| 1. | Epididymal duct was connected with efferent ducts
输出小管汇合后进入附睾管。 |
| 2. | Treatmeamt of infertile male by percutaneous epididymal sperm aspiration or testicular sperm extraction
附睾或睾丸取精术在男性不育症治疗中的应用 |
| 3. | Application of percutaneous epididymal sperm aspiration and testicular sperm extraction to the diagnosis and treatment of azoospermia
经皮附睾精子抽吸术和睾丸精子获取术在无精子症诊断和治疗中的应用 |
| 4. | The major function of the bovine seminal plasma protein is to accelerating the capacities of bovine epididymal sperm
Bsp蛋白家族是牛精浆的主要蛋白成分。 bsp家族的主要功能是促进精子的顶体反应及获能。 |
| 5. | Compared with the stage of mature , allof genital tubes changed much at the stages of immature and catagenetic . epididymal duct disappeared . the other tubes got smaller
在性未成熟时期和退化时期，附皋管消失，其他各管道变小，勃膜上皮不形成突起。 |
| 6. | Conclusion : seminal carnitine concentration may be an appropriate marker of sperm and epididymal function . l - carnitine / l - acetylcarnitine treatment may be an effective therapy to improve mainly functional seminal parameters
结论：精液中肉碱浓度可能可以作为一个指标用于检测精子和附睾功能。复合服用左旋肉碱加乙酰左旋肉碱，是提高精子质量和数量的主要参数的一种有效治疗方法。 |
| 7. | L - pgds expression was dramatically reduced in all of the rat epididymal regions after castration , which could be restored to control levels by testosterone propionate supplementation . des selectively eliminated mature leydig cells from rat testicular interstitium
大鼠睾丸切除后， l - pgdsmrna和蛋白在附睾各段的表达随手术后时间的增加而逐渐降低，睾酮处理可使其表达恢复。 |
| 8. | In the season of genesis , ( 1 ) testis - net ' s conduit was narrow and it was full of epithelial cell in the conduit . ( 2 ) the epithelial lining of efferent duct appeared phalangeal process and it was filled with secretory product in the efferent duct . ( 3 ) epididymal duct was small and round . it was full of secretory product in the epididymal
生殖殖季节时，精巢网的管腔狭长，腔内充满上皮细胞;输出小管的豁膜上皮呈指状突起，腔内充满脱落的上皮细胞和分泌物;附皋管的管腔较圆且小，腔内充满脱落的上皮细胞和分泌物;输精管的豁膜上皮呈指状突起，肌层明显。 |
| 9. | Primary culture of rat preadipocyte were prepared from the epididymal , inguinal and perirenal the fat pads of male normal , healthy , 15 - 20 days sprague - dawley rats . the preadipocyte grew better under the condition of 37 , 95 % humidity , 5 % co2 , ph 7 . 0 - 7 . 2 , centrifuged at 1000r / min , m199medium , and 10 % fetal bo vine serum , seeded at a density of 4 l04 , 5 l04 , / cm2 . oil red o staining was the special method to distinguish adipocyte from other cells , gimsa and he could determine the stage of the adiopcyte differentiation through the number of lipid drop , size and the position of the nucleolus of the staining fat cell
经过多次实验，确定本实验室大鼠前体脂肪细胞的最佳培养条件是：温度为37 ，湿度为95 ， co _ 2浓度为5 ， ph值为7 . 0 7 . 2 ，离心力为1000r / min ，培养基为m _ ( 199 )培养基，胎牛血清浓度为10 ，合适细胞接种密度为4 10 ~ 4 、 5 10 ~ 4个/ cm ~ 2 ，染色结果表明：油红o染色是鉴定脂肪细胞的特异方法， gimsa和he染色可根据不同区域染色程度、着色差别判断细胞核的位置及脂滴大小、多少，观察大鼠前体脂肪细胞分化过程中的形态变化，进而确定脂肪细胞的分化阶段。 |
