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1 iven by different sources of input to spinal alpha motor neurons.
2 correlate with the loss of force-generating alpha motor neurons.
3 the perikarya and proximal dendrites of host alpha motor neurons.
4 primarily characterized by the loss of lower alpha motor neurons.
5 organization secondary to deefferentation of alpha motor neurons.
6 s (ALS) is the selective loss of spinal cord alpha motor neurons.
7 protein, resulting in the selective loss of alpha-motor neurons.
8 approximately 72% of these motor neurons are alpha-motor neurons.
9 ctivity was observed within the ventral horn alpha-motor neurons.
10 of SCI-induced dendritic spine dysgenesis on alpha-motor neurons.
12 characterized by the degeneration of spinal alpha motor neurons (alphaMNs), associated with muscle p
13 spinal cords revealed preserved spinal cord alpha-motor neurons and preserved mitochondrial morpholo
14 urons into types that generate muscle force (alpha motor neurons) and types that modulate muscle prop
15 f the oculomotor nerve and its corresponding alpha motor neurons, and abnormalities of the levator pa
16 ity, decreased dendritic spine dysgenesis on alpha-motor neurons, and elevated the expression of the
17 and found that nerve endings terminating on alpha-motor neurons are affected during the symptomatic
19 trocyte-encoded Sema3a leads to dysregulated alpha-motor neuron axon initial segment orientation, mar
20 als reveals no degeneration of large caliber alpha-motor neurons beyond an age-dependent loss (initia
21 F staining demonstrated the dramatic loss of alpha-motor neurons characteristic of this disorder.
23 der SMN defective in this role, the specific alpha-motor neuron degenerative phenotype seen in the di
25 fiber electrical activity to decode accurate alpha-motor neuron discharges across five lumbosacral se
26 ponses of corticospinal axons and of plantar alpha-motor neurons following transcranial magnetic (TMS
29 disease characterized by degeneration of the alpha-motor neurons in the anterior horn of the spinal c
30 sease are caused by specific degeneration of alpha-motor neurons in the spinal cord, leading to muscl
32 uromuscular disease characterized by loss of alpha-motor neurons, leading to profound skeletal muscle
34 th impairment, and shortened life span, with alpha-motor neuron loss and abnormal neuromuscular junct
36 utosomal-recessive disorder characterized by alpha-motor neuron loss in the spinal cord anterior horn
37 h somal diameters > or = 25 microns) and non-alpha-motor neurons (< 25 microns somal diameters) also
38 Neuron 1 (SMN1), leading to degeneration of alpha motor neurons (MNs) but also affecting other cell
40 entiation of mouse embryonic stem cells into alpha motor neurons recapitulates the switch from matern
41 Reduced expression of SMN leads to loss of alpha-motor neurons, severe muscle weakness and often ea
43 llular responses were recorded in 23 plantar alpha motor neurons supplying intrinsic muscles of the f
44 rmore, p75NTR re-expression occurs in larger alpha motor neurons that express cleaved caspsase-3 and
45 Those in the ventral horn were identified as alpha motor neurons using retrograde tracing and/or doub
46 ed" adult mice to retrogradely infect spinal alpha-motor neurons, we observed significant restoration
47 00-800 microm(2) , suggesting that these are alpha motor neurons, which was confirmed after examinati
48 pinal cords was found primarily in lamina IX alpha motor neurons, while a weaker hybridization signal