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Truncating PICK1 Variant Identified in Azoospermia Affected Mitochondrial Dysfunction in Knockout Mice
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作者 yao-qiang du Chong-yi SHU +11 位作者 Min ZHENG Wei-de XU Yue SUN Lu SHEN Chen ZHANG Yu-xin ZHANG Qian-ni WANG Kai-qiang LI Bing-yu CHEN Ke HAO Jian-xin LYU Zhen WANG 《Current Medical Science》 SCIE CAS 2023年第2期313-323,共11页
Objective The protein interacting with C kinase 1(PICK1)plays a critical role in vesicle trafficking,and its deficiency in sperm cells results in abnormal vesicle trafficking from Golgi to acrosome,which eventually di... Objective The protein interacting with C kinase 1(PICK1)plays a critical role in vesicle trafficking,and its deficiency in sperm cells results in abnormal vesicle trafficking from Golgi to acrosome,which eventually disrupts acrosome formation and leads to male infertility.Methods An azoospermia sample was filtered,and the laboratory detection and clinical phenotype indicated typical azoospermia in the patient.We sequenced all of the exons in the PICK1 gene and found that there was a novel homozygous variant in the PICK1 gene,c.364delA(p.Lys122SerfsX8),and this protein structure truncating variant seriously affected the biological function.Then we constructed a PICK1 knockout mouse model using clustered regularly interspaced short palindromic repeat cutting technology(CRISPRc).Results The sperm from PICK1 knockout mice showed acrosome and nucleus abnormalities,as well as dysfunctional mitochondrial sheath formation.Both the total sperm and motility sperm counts were decreased in the PICK1 knockout mice compared to wild-type mice.Moreover,the mitochondrial dysfunction was verified in the mice.These defects in the male PICK1 knockout mice may have eventually led to complete infertility.Conclusion The c.364delA novel variant in the PICK1 gene associated with clinical infertility,and pathogenic variants in the PICK1 may cause azoospermia or asthenospermia by impairing mitochondrial function in both mice and humans. 展开更多
关键词 PICK1 AZOOSPERMIA truncating variant knockout mice mitochondrial dysfunction
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新生儿早发型无乳链球菌感染的风险因素及耐药分析(英文) 被引量:3
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作者 Ying-wei WANG yao-qiang du +9 位作者 Xiao-lin MIAO Guang-yong YE Yi-yun WANG Ai-bo XU Yun-zhong JING Yu TONG Kai XU Mei-qin ZHENG Dong CHEN Zhen WANG 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2018年第12期973-978,共6页
目的:新生儿早发型无乳链球菌(GBS)是一种可致婴儿脑、肺和眼部发生感染甚至死亡的细菌。筛查其感染风险因素并建立概率预测模型有助于疾病的预防和控制,进一步分析GBS菌株的耐药类型和耐药基因,为疾病的临床诊断和治疗提供指导意见。... 目的:新生儿早发型无乳链球菌(GBS)是一种可致婴儿脑、肺和眼部发生感染甚至死亡的细菌。筛查其感染风险因素并建立概率预测模型有助于疾病的预防和控制,进一步分析GBS菌株的耐药类型和耐药基因,为疾病的临床诊断和治疗提供指导意见。创新点:首次归类了新生儿感染GBS的众多因素,按照孕妇、分娩过程、胎儿因素分为三类,统计筛选出重要风险因素并建立Logistic回归的概率预测模型,并通过聚合酶链式反应(PCR)筛查到了相关耐药基因。方法:收集2007年1月至2015年12月,浙江大学医学院附属妇产科医院、温州医科大学附属眼视光医院和温州市人民医院的实验组135例早发型GBS感染和对照组234例无感染的新生儿及其母亲的临床资料和标本,进行数据统计分析并构建概率预测模型,采用传统的药敏实验对所有GBS阳性标本进行耐药分析,同时PCR筛查耐药基因并测定序列。结论:这9年间新生儿早发型GBS感染率呈上升趋势。孕妇泌尿系统感染、胎膜早破、胎龄这三项因素与感染GBS的结局存在显著关联,由此得出的Logistic回归模型可用于预测感染GBS的概率。135株GBS对克林霉素、红霉素、四环素的耐药菌株比例分别为51.11%、80.00%、91.11%,同时未发现对万古霉素、青霉素、呋喃妥因、力奈唑胺的耐药性。PCR筛查发现aac6、ant6-Ⅰ、aph3-Ⅲ和TEM四个耐药基因,其中aph3-Ⅲ仅存在于耐药株中,而测序发现aac6基因在非耐药株中相比耐药株存在一个缺失突变。临床上尽早对患者分离的GBS药敏试验,有助于合理用药和有效治疗。 展开更多
关键词 新生儿 无乳链球菌 风险因素 耐药性
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