Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.

By Chunjie Zhao, J. Takita, Yosuke Tanaka, M. Setou, Terunaga Nakagawa, S. Takeda, Hongwei Yang, S. Terada, T. Nakata, Yosuke Takei and 4 more. Cell, 2001

762 citations recorded by the source corpus.

Subfields: Cell Biology, Cellular and Molecular Neuroscience

View Paper: https://www.semanticscholar.org/paper/1671cdd20b35255acae61722c91043a20348f5cf

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In Cell Biology

1. Thomas Schwarz
2. R. Vale
3. D. C. Chan

In Cellular and Molecular Neuroscience

1. Ian A. Meinertzhagen
2. Thomas Schwarz
3. R. Vale

Citations in the corpus

• Axon degeneration mechanisms: commonality amid diversity (2005, neutral): “Genetic defects in kinesin family proteins often specifically cause axon degeneratio”
• The lipid binding pleckstrin homology domain in UNC-104 kinesin is necessary for synaptic vesicle transport in Caenorhabditis elegans. (2004, background): “Mutations in neuronal kinesin genes recently have been linked to human neurodegenerative diseases, most likely as the consequence of impaired ax- onal transport (Zhao et al., 2001; Reid et al., 2002).”
• AXONAL TRANSPORT: CARGO-SPECIFIC MECHANISMS OF MOTILITY AND REGULATION (2014, neutral): “…et al., 2013 Kinesin-13 KIF2A CDCBM3/MCD Poirier et al., 2013 Kinesin-3 KIF1A, KIF1B, KIF1C HSP (SPG30), CMT2A, HSN, MR, SPAX Erlich et al., 2011; Zhao et al., 2001; Rivière et al., 2011; Hamdan et al., 2011; Klebe et al., 2012; Dor et al., 2014; Novarino et al., 2014 Kinesin-4 KIF21A CFEOM…”
• Axonal transport of mitochondria to synapses depends on milton, a novel Drosophila protein. (2002, background): “In contrast, synaptic vesicles peripheral neuropathy that has an underlying defect incontinue to be transported to and concentrated at axonal transport (Zhao et al., 2001).synapses.”