课题基金 / 基金详情

Pharmacology of Lifespan Extension

Pharmacology of Lifespan Extension
延长寿命的药理学
批准号：
9521330
负责人：
Julie Kay Andersen
金额：
$19.4万
依托单位：
BUCK INSTITUTE FOR RESEARCH ON AGING
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
项目状态：
已结题
起止时间：
2008-02-15 至 2019-04-30
来源：
https://reporter.nih.gov/project-details/9521330
关键词：
Age of OnsetAgingAnimal ModelBiochemicalCaenorhabditisCaenorhabditis elegansCell LineChemicalsCholecalciferolChronic DiseaseClinical ResearchClinical TrialsCommunitiesDevelopmentDiseaseDoseDrug ModelingsElderlyEndoplasmic ReticulumExhibitsFunctional disorderFutureGeneticHealthHomeostasisIncidenceInterventionLeadLinkLongevityLongevity PathwayMammalian CellMammalsModelingNatural ProductsNematodaNeurodegenerative DisordersPathologyPathway interactionsPharmaceutical PreparationsPharmacologyPhenotypePlayPopulationPreventionPreventive therapyProteinsPublic HealthResearchRoleSecosteroidsSeriesStructureTechnologyTestingVitamin DVitamin D DeficiencyWorkage relatedamyloid formationcompound 30drug discoveryhigh throughput screeningimprovednovelpre-clinicalpre-clinical researchpreventprotein structureproteostasispublic health relevanceresponsesmall moleculesmall molecule librariessuccessful interventiontherapy outcometranslational study

项目摘要

项目成果

Julie Kay Andersen的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): We have discovered a series of chemical compounds that delay the onset of age-related pathology and extend lifespan. These compounds were identified in focused chemical screens and high throughput screens of both synthetic compounds and natural products. Here we propose to identify the mechanism of lifespan extension with a focus on vitamin D which we have shown maintains protein homeostasis and extends lifespan in C. elegans. This will uncover novel mechanisms for interventions in aging and age-related disease.
期刊论文(7)
专著(0)
科研奖励(0)
会议论文
Iron promotes protein insolubility and aging in C. elegans.
DOI： 10.18632/aging.100689
发表时间： 2014-11
期刊： Aging
影响因子： --
作者： [Klang IM, Schilling B, Sorensen DJ, Sahu AK, Kapahi P, Andersen JK, Swoboda P, Killilea DW, Gibson BW, Lithgow GJ]
通讯作者： Lithgow GJ
Kavain suppresses human Aβ-induced paralysis in C. elegans.
Kavain 抑制人 Aβ 诱导的线虫麻痹。
DOI： 10.17912/micropub.biology.000254
发表时间： 2020
期刊： microPublication biology
影响因子： --
作者： [Chamoli,Manish, Chinta,ShankarJ, Andersen,JulieK, Lithgow,GordonJ]
通讯作者： Lithgow,GordonJ
Vitamin D Promotes Protein Homeostasis and Longevity via the Stress Response Pathway Genes skn-1, ire-1, and xbp-1.
DOI： 10.1016/j.celrep.2016.09.086
发表时间： 2016-10-25
期刊： Cell reports
影响因子： 8.8
作者： [Mark KA, Dumas KJ, Bhaumik D, Schilling B, Davis S, Oron TR, Sorensen DJ, Lucanic M, Brem RB, Melov S, Ramanathan A, Gibson BW, Lithgow GJ]
通讯作者： Lithgow GJ
Zinc Levels Modulate Lifespan through Multiple Longevity Pathways in Caenorhabditis elegans.
DOI： 10.1371/journal.pone.0153513
发表时间： 2016
期刊： PloS one
影响因子： 3.7
作者： [Kumar J, Barhydt T, Awasthi A, Lithgow GJ, Killilea DW, Kapahi P]
通讯作者： Kapahi P
Novel mitochondria-to-lysosome crosstalk contributes to lysosomal dysfunction during aging
Neuronal FXR as a potential therapeutic target for Alzheimer's disease
Cellular senescence and Alzheimer's disease
Neuronal FXR as a potential therapeutic target for Alzheimer's disease
海外基金