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UnknownReduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations.
Not available
S-EPMC4502563 | biostudies-literature
UnknownHomotypic fibrillization of TMEM106B across diverse neurodegenerative diseases.
Not available
S-EPMC9018563 | biostudies-literature
UnknownC-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes.
Not available
S-EPMC10545506 | biostudies-literature
UnknownFluorescence grid analysis for the evaluation of piecemeal surgery in sinonasal inverted papilloma: a proof-of-concept study.
Not available
S-EPMC8940828 | biostudies-literature
UnknownIncreased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health.
Not available
S-EPMC12016085 | biostudies-literature
UnknownContribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
Not available
S-EPMC7881566 | biostudies-literature
UnknownAnalysis of the splicing landscape of the frontal cortex in FTLD-TDP reveals subtype specific patterns and cryptic splicing
Not available
S-EPMC12143990 | biostudies-literature
UnknownMutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Not available
S-EPMC7244618 | biostudies-literature
UnknownThe C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
Not available
S-EPMC4960451 | biostudies-literature
UnknownLoss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
Not available
S-EPMC4691687 | biostudies-literature
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