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Trends in Biochemical Sciences
|
February 9, 2000
A structure-based mechanism for drug binding by multidrug transporters
E E Zheleznova, P Markham, R Edgar, et al.
Biochemical Society Transactions
|
August 30, 2000
Recognition of multiple drugs by a single protein: a trivial solution of an old paradox
N Vazquez-Laslop, E E Zheleznova, P N Markham, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1992
Escherichia coli biotin holoenzyme synthetase/bio repressor crystal structure delineates the biotin- and DNA-binding domains
K P Wilson, L M Shewchuk, R G Brennan, et al.
The EMBO Journal
|
June 17, 1998
Crystal structures of Toxoplasma gondii uracil phosphoribosyltransferase reveal the atomic basis of pyrimidine discrimination and prodrug binding
M A Schumacher, D Carter, D M Scott, et al.
Science (New York, N.Y.)
|
December 12, 2001
Structural mechanisms of QacR induction and multidrug recognition
M A Schumacher, M C Miller, S Grkovic, et al.
Clinical Chemistry
|
January 1, 1980
Improved radiochemical method for measuring ferrochelatase activity
H L Williams, D J Johnson, M J Haut, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 22, 1997
Allosteric intermediates indicate R2 is the liganded hemoglobin end state
M A Schumacher, E E Zheleznova, K S Poundstone, et al.
The Journal of Biological Chemistry
|
November 18, 1994
Mutational analysis of the autoinhibitory domain of calmodulin kinase II
D A Brickey, J G Bann, Y L Fong, et al.
The Journal of Biological Chemistry
|
January 13, 2001
Consensus and variant cAMP-regulated enhancers have distinct CREB-binding properties
J C Craig, M A Schumacher, S E Mansoor, et al.
Molecular Microbiology
|
July 20, 1999
Characterization of the SarA virulence gene regulator of Staphylococcus aureus
T M Rechtin, A F Gillaspy, M A Schumacher, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 60) with videos related to
Sort By:
Page
of 6
Trends in Biochemical Sciences
|
February 9, 2000
A structure-based mechanism for drug binding by multidrug transporters
E E Zheleznova, P Markham, R Edgar, et al.
Biochemical Society Transactions
|
August 30, 2000
Recognition of multiple drugs by a single protein: a trivial solution of an old paradox
N Vazquez-Laslop, E E Zheleznova, P N Markham, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1992
Escherichia coli biotin holoenzyme synthetase/bio repressor crystal structure delineates the biotin- and DNA-binding domains
K P Wilson, L M Shewchuk, R G Brennan, et al.
The EMBO Journal
|
June 17, 1998
Crystal structures of Toxoplasma gondii uracil phosphoribosyltransferase reveal the atomic basis of pyrimidine discrimination and prodrug binding
M A Schumacher, D Carter, D M Scott, et al.
Science (New York, N.Y.)
|
December 12, 2001
Structural mechanisms of QacR induction and multidrug recognition
M A Schumacher, M C Miller, S Grkovic, et al.
Clinical Chemistry
|
January 1, 1980
Improved radiochemical method for measuring ferrochelatase activity
H L Williams, D J Johnson, M J Haut, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 22, 1997
Allosteric intermediates indicate R2 is the liganded hemoglobin end state
M A Schumacher, E E Zheleznova, K S Poundstone, et al.
The Journal of Biological Chemistry
|
November 18, 1994
Mutational analysis of the autoinhibitory domain of calmodulin kinase II
D A Brickey, J G Bann, Y L Fong, et al.
The Journal of Biological Chemistry
|
January 13, 2001
Consensus and variant cAMP-regulated enhancers have distinct CREB-binding properties
J C Craig, M A Schumacher, S E Mansoor, et al.
Molecular Microbiology
|
July 20, 1999
Characterization of the SarA virulence gene regulator of Staphylococcus aureus
T M Rechtin, A F Gillaspy, M A Schumacher, et al.
Page
of 6