serw-MX  [xml]  

 DeCS Categories

D08 Enzymes and Coenzymes .
D08.244 Cytochromes .
D08.244.453 Cytochrome P-450 Enzyme System .
D08.244.453.484 Cytochrome P450 Family 11 .
D08.244.453.484.250 Cholesterol Side-Chain Cleavage Enzyme .
D08.244.453.915 Steroid Hydroxylases .
D08.244.453.915.212 Cholesterol Side-Chain Cleavage Enzyme .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.656 Peptide Hydrolases .
D08.811.277.656.300 Endopeptidases .
D08.811.277.656.300.760 Serine Endopeptidases .
D08.811.277.656.300.760.315 Factor Xa .
D08.811.277.656.300.760.320 Factor XIa .
D08.811.277.656.300.760.324 Factor XIIa .
D08.811.277.656.959 Serine Proteases .
D08.811.277.656.959.350 Serine Endopeptidases .
D08.811.277.656.959.350.315 Factor Xa .
D08.811.277.656.959.350.320 Factor XIa .
D08.811.277.656.959.350.324 Factor XIIa .
D08.811.682 Oxidoreductases .
D08.811.682.690 Oxygenases .
D08.811.682.690.708 Mixed Function Oxygenases .
D08.811.682.690.708.170 Cytochrome P-450 Enzyme System .
D08.811.682.690.708.170.425 Cytochrome P450 Family 11 .
D08.811.682.690.708.170.425.250 Cholesterol Side-Chain Cleavage Enzyme .
D08.811.682.690.708.170.915 Steroid Hydroxylases .
D08.811.682.690.708.170.915.212 Cholesterol Side-Chain Cleavage Enzyme .
D08.811.913 Transferases .
D08.811.913.050 Acyltransferases .
D08.811.913.050.200 Aminoacyltransferases .
D08.811.913.050.200.800 Transglutaminases .
D08.811.913.050.200.800.300 Factor XIIIa .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.125 Blood Coagulation Factors .
D12.776.124.125.400 Factor X .
D12.776.124.125.400.315 Factor Xa .
D12.776.124.125.425 Factor XI .
D12.776.124.125.425.320 Factor XIa .
D12.776.124.125.450 Factor XII .
D12.776.124.125.450.324 Factor XIIa .
D12.776.124.125.475 Factor XIII .
D12.776.124.125.475.500 Factor XIIIa .
D12.776.422 Hemeproteins .
D12.776.422.220 Cytochromes .
D12.776.422.220.453 Cytochrome P-450 Enzyme System .
D12.776.422.220.453.484 Cytochrome P450 Family 11 .
D12.776.422.220.453.484.250 Cholesterol Side-Chain Cleavage Enzyme .
D12.776.422.220.453.915 Steroid Hydroxylases .
D12.776.422.220.453.915.212 Cholesterol Side-Chain Cleavage Enzyme .
D12.776.543 Membrane Proteins .
D12.776.543.750 Receptors, Cell Surface .
D12.776.543.750.705 Receptors, Immunologic .
D12.776.543.750.705.852 Receptors, Cytokine .
D12.776.543.750.705.852.760 Receptors, Tumor Necrosis Factor .
D12.776.543.750.705.852.760.345 Receptor Activator of Nuclear Factor-kappa B .
D23 Biological Factors .
D23.119 Blood Coagulation Factors .
D23.119.400 Factor X .
D23.119.400.315 Factor Xa .
D23.119.425 Factor XI .
D23.119.425.320 Factor XIa .
D23.119.450 Factor XII .
D23.119.450.324 Factor XIIa .
D23.119.475 Factor XIII .
D23.119.475.500 Factor XIIIa .
 Synonyms & Historicals
Factor XIa .
Activated Factor XI .
Blood Coagulation Factor XI, Activated .
Contact Activation Product .
Factor 11A .
Factor Eleven A .
Factor XIa, Coagulation .
Factor XI, Activated .
Coagulation Factor XIa .
Activated form of factor XI. In the intrinsic pathway, Factor XI is activated to XIa by factor XIIa in the presence of cofactor HMWK; (HIGH MOLECULAR WEIGHT KININOGEN). Factor XIa then activates factor IX to factor IXa in the presence of calcium. .
Factor X .
Blood Coagulation Factor X .
Factor 10 .
Factor Ten .
Stuart Prower Factor .
Factor X, Coagulation .
Autoprothrombin III .
Stuart Factor .
Stuart-Prower Factor .
Coagulation Factor X .
Storage-stable glycoprotein blood coagulation factor that can be activated to factor Xa by both the intrinsic and extrinsic pathways. A deficiency of factor X, sometimes called Stuart-Prower factor deficiency, may lead to a systemic coagulation disorder. .
Factor XII .
Factor 12 .
Factor Twelve .
Hageman Factor .
Coagulation Factor XII .
Stable blood coagulation factor activated by contact with the subendothelial surface of an injured vessel. Along with prekallikrein, it serves as the contact factor that initiates the intrinsic pathway of blood coagulation. Kallikrein activates factor XII to XIIa. Deficiency of factor XII, also called the Hageman trait, leads to increased incidence of thromboembolic disease. Mutations in the gene for factor XII that appear to increase factor XII amidolytic activity are associated with HEREDITARY ANGIOEDEMA TYPE III. .
Factor XI .
Blood Coagulation Factor XI .
Factor 11 .
Factor Eleven .
Antecedent, Plasma Thromboplastin .
Factor XI, Coagulation .
Thromboplastin Antecedent, Plasma .
Plasma Thromboplastin Antecedent .
Coagulation Factor XI .
Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C. .
Factor XIII .
Blood Coagulation Factor XIII .
Factor 13 .
Factor Thirteen .
Factor XIII A-Chain .
Laki Lorand Factor .
Factor XIII A Chain .
Factor XIII, Coagulation .
Stabilizing Factor, Fibrin .
Transamidase, Factor XIII .
XIII, Coagulation Factor .
Coagulation Factor XIII .
Factor XIII Transamidase .
Fibrin Stabilizing Factor .
Fibrinase .
Laki-Lorand Factor .
A fibrin-stabilizing plasma enzyme (TRANSGLUTAMINASES) that is activated by THROMBIN and CALCIUM to form FACTOR XIIIA. It is important for stabilizing the formation of the fibrin polymer (clot) which culminates the coagulation cascade. .
Cholesterol Side-Chain Cleavage Enzyme .
20,22-Desmolase .
CYP 11A1 .
Cytochrome P450 11A1 .
Cytochrome P450scc .
20,22 Desmolase .
Cholesterol Side Chain Cleavage Enzyme .
Cytochrome P 450 CYP11A1 .
CYP11A1 .
Cholesterol Desmolase .
Cholesterol Monooxygenase (Side-Chain-Cleaving) .
Cytochrome P-450 CYP11A1 .
Cytochrome P-450(scc) .
A mitochondrial cytochrome P450 enzyme that catalyzes the side-chain cleavage of C27 cholesterol to C21 pregnenolone in the presence of molecular oxygen and NADPH-FERRIHEMOPROTEIN REDUCTASE. This enzyme, encoded by CYP11A1 gene, catalyzes the breakage between C20 and C22 which is the initial and rate-limiting step in the biosynthesis of various gonadal and adrenal steroid hormones. .
Receptor Activator of Nuclear Factor-kappa B .
CD265 Antigen .
NF-KappaB Receptor Activator .
RANK Protein .
Receptor Activator of NF-kappa B .
Receptor Activator of NF-kappaB .
Receptor Activator of Nuclear Factor-kappaB .
TNFRSF11A Protein .
TRANCE Receptor .
Activator, NF-KappaB Receptor .
Antigen, CD265 .
NF Kappa B Receptor Activator .
NF KappaB Receptor Activator .
Receptor Activator of NF kappa B .
Receptor Activator of NF kappaB .
Receptor Activator of Nuclear Factor kappa B .
Receptor Activator of Nuclear Factor kappaB .
Receptor Activator, NF-KappaB .
NF-Kappa B Receptor Activator .
Receptors, Tumor Necrosis Factor, Member 11a .
Tumor Necrosis Factor Receptor Superfamily, Member 11a .
A tumor necrosis factor receptor family member that is specific for RANK LIGAND and plays a role in bone homeostasis by regulating osteoclastogenesis. It is also expressed on DENDRITIC CELLS where it plays a role in regulating dendritic cell survival. Signaling by the activated receptor occurs through its association with TNF RECEPTOR-ASSOCIATED FACTORS. .
Factor XIIa .
Activated Factor XII .
Blood Coagulation Factor XII, Activated .
Factor 12A .
Factor Twelve A .
Hageman-Factor Fragments .
Prekallikrein Activator .
Activator, Prekallikrein .
Factor XIIa, Coagulation .
Fragments, Hageman-Factor .
Hageman Factor Fragments .
Factor XII, Activated .
Coagulation Factor XIIa .
Activated form of factor XII. In the initial event in the intrinsic pathway of blood coagulation, kallikrein (with cofactor HIGH MOLECULAR WEIGHT KININOGEN) cleaves factor XII to XIIa. Factor XIIa is then further cleaved by kallikrein, plasmin, and trypsin to yield smaller factor XII fragments (Hageman-Factor fragments). These fragments increase the activity of prekallikrein to kallikrein but decrease the procoagulant activity of factor XII. .
Factor Xa .
Activated Factor X .
Blood Coagulation Factor X, Activated .
Factor 10A .
Factor Ten A .
Factor Xa, Coagulation .
Autoprothrombin C .
Factor X, Activated .
Thrombokinase .
Coagulation Factor Xa .
Activated form of factor X that participates in both the intrinsic and extrinsic pathways of blood coagulation. It catalyzes the conversion of prothrombin to thrombin in conjunction with other cofactors. .
Factor XIIIa .
Factor 13A .
Factor Thirteen A .
Activated Factor XIII .
Transglutaminase, Plasma .
Blood Coagulation Factor XIII, Activated .
Factor XIII, Activated .
Fibrinoligase .
Plasma Transglutaminase .
Activated form of FACTOR XIII, a transglutaminase, which stabilizes the formation of the fibrin polymer (clot) culminating the blood coagulation cascade. .