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D N Cooper

Showing results (171-180 of 205) with videos related to

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Blood|May 1, 1996
Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutationC J Formstone, P J Hallam, E G Tuddenham, et al.
Blood|May 1, 1991
A molecular genetic study of factor XI deficiencyJ F Hancock, K Wieland, R E Pugh, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 1, 1996
Aberrant RNA splicing of the protein C and protein S genes in healthy individualsL P Berg, J M Soria, C J Formstone, et al.
Radiation Research|February 24, 2006
Assessing radiation-associated mutational risk to the germline: repetitive DNA sequences as mutational targets and biomarkersS D Bouffler, B A Bridges, D N Cooper, et al.
Human Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.
Human Genetics|March 1, 1993
A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphismsR Williamson, A Bowcock, K Kidd, et al.
Human Genetics|January 5, 2001
Identification of an intronic regulatory element in the human protein C (PROC) geneM K Shamsher, N A Chuzhanova, B Friedman, et al.
Human Genetics|February 24, 2001
Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergenceH Winter, L Langbein, M Krawczak, et al.
Pageof 21

Showing results (171-180 of 205) with videos related to

Sort By:
Pageof 21
Blood|May 1, 1996
Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutationC J Formstone, P J Hallam, E G Tuddenham, et al.
Blood|May 1, 1991
A molecular genetic study of factor XI deficiencyJ F Hancock, K Wieland, R E Pugh, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 1, 1996
Aberrant RNA splicing of the protein C and protein S genes in healthy individualsL P Berg, J M Soria, C J Formstone, et al.
Radiation Research|February 24, 2006
Assessing radiation-associated mutational risk to the germline: repetitive DNA sequences as mutational targets and biomarkersS D Bouffler, B A Bridges, D N Cooper, et al.
Human Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.
Human Genetics|March 1, 1993
A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphismsR Williamson, A Bowcock, K Kidd, et al.
Human Genetics|January 5, 2001
Identification of an intronic regulatory element in the human protein C (PROC) geneM K Shamsher, N A Chuzhanova, B Friedman, et al.
Human Genetics|February 24, 2001
Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergenceH Winter, L Langbein, M Krawczak, et al.
Pageof 21