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Progress in Clinical and Biological Research
|
January 1, 1988
Role of ADP in platelet aggregation and fibrinogen binding induced by prostaglandin endoperoxides: studies in a patient with a selective defect of ADP-induced platelet aggregation
M Cattaneo, A M Randi, M T Canciani, et al.
International Journal of Clinical & Laboratory Research
|
January 1, 1992
Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center
E Sacchi, A M Randi, L Tagliavacca, et al.
Haematologica
|
September 1, 1990
Molecular analysis of severe von Willebrand disease in Italian patients
M Sampietro, A M Randi, E Sacchi, et al.
The Journal of Clinical Investigation
|
April 1, 1991
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences
A M Randi, I Rabinowitz, D J Mancuso, et al.
The Journal of Biological Chemistry
|
October 9, 1998
The I domain of integrin leukocyte function-associated antigen-1 is involved in a conformational change leading to high affinity binding to ligand intercellular adhesion molecule 1 (ICAM-1)
A McDowall, B Leitinger, P Stanley, et al.
La Ricerca in Clinica E in Laboratorio
|
January 1, 1989
Diagnosis of hemophilia A in a female subject by using restriction fragment length polymorphisms linked to the factor VIII gene
A M Randi, E Sacchi, M Sampietro, et al.
Blood
|
November 24, 2001
Combined genomic and antisense analysis reveals that the transcription factor Erg is implicated in endothelial cell differentiation
F McLaughlin, V J Ludbrook, J Cox, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Molecular biology of von Willebrand factor
J E Sadler, D J Mancuso, A M Randi, et al.
Blood
|
August 1, 1993
Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization method
A Inbal, T Englender, N Kornbrot, et al.
The Journal of Biological Chemistry
|
September 25, 1993
Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib
I Rabinowitz, A M Randi, K S Shindler, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Progress in Clinical and Biological Research
|
January 1, 1988
Role of ADP in platelet aggregation and fibrinogen binding induced by prostaglandin endoperoxides: studies in a patient with a selective defect of ADP-induced platelet aggregation
M Cattaneo, A M Randi, M T Canciani, et al.
International Journal of Clinical & Laboratory Research
|
January 1, 1992
Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center
E Sacchi, A M Randi, L Tagliavacca, et al.
Haematologica
|
September 1, 1990
Molecular analysis of severe von Willebrand disease in Italian patients
M Sampietro, A M Randi, E Sacchi, et al.
The Journal of Clinical Investigation
|
April 1, 1991
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences
A M Randi, I Rabinowitz, D J Mancuso, et al.
The Journal of Biological Chemistry
|
October 9, 1998
The I domain of integrin leukocyte function-associated antigen-1 is involved in a conformational change leading to high affinity binding to ligand intercellular adhesion molecule 1 (ICAM-1)
A McDowall, B Leitinger, P Stanley, et al.
La Ricerca in Clinica E in Laboratorio
|
January 1, 1989
Diagnosis of hemophilia A in a female subject by using restriction fragment length polymorphisms linked to the factor VIII gene
A M Randi, E Sacchi, M Sampietro, et al.
Blood
|
November 24, 2001
Combined genomic and antisense analysis reveals that the transcription factor Erg is implicated in endothelial cell differentiation
F McLaughlin, V J Ludbrook, J Cox, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Molecular biology of von Willebrand factor
J E Sadler, D J Mancuso, A M Randi, et al.
Blood
|
August 1, 1993
Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization method
A Inbal, T Englender, N Kornbrot, et al.
The Journal of Biological Chemistry
|
September 25, 1993
Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib
I Rabinowitz, A M Randi, K S Shindler, et al.
Page
of 3