Search Results - "Lasky, Joseph"
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Tubastatin ameliorates pulmonary fibrosis by targeting the TGFβ-PI3K-Akt pathway
Published in PloS one (18-10-2017)“…Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and fatal disease. Histone deacetylase 6 (HDAC6) alters function and fate of various proteins via…”
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2
Novel mediators of idiopathic pulmonary fibrosis
Published in Clinical science (1979) (31-08-2022)“…Fibrosis involving the lung may occur in many settings, including in association with known environmental agents, connective tissue diseases, and exposure to…”
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3
In search of druggable targets for GBM amino acid metabolism
Published in BMC cancer (28-02-2017)“…Amino acid (AA) pathways may contain druggable targets for glioblastoma (GBM). Literature reviews and GBM database ( http://r2.amc.nl ) analyses were carried…”
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4
Sirtuin 3 Deregulation Promotes Pulmonary Fibrosis
Published in The journals of gerontology. Series A, Biological sciences and medical sciences (01-05-2017)“…Oxidative stress leads to alveolar epithelial cell injury and fibroblast-myofibroblast differentiation (FMD), key events in the pathobiology of pulmonary…”
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NOTCH-ing up Surface Tension in the Fibrotic Lung
Published in American journal of respiratory and critical care medicine (01-02-2023)“…Lasky and Thannickal discuss the study by Wasnick and colleagues on surface tension in idiopathic pulmonary fibrosis (IPF). IPF occurs in a pattern that is…”
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A Phase 3 Trial of l-Glutamine in Sickle Cell Disease
Published in The New England journal of medicine (19-07-2018)“…A year-long, phase 3, randomized trial involving patients with sickle cell disease showed that the median number of pain crises was 25% lower and the median…”
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7
Prednisone, Azathioprine, and N-Acetylcysteine for Pulmonary Fibrosis
Published in The New England journal of medicine (24-05-2012)“…Many treatments used for idiopathic pulmonary fibrosis (IPF) have not been rigorously tested. This article reports discontinuation of treatment with…”
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Pharmacotherapy and adjunctive treatment for idiopathic pulmonary fibrosis (IPF)
Published in Journal of thoracic disease (01-09-2019)“…Idiopathic pulmonary fibrosis (IPF) is an advancing and fatal lung disease with increasing incidence and prevalence. Nintedanib and pirfenidone were approved…”
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Comparison of the antifibrotic effects of the pan-histone deacetylase-inhibitor panobinostat versus the IPF-drug pirfenidone in fibroblasts from patients with idiopathic pulmonary fibrosis
Published in PloS one (27-11-2018)“…Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease with a poor prognosis. Pirfenidone is the first antifibrotic agent to be approved for…”
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10
Update in Interstitial Lung Disease 2020
Published in American journal of respiratory and critical care medicine (01-06-2021)“…Podolanczuk et al provide an update in interstitial lung disease for 2020. The emergence of severe acute respiratory syndrome coronavirus 2…”
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Associations of circulating matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases with clinically relevant outcomes in idiopathic pulmonary fibrosis: Data from the IPF-PRO Registry
Published in PloS one (17-10-2024)“…We assessed the prognostic utility of circulating levels of matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs) in…”
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12
Safety, tolerability and appropriate use of nintedanib in idiopathic pulmonary fibrosis
Published in Respiratory research (24-09-2015)“…Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterised by dyspnea and loss of lung function. Using pooled data from the replicate,…”
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13
A New Piece to Help Solve the Interstitial Lung Disease Diagnostic Puzzle
Published in American journal of respiratory and critical care medicine (15-01-2021)“…Cosgrove and Lasky discuss the study of Richeldi et al which explored the use of a genomic classifier (GC) of lung tissue derived from pooled transbronchial…”
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14
HDAC8 inhibition ameliorates pulmonary fibrosis
Published in American journal of physiology. Lung cellular and molecular physiology (01-01-2019)“…Idiopathic pulmonary fibrosis (IPF) is a fibroproliferative lung disease, and fibroblast-myofibroblast differentiation (FMD) is thought to be a key event in…”
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15
Using Bronchoscopic Lung Cryobiopsy and a Genomic Classifier in the Multidisciplinary Diagnosis of Diffuse Interstitial Lung Diseases
Published in Chest (01-11-2020)“…Challenges remain for establishing a specific diagnosis in cases of interstitial lung disease (ILD). Bronchoscopic lung cryobiopsy (BLC) has impacted the…”
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Case Report: Blinatumomab as upfront consolidation and maintenance therapy in a pediatric patient with high-risk B-cell acute lymphoblastic leukemia
Published in Frontiers in oncology (01-11-2023)“…Introduction B-cell acute lymphoblastic leukemia (B-ALL) is the most common malignancy in children. The current conventional chemotherapy regimens have high…”
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A Phase II Clinical Trial of Low-Dose Inhaled Carbon Monoxide in Idiopathic Pulmonary Fibrosis
Published in Chest (01-01-2018)“…Preclinical studies have demonstrated that low-dose carbon monoxide (CO) can abrogate experimental lung fibrosis. To test the therapeutic role of inhaled CO,…”
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Imatinib Treatment for Idiopathic Pulmonary Fibrosis: Randomized Placebo-controlled Trial Results
Published in American journal of respiratory and critical care medicine (15-03-2010)“…Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with no known efficacious therapy. Imatinib is a tyrosine kinase inhibitor with potential…”
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Idiopathic Pulmonary Fibrosis in United States Automated Claims. Incidence, Prevalence, and Algorithm Validation
Published in American journal of respiratory and critical care medicine (15-11-2015)“…Estimates of idiopathic pulmonary fibrosis (IPF) incidence and prevalence from electronic databases without case validation may be inaccurate. Develop claims…”
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Safety of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis: Global Pharmacovigilance Data
Published in Advances in therapy (01-10-2020)“…Introduction The safety and tolerability of nintedanib in patients with idiopathic pulmonary fibrosis (IPF) have been characterized using data from clinical…”
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