Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.
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Recent advances in amyotrophic lateral sclerosisQuo vadis motor neuron disease?Clinical and genetic basis of familial amyotrophic lateral sclerosisOxidative stress and mitochondrial damage: importance in non-SOD1 ALSINaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS modelA Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During DiseaseWhole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohortPsychiatric genetics, neurogenetics, and neurodegenerationSingle-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese CohortNrf2--a therapeutic target for the treatment of neurodegenerative diseases.Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci.Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.Two familial ALS proteins function in prevention/repair of transcription-associated DNA damage.Development of Therapeutics for C9ORF72 ALS/FTD-Related Disorders.Mitochondria and endoplasmic reticulum crosstalk in amyotrophic lateral sclerosis.Paget's disease of bone-genetic and environmental factors.Targeting mitochondrial metal dyshomeostasis for the treatment of neurodegeneration.Stem cells therapy for ALS.RNA mis-splicing in disease.Critical issues in ALS case-control studies: the case of the Euro-MOTOR study.Amyotrophic Lateral Sclerosis, 2016: existing therapies and the ongoing search for neuroprotection.Further development of biomarkers in amyotrophic lateral sclerosis.Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity.Faulty RNA splicing: consequences and therapeutic opportunities in brain and muscle disorders.The Actin Cytoskeleton in SMA and ALS: How Does It Contribute to Motoneuron Degeneration?Motoneuron Disease: Basic Science.DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis.Investigation of vitamin D receptor polymorphisms in amyotrophic lateral sclerosis.Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers.Changes in the Excitability of Neocortical Neurons in a Mouse Model of Amyotrophic Lateral Sclerosis Are Not Specific to Corticospinal Neurons and Are Modulated by Advancing Disease.Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China.Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport.The role of TGF-β superfamily signaling in neurological disorders.Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.Correlating serum micrornas and clinical parameters in amyotrophic lateral sclerosis.Familial Amyotrophic Lateral Sclerosis.RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis.
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P2860
Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
Genetic causes of amyotrophic ...... opportunities and challenges.
@en
type
label
Genetic causes of amyotrophic ...... opportunities and challenges.
@en
prefLabel
Genetic causes of amyotrophic ...... opportunities and challenges.
@en
P2860
P1433
P1476
Genetic causes of amyotrophic ...... opportunities and challenges.
@en
P2093
Bryan J Traynor
Giuseppe Marangi
P2860
P356
10.1016/J.BRAINRES.2014.10.009
P407
P577
2014-10-12T00:00:00Z