Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Jiuqiao Zhao"'
Autor:
Xiaodong Wu, Yongqiang Wang, Jonna Liu, Xiaocheng Lv, Fei Chen, Izzie Wang, Jiuqiao Zhao, Yiping Rong
Publikováno v:
Regular and Young Investigator Award Abstracts.
Autor:
Bing Huang, Fangfang Du, Xiaocheng Lv, Jianxun Zhao, Fei Chen, Zailian Lu, Yang Zhang, Victor Chen, Xin Gan, Jiuqiao Zhao, Yun He, Xiaodong Wu, Yiping Rong
Publikováno v:
Regular and Young Investigator Award Abstracts.
Autor:
Xin Gan, Qianqian Shan, He Li, Rick Janssens, Yuqiang Shen, Yun He, Fei Chen, Rien van Haperen, Dubravka Drabek, Jin Li, Yang Zhang, Jiuqiao Zhao, Beibei Qin, Ming-Jin Jheng, Victor Chen, Jingsong Wang, Yiping Rong, Frank Grosveld
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 119(32):e2200879119. National Academy of Sciences
The value of anti-CTLA-4 antibodies in cancer therapy is well established. However, the broad application of currently available anti-CTLA-4 therapeutic antibodies is hampered by their narrow therapeutic index. It is therefore challenging and attract
Autor:
Andrew P. Degnan, Haiquan Fang, Tatyana Zvyaga, Zuzana Haarhoff, Claude A. Quesnelle, Melissa Kramer, Frank Marsilio, Richard A. Westhouse, John S. Tokarski, Shilpa Madari, Jiuqiao Zhao, Amy Wiebesiek, Chunhong Yan, Francis Y. Lee, Michael Sinz, John Morrison, Jean Simmermacher-Mayer, Carolynn Fanslau, Steven Sheriff, Lisa Huang, Ashvinikumar V. Gavai, Chunshan Xie, Matthew D. Hill, Gerry Everlof
Publikováno v:
Bioorganicmedicinal chemistry letters. 51
We describe our efforts to introduce structural diversity to a previously described triazole-containing N1-carboline series of bromodomain and extra-terminal (BET) inhibitors. N9 carbolines were designed to retain favorable binding interactions that
Autor:
Xin Gan, Qianqian Shan, He Li, Janssens, Rick, Yuqiang Shen, Yun He, Fei Chen, van Haperen, Rien, Drabek, Dubravka, Jin Li, Yang Zhang, Jiuqiao Zhao, Beibei Qin, Ming-Jin Jheng, Chen, Victor, Jingsong Wang, Yiping Rong, Grosveld, Frank
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 8/9/2022, Vol. 119 Issue 32, p1-27, 37p
Publikováno v:
Cancer Research. 79:4098-4098
Anti-CTLA-4 antibodies are one of the only three types of immune checkpoint inhibitors (together with anti-PD-1 and anti-PD-L1 antibodies) with proven monotherapy value in cancer therapy. Despite demonstrated efficacy, their broad application in mono
Autor:
Jack Pick, Mark Craighead, Heather A. Zanetakos, Jeffrey J. Letourneau, Rachel Milne, Hema Desai, Leigh Campbell-Wan, Jeremy Presland, Michael Ohlmeyer, James R. Baker, Nasrin Ansari, Ray Jui-Hsiang Chan, Cliona P MacSweeney, Douglas S. Auld, Maria L. Webb, Jiuqiao Zhao, Chris Riviello, J. Richard Morphy, Stuart A. Best, Irina Neagu, Susan Elizabeth Napier, Koc-Kan Ho
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:3813-3817
Synthesis and structure–activity relationships (SAR) of a novel series of vasopressin V1b antagonists are described. 2-(6-Aminomethylaryl-2-aryl-4-oxo-quinazolin-3(4H)-yl)acetamide have been identified with low nanomolar affinity for the V1b recept
Autor:
Herman D. Lim, Douglas S. Auld, Maria L. Webb, Jac C. H. M. Wijkmans, Jiuqiao Zhao, Luc Roumen, Rob Leurs, Chris de Graaf, Petra de Kruijf, Martine J. Smit, Véronique A. Renjaän, G.J.R. Zaman
Publikováno v:
Molecular Pharmacology, 80, 1108-1118. American Society for Pharmacology and Experimental Therapeutics
de Kruijf, P, Lim, H D, Roumen, L, Renjaan, V A, Zhao, J, Webb, M J, Auld, D A, Wijkmans, J C H M, Zaman, G J R, Smit, M J, de Graaf, C & Leurs, R 2011, ' Identification of a novel allosteric binding site in the CXCR2 chemokine receptor ', Molecular Pharmacology, vol. 80, pp. 1108-1118 . https://doi.org/10.1124/mol.111.073825
de Kruijf, P, Lim, H D, Roumen, L, Renjaan, V A, Zhao, J, Webb, M J, Auld, D A, Wijkmans, J C H M, Zaman, G J R, Smit, M J, de Graaf, C & Leurs, R 2011, ' Identification of a novel allosteric binding site in the CXCR2 chemokine receptor ', Molecular Pharmacology, vol. 80, pp. 1108-1118 . https://doi.org/10.1124/mol.111.073825
We have shown previously that different chemical classes of small-molecule antagonists of the human chemokine CXCR2 receptor interact with distinct binding sites of the receptor. Although an intracellular binding site for diarylurea CXCR2 antagonists
Autor:
Andrew G. Cole, Douglas S. Auld, Riviello Christopher, Hema Desai, Hong Li, Heather A. Zanetakos, Fiona Thomson, J. Richard Morphy, Jiuqiao Zhao, Susan Elizabeth Napier, Michael Ohlmeyer, Katharine A. Goan, Koc-Kan Ho, Maria L. Webb, Jeffrey J. Letourneau
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5394-5397
The discovery, synthesis, and preliminary structure–activity relationship (SAR) of a novel class of vasopressin V3 (V1b) receptor antagonists is described. Compound 1, identified by high throughput screening of a diverse, three million-member compo
Publikováno v:
Molecular Carcinogenesis. 26:32-36
A transgenic mouse model was developed in which ornithine decarboxylase (ODC) can be overexpressed in a tissue-specific and regulated manner. Hair follicle keratinocytes were targeted by use of a bovine keratin 6 (K6) promoter/regulatory region, and