Gina Rinetti

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
Area:
vestibular system, hair cells, exocytosis
Google:
"Gina Rinetti"
Mean distance: 14.26 (cluster 6)
 
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Publications

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Mock AF, Richardson JL, Hsieh JY, et al. (2010) Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels. Bmc Neuroscience. 11: 99
Rinetti GV, Schweizer FE. (2010) Ubiquitination acutely regulates presynaptic neurotransmitter release in mammalian neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 3157-66
Irwin M, Rinetti G, Redwine L, et al. (2004) Nocturnal proinflammatory cytokine-associated sleep disturbances in abstinent African American alcoholics. Brain, Behavior, and Immunity. 18: 349-60
Irwin MR, Rinetti G. (2004) Disordered sleep, nocturnal cytokines, and immunity: interactions between alcohol dependence and African-American ethnicity. Alcohol (Fayetteville, N.Y.). 32: 53-61
Nicolini H, Urraca N, Camarena B, et al. (2001) Lack of association of apolipoprotein E polymorphism in obsessive-compulsive disorder. Cns Spectrums. 6: 978-9, 992
Camarena B, Rinetti G, Cruz C, et al. (2001) Association study of the serotonin transporter gene polymorphism in obsessive-compulsive disorder. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 4: 269-72
Camarena B, Rinetti G, Cruz C, et al. (2001) Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder. American Journal of Medical Genetics. 105: 279-82
Rinetti G, Camarena B, Cruz C, et al. (2001) Dopamine D4 receptor (DRD4) gene polymorphism in the first psychotic episode. Archives of Medical Research. 32: 35-8
Weissbecker KA, Camarena B, Rinetti G, et al. (2001) Obsessive compulsive disorder with and without tics American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 639-640
Camarena B, Montiel F, Rinetti G, et al. (2001) Novelty seeking extreme phenotypes in ocd carriers: The low transcription allele of the MAO-A/uVNTR polymorphism American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 614-615
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