Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse model
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Rho family GTPases: key players in neuronal development, neuronal survival, and neurodegenerationIntricate effects of primary motor neuronopathy on contractile proteins and metabolic muscle enzymes as revealed by label-free mass spectrometry.Smads as muscle biomarkers in amyotrophic lateral sclerosisDrug repositioning for orphan genetic diseases through Conserved Anticoexpressed Gene Clusters (CAGCs)Activation of the endoplasmic reticulum stress response in skeletal muscle of G93A*SOD1 amyotrophic lateral sclerosis mice.Specific protein changes contribute to the differential muscle mass loss during ageing.State of the field: An informatics-based systematic review of the SOD1-G93A amyotrophic lateral sclerosis transgenic mouse model.Transcriptional activator TAp63 is upregulated in muscular atrophy during ALS and induces the pro-atrophic ubiquitin ligase Trim63.Proteomic profiling of the contractile apparatus from skeletal muscle.Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle.The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis.The Axon Guidance Protein Semaphorin 3A Is Increased in the Motor Cortex of Patients With Amyotrophic Lateral Sclerosis.Activation of AMP-activated protein kinase α1 mediates mislocalization of TDP-43 in amyotrophic lateral sclerosis.Early gene expression changes in skeletal muscle from SOD1(G93A) amyotrophic lateral sclerosis animal model.PGC-1α Silencing Compounds the Perturbation of Mitochondrial Function Caused by Mutant SOD1 in Skeletal Muscle of ALS Mouse Model.Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNFα.What is "Hyper" in the ALS Hypermetabolism?Specific induction of Akt3 in spinal cord motor neurons is neuroprotective in a mouse model of familial amyotrophic lateral sclerosis.Elucidating Cellular Metabolism and Protein Difference Data from DIGE Proteomics Experiments Using Enzyme Assays.Mapping the human skeletal muscle proteome: progress and potential.MRI reveals therapeutical efficacy of stem cells: An experimental study on the SOD1(G93A) animal model.A Novel Iron Chelator-Radical Scavenger Ameliorates Motor Dysfunction and Improves Life Span and Mitochondrial Biogenesis in SOD1G93A ALS Mice.Proteomic profiling of muscle fibre type shifting in neuromuscular diseases.Micro-computed tomography for non-invasive evaluation of muscle atrophy in mouse models of disease.Counteracting roles of MHCI and CD8 T cells in the peripheral and central nervous system of ALS SOD1 mice
P2860
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P2860
Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse model
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@ast
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@en
type
label
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@ast
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@en
prefLabel
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@ast
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@en
P2093
P2860
P50
P356
P1476
Molecular signatures of amyotr ...... s of an SOD1(G93A) mouse model
@en
P2093
Antonia Ratti
Cristina Daleno
Giuliano Grignaschi
P2860
P304
P356
10.1089/ARS.2012.4524
P50
P577
2012-06-13T00:00:00Z