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1 n innervated muscle and suppressed following muscle denervation.
2  mice, resulting in a progressive and severe muscle denervation.
3 macological inhibition significantly delayed muscle denervation.
4 tresses: fasting, muscle immobilization, and muscle denervation.
5 onduction abnormalities as well as extensive muscle denervation.
6 r NMJ-specific genes in a pattern resembling muscle denervation.
7 n underlying muscle phenotypic changes after muscle denervation.
8 g from oxidative stress generated in vivo by muscle denervation.
9  protein characteristic of their reaction to muscle denervation.
10 d apoptotic signalling is upregulated during muscle denervation.
11 etes, cancer, sepsis, burns, starvation, and muscle denervation.
12 pression during muscle development and after muscle denervation.
13 by progressive motor neuron degeneration and muscle denervation.
14 orial manner, driving cellular adaptation to muscle denervation.
15 injury resulting in long periods of skeletal muscle denervation.
16  progressive motor and sensory deficits, and muscle denervation.
17             However, there is no evidence of muscle denervation, a cardinal pathological feature of A
18 93A) mice in vivo, reductions in CRT precede muscle denervation and are restricted to vulnerable moto
19 rogressive motor neuron loss, gait problems, muscle denervation and atrophy, paralysis, and have dimi
20  characterized by motoneuron death, skeletal muscle denervation and atrophy.
21 ctions (NMJs), prolonged inactivity leads to muscle denervation and atrophy.
22 sorder characterized by progressive skeletal muscle denervation and loss of motor neurons that result
23 tor function or disease pathology, including muscle denervation and motor neuron loss.
24 expression causes a significant reduction in muscle denervation and neuromuscular junction degenerati
25 or neuron (SMN) protein, is characterized by muscle denervation and paralysis.
26 rized by progressive motor neuron (MN) loss, muscle denervation and paralysis.
27 ntally with the earliest detectable signs of muscle denervation and preceded physiologically measurab
28 ated muscle atrophy relates to the degree of muscle denervation and the capacity of successful reinne
29 ion, thus contributing to axon degeneration, muscle denervation, and motor neuron cell death in SMA.
30 changes in voluntary locomotion, markers for muscle denervation, and muscle atrophy.
31 e induced before muscle innervation or after muscle denervation, and this induction requires expressi
32  sequences within both these enhancers after muscle denervation, and this pattern of binding was very
33                                              Muscle denervation edema or atrophy along the distributi
34 on of angular muscle fibers, consistent with muscle denervation (from 7.6% to 15.6%), while angular m
35 tion of apoptotic signal transduction during muscle denervation has not been fully elucidated.
36 t also protected neuromuscular junction from muscle denervation in SOD1(G93A) mice clearly indicating
37                    Previous work showed that muscle denervation increases expression of AChR mRNAs du
38 es-stretch-sensitive mechanoreceptors, while muscle denervation induces extensive reactivation of the
39                                              Muscle denervation is a convenient model to examine expr
40 ein deficiency and/or subsequent to skeletal muscle denervation is unknown.
41                                Despite this, muscle denervation, motor axon degeneration, and disease
42 TD that shows decreased survival, paralysis, muscle denervation, motor neuron loss, anxiety-like beha
43 of SMA-related immobility, systemic illness, muscle denervation, or muscle atrophy.
44 event progressive motor neuron degeneration, muscle denervation, or paralysis in ALS.
45 s FRZB and Wnt signaling might be playing in muscle denervation/reinnervation.
46 uscular junctions that mimic the response to muscle denervation/reinnervation.
47                                              Muscle denervation resulting from injury, disease or agi
48 of motor neurons is accompanied by extensive muscle denervation, resulting in paralysis and ultimatel
49 ly restricted to the motor endplate in adult muscle, denervation results in its extrajunctional expre
50 ; (b) endplate-associated CGRP declines with muscle denervation several hours before any changes in A
51 s independently rated fascicular lesions and muscle denervation signs on a five-point scale and made
52                                              Muscle denervation signs were more prominent in ALS than
53 hat FRZB is part of a molecular signature of muscle denervation that may reflect disease progression
54                                         This muscle denervation was associated with early electrophys
55 The protective effect of hHsp27 on prolonged muscle denervation was examined by performing repeated s
56 l elderly women exhibited marked features of muscle denervation, whereas world class octogenarian fem