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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis
D S Millar, C B Grundy, P Bignell, et al.
British Journal of Haematology
|
November 1, 1993
A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++
A Girolami, P Simioni, B Girolami, et al.
Journal of Cellular Biochemistry
|
December 1, 1995
Prothrombin cleavage by human vascular smooth muscle cells: a potential alternative pathway to the coagulation cascade
O Benzakour, C Kanthou, F Lupu, et al.
The Biochemical Journal
|
June 1, 1995
Evidence for a protein S receptor(s) on human vascular smooth muscle cells. Analysis of the binding characteristics and mitogenic properties of protein S on human vascular smooth muscle cells
O Benzakour, C Formstone, S Rahman, et al.
Biochemical and Biophysical Research Communications
|
April 17, 1995
Galectin-1 modulates human melanoma cell adhesion to laminin
F A van den Brûle, C Buicu, M Baldet, et al.
Human Genetics
|
October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA
L P Berg, K Wieland, D S Millar, et al.
Human Genetics
|
November 1, 1994
Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis
D S Millar, A I Wacey, J Ribando, et al.
British Journal of Haematology
|
June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket
G Marchetti, P Patracchini, D Gemmati, et al.
Clinical Genetics
|
February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease
M A Martín, J C Rubio, A García, et al.
Molecular Psychiatry
|
May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease
C S Ku, C Polychronakos, E K Tan, et al.
Page
of 21
Search research articles
Search
Showing results (161-170 of 205) with videos related to
Sort By:
Page
of 21
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis
D S Millar, C B Grundy, P Bignell, et al.
British Journal of Haematology
|
November 1, 1993
A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++
A Girolami, P Simioni, B Girolami, et al.
Journal of Cellular Biochemistry
|
December 1, 1995
Prothrombin cleavage by human vascular smooth muscle cells: a potential alternative pathway to the coagulation cascade
O Benzakour, C Kanthou, F Lupu, et al.
The Biochemical Journal
|
June 1, 1995
Evidence for a protein S receptor(s) on human vascular smooth muscle cells. Analysis of the binding characteristics and mitogenic properties of protein S on human vascular smooth muscle cells
O Benzakour, C Formstone, S Rahman, et al.
Biochemical and Biophysical Research Communications
|
April 17, 1995
Galectin-1 modulates human melanoma cell adhesion to laminin
F A van den Brûle, C Buicu, M Baldet, et al.
Human Genetics
|
October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA
L P Berg, K Wieland, D S Millar, et al.
Human Genetics
|
November 1, 1994
Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis
D S Millar, A I Wacey, J Ribando, et al.
British Journal of Haematology
|
June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket
G Marchetti, P Patracchini, D Gemmati, et al.
Clinical Genetics
|
February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease
M A Martín, J C Rubio, A García, et al.
Molecular Psychiatry
|
May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease
C S Ku, C Polychronakos, E K Tan, et al.
Page
of 21