Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Qing, Kan"'
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 17, Iss 1, Pp 1-6 (2022)
Abstract Objective Congenital chylothorax (CC) is an uncommon congenital disease. The objective of this study was to analyze the clinical features, treatment, and outcome of infants with CC in a Chinese tertiary medical center. Methods CC was defined
Externí odkaz:
https://doaj.org/article/591f98ca37de45e794b40c8028e71a91
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 8, Pp 971-972 (2021)
Externí odkaz:
https://doaj.org/article/943ad80ecf5b4ccea38eeaab4954aa64
Autor:
Chenwei Zhang, Xianyou Wang, Hanwei Li, Jinying Wang, Qi Zeng, Wenting Huang, Haoqiang Huang, Yinshuai Xie, Shangzhen Yu, Qing Kan, Qi Wang, Yuqin Cheng
Publikováno v:
Plant Physiol
Grapevine leafroll-associated virus 2 (GLRaV-2) is a prevalent virus associated with grapevine leafroll disease, but the molecular mechanism underlying GLRaV-2 infection is largely unclear. Here, we report that 24-kDa protein (p24), an RNA-silencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fee0941173e921c4f538a33a7926c532
https://doi.org/10.1093/plphys/kiac181
https://doi.org/10.1093/plphys/kiac181
Publikováno v:
The Pediatric infectious disease journal. 41(5)
Elizabethkingia anophelis, originally isolated from the midgut of Anopheles gambiae in 2011, is an important cause of sepsis in adults and children and meningitis in newborns, with several reported outbreaks worldwide. Accumulating molecular biologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dba25d62dbcab54c4fe8177dcf865a3c
https://pubmed.ncbi.nlm.nih.gov/35067644
https://pubmed.ncbi.nlm.nih.gov/35067644
Publikováno v:
Chinese Journal of Chemical Engineering. 27:3017-3026
A new method for nitric oxide (NO) removal was developed by combining dielectric barrier discharge (DBD) and negative pulse corona (NPC). The effects of gas composition (O2, CO2, and H2O) on NO removal were investigated with this method, and the effe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e0dfb30f3243f342af8235d069083bd
https://doi.org/10.1016/j.cjche.2019.01.026
https://doi.org/10.1016/j.cjche.2019.01.026
Publikováno v:
Journal of cardiothoracic surgery. 17(1)
Objective Congenital chylothorax (CC) is an uncommon congenital disease. The objective of this study was to analyze the clinical features, treatment, and outcome of infants with CC in a Chinese tertiary medical center. Methods CC was defined as a non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::532a322f91c1bf953f6712ede2ada6cf
https://pubmed.ncbi.nlm.nih.gov/36303149
https://pubmed.ncbi.nlm.nih.gov/36303149
Publikováno v:
Zhongguo Dang Dai Er Ke Za Zhi
A healthy full-term female neonate, aged 3 days and born by vaginal delivery (with a 1-minute Apgar score of 10 and a 5-minute Apgar score of 10), had unexpected cardiac and respiratory arrests in the early morning on day 3 after birth and recovered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::005cefd0b8ebbb178d809c315cc490f3
https://pubmed.ncbi.nlm.nih.gov/33691923
https://pubmed.ncbi.nlm.nih.gov/33691923
Publikováno v:
Molecular Medicine Reports. 2015, Vol. 12 Issue 2, p2858-2864. 7p.
Publikováno v:
Molecular Medicine Reports.
Normal formation and function of the lungs are essential for the transition of the fetus to an air‑breathing environment at birth. The synthesis of pulmonary surfactant (PS), which is produced by type II alveolar epithelial cells (AECIIs), is requi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53cf55d20718bea299959f4d4ff86cbb
https://doi.org/10.3892/mmr.2018.8602
https://doi.org/10.3892/mmr.2018.8602
Autor:
Youyan Zhao, Li-Zhi Wu, Hong-Lu Liang, Qing Kan, Yun Liu, Xiao-Yu Zhou, Beibei Wang, Yang Yang, Zhao-Lan Cao
Publikováno v:
Experimental and Therapeutic Medicine. 11:235-238
Pompe disease, also known as glycogen storage disease type II, is caused by acid maltase deficiency, and can lead to lysosomal glycogen storage. The primal manifestations may be observed in children and adults, and also in infants. In general, the cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e901e4092df53313939bf2a1af98226b
https://doi.org/10.3892/etm.2015.2862
https://doi.org/10.3892/etm.2015.2862