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Toxicity of Familial ALS-Linked SOD1 Mutants from Selective Recruitment to Spinal Mitochondria
by Liu, Jian
Neuron (Cambridge, Mass.), 2004, Vol.43 (1), p.5-17
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Fusion and Fission: Interlinked Processes Critical for Mitochondrial Health
by Chan, David C
Annual review of genetics, 2012, Vol.46 (1), p.265-287
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Tau Promotes Neurodegeneration via DRP1 Mislocalization In Vivo
by DuBoff, Brian
Neuron (Cambridge, Mass.), 2012, Vol.75 (4), p.618-632
4.
Maintenance and Expression of Mammalian Mitochondrial DNA
by Gustafsson, Claes M
Annual review of biochemistry, 2016, Vol.85 (1), p.133-160
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RNA Editing in Plants and Its Evolution
by Takenaka, Mizuki
Annual review of genetics, 2013, Vol.47 (1), p.335-352
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VCP Is Essential for Mitochondrial Quality Control by PINK1/Parkin and this Function Is Impaired by VCP Mutations
by Kim, Nam Chul
Neuron (Cambridge, Mass.), 2013, Vol.78 (1), p.65-80
7.
Enjoy the Trip: Calcium in Mitochondria Back and Forth
by De Stefani, Diego
Annual review of biochemistry, 2016, Vol.85 (1), p.161-192
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Brown adipose tissue thermogenic adaptation requires Nrf1-mediated proteasomal activity
by Bartelt, Alexander
Nature medicine, 2018, Vol.24 (3), p.292-303
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A Fatal Mitochondrial Disease Is Associated with Defective NFU1 Function in the Maturation of a Subset of Mitochondrial Fe-S Proteins
by Navarro-Sastre, Aleix
American journal of human genetics, 2011, Vol.89 (5), p.656-667
10.
The mitochondrial proteome and human disease
by Calvo, Sarah E
Annual review of genomics and human genetics, 2010, Vol.11 (1), p.25-44
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The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders
by Houten, Sander M
Annual review of physiology, 2016, Vol.78 (1), p.23-44
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Mitochondria: The Next (Neurode)Generation
by Schon, Eric A
Neuron (Cambridge, Mass.), 2011, Vol.70 (6), p.1033-1053
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Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits
by Kraja, Aldi T. Aldi T.
American journal of human genetics, 2018, Vol.104 (1), p.112-138
14.
Structure and Function of the Mitochondrial Ribosome
by Greber, Basil J
Annual review of biochemistry, 2016, Vol.85 (1), p.103-132
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Autophagy deficiency leads to protection from obesity and insulin resistance by inducing Fgf21 as a mitokine
by Kim, Kook Hwan
Nature medicine, 2013, Vol.19 (1), p.83-92
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Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
by Beal, M. Flint
Nature, 2006, Vol.443 (7113), p.787-795
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Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome
by Pierce, Sarah B
American journal of human genetics, 2013, Vol.92 (4), p.614-620
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De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction
by Ehmke, Nadja
American journal of human genetics, 2017, Vol.101 (5), p.833-843
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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease
by Jenkinson, Emma M
American journal of human genetics, 2013, Vol.92 (4), p.605-613
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Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
by Suzuki, Tsutomu
Annual review of genetics, 2011, Vol.45 (1), p.299-329
