Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
Prothrombin is synthesized in the liver, specifically in the hepatocytes. It is then released into the bloodstream where it plays a critical role in the blood clotting cascade.
The independent variable in a study on blood clotting could be a factor that is manipulated or controlled by the researcher, such as the dosage of a medication, the presence of a certain gene mutation, or the concentration of a specific clotting factor.
Hemophilia is a genetic disorder caused by a deficiency or defect in clotting factor VIII (hemophilia A) or factor IX (hemophilia B). These clotting factors are essential for blood clot formation, and their deficiency leads to prolonged bleeding and poor clotting ability.
Fibrinogen is a protein present in plasma but not in serum. Serum is plasma without the clotting factors like fibrinogen, which is used up during the clotting process.
An enlarged spleen can interfere with blood clotting. The spleen is a multifunctional organ that helps produce platelets, which serve to clot the blood.
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
Most are made in the liver
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No,All are made in the liver except for Factor VIII (made by the vascular endothelium) and vonWillebrand's factor which is made in the endothelium (in the Weibel-Palade bodies), megakaryocytes (α-granules of platelets), and subendothelial connective tissue.
Haemophilia A - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor VIII Haemophilia B - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor IX Haemophilia C - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor XI -similar to- vonWillebrand's Disorder - an inhibition of clotting caused by a deficiency in a protein called the vonWillebrand's Factor
Prothrombin is synthesized in the liver, specifically in the hepatocytes. It is then released into the bloodstream where it plays a critical role in the blood clotting cascade.
contains nutrients
Protein factors required for clotting are synthesized by the liver. These proteins include fibrinogen, prothrombin, and factors V, VII, VIII, IX, X, XI, and XII. Their synthesis is regulated by various factors including vitamin K.
The most notable factor affecting how wounds heal is the clotting factor of plasma. If the clotting factor is weak, scars are more likely to form.
In the most common type, Hemophilia A, the person lacks clotting factor VIII. In Hemophilia B, clotting factor IX is lacking.
Serum, it lacks all of the elements needed for clotting. They have been separated out.