factor xiiib has been researched along with Deficiency, Factor 13 in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (4.76) | 18.7374 |
| 1990's | 5 (23.81) | 18.2507 |
| 2000's | 7 (33.33) | 29.6817 |
| 2010's | 7 (33.33) | 24.3611 |
| 2020's | 1 (4.76) | 2.80 |
| Authors | Studies |
|---|---|
| Conway, EM; Cullis, PR; Kastrup, CJ; Kulkarni, JA; Leung, J; Meixner, SC; Owens, AP; Palumbo, JS; Pryzdial, ELG; Russell, HM; Safikhan, NS; Strilchuk, AW; Sutherland, MR; van der Meel, R | 1 |
| Biswas, A; Garly, ML; Ivaškevičius, V; Oldenburg, J | 1 |
| Du, P; Hassan, R; Jiang, W; Liu, L; Luo, H; Sun, L; Wang, Y; Yan, Q | 1 |
| Ichinose, A; Matsumoto, R; Souri, M; Sugihara, T; Wada, H | 1 |
| Ahluwalia, J; Tahlan, A | 1 |
| Ajzner, E; Bereczky, Z; Boda, Z; Haramura, G; Katona, E; Kerényi, A; Muszbek, L; Schlammadinger, A | 1 |
| Bereczky, Z; Cohan, N; Karimi, M; Muszbek, L | 1 |
| Elloumi, M; Fakhfakh, F; Fendri-Kriaa, N; Hadjsalem, I; Kanoun, H; Louhichi, N; Medhaffar, M; Mkaouar-Rebai, E; Souissi, T; Yaïch, F | 1 |
| Biswas, A; Ivaskevicius, V; Kohler, HP; Krause, M; Loreth, R; Ohlenforst, S; Oldenburg, J; Rott, H; Scharrer, I; Schroeder, V | 1 |
| Biswas, A; Ivaskevicius, V; Oldenburg, J; Seitz, R; Thomas, A | 1 |
| Belvedere, MA; Blain, RC; Butine, MD; Ishak, LM; Lovejoy, AE; Nugent, DJ; Pederson, SM; Reynolds, TC; Visich, JE; Young, G | 1 |
| Degen, JL; Ichinose, A; Koseki-Kuno, S; Souri, M; Takeda, N | 1 |
| Degen, JL; Ichinose, A; Koseki-Kuno, S; Souri, M; Takeda, N; Takeishi, Y; Yamakawa, M | 1 |
| Ichinose, A | 1 |
| Ichinose, A; Souri, M | 1 |
| Fachet, J; Haramura, G; Kárpáti, L; Katona, E; Muszbek, L | 1 |
| Bertina, RM; Gómez García, EB; Kappers, M; Poort, SR; Schaap, MC; Stibbe, J; Sturk, A | 1 |
| Chitolie, A; Hutton, RA; Lee, CA; Murdock, PJ; Owens, DL | 1 |
| Girolami, A; Sartori, MT; Simioni, P | 1 |
| Asakura, H; Ito, K; Matsuda, T; Okafuji, K; Saito, M; Yoshida, T | 1 |
| Capellato, MG; Girolami, A; Lazzaro, AR; Marafioti, F; Polato, G | 1 |
5 review(s) available for factor xiiib and Deficiency, Factor 13
| Article | Year |
|---|---|
Factor XIII: congenital deficiency factor XIII, acquired deficiency, factor XIII A-subunit, and factor XIII B-subunit.
Topics: Coagulants; Factor VIII; Factor XIII; Factor XIII Deficiency; Fibrin; Fibrinogen; Humans; Protein Conformation; Protein Stability; Recombinant Proteins | 2014 |
Factor XIII Deficiency.
Topics: Ammonia; Enzyme-Linked Immunosorbent Assay; Factor XIII; Factor XIII Deficiency; Female; Fibrinolysin; Genotype; Glutamate Dehydrogenase; Humans; Infant, Newborn; Phenotype; Postpartum Hemorrhage; Pregnancy | 2009 |
An update of the mutation profile of Factor 13 A and B genes.
Topics: Animals; Databases, Genetic; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Genetic Heterogeneity; Humans; Internet; Mutation; Phenotype | 2011 |
[Molecular pathology of the b subunit deficiency for factor XIII].
Topics: Factor XIII; Factor XIII Deficiency; Humans | 1997 |
[Deficiency of A or B subunit for coagulation factor XIII].
Topics: Amino Acid Sequence; Diagnosis, Differential; Factor XIII; Factor XIII Deficiency; Genes, Recessive; Humans; Molecular Sequence Data; Transglutaminases | 1998 |
1 trial(s) available for factor xiiib and Deficiency, Factor 13
| Article | Year |
|---|---|
Safety and pharmacokinetics of recombinant factor XIII-A2 administration in patients with congenital factor XIII deficiency.
Topics: Adult; Aged; Blood Coagulation; Blood Coagulation Tests; Dimerization; Dose-Response Relationship, Drug; Drug-Related Side Effects and Adverse Reactions; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Female; Humans; Male; Middle Aged; Pilot Projects; Recombinant Proteins; Solubility; Thrombelastography; Time Factors | 2006 |
15 other study(ies) available for factor xiiib and Deficiency, Factor 13
| Article | Year |
|---|---|
Sustained depletion of FXIII-A by inducing acquired FXIII-B deficiency.
Topics: Animals; Blood Platelets; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Gene Knockdown Techniques; Hemorrhage; Mice; Mice, Knockout; Nanoparticles; Rabbits; RNA, Small Interfering | 2020 |
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A
Topics: Adolescent; Adult; Child; Child, Preschool; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Female; Humans; Infant; Male; Models, Molecular; Mutation; Protein Conformation; Recombinant Proteins; Young Adult | 2017 |
Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family.
Topics: 3' Untranslated Regions; Asian People; China; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Female; Humans; Male; Mutation, Missense; Polymorphism, Genetic; Prenatal Diagnosis | 2018 |
Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiency.
Topics: Aged; Blood Coagulation; Blood Coagulation Tests; Coagulants; Factor XIII; Factor XIII Deficiency; Genetic Predisposition to Disease; Humans; Isoantibodies; Male; Mutation; Phenotype; Time Factors; Treatment Outcome | 2013 |
Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency.
Topics: Adult; Antibodies, Monoclonal; Antibodies, Monoclonal, Murine-Derived; Autoantibodies; Autoantigens; Blotting, Western; Enzyme-Linked Immunosorbent Assay; Factor XIII; Factor XIII Deficiency; Female; Hemorrhage; Humans; Immunoglobulins, Intravenous; Immunologic Factors; Immunosuppressive Agents; Kidney Failure, Chronic; Lupus Erythematosus, Systemic; Plasmapheresis; Renal Dialysis; Rituximab | 2009 |
Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.
Topics: Amino Acid Sequence; Base Sequence; Factor XIII; Factor XIII Deficiency; Factor XIIIa; Female; Founder Effect; Frameshift Mutation; Haplotypes; Humans; Male; Microsatellite Repeats; Molecular Sequence Data; Pedigree; Tunisia | 2010 |
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency.
Topics: DNA Mutational Analysis; Factor XIII; Factor XIII Deficiency; Family; Female; Genotype; Germany; Humans; Male; Mutation; Phenotype | 2010 |
Administration of factor XIII B subunit increased plasma factor XIII A subunit levels in factor XIII B subunit knock-out mice.
Topics: Animals; Disease Models, Animal; Factor XIII; Factor XIII Deficiency; Humans; Mice; Mice, Knockout; Recombinant Proteins | 2008 |
Male-specific cardiac pathologies in mice lacking either the A or B subunit of factor XIII.
Topics: Age Factors; Aging; Animals; Echocardiography; Factor XIII; Factor XIII Deficiency; Female; Fibrosis; GTP-Binding Proteins; Heart Diseases; Hematoma; Hemorrhage; Hemosiderin; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Myocarditis; Myocardium; Protein Glutamine gamma Glutamyltransferase 2; Sex Factors; Transglutaminases | 2008 |
A simple, quick one-step ELISA assay for the determination of complex plasma factor XIII (A2B2).
Topics: Antibodies, Monoclonal; Biotinylation; Cross Reactions; Enzyme-Linked Immunosorbent Assay; Factor XIII; Factor XIII Deficiency; Fibrinogen; Horseradish Peroxidase; Humans; Protein Structure, Quaternary; Reference Standards; Reproducibility of Results; Sensitivity and Specificity; Spectrophotometry; Transglutaminases | 2000 |
Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency.
Topics: Adult; Animals; Autoantigens; Base Sequence; Child; DNA Primers; Factor XIII; Factor XIII Deficiency; Female; Humans; Molecular Sequence Data; Mutation, Missense; Netherlands; Point Mutation; Sequence Alignment; Sequence Analysis, DNA | 2001 |
Development and evaluation of ELISAs for factor XIIIA and XIIIB subunits in plasma.
Topics: Adult; Crohn Disease; Enzyme-Linked Immunosorbent Assay; Factor XIII; Factor XIII Deficiency; Humans; Liver Diseases; Male; Reference Values; Reproducibility of Results; Transglutaminases | 1992 |
An updated classification of factor XIII defect.
Topics: Factor XIII; Factor XIII Deficiency; Humans; Transglutaminases | 1991 |
A familial factor XIII subunit B deficiency.
Topics: Adult; Blood Coagulation Factors; Blood Coagulation Tests; Factor XIII; Factor XIII Deficiency; Family; Female; Humans; Male; Pedigree | 1990 |
A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiency.
Topics: Adult; Factor XIII; Factor XIII Deficiency; Female; Heterozygote; Humans; Immunoassay; Pedigree; Thrombelastography; Transglutaminases | 1987 |