Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aojie Cai"'
Autor:
Xiaofan Zhu, Aojie Cai, Jingjing Meng, Lina Liu, Siying Cui, Suzhen Qu, Junhong Zhao, Ning Liu, Xiangdong Kong
Publikováno v:
Stem Cell Research, Vol 32, Iss , Pp 47-50 (2018)
Duchenne muscular dystrophy (DMD) is a common X-linked recessive disorder for which there is no present cure. In this paper, we reported the generation of ZZUi008-A, an induced pluripotent stem cell(iPSC) line derived from chorionic villus(CV) cells
Externí odkaz:
https://doaj.org/article/aab3e3ebaa0546f28589ce5a0fa85ab1
Publikováno v:
Neurochemical Research. 48:72-81
Acitretin is an oral drug approved by the Food and Drug Administration that is commonly used to treat psoriasis. In recent years, acitretin has been identified as a candidate drug for the treatment of Alzheimer’s disease, but its role in neuronal d
Autor:
Xuechao Zhao, Haofeng Ning, Yanhong Wang, Ganye Zhao, Shiyue Mei, Ning Liu, Conghui Wang, Aojie Cai, Erhu Wei, Xiangdong Kong
Publikováno v:
Neurological Sciences. 43:4439-4451
We aimed to investigate the genetic etiology of epilepsy in children, and to analyze the nature of genetic variation, the function of related genes, and the genotype-phenotype relationship. Moreover, the impact of the genetic diagnosis on prognosis a
Publikováno v:
Neurochemical research. 47(12)
Neuroblastoma is a type of developmental childhood cancer that arises from the neural crest. It is the most common pediatric solid tumor in the world. AM580 is a powerful cyto-differentiating molecule on acute promyelocytic leukemia cells and induced
Autor:
Siying Cui, Ning Liu, Jingjing Meng, Xiaofan Zhu, Aojie Cai, Junhong Zhao, Xiangdong Kong, Li'na Liu, Suzhen Qu
Publikováno v:
Stem Cell Research, Vol 32, Iss, Pp 47-50 (2018)
Duchenne muscular dystrophy (DMD) is a common X-linked recessive disorder for which there is no present cure. In this paper, we reported the generation of ZZUi008-A, an induced pluripotent stem cell(iPSC) line derived from chorionic villus(CV) cells
Autor:
Suzhen Fan, Tianxiang Wei, Shuo Jin, Yun Tian, Hanqing Hong, Shujun Zhao, Nan Zhang, Yaping Wang, Yan Liu, Aojie Cai, Hai Zhu, Yuan Li, Yang Liu, Kaili Wang, Xiaofeng Lv, Yan Li, Hongyu Li, Qiaohong Qin
Publikováno v:
Cell Death & Disease
Cell Death and Disease, Vol 10, Iss 12, Pp 1-19 (2019)
Cell Death and Disease, Vol 10, Iss 12, Pp 1-19 (2019)
As a new class of non-coding RNA, circular RNAs (circRNAs) play crucial roles in the development and progression of various cancers. However, the detailed functions of circRNAs in cervical cancer have seldom been reported. In this study, circRNA sequ
Autor:
Yuxia, Yang, Suzhen, Qu, Li, Wang, Yilin, Guo, Shuwen, Xue, Aojie, Cai, Siying, Cui, Xiangdong, Kong
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 36(6)
To explore the prevalence and characteristics of chromosomal abnormalities in abortuses during early pregnancy with single nucleotide polymorphism microarray (SNP-array).For 520 abortuses, copy number variations (CNVs) in chorionic villi were analyze
Publikováno v:
European Journal of Medical Genetics. 64:104101
N-ethylmaleimide-sensitive factor attachment proteins (NAP: NAPA and NAPB) play a role in Soluble N-ethylmaleimide-sensitive accessory protein receptor (SNARE) complex dissociation and recycling, associated with neuronal regulation and brain developm
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 32(1)
The aim of this study is to explore the cause of miscarriage, providing risk assessment to guide the next pregnancy.Four hundred eighty-four products-of-conception (POC) samples were analyzed by single nucleotide polymorphism (SNP) array, and periphe
Autor:
Xinyu, Yang, Shiyue, Mei, Xiangdong, Kong, Zhenhua, Zhao, Aojie, Cai, Jiameng, Yao, Yiying, Li, Zhi, Qin
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 34(3)
To analyze mutations of IDUA gene in two pedigrees affected with mucopolysaccharidosis type I and provide prenatal diagnosis for them.The 14 exons of the IDUA gene were subjected to PCR amplification and Sanger sequencing.For pedigree 1, the proband