Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation - Wikidata - awgldk - TriplyDB

Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

http://www.wikidata.org/entity/Q36253321

about

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS Sumoylation of critical proteins in amyotrophic lateral sclerosis: emerging pathways of pathogenesis The involvement of the cerebellum in amyotrophic lateral sclerosis.Hippocampal sclerosis dementia with the C9ORF72 hexanucleotide repeat expansion An Assessment of Possible Neuropathology and Clinical Relationships in 46 Sporadic Amyotrophic Lateral Sclerosis Patient Autopsies Hippocampal sclerosis dementia: An amnesic variant of frontotemporal degeneration.Non-Alzheimer's disease-related memory impairment and dementia.C9ORF72 mutations in neurodegenerative diseases.C9ORF72 hexanucleotide repeats in behavioral and motor neuron disease: clinical heterogeneity and pathological diversity.Prevalence of brain and spinal cord inclusions, including dipeptide repeat proteins, in patients with the C9ORF72 hexanucleotide repeat expansion: a systematic neuropathological review.MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis.C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration.Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis.Reappraisal of TDP-43 pathology in FTLD-U subtypes.

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Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

http://www.wikidata.org/entity/Q36253321

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Frontotemporal lobar degenerat ...... clinicopathologic correlation

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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type

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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J.1440-1789.2012.01332.X

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Frontotemporal lobar degenerat ...... clinicopathologic correlation

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Alfred Rademaker

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Bing Bing Weitner

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Eileen H Bigio

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Kyung-Hwa Lee

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M-Marsel Mesulam

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Manjari Mishra

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Matt Baker

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Qinwen Mao

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Rakhee A Ganti

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Saman S Ahmadian

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P2860

A harmonized classification system for FTLD-TDP pathology

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

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

Neuropathological stageing of Alzheimer-related changes

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

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10.1111/J.1440-1789.2012.01332.X

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2

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Rosa Rademakers

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