The Columbia University Digestive and Liver Disease Research Center
哥伦比亚大学消化和肝脏疾病研究中心
基本信息
- 批准号:10612948
- 负责人:
- 金额:$ 121.89万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-04-30 至 2027-03-31
- 项目状态:未结题
- 来源:
- 关键词:AppointmentAutomobile DrivingBasic ScienceBioinformaticsBiologyCell CommunicationCellsClinicalClinical ResearchCollaborationsCollectionCommunitiesCore FacilityCreativenessDataDatabasesDetectionDigestive System DisordersDirect CostsDisciplineDiseaseEducationEducational workshopEffectivenessEnsureEnvironmentEpithelial CellsEpitheliumEsophagusEvolutionFunctional disorderFundingFutureGoalsGrantGrowthHomeostasisHospitalsInflammationInstitutionJointsLinkLiverLiver diseasesMeasuresMentorsMetabolismMissionMorbidity - disease rateNational Institute of Diabetes and Digestive and Kidney DiseasesNatural regenerationNeoplasmsNew YorkOrganOrganoidsPancreasPathway interactionsPatientsPhysiologyPresbyterian ChurchPreventionProductivityPublicationsResearchResearch MethodologyResearch PersonnelScienceScientistServicesStructureTrainingTraining and EducationTranslationsUnited States National Institutes of HealthUniversitiesVisionbasebioimagingclinical applicationclinical translationclinically relevantdiversity and equityempowermentequity, diversity, and inclusionforginggastrointestinalimprovedinnovationinter-institutionalmembermortalitymultidisciplinarynext generationnovel therapeutic interventionpatient populationprogramssingle cell analysissuccesssymposiumtherapeutic target
项目摘要
SUMMARY
Since its formal inception in 2019, the Columbia University Digestive and Liver Disease Research Center (CU-
DLDRC) has brought together an interdisciplinary group of highly accomplished basic, translational and clinical
researchers with complementary backgrounds from different departments and campuses and the New York
Presbyterian Hospital. The CU-DLDRC reflects vibrant growth in digestive disease science over the last two
decades, paired with exceptional institutional support and a dynamic scientific environment at Columbia
University. The CU-DLDRC’s vision is to contribute to improved prevention, detection and therapy of digestive
diseases through the application of creative concepts, cutting-edge research methods, innovation and multi-
disciplinary team science, with a strong emphasis on clinical relevance and translation. The CU-DLDRC includes
49 digestive-focused members (30 full, 19 associate) with NIH funding of $20.8M direct costs (35.6% from
NIDDK). The central theme “Epithelial cells and their interactions in digestive homeostasis and disease”, reflects
the passion and expertise of its members and its key role in digestive diseases. The broad coverage of digestive
organs under this theme is predicated upon the conceptual framework that many disease-driving pathways, cell-
cell interactions and therapeutic targets are shared across digestive organs. Guided by these principles,
digestive disease research at Columbia has witnessed significant growth and impact, fruitful collaborations and
joint publications and grants to a degree that would not have been achieved by studies in single digestive organs.
The Administrative Core ensures success and effectiveness of the CU-DLDRC through management of its
research base, operational oversight, scientific vision, innovation, and structures and activities that stimulate
translational digestive science with maximum member benefits (Aim 1). The four biomedical cores offer a suite
of closely linked state-of-the-art core facilities that span from clinical biospecimens and databases to cutting-
edge bioinformatics, organoid platforms and advanced bioimaging, empowering members to investigate
epithelial cells and their interactions; these powerful research methods will be linked the breadth of clinical
expertise and biospecimens via organ-focused clinical-basic teams (Aim 2). The Pilot and Feasibility program,
that to date has funded seven investigators with an exceptional rate of return, will promote impactful basic and
clinical projects, thereby promoting new investigators, innovation and the integration of excellence from other
fields (Aim 3). The Enrichment Program will stimulate intellectual exchange within our center and with the national
digestive community through seminars, an annual retreat, and basic-clinical symposia; support new investigators
and training through a formal mentoring program and workshops; and promote Diversity, Equity and Inclusion
(DEI) in all components and activities of the CU-DLDRC through a DEI delegate (Aim 4). Through these Aims,
the CU-DLDRC will make impactful contributions to digestive disease research and serve our patients.
概括
自2019年正式成立以来,哥伦比亚大学消化和肝病研究中心(Cu-
DLDRC)将一个高度成就的基本,翻译和临床的跨学科组汇集在一起
来自不同部门和校园以及纽约的完整背景的研究人员
长老会医院。 Cu-dldrc反映了过去两个消化疾病科学的鲜明生长
数十年来,搭配出色的机构支持和哥伦比亚的动态科学环境
大学。 Cu-DLDRC的愿景是为改善预防,检测和疗法做出贡献
通过应用创造性概念,尖端研究方法,创新和多种疾病疾病
纪律团队科学,非常重视临床相关性和翻译。 Cu-dldrc包括
49位以消化率的成员(30名完整,19个合伙人)为2080万美元的NIH资金(35.6%的资金
niddk)。中心主题“上皮细胞及其在消化稳态和疾病中的相互作用”反映了
其成员的热情和专家及其在消化疾病中的关键作用。消化的广泛覆盖范围
在此主题下的器官是根据许多驱动疾病的途径,细胞的概念框架预测的
细胞相互作用和治疗靶标在消化器官之间共享。在这些原则的指导下
哥伦比亚的消化疾病研究见证了显着的增长和影响,富有成果的合作和
单个消化器官研究无法实现的联合出版物和赠款。
行政核心通过管理核心确保Cu-dldrc的成功和有效性
研究基础,运营监督,科学愿景,创新以及刺激的结构和活动
具有最大会员益处的翻译消化科学(AIM 1)。这四个生物医学核心提供了一个套件
密切相关的最新核心设施,这些设施涉及从临床生物测量和数据库到剪切
边缘生物信息学,器官平台和高级生物成像,使成员有能力调查
上皮细胞及其相互作用;这些强大的研究方法将链接到临床的广度
通过有机临床基本团队的专业知识和生物测量(AIM 2)。飞行员和可行性计划,
迄今
临床项目,从而促进新的研究人员,创新和其他其他
字段(目标3)。丰富计划将刺激我们中心和国家的智力交流
通过SEMIAR,年度务虚会和基本临床专题讨论会消化社区;支持新的研究人员
并通过正式的心理计划和研讨会进行培训;并促进多样性,公平和包容性
(DEI)通过DEI代表在Cu-DLDRC的所有组件和活动中(AIM 4)。通过这些目标,
Cu-DLDRC将为消化疾病研究做出有影响力的贡献,并为我们的患者提供服务。
项目成果
期刊论文数量(20)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Two waves of coeliac disease incidence in Sweden: a nationwide population-based cohort study from 1990 to 2015.
- DOI:10.1136/gutjnl-2021-324209
- 发表时间:2022-06
- 期刊:
- 影响因子:24.5
- 作者:Bergman, David;King, James;Lebwohl, Benjamin;Clements, Mark S.;Roelstraete, Bjorn;Kaplan, Gilaad G.;Green, Peter H. R.;Murray, Joseph A.;Ludvigsson, Jonas F.
- 通讯作者:Ludvigsson, Jonas F.
Targeted Hsp70 fluorescence molecular endoscopy detects dysplasia in Barrett's esophagus.
- DOI:10.1007/s00259-021-05582-y
- 发表时间:2022-05
- 期刊:
- 影响因子:9.1
- 作者:Fang, Hsin-Yu;Stangl, Stefan;Marcazzan, Sabrina;Carvalho, Marcos J. Braz;Baumeister, Theresa;Anand, Akanksha;Strangmann, Julia;Huspenina, Julia Slotta;Wang, Timothy C.;Schmid, Roland M.;Feith, Marcus;Friess, Helmut;Ntziachristos, Vasilis;Multhoff, Gabriele;Gorpas, Dimitris;Quante, Michael
- 通讯作者:Quante, Michael
Histamine Signaling Is Essential for Tissue Macrophage Differentiation and Suppression of Bacterial Overgrowth in the Stomach.
- DOI:10.1016/j.jcmgh.2022.09.008
- 发表时间:2023
- 期刊:
- 影响因子:7.2
- 作者:Kim, Kwang H.;Park, Jihwan;Cho, Yejin;Cho, Soo Young;Lee, Buhyun;Jeong, Haengdueng;Lee, Yura;Yi, Ja-Woon;Oh, Yeseul;Lee, Jin-Jae;Wang, Timothy C.;Lim, Kyung-Min;Nam, Ki Taek
- 通讯作者:Nam, Ki Taek
Cost-Effectiveness of Liquid Biopsy for Colorectal Cancer Screening in Patients Who Are Unscreened.
- DOI:10.1001/jamanetworkopen.2023.43392
- 发表时间:2023-11-01
- 期刊:
- 影响因子:13.8
- 作者:Aziz, Zainab;Wagner, Sophie;Agyekum, Alice;Pumpalova, Yoanna S.;Prest, Matthew;Lim, Francesca;Rustgi, Sheila;Kastrinos, Fay;Grady, William M.;Hur, Chin
- 通讯作者:Hur, Chin
Nomenclature and diagnosis of seronegative coeliac disease and chronic non-coeliac enteropathies in adults: the Paris consensus.
- DOI:10.1136/gutjnl-2021-326645
- 发表时间:2022-11
- 期刊:
- 影响因子:24.5
- 作者:Schiepatti, Annalisa;Sanders, David S.;Baiardi, Paola;Caio, Giacomo;Ciacci, Carolina;Kaukinen, Katri;Lebwohl, Benjamin;Leffler, Daniel;Malamut, Georgia;Murray, Joseph A.;Rostami, Kamran;Rubio-Tapia, Alberto;Volta, Umberto;Biagi, Federico
- 通讯作者:Biagi, Federico
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Robert F. Schwabe其他文献
Prevention and treatment of hepatic fibrosis at the cellular level
从细胞水平预防和治疗肝纤维化
- DOI:
- 发表时间:
2004 - 期刊:
- 影响因子:0
- 作者:
B. Stefanovic;J. Lindquist;R. Rippe;B. Schnabl;Robert F. Schwabe;Ramón Bataller;D. Brenner - 通讯作者:
D. Brenner
CD40 activates NFKB and JNK and enhances IL-8 secretion on human hepatic myofibroblasts
- DOI:
10.1016/s0016-5085(00)86204-6 - 发表时间:
2000-04-01 - 期刊:
- 影响因子:
- 作者:
Robert F. Schwabe;Bernd Schnabl;David A. Brenner - 通讯作者:
David A. Brenner
OS-041-YI - X-box binding protein 1 (XBP1) in hepatic stellate cells (HSC) mitigates liver fibrosis
- DOI:
10.1016/s0168-8278(23)00497-x - 发表时间:
2023-06-01 - 期刊:
- 影响因子:
- 作者:
Hanghang Wu;Hui Ye;Juan Francisco Vilchez-Gómez;Marcos Fernandez Fondevila;Aveline Filliol;Robert F. Schwabe;Javier Vaquero;Rafael Bañares;Ruben Nogueiras;Eduardo Martínez-Naves;Scott Friedman;Yulia Nevzorova;Francisco Javier Cubero - 通讯作者:
Francisco Javier Cubero
Hepatic Stellate Cell Depletion and Genetic Manipulation.
肝星状细胞耗竭和基因操作。
- DOI:
10.1007/978-1-0716-3207-9_12 - 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
Qiuyan Sun;Robert F. Schwabe - 通讯作者:
Robert F. Schwabe
Modulation of soluble CD40 ligand bioactivity with anti-CD40 antibodies.
用抗 CD40 抗体调节可溶性 CD40 配体生物活性。
- DOI:
- 发表时间:
1997 - 期刊:
- 影响因子:0
- 作者:
Robert F. Schwabe;S. Hess;Judith P. Johnson;Hartmut Engelmann - 通讯作者:
Hartmut Engelmann
Robert F. Schwabe的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Robert F. Schwabe', 18)}}的其他基金
The Columbia University Digestive and Liver Disease Research Center
哥伦比亚大学消化和肝脏疾病研究中心
- 批准号:
10443133 - 财政年份:2022
- 资助金额:
$ 121.89万 - 项目类别:
Tumor-promoting and tumor-suppressive roles of Hepatic Stellate Cell Subpopulations in NASH-HCC
肝星状细胞亚群在 NASH-HCC 中的促肿瘤和抑肿瘤作用
- 批准号:
10278434 - 财政年份:2021
- 资助金额:
$ 121.89万 - 项目类别:
Protective and fibrosis-independent functions of hepatic stellate cells
肝星状细胞的保护性和纤维化独立功能
- 批准号:
10597076 - 财政年份:2021
- 资助金额:
$ 121.89万 - 项目类别:
Protective and fibrosis-independent functions of hepatic stellate cells
肝星状细胞的保护性和纤维化独立功能
- 批准号:
10378664 - 财政年份:2021
- 资助金额:
$ 121.89万 - 项目类别:
Tumor-promoting and tumor-suppressive roles of Hepatic Stellate Cell Subpopulations in NASH-HCC
肝星状细胞亚群在 NASH-HCC 中的促肿瘤和抑肿瘤作用
- 批准号:
10454375 - 财政年份:2021
- 资助金额:
$ 121.89万 - 项目类别:
Tumor-promoting and tumor-suppressive roles of Hepatic Stellate Cell Subpopulations in NASH-HCC
肝星状细胞亚群在 NASH-HCC 中的促肿瘤和抑肿瘤作用
- 批准号:
10654714 - 财政年份:2021
- 资助金额:
$ 121.89万 - 项目类别:
DAMPs and Their Receptors Link Hepatocyte Death to HSC Activation and Liver Fibrosis
DAMP 及其受体将肝细胞死亡与 HSC 激活和肝纤维化联系起来
- 批准号:
10224799 - 财政年份:2019
- 资助金额:
$ 121.89万 - 项目类别:
DAMPs and Their Receptors Link Hepatocyte Death to HSC Activation and Liver Fibrosis
DAMP 及其受体将肝细胞死亡与 HSC 激活和肝纤维化联系起来
- 批准号:
9917105 - 财政年份:2019
- 资助金额:
$ 121.89万 - 项目类别:
相似国自然基金
基于驾驶人行为理解的人机共驾型智能汽车驾驶权分配机制研究
- 批准号:52302494
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
有条件自动驾驶汽车驾驶人疲劳演化机理与协同调控方法
- 批准号:52372341
- 批准年份:2023
- 资助金额:49.00 万元
- 项目类别:面上项目
人机共驾汽车驾驶风险分析及控制权智能交互机理
- 批准号:
- 批准年份:2022
- 资助金额:54 万元
- 项目类别:面上项目
人机共驾汽车驾驶风险分析及控制权智能交互机理
- 批准号:52272413
- 批准年份:2022
- 资助金额:54.00 万元
- 项目类别:面上项目
定性与定量分析跟驰行驶中汽车驾驶员情感-行为交互作用机理
- 批准号:71901134
- 批准年份:2019
- 资助金额:19.0 万元
- 项目类别:青年科学基金项目
相似海外基金
BLRD Research Career Scientist Award Application
BLRD 研究职业科学家奖申请
- 批准号:
10701238 - 财政年份:2023
- 资助金额:
$ 121.89万 - 项目类别:
Functional ontogeny of pair bonding neural circuits
配对神经回路的功能个体发育
- 批准号:
10704079 - 财政年份:2022
- 资助金额:
$ 121.89万 - 项目类别:
The Columbia University Digestive and Liver Disease Research Center
哥伦比亚大学消化和肝脏疾病研究中心
- 批准号:
10443133 - 财政年份:2022
- 资助金额:
$ 121.89万 - 项目类别:
Functional ontogeny of pair bonding neural circuits
配对神经回路的功能个体发育
- 批准号:
10481368 - 财政年份:2022
- 资助金额:
$ 121.89万 - 项目类别:
Vanderbilt Network Lead Academic Participating Site for the NCTN
范德比尔特网络 (Vanderbilt Network) 主导 NCTN 学术参与网站
- 批准号:
10364747 - 财政年份:2019
- 资助金额:
$ 121.89万 - 项目类别: