Results 31 to 40 of about 550,801 (291)
Biochemical and functional studies on mouse ficolin-B, a novel pattern recognition molecule of the innate immune system [PDF]
Ficolins are members of the collectin family of proteins which in human and mice are able to recognize pathogen associated molecular patterns (PAMPs) on microbial surfaces.
Elumalai, Preetham
core +1 more source
Whooping cough, or pertussis, is a contagious disease of the respiratory tract that is re-emerging worldwide despite high vaccination coverage. The causative agent of this disease is the Gram-negative Bordetella pertussis. Knowledge on complement evasion
Elise S Hovingh +5 more
doaj +1 more source
BackgroundIschemia/reperfusion injury of lower extremities and associated lung damage may result from thrombotic occlusion, embolism, trauma, or surgical intervention with prolonged ischemia and subsequent restoration of blood flow.
Claudia Duehrkop +8 more
doaj +1 more source
Proteomic profiling of IgA nephropathy reveals distinct molecular prognostic subtypes
Summary: IgA nephropathy (IgAN) is a heterogeneous disease, which poses a series of challenges to accurate diagnosis and personalized therapy. Herein, we constructed a systematic quantitative proteome atlas from 59 IgAN and 19 normal control donors ...
Xizhao Chen +14 more
doaj +1 more source
C1-inhibitor treatment in patients with severe complement-mediated autoimmune hemolytic anemia [PDF]
Complement-mediated (CM) autoimmune hemolytic anemia (AIHA) is characterized by the destruction of red blood cells (RBCs) by autoantibodies that activate the classical complement pathway. These antibodies also reduce transfusion efficacy via the lysis of
Zeerleder, S. +14 more
core +1 more source
Background Immune-mediated hemolytic anemia (IMHA) is a common disease that affects all breeds of dogs and is associated with significant morbidity and mortality.
Robert Goggs, Erica Behling-Kelly
doaj +1 more source
IgG3 is unique among the IgG subclasses due to its extended hinge, allotypic diversity and enhanced effector functions, including highly efficient pathogen neutralisation and complement activation.
Leoni Abendstein +6 more
doaj +1 more source
BackgroundHereditary Angioedema with C1-inhibitor deficiency (C1-INH-HAE) is a rare disease characterized by recurrent subcutaneous and/or submucosal edematous (HAE) episodes, which may occur at any age.
Noémi Andrási +10 more
doaj +1 more source
The serpin C1 inhibitor (C1-INH) is the only regulator of classical complement activation as well as the major regulator of the contact system. Its importance is demonstrated by hereditary angioedema (HAE), a severe disease with potentially life ...
Ann-Kathrin Schoenfeld +2 more
doaj +1 more source
C1-inactivator is upregulated in glioblastoma.
BackgroundGlioblastoma is the most common and aggressive type of primary brain tumor in adults. A key problem is the capacity of glioma cells to inactivate the body's immune response.
Karolina Förnvik +5 more
doaj +1 more source

