Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1-Reference-Cited by-同舟云学术

Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1

Published:2018-07-24 Issue:9 Volume:96 Page:1576-1585
ISSN:0360-4012
Container-title:Journal of Neuroscience Research
language:en
Short-container-title:J Neuro Res

Author:

Ripolone Michela¹^ORCID,Lucchini Valeria¹,Ronchi Dario²,Fagiolari Gigliola¹,Bordoni Andreina²,Fortunato Francesco²,Mondello Stefania³,Bonato Sara²,Meregalli Mirella⁴,Torrente Yvan⁴,Corti Stefania²,Comi Giacomo P.²,Moggio Maurizio¹,Sciacco Monica¹

Affiliation:

1. Neuromuscular and Rare Diseases Unit, Department of Neuroscience; Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico; Milan, Italy

2. Neurology Unit, Neuroscience Section, Department of Pathophysiology and Transplantation, Dino Ferrari Centre, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico; University of Milan; Milan Italy

3. Department of Biomedical and Dental Sciences and Morphofunctional Imaging; University of Messina; Messina, Italy

4. Department of Pathophysiology and Transplantation, Stem Cell Laboratory; Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Centro Dino Ferrari; Milan Italy

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jnr.24263/fullpdf

Reference40 articles.

1. Altered age-related changes in bioenergetic properties and mitochondrial morphology in fibroblasts from sporadic amyotrophic lateral sclerosis patients;Allen;Neurobiology of Aging,2015

2. Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3;Barca;Clinical Genetics,2016

3. Electron cytochemistry of cristalline inclusions in human skeletal muscle mitochondria;Bonilla;Journal of Ultrastructure Research,1975

4. Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: Morphological, immunological and biochemical studies in muscle biopsies and autopsy tissues;Bresolin;Annals of Neurology,1987

5. SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat;Burright;Cell,1995

Cited by 15 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. Cerebellum in Alzheimer's disease and other neurodegenerative diseases: an emerging research frontier;MedComm;2024-07

2. Reviewing the Structure–Function Paradigm in Polyglutamine Disorders: A Synergistic Perspective on Theoretical and Experimental Approaches;International Journal of Molecular Sciences;2024-06-20

3. Lipid Metabolism: Key Determinant in Neurodegenerative Diseases;Altered Metabolism: A Major Contributor of Comorbidities in Neurodegenerative Diseases;2024

4. HD and SCA1: Tales from two 30-year journeys since gene discovery;Neuron;2023-11

5. Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1;Neuron;2023-11