International audienceSeveral cDNA clones coding for A alpha, B beta and gamma chains of fibrinogen have been isolated from a human liver cDNA library. They were selected by differential hybridization with probes raised against fractionated liver mRNA (positive probes) and muscle and albumin mRNA (negative probes), then firmly identified by positive hybridization selection. Three of these clones, encoding A alpha, B beta and gamma fibrinogen chain sequences, were further characterized by restriction mapping and used as probes to characterize fibrinogen mRNAs from adult and fetal liver and fibrinogen genes in normal individuals and two afibrinogenemic patients. The results indicate that there is a single copy of the fibrinogen genes which ar...
IntroductionFibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinog...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...
Congenital afibrinogenemia is a rare inherited coagulopathy, characterized by very low or unmeasurab...
Congenital afibrinogenemia is an autosomal recessive disorder characterized by the complete absence ...
Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functio...
Congenital afibrinogenemia is a rare coagulation disorder with autosomal recessive inheritance, char...
Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functio...
Fibrinogen is synthesized in hepatocytes in the form of a hexamer composed of two sets of three poly...
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by a hemorrhagic dia...
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by complete absence ...
This article reviews recent progress made in understanding the molecular basis of congenital afibrin...
Human fibrinogen cDNA probes for the alpha-, beta-, and gamma-polypeptide chains have been used to i...
Congenital fibrinogen disorders are caused by mutations in one of the three fibrinogen genes that af...
Congenital afibrinogenemia (Mendelian Inheritance in Man #202400) is a rare, autosomal recessive dis...
IntroductionFibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinog...
IntroductionFibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinog...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...
Congenital afibrinogenemia is a rare inherited coagulopathy, characterized by very low or unmeasurab...
Congenital afibrinogenemia is an autosomal recessive disorder characterized by the complete absence ...
Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functio...
Congenital afibrinogenemia is a rare coagulation disorder with autosomal recessive inheritance, char...
Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functio...
Fibrinogen is synthesized in hepatocytes in the form of a hexamer composed of two sets of three poly...
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by a hemorrhagic dia...
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by complete absence ...
This article reviews recent progress made in understanding the molecular basis of congenital afibrin...
Human fibrinogen cDNA probes for the alpha-, beta-, and gamma-polypeptide chains have been used to i...
Congenital fibrinogen disorders are caused by mutations in one of the three fibrinogen genes that af...
Congenital afibrinogenemia (Mendelian Inheritance in Man #202400) is a rare, autosomal recessive dis...
IntroductionFibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinog...
IntroductionFibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinog...
Hereditary fibrinogen disorders include type I deficiencies (afibrinogenemia and hypofibrinogenemia,...
Congenital afibrinogenemia is a rare inherited coagulopathy, characterized by very low or unmeasurab...