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Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1972
Crystallographic studies of chicken triose phosphate isomerase
D W Banner, A C Bloomer, G A Petsko, et al.
The Journal of Biological Chemistry
|
May 9, 1998
Coagulation factor VII Gln100 --> Arg. Amino acid substitution at the epidermal growth factor 2-protease domain interface results in severely reduced tissue factor binding and procoagulant function
G Kemball-Cook, D J Johnson, O Takamiya, et al.
Proteins
|
August 1, 1995
Activation of blood coagulation factor VIIa with cleaved tissue factor extracellular domain and crystallization of the active complex
D Kirchhofer, A Guha, Y Nemerson, et al.
Cell
|
May 7, 1993
Crystal structure of the soluble human 55 kd TNF receptor-human TNF beta complex: implications for TNF receptor activation
D W Banner, A D'Arcy, W Janes, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 26, 1981
On the three-dimensional structure and catalytic mechanism of triose phosphate isomerase
T Alber, D W Banner, A C Bloomer, et al.
Nature
|
March 7, 1996
The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor
D W Banner, A D'Arcy, C Chène, et al.
Journal of Molecular Biology
|
January 20, 1993
Crystallization and preliminary crystallographic analysis of a TNF-beta-55 kDa TNF receptor complex
A D'Arcy, D W Banner, W Janes, et al.
Journal of Medicinal Chemistry
|
June 1, 2001
2-(2-Oxo-1,4-dihydro-2H-quinazolin-3-yl)- and 2-(2,2-dioxo-1,4-dihydro-2H-2lambda6-benzo[1,2,6]thiadiazin-3-yl)-N-hydroxy-acetamides as potent and selective peptide deformylase inhibitors
C Apfel, D W Banner, D Bur, et al.
Journal of Medicinal Chemistry
|
November 11, 1994
Design and synthesis of potent and highly selective thrombin inhibitors
K Hilpert, J Ackermann, D W Banner, et al.
Journal of Medicinal Chemistry
|
July 6, 2000
Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents
C Apfel, D W Banner, D Bur, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1972
Crystallographic studies of chicken triose phosphate isomerase
D W Banner, A C Bloomer, G A Petsko, et al.
The Journal of Biological Chemistry
|
May 9, 1998
Coagulation factor VII Gln100 --> Arg. Amino acid substitution at the epidermal growth factor 2-protease domain interface results in severely reduced tissue factor binding and procoagulant function
G Kemball-Cook, D J Johnson, O Takamiya, et al.
Proteins
|
August 1, 1995
Activation of blood coagulation factor VIIa with cleaved tissue factor extracellular domain and crystallization of the active complex
D Kirchhofer, A Guha, Y Nemerson, et al.
Cell
|
May 7, 1993
Crystal structure of the soluble human 55 kd TNF receptor-human TNF beta complex: implications for TNF receptor activation
D W Banner, A D'Arcy, W Janes, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
June 26, 1981
On the three-dimensional structure and catalytic mechanism of triose phosphate isomerase
T Alber, D W Banner, A C Bloomer, et al.
Nature
|
March 7, 1996
The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor
D W Banner, A D'Arcy, C Chène, et al.
Journal of Molecular Biology
|
January 20, 1993
Crystallization and preliminary crystallographic analysis of a TNF-beta-55 kDa TNF receptor complex
A D'Arcy, D W Banner, W Janes, et al.
Journal of Medicinal Chemistry
|
June 1, 2001
2-(2-Oxo-1,4-dihydro-2H-quinazolin-3-yl)- and 2-(2,2-dioxo-1,4-dihydro-2H-2lambda6-benzo[1,2,6]thiadiazin-3-yl)-N-hydroxy-acetamides as potent and selective peptide deformylase inhibitors
C Apfel, D W Banner, D Bur, et al.
Journal of Medicinal Chemistry
|
November 11, 1994
Design and synthesis of potent and highly selective thrombin inhibitors
K Hilpert, J Ackermann, D W Banner, et al.
Journal of Medicinal Chemistry
|
July 6, 2000
Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents
C Apfel, D W Banner, D Bur, et al.
Page
of 4