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期刊名:Acta neuropathologica

缩写:ACTA NEUROPATHOL

ISSN:0001-6322

e-ISSN:1432-0533

IF/分区:10.3/Q1

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Matthew Pun,Akash Deogharkar,Siva Kumar Natarajan et al. Matthew Pun et al.
Chordomas are rare cancers that arise along the axial skeleton. Alterations in metabolism are a hallmark of cancer, and we sought to identify metabolic vulnerabilities in chordoma. We discovered that the tricarboxylic acid (TCA)-related enz...
Sonal Agrawal,Maude Wagner,Sue E Leurgans et al. Sonal Agrawal et al.
Cerebral amyloid angiopathy (CAA) is a common brain pathology in older people and has been recently recognized as a major risk factor for amyloid-related imaging abnormalities during anti-amyloid antibody therapy. CAA pathophysiology may in...
Hina Khan,Mary Gifford,Arash Kordbacheh et al. Hina Khan et al.
Parkinson's disease (PD) is characterized by progressive degeneration of nigrostriatal dopamine neurons and synucleinopathy, which is the accumulation of aggregated α-synuclein (α-syn). Increasing evidence implicates α-syn-associated neu...
Notash Shafiei,Daria Proniakova,Marija Simjanoska et al. Notash Shafiei et al.
Lewy body diseases, including Parkinson's disease (PD) and dementia with Lewy bodies (DLB), are defined by neuronal accumulation of misfolded α-synuclein (α-Syn), yet the ultrastructural diversity of these inclusions across brain regions ...
Chao Qi,Sofia Lövestam,Jenny Shi et al. Chao Qi et al.
Mutations in MAPT, the tau gene, give rise to forms of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17 T), with abundant filamentous tau inclusions in brain cells. Some mutations that encode missense and deletion v...
Courtney L Smith,John L Robinson,Edward B Lee Courtney L Smith
Annexin A11 (ANXA11) is a Ca2⁺-dependent phospholipid-binding protein that has recently emerged as a key player in neurodegeneration. Rare pathogenic ANXA11 variants were initially identified in cases of amyotrophic lateral sclerosis (ALS)...
Marika Bogdani,Vaishnavi S Jadhav,Brian C Kraemer et al. Marika Bogdani et al.
Autosomal-dominant frontotemporal lobar degeneration with tau pathology (FTLD-tau) is caused by pathogenic variants in the MAPT gene. Although abnormal tau aggregation is a shared endpoint, MAPT mutations produce distinct cellular phenotype...
Lea Altendorf,Anton Althammer,Rajanya Roy et al. Lea Altendorf et al.
Atypical teratoid/rhabdoid tumors (AT/RT) are the most common malignant brain tumors during infancy and associated with a dismal prognosis. The majority of patients suffer from tumor progression or recurrence, but underlying mechanisms rema...