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Propagation of TDP-43 proteinopathy in neurodegenerative disorders

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摘要 Neurodegenerative disorders are characterized by disruptions to neuronal function and circuitry,leading to a variety of clinical syndromes depending on the affected neuroanatomic regions(Geula,1998).Many proteinopathies implicated in neurodegenerative diseases are characterized by the pathologic accumulation of proteins into inclusions that are initially deposited in specific areas of the brain and spread widely with disease progression.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2022年第7期1498-1500,共3页 中国神经再生研究(英文版)
基金 supported by grants from the National Institute of Neurological Disorders and Stroke,No.NS085770 National Institute on Deafness and Other Communication Disorders No.DC008552 National Institute on Aging,No.AG062566 and AG065463 an institutional training grant from the National Institute of Neurological Disorders and Stroke,No.NS047987 an Alzheimer’s Disease Center Grant from the National Institute on Aging,No.AG013854。
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