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spermatozoa相关的网络例句

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与 spermatozoa 相关的网络例句 [注:此内容来源于网络,仅供参考]

The spermatozoa are embeded in a extracellalar matrix composed of high dense fibrils matrix and flocculent and concentric vesicles similar to that in the primary spermatophore layer, but the later lack of spermotozoa. The flocculent and concentric vesicles are often seen to release their contents around the main body of spermatozoa. The spermatozoa may absorb the contents to form vesicular zone and membrane zone in sperm nucleu. The secondary spermatophore layer is distinctly subdivided into inner region and outer region. The loose outer region consists of canaliculated reticulum and large flocculent vesicles.

输精管内的精荚为管状,由精子群、精荚基质及初级精荚壁和次级精荚壁组成,初级精荚壁与精荚基质是相连续的,它们之间无明显界限,两者均由电子密度较高的纤丝状基质和絮状泡和同心圆泡组成,但后者不含精子,后者中的絮状泡和同心圆泡常在精子主体部周围释放内含物,可能与形成精子细胞核中的泡状带和膜状带有关,在交配后的雌虾,其头胸部腹面上粘着的精荚中,其基质内已不见絮状和同心圆泡,仅见稀疏的纤丝。

The effects of cryopreservation (-196℃) on the antioxidant activities of enzymes (SOD, CAT, GSH-PX and GR) in seminal plasma and spermatozoa of Russian sturgeon Acipenser gueldenstaedti were studied by a reagent kit to clarify damage mechanism of spermatozoa.

为了探讨超低温(-196℃)对精子的损伤机理,采用试剂盒测定了冷冻前后俄罗斯鲟精浆和精子中超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和谷肽甘肽还原酶等酶活性。

Pregnancies resulted from 11 ICSI cycles with semen spermatozoa and 4 from 12 cycles with epididymal or testicular spermatozoa.

其中11例11个治疗周期采用精液精子行ICSI,4例妊娠;12例12个治疗周期采用附睾精子或睾丸精子,4例妊娠。

Inhibition of PP1 gamma 2 causes motility initiation in immature spermatozoa and motility stimulation and changes in flagellar beat parameters in mature spermatozoa.

抑制PP1γ2会起始未成熟精子的运动并刺激和改变成熟精子的鞭毛运动参数。

Results: The results showed that:(1) The three types of NOS immunoreactivity were not found in rat testis until 30 days after birth;(2) NOS1 immunoreactivity was found in a few spermatocytes in rat testes on postnatal 30 days, and in spermatozoa present at the lumen surface of seminiferous tubules and some Leydig cells on postnatal 60 days;(3) NOS2 immunoreactivity appeared in a few spermatocytes, Sertoli cells and peritubular myoid cells on postnatal 30 days. On postnatal 60 days, NOS2 immunoreactivity appeared in some Leydig cells, peritubular myoid cells, Sertoli cells, very few spermatocytes and the head of immature spermatozoa in some seminiferous tubules;(4) NOS3 immunoreactivity was detected in a few spermatocytes on postnatal 30 days, as well as in the smooth muscle cells of blood vessels on postnatal 30 days and 60 days.

结果:(1)生后4、7、14 d大鼠睾丸未见3种NOS免疫阳性反应;(2)生后30 d少数精母细胞及生后60 d生精小管腔面精子和间质细胞呈NOS1阳性;(3)生后30 d少数精母细胞、支持细胞和管周类肌细胞呈NOS2阳性,而生后60 d NOS2阳性反应见于睾丸间质细胞、管周类肌细胞、支持细胞、极少数精母细胞和不成熟精子头部;(4)生后30 d睾丸内少数精母细胞和血管壁呈NOS3阳性,生后60 d NOS3阳性反应仅见于血管壁。

The testis index, testis volumes were same as the annual changes of testis mass. The curves of annual variation were all unimodality.2 The spermatogenetic cycle of Myospalax cansus comprises seven stages with significant features: Stage I , from February to April, the testis were at the stage of spermatogonia proliferation. In this period, testis index and the number of spermatogonia began to rise. Other spermatogenic cells had not yet formed; Stage II to III, from March to April, primary spermatocyte meiosis period. The testis index was highest in this stage, and spermatogenic cells were in spermatocyte stage, the primary spermatocyte meiosis generated to secondary spermatocyte; Stage IV, from April to May, spermatocytes continued to split, germ cells appeared in seminiferous tubules; Stage V, in May, sperm formation, spermatids of seminiferous tubules were transformed to spermatozoa, a large number of sperms existed in the lumen; Stage VI, spermatozoa emission period, from May to June, testis index were a significant drop and mature spermatozoa excluded gradually; VII, the testicular activity ceased basically from July to September, November to January of the following year, the spermatogenic activity ceased completely. Therefore, Myospalax cansus are animals of seasonal reproduction, spermatogenesis cycle is discontinuous type.

睾丸系数、体积和重量的年周期变化规律一致,变化曲线呈现单峰型。2甘肃鼢鼠雄性生殖腺的年周期活动由7个特征明显的时期构成:Ⅰ期,2~3月份,精原细胞增殖期,睾丸系数开始上升,精原细胞进行有丝分裂,其他生精细胞尚未形成;3~4月份为Ⅱ~Ⅲ期,初级精母细胞成熟分裂期,睾丸系数达到最大,生精细胞大多处于精母细胞阶段,初级精母细胞减数分裂生成次级精母细胞;Ⅳ期,4~5月份精母细胞继续进行分裂,精细胞在生精小管内出现;Ⅴ期,5月份,精子形成期,曲细精管中精细胞变态成精子,在管腔中存在大量的精子;Ⅵ期,精子排放期,5~6月份,睾丸系数显著下降,成熟精子从生精小管上脱离,逐渐排除;Ⅶ期,精原细胞停滞期,7~9月份睾丸生精活动基本停滞,11~翌年1月,生精活动完全停止。

Whereas, as the special structure of rat spermatozoa, the successful cryopreservation protocol of its spermatozoa is very difficult.

而大鼠精子因为其结构的特殊性,目前仍未建立成熟的冷冻保存技术。

These critical spermatozoal functions are acquired in the epididymis where a specific luminal environment is created by the blood-epididymal barrier; proteins secreted by epididymal principal cells bind to maturing spermatozoa and regulate the maturational process of the spermatozoa.

精子功能在附睾特殊的管腔环境中获得,这一环境是由血-附睾屏障来维护。附睾主细胞分泌的蛋白与精子结合并调控精子的成熟。附睾中细胞-细胞间的相互作用通过粘附连接和紧密连接形成。

However, most experimental evidence is indirect and unassembled. In this paper the studies on LDH-C and energy metabolism of mammal spermatozoa were reviewed, We suggested that LDH-C played the multi-roles in energy metabolism of mammal spermatozoa, not only in directly the energy metabolism pathway but also in the signal pathway of spermatozoa.

综述了对哺乳动物精子能量代谢和LDH-C两个方面的研究,提出LDH-C在精子的能量代谢中扮演着多重角色,不仅直接参与精子的能量代谢,还可能参与哺乳动物精子获能的信号途径,LDH-C和哺乳动物精子的能量代谢密切相关。

Histologically, the seminiferous tubules contained numerous Sertoli cells and more Sertoli-spermatozoa complexes, accompanied by the depletion of Leydig cells with deeply stained nuclei. Mature spermatozoa were stored up in the epididymis, but only a few in the efferent ducts. In the second place was testicular atrophy(32/120; 26.7%). The seminiferous tubules showed moderate to severe inactivity of spermiogenesis with evidence of only spermatogonia, spermatocytes and Sertoli cells. The Leydig cells were obviously decreased in numbers associated with decrease of lipid droplets in their cytoplasms. Testicular hypoplasia was the third disorders(22/120; 18.3%). Only a few spermatogonia and Sertoli cells appeared without any spermiogenesis. The associated changes was decreased in Leydig cells and fibrous hyperplasia in the interstitium.Epididymal stones were sometimes found(12/120; 10%). Grossly, yellowish-white nodules with various sizes and firm in consistency were observed in the epididymis and the front efferent ducts. Microscopically, the epididymal ducts were dilated with voluminous spermatozoa storage, even showed calcification in severe cases. The deposited calcium salts were stained positively by Von Kossa and Alizarin red methods.Amyloidosis was also detected in 10 roosters(8.3%). Eosinophilic, homogeneous, amyloid-like substances were deposited mainly in the testicular interstitium and the periphery of blood vessels. These substances showed positive reaction by Congo red staining. Five roosters(4.2%)had Marek's lesions in the testis, epididymis and peripheral nerves with infiltration of pleomorphic lymphocytes. Only one case showed epithelial necrosis of seminiferous tubules accompanied by fibrous proliferation in the interstitium.

结果发现,在总共搜集的120个病例中,其中因年老所导致的产精力不佳为最多,占38例(31.7%),於镜下可见大量精虫黏附於Sertoli cell的表面,并可见Sertoli cell数量明显增多而Leydig cell明显减少,且其细胞核呈现浓染的现象,而在其副睪中仍可见到成熟精虫蓄留於管腔中,但在其输精管内却只有少量精虫存在;其次为睪丸萎缩,占32例(26.7%),镜下可见中度至重度无造精作用,其生精小管中只见到精母细胞、精原细胞及Sertoli cell存在,但Leydig cell数量明显减少且其细胞质内的脂质也明显减少;睪丸发育不全,占22例(18.3%),於生精小管内只见到精母细胞及少量Sertoli cell存在,不见造精细胞分化,於生精小管间质可见Leydig cell减少并伴随结缔组织增生;副睪结石,占12例(10%),肉眼下可在副睪及输精管前段见到黄白色大小不一的结节,触感坚硬,於镜下可见副睪管扩张并有大量成熟精虫蓄积,严重时可见钙化现象,以Von Kossa及茜素红染色均呈阳性反应;类淀粉沉著症,占10例(8.3%),镜下在睪丸间质及血管周围可见粉红均质样的物质沉积,以刚果红染色成阳性反应;马立克病,占5例(4.2%),镜下可在睪丸、副睪实质及周边神经内均可见到嗜碱性大小不一的淋巴样细胞浸润;睪丸坏死,占1例(0.8%),镜下可见生精小管上皮细胞坏死脱落及间质结缔组织增生。

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