Louis Saint-Amant
Affiliations: | University of Michigan, Ann Arbor, Ann Arbor, MI |
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| Gribble KD, Walker LJ, Saint-Amant L, et al. (2018) The synaptic receptor Lrp4 promotes peripheral nerve regeneration. Nature Communications. 9: 2389 |
| Knogler LD, Ryan J, Saint-Amant L, et al. (2015) A hybrid electrical and chemical circuit in the spinal cord generates a novel transient embryonic motor behavior. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 41-2 |
| Ogino K, Low SE, Yamada K, et al. (2015) RING finger protein 121 facilitates the degradation and membrane localization of voltage-gated sodium channels. Proceedings of the National Academy of Sciences of the United States of America. 112: 2859-64 |
| Horstick EJ, Linsley JW, Dowling JJ, et al. (2013) Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy. Nature Communications. 4: 1952 |
| Kokel D, Dunn TW, Ahrens MB, et al. (2013) Identification of nonvisual photomotor response cells in the vertebrate hindbrain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 3834-43 |
| Low SE, Woods IG, Lachance M, et al. (2012) Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1b. Journal of Neurophysiology. 108: 148-59 |
| Hirata H, Wen H, Kawakami Y, et al. (2012) Connexin 39.9 protein is necessary for coordinated activation of slow-twitch muscle and normal behavior in zebrafish. The Journal of Biological Chemistry. 287: 1080-9 |
| Dupre N, Valdmanis P, Stochmanski S, et al. (2012) A Mutation in the RNF170 Gene Causes Autosomal Dominant Sensory Ataxia (P05.014) Neurology. 78: P05.014-P05.014 |
| Low SE, Amburgey K, Horstick E, et al. (2011) TRPM7 is required within zebrafish sensory neurons for the activation of touch-evoked escape behaviors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 11633-44 |
| Valdmanis PN, Dupré N, Lachance M, et al. (2011) A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. Brain : a Journal of Neurology. 134: 602-7 |