Search research articles
Contact Us
Filters
Showing results (61-70 of 624) with videos related to
Page
of 63
Sort By:
The Journal of Biological Chemistry
|
June 2, 2011
Increasing hydrophobicity or disulfide bridging at the factor VIII A1 and C2 domain interface enhances procofactor stability
Hironao Wakabayashi, Amy E Griffiths, Philip J Fay
Advances in Experimental Medicine and Biology
|
February 23, 1999
All three vasopressin receptor sub-types are expressed by small-cell carcinoma
W G North, M J Fay, J Du
Journal of Thrombosis and Haemostasis : JTH
|
April 26, 2006
Epitope mapping factor VIII A2 domain by affinity-directed mass spectrometry: residues 497-510 and 584-593 comprise a discontinuous epitope for the monoclonal antibody R8B12
C Ansong, S M Miles, P J Fay
The Journal of Biological Chemistry
|
March 3, 1995
Nevirapine alters the cleavage specificity of ribonuclease H of human immunodeficiency virus 1 reverse transcriptase
C Palaniappan, P J Fay, R A Bambara
Methods in Enzymology
|
January 1, 1993
Factor VIII and factor VIIIa
P Lollar, P J Fay, D N Fass
Progress in Clinical and Biological Research
|
January 1, 1994
Bone marrow purging with etoposide/methylprednisolone in patients undergoing autologous bone marrow transplantation
L Pineiro, J Fay, R Collins, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 11, 2008
Combining mutations of charged residues at the A2 domain interface enhances factor VIII stability over single point mutations
H Wakabayashi, A E Griffiths, P J Fay
Biochemistry
|
November 1, 2006
Factor VIII A1 domain residues 97-105 represent a light chain-interactive site
Charles Ansong, Stephen M Miles, Philip J Fay
The Journal of Biological Chemistry
|
June 10, 2010
Factor VIII lacking the C2 domain retains cofactor activity in vitro
Hironao Wakabayashi, Amy E Griffiths, Philip J Fay
International Journal of Cell Cloning
|
September 1, 1991
Elimination of clonogenic tumor cells from bone marrow using methylprednisolone (MP) and etoposide VP16: an in vitro pharmacologic study
G Miller, T Brashear, M Stone, et al.
Page
of 63
Search research articles
Search
Showing results (61-70 of 624) with videos related to
Sort By:
Page
of 63
The Journal of Biological Chemistry
|
June 2, 2011
Increasing hydrophobicity or disulfide bridging at the factor VIII A1 and C2 domain interface enhances procofactor stability
Hironao Wakabayashi, Amy E Griffiths, Philip J Fay
Advances in Experimental Medicine and Biology
|
February 23, 1999
All three vasopressin receptor sub-types are expressed by small-cell carcinoma
W G North, M J Fay, J Du
Journal of Thrombosis and Haemostasis : JTH
|
April 26, 2006
Epitope mapping factor VIII A2 domain by affinity-directed mass spectrometry: residues 497-510 and 584-593 comprise a discontinuous epitope for the monoclonal antibody R8B12
C Ansong, S M Miles, P J Fay
The Journal of Biological Chemistry
|
March 3, 1995
Nevirapine alters the cleavage specificity of ribonuclease H of human immunodeficiency virus 1 reverse transcriptase
C Palaniappan, P J Fay, R A Bambara
Methods in Enzymology
|
January 1, 1993
Factor VIII and factor VIIIa
P Lollar, P J Fay, D N Fass
Progress in Clinical and Biological Research
|
January 1, 1994
Bone marrow purging with etoposide/methylprednisolone in patients undergoing autologous bone marrow transplantation
L Pineiro, J Fay, R Collins, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 11, 2008
Combining mutations of charged residues at the A2 domain interface enhances factor VIII stability over single point mutations
H Wakabayashi, A E Griffiths, P J Fay
Biochemistry
|
November 1, 2006
Factor VIII A1 domain residues 97-105 represent a light chain-interactive site
Charles Ansong, Stephen M Miles, Philip J Fay
The Journal of Biological Chemistry
|
June 10, 2010
Factor VIII lacking the C2 domain retains cofactor activity in vitro
Hironao Wakabayashi, Amy E Griffiths, Philip J Fay
International Journal of Cell Cloning
|
September 1, 1991
Elimination of clonogenic tumor cells from bone marrow using methylprednisolone (MP) and etoposide VP16: an in vitro pharmacologic study
G Miller, T Brashear, M Stone, et al.
Page
of 63