Motoneuron subtypes show specificity in glycine receptor channel abnormalities in a transgenic mouse model of amyotrophic lateral sclerosis.
about
Inhibitory synaptic regulation of motoneurons: a new target of disease mechanisms in amyotrophic lateral sclerosis.Generation and characterization of transgenic mice expressing mitochondrial targeted red fluorescent protein selectively in neurons: modeling mitochondriopathy in excitotoxicity and amyotrophic lateral sclerosis.Postactivation depression of the Ia EPSP in motoneurons is reduced in both the G127X SOD1 model of amyotrophic lateral sclerosis and in aged mice.Voltage-gated calcium channels are abnormal in cultured spinal motoneurons in the G93A-SOD1 transgenic mouse model of ALS.
P2860
Motoneuron subtypes show specificity in glycine receptor channel abnormalities in a transgenic mouse model of amyotrophic lateral sclerosis.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@ast
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@en
type
label
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@ast
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@en
prefLabel
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@ast
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@en
P2860
P356
P1433
P1476
Motoneuron subtypes show speci ...... amyotrophic lateral sclerosis.
@en
P2093
Lee J Martin
Qing Chang
P2860
P304
P356
10.4161/CHAN.5.4.16206
P577
2011-07-01T00:00:00Z