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i型肌纤维
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  type i muscle fiber
     Phospholipase D Is Involved in both Signal Pathways of Insulin-andContraction-induced Glucose Transport in Type I Muscle Fiber
     磷脂酶D参与胰岛素和收缩引起的I型肌纤维葡萄糖跨膜转运的信号转导体系
短句来源
     Objective To investigate whether phospholipase D (PLD) is involved in the signal pathways of insulin- or contraction-induced glucose transport in the type I muscle fiber.
     目的 :研究磷脂酶D(phospholipaseD ,PLD)是否参与胰岛素和收缩引起的I型肌纤维葡萄糖跨膜转运的信号转导体系。
短句来源
     Conclusion PLD is involved in the signal transduction processes triggered by insulin or contraction in glucose cross-membrance transportation in the type I muscle fiber, similarly as in type Ⅱ fiber.
     结论 :同在II型肌纤维中的作用一样 ,PDL也参与I型肌纤维中由胰岛素或肌肉收缩引起的肌细胞葡萄糖跨膜转运的信号转导系统。
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  “i型肌纤维”译为未确定词的双语例句
     But less BW gain were found in groups of different countermeasures, especially in SUS+HUT (4 h/d) and CEN (2.6 G) groups.
     两种对抗措施下,对抗效果显示明显的时间依赖性。 4h/d的STD或者HUT,己可完全防止模拟失重对SOL湿重与I、H型肌纤维CSA,I型肌纤维比例及MHC异构体比例的不良影响。
短句来源
     The cross sectional areas of both type I and II fibers were measured respectively.
     被检肌肉行ATP酶染色,测定I、I型肌纤维面积。
短句来源
     The specimens were applied for histological and histochemical staining. Results The most significant pathological features were appearance of central located nucli in numerous muscle fibers (15%~31%),involving more frequently the type I fibers.
     结果 肌肉病理发现在许多肌纤维的中心出现单个的肌核 ( 15 %~ 31%) ,主要累及 I型肌纤维 ,伴随 I型纤维呈病理性占优势和 I型肌纤维发育不良为主的肌型比例失调 ( I型肌纤维直径显著小于 II型肌纤维 )。
短句来源
     Results:The muscle spindle density was higher and the conjective forms were much more in the clavic part of pectoralis major and pectoralis minor than that in other parts,so was the proportion of type I fiber in them.
     结果 :胸大肌锁骨部和胸小肌肌梭密度较高 ,存在较多的肌梭联合体 ,I型肌纤维比例高于II型。
短句来源
     Methods Butanols, the inhibitors of PLD, were used to observe their effects on insulin- or contraction-induced glucose transport rates in soleus muscle of rat so as to find out the roles of PLD in cross-membrance the signal transduction processes.
     方法 :利用PLD的抑制剂丁醇 ,观察其对胰岛素和肌肉收缩引起的I型肌纤维占大多数的离体大鼠比目鱼肌葡萄糖跨膜转运的影响 ,了解PLD在信号转导体系中的作用。
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  相似匹配句对
     (2)C shape;
     C ;
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     (3)D shape.
     D
短句来源
     DISTRIBUTION OF MYOFIBER TYPES IN LEG MUSCLES
     小腿肌的肌纤维分布
短句来源
     The Study of Fiber Types in Human Masseter Muscles
     人类咬肌的肌纤维研究
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     brassii type; N.
     brassii ,N .
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  type i muscle fiber
Colchicine myopathy: a vacuolar myopathy with selective type I muscle fiber involvement
      
In agreement with the tracer data, a greater net decline in type I muscle fiber lipid content was observed in the LFA vs.
      


Twenty-four biopsy specimens of the gastrochemius muscles were taken from 12 surgical treated cases with spastic equina deformity. There were examined histochemically by myosin ATP ase method and studied ultra-structurally. The histochemical change is that the type I fibers, slow-twitch fibers, occupy a significantly higher proportion than control, and offten gather together to form type grouping. Ultra-structural abnormalities were found in all of the 24 specimens. The results showed that the surgical treatment...

Twenty-four biopsy specimens of the gastrochemius muscles were taken from 12 surgical treated cases with spastic equina deformity. There were examined histochemically by myosin ATP ase method and studied ultra-structurally. The histochemical change is that the type I fibers, slow-twitch fibers, occupy a significantly higher proportion than control, and offten gather together to form type grouping. Ultra-structural abnormalities were found in all of the 24 specimens. The results showed that the surgical treatment of spastic equina deformity was usually ineffective in long term, because there was not only disorder of the central nervous system but also the change of the muscle fiber types.

对24个脑瘫痉挛性马蹄足经手术治疗后的腓肠肌标本进行肌球蛋白ATP酶组化研究和超微结构观察。组织化学的主要改变是I型肌纤维(慢缩纤维)比例增多和I型肌纤维的聚集,全部标本均可见到超微结构异常。结果表明,脑瘫痉挛性马蹄足外科手术治疗远期效果不佳,除中枢神经系统失调外,还与腓肠肌肌纤维型转变有关。

Objective To study 20 cases of lipid storage myopathy (LSM) and to analyze them in clinical and pathological fields. Methods The clinical data of the 20 cases were collected and muscle biopsies were done with routine and histochemical staining. Light and electron microscopic studies were made.Results Combining clinical characters with pathologic changes, we divided these cases into two groups. The first group were acute or subacute onset. Muscle weakness occurred with increased muscle enzymes in the plasma....

Objective To study 20 cases of lipid storage myopathy (LSM) and to analyze them in clinical and pathological fields. Methods The clinical data of the 20 cases were collected and muscle biopsies were done with routine and histochemical staining. Light and electron microscopic studies were made.Results Combining clinical characters with pathologic changes, we divided these cases into two groups. The first group were acute or subacute onset. Muscle weakness occurred with increased muscle enzymes in the plasma. This group had dramatic responses to corticosteroid therapy. The second group were of chronic courses marked fatigue and muscle weakness. They were not sensitive to corticosteroid therapy. Mitochondrial abnormalities were obvious in this group. Muscle biopsies showed many vacuoles in the muscle fibers, especially in the type I fibers, with ORO staining positive. Electron microscopic observation demonstrated excessive accumulation of lipid droplets and with abnormal mitochondria in some cases. Conclusions LSM was a complex disease. It was considered to be a subgroup of mitochondrial myopathies. Fatigue and muscle weakness were the prominent symptoms with recurring courses in most cases. Muscle biopsy were of use to make the definite diagnosis of this disease.

目的从临床和肌肉病理的角度分析脂质沉积性肌病(LSM)的特点。方法收集20例LSM病人的临床资料,并做肌肉活检,采用常规组织学方法和组织化学方法染色,并在电镜下观察。结果结合临床和病理特点可将病例分为两组,第一组为急性或亚急性起病,四肢近端肌无力,肌酶谱明显升高,对激素治疗敏感;第二组呈慢性迁延性病程,表现肌无力和对运动不耐受,对激素治疗不敏感,肌纤维内线粒体异常比较明显。对20例病人的肌肉活检发现I型肌纤维为主的肌纤维空泡样变,油红“O”染色示脂滴明显增多,电镜也证实肌纤维内脂滴堆积,部分病例伴有异常线粒体增多。结论脂质沉积性肌病是一组生化方面十分复杂的疾病,属于线粒体肌病的一个类型,临床上以不能耐受运动和近端肌无力为主,病程呈波动性,部分可有自发缓解,肌肉病理检查有助于确诊。两组的临床病理差异可能提示脂肪代谢障碍的不同环节或不同酶的缺陷。

Objective To explore the change pattern of fibrillation potential amplitude in human denervated skeletal muscle and its relationship with denervated muscles. Methods 173 patients with brachial plexus injury were measured on their fibrillation potential amplitudes of biceps brachii muscles,among which 63 patients were taken biceps brachii muscle biopsies at the same site from Aug. 1995 to Dec. 1996.The biopsied muscles were processed with ATPase stain. The cross sectional areas of both type I and II fibers...

Objective To explore the change pattern of fibrillation potential amplitude in human denervated skeletal muscle and its relationship with denervated muscles. Methods 173 patients with brachial plexus injury were measured on their fibrillation potential amplitudes of biceps brachii muscles,among which 63 patients were taken biceps brachii muscle biopsies at the same site from Aug. 1995 to Dec. 1996.The biopsied muscles were processed with ATPase stain. The cross sectional areas of both type I and II fibers were measured respectively. Results It was observed that the fibrillation potential amplitudes and the cross sectional areas of muscle fibers decayed over time and correlated negatively with time. The fibrillation potential amplitude decreased significantly at the 5th,6th month and the time over 1 year( P <0.05). while the fiber cross sectional areas atrophyed apparently at the 4th month. The fibrillation potential amplitude correlated well with the fiber cross sectional areas.It was also seen that the fi brillation potential amplitude and type II fiber areas of males were higher than those of females ( P < 0.05 ). Conclusions The fibrillation potential amplitude changes in the same way as that of the fiber cross sectional areas,therefore it can be used as a quantitative index to estimate the atrophy state of muscle fibers.

目的研究失神经支配肱二头肌纤颤电位波幅的变化规律,并探索其与肌肉萎缩程度的关系。方法1995年8月~1996年12月,检测173块因臂丛神经损伤致完全失神经支配的肱二头肌纤颤电位并计算其波幅;63例在检测同一部位取肌组织送病理检查。被检肌肉行ATP酶染色,测定I、I型肌纤维面积。结果纤颤电位的波幅和肌纤维的横断面积与失神经时间呈负相关;失神经后第5、6个月及1年以后为纤颤电位波幅的显著下降期;失神经后第4个月为肌纤维的显著萎缩期。纤颤电位的波幅与肌纤维的横截面积呈正相关;男性纤颤电位的波幅及II型肌纤维面积均较女性为高(P<0.05)。结论纤颤电位波幅与肌纤维萎缩状态相一致,可作为评估肌肉萎缩程度的定量指标

 
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