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Subject : biology

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Novel deep intronic mutation in the coagulation factor XIII a chain gene leading to unexpected RNA splicing in a patient with factor XIII deficiency

Authors : Dan Li; Jun Deng; Heng Mei

Subjects: Adult; Male; 0301 basic medicine

Source: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)BMC Medical Genetics

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Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease

Authors : Robert Bernat; Jasna Leniček-Krleža; Sanja Dabelić

Subjects: 0301 basic medicine; medicine.medical_specialty; Plasmin

Source: Journal of Medical BiochemistryJournal of Medical Biochemistry, Vol 40, Iss 2, Pp 138-149 (2021)

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Important roles of the human leukocyte antigen class I and II molecules and their associated genes in the autoimmune coagulation factor XIII deficiency via whole-exome sequencing analysis

Authors : Tsukasa Osaki; Masayoshi Souri; Akitada Ichinose

Subjects: Male; Heredity; Physiology

Source: PLoS ONE, Vol 16, Iss 9, p e0257322 (2021)PLoS ONE

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The Structure of Blood Coagulation Factor XIII Is Adapted to Oxidation

Authors : L. V. Yurina; Maria I. Indeykina; Eugene N. Nikolaev

Subjects: 0301 basic medicine; Male; Lysis

Source: BiomoleculesVolume 10Issue 6Biomolecules, Vol 10, Iss 914, p 914 (2020)

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Inhibition of Fibrinolysis by Coagulation Factor XIII

Authors : Dingeman C. Rijken; Shirley Uitte de Willige; Hematology

Subjects: 0301 basic medicine; Plasmin; Coagulation factor XIII

Source: BioMed Research International, Vol 2017 (2017)BioMed Research InternationalBioMed Research International. Hindawi Publishing Corporation

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Biochemical characterization of a medaka (Oryzias latipes) orthologue for mammalian Factor XIII and establishment of a gene-edited mutant

Authors : Hideki Tatsukawa; Hisashi Hashimoto; Ryota Ogawa

Subjects: 0301 basic medicine; Fish Proteins; Tissue transglutaminase

Source: The FEBS Journal. 284(17):2843-2855

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Factor XIII and Fibrin Clot Properties in Acute Venous Thromboembolism

Authors : Joanna Natorska; Anetta Undas; Michał Ząbczyk

Subjects: 0301 basic medicine; Deep vein; Review

Source: International Journal of Molecular SciencesInternational Journal of Molecular Sciences, Vol 22, Iss 1607, p 1607 (2021)

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Spontaneous splenic rupture accompanied by hepatic arterial dissection in a patient with autoimmune haemorrhaphilia due to anti-factor XIII antibodies

Authors : D. Hidaka; E. Fujioka; Tsukasa Osaki

Subjects: Pathology; medicine.medical_specialty; Blood transfusion

Source: Haemophilia. 22:e314-e317

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Factor XIII: Congenital Deficiency Factor XIII, Acquired Deficiency, Factor XIII A-Subunit, and Factor XIII B-Subunit

Authors : Jasmina Ahluwalia; Anita Tahlan

Subjects: medicine.medical_specialty; Protein Conformation; Tissue transglutaminase

Source: Archives of Pathology & Laboratory Medicine. 138:278-281

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Development of anti-factor XIII antibodies in a patient with hereditary factor XIII deficiency receiving therapy for chronic hepatitis C

Authors : R. Sosa; A. T. Neff; David Gailani

Subjects: Pediatrics; medicine.medical_specialty; biology

Source: Haemophilia. 20:e429-e432

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فلترة النتائج

Novel deep intronic mutation in the coagulation factor XIII a chain gene leading to unexpected RNA splicing in a patient with factor XIII deficiency

Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease

Important roles of the human leukocyte antigen class I and II molecules and their associated genes in the autoimmune coagulation factor XIII deficiency via whole-exome sequencing analysis

The Structure of Blood Coagulation Factor XIII Is Adapted to Oxidation

Inhibition of Fibrinolysis by Coagulation Factor XIII

Biochemical characterization of a medaka (Oryzias latipes) orthologue for mammalian Factor XIII and establishment of a gene-edited mutant

Factor XIII and Fibrin Clot Properties in Acute Venous Thromboembolism

Spontaneous splenic rupture accompanied by hepatic arterial dissection in a patient with autoimmune haemorrhaphilia due to anti-factor XIII antibodies

Factor XIII: Congenital Deficiency Factor XIII, Acquired Deficiency, Factor XIII A-Subunit, and Factor XIII B-Subunit

Development of anti-factor XIII antibodies in a patient with hereditary factor XIII deficiency receiving therapy for chronic hepatitis C

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