Genome Targeted Inhibitors of Retroviruses

逆转录病毒基因组靶向抑制剂

基本信息

项目摘要

four pages) ............. 6-8 Other Biographical Sketches (Not to exceed four pages for each) ............................................... 9-31 Resources ...................................................................................................................................... 32 Research Plan 33-35 Introductionto Revised Application (Not to exceed 3 pages) ............................................................................................................................... Introduction to Supplemental Application (Notto exceed one page) .................................................................................................................... A. Specific Aims .......................................................................... _ ......................................................................................................... 36-60 B. Background and Significance ...................................................... !...................................................................................................... _._" C. Preliminary Studies/Progress Report/ _ (Items A-D: not to exceed 25 pages*) _K_ Phase I Progress Report (SBIPJSTTR Phase II ONLY) I * SBIR/STTR Phase I: Items A-D limited to 15 pages, t D. Research Design and Methods ............................................ _ ..................................................................................................... E Human Subjects ......................................................................................................................................................................................... Protection of Human Subjects (Required if Item 4 on the Face Page is marked "Yes") Inclusion of Women (Required if Item 4 on the Face Page is marked "Yes") ................................................................................... Inclusion of Minorities (Required if Item 4 on the Face Page is marked "Yes") ................................................................................ Inclusion of Children (Required if Item 4 on the Face Page is marked "Yes") ................................................................................... Data and Safety Monitoring Plan (Required if Item 4 on the Face Page is marked "Yes" anda Phase I, 11,or III clinical roposed trial is proposed ................................................................................................................................................................................ F. Vertebrate Animals ..................................................................................................................................................................................... 61 G, Literature Cited ........................................................................................................................................................................................... H. Consortium/Contractual Arrangements .................................................................................................................................................... I. Consultants ................................................................................................................................................................................................. 68-74 J. Product Development Plan (SBIR/STTR Phase I1and Fast-Track ONLY) ........................................................................................... Checklist ........................................................................................................................................ 75 Check if Appendix (Five collated sets_ No page numbering necessary for Appendix.) Appendix is Included Appendices NOT PERMITTED for Phase I SBIR/S TTR unless specifically solicited, 6 Number of publications and manuscripts accepted for publication (not to exceed 10) Other items (list): PHS 398 (Rev, 510 l) Page 3 Number pages consecutively at the bottom throughout the application. Do _t use suffixes such as 3a, 3b,
四页). 6-8 其他个人简介(每份不超过四页)... 9-31 资源...... 32 研究计划 33-35 经修订的申请简介(不超过3页)..... 补充申请简介(不超过一页).... A.具体目标...... _ ......................................................................................................... 36-60 B。背景及意义.... !...................................................................................................... _._ " C.初步研究/进度报告/ _(项目A-D:不超过25页 *)_K_ 第I阶段进度报告(仅限SBIPJSTTR第II阶段)I * SBIR/STTR第I阶段:项目A-D限于15页, D.研究设计和方法........ _ ..................................................................................................... E人类受试者......................................................................................................................................................................................... 人类受试者保护(如果正面页面上的第4项标记为“是”,则需要) 纳入女性(如果正面页面上的项目4标记为“是”,则需要)... 纳入少数群体(如果正面页项目4标记为“是”,则需要).... 包括儿童(如果正面页上的第4项标记为“是”,则需要)..... 数据和安全性监测计划(如果正面页面上的第4项标记为“是”,则需要,并且I、11或III期临床试验 建议试用................................................................................................................................................................................ F.脊椎动物..................................................................................................................................................................................... 61 G、引用的文献........................................................................................................................................................................................... H.联合会/合同安排.................................................................................................................................................... I.顾问................................................................................................................................................................................................. 68-74 J.产品开发计划(仅限SBIR/STTR阶段I1和快速通道)....... 核对表.. 75 检查是否 附录(五个整理集_附录无需页码。) 阑尾是 包括 附录不允许用于I期SBIR/S TTR,除非特别要求, 6 接受出版的出版物和手稿数量(不超过10份) 其他项目(列表): PHS 398(修订版,510 l)第3页 在整个应用程序的底部连续编号页面。不要使用后缀,如3a,3b,

项目成果

期刊论文数量(17)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A peptide nucleic acid-neamine conjugate that targets and cleaves HIV-1 TAR RNA inhibits viral replication.
靶向并切割 HIV-1 TAR RNA 的肽核酸-新胺缀合物可抑制病毒复制。
  • DOI:
    10.1021/jm049642d
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    7.3
  • 作者:
    Riguet,Emmanuel;Tripathi,Snehlata;Chaubey,Binay;Desire,Jerome;Pandey,VirendraN;Decout,Jean-Luc
  • 通讯作者:
    Decout,Jean-Luc
Inhibition of HIV Replication by Cyclic and Hairpin PNAs Targeting the HIV-1 TAR RNA Loop.
  • DOI:
    10.1155/2012/591025
  • 发表时间:
    2012
  • 期刊:
  • 影响因子:
    2.3
  • 作者:
    Upert G;Di Giorgio A;Upadhyay A;Manvar D;Pandey N;Pandey VN;Patino N
  • 通讯作者:
    Patino N
Anti-HIV-1 activity of anti-TAR polyamide nucleic acid conjugated with various membrane transducing peptides.
  • DOI:
    10.1093/nar/gki743
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    14.9
  • 作者:
    Tripathi S;Chaubey B;Ganguly S;Harris D;Casale RA;Pandey VN
  • 通讯作者:
    Pandey VN
A single deletion at position 134, 135, or 136 in the beta 7-beta 8 loop of the p51 subunit of HIV-1 RT disrupts the formation of heterodimeric enzyme.
HIV-1 RT p51 亚基的 β7-β8 环中第 134、135 或 136 位的单个缺失会破坏异二聚酶的形成。
  • DOI:
    10.1002/jcb.22439
  • 发表时间:
    2010
  • 期刊:
  • 影响因子:
    4
  • 作者:
    Upadhyay,Alok;Pandey,Nootan;Mishra,ChaturbhujA;Talele,TanajiT;Pandey,VirendraN
  • 通讯作者:
    Pandey,VirendraN
Immunological response to peptide nucleic acid and its peptide conjugate targeted to transactivation response (TAR) region of HIV-1 RNA genome.
针对 HIV-1 RNA 基因组反式激活反应 (TAR) 区域的肽核酸及其肽缀合物的免疫反应。
  • DOI:
    10.1089/oli.2008.0152
  • 发表时间:
    2008
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Upadhyay,Alok;Ponzio,NicholasM;Pandey,VirendraN
  • 通讯作者:
    Pandey,VirendraN
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Virendra Nath PANDEY其他文献

Virendra Nath PANDEY的其他文献

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{{ truncateString('Virendra Nath PANDEY', 18)}}的其他基金

Implication of RNase H domain on dimer stability and drug sensitivity of HIV-1 RT
RNase H 结构域对 HIV-1 RT 二聚体稳定性和药物敏感性的影响
  • 批准号:
    8707365
  • 财政年份:
    2013
  • 资助金额:
    $ 36.86万
  • 项目类别:
Implication of RNase H domain on dimer stability and drug sensitivity of HIV-1 RT
RNase H 结构域对 HIV-1 RT 二聚体稳定性和药物敏感性的影响
  • 批准号:
    8541412
  • 财政年份:
    2013
  • 资助金额:
    $ 36.86万
  • 项目类别:
FUSE Binding Protein As a Cellular Effector of HCV Replication
FUSE 结合蛋白作为 HCV 复制的细胞效应子
  • 批准号:
    7788343
  • 财政年份:
    2010
  • 资助金额:
    $ 36.86万
  • 项目类别:
FUSE Binding Protein As a Cellular Effector of HCV Replication
FUSE 结合蛋白作为 HCV 复制的细胞效应子
  • 批准号:
    8077981
  • 财政年份:
    2010
  • 资助金额:
    $ 36.86万
  • 项目类别:
Proteomics of HCV Replication Complex
HCV 复制复合物的蛋白质组学
  • 批准号:
    7828015
  • 财政年份:
    2009
  • 资助金额:
    $ 36.86万
  • 项目类别:
Structure-Based Development of nonnucleoside anti-HIV-1 RT Drugs
非核苷类抗 HIV-1 RT 药物的基于结构的开发
  • 批准号:
    7802045
  • 财政年份:
    2009
  • 资助金额:
    $ 36.86万
  • 项目类别:
Proteomics of HCV Replication Complex
HCV 复制复合物的蛋白质组学
  • 批准号:
    7385667
  • 财政年份:
    2009
  • 资助金额:
    $ 36.86万
  • 项目类别:
Structure-Based Development of nonnucleoside anti-HIV-1 RT Drugs
非核苷类抗 HIV-1 RT 药物的基于结构的开发
  • 批准号:
    7495273
  • 财政年份:
    2009
  • 资助金额:
    $ 36.86万
  • 项目类别:
Genome Targeted Inhibitors of Retroviruses
逆转录病毒基因组靶向抑制剂
  • 批准号:
    6842205
  • 财政年份:
    1999
  • 资助金额:
    $ 36.86万
  • 项目类别:
Genome Targeted Inhibitors of Retroviruses
逆转录病毒基因组靶向抑制剂
  • 批准号:
    7010743
  • 财政年份:
    1999
  • 资助金额:
    $ 36.86万
  • 项目类别:

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以三萜类化合物为药物发现模板,开发具有双重作用机制的抗 HIV 药物
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新型抗HIV药物的结构活性和结构性质关系
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    8466077
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新型抗HIV药物的结构活性和结构性质关系
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开发与宿主免疫压力发挥协同作用的抗HIV药物
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抑制 Pr55Gag 膜定位的抗 HIV 药物的设计和合成
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新型抗HIV药物的结构活性和结构性质关系
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开发宿主防御肽作为新型抗 HIV 药物
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设计和合成抑制 Vif 介导的 APOBEC3G 蛋白酶体降解的抗 HIV 药物
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基于病毒自我调节机制的化学基因组学抗HIV药物的开发
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