemi M.

Am J Respir Cell Mol Biol. 2010 May;42(5):626-32. doi: 10.1165/rcmb.2009-0021OC.


An inhibitor of NADPH oxidase-4 attenuates established pulmonary fibrosis in a rodent disease model.

Jarman ER, Khambata VS, Cope C, Jones P, Roger J, Ye LY, Duggan N, Head D, Pearce A, Press NJ, Bellenie B, Sohal B, Jarai G.

Am J Respir Cell Mol Biol. 2014 Jan;50(1):158-69. doi: 10.1165/rcmb.2013-0174OC.


The quest for the initial lesion in idiopathic pulmonary fibrosis: gene expression differences in IPF fibroblasts.

Eickelberg O, Laurent GJ.

Am J Respir Cell Mol Biol. 2010 Jan;42(1):1-2. doi: 10.1165/rcmb.2009-0245ED. No abstract available.


Increased FGF1-FGFRc expression in idiopathic pulmonary fibrosis.

MacKenzie B, Korfei M, Henneke I, Sibinska Z, Tian X, Hezel S, Dilai S, Wasnick R, Schneider B, Wilhelm J, El Agha E, Klepetko W, Seeger W, Schermuly R, Günther A, Bellusci S.

Respir Res. 2015 Jul 3;16:83. doi: 10.1186/s12931-015-0242-2.


Lung fibrotic tenascin-C upregulation is associated with other extracellular matrix proteins and induced by TGFβ1.

Estany S, Vicens-Zygmunt V, Llatjós R, Montes A, Penín R, Escobar I, Xaubet A, Santos S, Manresa F, Dorca J, Molina-Molina M.

BMC Pulm Med. 2014 Jul 26;14:120. doi: 10.1186/1471-2466-14-120.


Downregulation of FAK-related non-kinase mediates the migratory phenotype of human fibrotic lung fibroblasts.

Cai GQ, Zheng A, Tang Q, White ES, Chou CF, Gladson CL, Olman MA, Ding Q.

Exp Cell Res. 2010 May 15;316(9):1600-9. doi: 10.1016/j.yexcr.2010.01.021.


Reactive oxygen species are required for maintenance and differentiation of primary lung fibroblasts in idiopathic pulmonary fibrosis.

Bocchino M, Agnese S, Fagone E, Svegliati S, Grieco D, Vancheri C, Gabrielli A, Sanduzzi A, Avvedimento EV.

PLoS One. 2010 Nov 16;5(11):e14003. doi: 10.1371/journal.pone.0014003.


Increased fibroblast telomerase expression precedes myofibroblast α-smooth muscle actin expression in idiopathic pulmonary fibrosis.

Waisberg DR, Parra ER, Barbas-Filho JV, Fernezlian S, Capelozzi VL.

Clinics (Sao Paulo). 2012 Sep;67(9):1039-46.


Lung myofibroblasts are characterized by down-regulated cyclooxygenase-2 and its main metabolite, prostaglandin E2.

Gabasa M, Royo D, Molina-Molina M, Roca-Ferrer J, Pujols L, Picado C, Xaubet A, Pereda J.

PLoS One. 2013 Jun 3;8(6):e65445. doi: 10.1371/journal.pone.0065445.


Role of CD248 as a potential severity marker in idiopathic pulmonary fibrosis.

Bartis D, Crowley LE, D'Souza VK, Borthwick L, Fisher AJ, Croft AP, Pongrácz JE, Thompson R, Langman G, Buckley CD, Thickett DR.

BMC Pulm Med. 2016 Apr 14;16(1):51. doi: 10.1186/s12890-016-0211-7.


Matrices of physiologic stiffness potently inactivate idiopathic pulmonary fibrosis fibroblasts.

Marinković A, Liu F, Tschumperlin DJ.

Am J Respir Cell Mol Biol. 2013 Apr;48(4):422-30. doi: 10.1165/rcmb.2012-0335OC.


Forkhead Box F1 represses cell growth and inhibits COL1 and ARPC2 expression in lung fibroblasts in vitro.

Melboucy-Belkhir S, Pradère P, Tadbiri S, Habib S, Bacrot A, Brayer S, Mari B, Besnard V, Mailleux A, Guenther A, Castier Y, Mal H, Crestani B, Plantier L.

Am J Physiol Lung Cell Mol Physiol. 2014 Dec 1;307(11):L838-47. doi: 10.1152/ajplung.00012.2014.


Absence of Thy-1 results in TGF-β induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblasts.

Ramírez G, Hagood JS, Sanders Y, Ramírez R, Becerril C, Segura L, Barrera L, Selman M, Pardo A.

Lab Invest. 2011 Aug;91(8):1206-18. doi: 10.1038/labinvest.2011.80.


[Expressions of caveolin-1 and extracellular matrix in lung tissues of patients with idiopathic pulmonary fibrosis].

Wang XF, Ding H, Zhou FQ, Meng FQ, Cai HR.

Zhonghua Jie He He Hu Xi Za Zhi. 2012 May;35(5):336-9. Chinese.


Hypoxia-induced DNA hypermethylation in human pulmonary fibroblasts is associated with Thy-1 promoter methylation and the development of a pro-fibrotic phenotype.

Robinson CM, Neary R, Levendale A, Watson CJ, Baugh JA.

Respir Res. 2012 Aug 31;13:74. doi: 10.1186/1465-9921-13-74.


Up-regulation of heparan sulfate 6-O-sulfation in idiopathic pulmonary fibrosis.

Lu J, Auduong L, White ES, Yue X.

Am J Respir Cell Mol Biol. 2014 Jan;50(1):106-14. doi: 10.1165/rcmb.2013-0204OC.

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