-
1
-
-
0035895505
-
The sequence of the human genome
-
VENTER JC, ADAMS MD, MYERS EW et al.: The sequence of the human genome. Science (2001) 291:1304-1354.
-
(2001)
Science
, vol.291
, pp. 1304-1354
-
-
VENTER, J.C.1
ADAMS, M.D.2
MYERS, E.W.3
-
2
-
-
15944412467
-
Frontal affinity chromatography with MS detection (FAC-MS) in drug discovery
-
SLON-USUAKIEWICZ JJ, NG W, DAI J-R et al.: Frontal affinity chromatography with MS detection (FAC-MS) in drug discovery. Drug Discov. Today (2005) 10:409-416.
-
(2005)
Drug Discov. Today
, vol.10
, pp. 409-416
-
-
SLON-USUAKIEWICZ, J.J.1
DAI J-R, N.W.2
-
3
-
-
9644302954
-
A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures
-
ANNIS DA, NAZEF N, CHUANG Ch-Ch et al.: A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures. J. Am. Chem. Soc. (2004) 126:15495-15503.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 15495-15503
-
-
ANNIS, D.A.1
NAZEF, N.2
CHUANG, C.-C.3
-
4
-
-
33644934750
-
2 acetylcholine receptor ligands by affinity selection-mass spectrometry
-
2 acetylcholine receptor ligands by affinity selection-mass spectrometry. J. Biomol. Screen. (2006) 11:194-207.
-
(2006)
J. Biomol. Screen
, vol.11
, pp. 194-207
-
-
WHITEHURST, C.E.1
NAZEF, N.2
ANNIS, D.A.3
-
5
-
-
8444221197
-
An affinity selection-mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries. Discovery of a novel antagonist of E. coli dihydrofolate reductase
-
ANNIS DA, ATHANASOPOULOS J, CURRAN PJ et al.: An affinity selection-mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries. Discovery of a novel antagonist of E. coli dihydrofolate reductase. Int. J. Mass Spectrom. (2004) 238:77-83.
-
(2004)
Int. J. Mass Spectrom
, vol.238
, pp. 77-83
-
-
ANNIS, D.A.1
ATHANASOPOULOS, J.2
CURRAN, P.J.3
-
6
-
-
0347694626
-
SpeedScreen: Label-free, liquid-chromatography-mass spectrometry-based high-throughput screening for the discovery of orphan protein ligands
-
MUCKENSCHNABEL I, FALCHETTO R, MAYR LM et al.: SpeedScreen: label-free, liquid-chromatography-mass spectrometry-based high-throughput screening for the discovery of orphan protein ligands. Anal. Biochem. (2004) 324:241-249.
-
(2004)
Anal. Biochem
, vol.324
, pp. 241-249
-
-
MUCKENSCHNABEL, I.1
FALCHETTO, R.2
MAYR, L.M.3
-
7
-
-
6444220648
-
SpeedScreen: The 'missing link' between genomics and lead discovery
-
ZEHENDER H, LE GOFF F, LEHMANN N et al.: SpeedScreen: the 'missing link' between genomics and lead discovery. J. Biomol. Screen. (2004) 9(6):498-505.
-
(2004)
J. Biomol. Screen
, vol.9
, Issue.6
, pp. 498-505
-
-
ZEHENDER, H.1
LE GOFF, F.2
LEHMANN, N.3
-
9
-
-
0036006578
-
Drug screening of pharmaceutical discovery compounds by micro-size exclusion chromatography/mass spectrometry
-
WABNITZ PA, LOO JA: Drug screening of pharmaceutical discovery compounds by micro-size exclusion chromatography/mass spectrometry. Rapid Commun. Mass Spectrom. (2002) 16:85-91.
-
(2002)
Rapid Commun. Mass Spectrom
, vol.16
, pp. 85-91
-
-
WABNITZ, P.A.1
LOO, J.A.2
-
10
-
-
33749852183
-
An ultraefficient affinity-based high-throughput screening process: Application to bacterial cell wall biosynthesis enzyme murF
-
COMESS KM, SCHURDAK ME, VOORBACH MJ et al.: An ultraefficient affinity-based high-throughput screening process: application to bacterial cell wall biosynthesis enzyme murF. J. Biomol. Screen. (2006) 11:743:754.
-
(2006)
J. Biomol. Screen
, vol.11
, Issue.743
, pp. 754
-
-
COMESS, K.M.1
SCHURDAK, M.E.2
VOORBACH, M.J.3
-
11
-
-
33749856958
-
Kinase drug discovery by affinity selection/mass spectrometry (AS/MS): Application to DNA damage checkpoint kinase Chk1
-
COMESS KM, TRUMBULL JD, PARK C et al. Kinase drug discovery by affinity selection/mass spectrometry (AS/MS): Application to DNA damage checkpoint kinase Chk1. J. Biomol. Screen. (2006) 11:755-764.
-
(2006)
J. Biomol. Screen
, vol.11
, pp. 755-764
-
-
COMESS, K.M.1
TRUMBULL, J.D.2
PARK, C.3
-
12
-
-
33644938605
-
A Cheminformatics analysis of hit lists obtained from high-throughput afflnity-selection screening
-
BROWN N, ZEHENDER H, AZZAOUI K et al.: A Cheminformatics analysis of hit lists obtained from high-throughput afflnity-selection screening. J. Biomol. Screen. (2006) 11(2):123-130.
-
(2006)
J. Biomol. Screen
, vol.11
, Issue.2
, pp. 123-130
-
-
BROWN, N.1
ZEHENDER, H.2
AZZAOUI, K.3
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