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Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (pMet281Thr) 其他
检验科, Hamostaseologie;, 2020, 卷号: 40, 期号: 5, 页码: 687-690
作者:  Liu, Siqi;  Luo, Shasha;  Yang, Lihong;  Wang, Mingshan;  Jin, Yanhui
收藏  |  浏览/下载:21/0  |  提交时间:2023/12/08
Low Expression MCEMP1 Promoting Lung Adenocarcinoma Progression by and its Clinical Value 期刊论文
检验科, CURRENT CANCER DRUG TARGETS, 2024
作者:  Ling, Liqun;  Hu, Tianqi;  Zhou, Chenkang;  Chen, Shuhui;  Chou, Lunan
收藏  |  浏览/下载:13/0  |  提交时间:2024/05/20

A BERT-based approach for identifying anti-inflammatory peptides using sequence information 期刊论文
Wenzhou Medical University The First Clinical Medical Department of Clinical Laboratory, HELIYON, 2024, 卷号: 10, 期号: 12
作者:  Xu, Teng;  Wang, Qian;  Yang, Zhigang;  Ying, Jianchao
收藏  |  浏览/下载:16/0  |  提交时间:2024/07/10

First report of multidrug-resistant Escherichia coli isolates co-harbouring mcr-1 and bla(OXA-48) from clinical patients in China 其他
检验科, JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE, 2018, 卷号: 13, 页码: 94-95
作者:  Lu, Hong;  Zhang, Xiaoxiao;  Zhang, Yizhi;  Liu, Haiyang;  Xu, Chunquan
收藏  |  浏览/下载:39/0  |  提交时间:2022/03/30
Prevalence and characterisation of extended spectrum beta-lactamases genes in Shigella isolates, in Wenzhou, Southern China 其他
Wenzhou Medical University School of Laboratory Medicine, INDIAN JOURNAL OF MEDICAL MICROBIOLOGY, 2014, 卷号: 32, 期号: 1, 页码: 95-96
作者:  Cao, J.;  Zhang, X.;  Zhou, T.;  Lu, Y.;  Hou, J.
收藏  |  浏览/下载:15/0  |  提交时间:2022/03/30
Genome Sequence of the Human-Pathogenic Bacterium Vibrio vulnificus Type Strain ATCC 27562 (vol 194, pg 6954, 2012) 其他
Wenzhou Medical University The First Clinical Medical Department of Clinical Laboratory, JOURNAL OF BACTERIOLOGY, 2013, 卷号: 195, 期号: 7, 页码: 1622-1622
作者:  Li, Zhaoyun;  Chen, Huihong;  Chen, Xianjun;  Zhou, Tieli;  Zhao, Lei
收藏  |  浏览/下载:4/0  |  提交时间:2022/03/30
Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr) 其他
检验科, HAMOSTASEOLOGIE, 2020, 卷号: 40, 期号: 5, 页码: 687-690
作者:  Liu, Siqi;  Luo, Shasha;  Yang, Lihong;  Wang, Mingshan;  Jin, Yanhui
收藏  |  浏览/下载:14/0  |  提交时间:2022/03/30
Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication 其他
Wenzhou Medical University The First Clinical Medical Department of Clinical Laboratory, THROMBOSIS AND HAEMOSTASIS, 2011, 卷号: 106, 期号: 1, 页码: 180-181
作者:  Zheng, Fangxiu;  Jin, Yanhui;  Wang, Mingshan;  Niu, Zhenzhen;  Xu, Pengfei
收藏  |  浏览/下载:39/0  |  提交时间:2022/03/30
Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency 期刊论文
Wenzhou Medical University The First Clinical Medical Department of Clinical Laboratory, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2013, 卷号: 30, 期号: 3, 页码: 313-7.
作者:  Haixiao Xie;  Meiyan Lv;  Xiaoli Yang;  Liqing Zhu;  Lihong Yang
收藏  |  浏览/下载:13/0  |  提交时间:2022/04/08

ILver stiffness measurement: An alternative practical predictor for early kidney dysfunction in patients with non-alcoholic fatty liver disease 会议论文
Wenzhou Medical University First Affiliated Hospital, JOURNAL OF HEPATOLOGY, Vienna, AUSTRIA, APR 10-14, 2019
作者:  Sun, D. Q.;  Ye, Fang-Zhou;  Haluk Tarik, Kani;  Zheng, Chen-Fei;  Zhu, Pei-Wu
收藏  |  浏览/下载:85/0  |  提交时间:2022/03/28