English
|
正體中文
|
简体中文
|
全文筆數/總筆數 : 12189/12972 (94%)
造訪人次 : 955350 線上人數 : 685
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by
NTU Library IR team.
搜尋範圍
全部NHRI
生技與藥物研究所
蔣維棠
--期刊論文
查詢小技巧:
您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
進階搜尋
主頁
‧
登入
‧
上傳
‧
說明
‧
關於NHRI
‧
管理
國家衛生研究院 NHRI
>
生技與藥物研究所
>
蔣維棠
>
期刊論文
>
依題名瀏覽
依作者瀏覽
依日期瀏覽
依資料類型瀏覽
資料載入中.....
鄰近類別
會議論文/會議摘要
[
4
/5]
專利
[
0
/23]
類別統計
近3年內發表的文件:0(0.00%)
含全文筆數:37(97.37%)
文件下載次數統計
下載大於0次:37(100.00%)
下載大於100次:37(100.00%)
檔案下載總次數:28724(92.80%)
最後更新時間: 2024-12-03 04:10
上傳排行
資料載入中.....
下載排行
資料載入中.....
最近上傳
Xanthine derivatives reveal an allo...
DBPR108, a novel dipeptidyl peptida...
Potent and orally active purine-bas...
Identification of a multitargeted t...
Identification of novel anti-liver ...
Discovery of Conformational Control...
BPR1J373, a novel multitargeted kin...
Pyrazolylamine derivatives reveal t...
Identification of a potent 5-phenyl...
Fibroblast activation protein (FAP)...
跳至:
(選擇年份)
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009
2008
2007
2006
2005
2004
2003
2002
2001
2000
1999
1998
1997
1996
1995
1994
1993
1992
1991
1990
1985
1980
1975
1970
1960
1950
(選擇月份)
January
February
March
April
May
June
July
August
September
October
November
December
或輸入年份:
由新到舊排序
由最舊的開始
顯示項目11-20 / 38. (共4頁)
<<
<
1
2
3
4
>
>>
每頁顯示[
10
|
25
|
50
]項目
日期
題名
關聯
2014-02
Fibroblast activation protein (FAP) is essential for the migration of bone marrow mesenchymal stem cells through RhoA activation
PLoS ONE. 2014 Feb 13;9(2):Article number e88772.
2014-01-08
Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancer
PLoS ONE. 2014 Jan 8;9(1):Article number e83160.
2014-01
A novel dengue virus inhibitor, BP13944, discovered by high-throughput screening with dengue virus replicon cells selects for resistance in the viral NS2B/NS3 protease
Antimicrobial Agents and Chemotherapy. 2014 Jan;58(1):110-119.
2013-06-28
Optimization of ligand and lipophilic efficiency to identify an in vivo active furano-pyrimidine aurora kinase inhibitor
Journal of Medicinal Chemistry. 2013 Jun 28;56(13):5247-5260.
2013-06
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Bioorganic and Medicinal Chemistry. 2013 Jun;21(11):2856-2867.
2013-02
Resistance studies of a di-thiazol analogue, DBPR110, as a potential hepatitis C virus NS5A inhibitor in replicon systems
Antimicrobial Agents and Chemotherapy. 2013 Feb; 57(2):723-733.
2012-06-07
3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Bioorganic and Medicinal Chemistry Letters. 2012 Jun 7;22(14):4654-4659.
2012-01
Resistance analysis and characterization of a thiazole analogue, BP008, as a potent hepatitis C virus NS5A inhibitor
Antimicrobial Agents and Chemotherapy. 2012 Jan;56(1):44-53.
2012-01
BPR1J-097, a novel FLT3 kinase inhibitor, exerts potent inhibitory activity against AML
British Journal of Cancer. 2012 Jan;106(3):475-481.
2011-07
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Bioorganic and Medicinal Chemistry. 2011 Jul;19(14):4173-4182 .
顯示項目11-20 / 38. (共4頁)
<<
<
1
2
3
4
>
>>
每頁顯示[
10
|
25
|
50
]項目
DSpace Software
Copyright © 2002-2004
MIT
&
Hewlett-Packard
/
Enhanced by
NTU Library IR team
Copyright ©
-
回饋