Search Results - "Palmer, Scott M."
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Randomized, Double-Blind, Placebo-Controlled, Phase 2 Trial of BMS-986020, a Lysophosphatidic Acid Receptor Antagonist for the Treatment of Idiopathic Pulmonary Fibrosis
Published in Chest (01-11-2018)“…Idiopathic pulmonary fibrosis (IPF) causes irreversible loss of lung function. The lysophosphatidic acid receptor 1 (LPA1) pathway is implicated in IPF…”
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Advances in Human Lung Transplantation
Published in Annual review of medicine (27-01-2021)“…Lung transplantation improves survival and quality of life in patients with advanced pulmonary disease. Over the past several decades, the volume of lung…”
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An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
Published in American journal of respiratory and critical care medicine (01-07-2017)“…Idiopathic pulmonary fibrosis (IPF) is an increasingly recognized, often fatal lung disease of unknown etiology. The aim of this study was to use whole-exome…”
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LungMAP: The Molecular Atlas of Lung Development Program
Published in American journal of physiology. Lung cellular and molecular physiology (01-11-2017)“…The National Heart, Lung, and Blood Institute is funding an effort to create a molecular atlas of the developing lung (LungMAP) to serve as a research resource…”
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Clinical Risk Factors for Primary Graft Dysfunction after Lung Transplantation
Published in American journal of respiratory and critical care medicine (01-03-2013)“…Primary graft dysfunction (PGD) is the main cause of early morbidity and mortality after lung transplantation. Previous studies have yielded conflicting…”
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Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis
Published in American journal of respiratory and critical care medicine (01-07-2022)“…Genetic studies of idiopathic pulmonary fibrosis (IPF) have improved our understanding of this disease, but not all causal loci have been identified. To…”
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Prognostic implications of and clinical risk factors for acute lung injury and organizing pneumonia after lung transplantation: Data from a multicenter prospective cohort study
Published in American journal of transplantation (01-12-2022)“…We determined prognostic implications of acute lung injury (ALI) and organizing pneumonia (OP), including timing relative to transplantation, in a multicenter…”
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Impact of forced vital capacity loss on survival after the onset of chronic lung allograft dysfunction
Published in American journal of respiratory and critical care medicine (15-01-2014)“…Emerging evidence suggests a restrictive phenotype of chronic lung allograft dysfunction (CLAD) exists; however, the optimal approach to its diagnosis and…”
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Plasma microRNA signature as a noninvasive biomarker for acute graft-versus-host disease
Published in Blood (07-11-2013)“…Acute graft-versus-host disease (aGVHD) is the leading cause of morbidity and mortality after allogeneic hematopoietic cell transplantation (HCT)…”
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Peripheral blood proteomic profiling of idiopathic pulmonary fibrosis biomarkers in the multicentre IPF-PRO Registry
Published in Respiratory research (22-10-2019)“…Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease for which diagnosis and management remain challenging. Defining the circulating proteome in…”
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Body composition and mortality after adult lung transplantation in the United States
Published in American journal of respiratory and critical care medicine (01-11-2014)“…Obesity and underweight are contraindications to lung transplantation based on their associations with mortality in studies performed before implementation of…”
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Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort
Published in BMC pulmonary medicine (14-03-2020)“…Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) play important roles in the turnover of extracellular matrix and in the pathogenesis of…”
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Hyaluronan Contributes to Bronchiolitis Obliterans Syndrome and Stimulates Lung Allograft Rejection through Activation of Innate Immunity
Published in American journal of respiratory and critical care medicine (01-03-2014)“…Although innate immunity is increasingly recognized to contribute to lung allograft rejection, the significance of endogenous innate ligands, such as…”
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Lung function trajectories in patients with idiopathic pulmonary fibrosis
Published in Respiratory research (24-08-2023)“…Abstract Background Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease characterised by decline in lung function. We…”
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The utility of preoperative six-minute-walk distance in lung transplantation
Published in American journal of respiratory and critical care medicine (01-10-2015)“…The use of 6-minute-walk distance (6MWD) as an indicator of exercise capacity to predict postoperative survival in lung transplantation has not previously been…”
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Cytomegalovirus Pneumonitis Is a Risk for Bronchiolitis Obliterans Syndrome in Lung Transplantation
Published in American journal of respiratory and critical care medicine (15-06-2010)“…Cytomegalovirus pneumonitis is one of the most prevalent opportunistic infections after lung transplantation. Early studies reported that cytomegalovirus…”
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Circulating metabolic profile in idiopathic pulmonary fibrosis: data from the IPF-PRO Registry
Published in Respiratory research (25-01-2024)“…The circulating metabolome, reflecting underlying cellular processes and disease biology, has not been fully characterized in patients with idiopathic…”
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Survival after Bronchiolitis Obliterans Syndrome among Bilateral Lung Transplant Recipients
Published in American journal of respiratory and critical care medicine (15-09-2010)“…Despite the importance of bronchiolitis obliterans syndrome (BOS) in lung transplantation, little is known regarding the factors that influence survival after…”
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Integrative multi-omics analysis reveals novel idiopathic pulmonary fibrosis endotypes associated with disease progression
Published in Respiratory research (31-05-2023)“…Idiopathic pulmonary fibrosis (IPF) is characterized by the accumulation of extracellular matrix in the pulmonary interstitium and progressive functional…”
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