Genetics of familial and sporadic amyotrophic lateral sclerosis.
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Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosisExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSPhenotypic Heterogeneity of Monogenic Frontotemporal DementiaModeling neurological disorders by human induced pluripotent stem cellsFUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosisA perspective on stem cell modeling of amyotrophic lateral sclerosisFUS pathology in basophilic inclusion body diseaseTDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron diseaseProgressive Purkinje cell degeneration in tambaleante mutant mice is a consequence of a missense mutation in HERC1 E3 ubiquitin ligaseModification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS)β-amyloid triggers ALS-associated TDP-43 pathology in AD modelsThe sour side of neurodegenerative disorders: the effects of protein glycation.Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosisSporadic ALS Astrocytes Induce Neuronal Degeneration In Vivo.Development of the Huntington disease family concerns and strategies survey from focus group dataDNA-triggered aggregation of copper, zinc superoxide dismutase in the presence of ascorbate.Applying proteomics to the diagnosis and treatment of ALS and related diseases.Redox modifier genes and pathways in amyotrophic lateral sclerosis.Neurodegenerative diseases: exercising toward neurogenesis and neuroregeneration.Reduction in hSOD1 copy number significantly impacts ALS phenotype presentation in G37R (line 29) mice: implications for the assessment of putative therapeutic agentsCu,Zn-superoxide dismutase increases toxicity of mutant and zinc-deficient superoxide dismutase by enhancing protein stability.Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis.Persistent inward currents in spinal motoneurons: important for normal function but potentially harmful after spinal cord injury and in amyotrophic lateral sclerosis.Arylsulfanyl pyrazolones block mutant SOD1-G93A aggregation. Potential application for the treatment of amyotrophic lateral sclerosisGenetic rodent models of amyotrophic lateral sclerosisAssociation study on glutathione S-transferase omega 1 and 2 and familial ALS.Protein kinase Cepsilon binds peripherin and induces its aggregation, which is accompanied by apoptosis of neuroblastoma cells.Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.Immunoreactivity of the phosphorylated axonal neurofilament H subunit (pNF-H) in blood of ALS model rodents and ALS patients: evaluation of blood pNF-H as a potential ALS biomarker.Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patientsDietary Vitamin D3 Restriction Exacerbates Disease Pathophysiology in the Spinal Cord of the G93A Mouse Model of Amyotrophic Lateral SclerosisRNA-binding protein misregulation in microsatellite expansion disordersCommon molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis.Strategic approaches to developing drug treatments for ALS.TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysisEnrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosisEstablishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells.TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis.
P2860
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P2860
Genetics of familial and sporadic amyotrophic lateral sclerosis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@ast
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@en
type
label
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@ast
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@en
prefLabel
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@ast
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@en
P1476
Genetics of familial and sporadic amyotrophic lateral sclerosis.
@en
P2093
Claudia Gaspar
Francois Gros-Louis
P304
P356
10.1016/J.BBADIS.2006.01.004
P407
P577
2006-02-10T00:00:00Z