Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Qian Hua Phua"'
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-11 (2021)
Abstract The skin is made up of a plethora of cells arranged in multiple layers with complex and intricate vascular networks, creating a dynamic microenvironment of cells-to-matrix interactions. With limited donor sites, engineered skin substitute ha
Externí odkaz:
https://doaj.org/article/0d4c3277465940ce835e8cd5005d74f6
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-11 (2019)
Abstract Development of the complex human heart is tightly regulated at multiple levels, maintaining multipotency and proliferative state in the embryonic cardiovascular progenitors and thereafter suppressing progenitor characteristics to allow for t
Externí odkaz:
https://doaj.org/article/8bb10e14259a459e887383c7e097fcf2
Publikováno v:
Aging & Disease. Apr2024, Vol. 15 Issue 2, p503-516. 14p.
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-11 (2019)
Stem Cell Research & Therapy
Stem Cell Research & Therapy
Development of the complex human heart is tightly regulated at multiple levels, maintaining multipotency and proliferative state in the embryonic cardiovascular progenitors and thereafter suppressing progenitor characteristics to allow for terminal d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d401b2e2cc221aacf8eeacb4db9df48
http://link.springer.com/article/10.1186/s13287-019-1451-2
http://link.springer.com/article/10.1186/s13287-019-1451-2
Autor:
Qian Hua Phua, Jin-Hui Hor, Yang Yu, Shi-Yan Ng, Beatrice Xuan Ho, Jeremy Kah Sheng Pang, Nicole Min Qian Pek, Yong Fan, Henry He Yang, Boon Seng Soh, Omer An
Publikováno v:
Cell Death & Disease
Cell Death and Disease, Vol 10, Iss 11, Pp 1-16 (2019)
Cell Death and Disease, Vol 10, Iss 11, Pp 1-16 (2019)
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a mitochondrial disorder that is commonly caused by the m.3243A > G mutation in the MT-TL1 gene encoding for mitochondrial tRNA(Leu(UUR)). While clinical s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91f406aa4ed560ebf639bcce2d3db347
https://doi.org/10.1038/s41419-019-2036-9
https://doi.org/10.1038/s41419-019-2036-9