2011 Red Cells Gordon Research Conference
2011 红细胞戈登研究会议
基本信息
- 批准号:8198121
- 负责人:
- 金额:$ 1.3万
- 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:2011-07-01 至 2012-08-31
- 项目状态:已结题
- 来源:
- 关键词:AcademyAmerican Society of HematologyAnemiaAreaBasic ScienceBlood CellsCell MaturationCell Membrane StructuresChildhoodClinicalCollaborationsComplementCountryDefectDevelopmentDevelopmental BiologyDevelopmental ProcessDiagnosisDiamond-Blackfan anemiaDisabled PersonsDisciplineDiseaseEpigenetic ProcessErythrocytesErythroidErythroid CellsErythropoiesisEthnic OriginFundingFunding ApplicantFutureGenderGene ExpressionGeneticGenetic ResearchGenomicsGoalsGrowthHematological DiseaseHematologyHemeHeme IronHemoglobinHereditary DiseaseHumanInstitutesInternationalIronLeadLifeMalariaMembraneMembrane ProteinsMembrane Structure and FunctionMetabolismMethodologyMinorityMissionMolecularMolecular BiologyNational Heart, Lung, and Blood InstituteNational Human Genome Research InstituteNational Institute of Allergy and Infectious DiseaseNational Institute of Child Health and Human DevelopmentNational Institute of Diabetes and Digestive and Kidney DiseasesNatureNew HampshireParasitesParticipantPathologyPostdoctoral FellowProcessProductionPropertyRecording of previous eventsRegulationResearchResearch PersonnelScientistSeriesSickle Cell AnemiaSignal TransductionSpecialistStagingStem cellsStudentsSystems BiologyThalassemiaTranscriptional RegulationTransfusionUnited States National Institutes of HealthVariantWomanWorkcareergenome wide association studygraduate studenthuman diseaseimprovedinnovationinsightiron metabolismmeetingsnovelpostersprogenitorprogramsprotein structuresymposiumtrafficking
项目摘要
DESCRIPTION (provided by applicant): Funds are requested for partial support of the 2011 Gordon Research Conference (GRC) on Red Cells, the next in a series of meetings that have been held every other year since 1979. This conference assembles the top established and the most promising new investigators who are working on all aspects of erythroid cells, from the developmental/environmental control of its ontogeny, to cellular/morphogenic aspects related to its unique membrane structure, to transcriptional/epigenetic regulation of its gene expression, and to disorders following from variations in these normal processes. Sessions in 2011 will include Developmental Biology of Erythropoiesis; Transcriptional Control of Gene Expression; Epigenetics and Systems Biology of Red Cells; Erythropoiesis, Signaling and Red Cell Production; Erythrocyte Terminal Maturation; Membrane Protein Structures, Associations and Functions; Red Cell Disorders; Iron, Heme and the Red Cell; Parasite Interactions with Red Cells. By focusing on these topics, the Red Cells GRC continues to be the primary venue for presentation of the latest cutting edge basic science, novel insights into human disease, and innovations in methodology that it has covered throughout its history and for which it has become famous. The meeting attracts an international coterie of researchers and provides a lively forum for active participation and discussion within intimate surroundings that facilitates interactions between senior and junior investigators, and between investigators that normally may not readily interact. The meeting will be held on July 24-29, 2011 at Proctor Academy in Andover, New Hampshire, and will convene 52 speakers with a total of ~140 participants. The conference aims to be inclusive for women, minorities, and persons with disabilities; participants will include postdoctoral fellows and graduate students in addition to investigators who are early in their academic careers. Some postdoctoral fellow and student poster presenters will be selected for short talks. The opportunities for informal gatherings at meals and in the afternoons and evenings, provides an avenue for scientists from different disciplines to interact, promoting cross-disciplinary collaboration. By the nature of its subject matter, the Red Cells GRC remains fully relevant to enhancing the understanding of both the normal progression of erythroid cell maturation and the alterations that lead to its pathology.
PUBLIC HEALTH RELEVANCE: Defects in red blood cell formation and function can lead to anemias that range from mild to life-threatening. The 2011 Red Cells Gordon Research Conference is the primary means for investigators in the field to present their most recent findings, exchange ideas, and discuss future directions for investigating and understanding normal and aberrant modes of the erythroid cell. This exchange of new findings and ideas will accelerate development of improved diagnoses and therapies for human anemias.
描述(由申请人提供):申请资金用于2011年戈登红细胞研究会议(GRC)的部分支持,这是自1979年以来每隔一年举行一次的一系列会议中的下一个会议。本次会议汇集了顶尖和最有前途的新研究者,他们正在研究红系细胞的各个方面,从其个体发育/环境控制,到其独特膜结构相关的细胞/形态发生方面,到其基因表达的转录/表观遗传调控,以及这些正常过程变化引起的疾病。2011年的会议将包括红细胞生成发育生物学;基因表达的转录调控;红细胞的表观遗传学和系统生物学;红细胞生成、信号传导和红细胞生成;红细胞终末成熟;膜蛋白的结构、关联和功能;红细胞疾病;铁、血红素和红细胞;寄生虫与红细胞的相互作用。通过关注这些主题,红细胞GRC继续成为展示最新前沿基础科学、对人类疾病的新见解和方法创新的主要场所,这些内容贯穿其整个历史,并因此而闻名。会议吸引了一群国际研究人员,并提供了一个活跃的论坛,在亲密的环境中积极参与和讨论,促进了高级和初级研究人员之间的互动,以及通常不容易互动的研究人员之间的互动。会议将于2011年7月24日至29日在新罕布什尔州安多弗市的普罗科特学院举行,届时将有52位演讲嘉宾和140位参会者。会议旨在包容妇女、少数民族和残疾人;参与者将包括博士后研究员和研究生,以及处于学术生涯早期的研究人员。将选择一些博士后和学生海报演讲者进行简短的演讲。在用餐时间、下午和晚上举行非正式聚会的机会,为来自不同学科的科学家提供了一个互动的途径,促进了跨学科的合作。根据其主题的性质,红细胞GRC仍然与增强对红细胞成熟的正常进程和导致其病理变化的理解完全相关。
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 }}
Velia M Fowler其他文献
A Short Isoform of Tensin1 Is a Novel Regulator of F-Actin Assembly in Human Erythroblasts That Promotes Enucleation
- DOI:
10.1182/blood-2024-210773 - 发表时间:
2024-11-05 - 期刊:
- 影响因子:
- 作者:
Velia M Fowler;Arit Ghosh;Megan Coffin;Dimitri Diaz;Vincent P Schulz;Patrick G. Gallagher - 通讯作者:
Patrick G. Gallagher
Velia M Fowler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('Velia M Fowler', 18)}}的其他基金
Actin cytoskeleton regulation of lens architecture, transparency and mechanics
肌动蛋白细胞骨架对晶状体结构、透明度和力学的调节
- 批准号:
10405108 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane skeleton regulation of cell shape and interactions in lens development
细胞形状的膜骨架调节和晶状体发育中的相互作用
- 批准号:
8103870 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Actin cytoskeleton regulation of lens architecture, transparency and mechanics
肌动蛋白细胞骨架对晶状体结构、透明度和力学的调节
- 批准号:
10208583 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane Skeleton Regulation of Cell Shape and Interactions in Lens Development
晶状体发育中细胞形状和相互作用的膜骨架调节
- 批准号:
8400678 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane Skeleton Regulation of Cell Shape and Interactions in Lens Development
晶状体发育中细胞形状和相互作用的膜骨架调节
- 批准号:
8511653 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane skeleton regulation of cell shape and interactions in lens development
细胞形状的膜骨架调节和晶状体发育中的相互作用
- 批准号:
7528566 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane skeleton regulation of cell shape and interactions in lens development
细胞形状的膜骨架调节和晶状体发育中的相互作用
- 批准号:
7898748 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane Skeleton Regulation of Cell Shape and Interactions in Lens Development
晶状体发育中细胞形状和相互作用的膜骨架调节
- 批准号:
8680237 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Actin cytoskeleton regulation of lens architecture, transparency and mechanics
肌动蛋白细胞骨架对晶状体结构、透明度和力学的调节
- 批准号:
10630274 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:
Membrane skeleton regulation of cell shape and interactions in lens development
细胞形状的膜骨架调节和晶状体发育中的相互作用
- 批准号:
7680014 - 财政年份:2008
- 资助金额:
$ 1.3万 - 项目类别:














{{item.name}}会员




