日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Microbiome and metabolite signatures for cirrhosis to HCC risk stratification: progress, controversies, and gaps

微生物组和代谢物特征在肝硬化至肝细胞癌风险分层中的应用:进展、争议和差距

Duan, Yanan; Yang, Mengting; Li, Miaomiao; Sun, Yu; Liu, Shiguo

Characteristics of glucose-6-phosphate dehydrogenase mutations in newborns with deficiency from 2021 to 2022 in the Heze area of China

2021年至2022年中国菏泽地区新生儿葡萄糖-6-磷酸脱氢酶缺乏症基因突变特征

Zhang, Xin; Duan, Yanan; Zhang, Xiao; Li, Miaomiao; Li, Ling; Zhang, Renwei; Liu, Shiguo

Identification of common hub genes and construction of immune regulatory networks in aplastic anemia, myelodysplastic syndromes, and acute myeloid leukemia

鉴定再生障碍性贫血、骨髓增生异常综合征和急性髓系白血病中的共同枢纽基因并构建免疫调节网络

Shan, Mingliang; Xu, Li; Yang, Wenzhe; Sui, Lili; Sun, Ping; Zhuo, Xiumei; Liu, Shiguo

Identification of hub genes in congenital hypothyroidism and construction of the associated immune regulatory network

先天性甲状腺功能减退症关键基因的鉴定及相关免疫调节网络的构建

Shan, Mingliang; Xu, Li; Yang, Wenzhe; Liu, Shiguo

Corrigendum: Identification of hub genes and immune-related pathways in acute myeloid leukemia: insights from bioinformatics and experimental validation

更正:急性髓系白血病中枢基因和免疫相关通路鉴定:来自生物信息学和实验验证的见解

Shan, Mingliang; Xu, Li; Yang, Wenzhe; Liu, Shiguo; Cui, Zhaoqing

Relationship between TYG mediated pregnancy diabetes history and SII in American women: a retrospective cohort study of NHANES 2011-2018

TYG介导的妊娠糖尿病史与美国女性SII的关系:一项基于NHANES 2011-2018的回顾性队列研究

Duan, Yanan; Zhang, Ru; Zhang, Yan; Ma, Yuanxuan; Li, Miaomiao; Zhang, Wenke; Liu, Shiguo

Perioperative management of severe factor VII deficiency: a single-center experience in China

重度VII因子缺乏症的围手术期管理:中国单中心经验

Zhu, Chao; Zhao, Jinxia; Xu, Longqiang; Lu, Wenfei; Liu, Shiguo; Guan, Jialiang

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation

基于人群和家族验证的rs9789446基因型作为先天性甲状腺功能减退症的易感生物标志物

Zhong, Xue; Jia, Yaning; Liu, Wenmiao; Qiao, Mengfei; Li, Miaomiao; Yu, Xiaolong; Liu, Shiguo

Novel compound heterozygous DOCK6 variants expand the mutational spectrum in prenatal diagnosis of Adams-Oliver syndrome 2

新型复合杂合DOCK6变异体扩展了Adams-Oliver综合征2产前诊断的突变谱

Zhong, Xue; Zheng, Xuan; Xv, Yinglei; Cai, Kangxi; Wang, Qianqian; Liu, Shiguo

Identification of Novel IL-10RA Variant in Infantile-Onset Inflammatory Bowel Disease: A Case Series With Preliminary Genotype-Phenotype Correlation From Two Chinese Families

婴儿期发病炎症性肠病中新型IL-10RA变异体的鉴定:来自两个中国家庭的病例系列及初步基因型-表型相关性分析

Guan, Chengcheng; Ma, Yuanxuan; Zhang, Xiao; Zhang, Ru; Jiang, Yingjun; Liu, Shiguo