Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels-Reference-Cited by-同舟云学术

Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels

Published:2016-12 Issue: Volume:96 Page:115-126
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Sen Nesli Ece,Drost Jessica,Gispert Suzana,Torres-Odio Sylvia,Damrath Ewa,Klinkenberg Michael,Hamzeiy Hamid,Akdal Gülden,Güllüoğlu Halil,Başak A. Nazlı,Auburger Georg

Funder

DFG

Suna and İnan Kıraç Foundation

Bogazici University Research Funds

Publisher

Elsevier BV

Subject

Neurology

Reference138 articles.

1. Characterization of OPA1 isoforms isolated from mouse tissues;Akepati;J. Neurochem.,2008

2. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat. Genet.,2000

3. Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis;Almaguer-Mederos;Clin. Genet.,2010

4. Estimation of survival in spinocerebellar ataxia type 2 Cuban patients;Almaguer-Mederos;Clin. Genet.,2013

5. dAtaxin-2 mediates expanded ataxin-1-induced neurodegeneration in a Drosophila model of SCA1;Al-Ramahi;PLoS Genet.,2007

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Axonopathy Underlying Amyotrophic Lateral Sclerosis: Unraveling Complex Pathways and Therapeutic Insights;Neuroscience Bulletin;2024-08-04

2. The polyglutamine protein ATXN2: from its molecular functions to its involvement in disease;Cell Death & Disease;2024-06-14

3. The molecular mechanisms of spinocerebellar ataxias for DNA repeat expansion in disease;Emerging Topics in Life Sciences;2023-09-05

4. Pbp1 associates with Puf3 and promotes translation of its target mRNAs involved in mitochondrial biogenesis;PLOS Genetics;2023-05-22

5. Modeling amyotrophic lateral sclerosis through Ataxin-2 pathology;Handbook of Animal Models in Neurological Disorders;2023