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The Magic of Proteases: From a Procoagulant and Anticoagulant Factor V to an Equitable Treatment of Its Inherited Deficiency.
De Pablo-Moreno JA, Miguel-Batuecas A, de Sancha M, Liras A. De Pablo-Moreno JA, et al. Int J Mol Sci. 2023 Mar 26;24(7):6243. doi: 10.3390/ijms24076243. Int J Mol Sci. 2023. PMID: 37047215 Free PMC article. Review.
However, this magic has an insidious side to it, as it may also prevent the completion of the clinical value chain of factor V deficiency. This value chain encompasses the discovery of knowledge, the transfer of this knowledge, and its translation to clinical …
However, this magic has an insidious side to it, as it may also prevent the completion of the clinical value chain of factor V
Development and Characterization of a Factor V-Deficient CRISPR Cell Model for the Correction of Mutations.
Serrano LJ, Garcia-Arranz M, De Pablo-Moreno JA, Segovia JC, Olivera-Salazar R, Garcia-Olmo D, Liras A. Serrano LJ, et al. Int J Mol Sci. 2022 May 22;23(10):5802. doi: 10.3390/ijms23105802. Int J Mol Sci. 2022. PMID: 35628611 Free PMC article.
Factor V deficiency, an ultra-rare congenital coagulopathy, is characterized by bleeding episodes that may be more or less intense as a function of the levels of coagulation factor activity present in plasma. Fresh-frozen plasma, often used to treat patients
Factor V deficiency, an ultra-rare congenital coagulopathy, is characterized by bleeding episodes that may be more or l
Cell therapy for factor V deficiency: An approach based on human decidua mesenchymal stem cells.
Serrano LJ, de la Torre P, Liras A, Flores AI. Serrano LJ, et al. Biomed Pharmacother. 2021 Oct;142:112059. doi: 10.1016/j.biopha.2021.112059. Epub 2021 Aug 28. Biomed Pharmacother. 2021. PMID: 34467894 Free article.
This study was designed to lay the preliminary foundations for future cell-based therapy for patients with severe factor V deficiency. The study showed that hepatospheres, which produce coagulation factors VIII, IX, and V, synthetize and store intracellular g …
This study was designed to lay the preliminary foundations for future cell-based therapy for patients with severe factor V
Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 and two variants specific to East Asians.
Lin HY, Lin CY, Kuo SF, Lin JS, Lin PT, Huang YC, Hsieh HN, Shen MC. Lin HY, et al. Blood Coagul Fibrinolysis. 2023 Jan 1;34(1):8-13. doi: 10.1097/MBC.0000000000001162. Epub 2022 Aug 22. Blood Coagul Fibrinolysis. 2023. PMID: 35946468 Free PMC article.
Congenital coagulation factor V deficiency (FVD) is a rare, autosomal recessive bleeding disorder. ...
Congenital coagulation factor V deficiency (FVD) is a rare, autosomal recessive bleeding disorder. ...
Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report.
Al Khudari R, Batesh D, Habash R, Hamdn O. Al Khudari R, et al. J Med Case Rep. 2023 Nov 18;17(1):480. doi: 10.1186/s13256-023-04215-2. J Med Case Rep. 2023. PMID: 37978530 Free PMC article.
Hemophilia with Turner syndrome is a very rare case, but the combination of Turner syndrome, hemophilia, and factor V deficiency is an isolated case that has never been recorded in the medical literature. ...The lab tests showed: prolonged activated partial t …
Hemophilia with Turner syndrome is a very rare case, but the combination of Turner syndrome, hemophilia, and factor V defic
48 results