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血小板扫描电镜
platelet scanning microscopic
Observation of Platelet Scanning Microscopic Structure of Patients with Stagnation of Blood in Coronary Heart Disease 冠心病血瘀证患者血小板扫描电镜形态观察 短句来源 “血小板扫描电镜”译为未确定词的双语例句
ELECTRON MICROSCOPIC SCANNING OF PLATELETS AND DYNAMIC CHANGES OF SERUM 5-HT AND 5-HIAA IN HEMORRHAGICALLY SHOCKED DOGS 失血性休克犬血小板扫描电镜与血清5-HT、5-HIAA含量动态变化 短句来源 Scanning electron microscopic observation of platelets in normal rabbits 正常家兔血小板扫描电镜研究 短句来源 SCANNING ELECTRON MICROSCOPIC OBSERVATION OF PLATELETS IN EXPERIMENTAL DIABETIC RATS 实验性糖尿病大鼠血小板扫描电镜观察 短句来源 相似匹配句对
Scanning electron microscopic observation of platelets in normal rabbits 正常家兔血小板扫描电镜研究 短句来源 Scanning electron microscopic observation on platelets adhered to vessel wall 血小板与血管壁粘附的扫描电镜观察 短句来源 ②SEM. ②扫描电镜。 短句来源 Study of Cryopreservation of Human Platelets 血小板冷冻保存的研究 短句来源 SCANNING ELECTR ON MICR OSCOPIC OBSERVATION OF PARAMECIA 草履虫的扫描电镜观察 短句来源 
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Twelve adult hybrid dogs were used as the reconstructed model of hemor-rhagic shock.Arterial blood pressure was kept at 5.3-6.7 kPa by bleeding and infusion.The results showed that before bleeding, morphology of the platelets was normal without aggregation, at the first hour after bleeding, enlargement of the volume, reduction in the number of pseudopodia and mild degree of aggregation of the platelets were noticed, at the third hour after bleeding, not only the platelets became markedly enlarged and the nu... 以12只成年杂种犬复制失血性休克动物模型,经三通颈动脉插管放血至平均动脉血压于5.3～6.7kPa,在实验过程中经放、输血,使血压维持于该水平。血小板扫描电镜观察结果,失血前血小板形态正常、无聚集;失血后1h血小板体积明显胀大,伪足减少可见轻微聚集;失血后3h血小板不仅明显肿胀、伪足减少,而且聚集成团;失血后5h血小板聚集成团块,体积缩小,伪足消失,呈崩解型。血清5—HT含量,自失血后第2h起显著地高于失血前水平。5-HIAA含量,自失血后第3h起高于失血前水平(P<0.01)。 文摘来源 Objective The Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency caused by mutations in the WAS protein (WASP) gene. The disease is characterized by recurrent infections, eczema, and thrombocytopenia with small platelets, and it is known to be associated with extensive clinical variability, and mutation studies indicated that genotypes are also highly variant among WAS patients. The present study was conducted to identify the mutation types of Wiskott-Aldrich syndrome protein (WASP) ... 目的 明确 3例Wiskott Aldrich综合征 (WAS)患儿WAS蛋白 (WASP)基因突变的类型。方法 根据典型临床表现 (血小板减少、湿疹、反复感染 ) ,及淋巴细胞和血小板扫描电镜改变 ,采用PCR直接测序法 ,对 3例疑为WAS的患儿及其母亲的WASP基因进行序列分析。结果 以正义、反义引物扩增的PCR产物分别测序 ,发现两种新型WASP基因突变 :2例WAS孪生兄弟WASP基因第 10外显子 ,第 984位核苷酸C缺失突变 (984delC) ,导致 317位密码子后移码突变 ,于 4 4 4位密码子提前出现终止密码 (H317fsX4 4 4 ) ;其母亲为此突变WASP基因携带者。另 1例WAS患儿WASP基因第 11外显子 ,第 1388位核苷酸由G替换为T(1388G→T) ,为无义突变 ,使第 4 5 2位密码子提前变为终止密码(E4 5 2X)。其母亲无此突变WASP基因。结论 鉴定出两种新型WASP基因突变 ,WASP基因序列分析对于不典型和散发WAS的诊断及WASP突变基因携带者的检出有重要作用。 文摘来源 To explore the value of the clinical and genetic diagnosis for Wiskott-Aldrich syndrome(WAS).Methods Nine boys with clinical diagnosis of Wiskott-Aldrich syndrome,aged from 37 days to 3 years and 6 months,were recruited in this study.Scoring of the phenotype,analysis of the peripheral blood,immunological test,bone marrow examination,and scanning electron microscope(SEM) were done.While analysis of the WASP gene sequence by using PCR directed sequencing in 4 Wiskott-Aldrich syndrome patients and their moth... 目的探讨Wiskott-Aldrich综合征(WAS)的临床和基因诊断价值。方法对9例WAS患儿作临床表型评分和血常规、免疫学、骨髓常规、扫描电镜检查,并用PCR直接测序法分析4例患儿及其母亲基因组DNA中WAS蛋白(WASP)基因序列。结果9例患儿均为典型WAS,评4分,家庭史阳性者诊断年龄早于家族史阴性者;免疫学结果差异大;骨髓常规易误诊“特发性血小板减少性紫癜”,5例WAS患儿淋巴细胞、血小板扫描电镜有典型异常,其中4例存在WASP基因突变:缺失突变2例(984delC,P317fsX444),无义突变1例(1388G>T,E452X),拼接错误1例(IVIS+1G>T)。结论对怀疑WAS患儿应仔细询问家族史,临床评分,作扫描电镜检查可提高WAS的临床诊断准确率;WASP基因分析可确诊患者,发现携带者,为干细胞移植治疗患者提供依据。 文摘来源 << 更多相关文摘 
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