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Anja Roos

Showing results (61-70 of 71) with videos related to

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European Journal of Immunology|March 21, 2003
Biochemical and functional characterization of the interaction between pentraxin 3 and C1qAlma J Nauta, Barbara Bottazzi, Alberto Mantovani, et al.
Biochemistry|September 20, 2006
Structure and function of the long pentraxin PTX3 glycosidic moiety: fine-tuning of the interaction with C1q and complement activationAntonio Inforzato, Giuseppe Peri, Andrea Doni, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 28, 2009
Both complement and IgG fc receptors are required for development of attenuated antiglomerular basement membrane nephritis in miceMarielle A Otten, Tom W L Groeneveld, Roelof Flierman, et al.
Gastroenterology|August 9, 2005
Mannose binding lectin gene polymorphisms confer a major risk for severe infections after liver transplantationLee H Bouwman, Anja Roos, Onno T Terpstra, et al.
Clinical & Translational Immunology|November 8, 2021
A novel method to standardise serum IgA measurements shows an increased prevalence of IgA deficiency in young children with recurrent respiratory tract infectionsMischa H Koenen, Madeleen Bosma, Udo A Roorda, et al.
Journal of Hepatology|February 22, 2011
Mannose-binding lectin and ficolin-2 gene polymorphisms predispose to cytomegalovirus (re)infection after orthotopic liver transplantationBert-Jan F de Rooij, Martha T van der Beek, Bart van Hoek, et al.
European Journal of Immunology|August 13, 2004
Antibody-mediated activation of the classical pathway of complement may compensate for mannose-binding lectin deficiencyAnja Roos, Peter Garred, Manon E Wildenberg, et al.
Hepatology (Baltimore, Md.)|July 2, 2010
Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantationBert-Jan F de Rooij, Bart van Hoek, W Rogier ten Hove, et al.
Immunobiology|December 3, 2014
Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infectionsRosanne A van Schaarenburg, Nina A Daha, Joris J M Schonkeren, et al.
Pediatric Nephrology (Berlin, Germany)|October 9, 2016
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndromeDineke Westra, Elena B Volokhina, Renate G van der Molen, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
European Journal of Immunology|March 21, 2003
Biochemical and functional characterization of the interaction between pentraxin 3 and C1qAlma J Nauta, Barbara Bottazzi, Alberto Mantovani, et al.
Biochemistry|September 20, 2006
Structure and function of the long pentraxin PTX3 glycosidic moiety: fine-tuning of the interaction with C1q and complement activationAntonio Inforzato, Giuseppe Peri, Andrea Doni, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 28, 2009
Both complement and IgG fc receptors are required for development of attenuated antiglomerular basement membrane nephritis in miceMarielle A Otten, Tom W L Groeneveld, Roelof Flierman, et al.
Gastroenterology|August 9, 2005
Mannose binding lectin gene polymorphisms confer a major risk for severe infections after liver transplantationLee H Bouwman, Anja Roos, Onno T Terpstra, et al.
Clinical & Translational Immunology|November 8, 2021
A novel method to standardise serum IgA measurements shows an increased prevalence of IgA deficiency in young children with recurrent respiratory tract infectionsMischa H Koenen, Madeleen Bosma, Udo A Roorda, et al.
Journal of Hepatology|February 22, 2011
Mannose-binding lectin and ficolin-2 gene polymorphisms predispose to cytomegalovirus (re)infection after orthotopic liver transplantationBert-Jan F de Rooij, Martha T van der Beek, Bart van Hoek, et al.
European Journal of Immunology|August 13, 2004
Antibody-mediated activation of the classical pathway of complement may compensate for mannose-binding lectin deficiencyAnja Roos, Peter Garred, Manon E Wildenberg, et al.
Hepatology (Baltimore, Md.)|July 2, 2010
Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantationBert-Jan F de Rooij, Bart van Hoek, W Rogier ten Hove, et al.
Immunobiology|December 3, 2014
Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infectionsRosanne A van Schaarenburg, Nina A Daha, Joris J M Schonkeren, et al.
Pediatric Nephrology (Berlin, Germany)|October 9, 2016
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndromeDineke Westra, Elena B Volokhina, Renate G van der Molen, et al.
Pageof 8