Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ
Top Cited Papers
- 1 June 2001
- Vol. 105 (5), 587-597
- https://doi.org/10.1016/s0092-8674(01)00363-4
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 26 references indexed in Scilit:
- Kinesin Superfamily Motor Protein KIF17 and mLin-10 in NMDA Receptor-Containing Vesicle TransportScience, 2000
- SSCP analysis of long DNA fragments in low pH gelHuman Mutation, 1997
- The neuron-specific kinesin superfamily protein KIF1A is a uniqye monomeric motor for anterograde axonal transport of synaptic vesicle precursorsCell, 1995
- KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondriaCell, 1994
- Altered microtubule organization in small-calibre axons of mice lacking tau proteinNature, 1994
- Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic HeterogeneityGenomics, 1993
- The neuropathy of elderly miceActa Neuropathologica, 1993
- Brain dynein (MAP1C) localizes on both anterogradely and retrogradely transported membranous organelles in vivo.The Journal of cell biology, 1990
- Genetic aspects of hereditary motor and sensory neuropathy (types I and II)Journal of Medical Genetics, 1980
- The quantitative measurement of motor inco-ordination in naive mice using an accelerating rotarodJournal of Pharmacy and Pharmacology, 1968