Zobrazeno 1 - 4
of 4
pro vyhledávání: '"MEI XING G. ZUO"'
Autor:
Resat Cinar, Joshua K. Park, Charles N. Zawatsky, Nathan J. Coffey, Steven P. Bodine, Jasmina Abdalla, Tadafumi Yokoyama, Tony Jourdan, Lindsey Jay, Mei Xing G. Zuo, Kevin J. O'Brien, Junfeng Huang, Ken Mackie, Asaf Alimardanov, Malliga R. Iyer, William A. Gahl, George Kunos, Bernadette R. Gochuico, May Christine V. Malicdan
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 7, Pp n/a-n/a (2021)
Abstract Hermansky–Pudlak syndrome (HPS) is a rare genetic disorder which, in its most common and severe form, HPS‐1, leads to fatal adult‐onset pulmonary fibrosis (PF) with no effective treatment. We evaluated the role of the endocannabinoid/C
Externí odkaz:
https://doaj.org/article/6b58354bc8cd41de976ad8a5c91da796
Autor:
Bernadette R Gochuico, Mahin Hossain, Sara K Talvacchio, Mei Xing G Zuo, Mark Barton, An Ngoc Dang Do, Joan C Marini
Publikováno v:
Journal of Medical Genetics. :jmg-2022
PurposePulmonary disease is the major cause of morbidity and mortality in osteogenesis imperfecta (OI). We investigated the contribution of intrinsic lung factors to impaired pulmonary function in children and young adults with OI types III, IV, VI.M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26ad8c5b5f67ac4ea7d1143489a8d18a
https://doi.org/10.1136/jmg-2022-109009
https://doi.org/10.1136/jmg-2022-109009
Autor:
BERNADETTE GOCHUICO, MAHIN S HOSSAIN, SARA K TALVACCHIO, MEI XING G. ZUO, MARK BARTON, AN DANG DO, JOAN C. MARINI
Publikováno v:
Chest. 162:A2695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c9a509ab1acfaa660b39e8b6ee3957d
https://doi.org/10.1016/j.chest.2022.08.2193
https://doi.org/10.1016/j.chest.2022.08.2193
Autor:
George Kunos, Lindsey Jay, Charles N. Zawatsky, Resat Cinar, Ken Mackie, Joshua K. Park, Bernadette R. Gochuico, Mei Xing G. Zuo, Asaf Alimardanov, Steven P. Bodine, Tadafumi Yokoyama, Junfeng Huang, Nathan J. Coffey, Kevin J. O'Brien, William A. Gahl, May Christine V. Malicdan, Tony Jourdan, Malliga R. Iyer, Jasmina Abdalla
Publikováno v:
Clinical and Translational Medicine
Clinical and Translational Medicine, Vol 11, Iss 7, Pp n/a-n/a (2021)
Clinical and Translational Medicine, Vol 11, Iss 7, Pp n/a-n/a (2021)
Hermansky–Pudlak syndrome (HPS) is a rare genetic disorder which, in its most common and severe form, HPS‐1, leads to fatal adult‐onset pulmonary fibrosis (PF) with no effective treatment. We evaluated the role of the endocannabinoid/CB1R syste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4472d429dc98f3ca200c70bd67bf213
http://europepmc.org/articles/PMC8255071
http://europepmc.org/articles/PMC8255071