Carrie Louie, Ph.D.

Affiliations: 
2010 Biomedical Sciences University of California, San Diego, La Jolla, CA 
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"Carrie Louie"
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Joseph G. Gleeson grad student 2010 City of Hope
 (Ciliopathies: Molecular and genetic basis for Ahi1 function in retinal degeneration.)
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Publications

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Lopes VS, Boye SE, Louie CM, et al. (2013) Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus. Gene Therapy. 20: 824-33
Trivedi D, Colin E, Louie CM, et al. (2012) Live-cell imaging evidence for the ciliary transport of rod photoreceptor opsin by heterotrimeric kinesin-2. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 10587-93
Lee JE, Silhavy JL, Zaki MS, et al. (2012) CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium. Nature Genetics. 44: 193-9
Lancaster MA, Gopal DJ, Kim J, et al. (2011) Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome. Nature Medicine. 17: 726-31
Louie CM, Caridi G, Lopes VS, et al. (2010) AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis. Nature Genetics. 42: 175-80
Lancaster MA, Louie CM, Silhavy JL, et al. (2009) Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy. Nature Medicine. 15: 1046-54
Valente EM, Silhavy JL, Brancati F, et al. (2006) Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. Nature Genetics. 38: 623-5
Louie CM, Gleeson JG. (2005) Genetic basis of Joubert syndrome and related disorders of cerebellar development. Human Molecular Genetics. 14: R235-42
Dixon-Salazar T, Silhavy JL, Marsh SE, et al. (2004) Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria. American Journal of Human Genetics. 75: 979-87
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