Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Xueping Chen"'
Autor:
Yunpeng Yang, Xueping Chen, Qiongjie Zhou, Qiao Mei Wang, Yiping Zhang, Qun Xu, Zuoqi Peng, Y He, Yan Wang, Xinxiang Li, Xu Ma, Haiping Shen, Donghai Yan, Luhua Wang, Zongyu Xu
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 129:313-321
OBJECTIVE The antenatal screening strategy remains inadequate for eliminating congenital syphilis. To further eliminate maternal fetal transmission, preconception syphilis screening is considered an option. In this study, we investigated syphilis ser
Autor:
Xueping Chen, Ling Chen, Yue Wu, Yangli Zhang, Huili Bai, Xiaosong Li, Changlong He, Chengcheng Wei, Shi Chen, Jun Wen, Yifan Shen
Publikováno v:
Journal of Cancer Research and Clinical Oncology
Background By comparing the detection rate and type of targeted gene mutations in non-small cell lung cancer (NSCLC) between amplification refractory mutation system PCR (ARMS-PCR) and next-generation sequencing (NGS), the characteristics and applica
Autor:
Yongping Chen, Bei Cao, Xueping Chen, Xiaojing Gu, Chunyu Li, Bi Zhao, Huifang Shang, Yanbing Hou, Ying Wu, Kuncheng Liu, Ruwei Ou, Qianqian Wei, Lingyu Zhang, Wei Song
Publikováno v:
Parkinsonism & Related Disorders. 90:105-113
Amounting evidence has suggested the Tripartite Motif (TRIM) family proteins as related to Parkinson's disease (PD). However, many of the risk genes were still awaiting further explorations, and their genetic role in PD has not been investigated yet.
Publikováno v:
Journal of Nursing Management. 27:1546-1553
Aim This study aims to investigate the organisation and the workforce profile in long-term care facilities in Hangzhou City, China. Background Population ageing calls for an increase in the number of high-quality, long-term care services. Therefore,
Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study
Autor:
Yanbing Hou, Ying Wu, Xueping Chen, Yongping Chen, Wei Song, Lingyu Zhang, Chunyu Li, Tao Li, Bi Zhao, Huifang Shang, Qianqian Wei, Xianjun Dong, Bei Cao, Kuncheng Liu, Ruwei Ou, Xiaojing Gu
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 36(9)
Background Age at onset (AAO) is an essential feature of Parkinson's disease (PD) and can help predict disease progression and mortality. Identification of genetic variants influencing AAO of PD could lead to a better understanding of the disease's b
Autor:
Huifang Shang, Lingyu Zhang, Bei Cao, Xueping Chen, Qianqian Wei, Ruwei Ou, Yanbing Hou, Yongping Chen
Publikováno v:
Science China Life Sciences. 62:517-525
Continual discoveries of new genes and unraveling the genetic etiology in amyotrophic lateral sclerosis (ALS) have provided greater insight into the underlying pathogenesis in motor neuron degeneration, as well as facilitating the disease modeling an
Publikováno v:
Clinical Interventions in Aging
Bingbing Liu,1 Xueping Chen,1 Yang Li,1 Hui Liu,2 Shasha Guo,2 Ping Yu3 1Nursing Department, Qianjiang College, Hangzhou Normal University, Hangzhou, China; 2Medicine Department, Hangzhou Normal University, Hangzhou, China; 3School of Computing and I
Autor:
Wei Song, Yanbing Hou, Ying Wu, Yongping Chen, Huifang Shang, Ruwei Ou, Xueping Chen, Bi Zhao, Chunyu Li, Bei Cao, Kuncheng Liu, Xiaojing Gu, Qianqian Wei, Lingyu Zhang, Yi Liu
Publikováno v:
Neurobiology of aging. 101
Members of the transmembrane (TMEM) protein family have been identified to be associated with Parkinson's disease (PD) and other neurodegenerative disorders. However, most studies were based on the European-ancestry population and were still awaiting
Autor:
Yanbing Hou, Ying Wu, Bei Cao, Xiaojing Gu, Xueping Chen, Lingyu Zhang, Wei Song, Qianqian Wei, Ruwei Ou, Tao Li, Chunyu Li, Bi Zhao, Huifang Shang, Yongping Chen
Publikováno v:
Neurobiology of aging. 101
The glycosyltransferase 8 domain containing 1 (GLT8D1) gene was identified to be an amyotrophic lateral sclerosis (ALS)-causative gene via pedigree cosegregation and burden analysis. In the present study, 977 Chinese sporadic ALS (sALS) cases and 47
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Autor:
Yanbing Hou, Xiaoqin Yuan, Xueping Chen, Huifang Shang, Qianqian Wei, Bei Cao, Lingyu Zhang, Ru Wei Ou, Jiao Liu
Publikováno v:
BMC Neurology
BMC Neurology, Vol 20, Iss 1, Pp 1-8 (2020)
BMC Neurology, Vol 20, Iss 1, Pp 1-8 (2020)
Background Spastic paraplegia type 11 (SPG11) mutations are the most frequent cause of autosomal recessive hereditary spastic paraplegia (ARHSP). We are aiming to identify the causative mutations in SPG11 among families referred to our center with AR