Skeletal-muscle metabolic reprogramming in ALS-SOD1G93A mice
收藏NIAID Data Ecosystem2026-03-11 收录
官方服务：
资源简介：
Identify altered molecular markers in skeletal muscle during ALS progression
应用场景：
创建时间：
2020-04-07
相关数据集
RNAseq of oculomotor (OMN) and spinal motor neurons (SC) derived from mouse embryonic stem cells and purified by FACS
Oculomotor neurons, which regulate eye movement, are resilient to degeneration in the lethal motor neuron disease amyotrophic lateral sclerosis (ALS). It would be highly advantageous if motor neuron r
干细胞与再生医学数据中心2022-02-20 更新100
Cortical glia in SOD1(G93A) mice are subtly affected by ALS-like pathology
The role of glia in amyotrophic lateral sclerosis (ALS) is undeniable. Their disease-related activity has been extensively studied in the spinal cord, but only partly in the brain. We present herein a
NIAID Data Ecosystem50
DataSheet1_Untargeted muscle tissue metabolites profiling in young, adult, and old rats supplemented with tocotrienol-rich fraction.zip
The greatest significant influence on human life span and health is inevitable ageing. One of the distinguishing characteristics of ageing is the gradual decrease of muscle mass and physical function.
NIAID Data Ecosystem20
Growth based changes in amino acid isotopic composition in captive Pacific bluefin tuna ( Thunnus orientalis ).
Incorporation of 15N into amino acids of white muscle tissue as a function of relative growth (WR). A) Four source amino acids, glycine (unfilled circle), lysine (unfilled square), serine (unfilled tr
NIAID Data Ecosystem60
Proportion of mice obtained in the generation of ATF4+/+-SOD1G86R and ATF4−/−-SOD1G86R mice.
The percentage of mutant SOD1 transgenic mice obtained in relation to the equivalent ATF4 genotype of non-transgenic mice is indicated. Total animals obtained for each genotype is indicated.
Figshare2015-12-02 更新30
