Literature DB >> 22365247

Idiopathic pulmonary fibrosis: pathobiology of novel approaches to treatment.

Toby M Maher1.   

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive disease of unknown cause that conveys a dismal prognosis. In the United States there are currently no licensed therapies for treatment of IPF. The development of effective IPF clinical trials networks across the United States and Europe, however, has led to key developments in the treatment of IPF. Advances in understanding of the pathogenetic processes involved in the development of pulmonary fibrosis have led to novel therapeutic targets. These developments offer hope that there may, in the near future, be therapeutic options available for treatment of this devastating disease. Copyright Â
© 2012 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22365247     DOI: 10.1016/j.ccm.2011.11.002

Source DB:  PubMed          Journal:  Clin Chest Med        ISSN: 0272-5231            Impact factor:   2.878


  22 in total

1.  Lung surgery in interstitial lung disease-a safe and useful procedure?

Authors:  Martin Kolb; Yaron Shargall
Journal:  J Thorac Dis       Date:  2013-08       Impact factor: 2.895

2.  Skin Gene Expression Is Prognostic for the Trajectory of Skin Disease in Patients With Diffuse Cutaneous Systemic Sclerosis.

Authors:  Giuseppina Stifano; Thierry Sornasse; Lisa M Rice; Leo Na; Haiyin Chen-Harris; Dinesh Khanna; Angelika Jahreis; Yuqing Zhang; Jeff Siegel; Robert Lafyatis
Journal:  Arthritis Rheumatol       Date:  2018-06       Impact factor: 10.995

3.  Protein tyrosine phosphatase-α amplifies transforming growth factor-β-dependent profibrotic signaling in lung fibroblasts.

Authors:  Yael Aschner; Meghan Nelson; Matthew Brenner; Helen Roybal; Keriann Beke; Carly Meador; Daniel Foster; Kelly A Correll; Paul R Reynolds; Kelsey Anderson; Elizabeth F Redente; Jennifer Matsuda; David W H Riches; Steve D Groshong; Ambra Pozzi; Jan Sap; Qin Wang; Dhaarmini Rajshankar; Christopher A G McCulloch; Rachel L Zemans; Gregory P Downey
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2020-06-03       Impact factor: 5.464

4.  Fresolimumab treatment decreases biomarkers and improves clinical symptoms in systemic sclerosis patients.

Authors:  Lisa M Rice; Cristina M Padilla; Sarah R McLaughlin; Allison Mathes; Jessica Ziemek; Salma Goummih; Sashidhar Nakerakanti; Michael York; Giuseppina Farina; Michael L Whitfield; Robert F Spiera; Romy B Christmann; Jessica K Gordon; Janice Weinberg; Robert W Simms; Robert Lafyatis
Journal:  J Clin Invest       Date:  2015-06-22       Impact factor: 14.808

Review 5.  Idiopathic Pulmonary Fibrosis: New and Emerging Treatment Options.

Authors:  Richard J Hewitt; Toby M Maher
Journal:  Drugs Aging       Date:  2019-06       Impact factor: 3.923

6.  Increased survivin expression contributes to apoptosis-resistance in IPF fibroblasts.

Authors:  Thomas H Sisson; Toby M Maher; Iyabode O Ajayi; Jessie E King; Peter D R Higgins; Adam J Booth; Rommel L Sagana; Steven K Huang; Eric S White; Bethany B Moore; Jeffrey C Horowitz
Journal:  Adv Biosci Biotechnol       Date:  2012-10

Review 7.  Mitochondrial Dysfunction in Pulmonary Fibrosis.

Authors:  Sunad Rangarajan; Karen Bernard; Victor J Thannickal
Journal:  Ann Am Thorac Soc       Date:  2017-11

8.  Macrophage bone morphogenic protein receptor 2 depletion in idiopathic pulmonary fibrosis and Group III pulmonary hypertension.

Authors:  Ning-Yuan Chen; Scott D Collum; Fayong Luo; Tingting Weng; Thuy-Trahn Le; Adriana M Hernandez; Kemly Philip; Jose G Molina; Luis J Garcia-Morales; Yanna Cao; Tien C Ko; Javier Amione-Guerra; Odeaa Al-Jabbari; Raquel R Bunge; Keith Youker; Brian A Bruckner; Rizwan Hamid; Jonathan Davies; Neeraj Sinha; Harry Karmouty-Quintana
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2016-06-17       Impact factor: 5.464

Review 9.  Current and novel drug therapies for idiopathic pulmonary fibrosis.

Authors:  Huzaifa I Adamali; Toby M Maher
Journal:  Drug Des Devel Ther       Date:  2012-09-26       Impact factor: 4.162

10.  Bone marrow mesenchymal stem cells protect against bleomycin-induced pulmonary fibrosis in rat by activating Nrf2 signaling.

Authors:  Shirong Ni; Dexuan Wang; Xiaoxiao Qiu; Lingxia Pang; Zhangjuan Song; Kunyuan Guo
Journal:  Int J Clin Exp Pathol       Date:  2015-07-01
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