Training Program in Ion Channel and Transporter Biology
离子通道和转运生物学培训计划
基本信息
- 批准号:9976590
- 负责人:
- 金额:$ 17.08万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-07-20 至 2022-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Ion channels and transporter proteins are ubiquitous molecules that serve a variety of important physiological functions, provide targets for many types of pharmacological agents, and are encoded by genes that can be the basis for inherited diseases affecting the nervous system and other tissues. This proposal describes the continuation of a Training Program in Ion Channel and Transporter Biology that will provide multidisciplinary research training for postdoctoral scientists. This highly focused training program involves 28 NIH-funded preceptors (aggregate funding >$44,000,000 direct costs/year) affiliated with 13 different academic departments and 10 research centers at Vanderbilt University with strong records of accomplishments in the ion channel and transporter field, and with a deep commitment to training postdoctoral fellows. This interdepartmental training program capitalizes on a over 20-year history of institutional and multidisciplinary strength in ths research field. The program began initially in 2001 with only 19 faculty and has successfully filled all funded positions since that time. Although the training program originally included predoctoral training, since 2010 the program has focused solely on postdoctoral training. Postdoctoral trainees are selected from the pool of applicants that apply to preceptor laboratories as well as to participating centers and departments at Vanderbilt University. A multi-faceted recruitment strategy will continue to attract highly qualified individuals from underrepresented groups (URM). During the current funding cycle, 3/12 (25%) of trainees were URMs. In addition to intensive research experiences, trainees will have didactic course requirements that include a focused course on grant writing, an innovative program group meetings devoted to individualized training in grant writing, mentoring and career guidance. The high caliber of faculty mentors, the interdisciplinary nature of training opportunities, the strong
institutional strengths combine to foster a unique environment suited to the goal of the training program, which is to develop scientists with strong commitments to biomedical research in the area of ion channel and transporter biology.
描述(由申请人提供):离子通道和转运蛋白是普遍存在的分子,具有多种重要的生理功能,为许多类型的药理学试剂提供靶标,并且由基因编码,这些基因可能是影响神经系统和其他组织的遗传性疾病的基础。该提案描述了离子通道和转运蛋白生物学培训计划的延续,该计划将为博士后科学家提供多学科研究培训。这个高度集中的培训计划涉及28个NIH资助的导师(总资金> 44,000,000美元直接成本/年),隶属于范德比尔特大学的13个不同的学术部门和10个研究中心,在离子通道和转运蛋白领域取得了很好的成绩,并致力于培养博士后研究员。这个跨部门的培训计划利用了在研究领域超过20年的机构和多学科力量的历史。该计划最初于2001年开始,只有19名教师,并成功地填补了自那时以来所有资助的职位。虽然培训计划最初包括博士前培训,但自2010年以来,该计划只专注于博士后培训。博士后培训生是从申请导师实验室以及参与中心和部门在范德比尔特大学的申请人池中选择。一项多方面的征聘战略将继续从任职人数不足的群体中吸引高素质的个人。在本供资周期,3/12(25%)的受训人员是统一登记管理人员。除了密集的研究经验,学员将有教学课程的要求,其中包括一个重点课程的赠款写作,一个创新的程序组会议,致力于个性化的培训赠款写作,辅导和职业指导。高素质的教师导师,跨学科性质的培训机会,强大的
机构的优势联合收割机结合起来,以促进一个独特的环境,适合培训计划的目标,这是培养科学家与坚定的承诺,生物医学研究领域的离子通道和转运生物学。
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)
LTP in the mouse nucleus accumbens is developmentally regulated.
小鼠伏隔核中的 LTP 受到发育调节。
- DOI:10.1002/syn.10104
- 发表时间:2002
- 期刊:
- 影响因子:0
- 作者:Schramm,NicoleL;Egli,RegulaE;Winder,DannyG
- 通讯作者:Winder,DannyG
SN79, a sigma receptor antagonist, attenuates methamphetamine-induced astrogliosis through a blockade of OSMR/gp130 signaling and STAT3 phosphorylation.
SN79是一种Sigma受体拮抗剂,通过阻断OSMR/GP130信号传导和STAT3磷酸化,减弱了甲基苯丙胺诱导的星形胶质细胞增多症。
- DOI:10.1016/j.expneurol.2014.01.020
- 发表时间:2014-04
- 期刊:
- 影响因子:5.3
- 作者:Robson, Matthew J.;Turner, Ryan C.;Naser, Zachary J.;McCurdy, Christopher R.;O'Callaghan, James P.;Huber, Jason D.;Matsumoto, Rae R.
- 通讯作者:Matsumoto, Rae R.
Methamphetamine-induced toxicity: an updated review on issues related to hyperthermia.
- DOI:10.1016/j.pharmthera.2014.05.001
- 发表时间:2014-10
- 期刊:
- 影响因子:13.5
- 作者:Matsumoto RR;Seminerio MJ;Turner RC;Robson MJ;Nguyen L;Miller DB;O'Callaghan JP
- 通讯作者:O'Callaghan JP
Differential CaMKII regulation by voltage-gated calcium channels in the striatum.
- DOI:10.1016/j.mcn.2015.08.003
- 发表时间:2015-09
- 期刊:
- 影响因子:0
- 作者:Pasek JG;Wang X;Colbran RJ
- 通讯作者:Colbran RJ
Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).
- DOI:10.1016/j.yjmcc.2004.11.012
- 发表时间:2005-02-01
- 期刊:
- 影响因子:5
- 作者:Lundquist, Andrew L;Manderfield, Lauren J;George, Alfred L Jr
- 通讯作者:George, Alfred L Jr
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Jerod S. Denton其他文献
A LRRC8 chimera with native functional properties is a heptamer with a large lipid-blocked pore
- DOI:
10.1016/j.bpj.2022.11.2466 - 发表时间:
2023-02-10 - 期刊:
- 影响因子:
- 作者:
Hirohide Takahashi;Toshiki Yamada;Jerod S. Denton;Kevin Strange;Erkan Karakas - 通讯作者:
Erkan Karakas
55: Rational Synthesis of a Selective Renal Outer Medullary Potassium Channel (ROMK) Antagonist
- DOI:
10.1053/j.ajkd.2010.02.062 - 发表时间:
2010-04-01 - 期刊:
- 影响因子:
- 作者:
Gautam Bhave;Brian A. Chauder;Rishin Kadakia;Eric S. Dawson;Craig W. Lindsley;C. David Weaver;Jerod S. Denton - 通讯作者:
Jerod S. Denton
Development of Small-Molecule Inhibitors of Proton-Activated Chloride Channels
- DOI:
10.1016/j.bpj.2019.11.3197 - 发表时间:
2020-02-07 - 期刊:
- 影响因子:
- 作者:
Eric E. Figueroa;Jerod S. Denton - 通讯作者:
Jerod S. Denton
Oligomeric structure of LRRC8/VRAC channels: Arguments for a heptameric conformation
- DOI:
10.1016/j.bpj.2022.11.789 - 发表时间:
2023-02-10 - 期刊:
- 影响因子:
- 作者:
Jerod S. Denton;Toshiki Yamada;Hirohide Takahashi;Erkan Karakas;Kevin Strange - 通讯作者:
Kevin Strange
CysLT1 Receptor Antagonists Pranlukast and Zafirlukast Inhibit <em>LRRC8</em>-Mediated Volume Regulated Anion Channels Independently of the Receptor
- DOI:
10.1016/j.bpj.2019.11.3186 - 发表时间:
2020-02-07 - 期刊:
- 影响因子:
- 作者:
Eric E. Figueroa;Jerod S. Denton - 通讯作者:
Jerod S. Denton
Jerod S. Denton的其他文献
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{{ truncateString('Jerod S. Denton', 18)}}的其他基金
Preclinical validation of Kir4.1/5.1 inhibitors for overcoming diuretic resistance
Kir4.1/5.1 抑制剂克服利尿剂抵抗的临床前验证
- 批准号:
10740429 - 财政年份:2023
- 资助金额:
$ 17.08万 - 项目类别:
Development of Kv3.1 potentiators for correcting fast-spiking-interneuron hypofunction in schizophrenia and autism spectrum disorder
开发 Kv3.1 增效剂来纠正精神分裂症和自闭症谱系障碍的快速尖峰中间神经元功能减退
- 批准号:
10736465 - 财政年份:2023
- 资助金额:
$ 17.08万 - 项目类别:
Pharmacological Validation of Vascular KATP Channels for Modulating Ductus Arteriosus Tone
调节动脉导管张力的血管 KATP 通道的药理学验证
- 批准号:
10657531 - 财政年份:2020
- 资助金额:
$ 17.08万 - 项目类别:
Pharmacological Validation of Vascular KATP Channels for Modulating Ductus Arteriosus Tone
调节动脉导管张力的血管 KATP 通道的药理学验证
- 批准号:
10437919 - 财政年份:2020
- 资助金额:
$ 17.08万 - 项目类别:
Pharmacological Validation of Vascular KATP Channels for Modulating Ductus Arteriosus Tone
调节动脉导管张力的血管 KATP 通道的药理学验证
- 批准号:
10247076 - 财政年份:2020
- 资助金额:
$ 17.08万 - 项目类别:
Pharmacological Validation of Vascular KATP Channels for Modulating Ductus Arteriosus Tone
调节动脉导管张力的血管 KATP 通道的药理学验证
- 批准号:
10053976 - 财政年份:2020
- 资助金额:
$ 17.08万 - 项目类别:
Developing modulators of the sperm-specific potassium channel SLO3 for contraception
开发用于避孕的精子特异性钾通道 SLO3 调节剂
- 批准号:
10018521 - 财政年份:2019
- 资助金额:
$ 17.08万 - 项目类别:
Development of Distal Nephron Diuretics Targeting Kir4.1/5.1 Heteromeric Potassium Channels
针对 Kir4.1/5.1 异聚钾通道的远端肾单位利尿剂的开发
- 批准号:
10179370 - 财政年份:2019
- 资助金额:
$ 17.08万 - 项目类别:
Developing modulators of the sperm-specific potassium channel SLO3 for contraception
开发用于避孕的精子特异性钾通道 SLO3 调节剂
- 批准号:
10470966 - 财政年份:2019
- 资助金额:
$ 17.08万 - 项目类别:
Developing modulators of the sperm-specific potassium channel SLO3 for contraception
开发用于避孕的精子特异性钾通道 SLO3 调节剂
- 批准号:
10671550 - 财政年份:2019
- 资助金额:
$ 17.08万 - 项目类别:
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合作研究:FET:小型:基于离子通道忆阻器的储层计算
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