scholarly article | Q13442814 |
P2093 | author name string | E Johnson | |
F Tedesco | |||
C Casarsa | |||
H Langeggen | |||
M Pausa | |||
P2860 | cites work | Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 |
Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria | Q29616614 | ||
Two distinct abnormalities in patients with C8 alpha-gamma deficiency. Low level of C8 beta chain and presence of dysfunctional C8 alpha-gamma subunit | Q34260629 | ||
Regulation of the synthesis of C1 subcomponents and C1-inhibitor | Q34340423 | ||
Evolutionary conservation in the untranslated regions of actin mRNAs: DNA sequence of a human beta-actin cDNA. | Q35264401 | ||
The third component of complement is transcribed and secreted by cultured human endothelial cells | Q35856227 | ||
Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture | Q36355520 | ||
Complement biosynthesis by the human hepatoma-derived cell line HepG2 | Q36987205 | ||
Mononuclear phagocytes have the potential to synthesize the complete functional complement system | Q39643657 | ||
Effect of cytokines on the secretion of the fifth and eighth complement components by HepG2 cells | Q41498663 | ||
Endothelial cells in physiology and in the pathophysiology of vascular disorders | Q41757874 | ||
Reactive lysis: the complement-mediated lysis of unsensitized cells. II. The characterization of activated reactor as C56 and the participation of C8 and C9. | Q41762392 | ||
The cytolytically inactive terminal complement complex activates endothelial cells to express adhesion molecules and tissue factor procoagulant activity | Q41923727 | ||
In vitro biosynthesis of complement factor I by human endothelial cells | Q42459180 | ||
Biosynthesis of C3 by human mesangial cells. Modulation by proinflammatory cytokines | Q42477501 | ||
Monoclonal antibodies recognizing a neoantigen of poly(C9) detect the human terminal complement complex in tissue and plasma | Q43762567 | ||
The C5b-6 complex: formation, isolation, and inhibition of its activity by lipoprotein and the S-protein of human serum | Q43767406 | ||
Human umbilical vein endothelial cells synthesize functional C3, C5, C6, C8 and C9 in vitro | Q44091595 | ||
Complement activation occurs on subendothelial extracellular matrix in vitro and is initiated by retraction or removal of overlying endothelial cells | Q47936495 | ||
Biosynthesis of complement factor H by human umbilical vein endothelial cells. Regulation by T cell growth factor and IFN-gamma. | Q54357513 | ||
Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies | Q55670899 | ||
Organ-specific contribution to circulating C7 levels by the bone marrow and liver in humans | Q57089607 | ||
Differential regulation of complement factor H and C3 production in human umbilical vein endothelial cells by IFN-gamma and IL-1 | Q68416575 | ||
Expression of complement alternative pathway proteins by endothelial cells. Differential regulation by interleukin 1 and glucocorticoids | Q68428812 | ||
Synthesis of complement components C5, C6, C7, C8 and C9 in vitro by human monocytes and assembly of the terminal complement complex | Q69629002 | ||
Biosynthesis and secretion of the third component of complement by human endothelial cells in vitro | Q70341351 | ||
Interleukin-1 alpha, interleukin 6 and tumor necrosis factor alpha increase the synthesis and expression of the functional alternative and terminal complement pathways by human umbilical vein endothelial cells in vitro | Q71027197 | ||
How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusion | Q71446674 | ||
Human polymorphonuclear leukocytes store large amounts of terminal complement components C7 and C6, which may be released on stimulation | Q72169141 | ||
Paradoxical reconstitution of complement activity following plasma transfusion of an individual with deficiency of the seventh component of complement | Q72302250 | ||
Complement component C7. Assessment of in vivo synthesis after liver transplantation reveals that hepatocytes do not synthesize the majority of human C7 | Q72363605 | ||
Effect of gamma-interferon on the synthesis of the functional alternative and terminal complement pathways by human umbilical vein endothelial cells in vitro | Q72693834 | ||
P433 | issue | 1 | |
P304 | page(s) | 69-76 | |
P577 | publication date | 2000-07-01 | |
P1433 | published in | Clinical and Experimental Immunology | Q15716708 |
P1476 | title | The endothelium is an extrahepatic site of synthesis of the seventh component of the complement system | |
P478 | volume | 121 |
Q59791600 | Age and Sex-Associated Changes of Complement Activity and Complement Levels in a Healthy Caucasian Population |
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Q51076481 | Bispecific antibodies targeting tumor-associated antigens and neutralizing complement regulators increase the efficacy of antibody-based immunotherapy in mice. |
Q40669247 | Cloning and characterization of human complement component C7 promoter. |
Q33425421 | Complement Interactions with Blood Cells, Endothelial Cells and Microvesicles in Thrombotic and Inflammatory Conditions |
Q33217628 | Controlling complement resistance in cancer by using human monoclonal antibodies that neutralize complement-regulatory proteins CD55 and CD59. |
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Q37077537 | Decidual endothelial cells express surface-bound C1q as a molecular bridge between endovascular trophoblast and decidual endothelium |
Q52309394 | Extracellular Vesicles: Packages Sent With Complement. |
Q73343396 | HUVEC take up opsonized zymosan particles and secrete cytokines IL-6 and IL-8 in vitro |
Q28585139 | Hepatocyte nuclear factor 1alpha controls the expression of terminal complement genes |
Q56966003 | Hereditary complement C7 deficiency in nine families: Subtotal C7 deficiency revisited |
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Q35168168 | The interaction between circulating complement proteins and cutaneous microvascular endothelial cells in the development of childhood Henoch-Schönlein Purpura |
Q37154268 | Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. |
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