Publications by authors named "Adrian Flierl"

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The mitochondrial adenine nucleotide transporters in myogenesis.
Adrian Flierl, Samuel E Schriner, Saege Hancock, Pinar E Coskun, Douglas C Wallace

Free Radic Biol Med· August 2022

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LRRK2 p.Ile1371Val Mutation in a Case with Neuropathologically Confirmed Multi-System Atrophy.
Kelsey Lee, Khanh-Dung Nguyen, Chao Sun, Mei Liu, Faria Zafar, Adrian Flierl

J Parkinsons Dis· October 2019

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β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease.
Shuchi Mittal, Kjetil Bjørnevik, Doo Soon Im, Adrian Flierl, Xianjun Dong

Science· September 2017

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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.
Jason E Kokoszka, Katrina G Waymire, Adrian Flierl, Katelyn M Sweeney, Alessia Angelin

Biochim Biophys Acta· August 2016

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Higher vulnerability and stress sensitivity of neuronal precursor cells carrying an alpha-synuclein gene triplication.
Adrian Flierl, Luís M A Oliveira, Lisandro J Falomir-Lockhart, Sally K Mak, Jayne Hesley

PLoS One· July 2015

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Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
Mariella Simon, Elodie M Richard, Xinjian Wang, Mohsin Shahzad, Vincent H Huang, Adrian Flierl

PLoS Genet· March 2015

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