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Journal of Immunology (Baltimore, Md. : 1950)
|
February 28, 2018
FHR5 Binds to Laminins, Uses Separate C3b and Surface-Binding Sites, and Activates Complement on Malondialdehyde-Acetaldehyde Surfaces
Ramona B Rudnick, Qian Chen, Emma Diletta Stea, et al.
Frontiers in Immunology
|
December 12, 2019
Enolase From <i>Aspergillus fumigatus</i> Is a Moonlighting Protein That Binds the Human Plasma Complement Proteins Factor H, FHL-1, C4BP, and Plasminogen
Prasad Dasari, Naile Koleci, Iordana A Shopova, et al.
Molecular Immunology
|
May 2, 2015
The role of complement in C3 glomerulopathy
Peter F Zipfel, Christine Skerka, Qian Chen, et al.
Journal of Bacteriology
|
October 11, 2021
The Protease SplB of Staphylococcus aureus Targets Host Complement Components and Inhibits Complement-Mediated Bacterial Opsonophagocytosis
Prasad Dasari, Maria Nordengrün, Cláudia Vilhena, et al.
Human Molecular Genetics
|
September 17, 2010
An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)
Lars G Fritsche, Nadine Lauer, Andrea Hartmann, et al.
The Journal of Infectious Diseases
|
October 3, 2017
Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells
Christian Meinel, Giuseppina Spartà, Hans-Martin Dahse, et al.
The American Journal of Pathology
|
September 30, 2005
Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site
T Sakari Jokiranta, Zhu-Zhu Cheng, Harald Seeberger, et al.
Journal of the American Society of Nephrology : JASN
|
December 13, 2005
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions
Mihály Józsi, Stefan Heinen, Andrea Hartmann, et al.
Frontiers in Immunology
|
December 15, 2016
Complement Regulator FHR-3 Is Elevated either Locally or Systemically in a Selection of Autoimmune Diseases
Nicole Schäfer, Antje Grosche, Joerg Reinders, et al.
Frontiers in Plant Science
|
April 6, 2019
Recombinant Production of MFHR1, A Novel Synthetic Multitarget Complement Inhibitor, in Moss Bioreactors
Oguz Top, Juliana Parsons, Lennard L Bohlender, et al.
Page
of 28
Search research articles
Search
Showing results (211-220 of 273) with videos related to
Sort By:
Page
of 28
Journal of Immunology (Baltimore, Md. : 1950)
|
February 28, 2018
FHR5 Binds to Laminins, Uses Separate C3b and Surface-Binding Sites, and Activates Complement on Malondialdehyde-Acetaldehyde Surfaces
Ramona B Rudnick, Qian Chen, Emma Diletta Stea, et al.
Frontiers in Immunology
|
December 12, 2019
Enolase From <i>Aspergillus fumigatus</i> Is a Moonlighting Protein That Binds the Human Plasma Complement Proteins Factor H, FHL-1, C4BP, and Plasminogen
Prasad Dasari, Naile Koleci, Iordana A Shopova, et al.
Molecular Immunology
|
May 2, 2015
The role of complement in C3 glomerulopathy
Peter F Zipfel, Christine Skerka, Qian Chen, et al.
Journal of Bacteriology
|
October 11, 2021
The Protease SplB of Staphylococcus aureus Targets Host Complement Components and Inhibits Complement-Mediated Bacterial Opsonophagocytosis
Prasad Dasari, Maria Nordengrün, Cláudia Vilhena, et al.
Human Molecular Genetics
|
September 17, 2010
An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)
Lars G Fritsche, Nadine Lauer, Andrea Hartmann, et al.
The Journal of Infectious Diseases
|
October 3, 2017
Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells
Christian Meinel, Giuseppina Spartà, Hans-Martin Dahse, et al.
The American Journal of Pathology
|
September 30, 2005
Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site
T Sakari Jokiranta, Zhu-Zhu Cheng, Harald Seeberger, et al.
Journal of the American Society of Nephrology : JASN
|
December 13, 2005
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions
Mihály Józsi, Stefan Heinen, Andrea Hartmann, et al.
Frontiers in Immunology
|
December 15, 2016
Complement Regulator FHR-3 Is Elevated either Locally or Systemically in a Selection of Autoimmune Diseases
Nicole Schäfer, Antje Grosche, Joerg Reinders, et al.
Frontiers in Plant Science
|
April 6, 2019
Recombinant Production of MFHR1, A Novel Synthetic Multitarget Complement Inhibitor, in Moss Bioreactors
Oguz Top, Juliana Parsons, Lennard L Bohlender, et al.
Page
of 28