Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Habtamu B, Derseh"'
Autor:
Udari Eshani Perera, Louise Organ, Simon G. Royce, Chrishan S. Samuel, Habtamu B. Derseh, Sasika N. V. Dewage, Emmanuel Koumoundouros, Andrew Stent, Kenneth J. Snibson
Publikováno v:
Canadian Respiratory Journal, Vol 2023 (2023)
Idiopathic pulmonary fibrosis (IPF) is a chronic disease characterized by excessive deposition of extracellular matrix in the interstitial lung parenchyma, often manifested by dyspnea and progressive loss of lung function. The role of inflammation in
Externí odkaz:
https://doaj.org/article/c4cdbb816e0647ad8668c4493bf7d4c0
Autor:
Udari Eshani Perera, Habtamu B. Derseh, Sasika N. V. Dewage, Andrew Stent, Rukmali Wijayarathna, Kenneth J. Snibson
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-13 (2021)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a chronic progressive fibroproliferative disorder that has one of the poorest prognoses amongst interstitial lung diseases. Recently, the finding of aberrant expression levels of miRNAs in IP
Externí odkaz:
https://doaj.org/article/bd64d6e6b5a24b0698ab269167819e9e
Autor:
Habtamu B. Derseh, Sasika N. Vithana Dewage, Kopiyawaththage U. E. Perera, Charles N. Pagel, Emmanuel Koumoundouros, Louise Organ, Ken J. Snibson
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Abstract Idiopathic pulmonary fibrosis (IPF) is a chronic progressive lung disease with limited therapeutic options and poor prognosis. IPF has been associated with aberrant vascular remodelling, however the role of vascular remodelling in pulmonary
Externí odkaz:
https://doaj.org/article/18bd2ab7a74e400796b59f1eeaf6c5b4
Autor:
Habtamu B. Derseh, Kopiyawaththage U. E. Perera, Sasika N. Vithana Dewage, Andrew Stent, Emmanuel Koumoundouros, Louise Organ, Charles N. Pagel, Ken J. Snibson
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Idiopathic pulmonary fibrosis (IPF) is a progressive chronic lung disease characterized by excessive extracellular matrix (ECM) deposition in the parenchyma of the lung. Accompanying the fibrotic remodeling, dysregulated angiogenesis has been observe
Externí odkaz:
https://doaj.org/article/bd205fb8776e4e3fa911e8440c80dcab
Autor:
Udari E. Perera, Louise Organ, Sasika N. V. Dewage, Habtamu B. Derseh, Andrew Stent, Kenneth J. Snibson
Publikováno v:
Canadian Respiratory Journal, Vol 2021 (2021)
Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease, characterized by progressive damage to the lung tissues. Apoptosis and endoplasmic reticulum stress (ER stress) in type II alveolar epithelial cells (AECs) and lung macrophages
Externí odkaz:
https://doaj.org/article/908789700f3c4800baa20f46f7156b29
Autor:
Habtamu B Derseh, Jason Q D Goodger, Jean-Pierre Y Scheerlinck, Chrishan S Samuel, Ian E Woodrow, Enzo A Palombo, Alistair Cumming, Ken Snibson
Publikováno v:
PLoS ONE, Vol 16, Iss 12, p e0260719 (2021)
The primary flavonoid, pinocembrin, is thought to have a variety of medical uses which relate to its reported anti-oxidant, anti-inflammatory, anti-microbial and anti-cancer properties. Some studies have reported that this flavonoid has anti-fibrotic
Externí odkaz:
https://doaj.org/article/a6621f800b28464e8fd74e3032cbad04
Autor:
Rukmali Wijayarathna, Kenneth J. Snibson, Sasika N V Dewage, Udari Eshani Perera, Andrew Stent, Habtamu B Derseh
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-13 (2021)
BMC Genomics
BMC Genomics
Background Idiopathic pulmonary fibrosis (IPF) is a chronic progressive fibroproliferative disorder that has one of the poorest prognoses amongst interstitial lung diseases. Recently, the finding of aberrant expression levels of miRNAs in IPF patient
Autor:
Charles N. Pagel, Emmanuel Koumoundouros, Kenneth J. Snibson, Louise Organ, Sasika N. Vithana Dewage, Habtamu B Derseh, Udari Eshani Perera
Publikováno v:
Experimental Lung Research. 46:409-419
Background Although IPF is described traditionally as a disease affecting lung parenchyma, there is renewed interest in the alterations in the structure and function of the small airways in both IPF patients, and animal models of pulmonary fibrosis.
Autor:
Charles N. Pagel, Louise Organ, Kopiyawaththage U. E. Perera, Emmanuel Koumoundouros, Kenneth J. Snibson, Sasika N. Vithana Dewage, Habtamu B Derseh
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reports
Scientific Reports
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive lung disease with limited therapeutic options and poor prognosis. IPF has been associated with aberrant vascular remodelling, however the role of vascular remodelling in pulmonary fibrosis
Autor:
Glenn F. Browning, Amir H. Noormohammadi, Nadeeka K. Wawegama, Mauricio J. C. Coppo, O.S. Omotainse, Habtamu B Derseh, Anna Kanci Condello, Paola K. Vaz, Sathya N Kulappu Arachchige
Publikováno v:
Cellular Microbiology. 23
Tracheitis associated with the chronic respiratory disease in chickens caused by Mycoplasma gallisepticum is marked by infiltration of leukocytes into the mucosa. Although cytokines/chemokines are known to play a key role in the recruitment, differen