Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Pei-Pei Liu"'
Autor:
Xiao-Yan Meng, Hui-Fang Sun, Ying-Jie Zhang, Wen-Xiu Li, Dian-Dian Wang, Dan-Hua Liu, Sen-Miao Li, Yue Wu, Jia-Kang Li, Xiao-Hui Liu, Pei-Pei Liu, Run-Zhou Yang, Shu-Ang Li, Jian-Sheng Kang
Publikováno v:
Stem Cell Research, Vol 79, Iss , Pp 103486- (2024)
Pluripotent stem cells were generated through the electroporation of episomal plasmids, containing crucial reprogramming factors, into skin fibroblasts extracted from a female Alzheimer’s patient harboring the PSEN1 709 T > C (p.Phe237Leu) heterozy
Externí odkaz:
https://doaj.org/article/acc8f8cafa764c16ad104ab82ec746d0
Autor:
Sen‐Miao Li, Dian‐Dian Wang, Dan‐Hua Liu, Xiao‐Yan Meng, Zhizhong Wang, Xitong Guo, Qian Liu, Pei‐Pei Liu, Shu‐Ang Li, Songwei Wang, Run‐Zhou Yang, Yuming Xu, Longde Wang, Jian‐Sheng Kang
Publikováno v:
MedComm, Vol 5, Iss 6, Pp n/a-n/a (2024)
Abstract Parkinson's disease (PD) is a mitochondria‐related neurodegenerative disease characterized by locomotor deficits and loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc). Majority of PD research primarily focused o
Externí odkaz:
https://doaj.org/article/62f42c40c5de4a5db3198e57338533c3
Publikováno v:
Journal of Integrative Neuroscience, Vol 23, Iss 9, p 180 (2024)
Objective: To explore the relationship between YKL-40 level, telomere length, and different subtypes of insomnia disorder. Methods: A total of 145 individuals suffering from insomnia were enrolled and divided into four groups according to the insomni
Externí odkaz:
https://doaj.org/article/e9ea4a0633ca41f9a284296921c69dd2
Generation of induced pluripotent stem cells (ZZUCSBi001-A) from skin fibroblasts of a healthy donor
Publikováno v:
Stem Cell Research, Vol 76, Iss , Pp 103328- (2024)
Fibroblasts were extracted from the scalp of a healthy 55-year-old male and subsequently transformed into pluripotent stem cells by introducing episomal plasmids harboring essential reprogramming factors. These induced pluripotent stem cells exhibite
Externí odkaz:
https://doaj.org/article/16bc0078ebed49e1991be72222ad8650
Autor:
Shu-Ang Li, Xiao-Yan Meng, Ying-Jie Zhang, Cai-Li Chen, Yu-Xue Jiao, Yong-Qing Zhu, Pei-Pei Liu, Wei Sun
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2024)
pH-sensitive fluorescent proteins have revolutionized the field of cellular imaging and physiology, offering insight into the dynamic pH changes that underlie fundamental cellular processes. This comprehensive review explores the diverse applications
Externí odkaz:
https://doaj.org/article/38dc691be8834714895d00ba310e17f0
Autor:
Ya-Jie Xu, Pei-Pei Liu, Zhong-Ze Yan, Ting-Wei Mi, Ying-Ying Wang, Qian Li, Zhao-Qian Teng, Chang-Mei Liu
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-16 (2022)
Abstract Background Rett syndrome (RTT), mainly caused by mutations in methyl-CpG binding protein 2 (MECP2), is one of the most prevalent neurodevelopmental disorders in girls. However, the underlying mechanism of MECP2 remains largely unknown and cu
Externí odkaz:
https://doaj.org/article/9141a8097db34f22a03cf62751e12afa
Publikováno v:
Videosurgery and Other Miniinvasive Techniques, Vol 17, Iss 4, Pp 710-715 (2022)
Externí odkaz:
https://doaj.org/article/1254942591d9401982c51d8cfb3a7701
Publikováno v:
Guoji Yanke Zazhi, Vol 22, Iss 7, Pp 1224-1227 (2022)
AIM: To provide guidance for more accurate measurement of axial length(AL)of difficult measuring eyes by comparing the differences in the AL of the patient's difficult measuring eye with three methods of the sitting position, supine position A-scan a
Externí odkaz:
https://doaj.org/article/104e853197794e1596a1e08101cc8cd4
Publikováno v:
Reproductive Biology and Endocrinology, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Several surveys have reported that patients treated with gonadotropin-releasing hormone antagonist (GnRH-ant) protocol showed a significantly lower rate of implantation and clinical pregnancy compared to GnRH agonist (GnRH-a) prot
Externí odkaz:
https://doaj.org/article/73b35407399a45e08918ab704a65fb3e
Autor:
Pei‐Pei Liu, Shang‐Kun Dai, Ting‐Wei Mi, Gang‐Bin Tang, Zhuo Wang, Hui Wang, Hong‐Zhen Du, Yi Tang, Zhao‐Qian Teng, Chang‐Mei Liu
Publikováno v:
EMBO Molecular Medicine, Vol 14, Iss 12, Pp n/a-n/a (2022)
Abstract Mutations in AT‐rich interactive domain‐containing protein 1A (ARID1A) cause Coffin‐Siris syndrome (CSS), a rare genetic disorder that results in mild to severe intellectual disabilities. However, the biological role of ARID1A in the b
Externí odkaz:
https://doaj.org/article/b4f7592562874eeaa694011fbfd342d4