Search research articles
Contact Us
Filters
Showing results (61-70 of 71) with videos related to
Page
of 8
Sort By:
European Journal of Immunology
|
March 21, 2003
Biochemical and functional characterization of the interaction between pentraxin 3 and C1q
Alma 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 activation
Antonio 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 mice
Marielle 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 transplantation
Lee 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 infections
Mischa 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 transplantation
Bert-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 deficiency
Anja 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 transplantation
Bert-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 infections
Rosanne 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 syndrome
Dineke Westra, Elena B Volokhina, Renate G van der Molen, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
European Journal of Immunology
|
March 21, 2003
Biochemical and functional characterization of the interaction between pentraxin 3 and C1q
Alma 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 activation
Antonio 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 mice
Marielle 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 transplantation
Lee 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 infections
Mischa 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 transplantation
Bert-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 deficiency
Anja 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 transplantation
Bert-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 infections
Rosanne 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 syndrome
Dineke Westra, Elena B Volokhina, Renate G van der Molen, et al.
Page
of 8