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Investigative Ophthalmology & Visual Science
|
December 1, 1996
Comparison of psychophysical and electrophysiological testing in early glaucoma
S L Graham, S M Drance, B C Chauhan, et al.
Current Opinion in Chemical Biology
|
August 1, 1997
Farnesyltransferase inhibitors versus Ras inhibitors
J B Gibbs, S L Graham, G D Hartman, et al.
British Journal of Pharmacology
|
January 1, 1990
L-662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals
M F Sugrue, P Gautheron, P Mallorga, et al.
Molecular and Cellular Biology
|
June 1, 1994
Farnesyltransferase inhibition causes morphological reversion of ras-transformed cells by a complex mechanism that involves regulation of the actin cytoskeleton
G C Prendergast, J P Davide, S J deSolms, et al.
Journal of Medicinal Chemistry
|
July 23, 1993
Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase
T H Scholz, J M Sondey, W C Randall, et al.
Journal of Epidemiology and Community Health
|
February 1, 1996
Geographical distribution of risk factors and incidence of invasive cervical cancer in south east China
Z F Zhang, Z Z Zhang, S Z Yu, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Potent, non-thiol inhibitors of farnesyltransferase
M J Breslin, S J deSolms, E A Giuliani, et al.
Journal of Medicinal Chemistry
|
February 1, 1990
Topically active carbonic anhydrase inhibitors. 3. Benzofuran- and indole-2-sulfonamides
S L Graham, J M Hoffman, P Gautheron, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 6, 2018
Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentials
V Jayanetti, A I Klistorner, S L Graham, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity
S D Young, L S Payne, W J Thompson, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
Investigative Ophthalmology & Visual Science
|
December 1, 1996
Comparison of psychophysical and electrophysiological testing in early glaucoma
S L Graham, S M Drance, B C Chauhan, et al.
Current Opinion in Chemical Biology
|
August 1, 1997
Farnesyltransferase inhibitors versus Ras inhibitors
J B Gibbs, S L Graham, G D Hartman, et al.
British Journal of Pharmacology
|
January 1, 1990
L-662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals
M F Sugrue, P Gautheron, P Mallorga, et al.
Molecular and Cellular Biology
|
June 1, 1994
Farnesyltransferase inhibition causes morphological reversion of ras-transformed cells by a complex mechanism that involves regulation of the actin cytoskeleton
G C Prendergast, J P Davide, S J deSolms, et al.
Journal of Medicinal Chemistry
|
July 23, 1993
Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase
T H Scholz, J M Sondey, W C Randall, et al.
Journal of Epidemiology and Community Health
|
February 1, 1996
Geographical distribution of risk factors and incidence of invasive cervical cancer in south east China
Z F Zhang, Z Z Zhang, S Z Yu, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Potent, non-thiol inhibitors of farnesyltransferase
M J Breslin, S J deSolms, E A Giuliani, et al.
Journal of Medicinal Chemistry
|
February 1, 1990
Topically active carbonic anhydrase inhibitors. 3. Benzofuran- and indole-2-sulfonamides
S L Graham, J M Hoffman, P Gautheron, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 6, 2018
Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentials
V Jayanetti, A I Klistorner, S L Graham, et al.
Journal of Medicinal Chemistry
|
May 15, 1992
HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity
S D Young, L S Payne, W J Thompson, et al.
Page
of 10