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Integration of resources and studies to elucidate neuropeptide signaling Abstract Elucidating the mechanisms governing drug addiction requires knowledge of the role of neuropeptides on the neuronal networks. These signaling peptides mediate responses to environmental stimuli and influence addiction behaviors. Many drugs of abuse directly interact with neuropeptide receptors, and others appear to mediate peptide responses. NIDA has a long tradition of supporting fundamental neuroscience research that has lead to the elucidation of signaling systems and provided critical insights into substance abuse and behavior. Signaling peptides have been studied using a wide range of techniques and model organisms. Multiple complementary neuropeptide repositories and peptidomic and transcriptomic experiments are now available. Even with such information, the challenge remains to gain a complete and systematic understanding of the neuropeptidome and its association with drug escalation and abuse. We propose to address this challenge by developing a public and comprehensive neuropeptide resource much needed by the research community and by collectively analyzing proteomic and transcriptomic experiments to augment the understanding of extracellular signaling peptides both at the fundamental neuroscience as well as the applied substance abuse levels. To accomplish these objectives, we plan to (Aim 1) integrate complementary peptide repositories and develop tools to assemble and effectively query a comprehensive and public resource of experimental and in silico predictions; mine this resource to (Aim 2) perform secondary and joint analysis of available high proteomic experiments; and (Aim 3) perform integrated analysis of proteomic and transcriptomic experiments. The overarching strategy is to integrate complementary information across databases, experiments and platforms to provide a unique and comprehensive understanding of the dynamic neuropeptide complement. The outcome of this project will be resources, tools and information that will fill critical gaps in the knowledge on intercellular signaling systems and suggest targets for prevention, diagnosis and cure of substance abuse.
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Common and novel transcriptional routes to behavioral maturation in worker and male honey bees.
工蜂和雄性蜜蜂行为成熟的常见和新颖的转录途径。
DOI: 10.1111/j.1601-183x.2011.00750.x
发表时间: 2012
期刊: Genes, brain, and behavior
影响因子: --
作者: [Zayed,A, Naeger,NL, Rodriguez-Zas,SL, Robinson,GE]
通讯作者: Robinson,GE
Synergistic and antagonistic interplay between myostatin gene expression and physical activity levels on gene expression patterns in triceps Brachii muscles of C57/BL6 mice.
肌生长抑制素基因表达和体力活动水平之间对 C57/BL6 小鼠肱三头肌基因表达模式的协同和拮抗相互作用。
DOI: 10.1371/journal.pone.0116828
发表时间: 2015
期刊: PloS one
影响因子: 3.7
作者: [Caetano-Anollés,Kelsey, Mishra,Sanjibita, Rodriguez-Zas,SandraL]
通讯作者: Rodriguez-Zas,SandraL
DOI: 10.1371/journal.pone.0058608
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Delfino KR, Rodriguez-Zas SL]
通讯作者: Rodriguez-Zas SL
Inflammation-Induced Behavioral Alterations: A Psychogenomic Approach
Inflammation-Induced Behavioral Alterations: A Psychogenomic Approach
Discovery of exon, microRNA and clinical prognostic markers of glioblastoma survi
Discovery of exon, microRNA and clinical prognostic markers of glioblastoma survi
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