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Scientific Reports
|
December 18, 2019
Ten-Second Electrophysiology: Evaluation of the 3DEP Platform for high-speed, high-accuracy cell analysis
Kai F Hoettges, Erin A Henslee, Ruth M Torcal Serrano, et al.
Journal of Racial and Ethnic Health Disparities
|
June 18, 2025
Health Status And Delays In Referral-To-Treatment Waiting Times for Elective Admissions of Adults From Deprived Areas And Ethnic Minority Backgrounds: A Study of Healthcare Inequalities
David Fluck, Emma Jackson, Ana Llamas-Montoya, et al.
Endocrine-Related Cancer
|
March 12, 2015
Transcription of Nrdp1 by the androgen receptor is regulated by nuclear filamin A in prostate cancer
Rosalinda M Savoy, Liqun Chen, Salma Siddiqui, et al.
Protein Science : a Publication of the Protein Society
|
December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closure
Kenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 22, 2017
Three-dimensional culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer
Cunxi Li, Bhuminder Singh, Ramona Graves-Deal, et al.
Biochemistry
|
June 14, 2006
Crystal structures of DPP-IV (CD26) from rat kidney exhibit flexible accommodation of peptidase-selective inhibitors
Kenton L Longenecker, Kent D Stewart, David J Madar, et al.
Chemical Biology & Drug Design
|
February 24, 2006
Structure-based optimization of MurF inhibitors
Geoffrey F Stamper, Kenton L Longenecker, Elizabeth H Fry, et al.
Journal of Medicinal Chemistry
|
July 21, 2006
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors
Hongyu Zhao, Michael D Serby, Zhili Xin, et al.
Journal of Medicinal Chemistry
|
March 27, 2010
Optimization of phenyl-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase inhibitors: identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a highly potent and efficacious inhibitor
Thomas D Penning, Gui-Dong Zhu, Jianchun Gong, et al.
Bioorganic & Medicinal Chemistry
|
June 11, 2008
Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer
Thomas D Penning, Gui-Dong Zhu, Viraj B Gandhi, et al.
Page
of 31
Search research articles
Search
Showing results (291-300 of 305) with videos related to
Sort By:
Page
of 31
Scientific Reports
|
December 18, 2019
Ten-Second Electrophysiology: Evaluation of the 3DEP Platform for high-speed, high-accuracy cell analysis
Kai F Hoettges, Erin A Henslee, Ruth M Torcal Serrano, et al.
Journal of Racial and Ethnic Health Disparities
|
June 18, 2025
Health Status And Delays In Referral-To-Treatment Waiting Times for Elective Admissions of Adults From Deprived Areas And Ethnic Minority Backgrounds: A Study of Healthcare Inequalities
David Fluck, Emma Jackson, Ana Llamas-Montoya, et al.
Endocrine-Related Cancer
|
March 12, 2015
Transcription of Nrdp1 by the androgen receptor is regulated by nuclear filamin A in prostate cancer
Rosalinda M Savoy, Liqun Chen, Salma Siddiqui, et al.
Protein Science : a Publication of the Protein Society
|
December 3, 2005
Structure of MurF from Streptococcus pneumoniae co-crystallized with a small molecule inhibitor exhibits interdomain closure
Kenton L Longenecker, Geoffrey F Stamper, Philip J Hajduk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 22, 2017
Three-dimensional culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer
Cunxi Li, Bhuminder Singh, Ramona Graves-Deal, et al.
Biochemistry
|
June 14, 2006
Crystal structures of DPP-IV (CD26) from rat kidney exhibit flexible accommodation of peptidase-selective inhibitors
Kenton L Longenecker, Kent D Stewart, David J Madar, et al.
Chemical Biology & Drug Design
|
February 24, 2006
Structure-based optimization of MurF inhibitors
Geoffrey F Stamper, Kenton L Longenecker, Elizabeth H Fry, et al.
Journal of Medicinal Chemistry
|
July 21, 2006
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors
Hongyu Zhao, Michael D Serby, Zhili Xin, et al.
Journal of Medicinal Chemistry
|
March 27, 2010
Optimization of phenyl-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase inhibitors: identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a highly potent and efficacious inhibitor
Thomas D Penning, Gui-Dong Zhu, Jianchun Gong, et al.
Bioorganic & Medicinal Chemistry
|
June 11, 2008
Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer
Thomas D Penning, Gui-Dong Zhu, Viraj B Gandhi, et al.
Page
of 31