相关实验视频
Updated: Jul 10, 2025

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
源自MUSK基因突变的先天性肌痛综合征
1Neurology, Cairns Hospital, Cairns, Queensland, Australia antonia.mclean2@health.qld.gov.au.
遗传突变可以导致缓慢进展的神经肌肉症状. 一名妇女在发现MUSK基因突变后被诊断出患有先天性肌肌综合征,突出显示了罕见神经肌肉疾病中的遗传联系.
科学领域:
- 神经学 神经学
- 遗传学 遗传学是一种遗传学.
- 分子生物学分子生物学
背景情况:
- 缓慢进展的神经肌肉症状经常源于遗传基础.
- 在没有明确的遗传识别的情况下,罕见的神经肌肉疾病的诊断挑战仍然存在.
更多相关视频
06:51Systemic Delivery of MicroRNA Using Recombinant Adeno-associated Virus Serotype 9 to Treat Neuromuscular Diseases in Rodents
Published on: August 10, 2018
14:10Isometric and Eccentric Force Generation Assessment of Skeletal Muscles Isolated from Murine Models of Muscular Dystrophies
Published on: January 31, 2013
相关概念视频
Myasthenia Gravis: Overview and Treatment
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
Myasthenia Gravis: Diagnostic Tests
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
Disorders of the Skeletal Muscle
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
Satellite Stem Cells and Muscular Dystrophy
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Sex-linked Disorders