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D N Cooper

Showing results (131-140 of 205) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.
Journal of Medical Genetics|February 5, 2008
Human Gene Mutation Database: towards a comprehensive central mutation databaseP D Stenson, E Ball, K Howells, et al.
Human Molecular Genetics|December 1, 1994
Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophiliaL P Berg, D A Scopes, A Alhaq, et al.
Thrombosis Research|February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolismC Grundy, H Plendl, W Grote, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Mutation|January 1, 1995
Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selectionM Krawczak, B Smith-Sorensen, J Schmidtke, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi JewsL P Berg, D Varon, U Martinowitz, et al.
Human Genetics|January 1, 1984
Restriction fragment length polymorphisms at the human parathyroid hormone gene locusJ Schmidtke, B Pape, U Krengel, et al.
Human Genetics|January 1, 1997
Mutational and functional analysis of the neurofibromatosis type 1 (NF1) geneM Upadhyaya, M J Osborn, J Maynard, et al.
Human Genetics|February 1, 1987
Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysisA M Goate, D N Cooper, C Hall, et al.
Pageof 21

Showing results (131-140 of 205) with videos related to

Sort By:
Pageof 21
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.
Journal of Medical Genetics|February 5, 2008
Human Gene Mutation Database: towards a comprehensive central mutation databaseP D Stenson, E Ball, K Howells, et al.
Human Molecular Genetics|December 1, 1994
Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophiliaL P Berg, D A Scopes, A Alhaq, et al.
Thrombosis Research|February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolismC Grundy, H Plendl, W Grote, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Mutation|January 1, 1995
Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selectionM Krawczak, B Smith-Sorensen, J Schmidtke, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi JewsL P Berg, D Varon, U Martinowitz, et al.
Human Genetics|January 1, 1984
Restriction fragment length polymorphisms at the human parathyroid hormone gene locusJ Schmidtke, B Pape, U Krengel, et al.
Human Genetics|January 1, 1997
Mutational and functional analysis of the neurofibromatosis type 1 (NF1) geneM Upadhyaya, M J Osborn, J Maynard, et al.
Human Genetics|February 1, 1987
Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysisA M Goate, D N Cooper, C Hall, et al.
Pageof 21