A protein S gene polymorphism, detectable by restriction analysis (BstXI) of amplified exonic sequences (exon 15), was studied in seven Italian families with protein S deficiency. In the 17 individuals heterozygous for the polymorphism the study was extended to platelet mRNA through reverse transcription, amplification and densitometric analysis. mRNA produced by the putative defective protein S genes was absent in three families and reduced to a different extent (as expressed by altered allelic ratios) in four families. The allelic ratios helped to distinguish total protein S deficiency (type I) for free protein S deficiency (type IIa) in families with equivocal phenotypes. This study indicates that the study of platelet mRNA, in associati...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Abstract Protein S deficiency is an autosomal dominant disorder that results from mutations in the p...
A protein S gene polymorphism, detectable by restriction analysis of amplified exonic sequences, was...
The molecular basis of protein S (PS) deficiency was investigated in seven of eight donors identifie...
Hereditary protein S deficiency is a risk factor for developing recurrent venous thromboembolic dise...
The molecular genetic analysis of protein S deficiency has been hampered by the complexity of the pr...
The Protein S Italian Team (PROSIT) enrolled 79 protein S (PS) deficient families and found 38 PROS1...
Protein S deficiency is a known risk factor for thrombosis. The coexistence of phenotypic type I (re...
Protein S (PS) deficiency is a risk factor for venous thromboembolism (VTE) and can be caused by var...
By single strand conformational polymorphism, nucleotide sequencing and enzyme restriction, we analy...
A dimorphism in PROS1 gene (c.A2001G, p.Pro667Pro) has been associated with significantly reduced le...
The molecular genetic analysis of protein S deficiency has been hampered by the complexity of the pr...
International audienceOnly a few mutations associated with qualitative protein S deficiency have alr...
Protein S deficiency is a recognized risk factor for venous thrombosis. Of all the inherited thrombo...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Abstract Protein S deficiency is an autosomal dominant disorder that results from mutations in the p...
A protein S gene polymorphism, detectable by restriction analysis of amplified exonic sequences, was...
The molecular basis of protein S (PS) deficiency was investigated in seven of eight donors identifie...
Hereditary protein S deficiency is a risk factor for developing recurrent venous thromboembolic dise...
The molecular genetic analysis of protein S deficiency has been hampered by the complexity of the pr...
The Protein S Italian Team (PROSIT) enrolled 79 protein S (PS) deficient families and found 38 PROS1...
Protein S deficiency is a known risk factor for thrombosis. The coexistence of phenotypic type I (re...
Protein S (PS) deficiency is a risk factor for venous thromboembolism (VTE) and can be caused by var...
By single strand conformational polymorphism, nucleotide sequencing and enzyme restriction, we analy...
A dimorphism in PROS1 gene (c.A2001G, p.Pro667Pro) has been associated with significantly reduced le...
The molecular genetic analysis of protein S deficiency has been hampered by the complexity of the pr...
International audienceOnly a few mutations associated with qualitative protein S deficiency have alr...
Protein S deficiency is a recognized risk factor for venous thrombosis. Of all the inherited thrombo...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Background and Objectives. Hereditary protein S (PS) deficiency is a rare autosomal disorder of the ...
Abstract Protein S deficiency is an autosomal dominant disorder that results from mutations in the p...