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Robert W. Burgess

University of Maine

107

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p53-mediated neurodegeneration in the absence of the nuclear protein Akirin2

2021 bioRxiv
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A longitudinal and cross-sectional study of plasma neurofilament light chain concentration in Charcot-Marie-Tooth disease.

2021 Journal of The Peripheral Nervous System
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An allelic series of spontaneous mutations in Rorb cause a gait phenotype, retinal abnormalities, and transcriptomic changes relevant to human neurodevelopmental conditions

2021 bioRxiv
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Structural variant in mitochondrial-associated gene (MRPL3) induces adult-onset neurodegeneration with memory impairment in the mouse.

2020 The Journal of Neuroscience
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Allele-specific RNA interference prevents neuropathy in Charcot-Marie-Tooth disease type 2D mouse models

2019 Journal of Clinical Investigation
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CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4

2019 bioRxiv
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Aberrant GlyRS-HDAC6 interaction linked to axonal transport deficits in Charcot-Marie-Tooth neuropathy

2018 Nature Communications
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DSCAM promotes self-avoidance in the developing mouse retina by masking the functions of cadherin superfamily members

2018 Proceedings of the National Academy of Sciences of the United States of America
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Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes.

2017 Cell Reports
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Accumulating Evidence for Axonal Translation in Neuronal Homeostasis

2017 Frontiers in Neuroscience
- Emily L. Spaulding
- Robert W. Burgess
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Citations (29)