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Carbon nanomaterials affect carbon cycle-related functions of the soil microbial community and the coupling of nutrient cycles 期刊论文
JOURNAL OF HAZARDOUS MATERIALS, 2020, 卷号: 390
Authors:  Wu, Fan;  You, Yaqi;  Werner, David;  Jiao, Shuo;  Hu, Jing;  Zhang, Xinyu;  Wan, Yi;  Liu, Junfeng;  Wang, Bin;  Wang, Xilong
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Carbon nanomaterials  ORGANIC-COMPOUNDS  Soil microbial community  ENZYME-ACTIVITY  Nutrient cycle  NANOTUBES  Coupling of nutrient cycles  NITROGEN  Metagenomics  PHOSPHORUS  Gene networks  TOXICITY  IMPACT  CYTOTOXICITY  ENVIRONMENT  MECHANISMS  
Congenital muscular dystrophies in China 期刊论文
CLINICAL GENETICS, 2019, 卷号: 96, 期号: 3, 页码: 207-215
Authors:  Ge, Lin;  Zhang, Cheng;  Wang, Zhaoxia;  Chan, Sophelia H. S.;  Zhu, Wenhua;  Han, Chunxi;  Zhang, Xiaoli;  Zheng, Hong;  Wu, Liwen;  Jin, Bo;  Shan, Jingli;  Mao, Bing;  Zhong, Jianmin;  Peng, Xiaoyin;  Cheng, Yaying;  Hu, Jun;  Sun, Yan;  Lu, Junlan;  Hua, Ying;  Zhu, Sainan;  Wei, Cuijie;  Wang, Shuo;  Jiao, Hui;  Yang, Haipo;  Fu, Xiaona;  Fan, Yanbin;  Chang, Xingzhi;  Wang, Shuang;  Bao, Xinhua;  Zhang, Yuehua;  Wang, Jingmin;  Wu, Ye;  Jiang, Yuwu;  Yuan, Yun;  Rutkowski, Anne;  Bonnemann, Carsten G.;  Wei, Wei;  Wu, Xiru;  Xiong, Hui
Favorite  |  View/Download:3/0  |  Submit date:2019/09/23
Congenital Muscular Dystrophy  Founder Mutation  Nationwide Population Study  Prevalence  Prevalence  Diagnosis  Phenotype  Etiology  Genotype  Spectrum  Disease  
心肺复苏后严重心功能不全患者目标温度管理治疗2例并文献复习 期刊论文
临床急诊杂志, 2019, 卷号: 20, 期号: 1, 页码: 36-39
Authors:  陈玉娇;  马青变;  李硕;  杜兰芳;  李姝
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目标温度管理  心肺复苏  心肌保护  心功能  
Body mass index and basal androstenedione are independent risk factors for miscarriage in polycystic ovary syndrome 期刊论文
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2018, 卷号: 16
Authors:  Yang, Wan;  Yang, Rui;  Lin, Mingmei;  Yang, Yan;  Song, Xueling;  Zhang, Jiajia;  Yang, Shuo;  Song, Ying;  Li, Jia;  Pang, Tianshu;  Deng, Feng;  Zhang, Hua;  Wang, Ying;  Li, Rong;  Jiao, Jie
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Gonadotropin-releasing hormone antagonist  Polycystic ovary syndrome  Hyperandrogenism  Body mass index  In vitro fertilization  
Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing 期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
Authors:  Fu, Xiaona;  Yang, Haipo;  Jiao, Hui;  Wang, Shuo;  Liu, Aijie;  Li, Xiaoqing;  Xiao, Jiangxi;  Yang, Yanling;  Wu, Xiru;  Xiong, Hui
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FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies 期刊论文
JOURNAL OF HUMAN GENETICS, 2016, 卷号: 61, 期号: 12, 页码: 1013-1020
Authors:  Fu, Xiaona;  Yang, Haipo;  Wei, Cuijie;  Jiao, Hui;  Wang, Shuo;  Yang, Yanling;  Han, Chunxi;  Wu, Xiru;  Xiong, Hui
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Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients 期刊论文
BRAIN & DEVELOPMENT, 2015, 卷号: 37, 期号: 9, 页码: 880-886
Authors:  Yang, Haipo;  Kobayashi, Kazuhiro;  Wang, Shuo;  Jiao, Hui;  Xiao, Jiangxi;  Toda, Tatsushi;  Wu, Xiru;  Xiong, Hui
Adobe PDF(1248Kb)  |  Favorite  |  View/Download:12/0  |  Submit date:2016/10/21
Fukuyama Congenital Muscular Dystrophy  Fktn  3-kb Insertion  Haplotype Analysis  Founder Mutation  
Walker-Warburg综合征的临床表型与POMT1基因突变分析 期刊论文
中华实用儿科临床杂志, 2014, 卷号: 29, 期号: 5, 页码: 368-370
Authors:  杨海坡;  王硕;  焦辉;  肖江喜;  熊晖
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先天性肌营养不良  Walker-warburg综合征  Pomt1基因  Congenital Muscular Dystrophy  Walker-warburg Syndrome  Pomt1 Gene  
Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients 期刊论文
MOLECULAR GENETICS AND GENOMICS, 2013, 卷号: 288, 期号: 7-8, 页码: 297-308
Authors:  Jiao, Hui;  Manya, Hiroshi;  Wang, Shuo;  Zhang, Yanzhi;  Li, Xiaoqing;  Xiao, Jiangxi;  Yang, Yanling;  Kobayashi, Kazuhiro;  Toda, Tatsushi;  Endo, Tamao;  Wu, Xiru;  Xiong, Hui
Adobe PDF(835Kb)  |  Favorite  |  View/Download:6/0  |  Submit date:2016/11/04
Muscle-eye-brain Disease  Pomgnt1 Mutation  Alpha-dystroglycanopathy  Enzyme Activity  
一个正常血钾型周期性瘫痪家系临床及分子遗传学研究 期刊论文
中华儿科杂志, 2013, 卷号: 51, 期号: 1, 页码: 47-51
Authors:  魏翠洁;  汪东;  王硕;  焦辉;  洪道俊;  蒲利华;  熊晖
Favorite  |  View/Download:7/0  |  Submit date:2016/04/25
离子通道病  常染色体显性  正常血钾型周期性瘫痪  Channelopathies  Autosomal Dominant  Normokalemic Periodic Paralysis