Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yingxi Cao"'
Autor:
Yu Xia, Sierra Duca, Björn Perder, Friederike Dündar, Paul Zumbo, Miaoyan Qiu, Jun Yao, Yingxi Cao, Michael R. M. Harrison, Lior Zangi, Doron Betel, Jingli Cao
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
The epicardium supports heart regeneration, though precisely how is unclear. Here the authors define an activated epicardial progenitor population as the source of essential cell types and paracrine factors for successful heart regeneration in zebraf
Externí odkaz:
https://doaj.org/article/3ae641996c0f41c8ae565e948ca8a1a7
Autor:
Yingxi Cao, Jingli Cao
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 6, Iss 1, p 3 (2018)
The epicardium, a mesothelial layer that envelops vertebrate hearts, has become a therapeutic target in cardiac repair strategies because of its vital role in heart development and cardiac injury response. Epicardial cells serve as a progenitor cell
Externí odkaz:
https://doaj.org/article/38a116865c2c4db6a88c50d07acbbe1c
Autor:
Yu Xia, Sierra Duca, Björn Perder, Friederike Dündar, Paul Zumbo, Miaoyan Qiu, Jun Yao, Yingxi Cao, Michael R. Harrison, Lior Zangi, Doron Betel, Jingli Cao
The epicardium, a mesothelial cell tissue that encompasses vertebrate hearts, supports heart regeneration after injury through paracrine effects and as a source of multipotent progenitors. However, the progenitor state in the adult epicardium has yet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dfaa29b73758acb5707b61530285dea
https://doi.org/10.1101/2022.10.26.513031
https://doi.org/10.1101/2022.10.26.513031
Autor:
Lingyun Song, Alexias Safi, Kenneth D. Poss, Yu Xia, Jingli Cao, Timothy Curtis, Jianhong Ou, Yingxi Cao, Gregory E. Crawford, Joseph B. Balowski
Publikováno v:
Development
The epicardium is a mesothelial tissue layer that envelops the heart. Cardiac injury activates dynamic gene expression programs in epicardial tissue, which in zebrafish enables subsequent regeneration through paracrine and vascularizing effects. To i
Publikováno v:
Gene. 710:9-16
Maple syrup urine disease (MSUD) is a rare autosomal recessive genetic metabolic disease, with a high incidence rate in infants. We analyzed the data of molecular genetic analysis of five infants whose metabolism screening suspected MSUD and describe
Autor:
Yingxi Cao, Jing Liu, Jianyan Pan, Yanling Teng, Lingqian Wu, Siyuan Linpeng, Zhuo Li, Desheng Liang
Publikováno v:
BioMed Research International, Vol 2018 (2018)
Joubert syndrome (JBTS) is a clinically and genetically heterogeneous group of ciliary diseases. To date, 34 subtypes of JBTS have been classified due to different causative genes or extra clinical features. Most of them are autosomal recessive, whil
Publikováno v:
International Heart Journal. 59:1059-1068
There are many inherited disorders associated with thoracic aortic aneurysms and dissections (TAADs), like Marfan syndrome and Loeys-Dietz syndrome (LDS). The 4 patients in this study all had TAADs and were initially diagnosed with suspected Marfan s
Publikováno v:
Cold Spring Harb Perspect Biol
The epicardium, the outermost tissue layer that envelops all vertebrate hearts, plays a crucial role in cardiac development and regeneration and has been implicated in potential strategies for cardiac repair. The heterogenous cell population that com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cbff1b3a837e6892d156bf2c83cbd01
https://europepmc.org/articles/PMC6996450/
https://europepmc.org/articles/PMC6996450/
Publikováno v:
Gene. 669:42-46
Idiopathic hypogonadotropic hypogonadism (IHH) is characterized by low levels of gonadotropins and delayed or absent sexual development. Most of the patients are diagnosed in late adolescence or early adulthood. Determining the diagnosis of IHH in pr
Autor:
Zhuo Li, Hu Tan, Rui Zhang, Siyuan Linpeng, Yanru Huang, Lingqian Wu, Weigang Lv, Desheng Liang, Haoxian Li, Xigui Long, Yingxi Cao
Publikováno v:
Eye
Purpose To detect the underlying pathogenesis of congenital cataract in a four-generation Chinese family. Methods Whole-exome sequencing (WES) of family members (III:4, IV:4, and IV:6) was performed. Sanger sequencing and bioinformatics analysis were