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Agustín Tortajada

Showing results (1-10 of 23) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 1, 2013
Structural basis for the stabilization of the complement alternative pathway C3 convertase by properdinMartín Alcorlo, Agustín Tortajada, Santiago Rodríguez de Córdoba, et al.
Seminars in Thrombosis and Hemostasis|May 7, 2014
Genetics of atypical hemolytic uremic syndrome (aHUS)Santiago Rodríguez de Córdoba, Marta Subías Hidalgo, Sheila Pinto, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2009
3D structure of the C3bB complex provides insights into the activation and regulation of the complement alternative pathway convertaseEva Torreira, Agustín Tortajada, Tamara Montes, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 6, 2009
Coexistence of closed and open conformations of complement factor B in the alternative pathway C3bB(Mg2+) proconvertaseEva Torreira, Agustín Tortajada, Tamara Montes, et al.
Kidney International|August 13, 2010
Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndromeSvetlana Hakobyan, Agustín Tortajada, Claire L Harris, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2009
Functional basis of protection against age-related macular degeneration conferred by a common polymorphism in complement factor BTamara Montes, Agustín Tortajada, B Paul Morgan, et al.
Seminars in Immunopathology|August 16, 2017
How novel structures inform understanding of complement functionElena Goicoechea de Jorge, Hugo Yebenes, Marina Serna, et al.
Immunobiology|May 9, 2026
Factor H-related proteins as a protective evolutionary mechanism against microbial infectionsRosario García-Sánchez, Alberto López-Lera, Laura González-Sánchez, et al.
Human Molecular Genetics|June 25, 2009
The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activityAgustín Tortajada, Tamara Montes, Rubén Martínez-Barricarte, et al.
Kidney International|September 2, 2011
Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significanceAgustín Tortajada, Sheila Pinto, Jorge Martínez-Ara, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|August 1, 2013
Structural basis for the stabilization of the complement alternative pathway C3 convertase by properdinMartín Alcorlo, Agustín Tortajada, Santiago Rodríguez de Córdoba, et al.
Seminars in Thrombosis and Hemostasis|May 7, 2014
Genetics of atypical hemolytic uremic syndrome (aHUS)Santiago Rodríguez de Córdoba, Marta Subías Hidalgo, Sheila Pinto, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2009
3D structure of the C3bB complex provides insights into the activation and regulation of the complement alternative pathway convertaseEva Torreira, Agustín Tortajada, Tamara Montes, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 6, 2009
Coexistence of closed and open conformations of complement factor B in the alternative pathway C3bB(Mg2+) proconvertaseEva Torreira, Agustín Tortajada, Tamara Montes, et al.
Kidney International|August 13, 2010
Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndromeSvetlana Hakobyan, Agustín Tortajada, Claire L Harris, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2009
Functional basis of protection against age-related macular degeneration conferred by a common polymorphism in complement factor BTamara Montes, Agustín Tortajada, B Paul Morgan, et al.
Seminars in Immunopathology|August 16, 2017
How novel structures inform understanding of complement functionElena Goicoechea de Jorge, Hugo Yebenes, Marina Serna, et al.
Immunobiology|May 9, 2026
Factor H-related proteins as a protective evolutionary mechanism against microbial infectionsRosario García-Sánchez, Alberto López-Lera, Laura González-Sánchez, et al.
Human Molecular Genetics|June 25, 2009
The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activityAgustín Tortajada, Tamara Montes, Rubén Martínez-Barricarte, et al.
Kidney International|September 2, 2011
Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significanceAgustín Tortajada, Sheila Pinto, Jorge Martínez-Ara, et al.
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