Fingerprint analysis of Huolingshengji Formula and its neuroprotective effects in SOD1G93A mouse model of amyotrophic lateral sclerosis
Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease characterized by progressive loss of motor neurons. There are no definitive pathogenic mechanisms and effective treatments for ALS now. Traditional Chinese medicine (TCM) plays an important role in Chinese health care syste...
Guardado en:
Autores principales: | Qinming Zhou, Youjie Wang, Jingjing Zhang, Yaping Shao, Song Li, Yuan Wang, Huaibin Cai, Yi Feng, Weidong Le |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/66e495b882f24c34ba9bf015a522c762 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral Sclerosis
por: Luca Muzio, et al.
Publicado: (2020) -
Early detection of motor dysfunction in the SOD1G93A mouse model of Amyotrophic Lateral Sclerosis (ALS) using home cage running wheels.
por: Ellen J Bennett, et al.
Publicado: (2014) -
Amyotrophic lateral sclerosis and frontotemporal degeneration
Publicado: (2000) -
The cortical signature of amyotrophic lateral sclerosis.
por: Federica Agosta, et al.
Publicado: (2012) -
c-Abl inhibition delays motor neuron degeneration in the G93A mouse, an animal model of amyotrophic lateral sclerosis.
por: Ryu Katsumata, et al.
Publicado: (2012)