IDENTIFICATION OF THE PHYSIOLOGICALLY RELEVANT ENDOGENOUS LIGAND FOR PPAR?
PPAR 的生理相关内源性配体的鉴定?
基本信息
- 批准号:8361385
- 负责人:
- 金额:$ 0.81万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2011
- 资助国家:美国
- 起止时间:2011-01-01 至 2011-12-31
- 项目状态:已结题
- 来源:
- 关键词:DiseaseFatty-acid synthaseFundingGene ExpressionGenerationsGrantHumanLigandsMass Spectrum AnalysisNational Center for Research ResourcesNuclear ReceptorsPPAR alphaPeroxisome Proliferator-Activated ReceptorsPharmaceutical PreparationsPrincipal InvestigatorResearchResearch InfrastructureResourcesSourceUnited States National Institutes of Healthbiomedical resourcecostlipid metabolism
项目摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
The nuclear receptor PPARalpha is activated by drugs to treat human disorders of lipid metabolism. Its endogenous ligand is unknown. PPARalpha-dependent gene expression is impaired with inactivation of fatty acid synthase (FAS), suggesting that FAS is involved in generation of a PPARalpha ligand.
这个子项目是利用这些资源的众多研究子项目之一
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Manu V. Chakravarthy其他文献
848 A NOVEL, PRECISION-ENGINEERED AMINO ACID COMPOSITION, AXA1665, IS SAFE, WELL-TOLERATED AND IMPROVES NEUROCOGNITION AND PHYSICAL FUNCTION IN CHILD-PUGH A AND B SUBJECTS
- DOI:
10.1016/s0016-5085(21)02620-2 - 发表时间:
2021-05-01 - 期刊:
- 影响因子:
- 作者:
Arun J. Sanyal;Scharmen Confer;Robert G. Perry;Joel M. Neutel;Eric Lawitz;Jasmohan S. Bajaj;Andres Duarte-Rojo;William Comb;Jeff Zhao;Manu V. Chakravarthy - 通讯作者:
Manu V. Chakravarthy
Biased agonism of GLP-1R and GIPR enhances glucose lowering and weight loss, with dual GLP-1R/GIPR biased agonism yielding greater efficacy
GLP-1R 和 GIPR 的偏向激动作用增强了降糖和减重效果,而双重 GLP-1R/GIPR 偏向激动作用产生了更大的疗效。
- DOI:
10.1016/j.xcrm.2025.102156 - 发表时间:
2025-06-17 - 期刊:
- 影响因子:10.600
- 作者:
Ruben Rodriguez;Anne Hergarden;Shyam Krishnan;Marikris Morales;Davina Lam;Ted Tracy;Teresa Tang;Avalon Patton;Craig Lee;Asmita Pant;Daniel A. Erlanson;Johan Enquist;Derek Bone;Ray Fucini;Damian Bialonczyk;Stig K. Hansen;Jian Luo;Manu V. Chakravarthy - 通讯作者:
Manu V. Chakravarthy
Manu V. Chakravarthy的其他文献
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{{ truncateString('Manu V. Chakravarthy', 18)}}的其他基金
IDENTIFICATION OF THE PHYSIOLOGICALLY RELEVANT ENDOGENOUS LIGAND FOR PPAR?
PPAR 的生理相关内源性配体的鉴定?
- 批准号:
8168779 - 财政年份:2010
- 资助金额:
$ 0.81万 - 项目类别:
IDENTIFICATION OF THE PHYSIOLOGICALLY RELEVANT ENDOGENOUS LIGAND FOR PPAR?
PPAR 的生理相关内源性配体的鉴定?
- 批准号:
7954028 - 财政年份:2009
- 资助金额:
$ 0.81万 - 项目类别:
NEW HEPATIC FAT ACTIVATES PPARA TO MAINTAIN GLUCOSE LIPID CHOLESTEROL HOMEO
新的肝脂肪激活 PPARA 来维持葡萄糖脂质胆固醇 Homeo
- 批准号:
7355230 - 财政年份:2006
- 资助金额:
$ 0.81万 - 项目类别:
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