Works matching DE "BLOOD coagulation factor XIII"
Results: 464
Dynamics of Factor XIII Levels After Open Heart Surgery for Congenital Heart Defects: Do Cyanotic and Acyanotic Patients Differ?
- Published in:
- Pediatric Cardiology, 2014, v. 35, n. 7, p. 1108, doi. 10.1007/s00246-014-0903-9
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- Publication type:
- Article
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency (Communicated by Edward Tuddenham) Online Citation: Human Mutation, Mutation in Brief #677 (2003) Online http://www.interscience.wiley.com/homepages/38515/pdf/mutation/677.pdf)
- Published in:
- Human Mutation, 2004, v. 23, n. 1, p. 98, doi. 10.1002/humu.9206
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- Publication type:
- Article
Diagnostic Approach to Patients with Low Serum Alkaline Phosphatase.
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- Calcified Tissue International, 2023, v. 112, n. 3, p. 289, doi. 10.1007/s00223-022-01039-y
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- Publication type:
- Article
Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 2135, doi. 10.3906/sag-2006-107
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- Publication type:
- Article
Precise CRISPR-Cas9 gene repair in autologous memory T cells to treat familial hemophagocytic lymphohistiocytosis.
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- Science Immunology, 2024, v. 9, n. 92, p. 1, doi. 10.1126/sciimmunol.adi0042
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- Article
Screening for Celiac Disease Using Anti Tissue ransglutaminase in Patients with Esophageal SCC between 2004 and 2009.
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- Journal of Cardio-Thoracic Medicine, 2015, v. 3, n. 1, p. 254
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- Publication type:
- Article
DETERMINATION OF CYTOKINE STATUS INDICATORS AND ANGIOGENESIS FACTORS IN PATIENTS WITH EXTERNAL GENITAL ENDOMETRIOSIS AND VITAMIN D DEFICIENCY.
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- Periódico Tchê Química, 2020, v. 17, n. 34, p. 251, doi. 10.52571/ptq.v17.n34.2020.268_p34_pgs_251_259.pdf
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- Publication type:
- Article
A Comprehensive Update on Late-Onset Pompe Disease.
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- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1279, doi. 10.3390/biom13091279
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- Publication type:
- Article
Type I interferon receptor (IFNAR2) deficiency reveals Zika virus cytopathicity in human macrophages and microglia.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.1035532
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- Publication type:
- Article
Endothelial deletion of PTBP1 disrupts ventricular chamber development.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37409-9
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- Publication type:
- Article
Lewis Ayres und H. Clifton Ward, Hgg.: The Rise of the Early Christian Intellectual, Arbeiten zur Kirchengeschichte 139, Berlin (de Gruyter) 2020, XIII + 272 S., ISBN 978-3-11-060755-0, € 86,95.
- Published in:
- 2021
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- Publication type:
- Book Review
Compilation of Genotype and Phenotype Data in GCDH -LOVD for Variant Classification and Further Application.
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- Genes, 2023, v. 14, n. 12, p. 2218, doi. 10.3390/genes14122218
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- Publication type:
- Article
Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation.
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- 2022
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- Publication type:
- Case Study
A Common Missense Variant Causing Factor XI Deficiency and Increased Bleeding Tendency in Maine Coon Cats.
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- Genes, 2022, v. 13, n. 5, p. 792, doi. 10.3390/genes13050792
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- Publication type:
- Article
Detection of 46, XY Disorder of Sex Development (DSD) Based on Plasma Cell-Free DNA and Targeted Next-Generation Sequencing.
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- Genes, 2021, v. 12, n. 12, p. 1890, doi. 10.3390/genes12121890
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- Publication type:
- Article
Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese Pedigree.
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- Genes, 2021, v. 12, n. 10, p. 1521, doi. 10.3390/genes12101521
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- Publication type:
- Article
Effects of Cocoa Genotypes on Coat Color, Platelets and Coagulation Parameters in French Bulldogs.
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- Genes, 2021, v. 12, n. 7, p. 1092, doi. 10.3390/genes12071092
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- Publication type:
- Article
Somatostatin- and Factor XIIIa-immunoreactive Cells in Psoriasis during Clobetasol Propionate and Calcipotriol treatment.
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- Acta Dermato-Venereologica, 1999, v. 79, n. 1, p. 44, doi. 10.1080/000155599750011697
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- Publication type:
- Article
Valproate induces reversible factor XIII deficiency with risk of perioperative bleeding.
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- Acta Neurologica Scandinavica, 2003, v. 108, n. 2, p. 142, doi. 10.1034/j.1600-0404.2003.00149.x
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- Publication type:
- Article
How an engineered therapy could replace the need for potentially harmful plasma infusions.
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- Expert Review of Clinical Pharmacology, 2019, v. 12, n. 4, p. 289, doi. 10.1080/17512433.2019.1588109
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- Publication type:
- Article
Vitamin B12 deficiency in diabetic patients treated with metformin: A cross-sectional study.
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- PLoS ONE, 2024, v. 19, n. 4, p. 1, doi. 10.1371/journal.pone.0302500
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- Publication type:
- Article
The contact system in liver injury.
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- Seminars in Immunopathology, 2021, v. 43, n. 4, p. 507, doi. 10.1007/s00281-021-00876-7
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- Publication type:
- Article
The procoagulant and proinflammatory plasma contact system.
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- Seminars in Immunopathology, 2012, v. 34, n. 1, p. 31, doi. 10.1007/s00281-011-0288-2
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- Publication type:
- Article
Biomarkers Involved in the Pathogenesis of Hemophilic Arthropathy.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 18, p. 9897, doi. 10.3390/ijms25189897
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- Publication type:
- Article
Morquio A Syndrome: Identification of Differential Patterns of Molecular Pathway Interactions in Bone Lesions.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 6, p. 3232, doi. 10.3390/ijms25063232
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- Publication type:
- Article
Late-Onset Pompe Disease with Normal Creatine Kinase Levels: The Importance of Rheumatological Suspicion.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 21, p. 15924, doi. 10.3390/ijms242115924
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- Publication type:
- Article
Computational Exploration of the Effects of Mutations on GABA Aminotransferase in GABA Aminotransferase Deficiency.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 13, p. 10933, doi. 10.3390/ijms241310933
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- Publication type:
- Article
The Magic of Proteases: From a Procoagulant and Anticoagulant Factor V to an Equitable Treatment of Its Inherited Deficiency.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6243, doi. 10.3390/ijms24076243
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- Publication type:
- Article
Autoimmune Diseases Affecting Hemostasis: A Narrative Review.
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- 2022
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- Publication type:
- Literature Review
The Effect of Activated FXIII, a Transglutaminase, on Vascular Smooth Muscle Cells.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 10, p. 5845, doi. 10.3390/ijms23105845
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- Publication type:
- Article
Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 4725, doi. 10.3390/ijms23094725
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- Publication type:
- Article
The Role of GRP and MGP in the Development of Non-Hemorrhagic VKCFD1 Phenotypes.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 2, p. 798, doi. 10.3390/ijms23020798
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- Publication type:
- Article
A Brief Review on Vitamin B 12 Deficiency Looking at Some Case Study Reports in Adults.
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- 2021
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- Publication type:
- Case Study
Investigating Immune Responses to the scAAV9- HEXM Gene Therapy Treatment in Tay–Sachs Disease and Sandhoff Disease Mouse Models.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6751, doi. 10.3390/ijms22136751
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- Publication type:
- Article
Clinical Validation of an Automated Fluorogenic Factor XIII Activity Assay Based on Isopeptidase Activity.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1002, doi. 10.3390/ijms22031002
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- Publication type:
- Article
Effect of Mitochondrial and Cytosolic FXN Isoform Expression on Mitochondrial Dynamics and Metabolism.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 21, p. 8251, doi. 10.3390/ijms21218251
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- Publication type:
- Article
Protein Degradation and the Pathologic Basis of Phenylketonuria and Hereditary Tyrosinemia.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 14, p. 4996, doi. 10.3390/ijms21144996
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- Publication type:
- Article
Acid Sphingomyelinase Deficiency Ameliorates Farber Disease.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 24, p. 6253, doi. 10.3390/ijms20246253
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- Publication type:
- Article
Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 23, p. 5963, doi. 10.3390/ijms20235963
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- Publication type:
- Article
Characterization of L-amino Acid Oxidase Derived from Crotalus adamanteus Venom: Procoagulant and Anticoagulant Activities.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4853, doi. 10.3390/ijms20194853
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- Publication type:
- Article
Identification of Potential Novel Interacting Partners for Coagulation Factor XIII B (FXIII-B) Subunit, a Protein Associated with a Rare Bleeding Disorder.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 11, p. 2682, doi. 10.3390/ijms20112682
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- Publication type:
- Article
Extravascular fibrin, plasminogen activator, plasminogen activator inhibitors, and airway hyperresponsiveness.
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- 2004
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- Publication type:
- journal article
The Effects of Fibrin on Intraperitoneal Tumour Growth; The Tumour Cell Entrapment Theory Revisited.
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- European Surgical Research, 2004, v. 36, p. 119
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- Publication type:
- Article
Effectiveness of Coagulation Factor XIII Concentrate for Reversing Loss of Tensile Strength of Rat Intestinal Anastomoses.
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- European Surgical Research, 2004, v. 36, n. 1, p. 53, doi. 10.1159/000075075
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- Publication type:
- Article
Navigating thrombotic terrain: unveiling a novel homocystinuria mutation associated with thrombophilia in a 16 year old.
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- Bulletin of the National Research Centre, 2024, v. 48, n. 1, p. 1, doi. 10.1186/s42269-024-01198-y
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- Publication type:
- Article
Poruchy cyklu močoviny, Arginin Chlorid v léčbě hyperamonémie.
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- Klinická Biochemie a Metabolismus, 2021, v. 29, n. 4, p. 209
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- Publication type:
- Article
Transglutaminase 2 contributes to a TP53-induced autophagy program to prevent oncogenic transformation.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.07101
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- Publication type:
- Article
Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation.
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- British Journal of Dermatology, 2009, v. 161, n. 2, p. 456, doi. 10.1111/j.1365-2133.2009.09277.x
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- Publication type:
- Article
Impaired B-cell function in ERCC2 deficiency.
- Published in:
- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1423141
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- Publication type:
- Article
DNA and histones impair the mechanical stability and lytic susceptibility of fibrin formed by staphylocoagulase.
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- Frontiers in Immunology, 2023, p. 01, doi. 10.3389/fimmu.2023.1233128
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- Publication type:
- Article