Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Peina Jin"'
Publikováno v:
Cell Transplantation, Vol 30 (2021)
Pneumonia is a serious respiratory tract infection disease in children, which threatens to the health or life of children patients. Ginsenoside Rb1 (Rb1) is a principle active ingredient extracted from the root of Panax notoginseng (Burk.) F.H. Chen
Externí odkaz:
https://doaj.org/article/9afc16de918f4071ac12bf9b35f1e55b
Autor:
Yao, Wang, Huimin, Kong, Yue, Wang, Peina, Jin, Juan, Ding, Hongwei, Li, Huaili, Wang, Zhihong, Zhuo
Publikováno v:
Pediatric Neurology. 138:17-24
Childhood moyamoya disease (MMD) can lead to progressive and irreversible neurological impairment. Early age at onset is likely associated with a worst prognosis of the disease. The study aims to summarize the clinical characteristics of childhood MM
Publikováno v:
General Physiology & Biophysics; 2022, Vol. 41 Issue 6, p499-509, 11p
Publikováno v:
Cell Transplantation
Cell Transplantation, Vol 30 (2021)
Cell Transplantation, Vol 30 (2021)
Background Pneumonia is a serious respiratory tract infection disease in children, which threatens to the health or life of children patients. Ginsenoside Rb1 (Rb1) is a principle active ingredient extracted from the root of Panax notoginseng (Burk.)
Supplemental Material, sj-docx-1-cll-10.1177_09636897211002787 for Ginsenoside Rb1 Alleviates Lipopolysaccharide-Induced Inflammatory Injury by Downregulating miR-222 in WI-38 Cells by Erhu Wei, Xiao Fang, Peisheng Jia, Mingxia Li, Peina Jin, Fengyan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a65380e353b65f8874be9973cd0758
Autor:
Zhihong, Zhuo, Yiwen, Zhai, Peina, Jin, Wenhao, Yan, Huimin, Kong, Xiao, Fang, Fengyan, Li, Qiang, Luo, Xiangdong, Kong, Huaili, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 35(6)
To detect potential mutation in a Chinese pedigree affected with split hand/split foot malformation (SHFM).The patients were screened for genome-wide copy number variations with single nucleotide polymorphism (SNP) microarray. Copy number variations
Publikováno v:
Journal of the Neurological Sciences. 353:84-86
We report a novel mutation in the electron transfer flavoprotein dehydrogenase (EFTDH) gene in an adolescent Chinese patient with late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD) characterized by muscle weakness as e
Publikováno v:
Molecular bioSystems. 12(8)
Human mitogen-activated protein kinase (MAPK) family members JNK and p38 are two homologous protein-serine/threonine kinases but play distinct roles in the pathological process of neurological disorders. Selective targeting of JNK over p38 has been e