Cargando…
Corrigendum: Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells
Autores principales: | Tu, Jiajie, Wan, Chao, Zhang, Fengjie, Cao, Lianbao, Nok Law, Patrick Wai, Tian, Yuyao, Lu, Gang, Rennert, Owen M., Chan, Wai‐Yee, Cheung, Hoi‐Hung |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753979/ http://dx.doi.org/10.1111/acel.13227 |
Ejemplares similares
-
Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells
por: Tu, Jiajie, et al.
Publicado: (2020) -
WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome
por: Tian, Yuyao, et al.
Publicado: (2022) -
Corrigendum to “Expression of HGF and c-Met Proteins in Human Keratoconus Corneas”
por: You, Jingjing, et al.
Publicado: (2016) -
Corrigendum to: Regorafenib reverses HGF‐induced sorafenib resistance by inhibiting epithelial‐mesenchymal transition in hepatocellular carcinoma
Publicado: (2022) -
Corrigendum to “SIRT1 Inhibition Affects Angiogenic Properties of Human MSCs”
por: Botti, Chiara, et al.
Publicado: (2015)