Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ankita Burman"'
Autor:
Jiurong Liang, Guanling Huang, Xue Liu, Forough Taghavifar, Ningshan Liu, Yizhou Wang, Nan Deng, Changfu Yao, Ting Xie, Vrishika Kulur, Kristy Dai, Ankita Burman, Simon C. Rowan, S. Samuel Weigt, John Belperio, Barry Stripp, William C. Parks, Dianhua Jiang, Paul W. Noble
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 11 (2022)
Type 2 alveolar epithelial cells (AEC2s) function as progenitor cells in the lung. We have shown previously that failure of AEC2 regeneration results in progressive lung fibrosis in mice and is a cardinal feature of idiopathic pulmonary fibrosis (IPF
Externí odkaz:
https://doaj.org/article/f7539cbaaa2b4928beaa1bce4118eb7f
Autor:
Xue Liu, Simon C. Rowan, Jiurong Liang, Changfu Yao, Guanling Huang, Nan Deng, Ting Xie, Di Wu, Yizhou Wang, Ankita Burman, Tanyalak Parimon, Zea Borok, Peter Chen, William C. Parks, Cory M. Hogaboam, S. Samuel Weigt, John Belperio, Barry R. Stripp, Paul W. Noble, Dianhua Jiang
Publikováno v:
iScience, Vol 24, Iss 6, Pp 102551- (2021)
Summary: Pulmonary mesenchymal cells are critical players in both the mouse and human during lung development and disease states. They are increasingly recognized as highly heterogeneous, but there is no consensus on subpopulations or discriminative
Externí odkaz:
https://doaj.org/article/61fae4523109433c93b49fa80896a3e0
Publikováno v:
Am J Med Sci
Idiopathic pulmonary fibrosis (IPF) is a disease of older adults leading to progressive dyspnea and reduced exercise capacity, typically resulting in death within 3–5 years of diagnosis. Underlying genetic susceptibility combined with environmental
Autor:
Di Wu, Zea Borok, Simon C. Rowan, Ankita Burman, Jiurong Liang, Ting Xie, Dianhua Jiang, Guanling Huang, William C. Parks, Cory M. Hogaboam, Xue Liu, Peter Chen, Tanyalak Parimon, Changfu Yao, Barry R. Stripp, Paul W. Noble, John A. Belperio, S. Samuel Weigt, Nan Deng, Yizhou Wang
Publikováno v:
iScience
iScience, Vol 24, Iss 6, Pp 102551-(2021)
iScience, Vol 24, Iss 6, Pp 102551-(2021)
Summary Pulmonary mesenchymal cells are critical players in both the mouse and human during lung development and disease states. They are increasingly recognized as highly heterogeneous, but there is no consensus on subpopulations or discriminative m
Autor:
Ankita Burman, Huang, G., Liang, C. J., Liu, N., Taghavifar, F., Kulur, V., Jiang, D., Noble, P. W.
Publikováno v:
Web of Science
Autor:
Simon C. Rowan, S. Samuel Weigt, Yizhou Wang, Barry R. Stripp, John A. Belperio, Ankita Burman, Dianhua Jiang, Forough Taghavifar, Xue Liu, William C. Parks, Paul W. Noble, Changfu Yao, Nan Deng, Ting Xie, Jiurong Liang, Ningshan Liu, Guanling Huang
SUMMARY Idiopathic pulmonary fibrosis (IPF) is a fatal form of interstitial lung disease and aging has been identified as a risk factor to the disease. Alveolar type II cells (AEC2s) function as progenitor cells in the lung. Growing evidences indicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::848b6cc4397e30075518fd6eb24aa71b
https://doi.org/10.1101/2020.07.30.229567
https://doi.org/10.1101/2020.07.30.229567
Autor:
William C. Parks, Ankita Burman, Simon C. Rowan, Changfu Yao, Nan Deng, Yizhou Wang, John A. Belperio, Barry R. Stripp, Paul W. Noble, Cory M. Hogaboam, Guanling Huang, Ningshan Liu, S. Samuel Weigt, Dianhua Jiang, Forough Taghavifar, Xue Liu, Peter Chen, Ting Xie, Jiurong Liang
Aging is a critical risk factor in progressive lung fibrotic diseases such as idiopathic pulmonary fibrosis (IPF). Loss of integrity of type 2 alveolar epithelial cells (AEC2s) is the main causal event in the pathogenesis of IPF. To systematically ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb1fd518cec39c6ca9fb173b5de125b3
https://doi.org/10.1101/2020.07.30.227892
https://doi.org/10.1101/2020.07.30.227892
Definition and Signatures of Lung Fibroblast Populations in Development and Fibrosis in Mice and Men
Autor:
Ankita Burman, Ting Xie, S. Samuel Weigt, Jiurong Liang, Di Wu, Simon C. Rowan, Paul W. Noble, Xue Liu, John A. Belperio, Peter Chen, Tanyalak Parimon, Changfu Yao, Guanling Huang, Dianhua Jiang, Cory M. Hogaboam, Zea Borok, Yizhou Wang, Barry R. Stripp, Nan Deng, William C. Parks
The heterogeneity of fibroblasts in the murine and human lung during homeostasis and disease is increasingly recognized. It remains unclear if the different phenotypes identified to date are characteristic of unique subpopulations with unique progeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f259a115e939205425967ecacbce3455
https://doi.org/10.1101/2020.07.15.203141
https://doi.org/10.1101/2020.07.15.203141
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology
Autor:
Lucas J. McClellan, Melinda E. McConaha, Ankita Burman, Joshua P. Fessel, Andrew Bryant, Thomas R. Blackwell, Harikrishna Tanjore, Christy Moore, Linda Robinson, Niki Penner, Megha Talati, James West, Anna R. Hemnes, Vasiliy V. Polosukhin, Linda A. Gleaves, William Lawson, Santhi Gladson, Timothy S. Blackwell
Publikováno v:
Pulmonary Circulation. 5:681-690
Pulmonary fibrosis is often complicated by pulmonary hypertension (PH), and previous studies have shown a potential link between bone morphogenetic protein receptor II (BMPR2) and PH secondary to pulmonary fibrosis. We exposed transgenic mice express