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D N Cooper

Showing results (151-160 of 205) with videos related to

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Human Genetics|August 1, 1992
Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcriptsR Slomski, M Schloesser, L P Berg, 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.
Human Genetics|December 29, 2000
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsM Krawczak, N A Chuzhanova, P D Stenson, 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.
Human Genetics|January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IXB Zoll, J Arnemann, M Krawczak, et al.
The Biochemical Journal|July 15, 1995
Evaluation of the use of the luciferase-reporter-gene system for gene-regulation studies involving cyclic AMP-elevating agentsO Benzakour, C Kanthou, U Dennehy, et al.
Human Genetics|February 24, 2001
The Frequency of Inherited Disorders DatabaseL N Al-Jader, P S Harper, M Krawczak, et al.
Clinical Genetics|October 27, 1998
Three novel PROC gene lesions causing protein C deficiencyP J Hallam, P Mannucci, A Tripodi, et al.
Thrombosis and Haemostasis|June 1, 1996
Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC geneJ M Soria, L P Berg, J Fontcuberta, et al.
Thrombosis and Haemostasis|January 11, 1993
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisP H Reitsma, S R Poort, F Bernardi, et al.
Pageof 21

Showing results (151-160 of 205) with videos related to

Sort By:
Pageof 21
Human Genetics|August 1, 1992
Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcriptsR Slomski, M Schloesser, L P Berg, 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.
Human Genetics|December 29, 2000
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsM Krawczak, N A Chuzhanova, P D Stenson, 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.
Human Genetics|January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IXB Zoll, J Arnemann, M Krawczak, et al.
The Biochemical Journal|July 15, 1995
Evaluation of the use of the luciferase-reporter-gene system for gene-regulation studies involving cyclic AMP-elevating agentsO Benzakour, C Kanthou, U Dennehy, et al.
Human Genetics|February 24, 2001
The Frequency of Inherited Disorders DatabaseL N Al-Jader, P S Harper, M Krawczak, et al.
Clinical Genetics|October 27, 1998
Three novel PROC gene lesions causing protein C deficiencyP J Hallam, P Mannucci, A Tripodi, et al.
Thrombosis and Haemostasis|June 1, 1996
Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC geneJ M Soria, L P Berg, J Fontcuberta, et al.
Thrombosis and Haemostasis|January 11, 1993
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisP H Reitsma, S R Poort, F Bernardi, et al.
Pageof 21