Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Yucui Zang"'
Autor:
Jingli Wang, Chengcheng Guan, Jing Sui, Yucui Zang, Yuwen Wu, Ru Zhang, Xiaoying Qi, Shunfu Piao
Publikováno v:
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Xeroderma pigmentosum complementation group C (XPC) is a DNA damage recognition protein that plays an important role in nucleotide excision repair and can reduce oxidative stress, which may be involved in the development of preecl
Externí odkaz:
https://doaj.org/article/f2cd2305238a488cb513c2f492c6d022
Autor:
Fengqi Wang, Yucui Zang, Miaomiao Li, Wenmiao Liu, Yangang Wang, Xiaolong Yu, Hua Li, Fang Wang, Shiguo Liu
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Background: Thyroid dysgenesis (TD), which is caused by gland developmental abnormalities, is the most common cause of congenital hypothyroidism (CH). In addition, advances in diagnostic techniques have facilitated the identification of mild CH patie
Externí odkaz:
https://doaj.org/article/f15a357bba1a4f96ac6854a432dc9497
Autor:
Shiguo Liu, Wenxiu Han, Yucui Zang, Hongwei Zang, Fang Wang, Pei Jiang, Hongwei Wei, Xiangju Liu, Yangang Wang, Xu Ma, Yinlin Ge
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Context: The DUOX/DUOXA systems play a key role in H2O2 generation in thyroid cells, which is required for iodine organification and thyroid hormone synthesis. DUOX2/DUOXA2 defects can cause congenital hypothyroidism (CH), but it is unknown whether D
Externí odkaz:
https://doaj.org/article/86dfd42061694342bf2f401e3b89d134
Autor:
Xiao, Zhang, Miaomiao, Li, Jianhua, Ma, Yucui, Zang, Jingli, Wang, Yinglei, Xu, Lu, Shen, Shiguo, Liu
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(10)
To explore the genetic basis for a child with metachromatic leukodystrophy (MLD).Clinical data of the patient was collected. Genomic DNA was extracted from peripheral blood samples of the child and his family members. Potential variant was screened b
Autor:
Fan He, Wenhan Luo, Zuzhou Huang, Xueying Feng, Yuze Yan, Yanzhao Wei, Fengyuan Che, Mengmeng Han, Chunmei Wu, Yi Zheng, Xue Sun, Hong Xie, Ji-Song Guan, Jinchuan Xing, Xuzhan Zhang, Lang Chen, Ni Ran, Miaomiao Tian, Huanhuan Huang, Jiani Li, Yixia Guo, Hui Li, Hongzai Guan, Mingji Yi, Chuanyue Wang, Lanlan Zheng, Yinlin Ge, Zhaochuan Yang, Tao Zhu, Xueping Zheng, Xiuhai Wang, Xu Ma, Christian P. Schaaf, Fuli Yu, Guiju Wang, Haiyan Wang, Yeting Zhang, Yinglei Xu, Qinan Chen, Zhongcui Jing, Wenmiao Liu, Yucui Zang, Hui Liang, Hao Deng, Shiguo Liu, Xiangrong Sun, Ru Zhang, Jingli Wang
Publikováno v:
Molecular Psychiatry. 25:476-490
Tourette syndrome (TS) is a childhood-onset neuropsychiatric disorder characterized by repetitive motor movements and vocal tics. The clinical manifestations of TS are complex and often overlap with other neuropsychiatric disorders. TS is highly heri
Autor:
Jing Sui, Chengcheng Guan, Yucui Zang, Shunfu Piao, Xiaoying Qi, Jingli Wang, Ru Zhang, Yuwen Wu
Publikováno v:
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-7 (2021)
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-7 (2021)
Background Xeroderma pigmentosum complementation group C (XPC) is a DNA damage recognition protein that plays an important role in nucleotide excision repair and can reduce oxidative stress, which may be involved in the development of preeclampsia (P
Autor:
Jingjing Niu, Liangshan Li, Yangang Wang, Liqin Zhang, Fang Wang, Dehua Zhao, Maosheng Gu, Hui Zou, Wei Li, Longfang Xu, Fengqi Wang, Miaomiao Li, Yucui Zang, Weibing Tian, Yulin Zhou, Wenbin Zhu, Quanqi Zhang, Shiguo Liu
Publikováno v:
SSRN Electronic Journal.
Autor:
Fuyan Lv, Chengyu Yang, Fang Wang, Shengli Yan, Yucui Zang, Miaomiao Li, Shiguo Liu, Wenmiao Liu, Hongwei Zang, Zhixia Zhou
Publikováno v:
Journal of Cellular Biochemistry. 119:9474-9482
Thyroid dysgenesis (TD) accounts for most cases of congenital hypothyroidism. Although mutations in thyroid hormone receptor β (THRB) have been identified in TD, the mutational spectrum of THRB and phenotype-genotype correlations have not been fully
Autor:
Qian Tang, Yucui Zang, Fengqi Wang, Dehua Zhao, Fang Wang, Xiuli Wang, Wenmiao Liu, Shiguo Liu, Lu Zhang, Miaomiao Li
Publikováno v:
Endokrynologia Polska. 71(2)
Introduction: Thyroid dysgenesis (TD) is the main cause of congenital hypothyroidism (CH), affecting nearly 1 in 2000–3000 newborns worldwide, as the most common neonatal endocrine disorder. Paired box gene 8 ( PAX8 ), expressed during all stages o
Autor:
Yuze Yan, Yinlin Ge, Hui Liang, Tao Zhu, Jingli Wang, Yanzhao Wei, Xueping Zheng, Fuli Yu, Yinglei Xu, Xu Ma, Zhongcui Jing, Xiuhai Wang, Haiyan Wang, Christian P. Schaaf, Wenmiao Liu, Chunmei Wu, Zhaochuan Yang, Yeting Zhang, Huanhuan Huang, Miaomiao Tian, Zuzhou Huang, Qinan Chen, Ru Zhang, Xue Sun, Hongzai Guan, Lanlan Zheng, Chuanyue Wang, Ni Ran, Ji-Song Guan, Yixia Guo, Hui Li, Jinchuan Xing, Shiguo Liu, Hao Deng, Mingji Yi, Xueying Feng, Mengmeng Han, Wenhan Luo, Jiani Li, Guiju Wang, Yucui Zang, Xiangrong Sun, Xuzhan Zhang, Lang Chen, Fan He, Fengyuan Che, Yi Zheng, Hong Xie
Publikováno v:
Molecular Psychiatry. 25:241-242