2017 Mammary Gland Biology Gordon Research Conference & Gordon Research Seminar
2017年乳腺生物学戈登研究会议
基本信息
- 批准号:9324532
- 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:2017
- 资助国家:美国
- 起止时间:2017-03-03 至 2018-03-02
- 项目状态:已结题
- 来源:
- 关键词:AddressAreaBasic ScienceBiologicalBiologyBreastBreast Cancer PreventionBreast DiseasesBreast Epithelial CellsCancer BiologyCell CommunicationCellsCellular biologyCollaborationsDataDevelopmentDiseaseEndocrinologistEnvironmentEpithelial CellsEquilibriumEventFeesFertilizationFosteringFundingFutureGenomeGoalsHeterogeneityHumanImmune systemInternationalItalyKnowledgeLactationMalignant NeoplasmsMammary TumorigenesisMammary glandMolecularNatureNeoplasm MetastasisOncologistOralOrganogenesisParticipantPathologistPhysiologyPostdoctoral FellowPreventionRecording of previous eventsRecurrenceRegulationResearchResearch PersonnelRoleScienceScientistStem Cell DevelopmentStem cellsStudentsThinkingTimeTrainingTranslational ResearchTravelUnited States National Institutes of HealthWorkbasecancer preventioncancer riskcancer therapycarcinogenesiscareer developmentcell behaviordesignepigenomegraduate studentinformal supportinnovationinsightinterestmalignant breast neoplasmmammary gland developmentmathematical modelmeetingsmouse modelnext generationpeer coachingpostersprogramssocialstudent trainingsuccesssymposiumtherapeutic targettherapy resistanttumor heterogeneitytumor initiationtumor progression
项目摘要
Project Summary/Abstract
This application seeks conference funding to provide partial support for registration fee and/or travel support for
participants to attend the 2017 meetings of the Mammary Gland Biology Gordon Research Conference (GRC)
and the newly established and already highly successful Gordon Research Seminar (GRS). The unique
contribution and significance of this long-standing conference is that it will bring together developmental
biologists, experts in breast cancer risk and prevention, stem cell biologists, lactation physiologists, breast
pathologists, endocrinologists, cancer biologists and oncologists to collectively tackle important issues in
mammary biology, breast cancer prevention and treatment. The goals for a successful program are to inspire
important insights, energize new scientists and foster creative collaborations that will deepen our understanding
of normal breast physiology and accelerate the eradication of breast cancer. The multipronged nature of these
meetings guarantees a high degree of scientific cross-fertilization. The specific aims of the meeting will be to 1)
provide a program of highly qualified, internationally recognized speakers to address outstanding scientific
questions and controversies, 2) foster discussion, unfettered dialog and promote collaborations, and 3)
contribute to the training and development of the next generation of scientists.
The 2017 conference will focus on outstanding, and understudied, questions and recent discoveries related to
breast cancer risk and prevention, the mammary gland genome and epigenome in development and breast
cancer, mammary stem cells and development, lactation biology, mouse models of mammary tumorigenesis and
their relevance to human cancer, tumor heterogeneity, dormancy and metastasis, the role of the stroma and the
immune system. Experts in these fields were invited to share their most recent findings and discuss emerging
challenges. These are important issues, and the innovative approach of pairing research into development,
prevention and cancer within the same meeting will stimulate new and creative thinking. Short talks highlighting
outstanding work by young investigators and trainees will be chosen from the submitted abstracts.
Other unique features of this meeting include: (i) a tradition of sharing unpublished data; (ii) a program that
includes substantial time for questions and open discussion, (iii) an environment that supports informal
discussions outside of formal presentations; (iv) active participation and training environment for students and
post-docs through the Gordon Research Seminar and the Gordon Research Conference; and (v) the
encouragement of international collaborations and perspectives. In 2017, we will hold a “meet the expert” session
at the end of the GRS, in which senior leaders meet with small groups of students and post-doctoral fellows to
discuss science and career development. This session will be coordinated by GRC and GRS chairs
项目总结/摘要
本申请寻求会议资金,以提供部分注册费和/或差旅费支持,
参加2017年乳腺生物学戈登研究会议(GRC)的与会者
以及新成立的、已经非常成功的戈登研究研讨会(GRS)。独特的
这一长期会议的贡献和意义在于,它将汇集发展中国家,
生物学家,乳腺癌风险和预防专家,干细胞生物学家,哺乳生理学家,乳腺癌
病理学家,内分泌学家,癌症生物学家和肿瘤学家共同解决
乳腺生物学、乳腺癌防治。一个成功的计划的目标是激励
重要的见解,激励新的科学家和促进创造性的合作,将加深我们的理解
正常乳腺生理机能的改变,加速乳腺癌的根除。这些问题的多管齐下性质
会议保证了高度的科学交叉。会议的具体目标是:(1)
提供一个高素质的,国际公认的演讲者计划,以解决杰出的科学
问题和争议,2)促进讨论,自由对话,促进合作,以及3)
为下一代科学家的培养和发展做出贡献。
2017年会议将重点关注与以下方面有关的突出和未充分研究的问题和最新发现:
乳腺癌的风险和预防,乳腺基因组和表观基因组在发育和乳腺癌
癌症,乳腺干细胞和发育,哺乳生物学,乳腺肿瘤发生的小鼠模型,
它们与人类癌症、肿瘤异质性、休眠和转移的相关性,基质的作用和肿瘤细胞的增殖,
免疫系统这些领域的专家应邀分享了他们的最新研究结果,并讨论了新出现的
挑战这些都是重要的问题,将研究与发展结合起来的创新方法,
在同一次会议上讨论预防和癌症问题将激发新的创造性思维。简短的谈话强调
将从提交的摘要中选出年轻研究人员和受训人员的杰出工作。
本次会议的其他独特之处包括:(一)分享未公布数据的传统;(二)
包括大量的提问和公开讨论的时间,(iii)支持非正式讨论的环境
(四)积极参与,为学生提供培训环境,
(v)研究院的研究计划;及
鼓励国际合作和展望。2017年,我们将举办“会见专家”会议
在GRS结束时,高级领导人与学生和博士后研究员小组会面,
讨论科学和职业发展。本次会议将由GRC和GRS主席协调
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 }}
Heide L. Ford其他文献
All eyes on Eya: A unique transcriptional co-activator and phosphatase in cancer
聚焦Eya:癌症中一种独特的转录共激活因子和磷酸酶
- DOI:
10.1016/j.bbcan.2024.189098 - 发表时间:
2024-05-01 - 期刊:
- 影响因子:8.300
- 作者:
Connor J. Hughes;Christopher Alderman;Arthur R. Wolin;Kaiah M. Fields;Rui Zhao;Heide L. Ford - 通讯作者:
Heide L. Ford
Transcriptional Control of the Cell Cycle in Mammary Gland Development and Tumorigenesis
- DOI:
10.1023/b:jomg.0000023587.40966.f6 - 发表时间:
2004-01-01 - 期刊:
- 影响因子:3.600
- 作者:
Ricardo D. Coletta;Paul Jedlicka;Arthur Gutierrez-Hartmann;Heide L. Ford - 通讯作者:
Heide L. Ford
MIRO2 promotes cancer invasion and metastasis via MYO9B suppression of RhoA activity
Miro2 通过抑制 RhoA 活性的 Myo9b 促进癌症侵袭和转移
- DOI:
10.1016/j.celrep.2024.115120 - 发表时间:
2025-01-28 - 期刊:
- 影响因子:6.900
- 作者:
Dillon P. Boulton;Connor J. Hughes;Valentina Vaira;Alessandro Del Gobbo;Alessandro Palleschi;Marco Locatelli;Etienne Danis;Masoom Raza;Andrew J. Neumann;Stephen Connor Purdy;Raymundo Lerma;John Meshki;Heide L. Ford;Rytis Prekeris;Colm Morrissey;M. Cecilia Caino - 通讯作者:
M. Cecilia Caino
Guidelines and definitions for research on epithelial–mesenchymal transition
上皮-间充质转化研究的指南和定义
- DOI:
10.1038/s41580-020-0237-9 - 发表时间:
2020-04-16 - 期刊:
- 影响因子:90.200
- 作者:
Jing Yang;Parker Antin;Geert Berx;Cédric Blanpain;Thomas Brabletz;Marianne Bronner;Kyra Campbell;Amparo Cano;Jordi Casanova;Gerhard Christofori;Shoukat Dedhar;Rik Derynck;Heide L. Ford;Jonas Fuxe;Antonio García de Herreros;Gregory J. Goodall;Anna-Katerina Hadjantonakis;Ruby Y. J. Huang;Chaya Kalcheim;Raghu Kalluri;Yibin Kang;Yeesim Khew-Goodall;Herbert Levine;Jinsong Liu;Gregory D. Longmore;Sendurai A. Mani;Joan Massagué;Roberto Mayor;David McClay;Keith E. Mostov;Donald F. Newgreen;M. Angela Nieto;Alain Puisieux;Raymond Runyan;Pierre Savagner;Ben Stanger;Marc P. Stemmler;Yoshiko Takahashi;Masatoshi Takeichi;Eric Theveneau;Jean Paul Thiery;Erik W. Thompson;Robert A. Weinberg;Elizabeth D. Williams;Jianhua Xing;Binhua P. Zhou;Guojun Sheng - 通讯作者:
Guojun Sheng
Heide L. Ford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('Heide L. Ford', 18)}}的其他基金
Deciphering Mechanisms by which Tumor Cells Collaborate to Mediate Metastasis
破译肿瘤细胞协作介导转移的机制
- 批准号:
9900185 - 财政年份:2019
- 资助金额:
$ 1万 - 项目类别:
Examining the EYA2/MYC axis in Group 3 Medulloblastoma
检查第 3 组髓母细胞瘤中的 EYA2/MYC 轴
- 批准号:
9753388 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Deciphering Mechanisms by which Tumor Cells Collaborate to Mediate Metastasis
破译肿瘤细胞协作介导转移的机制
- 批准号:
10296675 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Deciphering Mechanisms by which Tumor Cells Collaborate to Mediate Metastasis
破译肿瘤细胞协作介导转移的机制
- 批准号:
10531902 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Examining the EYA2/MYC axis in Group 3 Medulloblastoma
检查第 3 组髓母细胞瘤中的 EYA2/MYC 轴
- 批准号:
10172986 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Deciphering Mechanisms by which Tumor Cells Collaborate to Mediate Metastasis
破译肿瘤细胞协作介导转移的机制
- 批准号:
10053325 - 财政年份:2018
- 资助金额:
$ 1万 - 项目类别:
Role of Eya3 in regulating the immune microenvironment to promote breast tumor progression
Eya3在调节免疫微环境促进乳腺肿瘤进展中的作用
- 批准号:
10218071 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
Role of Eya3 in regulating the immune microenvironment to promote breast tumor progression
Eya3在调节免疫微环境促进乳腺肿瘤进展中的作用
- 批准号:
9751261 - 财政年份:2017
- 资助金额:
$ 1万 - 项目类别:
Developing cancer therapies through targeting the Six1/Eya transcriptional complex
通过靶向 Six1/Eya 转录复合物开发癌症疗法
- 批准号:
8989081 - 财政年份:2014
- 资助金额:
$ 1万 - 项目类别:
The anti-tumorigenic and anti-metastatic potential of Eya phosphatase inhibitors
Eya 磷酸酶抑制剂的抗肿瘤发生和抗转移潜力
- 批准号:
8592626 - 财政年份:2013
- 资助金额:
$ 1万 - 项目类别:
相似国自然基金
层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
- 批准号:2021JJ40433
- 批准年份:2021
- 资助金额:0.0 万元
- 项目类别:省市级项目
寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
- 批准号:32001603
- 批准年份:2020
- 资助金额:24.0 万元
- 项目类别:青年科学基金项目
AREA国际经济模型的移植.改进和应用
- 批准号:18870435
- 批准年份:1988
- 资助金额:2.0 万元
- 项目类别:面上项目
相似海外基金
Onboarding Rural Area Mathematics and Physical Science Scholars
农村地区数学和物理科学学者的入职
- 批准号:
2322614 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant
Point-scanning confocal with area detector
点扫描共焦与区域检测器
- 批准号:
534092360 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Major Research Instrumentation
TRACK-UK: Synthesized Census and Small Area Statistics for Transport and Energy
TRACK-UK:交通和能源综合人口普查和小区域统计
- 批准号:
ES/Z50290X/1 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Research Grant
Wide-area low-cost sustainable ocean temperature and velocity structure extraction using distributed fibre optic sensing within legacy seafloor cables
使用传统海底电缆中的分布式光纤传感进行广域低成本可持续海洋温度和速度结构提取
- 批准号:
NE/Y003365/1 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Research Grant
Collaborative Research: Scalable Manufacturing of Large-Area Thin Films of Metal-Organic Frameworks for Separations Applications
合作研究:用于分离应用的大面积金属有机框架薄膜的可扩展制造
- 批准号:
2326714 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant
Collaborative Research: Scalable Manufacturing of Large-Area Thin Films of Metal-Organic Frameworks for Separations Applications
合作研究:用于分离应用的大面积金属有机框架薄膜的可扩展制造
- 批准号:
2326713 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant
Unlicensed Low-Power Wide Area Networks for Location-based Services
用于基于位置的服务的免许可低功耗广域网
- 批准号:
24K20765 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
RAPID: Collaborative Research: Multifaceted Data Collection on the Aftermath of the March 26, 2024 Francis Scott Key Bridge Collapse in the DC-Maryland-Virginia Area
RAPID:协作研究:2024 年 3 月 26 日 DC-马里兰-弗吉尼亚地区 Francis Scott Key 大桥倒塌事故后果的多方面数据收集
- 批准号:
2427233 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant
RAPID: Collaborative Research: Multifaceted Data Collection on the Aftermath of the March 26, 2024 Francis Scott Key Bridge Collapse in the DC-Maryland-Virginia Area
RAPID:协作研究:2024 年 3 月 26 日 DC-马里兰-弗吉尼亚地区 Francis Scott Key 大桥倒塌事故后果的多方面数据收集
- 批准号:
2427232 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant
RAPID: Collaborative Research: Multifaceted Data Collection on the Aftermath of the March 26, 2024 Francis Scott Key Bridge Collapse in the DC-Maryland-Virginia Area
RAPID:协作研究:2024 年 3 月 26 日 DC-马里兰-弗吉尼亚地区 Francis Scott Key 大桥倒塌事故后果的多方面数据收集
- 批准号:
2427231 - 财政年份:2024
- 资助金额:
$ 1万 - 项目类别:
Standard Grant