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检索条件"主题词= Chinese"
76085 条 记 录,以下是1-10 订阅
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Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals
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Transfusion 2015年 第1期55卷 137-143页
作者: He, Ji Ying, Yanling Hong, Xiaozhen Xu, Xianguo Zhu, Faming Lv, Hangjun Blood Center of Zhejiang Province Key Laboratory of Blood Safety Research of MOH Wulin Road 345 Hangzhou Zhejiang Province 310006 China Key Laboratory of Blood Safety Research Ministry of Health Hangzhou Zhejiang China
Background The frequency and molecular basis of the D variants have been reported in the Caucasian and African populations, but relatively little information was known in the Chinese population. Here, a study was inve... 详细信息
来源: EBSCOASC期刊 EBSCOASC期刊 评论
Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia
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Asian Journal of Andrology 2007年 第1期9卷 57-62页
作者: A Z.-C. Yang Y. Zhang S.-Z. Li N. Zhang W. 2Department of Chemistry and biology Dali College Dali 610041 China 1Department of Medical Genetics West China Hospital Sichuan University and Division of Human Morbid Genomics State Key Laboratory of Biotherapy Chengdu 610041 China 1Department of Medical Genetics West China Hospital Sichuan University and Division of Human Morbid Genomics State Key Laboratory of Biotherapy Chengdu 610041 China 1Department of Medical Genetics West China Hospital Sichuan University and Division of Human Morbid Genomics State Key Laboratory of Biotherapy Chengdu 610041 China 1Department of Medical Genetics West China Hospital Sichuan University and Division of Human Morbid Genomics State Key Laboratory of Biotherapy Chengdu 610041 China
Aim: To analyze the distribution of the single nucleotide polymorphism (SNP) C677T in the methylenetetrahydrofolate reductase (MTHFR) gene in 355 infertile Chinese patients with idiopathic azoospermia or severe oligoz... 详细信息
来源: Wiley期刊 Wiley期刊 评论
Risk factors for the prevalence of musculoskeletal disorders among Chinese foundry workers
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International Journal of Industrial Ergonomics 2005年 第3期35卷 197-204页
作者: Lei, Ling Dempsey, Patrick G. patrick.demspey@libertymutual.com Xu, Jian-guo Ge, Lin-na Liang, You-xin School of Public Health Liberty Mutual SafeWork Center at Fudan University Shanghai 200032 P.R. China Cixi Municipal Center for Disease Control and Prevention Cixi P.R. China Liberty Mutual Research Institute for Safety and Health 71 Frankland Road Hopkinton MA 01748 USA
Abstract: The goal of the study was to investigate risk factors for the prevalence of musculoskeletal symptoms (ache, pain, or discomfort) among foundry workers in China using the standardized Nordic questionnaire. In... 详细信息
来源: ElsevierScienceDirect期刊 ElsevierScienceDirec... EBSCOBSC期刊 EBSCOBSC期刊 评论
HBV 天然免疫的研究进展
Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi
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Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi 2016年 第5期32卷 992-996页
作者: 李凤莉 华 娟 卢银平 杨东亮 华中科技大学同济医学院附属协和医院感染科,感染病与免疫研究所,武汉 430022
When hepatitis B virus( HBV) invades the human body,innate immunity acts the earliest and plays an important role. When an adult is infected with HBV,HBV can often be eliminated spontaneously. However,if HBV infection... 详细信息
来源: EBSCOASC期刊 EBSCOASC期刊 评论
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss
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Biochemical and Biophysical Research Communications;Biochemical and biophysical research communications 2007年 第1期362卷 94-100页
作者: Yuan, Huijun Chen, Jing Liu, Xin Cheng, Jing Wang, Xinjian Yang, Li Yang, Shuzhi Cao, Juyang Kang, Dongyang Dai, Pu Zhai, Suoqiang Han, Dongyi HDY301@263.com Young, Wie-Yen YWY@263.com Guan, Min-Xin min-xin.guan@cchmc.org Institute of Otolaryngology Chinese PLA General Hospital Beijing China. Division of Human Genetics and Center for Hearing and Deafness Research Cincinnati Children's Hospital Medical Center 3333 Burnet Avenue Cincinnati OH 45229-3039 USA. Institute of Otolaryngology Chinese PLA General Hospital Beijing China. Electronic address: HDY301@263.com. Institute of Otolaryngology Chinese PLA General Hospital Beijing China. Electronic address: YWY@263.com. Division of Human Genetics and Center for Hearing and Deafness Research Cincinnati Children's Hospital Medical Center 3333 Burnet Avenue Cincinnati OH 45229-3039 USA Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH USA. Electronic address: min-xin.guan@cchmc.org.
Mutations in mitochondrial DNA are one of the important causes of hearing loss. We report here the clinical, genetic, and molecular characterization of two Han Chinese pedigrees with maternally transmitted aminoglycos... 详细信息
来源: ElsevierScienceDirect期刊 ElsevierScienceDirec... EBSCOASC期刊 EBSCOASC期刊 评论
Association of distal hyperplastic polyps and proximal neoplastic lesions: a prospective study of 5613 subjects
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Gastrointestinal Endoscopy 2016年 第3期83卷 555-562页
作者: Wong, Martin C.S., MD, MPH Ching, Jessica Y.L., MPH Chan, Victor C.W., BSc Lam, Thomas Y.T., MSc Luk, Arthur K.C., BA Wong, Sunny H., PhD Ng, Siew C., PhD Ng, Simon S.M., MD Wu, Justin C.Y., MD Chan, Francis K.L., MD Sung, Joseph J.Y., MD, PhD Institute of Digestive Disease Chinese University of Hong Kong Lui Che Woo Clinical Sciences Building Prince of Wales Hospital Shatin Hong Kong School of Public Health and Primary Care Chinese University of Hong Kong Shatin Hong Kong
Background and Aims Current evidence of whether distal hyperplastic polyps (HPs) are markers of proximal neoplasia (PN) is mixed. We evaluated the association between distal neoplasia and synchronous PN in asymptomati... 详细信息
来源: ElsevierScienceDirect期刊 ElsevierScienceDirec... 评论
Identification of a Novel NHS Mutation in a Chinese Family with Nance-Horan Syndrome
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Current Eye Research 2015年 第4期40卷 434-438页
作者: Li, Aijun Li, Bingzhen Wu, Lemeng Yang, Liping Chen, Ningning Ma, Zhizhong Key Laboratory of Vision Loss and Restoration Ministry of Education Peking University Eye Center Peking University Third Hospital Beijing P. R. China Key Laboratory of Vision Loss and Restoration Ministry of Education Peking University Eye Center Peking University Third Hospital Beijing P. R. ChinaCorrespondencemazzpuh3@163.com
Abstract Purpose: To identiy the disease causing mutation in a Chinese family presenting with early-onset cataract and dental anomalies. Materials and Methods: A specific Hereditary Eye Disease Enrichment Panel (HEDEP... 详细信息
来源: EBSCOASC期刊 EBSCOASC期刊 T&F期刊 评论
无干扰素,口服治疗,全面治愈 ——迈向慢性丙型肝炎治疗新纪元
Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi
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Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi 2015年 第11期31卷 1747-1751页
作者: 胡克勤 美国尔湾加州大学医学中心胃肠/ 肝病科,美国 尔湾 92868
Hepatitis C Virus (HCV) Infection affects approximately 170 million people globally, that causes chronic hepatitis C and has been associated with cirrhosis and hepatocellular carcinoma. In the past few years, signific... 详细信息
来源: EBSCOASC期刊 EBSCOASC期刊 评论
The genetic polymorphisms of POU5F1 gene are associated with psoriasis vulgaris in Chinese
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Journal of Dermatological Science 2007年 第2期46卷 153-156页
作者: Chang Y.-T. Hsu C.-Y. Chou C.-T. Lin M.-W. Shiao Y.-M. Tsai C.-Y. Yu C.-W. Shiue J.-J. Lee Y.-F. Huang C.-H. Chen C.-C. Lee D.-D. Wang W.-J. Liu H.-N. Tsai S.-F. Department of Dermatology Taipei Veterans General Hospital No. 201 Sec. 2 Shih-Pai Road Taipei 11217 Taiwan Department of Dermatology National Yang-Ming University Taipei Taiwan Department of Pathology Taipei Veterans General Hospital No. 201 Sec. 2 Shih-Pai Road Taipei 11217 Taiwan Division of Allergy-Immunology-Rheumatology Taipei Veterans General Hospital No. 201 Sec. 2 Shih-Pai Road Taipei 11217 Taiwan Department of Medical Research and Education Taipei Veterans General Hospital No. 201 Sec. 2 Shih-Pai Road Taipei 11217 Taiwan Institute of Public Health National Yang-Ming University Taipei Taiwan Faculty of Life Sciences Institute of Genome Sciences National Yang-Ming University Taipei Taiwan Department of Dermatology National Defence Medical Center Taipei Taiwan Division of Molecular and Genomic Medicine National Health Research Institutes Taipei Taiwan
来源: ElsevierScienceDirect期刊 ElsevierScienceDirec... 评论
SORL1 gene polymorphism association with late-onset Alzheimer’s disease
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Neuroscience Letters 2015年 584卷 382-389页
作者: Feng, Xialu tjxialu@163.com Hou, Deren hou0718@126.com Deng, Yanyao 530046717@qq.com Li, Wei 750724354@qq.com Tian, Mi 506535410@qq.com Yu, Zhuling 969653601@qq.com Department of Neurology The Third Xiangya Hospital Central South University 138 Tongzipo Road Changsha HN410013 China
Highlights • SORL1 gene, as a candidate gene in lipid metabolic pathways is involved in AD onset. • We examined on the relationship between SORL1 gene and Alzheimer’s disease onset. • SORL1 gene SNPs at rs689021 and ... 详细信息
来源: ElsevierScienceDirect期刊 ElsevierScienceDirec... EBSCOASC期刊 EBSCOASC期刊 评论