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Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death. [electronic resource] by
- Elstner, Matthias
- Morris, Christopher M
- Heim, Katharina
- Bender, Andreas
- Mehta, Divya
- Jaros, Evelyn
- Klopstock, Thomas
- Meitinger, Thomas
- Turnbull, Douglass M
- Prokisch, Holger
Producer: 20111013
In:
Acta neuropathologica vol. 122
Availability: No items available.
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15.
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TOM40 mediates mitochondrial dysfunction induced by α-synuclein accumulation in Parkinson's disease. [electronic resource] by
- Bender, Andreas
- Desplats, Paula
- Spencer, Brian
- Rockenstein, Edward
- Adame, Anthony
- Elstner, Matthias
- Laub, Christoph
- Mueller, Sarina
- Koob, Andrew O
- Mante, Michael
- Pham, Emily
- Klopstock, Thomas
- Masliah, Eliezer
Producer: 20131126
In:
PloS one vol. 8
Availability: No items available.
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16.
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Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants. [electronic resource] by
- Pye, Deborah
- Kyriakouli, Dimitra S
- Taylor, Geoffrey A
- Johnson, Riem
- Elstner, Matthias
- Meunier, Brigitte
- Chrzanowska-Lightowlers, Zofia M A
- Taylor, Robert W
- Turnbull, Douglass M
- Lightowlers, Robert N
Producer: 20060816
In:
Nucleic acids research vol. 34
Availability: No items available.
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17.
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Neuromelanin, neurotransmitter status and brainstem location determine the differential vulnerability of catecholaminergic neurons to mitochondrial DNA deletions. [electronic resource] by
- Elstner, Matthias
- Müller, Sarina K
- Leidolt, Lars
- Laub, Christoph
- Krieg, Lena
- Schlaudraff, Falk
- Liss, Birgit
- Morris, Chris
- Turnbull, Douglass M
- Masliah, Eliezer
- Prokisch, Holger
- Klopstock, Thomas
- Bender, Andreas
Producer: 20120605
In:
Molecular brain vol. 4
Availability: No items available.
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18.
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A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one? [electronic resource] by
- Swalwell, Helen
- Blakely, Emma L
- Sutton, Ruth
- Tonska, Kasia
- Elstner, Matthias
- He, Langping
- Taivassalo, Tanja
- Burns, Dennis K
- Turnbull, Douglass M
- Haller, Ronald G
- Davidson, Mercy M
- Taylor, Robert W
Producer: 20081105
In:
European journal of human genetics : EJHG vol. 16
Availability: No items available.
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19.
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Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms. [electronic resource] by
- Perier, Celine
- Bender, Andreas
- García-Arumí, Elena
- Melià, Ma Jesus
- Bové, Jordi
- Laub, Christoph
- Klopstock, Thomas
- Elstner, Matthias
- Mounsey, Ross B
- Teismann, Peter
- Prolla, Tomas
- Andreu, Antoni L
- Vila, Miquel
Producer: 20131030
In:
Brain : a journal of neurology vol. 136
Availability: No items available.
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20.
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Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. [electronic resource] by
- Hartig, Monika B
- Iuso, Arcangela
- Haack, Tobias
- Kmiec, Tomasz
- Jurkiewicz, Elzbieta
- Heim, Katharina
- Roeber, Sigrun
- Tarabin, Victoria
- Dusi, Sabrina
- Krajewska-Walasek, Malgorzata
- Jozwiak, Sergiusz
- Hempel, Maja
- Winkelmann, Juliane
- Elstner, Matthias
- Oexle, Konrad
- Klopstock, Thomas
- Mueller-Felber, Wolfgang
- Gasser, Thomas
- Trenkwalder, Claudia
- Tiranti, Valeria
- Kretzschmar, Hans
- Schmitz, Gerd
- Strom, Tim M
- Meitinger, Thomas
- Prokisch, Holger
Producer: 20111212
In:
American journal of human genetics vol. 89
Availability: No items available.
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