Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Xiajing Chen"'
Autor:
Xiajing Chen, Yanan Zhang, Hui Zhang, Liang Zhang, Lingjuan Liu, Yang Cao, Haitao Ran, Jie Tian
Publikováno v:
Journal of Nanobiotechnology, Vol 20, Iss 1, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/fe33b09c98804575a9000f40b86b41a3
Autor:
Xiajing Chen, Yanan Zhang, Hui Zhang, Liang Zhang, Lingjuan Liu, Yang Cao, Haitao Ran, Jie Tian
Publikováno v:
Journal of Nanobiotechnology, Vol 19, Iss 1, Pp 1-18 (2021)
Abstract Background Ischemic heart disease (IHD) is the leading cause of morbidity and mortality worldwide, and imposes a serious economic load. Thus, it is crucial to perform a timely and accurate diagnosis and monitoring in the early stage of myoca
Externí odkaz:
https://doaj.org/article/3373098f967e484b985b9ca61f2d72eb
Autor:
Jie Tian, Yang Cao, Yanan Zhang, Haitao Ran, Xiajing Chen, Liang Zhang, Hui Zhang, Lingjuan Liu
Publikováno v:
Journal of Nanobiotechnology
Journal of Nanobiotechnology, Vol 19, Iss 1, Pp 1-18 (2021)
Journal of Nanobiotechnology, Vol 19, Iss 1, Pp 1-18 (2021)
Background Ischemic heart disease (IHD) is the leading cause of morbidity and mortality worldwide, and imposes a serious economic load. Thus, it is crucial to perform a timely and accurate diagnosis and monitoring in the early stage of myocardial isc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab05da1aa280a8d537a0f65e8d1637f
http://europepmc.org/articles/PMC7986298
http://europepmc.org/articles/PMC7986298
Autor:
Xiajing Chen, Yanan Zhang, Zhang, Hui, Zhang, Liang, Lingjuan Liu, Cao, Yang, Haitao Ran, Tian, Jie
Additional file 1: Figure S1. The size changes of IMTP-Fe3O4-PFH NPs for different days. Figure S2. The iron standard curves by atomic absorption spectroscopy. Figure S3. The routine blood indexes in the control group and the experimental groups. Fig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14be6b4dd3178c533f9020f852bf06cc
Publikováno v:
International Journal of Nanomedicine
Yanan Zhang,1,2 Xiajing Chen,1,2 Lingjuan Liu,1,2 Jie Tian,1,2 Lan Hao,3 Hai-tao Ran3 1Department of Cardiology, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b7b0dcfe7751f888032661ce8dc05cf
https://pubmed.ncbi.nlm.nih.gov/33628023
https://pubmed.ncbi.nlm.nih.gov/33628023
Publikováno v:
DNA and cell biology.
Long noncoding RNAs (lncRNAs) may serve as potential molecular diagnostic markers to improve the capacity of earlier and more accurate diagnosis of dilated cardiomyopathy (DCM). We integrated five independent transcriptomic datasets (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28389e3912446b646a1174343ae49933
https://pubmed.ncbi.nlm.nih.gov/33146560
https://pubmed.ncbi.nlm.nih.gov/33146560
Autor:
Lingzhang, Meng, Shan, Cao, Na, Lin, Jingjie, Zhao, Xulong, Cai, Yonghua, Liang, Ken, Huang, Mali, Lin, Xiajing, Chen, Dongming, Li, Junli, Wang, Lijuan, Yang, Aibo, Wei, Genliang, Li, Qingmei, Lu, Yuxiu, Guo, Qiuju, Wei, Junhua, Tan, Meiying, Huang, Yuming, Huang, Jie, Wang, Yunguang, Liu
Publikováno v:
BioMed Research International
ACTN4, a gene which codes for the protein α-actinin-4, is critical for the maintenance of the renal filtration barrier. It is well known that ACTN4 mutations can lead to kidney dysfunction, such as familial focal segmental glomerulosclerosis (FSGS),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a31049b89661b99d66c8f63d389ad02
https://pubmed.ncbi.nlm.nih.gov/31930129
https://pubmed.ncbi.nlm.nih.gov/31930129
Autor:
Jingjie Zhao, Mali Lin, Aibo Wei, Xiajing Chen, Dongming Li, Junhua Tan, Qiuju Wei, Junli Wang, Xulong Cai, Na Lin, Lingzhang Meng, Yuming Huang, Yuxiu Guo, Jie Wang, Shan Cao, Ken Huang, Yonghua Liang, Lijuan Yang, Genliang Li, Meiying Huang, Yunguang Liu, Qingmei Lu
Publikováno v:
BioMed Research International, Vol 2019 (2019)
ACTN4, a gene which codes for the protein α-actinin-4, is critical for the maintenance of the renal filtration barrier. It is well known that ACTN4 mutations can lead to kidney dysfunction, such as familial focal segmental glomerulosclerosis (FSGS),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fad0b98c72973b30cfa0fcc5a1879ac7
https://doaj.org/article/da62753665274fc29f14d11aa196bf88
https://doaj.org/article/da62753665274fc29f14d11aa196bf88