C9ORF72 mutations in neurodegenerative diseases. - Wikidata - thesis-toulmin - TriplyDB

C9ORF72 mutations in neurodegenerative diseases.

C9ORF72 mutations in neurodegenerative diseases.

http://www.wikidata.org/entity/Q38128241

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ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease Intermediate CAG repeat expansion in the ATXN2 gene is a unique genetic risk factor for ALS--a systematic review and meta-analysis of observational studies.The Association between C9orf72 Repeats and Risk of Alzheimer's Disease and Amyotrophic Lateral Sclerosis: A Meta-Analysis.Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic.Simple animal models for amyotrophic lateral sclerosis drug discovery.Molecular Genetics of Neurodegenerative Dementias.Linking amyotrophic lateral sclerosis and spinal muscular atrophy through RNA-transcriptome homeostasis: a genomics perspective.Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease.Frontotemporal dementia.

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C9ORF72 mutations in neurodegenerative diseases.

http://www.wikidata.org/entity/Q38128241

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article científic

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C9ORF72 mutations in neurodegenerative diseases.

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C9ORF72 mutations in neurodegenerative diseases.

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C9ORF72 mutations in neurodegenerative diseases.

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Molecular Neurobiology

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C9ORF72 mutations in neurodegenerative diseases.

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Jing Zhou

http://www.w3.org/2001/XMLSchema#string

Ying Liu

http://www.w3.org/2001/XMLSchema#string

Yu Zong

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P2860

Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Cognitive and behavioral features of c9FTD/ALS

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386-398

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10.1007/S12035-013-8528-1

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1

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2013-08-10T00:00:00Z

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1019307424

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23934648

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neurodegeneration