[Platelet factor XIII as the collagen receptor].
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Factor XIII↗
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Congenital deficiency of clotting factor XIII.
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Adolescent↗
[Importance of factor XIII for hemostasis and wound healing].
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Blood Coagulation Disorders↗
[Preventive and therapeutic effects of fresh-frozen plasma in patients with inborn deficiency of the coagulation factor XIII].
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Blood Transfusion↗
[Congenital deficiency of fibrin stabilizing factor (factor XIII)].
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Blood Coagulation Tests↗
Congenital deficiency of factor XIII.
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Blood Coagulation Disorders↗
Congenital factor XIII deficiency.
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Child↗
Factor XIII does not stimulate growth of human cultured tumor cells.
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Cell Division↗
[Influence of fibrinolysis on factor XIII assay].
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Blood Coagulation Disorders↗
[Case suspected to be factor XIII deficiency].
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Adult↗
Deproteinized calf-blood extract, and influence of fibrin stabilising factor (Factor XIII) activity in cirrhosis of the liver.
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Animals↗
[Influence of fibrinolytic activation on the determination of factor XIII].
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Amino Alcohols↗
Functional modifications of alpha 2-macroglobulin by primary amines. I. Characterization of alpha 2 M after derivatization by methylamine and by factor XIII.
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Endocytosis↗
Acquired deficiency of factor XIII.
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Factor XIII Deficiency↗
[Clinical evaluation of factor XIII for postoperative stomal leakage and fistulae after gastrointestinal surgery].
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Factor XIII↗
[Factor XIII Val34Leu polymorphism and premature myocardial infarction].
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Adult↗
Factor XIII cross-linking and the rate of fibrinolysis induced by streptokinase and urokinase.
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Endopeptidases↗
Decay accelerating factor (DAF) peptide sequences share homology with a consensus sequence found in the superfamily of structurally related complement proteins and other proteins including haptoglobin, factor XIII, beta 2-glycoprotein I, and the IL-2 receptor.
Amino acid sequence data derived from tryptic peptides of the decay accelerating factor indicate that this complement regulatory protein contains a sequence with homology to the superfamily of structurally related complement proteins, including the C4 binding protein, factor H, complement receptor type 1, complement receptor type 2, Ba, C1r, and to their non-complement relatives, including beta 2-glycoprotein I, factor XIIIb, the alpha 1 chain of haptoglobin, and the interleukin 2 receptor. Identifying DAF as a member of the superfamily of structurally related complement proteins provides evidence that DAF may contain a functionally important C4b and C3b binding domain.
Amino Acid Sequence↗