Articles with "ipf" as a keyword



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Targeting anti‐aging protein sirtuin (Sirt) in the diagnosis of idiopathic pulmonary fibrosis

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Published in 2018 at "Journal of Cellular Biochemistry"

DOI: 10.1002/jcb.28033

Abstract: Idiopathic pulmonary fibrosis (IPF) is a severe, incurable, age‐associated respiratory disorder that has gained significance because of its unknown etiology and lack of therapeutic approaches. IPF causes maximum damage to the alveolar epithelial cells, thereby… read more here.

Keywords: protein; fibrosis; diagnosis; idiopathic pulmonary ... See more keywords
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Proteomic analysis of the IPF mesenchymal progenitor cell nuclear proteome identifies abnormalities in key nodal proteins that underlie their fibrogenic phenotype

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Published in 2022 at "Proteomics"

DOI: 10.1002/pmic.202200018

Abstract: IPF is a progressive fibrotic lung disease whose pathogenesis remains incompletely understood. We have previously discovered pathologic mesenchymal progenitor cells (MPCs) in the lungs of IPF patients. IPF MPCs display a distinct transcriptome and create… read more here.

Keywords: ipf; phenotype; progenitor; mesenchymal progenitor ... See more keywords
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Pharmacologic Treatment of IPF

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Published in 2018 at "Respiratory Medicine"

DOI: 10.1007/978-3-319-99975-3_13

Abstract: The pathogenetic mechanisms leading to lung fibrosis in idiopathic pulmonary fibrosis (IPF) are mostly unknown. The old paradigm of inflammation has been substantially replaced by hypotheses of dysregulated wound healing with an excessive production of… read more here.

Keywords: guideline; pharmacologic treatment; treatment; treatment ipf ... See more keywords
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Risk of progression of idiopathic pulmonary fibrosis to connective tissue disease: a long-term observational study in 527 patients

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Published in 2021 at "Clinical Rheumatology"

DOI: 10.1007/s10067-021-05659-x

Abstract: Connective tissue disease (CTD) might occur during the course of idiopathic pulmonary fibrosis (IPF). Clinical factors associated with CTD development in IPF patients have still not been identified. We investigated which antibodies have a significant… read more here.

Keywords: acpa mpo; ctd; mpo anca; ipf patients ... See more keywords
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Survival and outcomes after lung transplantation for connective tissue disease-associated interstitial lung diseases

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Published in 2021 at "Clinical Rheumatology"

DOI: 10.1007/s10067-021-05704-9

Abstract: Lung transplantation (LTx) is the most important treatment for end-stage lung diseases. However, the treatment of connective tissue disease-associated interstitial lung diseases (CTD-ILD) using LTx is still controversial especially for polymyositis/dermatomyositis-associated interstitial lung disease (PM/DM-ILD).… read more here.

Keywords: connective tissue; associated interstitial; lung diseases; ipf ... See more keywords
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Decrypting the crosstalk of noncoding RNAs in the progression of IPF

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Published in 2020 at "Molecular Biology Reports"

DOI: 10.1007/s11033-020-05368-9

Abstract: Idiopathic pulmonary fibrosis (IPF) is an agnogenic, rare, and lethal disease, with high mortality and poor prognosis and a median survival time as short as 3 to 5 years after diagnosis. No effective therapeutic drugs… read more here.

Keywords: ipf; decrypting crosstalk; progression ipf; noncoding rnas ... See more keywords
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Impact of gender on immature platelet count and its relationship with coronary artery disease

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Published in 2020 at "Journal of Thrombosis and Thrombolysis"

DOI: 10.1007/s11239-020-02080-0

Abstract: The impact of platelet parameters on the cardiovascular risk is still debated. Gender differences in platelet volume indexes and turnover have been previously reported, potentially conditioning their role in the development of coronary artery disease… read more here.

Keywords: gender; cad; prevalence; ipf ... See more keywords
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Epidemiology of idiopathic pulmonary fibrosis: a population-based study in primary care

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Published in 2019 at "Internal and Emergency Medicine"

DOI: 10.1007/s11739-019-02195-0

Abstract: Idiopathic pulmonary fibrosis (IPF) is a chronic disease with unknown etiology and poor prognosis. Little is known about the epidemiology of this disease; most of the studies are limited by small and restricted cohort studies.… read more here.

Keywords: incidence; primary care; epidemiology; using algorithm ... See more keywords
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Association between C-reactive protein and carotid plaque in mild-to-moderate idiopathic pulmonary fibrosis

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Published in 2021 at "Internal and Emergency Medicine"

DOI: 10.1007/s11739-020-02607-6

Abstract: An association between C-reactive protein (CRP) levels and carotid plaque has never been investigated in idiopathic pulmonary fibrosis (IPF). The aim of this study was to evaluate the extent of carotid atherosclerosis in mild-to-moderate IPF… read more here.

Keywords: crp levels; carotid; carotid plaque; ipf ... See more keywords
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Immature platelet fraction (IPF) as a predictive value for thrombopoietic recovery after allogeneic stem cell transplantation

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Published in 2017 at "International Journal of Hematology"

DOI: 10.1007/s12185-017-2344-8

Abstract: We consecutively examined the utility of measurements of percentage of immature platelet fraction (IPF%) and absolute IPF number (A-IPF) in predicting thrombopoietic recovery in 15 adult patients who underwent allogeneic hematopoietic stem cell transplantation (allo-SCT).… read more here.

Keywords: recovery; thrombopoietic recovery; platelet fraction; ipf ... See more keywords
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Meta‐analysis of Gastroesophageal Reflux Disease and Idiopathic Pulmonary Fibrosis

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Published in 2019 at "Chest"

DOI: 10.1016/j.chest.2018.07.038

Abstract: BACKGROUND: The relationship between gastroesophageal reflux disease (GERD) and idiopathic pulmonary fibrosis (IPF) is controversial. Current guidelines recommend that clinicians use regular antacid treatment, while two recent meta‐analyses of antacid therapy in IPF were inconclusive.… read more here.

Keywords: control; disease; meta; ipf ... See more keywords