Homo sapiens Genome sequencing and assembly. Homo sapiens

NIAID Data Ecosystem2026-03-13 收录

帕金森病转录组

神经退行性疾病

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA792712 数据链接链接失效反馈

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The aim of this study was to characterize the transcriptome characteristics of patients with Parkinson's disease.

创建时间：

2021-12-28

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

线粒体功能障碍

神经退行性疾病

Although exact causes of Parkinson disease (PD) remain enigmatic, mitochondrial dysfunction is increasingly appreciated as a key determinant of dopaminergic neuron susceptibility in both familial and

DataCite Commons2020-08-28 更新100

Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: Evidence for involvement of splicing regulatory proteins

基因剪接

神经退行性疾病

Spinal Muscular Atrophy (SMA) is caused by deletions or mutations in the Survival Motor Neuron 1 ( SMN1 ) gene. The second gene copy, SMN2 , produces some, but not enough, functional SMN pr

DataCite Commons2020-09-04 更新60

Additional file 3 of Targeting the glycine-rich domain of TDP-43 with antibodies prevents its aggregation in vitro and reduces neurofilament levels in vivo

神经退行性疾病

基因表达分析

Additional file 3: Table S2. Full Gene Ontology enrichment analysis for differentially expressed genes from TargetALS patients in spinal cord and genes expressed in rNLS8 mice, each both compared to n

DataCite Commons2024-08-14 更新50

Additional file 2 of Identification and validation of a tear fluid-derived protein biomarker signature in patients with amyotrophic lateral sclerosis

神经退行性疾病

生物标志物

Supplementary Material 2

DataCite Commons2025-09-03 更新70

UBA5 mutations cause a new form of autosomal recessive cerebellar ataxia

遗传学

神经退行性疾病

Autosomal recessive cerebellar ataxia (ARCA) comprises a large and heterogeneous group of neurodegenerative disorders. Through whole-exome sequencing, we identified compound heterozygous mutations in

DataCite Commons2020-09-04 更新50

Homo sapiens Genome sequencing and assembly. Homo sapiens

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