-
1
-
-
0034972445
-
The ears of the hippopotamus: Manifestations, determinants, and estimates of the malaria burden
-
BREMAN JG: The ears of the hippopotamus: manifestations, determinants, and estimates of the malaria burden. Am. J. Trop. Med. Hyg. (2001) 64(Suppl. 1-2):1-11.
-
(2001)
Am. J. Trop. Med. Hyg.
, vol.64
, Issue.SUPPL. 1-2
, pp. 1-11
-
-
Breman, J.G.1
-
3
-
-
0036188537
-
Clinical status and implications of antimalarial drug resistance
-
WINSTANLEY PA, WARD SA, SNOW RW. Clinical status and implications of antimalarial drug resistance. Microbes Infect. (2002) 4:157-164.
-
(2002)
Microbes Infect.
, vol.4
, pp. 157-164
-
-
Winstanley, P.A.1
Ward, S.A.2
Snow, R.W.3
-
5
-
-
0027401399
-
Beyond chloroquine: Implications of drug resistance for evaluating malaria therapy efficacy and treatment policy in Africa
-
BLOLAND PB, LACKRITZ EM, KAZEMBE PN et al.: Beyond chloroquine: implications of drug resistance for evaluating malaria therapy efficacy and treatment policy in Africa. J. Infect. Dis. (1993) 167:932-937.
-
(1993)
J. Infect. Dis.
, vol.167
, pp. 932-937
-
-
Bloland, P.B.1
Lackritz, E.M.2
Kazembe, P.N.3
-
6
-
-
0034536076
-
Using evidence to change antimalarial drug policy in Kenya
-
SHRETTA R, OMUMBO J, RAPUODA B et al.: Using evidence to change antimalarial drug policy in Kenya. Trop. Med. Int. Health (2000) 5:755-764.
-
(2000)
Trop. Med. Int. Health
, vol.5
, pp. 755-764
-
-
Shretta, R.1
Omumbo, J.2
Rapuoda, B.3
-
7
-
-
0035702490
-
Pyrimethamine-sulfadoxine resistance in Plasmodium falciparum: What next?
-
SIBLEY CH, HYDE JE, SIMS PF et al.: Pyrimethamine-sulfadoxine resistance in Plasmodium falciparum: what next? Trends Parasitol. (2001) 17:582-588.
-
(2001)
Trends Parasitol.
, vol.17
, pp. 582-588
-
-
Sibley, C.H.1
Hyde, J.E.2
Sims, P.F.3
-
8
-
-
0036188538
-
Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs
-
HYDE JE: Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs. Microbes Infect. (2002) 4:165-174.
-
(2002)
Microbes Infect.
, vol.4
, pp. 165-174
-
-
Hyde, J.E.1
-
9
-
-
0031282305
-
Plasmodium: Drug discovery and development - An industrial perspective
-
RIDLEY RG: Plasmodium: drug discovery and development - an industrial perspective. Exp. Parasitol. (1997) 87:293-304.
-
(1997)
Exp. Parasitol.
, vol.87
, pp. 293-304
-
-
Ridley, R.G.1
-
10
-
-
0033004991
-
An overview of chemotherapeutic targets for antimalarial drug discovery
-
OLLIARO PL, YUTHAVONG Y: An overview of chemotherapeutic targets for antimalarial drug discovery. Pharmacol. Ther. (1999) 81:91-110.
-
(1999)
Pharmacol. Ther.
, vol.81
, pp. 91-110
-
-
Olliaro, P.L.1
Yuthavong, Y.2
-
11
-
-
0034127436
-
Chemical inhibitors of cyclic-dependent kinases: Preclinical and clinical study
-
DAMIENS E, MEIJER L: Chemical inhibitors of cyclic-dependent kinases: preclinical and clinical study. Pathol. Biol. (2000) 48:340-351.
-
(2000)
Pathol. Biol.
, vol.48
, pp. 340-351
-
-
Damiens, E.1
Meijer, L.2
-
12
-
-
0033402254
-
Discovering novel chemotherapeutic drugs for the third millennium
-
GARRETT MD, WORKMAN P: Discovering novel chemotherapeutic drugs for the third millennium. Eur. J. Cancer (1999) 35:2010-2030.
-
(1999)
Eur. J. Cancer
, vol.35
, pp. 2010-2030
-
-
Garrett, M.D.1
Workman, P.2
-
13
-
-
0032605463
-
Synthetic cyclin-dependent kinase inhibitors. New generation of potent anti-cancer drugs
-
HAJDUCH M, HAVLIEEK L, VESELY J et al.: Synthetic cyclin-dependent kinase inhibitors. New generation of potent anti-cancer drugs. Adv. Exp. Med. Biol. (1999) 457:341-353.
-
(1999)
Adv. Exp. Med. Biol.
, vol.457
, pp. 341-353
-
-
Hajduch, M.1
Havlieek, L.2
Vesely, J.3
-
14
-
-
0033036758
-
Properties and potential-applications of chemical inhibitors of cyclin-dependent kinases
-
MEIJER L, LECLERC S, LEOST M: Properties and potential-applications of chemical inhibitors of cyclin-dependent kinases. Pharmacol. Ther. (1999) 82:279-284.
-
(1999)
Pharmacol. Ther.
, vol.82
, pp. 279-284
-
-
Meijer, L.1
Leclerc, S.2
Leost, M.3
-
15
-
-
0344809977
-
ATP-site directed inhibitors of cyclin-dependent kinases
-
GRAY N, DETIVAUD L, DOERIG C et al.: ATP-site directed inhibitors of cyclin-dependent kinases. Curr. Med. Chem. (1999) 6:859-875.
-
(1999)
Curr. Med. Chem.
, vol.6
, pp. 859-875
-
-
Gray, N.1
Detivaud, L.2
Doerig, C.3
-
16
-
-
0031466305
-
Cyclin-dependent kinases: Engines, clocks, and microprocessors
-
MORGAN DO: Cyclin-dependent kinases: engines, clocks, and microprocessors. Ann. Rev. Cell Dev. Biol. (1997) 13:261-291.
-
(1997)
Ann. Rev. Cell Dev. Biol.
, vol.13
, pp. 261-291
-
-
Morgan, D.O.1
-
17
-
-
0027938207
-
Ordering S phase and M phase in the cell cycle
-
NURSE P: Ordering S phase and M phase in the cell cycle. Cell (1994) 79:547-550.
-
(1994)
Cell
, vol.79
, pp. 547-550
-
-
Nurse, P.1
-
18
-
-
0028931265
-
Principles of CDK regulation
-
MORGAN DO: Principles of CDK regulation. Nature (1995) 374:131-134.
-
(1995)
Nature
, vol.374
, pp. 131-134
-
-
Morgan, D.O.1
-
19
-
-
0029029617
-
Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex
-
JEFFREY PD, RUSSO AA, POLYAK K et al.: Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex. Nature (1995) 376:313-320.
-
(1995)
Nature
, vol.376
, pp. 313-320
-
-
Jeffrey, P.D.1
Russo, A.A.2
Polyak, K.3
-
20
-
-
0027182223
-
Crystal structure of cyclin-dependent kinase 2
-
DE BONDT HL, ROSENBLATT J, JANCARIK J et al.: Crystal structure of cyclin-dependent kinase 2. Nature (1993) 363:595-602.
-
(1993)
Nature
, vol.363
, pp. 595-602
-
-
De Bondt, H.L.1
Rosenblatt, J.2
Jancarik, J.3
-
21
-
-
0033574614
-
Mechanisms of cyclin-dependent kinase regulation: Structures of Cdks, their cyclin activators, and Cip and INK4 inhibitors
-
PAVLETICH NP: Mechanisms of cyclin-dependent kinase regulation: structures of Cdks, their cyclin activators, and Cip and INK4 inhibitors. J. Mol. Biol. (1999) 287:821-828.
-
(1999)
J. Mol. Biol.
, vol.287
, pp. 821-828
-
-
Pavletich, N.P.1
-
22
-
-
0023647143
-
Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2
-
(6117)
-
LEE MG, NURSE P: Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2. Nature (1987) 327(6117):31-35.
-
(1987)
Nature
, vol.327
, pp. 31-35
-
-
Lee, M.G.1
Nurse, P.2
-
23
-
-
0029417882
-
Chemical inhibitors of cyclin-dependent kinases
-
MEIJER L: Chemical inhibitors of cyclin-dependent kinases. Prog. Cell Cycle Res. (1995) 1:351-363.
-
(1995)
Prog. Cell Cycle Res.
, vol.1
, pp. 351-363
-
-
Meijer, L.1
-
24
-
-
0033760789
-
Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics
-
FISCHER PM, LANE DP: Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics. Curr. Med. Chem. (2000) 7:1213-1245.
-
(2000)
Curr. Med. Chem.
, vol.7
, pp. 1213-1245
-
-
Fischer, P.M.1
Lane, D.P.2
-
26
-
-
17944375799
-
Identification of selective inhibitors of cyclin-dependent kinase 4
-
CARINI DJ, KALTENBACH RF, LIU J et al.: Identification of selective inhibitors of cyclin-dependent kinase 4. Bioorg. Med. Chem. Lett (2001) 11:2209-2211.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 2209-2211
-
-
Carini, D.J.1
Kaltenbach, R.F.2
Liu, J.3
-
27
-
-
0034597571
-
Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: Synthesis and biological effects
-
KIM KS, SACK JS, TOKARSKI JS et al.: Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects. J. Med. Chem. (2000) 43:4126-4134.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4126-4134
-
-
Kim, K.S.1
Sack, J.S.2
Tokarski, J.S.3
-
28
-
-
0032087856
-
The Plasmodium cell-cycle: Facts and questions
-
ARNOT DE, GULL K: The Plasmodium cell-cycle: facts and questions. Ann. Trop. Med. Parasitol. (1998) 92:361-365.
-
(1998)
Ann. Trop. Med. Parasitol.
, vol.92
, pp. 361-365
-
-
Arnot, D.E.1
Gull, K.2
-
29
-
-
0030296465
-
Malaria and the cell cycle
-
LEETE TH, RUBIN H: Malaria and the cell cycle. Parasitol. Today (1996) 12:442-444.
-
(1996)
Parasitol. Today
, vol.12
, pp. 442-444
-
-
Leete, T.H.1
Rubin, H.2
-
31
-
-
0028988027
-
Pfcrk-1, a developmentally regulated cdc2-related protein kinase of Plasmodium falciparum
-
DOERIG C, HORROCKS P, COYLE J et al.: Pfcrk-1, a developmentally regulated cdc2-related protein kinase of Plasmodium falciparum. Mol. Biochem. Parasitol. (1995) 70:167-174.
-
(1995)
Mol. Biochem. Parasitol.
, vol.70
, pp. 167-174
-
-
Doerig, C.1
Horrocks, P.2
Coyle, J.3
-
32
-
-
0028224015
-
Isolation and expression of a gene specifying a cdc2-like protein kinase from the human malaria parasite Plasmodium falciparum
-
ROSS-MACDONALD PB, GRAESER R, KAPPES B et al.: Isolation and expression of a gene specifying a cdc2-like protein kinase from the human malaria parasite Plasmodium falciparum. Eur. J. Biochem. (1994) 220:693-701.
-
(1994)
Eur. J. Biochem.
, vol.220
, pp. 693-701
-
-
Ross-Macdonald, P.B.1
Graeser, R.2
Kappes, B.3
-
33
-
-
0030200306
-
Mechanisms of activation of the cdc2-related kinase PfPK5 from Plasmodium falciparum
-
GRAESER R, FRANKLIN RM, KAPPES B: Mechanisms of activation of the cdc2-related kinase PfPK5 from Plasmodium falciparum. Mol. Biochem. Parasitol. (1996) 79:125-127.
-
(1996)
Mol. Biochem. Parasitol.
, vol.79
, pp. 125-127
-
-
Graeser, R.1
Franklin, R.M.2
Kappes, B.3
-
34
-
-
0030581694
-
Plasmodium: Falciparum protein kinase 5 and the malarial nuclear division cycles
-
GRAESER R, WERNLI B, FRANKLIN RM et al.: Plasmodium falciparum protein kinase 5 and the malarial nuclear division cycles. Mol. Biochem. Parasitol. (1996) 82:37-49.
-
(1996)
Mol. Biochem. Parasitol.
, vol.82
, pp. 37-49
-
-
Graeser, R.1
Wernli, B.2
Franklin, R.M.3
-
35
-
-
0034176923
-
PfPK6, a novel cyclin-dependent kinase/mitogen-activated protein kinase-related protein kinase from Plasmodium falciparum
-
BRACCHI-RICARD V, BARIK S, DELVECCHI0 C et al.: PfPK6, a novel cyclin-dependent kinase/mitogen-activated protein kinase-related protein kinase from Plasmodium falciparum. Biochem. J. (2000) 347 Pt 1:255-263.
-
(2000)
Biochem. J.
, vol.347
, Issue.PART 1
, pp. 255-263
-
-
Bracchi-Ricard, V.1
Barik, S.2
Delvecchio, C.3
-
36
-
-
0034708437
-
Activation of a Plasmodium falciparum cdc2-related kinase by heterologous p25 and cyclin H. Functional characterization of a P. falciparum cyclin homologue
-
LE ROCH K, SESTIER C, DORIN D et al.: Activation of a Plasmodium falciparum cdc2-related kinase by heterologous p25 and cyclin H. Functional characterization of a P. falciparum cyclin homologue. J. Biol. Chem. (2000) 275:8952-8958.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 8952-8958
-
-
Le Roch, K.1
Sestier, C.2
Dorin, D.3
-
37
-
-
0029862051
-
Pfmrk, a MO15-related protein kinase from Plasmodium falciparum. Gene cloning, sequence, stage-specific expression and chromosome localization
-
LI JL, ROBSON KJ, CHEN JL et al.: Pfmrk, a MO15-related protein kinase from Plasmodium falciparum. Gene cloning, sequence, stage-specific expression and chromosome localization. Eur. J. Biochem. (1996) 241:805-813.
-
(1996)
Eur. J. Biochem.
, vol.241
, pp. 805-813
-
-
Li, J.L.1
Robson, K.J.2
Chen, J.L.3
-
38
-
-
0034654447
-
Cyclin H activation and drug susceptibility of the Pfmrk cyclin-dependent protein kinase from Plasmodium falciparum
-
WATERS NC, WOODARD CL, PRIGGE ST: Cyclin H activation and drug susceptibility of the Pfmrk cyclin-dependent protein kinase from Plasmodium falciparum. Mol. Biochem. Parasitol. (2000) 107:45-55.
-
(2000)
Mol. Biochem. Parasitol.
, vol.107
, pp. 45-55
-
-
Waters, N.C.1
Woodard, C.L.2
Prigge, S.T.3
-
39
-
-
0029418115
-
The regulation and functions of cdk7
-
SHUTTLEWORTH J: The regulation and functions of cdk7. Prog. Cell Cycle Res. (1995) 1:229-240.
-
(1995)
Prog. Cell Cycle Res.
, vol.1
, pp. 229-240
-
-
Shuttleworth, J.1
-
40
-
-
0028958673
-
Association of Cdk-activating kinase subunits with transcription factor TFIIH
-
SERIZAWA H, MAKELA TP, CONAWAY JW et al.: Association of Cdk-activating kinase subunits with transcription factor TFIIH. Nature (1995) 374:280-282.
-
(1995)
Nature
, vol.374
, pp. 280-282
-
-
Serizawa, H.1
Makela, T.P.2
Conaway, J.W.3
-
41
-
-
0030598865
-
The Cdk-activating kinase (CAK) from budding yeast
-
KALDIS P. SUTTON A, SOLOMON MJ: The Cdk-activating kinase (CAK) from budding yeast. Cell (1996) 86:553-564.
-
(1996)
Cell
, vol.86
, pp. 553-564
-
-
Kaldis, P.1
Sutton, A.2
Solomon, M.J.3
-
42
-
-
0031686960
-
Human and yeast cdk-activating kinases (CAKs) display distinct substrate specificities
-
KALDIS P, RUSSO AA, CHOU HS et al.: Human and yeast cdk-activating kinases (CAKs) display distinct substrate specificities. Mol. Biol. Cell (1998) 9:2545-2560.
-
(1998)
Mol. Biol. Cell
, vol.9
, pp. 2545-2560
-
-
Kaldis, P.1
Russo, A.A.2
Chou, H.S.3
-
43
-
-
0029066929
-
KIN28 encodes a C-terminal domain kinase that controls mRNA transcription in Saccharomyces cerevisiae but lacks cyclin-dependent kinase-activating kinase (CAK) activity
-
CISMOWSKI MJ, LAFF GM, SOLOMON MJ et al.: KIN28 encodes a C-terminal domain kinase that controls mRNA transcription in Saccharomyces cerevisiae but lacks cyclin-dependent kinase-activating kinase (CAK) activity. Mol. Cell. Biol. (1995) 15:2983-2992.
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 2983-2992
-
-
Cismowski, M.J.1
Laff, G.M.2
Solomon, M.J.3
-
44
-
-
0035900603
-
Influence of human p16(INK4) and p21(CIP1) on the in vitro activity of recombinant Plasmodium falciparum cyclin-dependent protein kinases
-
LI Z, LE ROCH K, GEYER JA et al.: Influence of human p16(INK4) and p21(CIP1) on the in vitro activity of recombinant Plasmodium falciparum cyclin-dependent protein kinases. Biochem. Biophys. Res. Commun. (2001) 288:1207-1211.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.288
, pp. 1207-1211
-
-
Li, Z.1
Le Roch, K.2
Geyer, J.A.3
-
45
-
-
0033605643
-
Effects of phosphorylation of threonine 160 on cyclin-dependent kinase 2 structure and activity
-
BROWN NR, NOBLE ME, LAWRIE AM et al.: Effects of phosphorylation of threonine 160 on cyclin-dependent kinase 2 structure and activity. J. Biol. Chem. (1999) 274:8746-8756.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 8746-8756
-
-
Brown, N.R.1
Noble, M.E.2
Lawrie, A.M.3
-
46
-
-
0029767016
-
Structural basis of cyclin-dependent kinase activation by phosphorylation
-
RUSSO AA, JEFFREY PD, PAVLETICH NP: Structural basis of cyclin-dependent kinase activation by phosphorylation. Nat. Struct. Biol. (1996) 3:696-700.
-
(1996)
Nat. Struct. Biol.
, vol.3
, pp. 696-700
-
-
Russo, A.A.1
Jeffrey, P.D.2
Pavletich, N.P.3
-
47
-
-
0035427503
-
Structure-activity relationships and inhibitory effects of various purine derivatives on the in vitro growth of Plasmodium falciparum
-
HARMSE L, VAN ZYL R, GRAY N et al.: Structure-activity relationships and inhibitory effects of various purine derivatives on the in vitro growth of Plasmodium falciparum. Biochem. Pharmacol. (2001) 62:341-348.
-
(2001)
Biochem. Pharmacol.
, vol.62
, pp. 341-348
-
-
Harmse, L.1
Van Zyl, R.2
Gray, N.3
-
48
-
-
0035924240
-
A novel approach for the development of selective Cdk4 inhibitors: Library design based on locations of Cdk4 specific amino acid residues
-
HONMA T, YOSHIZUMI T, HASHIMOTO N et al.: A novel approach for the development of selective Cdk4 inhibitors: library design based on locations of Cdk4 specific amino acid residues. J. Med. Chem. (2001) 44:4628-4640.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4628-4640
-
-
Honma, T.1
Yoshizumi, T.2
Hashimoto, N.3
-
49
-
-
0028093182
-
Inhibition of cyclin-dependent kinases by purine analogues
-
VESELY J, HAVLICEK L, STRNAD M et al.: Inhibition of cyclin-dependent kinases by purine analogues. Eur. J. Biochem. (1994) 224:771-786.
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 771-786
-
-
Vesely, J.1
Havlicek, L.2
Strnad, M.3
-
50
-
-
0034642532
-
Cyclin-dependent kinase inhibitors: Useful targets in cell cycle regulation
-
SIELECKI TM, BOYLAN JF, BENFIELD PA et al.: Cyclin-dependent kinase inhibitors: useful targets in cell cycle regulation. J. Med. Chem. (2000) 43:1-18.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1-18
-
-
Sielecki, T.M.1
Boylan, J.F.2
Benfield, P.A.3
-
51
-
-
0034721195
-
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
-
ARRIS CE, BOYLE FT, CALVERT AH et al.: Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles. J. Med. Chem. (2000) 43:2797-2804.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2797-2804
-
-
Arris, C.E.1
Boyle, F.T.2
Calvert, A.H.3
-
52
-
-
0034736093
-
Pyrido [2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases
-
BARVIAN M, BOSCHELLI DH, COSSROW J et al.: Pyrido [2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases. J. Med. Chem. (2000) 43:4606-4616.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4606-4616
-
-
Barvian, M.1
Boschelli, D.H.2
Cossrow, J.3
-
53
-
-
0034618674
-
Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product
-
SONI R, MULLER L, FURET P et al.: Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product. Biochem. Biophys. Res. Commun. (2000) 275:877-884.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.275
, pp. 877-884
-
-
Soni, R.1
Muller, L.2
Furet, P.3
-
54
-
-
0035920248
-
Crystallographic approach to identification of cyclin-dependent kinase 4 (CDK4)-specific inhibitors by using CDK4 mimic CDK2 protein
-
IKUTA M, KAMATA K, FUKASAWA K et al.: Crystallographic approach to identification of cyclin-dependent kinase 4 (CDK4)-specific inhibitors by using CDK4 mimic CDK2 protein. J. Biol. Chem. (2001) 276:27548-27554.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 27548-27554
-
-
Ikuta, M.1
Kamata, K.2
Fukasawa, K.3
-
55
-
-
0035818942
-
Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): Design, synthesis, enzymatic activities, and X-ray crystallographic analysis
-
BRAMSON HN, CORONA J, DAVIS ST et al.: Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): design, synthesis, enzymatic activities, and X-ray crystallographic analysis. J. Med. Chem. (2001) 44:4339-4358.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4339-4358
-
-
Bramson, H.N.1
Corona, J.2
Davis, S.T.3
-
56
-
-
0035924235
-
Structure-based generation of a new class of potent Cdk4 inhibitors: New de novo design strategy and library design
-
HONMA T, HAYASHI K, AOYAMA T et al.: Structure-based generation of a new class of potent Cdk4 inhibitors: new de novo design strategy and library design. J. Med. Chem. (2001) 44:4615-4627.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4615-4627
-
-
Honma, T.1
Hayashi, K.2
Aoyama, T.3
-
57
-
-
0033028071
-
Chemical inhibitors of cyclin-dependent kinases: Insights into design from X-ray crystallographic studies
-
NOBLE ME, ENDICOTT JA: Chemical inhibitors of cyclin-dependent kinases: insights into design from X-ray crystallographic studies. Pharmacol. Ther. (1999) 82:269-278.
-
(1999)
Pharmacol. Ther.
, vol.82
, pp. 269-278
-
-
Noble, M.E.1
Endicott, J.A.2
-
58
-
-
0034162636
-
Preclinical and clinical development of cyclin-dependent kinase modulators
-
SENDEROWICZ AM, SAUSVILLE EA: Preclinical and clinical development of cyclin-dependent kinase modulators. J. Natl. Cancer Inst. (2000) 92:376-387.
-
(2000)
J. Natl. Cancer Inst.
, vol.92
, pp. 376-387
-
-
Senderowicz, A.M.1
Sausville, E.A.2
-
59
-
-
0035808599
-
Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors
-
DAVIS ST, BENSON BG, BRAMSON HN et al.: Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors. Science (2001) 291:134-137.
-
(2001)
Science
, vol.291
, pp. 134-137
-
-
Davis, S.T.1
Benson, B.G.2
Bramson, H.N.3
-
60
-
-
0031028163
-
Inhibition of cyclin-dependent kinases by purine analogues: Crystal structure of human cdk2 complexed with roscovitine
-
DE AZEVEDO WF, LECLERC S, MEIJER L et al.: Inhibition of cyclin-dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitine. Eur. J. Biochem. (1997) 243:518-526.
-
(1997)
Eur. J. Biochem.
, vol.243
, pp. 518-526
-
-
De Azevedo, W.F.1
Leclerc, S.2
Meijer, L.3
-
61
-
-
0035814077
-
Design and synthesis of Pfmrk inhibitors as potential antimalarial agents
-
XIAO Z, WATERS NC, WOODARD CL et al.: Design and synthesis of Pfmrk inhibitors as potential antimalarial agents. Bioorg. Med. Chem. Lett (2001) 11:2875-2878.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2875-2878
-
-
Xiao, Z.1
Waters, N.C.2
Woodard, C.L.3
-
62
-
-
16044363907
-
Structure-based design of parasitic protease inhibitors
-
LI R, CHEN X, GONG B et al.: Structure-based design of parasitic protease inhibitors. Bioorg. Med. Chem. (1996) 4:1421-1427.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1421-1427
-
-
Li, R.1
Chen, X.2
Gong, B.3
-
63
-
-
0029594562
-
In vitro antimalarial activity of chalcones and their derivatives
-
LI R, KENYON GL, COHEN FE et al.: In vitro antimalarial activity of chalcones and their derivatives. J. Med. Chem. (1995) 38:5031-5037.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 5031-5037
-
-
Li, R.1
Kenyon, G.L.2
Cohen, F.E.3
-
64
-
-
0035818913
-
Antimalarial alkoxylated and hydroxylated chalcones: Structure-activity relationship analysis
-
LIU M, WILAIRAT P, GO ML: Antimalarial alkoxylated and hydroxylated chalcones: structure-activity relationship analysis. J. Med. Chem. (2001) 44:4443-4452.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4443-4452
-
-
Liu, M.1
Wilairat, P.2
Go, M.L.3
-
65
-
-
0035357889
-
Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity
-
DOMINGUEZ JN, CHARRIS JE, LOBO G et al.: Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity. Eur. J. Med. Chem. (2001) 36:555-560.
-
(2001)
Eur. J. Med. Chem.
, vol.36
, pp. 555-560
-
-
Dominguez, J.N.1
Charris, J.E.2
Lobo, G.3
-
66
-
-
0035126479
-
Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparum
-
SUROLIA N, SUROLIA A: Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparum. Nat. Med. (2001) 7:167-173.
-
(2001)
Nat. Med.
, vol.7
, pp. 167-173
-
-
Surolia, N.1
Surolia, A.2
|