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Matthias Elstner

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Plos One|April 30, 2013
TOM40 mediates mitochondrial dysfunction induced by α-synuclein accumulation in Parkinson's diseaseAndreas Bender, Paula Desplats, Brian Spencer, et al.
Nucleic Acids Research|August 4, 2006
Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variantsDeborah Pye, Dimitra S Kyriakouli, Geoffrey A Taylor, et al.
Molecular Brain|December 23, 2011
Neuromelanin, neurotransmitter status and brainstem location determine the differential vulnerability of catecholaminergic neurons to mitochondrial DNA deletionsMatthias Elstner, Sarina K Müller, Lars Leidolt, et al.
Brain : a Journal of Neurology|July 26, 2013
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanismsCeline Perier, Andreas Bender, Elena García-Arumí, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?Helen Swalwell, Emma L Blakely, Ruth Sutton, et al.
Brain : a Journal of Neurology|September 22, 2022
The phenotypic spectrum of COX20-associated mitochondrial disorderRui Ban, Robert Kopajtich, Junlan Lv, et al.
Journal of Medical Genetics|April 3, 2021
Whole genome and exome sequencing identify <i>NDUFV2</i> mutations as a new cause of progressive cavitating leukoencephalopathyZhimei Liu, Li Zhang, Changhong Ren, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Acta Neuropathologica Communications|July 1, 2016
Analysis of primary visual cortex in dementia with Lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinationsAhmad A Khundakar, Peter S Hanson, Daniel Erskine, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Plos One|April 30, 2013
TOM40 mediates mitochondrial dysfunction induced by α-synuclein accumulation in Parkinson's diseaseAndreas Bender, Paula Desplats, Brian Spencer, et al.
Nucleic Acids Research|August 4, 2006
Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variantsDeborah Pye, Dimitra S Kyriakouli, Geoffrey A Taylor, et al.
Molecular Brain|December 23, 2011
Neuromelanin, neurotransmitter status and brainstem location determine the differential vulnerability of catecholaminergic neurons to mitochondrial DNA deletionsMatthias Elstner, Sarina K Müller, Lars Leidolt, et al.
Brain : a Journal of Neurology|July 26, 2013
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanismsCeline Perier, Andreas Bender, Elena García-Arumí, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?Helen Swalwell, Emma L Blakely, Ruth Sutton, et al.
Brain : a Journal of Neurology|September 22, 2022
The phenotypic spectrum of COX20-associated mitochondrial disorderRui Ban, Robert Kopajtich, Junlan Lv, et al.
Journal of Medical Genetics|April 3, 2021
Whole genome and exome sequencing identify <i>NDUFV2</i> mutations as a new cause of progressive cavitating leukoencephalopathyZhimei Liu, Li Zhang, Changhong Ren, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Acta Neuropathologica Communications|July 1, 2016
Analysis of primary visual cortex in dementia with Lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinationsAhmad A Khundakar, Peter S Hanson, Daniel Erskine, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Pageof 3