Human-specific translational control of neuronal mitochondria and excitability

Lane et al. Neuron (2023)

111: 3901-3903

Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants

Zlatic et al. Human Molecular Genetics. (2023)

https://doi.org/10.1093/hmg/ddad154

APOE expression and secretion are modulated by mitochondrial dysfunction

Wynne et al. eLife (2023)

https://elifesciences.org/articles/85779

Convergent Cerebrospinal Fluid Proteomes and Metabolic Ontologies in Humans and Animal Models of Rett Syndrome

Zlatic et al. iScience(2022)

https://doi.org/10.1016/j.isci.2022.104966

Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus

Gokhale et al. J Neurosci. 2021 Aug 4;41(31):6596-6616. doi: 10.1523/JNEUROSCI.2197-20.2021.

Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory Neurons

Wynne et al. eNeuro. 2021 Aug 9;8(4):ENEURO.0232-21.2021. doi: 10.1523/ENEURO.0232-21.2021

Mitochondrial Protein Synthesis and the Bioenergetic Cost of Neurodevelopment

Bülow SA et al. iScience.(2022)

https://doi.org/10.1016/j.isci.2022.104966

The Physician-Scientist, 75 Years After Vannevar Bush-rethinking the 'Bench' and 'Bedside' Dichotomy

Sarma G et al. Nature Medicine 26(4):461-462.  doi: 10.1038/s41591-020-0828-1.

Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content

Hartwig, C et al. J Neurosci 2021 Jan 13;41(2):215-233. doi: 10.1523/JNEUROSCI.1284-20.2020

The Mitochondrial RNA Granule Modulates Manganese-Dependent Cell Toxicity

Werner E et al. Mol Biol Cell. (2022)

https://www.molbiolcell.org/doi/10.1091/mbc.E22-03-0096

Rare Genetic Diseases: Nature's Experiments on Human Development

Chelsea E. Lee iScience. 2020 May 22;23(5):101123. doi: 10.1016/j.isci.2020.101123.

FMRP attenuates activity dependent modifications in the mitochondrial proteome

Mol Brain 14, 75 (2021) https://doi.org/10.1186/s13041-021-00783-w