F9 wt Allele

Human F9 wild-type allele is located within Xq27.1-q27.2 and is approximately 33 kb in length. This allele, which encodes coagulation factor IX protein, plays a role in the intrinsic blood coagulation cascade. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency. This is a recessive X-linked disorder, also called hemophilia B or Christmas disease. (NCI Thesaurus)

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F9 Gene

This gene plays a role in the regulation of blood coagulation and is modulated by Ca+2 ions, membrane phospholipids, and factor…

F8 wt Allele

Human F8 wild-type allele is located within Xq28 and is approximately 548 kb in length. This allele, which encodes coagulation factor VIII…

F8 Gene

This gene plays an important role in blood coagulation.

F7 wt Allele

Human F7 wild-type allele is located within 13q34 and is approximately 14 kb in length. This allele, which encodes coagulation factor VII…

F7 Gene

This gene plays an essential role in the maintenance of cellular homeostasis.

F511 cream

A substance being studied in the prevention of palmar-plantar erythrodysesthesia (pain, swelling, numbness, tingling, or redness of the palms of the hands…