1) Muscular atrophy/genet
肌萎缩/遗传学
2) Werding-Hoffmann atrophy(paralysis,type)
专-霍二氏萎缩(麻痹，型)，遗传早发性脊髓肌萎缩
3) X-linked spinal and bulbar muscular atrophy
X-连锁隐性遗传性脊髓延髓型肌萎缩
4) Muscular atrophy/pathol
肌萎缩/病理学
5) muscle atrophy
肌萎缩
1.
Preventive and therapeutic effects of proteasome inhibitor MG-132 on dener-vated muscle atrophy of rats;
蛋白酶体抑制剂MG-132对大鼠失神经肌萎缩的防治作用
2.
Rabbit masseteric muscle atrophy resulting from triamcinolone for injection;
曲安奈德肌内注射诱导兔咬肌萎缩的实验研究
3.
Objective To investigate the intervention of ciliary enurotrophic factors(CNTF)on weightlessness-induced muscle atrophy and its myofiber phenotype transition.
目的探讨CNTF对失重性肌萎缩及其纤维表型转换的干预作用。
6) Muscle atrophy
肌肉萎缩
1.
Purpose To study limb immobilization influencing on denervated muscle atrophy.
结论 肢体制动加速了失神经支配肌肉萎缩的发展。
2.
This paper reviews two main signaling pathways in order to introduce the key role of Akt in it,one is Akt1/FOXOs/MAFbx/MuRF1 signaling path- way which associated with muscle atrophy;the other is PI3K/Akt/mTOR/S6K1 signaling pathway which associated with muscle hypertrophy.
综述与骨骼肌质量变化相关的两个主要信号通路:一方面是与肌肉萎缩相关的Akt1/FOXOs/MAFbx/MuRF1信号通路;另一方面为与肌肉肥大相关的PI3K/Akt/mTOR/S6K1信号通路,从两方面介绍Akt在骨骼肌质量变化中所处的核心地位。
3.
Methods: In order to establish the cell model of using GCs to cause the muscle atrophy,we examined the total protein of the C2C12 muscle tube which was fed with Dexamethasone(DEX,100 nMs) for 1 to 4 days using BCA method.
目的:建立高剂量或长期服用糖皮质激素会引起肌肉萎缩的细胞模型。
补充资料：肌萎缩
肌萎缩
myoatrophy
肌肉体积缩小，肌纤维变细的一种表现。多由肌肉本身疾患或神经系统功能障碍所致。部分因肢体活动减少所致者称为废用性萎缩。本病常伴有肌纤维数目减少和肌张力减弱。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条