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Adam Siddiqui-Jain

Showing results (1-10 of 24) with videos related to

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Nature Chemistry|February 21, 2013
DNA structure: Visualizing the quadruplexAdam Siddiqui-Jain, Laurence H Hurley
Seminars in Oncology|August 8, 2006
Drug targeting of the c-MYC promoter to repress gene expression via a G-quadruplex silencer elementLaurence H Hurley, Daniel D Von Hoff, Adam Siddiqui-Jain, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2002
Direct evidence for a G-quadruplex in a promoter region and its targeting with a small molecule to repress c-MYC transcriptionAdam Siddiqui-Jain, Cory L Grand, David J Bearss, et al.
Bioorganic & Medicinal Chemistry Letters|February 14, 2018
Pharmacology and in vivo efficacy of pyridine-pyrimidine amides that inhibit microtubule polymerizationAdam Siddiqui-Jain, Jacob P Hoj, David W Cescon, et al.
Journal of Medicinal Chemistry|April 15, 2005
Conformationally restricted analogues of psorospermin: design, synthesis, and bioactivity of natural-product-related bisfuranoxanthonesRobert A Heald, Thomas S Dexheimer, Hariprasad Vankayalapati, et al.
Journal of the American Chemical Society|July 15, 2004
The dynamic character of the G-quadruplex element in the c-MYC promoter and modification by TMPyP4Jeyaprakashnarayanan Seenisamy, Evonne M Rezler, Tiffanie J Powell, et al.
Journal of the American Chemical Society|March 3, 2005
Design and synthesis of an expanded porphyrin that has selectivity for the c-MYC G-quadruplex structureJeyaprakashnarayanan Seenisamy, Sridevi Bashyam, Vijay Gokhale, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 2012
Novel potent dual inhibitors of CK2 and Pim kinases with antiproliferative activity against cancer cellsFabrice Pierre, Collin F Regan, Marie-Claire Chevrel, et al.
Biochemistry|August 30, 2011
Unprecedented selectivity and structural determinants of a new class of protein kinase CK2 inhibitors in clinical trials for the treatment of cancerRoberto Battistutta, Giorgio Cozza, Fabrice Pierre, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2017
Pyridine-pyrimidine amides that prevent HGF-induced epithelial scattering by two distinct mechanismsAdam Siddiqui-Jain, Jacob P Hoj, J Blade Hargiss, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Nature Chemistry|February 21, 2013
DNA structure: Visualizing the quadruplexAdam Siddiqui-Jain, Laurence H Hurley
Seminars in Oncology|August 8, 2006
Drug targeting of the c-MYC promoter to repress gene expression via a G-quadruplex silencer elementLaurence H Hurley, Daniel D Von Hoff, Adam Siddiqui-Jain, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2002
Direct evidence for a G-quadruplex in a promoter region and its targeting with a small molecule to repress c-MYC transcriptionAdam Siddiqui-Jain, Cory L Grand, David J Bearss, et al.
Bioorganic & Medicinal Chemistry Letters|February 14, 2018
Pharmacology and in vivo efficacy of pyridine-pyrimidine amides that inhibit microtubule polymerizationAdam Siddiqui-Jain, Jacob P Hoj, David W Cescon, et al.
Journal of Medicinal Chemistry|April 15, 2005
Conformationally restricted analogues of psorospermin: design, synthesis, and bioactivity of natural-product-related bisfuranoxanthonesRobert A Heald, Thomas S Dexheimer, Hariprasad Vankayalapati, et al.
Journal of the American Chemical Society|July 15, 2004
The dynamic character of the G-quadruplex element in the c-MYC promoter and modification by TMPyP4Jeyaprakashnarayanan Seenisamy, Evonne M Rezler, Tiffanie J Powell, et al.
Journal of the American Chemical Society|March 3, 2005
Design and synthesis of an expanded porphyrin that has selectivity for the c-MYC G-quadruplex structureJeyaprakashnarayanan Seenisamy, Sridevi Bashyam, Vijay Gokhale, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 2012
Novel potent dual inhibitors of CK2 and Pim kinases with antiproliferative activity against cancer cellsFabrice Pierre, Collin F Regan, Marie-Claire Chevrel, et al.
Biochemistry|August 30, 2011
Unprecedented selectivity and structural determinants of a new class of protein kinase CK2 inhibitors in clinical trials for the treatment of cancerRoberto Battistutta, Giorgio Cozza, Fabrice Pierre, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2017
Pyridine-pyrimidine amides that prevent HGF-induced epithelial scattering by two distinct mechanismsAdam Siddiqui-Jain, Jacob P Hoj, J Blade Hargiss, et al.
Pageof 3