FASEB's The Molecular Mechanisms of Immune Cell Development and Function Conference
FASEB 免疫细胞发育和功能的分子机制会议
基本信息
- 批准号:10224401
- 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:2021
- 资助国家:美国
- 起止时间:2021-06-01 至 2022-11-30
- 项目状态:已结题
- 来源:
- 关键词:AmericanAntigen ReceptorsArchitectureAreaAutoimmunityB cell differentiationBiologicalBiological ModelsBiologyBudgetsBusinessesCaliforniaCanadaCareer MobilityCell CommunicationCellsChromatinClinicalCollaborationsDNA RepairDevelopmentDevelopmental ProcessDiseaseEducational workshopEffector CellEnsureEnvironmentEvaluationFacultyFeedbackFinancial SupportFosteringFunctional disorderFundingFutureGene ExpressionGene Expression RegulationGene RearrangementGenesGenetic RecombinationGenomeGenomic DNAGenomicsHealthHematopoieticHematopoietic stem cellsHomeostasisHumanImmuneImmune responseImmune systemImmunologic ReceptorsImmunologyImmunooncologyIndividualInnate Immune SystemInternationalIslandKnowledgeLaboratoriesLettersLymphocyteMalignant NeoplasmsMentorsModelingMolecularMolecular BiologyMolecular ImmunologyNova ScotiaOralPatternPostdoctoral FellowReceptor GeneRegulationRequest for ProposalsResearchResearch PersonnelScientistSenior ScientistSeriesSignal PathwaySignal TransductionSocietiesStem Cell DevelopmentSystemT-Cell DevelopmentThinkingTimeTrainingTranscriptional RegulationTravelUnderrepresented MinorityUnited States National Institutes of HealthWomanWorkbiological researchcareercareer developmentcostdesignepigenomicsexperiencegene functiongenome integritygenome-widegraduate studentgut homeostasisimmune functioninformation processinginsightleukemiameetingsmicroorganismminority scientistposterspre-doctoralprogramsresponsescientific atmospheresummer researchsymposiumsynergismtranscriptomics
项目摘要
PROJECT SUMMARY
This proposal requests partial support for a 2021 Summer Research Conference sponsored by the Federation
of American Societies for Experimental Biology (FASEB) on the subject of “Molecular Mechanisms of Immune
Cell Development and Function”, the 10th conference in this highly successful series. This conference has been
chosen for sponsorship by FASEB after a competitive re-evaluation every other year since its inception in
summer 2003. The distinctive features of this conference are: (1) A strong emphasis on molecular biology of
gene regulation in immune cell development and function, including new insights emerging from genome-wide
and systems approaches; (2) Close integration of the study of molecular mechanisms of immune receptor gene
recombination and diversification with concepts in genomic architecture and long-range genomic control; (3)
Deliberate juxtaposition of research on different classes of immune cells to reveal larger patterns of shared use
of molecular and developmental mechanisms; (4) An explicit focus on gene network and signaling network
connections rather than “one gene at a time” studies to provide a comprehensive explanation of biological
regulation; (5) Creation of new sessions that integrate the major molecular/mechanistic themes of the meeting
with immuno-oncology, gut homeostasis, and autoimmunity; (6) Integration of presentations from scientists at
many career levels, from internationally renowned experts to junior postdoctoral and graduate students, in an
intensive, all-plenary program—allowing trainees easy access to experienced senior scientists who in turn gain
an appreciation of the young people’s individual ideas. (7) Implementation of our unique financial model in which
invited speakers forego financial support for their participation to allow the use of the majority of funds to support
trainees and young investigators who are establishing their independent careers. These distinctive features are
designed around three specific aims: Aim 1—To disseminate the most recent and important advances and new
paradigms in molecular immunology; Aim 2—To create a highly interactive, supportive, and collegial
environment for the sharing of scientific knowledge between scientists at many different stages of training and
career development, thereby facilitating new collaborations, broadening of professional and mentoring networks,
and career development; and Aim 3—To enhance diversity among the individuals who participate in, contribute
to, and achieve career advancement in the field of immunology and biological research more broadly.
Many laboratories are unwilling or unable to send promising trainees to important conferences and young
investigators attempting to establish their independent careers are often unable to cover the costs of conference
attendance. The support requested is crucial to make it possible for the most promising trainees and junior faculty
in molecular immunology to publicly present their work and interact in an intimate setting with leaders in their
field. This meeting has received enthusiastic feedback from conference attendees of previous meetings and a
strong mandate for long-term continuation.
项目摘要
该提案要求对联邦赞助的2021年夏季研究会议进行部分支持
美国实验生物学社会(FASEB)关于“免疫分子机制的主题
细胞开发和功能”,这个非常成功的系列中的第十次会议。这次会议是
自一年以来,每隔一年就选择了FaseB的赞助
2003年夏季。这次会议的独特特征是:(1)非常强调
免疫细胞发育和功能中的基因调节,包括全基因组出现的新见解
和系统方法; (2)紧密整合免疫受体基因的分子机制
重组和多样化,具有基因组结构和远程基因组控制中的概念; (3)
故意对不同类别的免疫细胞的研究并置,以揭示更大的共享使用模式
分子和发育机制; (4)明确关注基因网络和信号网络
连接而不是“一次基因”研究,以提供对生物学的全面解释
规定; (5)创建整合会议的主要分子/机械主题的新会议
具有免疫肿瘤,肠道稳态和自身免疫性; (6)从科学家的演讲整合
从国际知名的专家到初级博士后和研究生,许多职业级别
密集的全样计划 - 允许学员轻松进入经验丰富的高级科学家
对年轻人的个人想法的欣赏。 (7)实施我们独特的财务模型
邀请演讲者放弃参与的财政支持,以允许使用大多数资金来支持
正在建立独立职业的学员和年轻的调查员。这些独特的特征是
围绕三个特定目标设计:目标1-传播最新和重要的进步和新的进步
分子免疫学范例;目标2 - 创建一个高度互动,支持和大学
在培训的许多不同阶段,科学家之间分享科学知识的环境和
职业发展,从而支持新的合作,扩大专业和心理网络,
和职业发展;和目标3-增强参与个人的多样性,做出贡献
更广泛地在免疫学和生物学研究领域实现职业发展。
许多实验室不愿意或无法向重要的会议发送诺言培训
试图建立独立职业的调查人员通常无法支付会议的费用
出勤。要求的支持对于使最有前途的培训和初级教师成为可能
在分子免疫学中,公开介绍他们的工作,并在与领导者的亲密环境中进行互动
场地。这次会议收到了以前会议的会议与会者的热情反馈和
长期延续的强大任务。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
David G. Schatz其他文献
cDNA representational difference analysis: a sensitive and flexible method for identification of differentially expressed genes.
cDNA代表性差异分析:一种灵敏且灵活的差异表达基因鉴定方法。
- DOI:
- 发表时间:
1999 - 期刊:
- 影响因子:0
- 作者:
Michael Hubank;David G. Schatz - 通讯作者:
David G. Schatz
Systeme autoregule, regule par la tetracycline, pour l'expression inductible des genes dans les eucaryotes
系统自动调节、四环素调节、真核生物基因诱导表达
- DOI:
- 发表时间:
1996 - 期刊:
- 影响因子:0
- 作者:
David G. Schatz - 通讯作者:
David G. Schatz
The SV40 virus enhancer functions as a somatic hypermutation-targeting element with potential tumorigenic activity
- DOI:
10.1016/j.tvr.2024.200293 - 发表时间:
2024-12-01 - 期刊:
- 影响因子:
- 作者:
Filip Šenigl;Anni I. Soikkeli;Salomé Prost;David G. Schatz;Martina Slavková;Jiří Hejnar;Jukka Alinikula - 通讯作者:
Jukka Alinikula
Skewing the Playing Field: A Single-Molecule Study on how RSS Sequence Influences Gene Segment Selection
- DOI:
10.1016/j.bpj.2017.11.511 - 发表时间:
2018-02-02 - 期刊:
- 影响因子:
- 作者:
Soichi Hirokawa;Nathan M. Belliveau;Geoffrey A. Lovely;Michael Anaya;David G. Schatz;David Baltimore;Rob Phillips - 通讯作者:
Rob Phillips
David G. Schatz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('David G. Schatz', 18)}}的其他基金
Genome Architecture in Human Germinal Center B Cell Development, Malignancy, and Somatic Hypermutation
人类生发中心 B 细胞发育、恶性肿瘤和体细胞超突变中的基因组结构
- 批准号:
10478178 - 财政年份:2020
- 资助金额:
$ 1万 - 项目类别:
Genome Architecture in Human Germinal Center B Cell Development, Malignancy, and Somatic Hypermutation
人类生发中心 B 细胞发育、恶性肿瘤和体细胞超突变中的基因组结构
- 批准号:
10706308 - 财政年份:2020
- 资助金额:
$ 1万 - 项目类别:
Genome Architecture in Human Germinal Center B Cell Development, Malignancy, and Somatic Hypermutation
人类生发中心 B 细胞发育、恶性肿瘤和体细胞超突变中的基因组结构
- 批准号:
10117444 - 财政年份:2020
- 资助金额:
$ 1万 - 项目类别:
Genome Architecture in Human Germinal Center B Cell Development, Malignancy, and Somatic Hypermutation
人类生发中心 B 细胞发育、恶性肿瘤和体细胞超突变中的基因组结构
- 批准号:
10264152 - 财政年份:2020
- 资助金额:
$ 1万 - 项目类别:
Function and Evolutionary Origins of the RAG Endonuclease
RAG 核酸内切酶的功能和进化起源
- 批准号:
10460993 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Function and Evolutionary Origins of the RAG Endonuclease
RAG 核酸内切酶的功能和进化起源
- 批准号:
10231071 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Function and Evolutionary Origins of the RAG Endonuclease
RAG 核酸内切酶的功能和进化起源
- 批准号:
10801641 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
The role of AID/APOBEC3 proteins in genome instability in multiple myeloma
AID/APOBEC3 蛋白在多发性骨髓瘤基因组不稳定中的作用
- 批准号:
10165658 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
相似国自然基金
嵌合抗原受体巨噬细胞(CAR-M)微马达的制备及其血管蜂窝网络磁驱行为机理与控制方法研究
- 批准号:52375565
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
体内构建嵌合抗原受体Kupffer细胞(CAR-KC)并借助“细胞变装”策略实现肝癌双靶杀伤
- 批准号:82304398
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
双靶向CSPG4/CD126嵌合抗原受体修饰的复制缺失型弓形虫减毒活疫苗(CAR-Tg)抗恶性黑色素瘤的效应及机制研究
- 批准号:32370997
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
靶向c-MET以及CD133的串联双靶点嵌合抗原受体—巨噬细胞(CAR-M)对胰腺癌的杀伤及化疗协同增效作用及机制研究
- 批准号:82373230
- 批准年份:2023
- 资助金额:49.00 万元
- 项目类别:面上项目
脂质纳米粒体内介导嵌合抗原受体-M1型巨噬细胞协同TLR激动剂治疗实体瘤的研究
- 批准号:82304418
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
相似海外基金
Impact of novel enhancers on Igh repertoire diversity
新型增强子对 Igh 库多样性的影响
- 批准号:
10716628 - 财政年份:2023
- 资助金额:
$ 1万 - 项目类别:
ILC3 Syndecan-4 in the Regulation of Intestinal Health and Inflammation
ILC3 Syndecan-4 在肠道健康和炎症调节中的作用
- 批准号:
10678494 - 财政年份:2023
- 资助金额:
$ 1万 - 项目类别:
Developing robust and scalable genomics tools and databases to analyze immune receptor repertoires across diverse populations
开发强大且可扩展的基因组学工具和数据库来分析不同人群的免疫受体库
- 批准号:
10656981 - 财政年份:2023
- 资助金额:
$ 1万 - 项目类别:
The Molecular Mechanisms of Immune Cell Development and Function
免疫细胞发育和功能的分子机制
- 批准号:
10751580 - 财政年份:2023
- 资助金额:
$ 1万 - 项目类别: