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   azoospermia 在 泌尿科学 分类中 的翻译结果: 查询用时:0.012秒
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azoospermia     
相关语句
  无精子症
    Study of CFTR Gene Mutations and Testicular Ultrastructure and ICSI of Congenital Obstructive Azoospermia
    先天性梗阻性无精子症患者CFTR基因突变及其睾丸超微结构的研究和ICSI治疗的临床观察
短句来源
    ETIOLOGICAL DIAGNOSIS OF 263 CASES OF AZOOSPERMIA
    无精子症263例病因诊断分析
短句来源
    Azoospermia: Analysis of 21 Cases with Deferentiovesiculography
    无精子症精路造影21例分析
短句来源
    Analysis of the disease causes and diagnostic and treating experience in 126 cases of azoospermia
    126例无精子症病因分析和诊治体会
短句来源
    Methods Detect the chromosome and serum reproductive hormones of 86 azoospermia cases and 35 normal controls.
    方法:检测86例无精子症患者与35例正常对照男性的外周血染色体、血清生殖激素(FSH、LH、T、PRL、T/LH);
短句来源
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  无精症
    Study on Testicular Multibiopsy and Quantitative Determination of Expression of the Protamine-2 and hspA2 mRNA of Testicular Tissue in Patients with Azoospermia
    无精症患者睾丸组织多点活检及测定鱼精蛋白-2与hspA2 mRNA表达量的意义
短句来源
    Analysis of YRRM gene in azoospermia
    YRRM1基因检测在无精症病因分析中的应用
短句来源
    Conclusion AZF microdeletion is one of the important cause of nonobstructive azoospermia.
    结论AZF微缺失导致男性非梗阻性无精症的重要原因之一。
短句来源
    Study on YRRM1,DYS240 genes and karytype in the 5 patients with azoospermia
    5例无精症病人染色体核型及YRRM1、DYS240基因检测
短句来源
    Cloning of the idiopathic azoospermia related genes with mRNA differential display method
    mRNA差异显示法克隆原发无精症相关基因
短句来源
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  无精子
    Pathological analysis of 104 cases with azoospermia infertility by testicular biopsy
    104例无精子不育症睾丸活检病理分析
短句来源
    MethodsMultiplex PCR amplification of 6 sequence-tagged sites in AZF regions of the Y chromosome was examined among 100 normal karyotype male patients with azoospermia or oligozoospermia.
    方法:采用多重PCR技术,对100例染色体核型正常的、无精子症和少弱精子症患者Y染色体无精子因子(azoospermia factor,AZF)区域的6个序列标签位点进行检测。
短句来源
    PCR screening of AZF microideletion in patients with azoospermia and sever oligozoospermia
    无精子和严重少精子患者Y染色体AZF微缺失的PCR筛查
短句来源
    Analysis on the result of testis and reproductive hormones measurement in 272 azoospermia patients.
    272例无精子男性睾丸与生殖激素测量结果分析
短句来源
    Screening of AZF microdeletion in the patients with azoospermia or severe oligozoospermia
    严重少精、无精患者无精子因子(AZF)的检测及意义
短句来源
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  精子缺乏
    Etiology of azoospermia in a large nonreferral inner-city population
    在大规模非转诊城内人群中精子缺乏的病因学
短句来源

 

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  azoospermia
The highest frequency of abnormal karyotypes (10%) was found among patients with azoospermia and the most frequent anomaly was 47, XXY chromosomal constitution, found in 6 (8.57%) patients.
      
All patients with numerical chromosomal anomalies had azoospermia.
      
We suggest that men with azoospermia should be considered for cytogenetic investigation and we report that "variants of the Y chromosome" have no influence on the sperm count (million/ml) and fertility of men.
      
The frequencies of AZF deletions in patients with azoospermia and severe oligozoospermia amounted to 12.2 and 8.1%, respectively.
      
Ninety patients with normal cytogenetic findings with azoospermia and severe oligozoospermia were included in the study.
      
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Testicular dysfunction is one of the primary causes of male infertility.Ultrastruc-tural observation of testicular biopsies provides useful approach to the diagnosis of male in-fertiaity.This paper presents an ultrastructural study on tesicular biopsies from 25 caseswith oligospermia or azoospermia.Five kinds of changes were noted in the limiting mem-brane of the seminiferous tubule:(1)thickening and layering of the basal lamina or fold-ing into the seminiferous tubule;(2)thickening of the peritubular...

Testicular dysfunction is one of the primary causes of male infertility.Ultrastruc-tural observation of testicular biopsies provides useful approach to the diagnosis of male in-fertiaity.This paper presents an ultrastructural study on tesicular biopsies from 25 caseswith oligospermia or azoospermia.Five kinds of changes were noted in the limiting mem-brane of the seminiferous tubule:(1)thickening and layering of the basal lamina or fold-ing into the seminiferous tubule;(2)thickening of the peritubular tissue resulting fromincseased intercellular matenials;(3)degeneration of myoid cells;(4)widening of the limit-ing membrane due to diffuse deposition of basement membranoid substance;(5)mast cellsexisting in the lim(?)ting membrane.The endothelial cells of small blood vessels showed sig-nificant thickening,which led to progressive encroachement upon the lumen.The Ser-toli cells contained large amounts of lipid droplets and two kinds of Sertoli cells could beseen:mature and immature Sertoli cells.The mature sertoli cells were joined by typicalSertoli-Sertoli junctions,while the immature Sertoli cells were connected simply by inter-digitating processes and without any blood-testis barrier.The possible significance of thesechanges was discussed.

本文对25例男性不育症患者的睾丸活检组织进行了超微结构观察。结果表明不育症患者睾丸曲细精管界膜有显著变化,主要为界膜增厚、界膜纤维化、基膜样物质沉积、肌样细胞变性及肥大细胞增多。间质中可见结缔组织增生或小血管内皮细胞肿胀。支持细胞有空泡变性,支持细胞综合症患者的支持细胞呈未成熟型,支持细胞间未形成复合连接,而在其它病例,则有血睾屏障存在。

Certain effect of gossypol has been proved clinically on man's fertility. In order to study the reverslbility of fertility,regular semen examinations after withdrawl of gossypol were made.The subjects were followed up for an average of 3_(12)~1 years(1~6.5 years).The results revealed an azoospermia rate ot 5.42%(18/332).It is likely that gossypol exerts a sterilizing offect on a few subjects.

临床应用棉酚节制男子生育已取得了肯定的效果.为了探讨棉酚节制生育的可逆性,作者对停服棉酚者进行了定期的精液检查,332例平均随访3 1/(12)年(1~6.5年),18例(5.42%)精子数始终为0或接近于0,提示棉酚可能对少数服药者呈绝育作用.

C-band heteromorphism was studied quantitatively in 80 cases of infertile males, 30 cases of normal fertile males and 12 members of Yqh+ bearing families. Relative lengths of qh/16p ratios of 1, 9, 16, and the Y chromosome were measured by a computerized micro-videomat system. The popular frequencies of 1qh+ and 9qh+in infertile males were similar to those in fertile males; Yqh/16p relation lengths were of the 3rd level in both groups; Yqh+ frequencies of both groups were significantly different (16.25% and...

C-band heteromorphism was studied quantitatively in 80 cases of infertile males, 30 cases of normal fertile males and 12 members of Yqh+ bearing families. Relative lengths of qh/16p ratios of 1, 9, 16, and the Y chromosome were measured by a computerized micro-videomat system. The popular frequencies of 1qh+ and 9qh+in infertile males were similar to those in fertile males; Yqh/16p relation lengths were of the 3rd level in both groups; Yqh+ frequencies of both groups were significantly different (16.25% and 26.67% respectively). No positive correlation between size of testis, azoospermia and oligozoospermia etc. in male infertility were observed. 12 males from families carrying Yqh+ were fertile (except Yqh+ probans with infertility). Indicating that Yqh+ is not a direct cause of male infertility.

对80例不育男性和30例正常生育男性及12例Yqh~+携带者家系作了染色体C带异态性定量研究。用显微图象测量仪微机控制半自动描迹测量1、9、16和Y染色体的qh/16p相对长度比率。不育组和生育组1qh~+和9qh~+群体频率接近;两组Yqh/16p众数均为3级;两组Yqh~+频率(16.25%和26.67%)虽有差异,但与不育表型(睾丸大小、无精、少精等)并无正相关。12例家系男性Yqh~+携带者都能生育(不育男性Yqh~+先证者除外),表明Yqh~+并不直接导致男性不育。

 
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