-
1
-
-
38749114995
-
Oncogenes and cancer
-
COI: 1:CAS:528:DC%2BD1cXhtlWlur8%3D, PID: 18234754
-
Croce CM. Oncogenes and cancer. N Engl J Med. 2008;358(5):502–11.
-
(2008)
N. Engl. J. Med.
, vol.358
, Issue.5
, pp. 502-511
-
-
Croce, C.M.1
-
2
-
-
84971360233
-
Breakthroughs in epigenetics
-
COI: 1:CAS:528:DC%2BC28XmtlCrsLk%3D
-
Anand SS, Gill BS. Breakthroughs in epigenetics. Pharm Tutor. 2015;3(7):16–24.
-
(2015)
Pharm Tutor
, vol.3
, Issue.7
, pp. 16-24
-
-
Anand, S.S.1
Gill, B.S.2
-
3
-
-
0025343230
-
Signal transduction by receptors with tyrosine kinase activity
-
COI: 1:CAS:528:DyaK3cXktlKnu74%3D, PID: 2158859
-
Ullrich A, Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell. 1990;61(2):203–12.
-
(1990)
Cell
, vol.61
, Issue.2
, pp. 203-212
-
-
Ullrich, A.1
Schlessinger, J.2
-
4
-
-
84971240326
-
Success stories of enolate form of drugs
-
Negi A, Gill B. Success stories of enolate form of drugs. Pharm Tutor. 2013;1(2):45–53.
-
(2013)
Pharm Tutor
, vol.1
, Issue.2
, pp. 45-53
-
-
Negi, A.1
Gill, B.2
-
5
-
-
0034789517
-
Receptor tyrosine kinase signalling as a target for cancer intervention strategies
-
COI: 1:CAS:528:DC%2BD3MXotlCqsL0%3D, PID: 11566607
-
Zwick E, Bange J, Ullrich A. Receptor tyrosine kinase signalling as a target for cancer intervention strategies. Endocr Relat Cancer. 2001;8(3):161–73.
-
(2001)
Endocr Relat Cancer
, vol.8
, Issue.3
, pp. 161-173
-
-
Zwick, E.1
Bange, J.2
Ullrich, A.3
-
6
-
-
84976276835
-
Triterpenes in cancer: significance and their influence
-
COI: 1:CAS:528:DC%2BC28XhtVKnsLzM, PID: 27344437
-
Gill BS, Kumar S. Triterpenes in cancer: significance and their influence. Mol Biol Rep. 2016;43(9):881–96. doi:10.1007/s11033-016-4032-9.
-
(2016)
Mol. Biol. Rep.
, vol.43
, Issue.9
, pp. 881-896
-
-
Gill, B.S.1
Kumar, S.2
-
7
-
-
0034644539
-
Cell signaling by receptor tyrosine kinases
-
COI: 1:CAS:528:DC%2BD3cXns1Cltrs%3D, PID: 11057895
-
Schlessinger J. Cell signaling by receptor tyrosine kinases. Cell. 2000;103(2):211–25.
-
(2000)
Cell
, vol.103
, Issue.2
, pp. 211-225
-
-
Schlessinger, J.1
-
8
-
-
84955614581
-
Missing link between microRNA and prostate cancer
-
COI: 1:CAS:528:DC%2BC28XitFCjs7k%3D
-
Gill BS, Alex JM, Kumar S. Missing link between microRNA and prostate cancer. Tumor Biol. 2016;37(5):5683–704.
-
(2016)
Tumor Biol.
, vol.37
, Issue.5
, pp. 5683-5704
-
-
Gill, B.S.1
Alex, J.M.2
Kumar, S.3
-
9
-
-
0027401607
-
The multistep nature of cancer
-
COI: 1:STN:280:DyaK3s3ps1yrtw%3D%3D, PID: 8516849
-
Vogelstein B, Kinzler KW. The multistep nature of cancer. Trends Genet. 1993;9(4):138–41.
-
(1993)
Trends Genet.
, vol.9
, Issue.4
, pp. 138-141
-
-
Vogelstein, B.1
Kinzler, K.W.2
-
10
-
-
84971253579
-
Tilling: versatile reverse genetic tool
-
Negi ABG, Anand SS. Tilling: versatile reverse genetic tool. Pharma Tutor. 2014;2(1):26–32.
-
(2014)
Pharma Tutor
, vol.2
, Issue.1
, pp. 26-32
-
-
Negi, A.B.G.1
Anand, S.S.2
-
11
-
-
1642617115
-
Plant-derived protein tyrosine kinase inhibitors as anticancer agents
-
COI: 1:CAS:528:DC%2BD2cXivVSlurc%3D, PID: 15032721
-
Hollosy F, Keri G. Plant-derived protein tyrosine kinase inhibitors as anticancer agents. Curr Med Chem Anticancer Agents. 2004;4(2):173–97.
-
(2004)
Curr Med Chem Anticancer Agents
, vol.4
, Issue.2
, pp. 173-197
-
-
Hollosy, F.1
Keri, G.2
-
12
-
-
84952066998
-
Misconstrued versatility of Ganoderma lucidum: a key player in multi-targeted cellular signaling
-
Gill BS, Sharma P, Kumar R, Kumar S. Misconstrued versatility of Ganoderma lucidum: a key player in multi-targeted cellular signaling. Tumor Biol. 2015;37(3):2789–804.
-
(2015)
Tumor Biol.
, vol.37
, Issue.3
, pp. 2789-2804
-
-
Gill, B.S.1
Sharma, P.2
Kumar, R.3
Kumar, S.4
-
13
-
-
30344482855
-
Anticancer effects of Ganoderma lucidum: a review of scientific evidence
-
COI: 1:CAS:528:DC%2BD28XptF2ksQ%3D%3D, PID: 16351502
-
Yuen JW, Gohel MDI. Anticancer effects of Ganoderma lucidum: a review of scientific evidence. Nutr Cancer. 2005;53(1):11–7.
-
(2005)
Nutr. Cancer
, vol.53
, Issue.1
, pp. 11-17
-
-
Yuen, J.W.1
Gohel, M.D.I.2
-
14
-
-
84937973345
-
Differential algorithms-assisted molecular modeling-based identification of mechanistic binding of ganoderic acids
-
COI: 1:CAS:528:DC%2BC2MXhtFGgur%2FP
-
Gill BS, Kumar S. Differential algorithms-assisted molecular modeling-based identification of mechanistic binding of ganoderic acids. Med Chem Res. 2015;24(9):3483–93.
-
(2015)
Med Chem Res
, vol.24
, Issue.9
, pp. 3483-3493
-
-
Gill, B.S.1
Kumar, S.2
-
15
-
-
63149183342
-
Ganoderic acid DM: anti-androgenic osteoclastogenesis inhibitor
-
COI: 1:CAS:528:DC%2BD1MXkt1Sjsbs%3D, PID: 19289282
-
Liu J, Shiono J, Shimizu K, Kukita A, Kukita T, Kondo R. Ganoderic acid DM: anti-androgenic osteoclastogenesis inhibitor. Bioorg Med Chem Lett. 2009;19(8):2154–7.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, Issue.8
, pp. 2154-2157
-
-
Liu, J.1
Shiono, J.2
Shimizu, K.3
Kukita, A.4
Kukita, T.5
Kondo, R.6
-
16
-
-
84868624596
-
Inhibition of the JAK-STAT3 signaling pathway by ganoderic acid A enhances chemosensitivity of HepG2 cells to cisplatin
-
COI: 1:CAS:528:DC%2BC3sXitFCisQ%3D%3D, PID: 22961117
-
Yao X, Li G, Xu H, Lü C. Inhibition of the JAK-STAT3 signaling pathway by ganoderic acid A enhances chemosensitivity of HepG2 cells to cisplatin. Planta Med. 2012;78(16):1740–8.
-
(2012)
Planta Med.
, vol.78
, Issue.16
, pp. 1740-1748
-
-
Yao, X.1
Li, G.2
Xu, H.3
Lü, C.4
-
17
-
-
55549103741
-
Ganoderic acid Me inhibits tumor invasion through down-regulating matrix metalloproteinases 2/9 gene expression
-
COI: 1:CAS:528:DC%2BD1cXhtlehs7%2FM, PID: 18946196
-
Chen N-H, Liu J-W, Zhong J-J. Ganoderic acid Me inhibits tumor invasion through down-regulating matrix metalloproteinases 2/9 gene expression. J Pharmacol Sci. 2008;108(2):212–6.
-
(2008)
J. Pharmacol. Sci.
, vol.108
, Issue.2
, pp. 212-216
-
-
Chen, N.-H.1
Liu, J.-W.2
Zhong, J.-J.3
-
18
-
-
0032789660
-
Curcumin inhibits tyrosine kinase activity of p185neu and also depletes p185neu
-
COI: 1:CAS:528:DyaK1MXltVCqt7g%3D, PID: 10430096
-
Hong R-L, Spohn WH, Hung M-C. Curcumin inhibits tyrosine kinase activity of p185neu and also depletes p185neu. Clin Cancer Res. 1999;5(7):1884–91.
-
(1999)
Clin. Cancer Res.
, vol.5
, Issue.7
, pp. 1884-1891
-
-
Hong, R.-L.1
Spohn, W.H.2
Hung, M.-C.3
-
19
-
-
0032756794
-
Effects of luteolin and quercetin, inhibitors of tyrosine kinase, on cell growth and metastasis‐associated properties in A431 cells overexpressing epidermal growth factor receptor
-
COI: 1:CAS:528:DyaK1MXnt1WltL8%3D, PID: 10556937
-
Huang YT, Hwang JJ, Lee PP, Ke FC, Huang JH, Huang CJ, et al. Effects of luteolin and quercetin, inhibitors of tyrosine kinase, on cell growth and metastasis‐associated properties in A431 cells overexpressing epidermal growth factor receptor. Br J Pharmacol. 1999;128(5):999–1010.
-
(1999)
Br. J. Pharmacol.
, vol.128
, Issue.5
, pp. 999-1010
-
-
Huang, Y.T.1
Hwang, J.J.2
Lee, P.P.3
Ke, F.C.4
Huang, J.H.5
Huang, C.J.6
-
20
-
-
0036244345
-
Betulinic acid inhibits growth factor‐induced in vitro angiogenesis via the modulation of mitochondrial function in endothelial cells
-
COI: 1:CAS:528:DC%2BD38Xks1Ojt7Y%3D
-
Kwon HJ, Shim JS, Kim JH, Cho HY, Yum YN, Kim SH, et al. Betulinic acid inhibits growth factor‐induced in vitro angiogenesis via the modulation of mitochondrial function in endothelial cells. Cancer Sci. 2002;93(4):417–25.
-
(2002)
Cancer Sci.
, vol.93
, Issue.4
, pp. 417-425
-
-
Kwon, H.J.1
Shim, J.S.2
Kim, J.H.3
Cho, H.Y.4
Yum, Y.N.5
Kim, S.H.6
-
21
-
-
80053534321
-
Down-regulation of estrogen receptor-alpha and rearranged during transfection tyrosine kinase is associated with withaferin a-induced apoptosis in MCF-7 breast cancer cells
-
COI: 1:CAS:528:DC%2BC3MXhtlynt7rL, PID: 21978374
-
Zhang X, Mukerji R, Samadi AK, Cohen MS. Down-regulation of estrogen receptor-alpha and rearranged during transfection tyrosine kinase is associated with withaferin a-induced apoptosis in MCF-7 breast cancer cells. BMC Complement Altern Med. 2011;11(1):84.
-
(2011)
BMC Complement. Altern. Med.
, vol.11
, Issue.1
, pp. 84
-
-
Zhang, X.1
Mukerji, R.2
Samadi, A.K.3
Cohen, M.S.4
-
22
-
-
33748882713
-
Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake
-
COI: 1:CAS:528:DC%2BD28XhtVagtL3O
-
Zhang W, Hong D, Zhou Y, Zhang Y, Shen Q, Li J-Y, et al. Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake. BBA Gen Subjects. 2006;1760(10):1505–12.
-
(2006)
BBA Gen Subjects
, vol.1760
, Issue.10
, pp. 1505-1512
-
-
Zhang, W.1
Hong, D.2
Zhou, Y.3
Zhang, Y.4
Shen, Q.5
Li, J.-Y.6
-
23
-
-
84863000261
-
Pristimerin, a triterpenoid, inhibits tumor angiogenesis by targeting VEGFR2 activation
-
COI: 1:CAS:528:DC%2BC38XptVert70%3D, PID: 22669041
-
Mu X, Shi W, Sun L, Li H, Jiang Z, Zhang L. Pristimerin, a triterpenoid, inhibits tumor angiogenesis by targeting VEGFR2 activation. Molecules. 2012;17(6):6854–68.
-
(2012)
Molecules
, vol.17
, Issue.6
, pp. 6854-6868
-
-
Mu, X.1
Shi, W.2
Sun, L.3
Li, H.4
Jiang, Z.5
Zhang, L.6
-
24
-
-
0029912748
-
Development and testing of the OPLS all-atom force field on conformational energetics and properties of organic liquids
-
COI: 1:CAS:528:DyaK28XmtlOitrs%3D
-
Jorgensen WL, Maxwell DS, Tirado-Rives J. Development and testing of the OPLS all-atom force field on conformational energetics and properties of organic liquids. J Am Chem Soc. 1996;118(45):11225–36.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, Issue.45
, pp. 11225-11236
-
-
Jorgensen, W.L.1
Maxwell, D.S.2
Tirado-Rives, J.3
-
25
-
-
33645941402
-
The OPLS [optimized potentials for liquid simulations] potential functions for proteins, energy minimizations for crystals of cyclic peptides and crambin
-
COI: 1:CAS:528:DyaL1cXht1yjt7Y%3D, PID: 27557051
-
Jorgensen WL, Tirado-Rives J. The OPLS [optimized potentials for liquid simulations] potential functions for proteins, energy minimizations for crystals of cyclic peptides and crambin. J Am Chem Soc. 1988;110(6):1657–66.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, Issue.6
, pp. 1657-1666
-
-
Jorgensen, W.L.1
Tirado-Rives, J.2
-
26
-
-
77952415408
-
Prediction of absolute solvation free energies using molecular dynamics free energy perturbation and the OPLS force field
-
COI: 1:CAS:528:DC%2BC3cXkslKhu7g%3D, PID: 26615687
-
Shivakumar D, Williams J, Wu Y, Damm W, Shelley J, Sherman W. Prediction of absolute solvation free energies using molecular dynamics free energy perturbation and the OPLS force field. J Chem Theory Comput. 2010;6(5):1509–19.
-
(2010)
J. Chem. Theory Comput.
, vol.6
, Issue.5
, pp. 1509-1519
-
-
Shivakumar, D.1
Williams, J.2
Wu, Y.3
Damm, W.4
Shelley, J.5
Sherman, W.6
-
28
-
-
12144289984
-
GLIDE: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy
-
COI: 1:CAS:528:DC%2BD2cXhsFyit74%3D, PID: 15027865
-
Friesner RA, Banks JL, Murphy RB, Halgren TA, Klicic JJ, Mainz DT, et al. GLIDE: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy. J Med Chem. 2004;47(7):1739–49.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.7
, pp. 1739-1749
-
-
Friesner, R.A.1
Banks, J.L.2
Murphy, R.B.3
Halgren, T.A.4
Klicic, J.J.5
Mainz, D.T.6
-
29
-
-
33750124980
-
Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes
-
COI: 1:CAS:528:DC%2BD28XpvVGmurg%3D, PID: 17034125
-
Friesner RA, Murphy RB, Repasky MP, Frye LL, Greenwood JR, Halgren TA, et al. Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. J Med Chem. 2006;49(21):6177–96.
-
(2006)
J. Med. Chem.
, vol.49
, Issue.21
, pp. 6177-6196
-
-
Friesner, R.A.1
Murphy, R.B.2
Repasky, M.P.3
Frye, L.L.4
Greenwood, J.R.5
Halgren, T.A.6
-
30
-
-
0037204544
-
Prediction of drug solubility from structure
-
COI: 1:CAS:528:DC%2BD38Xitlartbc%3D, PID: 11922952
-
Jorgensen WL, Duffy EM. Prediction of drug solubility from structure. Adv Drug Deliv Rev. 2002;54(3):355–66.
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, Issue.3
, pp. 355-366
-
-
Jorgensen, W.L.1
Duffy, E.M.2
-
31
-
-
84930927156
-
High-throughput virtual screening, identification and in vitro biological evaluation of novel inhibitors of signal transducer and activator of transcription 3
-
COI: 1:CAS:528:DC%2BC2MXhvV2rsro%3D
-
Singh P, Bast F. High-throughput virtual screening, identification and in vitro biological evaluation of novel inhibitors of signal transducer and activator of transcription 3. Med Chem Res. 2015;24(6):2694–708.
-
(2015)
Med Chem Res
, vol.24
, Issue.6
, pp. 2694-2708
-
-
Singh, P.1
Bast, F.2
-
32
-
-
85041671135
-
Ganoderic acid A targeting β-catenin in Wnt signaling pathway: in silico and in vitro study
-
Gill BS, Navgeet, Kumar S. Ganoderic acid A targeting β-catenin in Wnt signaling pathway: in silico and in vitro study. Interdisciplinar Sci Comput Life Sci. 2016. doi:10.1007/s12539-016-0182-7.
-
(2016)
Interdisciplinar Sci Comput Life Sci
-
-
Gill, B.S.1
Navgeet2
Kumar, S.3
|