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M E de la Morena-Barrio

Showing results (1-10 of 12) with videos related to

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IEEE Journal of Biomedical and Health Informatics|August 23, 2022
Using Machine Learning for Predicting the Effect of Mutations in the Initiation CodonJ Castell-Diaz, F Abad-Navarro, M E de la Morena-Barrio, et al.
Journal of Thrombosis and Haemostasis : JTH|October 23, 2012
Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophiliaM E de la Morena-Barrio, T S Sevivas, I Martinez-Martinez, et al.
Journal of Thrombosis and Haemostasis : JTH|May 15, 2014
Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutationsS Aguila, J Navarro-Fernández, N Bohdan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 30, 2017
High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla studyJ Esteban, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Thrombosis Research|December 4, 2010
Heparin affinity of factor VIIa: implications on the physiological inhibition by antithrombin and clearance of recombinant factor VIIaI Martínez-Martínez, A Ordóñez, S Pedersen, et al.
Medical Hypotheses|April 13, 2020
When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish ReconquistaF Bauduer, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Thrombosis Research|July 19, 2015
A new method to quantify β-antithrombin glycoform in plasma reveals increased levels during the acute stroke eventM E de la Morena-Barrio, A García, I Martínez-Martínez, et al.
Clinical Reviews in Allergy & Immunology|March 16, 2021
Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys VariantR López-Gálvez, M E de la Morena-Barrio, A Miñano, et al.
Thrombosis Research|January 7, 2014
Proteomic analysis of platelet N-glycoproteins in PMM2-CDG patientsM E de la Morena-Barrio, M Di Michele, M L Lozano, et al.
British Journal of Haematology|July 21, 2020
Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryoC Bravo-Pérez, M E de la Morena-Barrio, A Palomo, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
IEEE Journal of Biomedical and Health Informatics|August 23, 2022
Using Machine Learning for Predicting the Effect of Mutations in the Initiation CodonJ Castell-Diaz, F Abad-Navarro, M E de la Morena-Barrio, et al.
Journal of Thrombosis and Haemostasis : JTH|October 23, 2012
Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophiliaM E de la Morena-Barrio, T S Sevivas, I Martinez-Martinez, et al.
Journal of Thrombosis and Haemostasis : JTH|May 15, 2014
Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutationsS Aguila, J Navarro-Fernández, N Bohdan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 30, 2017
High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla studyJ Esteban, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Thrombosis Research|December 4, 2010
Heparin affinity of factor VIIa: implications on the physiological inhibition by antithrombin and clearance of recombinant factor VIIaI Martínez-Martínez, A Ordóñez, S Pedersen, et al.
Medical Hypotheses|April 13, 2020
When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish ReconquistaF Bauduer, M E de la Morena-Barrio, S Salloum-Asfar, et al.
Thrombosis Research|July 19, 2015
A new method to quantify β-antithrombin glycoform in plasma reveals increased levels during the acute stroke eventM E de la Morena-Barrio, A García, I Martínez-Martínez, et al.
Clinical Reviews in Allergy & Immunology|March 16, 2021
Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys VariantR López-Gálvez, M E de la Morena-Barrio, A Miñano, et al.
Thrombosis Research|January 7, 2014
Proteomic analysis of platelet N-glycoproteins in PMM2-CDG patientsM E de la Morena-Barrio, M Di Michele, M L Lozano, et al.
British Journal of Haematology|July 21, 2020
Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryoC Bravo-Pérez, M E de la Morena-Barrio, A Palomo, et al.
Pageof 2