B R Bahnak - JoVE Visualize

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1992

Molecular study of von Willebrand disease: identification of potential mutations in patients with type IIA and type IIBG Piétu, A S Ribba, L de Paillette, et al.

British Journal of Haematology|September 1, 1992

Defects in type IIA von Willebrand disease: a cysteine 509 to arginine substitution in the mature von Willebrand factor disrupts a disulphide loop involved in the interaction with platelet glycoprotein Ib-IXJ M Lavergne, L De Paillette, B R Bahnak, et al.

Thrombosis and Haemostasis|October 31, 1988

Carrier detection in severe (type III) von Willebrand disease using two intragenic restriction fragment length polymorphismsB R Bahnak, J M Lavergne, C L Verweij, et al.

Human Genetics|February 1, 1994

A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWDV Siguret, J M Lavergne, G Chérel, et al.

European Journal of Human Genetics : EJHG|January 1, 1993

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.

Journal of Cellular Physiology|February 1, 1989

Expression of von Willebrand factor in porcine vessels: heterogeneity at the level of von Willebrand factor mRNAB R Bahnak, Q Y Wu, L Coulombel, et al.

Blood|January 1, 1987

Steady state levels of factor X mRNA in liver and Hep G2 cellsB R Bahnak, R Howk, J H Morrissey, et al.

British Journal of Haematology|August 1, 1993

Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresisM Tartary, D Vidaud, Y Piao, et al.

Human Genetics|April 1, 1993

Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counselingD Vidaud, M Tartary, J M Costa, et al.

Blood|May 1, 1988

Analysis of von Willebrand factor mRNA from the lung of pigs with severe von Willebrand disease by using a human cDNA probeQ Y Wu, B R Bahnak, L Coulombel, et al.

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1992

Molecular study of von Willebrand disease: identification of potential mutations in patients with type IIA and type IIBG Piétu, A S Ribba, L de Paillette, et al.

British Journal of Haematology|September 1, 1992

Defects in type IIA von Willebrand disease: a cysteine 509 to arginine substitution in the mature von Willebrand factor disrupts a disulphide loop involved in the interaction with platelet glycoprotein Ib-IXJ M Lavergne, L De Paillette, B R Bahnak, et al.

Thrombosis and Haemostasis|October 31, 1988

Carrier detection in severe (type III) von Willebrand disease using two intragenic restriction fragment length polymorphismsB R Bahnak, J M Lavergne, C L Verweij, et al.

Human Genetics|February 1, 1994

A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWDV Siguret, J M Lavergne, G Chérel, et al.

European Journal of Human Genetics : EJHG|January 1, 1993

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.

Journal of Cellular Physiology|February 1, 1989

Expression of von Willebrand factor in porcine vessels: heterogeneity at the level of von Willebrand factor mRNAB R Bahnak, Q Y Wu, L Coulombel, et al.

Blood|January 1, 1987

Steady state levels of factor X mRNA in liver and Hep G2 cellsB R Bahnak, R Howk, J H Morrissey, et al.

British Journal of Haematology|August 1, 1993

Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresisM Tartary, D Vidaud, Y Piao, et al.

Human Genetics|April 1, 1993

Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counselingD Vidaud, M Tartary, J M Costa, et al.

Blood|May 1, 1988

Analysis of von Willebrand factor mRNA from the lung of pigs with severe von Willebrand disease by using a human cDNA probeQ Y Wu, B R Bahnak, L Coulombel, et al.

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