Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Anmao, Li"'
Autor:
Lei Gu, Anmao Li, Chunyan He, Rui Xiao, Jiaxin Liao, Li Xu, Junhao Mu, Xiaohui Wang, Mingjin Yang, Jinyue Jiang, Yang Bai, Xingxing Jin, Meiling Xiao, Xia Zhang, Tairong Tan, Yang Xiao, Jing Lin, Yishi Li, Shuliang Guo
Publikováno v:
Genes and Diseases, Vol 11, Iss 5, Pp 101040- (2024)
Fibroblast activation and extracellular matrix (ECM) deposition play an important role in the tracheal abnormal repair process and fibrosis. As a transcription factor, SOX9 is involved in fibroblast activation and ECM deposition. However, the mechani
Externí odkaz:
https://doaj.org/article/e2085c8c86c94e0d966bcdcb0a8b1600
Autor:
Chunyan He, Lei Gu, Anmao Li, Yishi Li, Rui Xiao, Jiaxin Liao, Junhao Mu, Yiling Gan, Mingyu Peng, Giri Mohan, Wei Liu, Li Xu, Shuliang Guo
Publikováno v:
Molecular and Cellular Probes, Vol 73, Iss , Pp 101947- (2024)
Airway fibrosis is among the pathological manifestations of benign central airway obstruction noted in the absence of effective treatments and requires new drug targets to be developed. Slit guidance ligand 2–roundabout guidance receptor 1 (Slit2
Externí odkaz:
https://doaj.org/article/93a1cb95e7ec48248f68ad16e486388a
Autor:
Chunyan He, Anmao Li, Lei Gu, Rui Xiao, Jiaxin Liao, Yiling Gan, Mingyu Peng, Shuliang Guo, Xiangxiang Pan, Peifang Wei
Publikováno v:
Chinese Medical Journal, Vol 136, Iss 17, Pp 2125-2127 (2023)
Externí odkaz:
https://doaj.org/article/e716e1b015a6435c8c54bc5f5ec0f0ef
Publikováno v:
FEBS Open Bio, Vol 11, Iss 2, Pp 519-528 (2021)
Multiple myeloma (MM) is a heterogeneous disease with poor prognosis. Increasing evidence has revealed that microRNAs (miRNAs) are strongly associated with the pathogenesis and progression of MM. Here, we investigated the role of microRNA‐637 (miR
Externí odkaz:
https://doaj.org/article/3f2f4c22e8c14b539208e72d534550f6
Publikováno v:
FEBS Open Bio, Vol 10, Iss 10, Pp 2097-2106 (2020)
Multiple myeloma (MM) is the second most common hematologic malignancy of immunoglobulin‐secreting plasma cells. Recent modern combination therapies have improved survival rates, but many patients develop resistance to novel drugs, leading to relap
Externí odkaz:
https://doaj.org/article/642fc25d382d4ee6816bf22ac0231f26
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102391- (2021)
Induced pluripotent stem cell lines (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) isolated from the peripheral blood of a two month-old boy and the parents. Jervell and Lange-Nielsen syndrome (JLNS) was diagnosed in the boy c
Externí odkaz:
https://doaj.org/article/907fed5105374be1b1a1e65587a363e0
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101912- (2020)
Induced pluripotent stem cell lines (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) isolated from the peripheral blood of a 14 year-old boy and his mother using same protocols. Diagnosis of combined oxidative phosphorylation de
Externí odkaz:
https://doaj.org/article/d0f449ad43174617b89ae98387fcfdea
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) isolated from the peripheral blood of a five months-old boy with glycogen storage disease type II(GSD II, also known as Pompe disease, PD) carries c
Externí odkaz:
https://doaj.org/article/57e3553beb2f4793b26391604d60b93d
Publikováno v:
Stem Cell Research, Vol 39, Iss , Pp - (2019)
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) isolated from the peripheral blood of a 4 month-old boy with catecholaminergic polymorphic ventricular tachycardia carrying the double heterozygous
Externí odkaz:
https://doaj.org/article/3cc6d8287dcb4ea79633c02d7adca2bd
Autor:
Yafei Zhou, Wenjun Huang, Leiying Liu, Anmao Li, Congshan Jiang, Rui Zhou, Jie Wang, Xiaoqiu Tan, Christopher L.-H. Huang, Yanmin Zhang
Publikováno v:
Philosophical Transactions of the Royal Society B: Biological Sciences. 378
We illustrate use of induced pluripotent stem cells (iPSCs) as platforms for investigating cardiomyocyte phenotypes in a human family pedigree exemplified by novel heterozygous RYR2-A1855D and SCN10A-Q1362H variants occurring alone and in combination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12a2394533969ece88ccedbd0a0b782e
https://doi.org/10.1098/rstb.2022.0175
https://doi.org/10.1098/rstb.2022.0175