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D S Millar

Showing results (11-20 of 38) with videos related to

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Prenatal Diagnosis|November 1, 1985
Normal blood cell values in the early mid-trimester fetusD S Millar, L R Davis, C H Rodeck, et al.
Analytical Biochemistry|April 10, 1995
Solid-phase hybridization capture of low-abundance target DNA sequences: application to the polymerase chain reaction detection of Mycobacterium paratuberculosis and Mycobacterium avium subsp. silvaticumD S Millar, S J Withey, M L Tizard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1995
Three novel mutations in the protein C (PROC) gene causing venous thrombosisD S Millar, D Bevan, A Chitolie, et al.
Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.
Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.
Nucleic Acids Research|October 23, 1997
Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNAP M Warnecke, C Stirzaker, J R Melki, et al.
Oncogene|February 18, 1999
Detailed methylation analysis of the glutathione S-transferase pi (GSTP1) gene in prostate cancerD S Millar, K K Ow, C L Paul, et al.
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 thrombosisD 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.
Human Genetics|October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNAL P Berg, K Wieland, D S Millar, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|November 1, 1985
Normal blood cell values in the early mid-trimester fetusD S Millar, L R Davis, C H Rodeck, et al.
Analytical Biochemistry|April 10, 1995
Solid-phase hybridization capture of low-abundance target DNA sequences: application to the polymerase chain reaction detection of Mycobacterium paratuberculosis and Mycobacterium avium subsp. silvaticumD S Millar, S J Withey, M L Tizard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1995
Three novel mutations in the protein C (PROC) gene causing venous thrombosisD S Millar, D Bevan, A Chitolie, et al.
Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.
Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.
Nucleic Acids Research|October 23, 1997
Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNAP M Warnecke, C Stirzaker, J R Melki, et al.
Oncogene|February 18, 1999
Detailed methylation analysis of the glutathione S-transferase pi (GSTP1) gene in prostate cancerD S Millar, K K Ow, C L Paul, et al.
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 thrombosisD 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.
Human Genetics|October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNAL P Berg, K Wieland, D S Millar, et al.
Pageof 4