Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Shiguo Liu"'
Publikováno v:
Developmental Neurobiology
Ash1l potentially contributes to neurodevelopmental diseases. Although specific Ash1l mutations are rare, they have led to informative studies in animal models that may bring therapeutic advances. Ash1l is highly expressed in the brain and correlates
Autor:
Yinglei Xu, Lu Zhang, Huabin Hou, Cuijiao Wu, Chunlian Wei, Mengmeng Han, Jingli Wang, Shiguo Liu, Ying Chen
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-8 (2020)
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth
Background Gestational diabetes mellitus (GDM) is a pregnancy-specific carbohydrate intolerance Which can cause a large number of perinatal and postpartum complications. The members of Transforming growth factor-β (TGF-β) superfamily play key roles
Publikováno v:
Human Genomics, Vol 14, Iss 1, Pp 1-9 (2020)
Human Genomics
Human Genomics
Background Several genome-wide association studies have identified single-nucleotide polymorphisms (SNPs), such as rs4409766, rs1004467, and rs3824755 in CYP17A1 and rs2021783 in CYP21A2, as new hypertension susceptibility genetic variants in the Chi
Autor:
Fang Wang, Wenmiao Liu, Liangshan Li, Fengqi Wang, Liqin Zhang, Xiuli Wang, Shiguo Liu, Maosheng Gu
Publikováno v:
Endocrine. 72:147-156
Mutations in DUOX2 are the frequent cause of congenital hypothyroidism (CH), a common neonatal metabolic disorder characterized by great phenotypic variability. CH can be traditionally subclassified into two subtypes: thyroid dysgenesis (TD) and thyr
Autor:
Qin Zhou, Mingwei Zhang, Jianjun Zhang, Wei Wei, Kuangyu Li, Wei An, Yafang Zhang, Ping Yang, Shiguo Liu, Yaling Liao, Jialin Liu, Min Chen, Xin Xu, Guowei Zhang, Tao Qin, Fei Xia, Shasha Fang
Publikováno v:
Journal of Medical Virology
This study aims to observe the clinical characteristics of recovered patients from Coronavirus Disease 2019 (COVID-19) with positive in reverse transcription-polymerase chain reaction (RT-PCR) or serum antibody. The profile, clinical symptoms, labora
Autor:
Aiping Chen, Xin Zhao, Congying Li, Xueying Li, Chao Liu, Ru Zhang, Xuewen Jia, Mingzhen Guo, Yan Lin, Huifang Zhao, Jingli Wang, Shiguo Liu, Sai Li, Yuan Li, Jingjing Liu
Publikováno v:
Journal of Immunology Research
Journal of Immunology Research, Vol 2020 (2020)
Journal of Immunology Research, Vol 2020 (2020)
Unbalanced inflammatory reactions and oxidative stress are inseparably interconnected, and both may play crucial roles in the pathophysiological mechanisms of preeclampsia (PE). In the published previous studies, we have genotyped for SNPs that relat
Family-Based Analysis Combined with Case–Controls Study Implicate Roles of PCNT in Tourette Syndrome
Autor:
Hao Deng, Wenmiao Liu, Mingji Yi, Xiumei Liu, Jicheng Dong, Yixia Guo, Shiguo Liu, Ru Zhang, Fan He, Fengyuan Che
Publikováno v:
Neuropsychiatric Disease and Treatment. 16:349-354
Objective Tourette syndrome (TS) is a childhood-onset neuro-developmental disorder and the genetic factors play an important role in its etiology. As pericentrin (PCNT) binds to disruption-in-schizophrenia 1 (DISC1) and is a risk factor for many ment
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:
Yue-Shuai Pan, Zong-Jun Yang, Lu Zhang, Qian Tang, Wei-Qing Song, Li-Li Wei, Yu-Fang Gao, Shiguo Liu, Jing Li
Publikováno v:
Hypertension Research. 43:13-22
Preeclampsia (PE) is a major obstetrical complication that results in maternal and fetal morbidity and mortality. Aberrant epigenetic modifications are widely involved in the pathogenesis of PE. Previously, the activated leukocyte cell adhesion molec
Publikováno v:
Reproductive Biology and Endocrinology : RB&E
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-20 (2021)
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-20 (2021)
Preeclampsia (PE) is an idiopathic disease that occurs during pregnancy. It comprises multiple organ and system damage, and can seriously threaten the safety of the mother and infant throughout the perinatal period. As the pathogenesis of PE is uncle