Detalhe da pesquisa
1.
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease.
Mov Disord
; 37(2): 302-314, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34779538
2.
Hippocampal network hyperexcitability in young transgenic mice expressing human mutant alpha-synuclein.
Neurobiol Dis
; 149: 105226, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33347975
3.
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level.
Nucleic Acids Res
; 47(14): 7430-7443, 2019 08 22.
Artigo
Inglês
| MEDLINE | ID: mdl-31147703
4.
Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues.
Neurobiol Dis
; 134: 104631, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31689514
5.
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle.
Ann Neurol
; 84(2): 289-301, 2018 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30014514
6.
Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.
Nucleic Acids Res
; 44(11): 5313-29, 2016 06 20.
Artigo
Inglês
| MEDLINE | ID: mdl-27131788
7.
Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls.
Acta Neuropathol
; 139(1): 219-221, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31781911
8.
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
Nat Genet
; 38(5): 515-7, 2006 May.
Artigo
Inglês
| MEDLINE | ID: mdl-16604074
9.
A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders.
Biochim Biophys Acta Mol Basis Dis
; 1870(5): 167131, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38521420
10.
No excess of mitochondrial DNA deletions within muscle in progressive multiple sclerosis.
Mult Scler
; 19(14): 1858-66, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-23787892
11.
Mitochondrial DNA and disease.
J Pathol
; 226(2): 274-86, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-21989606
12.
Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.
Brain
; 135(Pt 6): 1736-50, 2012 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22577219
13.
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.
Brain
; 135(Pt 1): 62-71, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22189570
14.
Single Cell Analysis of Mitochondrial DNA Deletions.
Methods Mol Biol
; 2615: 443-463, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36807808
15.
Parkinson's disease neurons exhibit alterations in mitochondrial quality control proteins.
NPJ Parkinsons Dis
; 9(1): 120, 2023 Aug 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37553379
16.
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.
Hum Mol Genet
; 19(15): 3043-52, 2010 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20484224
17.
Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis.
Ann Neurol
; 69(3): 481-92, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21446022
18.
Nature of mitochondrial DNA deletions in substantia nigra neurons.
Am J Hum Genet
; 82(1): 228-35, 2008 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-18179904
19.
3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampus.
Cell Rep
; 36(6): 109509, 2021 08 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34380033
20.
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson's disease.
NPJ Parkinsons Dis
; 7(1): 39, 2021 May 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33980828