The Administrative Core
行政核心
基本信息
- 批准号:10443134
- 负责人:
- 金额:$ 24.56万
- 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:AdministratorAdultBasic ScienceBioinformaticsBiologyCaringCell Culture TechniquesCellsChildhoodClinicalClinical ResearchCollaborationsCommunicationCommunitiesCommunity OutreachDigestive System DisordersDiseaseDoctor of PhilosophyEducationEducational ActivitiesEducational workshopEffectivenessEnsureEnvironmentEpithelialEpithelial CellsEvaluationEvolutionExpenditureFeedbackFeesFosteringFoundationsFundingFutureGrantGrowthHealthHomeostasisImageInflammationLeadershipLinkLiver diseasesLongevityMentorsMentorshipMetabolismMissionMonitorNational Institute of Diabetes and Digestive and Kidney DiseasesNatural regenerationOrganOrganoidsPlant RootsProductivityPublicationsRecording of previous eventsResearchResearch PersonnelResearch SupportResourcesSchoolsScienceScientistServicesStructureSurveysTechnologyTraining and EducationTranslational ResearchUniversitiesVisionWorkbasebioimagingbiomedical resourcecareer developmentcommunity engagementdiversity and equityempoweredexperienceinnovationinterestmembermultidisciplinarynew technologynext generationoperationprogramsresearch and developmentsingle cell analysissocial mediasuccessweb site
项目摘要
SUMMARY
The inception of the Columbia University Digestive and Disease Research Center (CU-DLDRC) in 2019 has its
foundational roots over the past 15 years through the resounding growth of basic, translational and clinical
research. The CU-DLDRC reflects the enthusiasm, collaborations, productivity and success of its members as
well as the long-term institutional support of digestive disease research at Columbia University. The CU-DLDRC
comprises an interactive group of 49 highly productive members (30 full and 19 associate), united by their strive
for excellence in adult and pediatric digestive disease research and care. Since the CU-DLDRC’s inception, the
Administrative Core (AC) has enhanced the collaborative research culture through the following endeavors: (i)
Fostering interdisciplinary networks and team science, and collaborations between basic and clinical
researchers; (ii) promoting education, training, mentorship and diversity, equity and inclusion (DEI); and (iii)
supporting new investigators. The CU-DLDRC’ central research theme “Epithelial Cells and their Interactions in
Digestive Homeostasis and Disease” encompasses two interrelated subthemes with major impact on digestive
health: “Epithelial Homeostasis, Metabolism and Regeneration” (Subtheme 1) and “Epithelial Interactions in
Inflammation and Preneoplasia” (Subtheme 2). Four Biomedical Cores provide access to cutting-edge
technologies and facilities: Clinical Research and Biospecimen; Organoid and Cell Culture; Bioimaging; and
Bioinformatics and Single Cell Analysis. The CU-DLDRC includes active Pilot and Feasibility (P/F) and
Enrichment (EP) Programs, empowering the next generation of scientists and promoting education and
intellectual exchange. The AC, as central component of the CU-DLDRC, will contribute to the collation and
implementation of its mission, activities and success via optimal organization of the research base; fiscal
management; coordination, evaluation and continuous evolution of its components; and communication with
oversight committees, the NIDDK and other DDRCCs. The AC is directed by experienced leaders with
complementary expertise: Robert Schwabe, MD, PhD (Director); Timothy Wang, MD and Kara Margolis, MD
(Associate Directors), supported by AC administrator Seetha Srinivasan, PhD. The AC will promote the mission
and success of the CU-DLDRC through these Specific Aims: To provide governance through efficient
administration, budgetary oversight, scientific leadership and interactions with oversight committees (Aim 1). To
ensure state-of-the-art services, efficient operation and cross-core collaboration by the Biomedical Cores (Aim
2). To promote the next generation of scientists and monitor their success via the P/F Program (Aim 3). To foster
a fertile environment and intellectual exchange through seminars and retreats, and to promote DEI via the EP
(Aim 4). To highlight the CU-DLDRC, its cores, educational activities and accomplishments on our website (Aim
5). Successful realization of these Aims will contribute to the effectiveness and success of the CU-DLDRC.
总结
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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Robert F. Schwabe其他文献
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 cells control liver zonation, size and functions via R-spondin 3
肝星状细胞通过 R-spondin 3 控制肝脏分区、大小和功能
- DOI:
10.1038/s41586-025-08677-w - 发表时间:
2025-03-12 - 期刊:
- 影响因子:48.500
- 作者:
Atsushi Sugimoto;Yoshinobu Saito;Guanxiong Wang;Qiuyan Sun;Chuan Yin;Ki Hong Lee;Yana Geng;Presha Rajbhandari;Celine Hernandez;Marcella Steffani;Jingran Qie;Thomas Savage;Dhruv M. Goyal;Kevin C. Ray;Taruna V. Neelakantan;Deqi Yin;Johannes Melms;Brandon M. Lehrich;Tyler M. Yasaka;Silvia Liu;Michael Oertel;Tian Lan;Adrien Guillot;Moritz Peiseler;Aveline Filliol;Hiroaki Kanzaki;Naoto Fujiwara;Samhita Ravi;Benjamin Izar;Mario Brosch;Jochen Hampe;Helen Remotti;Josepmaria Argemi;Zhaoli Sun;Timothy J. Kendall;Yujin Hoshida;Frank Tacke;Jonathan A. Fallowfield;Storm K. Blockley-Powell;Rebecca A. Haeusler;Jonathan B. Steinman;Utpal B. Pajvani;Satdarshan P. Monga;Ramon Bataller;Mojgan Masoodi;Nicholas Arpaia;Youngmin A. Lee;Brent R. Stockwell;Hellmut G. Augustin;Robert F. Schwabe - 通讯作者:
Robert F. Schwabe
Hepatic stellate cells: balancing homeostasis, hepatoprotection and fibrogenesis in health and disease
肝星状细胞:在健康和疾病中平衡稳态、肝保护和纤维化
- DOI:
10.1038/s41575-025-01068-6 - 发表时间:
2025-05-22 - 期刊:
- 影响因子:51.000
- 作者:
Robert F. Schwabe;David A. Brenner - 通讯作者:
David A. Brenner
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
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{{ 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:
10612948 - 财政年份:2022
- 资助金额:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 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:
$ 24.56万 - 项目类别:
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