Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Shayi Jiang"'
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0306863 (2024)
BackgroundAlthough clear cell sarcoma of kidney (CCSK) is rare, it is the second most common renal tumor in children after Wilms' tumor. NWTS and SIOP are two major groups which had made tremendous efforts on renal tumors, but the strategies are diff
Externí odkaz:
https://doaj.org/article/4cf30ef58af54688b3f4d21b8599bff3
Autor:
Shayi Jiang, Can Huang, Shan shan Li, Jing Yang, Xue lian Liao, Yangyang Jiao, Ting Zhang, Shuanglong Lu, Yan hua Li, Hui Jiang, Fanyi Zeng
A series of immune abnormalities presenting in aplastic anemia (AA) support the immune pathogenesis of AA. However, how abnormal immunity specifically damages hematopoietic stem cells (HSCs) remains ambiguous. The discovery of bone marrow immune priv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d7ef01f772184e4ebf3840e0379f57c
https://doi.org/10.22541/au.168235933.30161467/v1
https://doi.org/10.22541/au.168235933.30161467/v1
Neuroblastoma (NBL) is clinically and biologically heterogeneous, and novel therapies are desperately needed as the poor prognosis of high-risk NBL cases. Increasingly, studies about metabolic reprogramming and tumor microenvironment (TME) open the w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3abddabe4d4024a6aa20d13b108c69fc
https://doi.org/10.21203/rs.3.rs-2748220/v1
https://doi.org/10.21203/rs.3.rs-2748220/v1
Publikováno v:
Annals of Hematology. 101:617-619
HBB gene mutations lead to many kinds of diseases, of which, except for the two most common diseases of thalassemia and sickle cell anemia, rare kinds of hemolytic anemia, such as hemoglobin Bristol-Alesha, are rarely reported, no ideal treatment in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38bdbc1041eff3216cd9b100593256c5
https://doi.org/10.1007/s00277-021-04721-7
https://doi.org/10.1007/s00277-021-04721-7
Autor:
Jing Ma, Nan Jiang, Jin Zhang, Qing Chen, Kaiyue Jin, Jichun Yang, Yanlin Wang, Jianbo Huang, Shayi Jiang, Wenjun Xia, Duan Ma, Yu Xiong
Publikováno v:
Journal of Cellular Physiology. 233:6841-6852
Plant homeodomain finger 2 (PHF2) is a JmjC family histone demethylase that demethylates H3K9me2, a repressive gene marker. PHF2 was found to play a role in the differentiation of several tissue types such as osteoblast and adipocyte differentiation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b2c0840e336ec7330b612978d91c39a
https://doi.org/10.1002/jcp.26438
https://doi.org/10.1002/jcp.26438
Autor:
Hongwu Wang, Lian Ma, Ting Zhang, Jingbo Shao, Shayi Jiang, Jingwei Yang, Chiju Wei, Tianyou Wang, Hui Jiang
Publikováno v:
Experimental and Therapeutic Medicine
It has been indicated that the combination of pancreatic and duodenal homeobox 1 (Pdx1), MAF bZIP transcription factor A (MafA) and neurogenin 3 (Ngn3) was able to reprogram various cell types towards pancreatic β-like cells (pβLCs). Paired box 4 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80bea6505dded559f929d9884c7da35d
https://doi.org/10.3892/etm.2019.7854
https://doi.org/10.3892/etm.2019.7854
Autor:
Ting C. Zhao, Huadong Li, Wenxia Ma, Chunxiang Zhang, Eric Zhang, Hongyu Qiu, Qinghua Liu, Chan Boriboun, Shayi Jiang, Junlan Zhou, Shiyue Xu, Dauren Biyashev, Aijun Qiao, Jianyi Zhang, Gangjian Qin, Liu Yang, Stéphane Richard, Prasanna Krishnamurthy, Shuling Han
Publikováno v:
J Mol Cell Cardiol
Objective The role of Src-associated-in-mitosis-68-kDa (Sam68) in cardiovascular biology has not been studied. A recent report suggests that Sam68 promotes TNF-α–induced NF-κB activation in fibroblasts. Here we sought to dissect the molecular mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9d3bacb3f5f35a5f30b228a6c406037
https://pubmed.ncbi.nlm.nih.gov/31639388
https://pubmed.ncbi.nlm.nih.gov/31639388
Autor:
SHAYI JIANG1, MIN XIA1, JINGWEI YANG1, JINGBO SHAO1, XUELIAN LIAO1, JIASHI ZHU1, HUI JIANG1 hjiang_1@163.com
Publikováno v:
Molecular Medicine Reports. 2015, Vol. 12 Issue 6, p7877-7882. 6p.
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 9, Pp 1072-1077 (2016)
Chinese Medical Journal
Chinese Medical Journal
Background: Gaucher's disease (GD) is an autosomal recessive disorder caused by a deficiency of acid β-glucosidase (glucocerebrosidase [GBA]) that results in the accumulation of glucocerebroside within macrophages. Many mutations have been reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05615f316ce83a1e76af115a9dd24f8c
https://doi.org/10.4103/0366-6999.180523
https://doi.org/10.4103/0366-6999.180523