Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis
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Therapeutic potential of mood stabilizers lithium and valproic acid: beyond bipolar disorderCopy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative DiseasesThe function of RNA-binding proteins at the synapse: implications for neurodegenerationAmyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic TrialsThe role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.Complex genetics of amyotrophic lateral sclerosis.Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population.Therapeutic developments in the treatment of amyotrophic lateral sclerosis.The importance of the SMN genes in the genetics of sporadic ALS.Molecular and cellular pathways of neurodegeneration in motor neurone diseaseSMN1 gene duplications are associated with sporadic ALS.Homozygous SMN2 deletion is a protective factor in the Swedish ALS population.Amyotrophic lateral sclerosis: contemporary concepts in etiopathogenesis and pharmacotherapy.Measures and markers in amyotrophic lateral sclerosis.Skeletal muscle in motor neuron diseases: therapeutic target and delivery route for potential treatments.Genetics of amyotrophic lateral sclerosis: an update.The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice.Homozygous survival motor neuron 2 gene deletion and sporadic lower motor neuron disease in children: case report and literature review.Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis.Stress granules in neurodegeneration--lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma.New therapy options for amyotrophic lateral sclerosis.SMA carrier testing: a meta-analysis of differences in test performance by ethnic group.Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing.Further development of biomarkers in amyotrophic lateral sclerosis.Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers.SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter.A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population.Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.Familial Amyotrophic Lateral Sclerosis.Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutationAssociation study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS
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Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis
description
article
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im Januar 2002 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в січні 2002
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name
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
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Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
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type
label
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
@en
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
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prefLabel
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
@en
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
@nl
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P1433
P1476
Abnormal SMN1 gene copy number ...... amyotrophic lateral sclerosis
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Alain Autret
Christian Andres
Jawad Khoris
Jean-Pierre Müh
Véronique Mayeux-Portas
William Camu
the French ALS Research Group
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P304
P356
10.1002/ANA.10104
P577
2002-01-31T00:00:00Z