FASEB SRC on Acute Kidney Injury: from beside to bench (and back again)
FASEB SRC 关于急性肾损伤:从旁边到替补(然后再回来)
基本信息
- 批准号:9752908
- 负责人:
- 金额:$ 1万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-07-01 至 2020-06-30
- 项目状态:已结题
- 来源:
- 关键词:AcademiaAcute Renal Failure with Renal Papillary NecrosisAgeAmericanAreaBackBasic ScienceBiological MarkersCareer ChoiceChronic Kidney FailureClinicalClinical InvestigatorClinical ResearchClinical SciencesClinical TrialsCollaborationsCommunitiesComorbidityComplexDevelopmentDiabetes MellitusDisciplineDoctor of PhilosophyDrug ScreeningEducational workshopEnvironmentFemaleFibrosisFosteringFunctional disorderGoalsGovernmentGovernment AgenciesHearingHeterogeneityHumanIndustryInternationalKidneyMarinesMedicineMolecularMorbidity - disease rateNephrologyPatientsPhenotypePre-Clinical ModelRecoveryResearchResearch DesignResearch PersonnelRiskScientistSocietiesTestingTimeTissuesWorkWorkforce Developmentbasebench to bedsidecareerclinical phenotypeclinically relevantdata integrationdesigndrug developmentdrug discoveryevidence basehuman diseasehuman tissueinjury and repairinnovationinterestinvestigator trainingmeetingsmortalitynew technologynovel strategiesnovel therapeutic interventionnovel therapeuticspostersprecision medicinepreventprogramsresponsesymposiumtherapeutic developmenttranslational approach
项目摘要
6. Project Summary/Abstract
Acute kidney injury (AKI) is an increasingly prevalent worldwide problem that has a significant impact on patient
mortality and morbidity, including a marked increased risk of progressive chronic kidney disease (CKD). AKI is
also an active area of basic and clinical research. Despite this, no therapies have been definitively shown to
accelerate recovery or prevent progression to CKD in patients with AKI. There are a number of reasons for this,
but a major factor is the lack of effective collaborative pipelines between bench researchers studying the
mechanisms and new therapeutic approaches to treat AKI, and clinical scientists studying the human disease
and implementing hypothesis testing clinical trials to evaluate new therapeutics in patients with AKI. However,
aside from the annual scientific meeting of the American Society of Nephrology (ASN), there are few established
forums that promote direct exchange of ideas across the clinical and basic science AKI research communities
in academia and industry. The concept of this new conference is therefore to develop scientific
interactions and collaborations across the bench to bedside divide, and to use this as a forum to help
develop a pipeline of investigators trained to think in a more translational way about the problem of AKI.
To achieve this, the organizers have designed a three and a half day FASEB Scientific Research Conference.
Experts from academic medicine and industry have been invited to provide state of the art talks on key, topical
aspects of research in both the basic and clinical science of AKI, as well as recent advances in drug and
therapeutic development for AKI. This will also provide the first evidence-based forum to discuss new
approaches to study human AKI, and to develop better pre-clinical modeling that reflects the observed cellular
and molecular heterogeneity of AKI in humans. We anticipate that this meeting will attract investigators and
trainees from academia, industry and government agencies involved in different aspects of AKI research, and
as such will provide a unique opportunity to foster new collaborative interactions between these stakeholders.
6. 项目总结/摘要
急性肾损伤(AKI)是一个日益普遍的世界性问题,对患者产生重大影响
死亡率和发病率,包括进行性慢性肾病(CKD)的风险显着增加。 AKI 是
也是基础和临床研究的活跃领域。尽管如此,目前还没有明确的治疗方法可以证明
加速 AKI 患者的康复或预防进展为 CKD。造成这种情况的原因有很多,
但一个主要因素是研究该领域的实验室研究人员之间缺乏有效的合作渠道
治疗 AKI 的机制和新治疗方法,以及研究人类疾病的临床科学家
实施假设检验临床试验来评估 AKI 患者的新疗法。然而,
除了美国肾脏病学会 (ASN) 的年度科学会议外,很少有既定的会议
促进临床和基础科学 AKI 研究社区直接交流思想的论坛
在学术界和工业界。因此,这次新会议的理念是发展科学
跨工作台到床边的互动和协作,并以此为论坛来提供帮助
培养一批经过培训的调查人员,以更加转化的方式思考 AKI 问题。
为了实现这一目标,主办方设计了为期三天半的FASEB科学研究会议。
来自医学界和工业界的专家受邀就关键、专题提供最先进的演讲
AKI 基础和临床科学研究的各个方面,以及药物和治疗的最新进展
AKI 的治疗开发。这也将提供第一个基于证据的论坛来讨论新的
研究人类 AKI 的方法,并开发更好的临床前模型来反映观察到的细胞
以及人类 AKI 的分子异质性。我们预计这次会议将吸引调查人员和
来自学术界、工业界和政府机构的学员参与 AKI 研究的不同方面,以及
因此,这将为促进这些利益相关者之间新的协作互动提供独特的机会。
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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Mark P. de Caestecker其他文献
Transcriptional Cross-talk between Smad, ERK1/2, and p38 Mitogen-activated Protein Kinase Pathways Regulates Transforming Growth Factor-β-induced Aggrecan Gene Expression in Chondrogenic ATDC5 Cells*
Smad、ERK1/2 和 p38 丝裂原激活蛋白激酶途径之间的转录串扰调节软骨形成 ATDC5 细胞中转化生长因子-β 诱导的聚集蛋白聚糖基因表达*
- DOI:
- 发表时间:
2001 - 期刊:
- 影响因子:4.8
- 作者:
Hideto Watanabe;Mark P. de Caestecker;Yoshihiko Yamada - 通讯作者:
Yoshihiko Yamada
Hyperoxia Increases Kidney Injury During Renal Ischemia and Reperfusion in Mice
高氧会增加小鼠肾缺血和再灌注期间的肾脏损伤
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:5.7
- 作者:
M. Kimlinger;Tom J. No;Eric H. Mace;R. Delgado;Marcos G. Lopez;Mark P. de Caestecker;F. Billings - 通讯作者:
F. Billings
FGF/EGF signaling regulates the renewal of early nephron progenitors during embryonic development
FGF/EGF 信号传导调节胚胎发育过程中早期肾单位祖细胞的更新
- DOI:
- 发表时间:
2011 - 期刊:
- 影响因子:4.6
- 作者:
Aaron C. Brown;Derek C. Adams;Mark P. de Caestecker;Xuehui Yang;R. Friesel;Leif Oxburgh - 通讯作者:
Leif Oxburgh
Detection of abnormal peripheral blood mononuclear cell cytokine networks in human IgA nephropathy.
人 IgA 肾病外周血单核细胞细胞因子网络异常的检测。
- DOI:
- 发表时间:
1993 - 期刊:
- 影响因子:19.6
- 作者:
Mark P. de Caestecker;Martin Bottomley;Brian A. Telfer;Ian V. Hutchinson;Brent M. Vose;Francis W. Ballardie - 通讯作者:
Francis W. Ballardie
Mark P. de Caestecker的其他文献
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{{ truncateString('Mark P. de Caestecker', 18)}}的其他基金
Mechanisms and therapeutic manipulation of retinoic acid signaling in Acute Kidney Injury
急性肾损伤中视黄酸信号传导的机制和治疗操作
- 批准号:
9924588 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
Vanderbilt Kidney O'brien Center - Enrichment Program
范德比尔特肾脏奥布莱恩中心 - 浓缩计划
- 批准号:
10163171 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
Mechanisms and therapeutic manipulation of retinoic acid signaling in Acute Kidney Injury
急性肾损伤中视黄酸信号传导的机制和治疗操作
- 批准号:
9332756 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
Mutation Specific Therapies in Patients with HPAH
HPAH 患者的突变特异性治疗
- 批准号:
8518456 - 财政年份:2012
- 资助金额:
$ 1万 - 项目类别:
Mutation Specific Therapies in Patients with HPAH
HPAH 患者的突变特异性治疗
- 批准号:
8356472 - 财政年份:2012
- 资助金额:
$ 1万 - 项目类别:
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