Ali G. Fenstermaker

University of California, San Diego, La Jolla, CA 
developmental neuroscience
"Ali Fenstermaker"
Mean distance: 16.51 (cluster 11)


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Yimin Zou grad student 2004-2010 UCSD
 (Mechanisms of axon pathfinding and survival.)
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Zaki MS, Selim L, Mansour L, et al. (2015) Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis. Clinical Genetics. 88: 95-7
Baek ST, Kerjan G, Bielas SL, et al. (2014) Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous microRNA dysregulation. Neuron. 82: 1255-62
Novarino G, Fenstermaker AG, Zaki MS, et al. (2014) Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science (New York, N.Y.). 343: 506-11
Akizu N, Silhavy JL, Rosti RO, et al. (2014) Mutations in CSPP1 lead to classical Joubert syndrome. American Journal of Human Genetics. 94: 80-6
Akizu N, Cantagrel V, Schroth J, et al. (2013) AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder. Cell. 154: 505-17
Lin W, Lin Y, Li J, et al. (2013) Oligodendrocyte-specific activation of PERK signaling protects mice against experimental autoimmune encephalomyelitis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 5980-91
Dixon-Salazar TJ, Silhavy JL, Udpa N, et al. (2012) Exome sequencing can improve diagnosis and alter patient management. Science Translational Medicine. 4: 138ra78
Fenstermaker AG, Prasad AA, Bechara A, et al. (2010) Wnt/planar cell polarity signaling controls the anterior-posterior organization of monoaminergic axons in the brainstem. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 16053-64
Wolf AM, Lyuksyutova AI, Fenstermaker AG, et al. (2008) Phosphatidylinositol-3-kinase-atypical protein kinase C signaling is required for Wnt attraction and anterior-posterior axon guidance. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 3456-67
Fortun J, Li J, Go J, et al. (2005) Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model. Journal of Neurochemistry. 92: 1531-41
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