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Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich's ataxia patients

ChEBI2017-10-18 更新2026-07-12 收录

神经退行性疾病生物标志物

循环miRNA测序分析

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-105052 数据链接链接失效反馈

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资源简介：

Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich's ataxia patients

应用场景：

创建时间：

2017-10-18

神经退行性疾病生物标志物

miRNA表达分析

Repetitive head impacts (RHI) and traumatic brain injuries are risk factors for the neurodegenerative diseases chronic traumatic encephalopathy (CTE) and amyotrophic lateral sclerosis (ALS). ALS and C

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Table_2_Genetic Variability in Molecular Pathways Implicated in Alzheimer's Disease: A Comprehensive Review.XLSX

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神经退行性疾病生物标志物

Alzheimer's disease (AD) is a complex neurodegenerative disease, affecting a significant part of the population. The majority of AD cases occur in the elderly with a typical age of onset of the diseas

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HDAC concentrations in human neural retina.

神经退行性疾病生物标志物

组蛋白去乙酰化酶定量分析

aMeasurements were performed on supernatant of retina from control (n = 4), AD-affected (n = 3), and AMD (n = 4) human donor pools (S4 Table) supplemented with QconCAT standards after high-speed centr

NIAID Data Ecosystem50

Additional file 3 of An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease

神经退行性疾病生物标志物

RNA-seq数据分析

Supplementary Material 3

DataCite Commons2024-08-17 更新80

Alterations in the tyrosine and phenylalanine pathways revealed by biochemical profiling in cerebrospinal fluid of Huntington’s disease subjects

亨廷顿病代谢组学

神经退行性疾病生物标志物

Huntington's disease (HD) is a severe neurological disease leading to psychiatric symptoms, motor impairment and cognitive decline. The disease is caused by a CAG expansion in the huntingtin (HTT) gen

NIAID Data Ecosystem50

Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich's ataxia patients

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