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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
January 1, 1996
Factor X Stockton: a mild bleeding diathesis associated with an active site mutation in factor X
T L Messier, C Y Wong, E G Bovill, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 20, 2001
Quantum computing
S S Li, G L Long, F S Bai, et al.
Biochemistry
|
August 28, 1990
Organization of the human protein S genes
D K Schmidel, A V Tatro, L G Phelps, et al.
Blood
|
June 1, 1996
Proteolytic events that regulate factor V activity in whole plasma from normal and activated protein C (APC)-resistant individuals during clotting: an insight into the APC-resistance assay
M Kalafatis, P E Haley, D Lu, et al.
Thrombosis and Haemostasis
|
October 1, 1994
Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations
G L Long, J A Tomczak, I R Rainville, et al.
Nucleic Acids Research
|
July 25, 1985
The structure and evolution of a 461 amino acid human protein C precursor and its messenger RNA, based upon the DNA sequence of cloned human liver cDNAs
R J Beckmann, R J Schmidt, R F Santerre, et al.
Journal of Cellular Biochemistry
|
November 1, 1995
Glucocorticoids coordinately regulate type I collagen pro alpha 1 promoter activity through both the glucocorticoid and transforming growth factor beta response elements: a novel mechanism of glucocorticoid regulation of eukaryotic genes
N Meisler, S Shull, R Xie, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 29, 2007
A genetic basis for the interrelation of coagulation factors
C Y Vossen, P W Callas, S J Hasstedt, et al.
Blood
|
March 15, 1992
Protein CVermont: symptomatic type II protein C deficiency associated with two GLA domain mutations
E G Bovill, J A Tomczak, B Grant, et al.
Blood
|
February 11, 1991
A 5.3-kb deletion including exon XIII of the protein S alpha gene occurs in two protein S-deficient families
D K Schmidel, R M Nelson, E H Broxson, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 85) with videos related to
Sort By:
Page
of 9
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
January 1, 1996
Factor X Stockton: a mild bleeding diathesis associated with an active site mutation in factor X
T L Messier, C Y Wong, E G Bovill, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 20, 2001
Quantum computing
S S Li, G L Long, F S Bai, et al.
Biochemistry
|
August 28, 1990
Organization of the human protein S genes
D K Schmidel, A V Tatro, L G Phelps, et al.
Blood
|
June 1, 1996
Proteolytic events that regulate factor V activity in whole plasma from normal and activated protein C (APC)-resistant individuals during clotting: an insight into the APC-resistance assay
M Kalafatis, P E Haley, D Lu, et al.
Thrombosis and Haemostasis
|
October 1, 1994
Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations
G L Long, J A Tomczak, I R Rainville, et al.
Nucleic Acids Research
|
July 25, 1985
The structure and evolution of a 461 amino acid human protein C precursor and its messenger RNA, based upon the DNA sequence of cloned human liver cDNAs
R J Beckmann, R J Schmidt, R F Santerre, et al.
Journal of Cellular Biochemistry
|
November 1, 1995
Glucocorticoids coordinately regulate type I collagen pro alpha 1 promoter activity through both the glucocorticoid and transforming growth factor beta response elements: a novel mechanism of glucocorticoid regulation of eukaryotic genes
N Meisler, S Shull, R Xie, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 29, 2007
A genetic basis for the interrelation of coagulation factors
C Y Vossen, P W Callas, S J Hasstedt, et al.
Blood
|
March 15, 1992
Protein CVermont: symptomatic type II protein C deficiency associated with two GLA domain mutations
E G Bovill, J A Tomczak, B Grant, et al.
Blood
|
February 11, 1991
A 5.3-kb deletion including exon XIII of the protein S alpha gene occurs in two protein S-deficient families
D K Schmidel, R M Nelson, E H Broxson, et al.
Page
of 9