Digitale Bibliotheek
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                             205 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A complement-dependent human long-noncoding RNA induced by Staphylococcus aureus Karlsen, Bård O.
2017
89 C p. 151-
1 p.
artikel
2 Acquisition of C1 inhibitor by Bordetella pertussis Vag8 results in C2 and C4 consumption away from the bacterial surface Hovingh, Elise S.
2017
89 C p. 152-153
2 p.
artikel
3 A cryptic non-GPI anchored form of CD59 facilitates insulin secretion from pancreatic beta cells King, Ben C.
2017
89 C p. 135-
1 p.
artikel
4 Activation of alternative complement pathway without complement factor D Zhang, Yuzhou
2017
89 C p. 173-
1 p.
artikel
5 Activation of complement by pigment epithelium-derived factor (PEDF) in rheumatoid arthritis Vogt, Leonie M.
2017
89 C p. 116-117
2 p.
artikel
6 Activation of C1, the complex initiating the classical pathway of the complement cascade, through cross-complex activation of proteases Thiel, Steffen
2017
89 C p. 141-142
2 p.
artikel
7 Activation of the alternative pathway of complement, represented by factor Bb, is longitudinally associated with late β-cell conservation in type 2 diabetes: The CODAM study van Greevenbroek, Marleen
2017
89 C p. 189-
1 p.
artikel
8 Administration of intravenous iron preparations induces complement activation in anemic patients Faria, B.
2017
89 C p. 180-
1 p.
artikel
9 Altered expression of complement factors in patients with nasal polyps in response to the TLR3 ligand PolyI:C Werner, Ulrike
2017
89 C p. 138-139
2 p.
artikel
10 A multi-center method comparison for detection of autoantibodies to human complement Factor H (AFH) Willrich, Maria Alice
2017
89 C p. 118-
1 p.
artikel
11 Analysis of C3 gene variants in patients with idiopathic, recurrent, spontaneous pregnancy loss Mohlin, Frida C.
2017
89 C p. 147-
1 p.
artikel
12 Analysis of complement gene variants in the clinical laboratory: Comparison of Next-Generation Sequencing (NGS) and Sanger methods Lagerstedt, Susan A.
2017
89 C p. 149-
1 p.
artikel
13 Analysis of Factor D isoforms in 3MC patients highlights the role of MASP-3 as a maturase in the alternative pathway of complement Pihl, Rasmus
2017
89 C p. 144-
1 p.
artikel
14 A new complement evasion strategy: How S. pyogenes exploits IgGs to recruit more C4BP Ermert, David
2017
89 C p. 155-
1 p.
artikel
15 A novel endothelial cell based complement dependent cytotoxicity test in kidney transplantation Lammerts, R.G.M.
2017
89 C p. 209-
1 p.
artikel
16 A novel model for complement studies and intervention in kidney ischemia/reperfusion injury Schjalm, Camilla
2017
89 C p. 208-209
2 p.
artikel
17 A novel nanobody inhibitor of the alternative pathway Jensen, Rasmus Kjeldsen
2017
89 C p. 198-
1 p.
artikel
18 Anti-factor H autoantibodies in Tunisian aHUS patients Sellami, M. Kallel
2017
89 C p. 184-
1 p.
artikel
19 Anti-H-factor autoantibodies in inflammatory myopathies Marie, Senant
2017
89 C p. 119-
1 p.
artikel
20 Antimicrobial peptides of invertebrates influence on the complement activity Umnyakova, Ekaterina S.
2017
89 C p. 196-
1 p.
artikel
21 APL-2, a complement C3 inhibitor, may potentially reduce both intravascular and extravascular hemolysis in patients with paroxysmal nocturnal hemoglobinuria Mehdi, Delphine El
2017
89 C p. 115-
1 p.
artikel
22 A protective role of complement regulators linked to a PEG phospholipid construct in reducing ischemic reperfusion injury in transplantation Nilsson, Bo
2017
89 C p. 208-
1 p.
artikel
23 Assessment of complement and NK cell activation in GalTKO/hCD46/HLA-E porcine hearts ex vivo xenoperfused with human blood Rieben, Robert
2017
89 C p. 207-
1 p.
artikel
24 Association of lectin pathway protein levels and genetic variants early after injury with outcomes after severe traumatic brain injury. A prospective cohort study Trendelenburg, Marten
2017
89 C p. 212-213
2 p.
artikel
25 Associations of the alternative pathway and classical pathway of complement activation with incident metabolic syndrome: The CODAM study Xin, Ying
2017
89 C p. 190-
1 p.
artikel
26 A teenager with primary pneumococcal peritonitis Ugrinovic, S.
2017
89 C p. 156-
1 p.
artikel
27 Atypical hemolytic uremic syndrome – Why the kidney? Roumenina, Lubka T.
2017
89 C p. 172-173
2 p.
artikel
28 Author Index 2017
89 C p. I-VI
nvt p.
artikel
29 Auto-regulation of Th1 responses through carboxypeptidase M-generated C5a-desArg West, Erin E.
2017
89 C p. 135-
1 p.
artikel
30 BET inhibitor apabetalone (RVX-208) downregulates the complement cascade in primary human hepatocytes, in mice and in cardiovascular disease human patients Wasiak, Sylwia
2017
89 C p. 127-128
2 p.
artikel
31 Binding of von Willebrand factor to complement C1q on a cholesterol crystal surface Donat, Claudia
2017
89 C p. 137-
1 p.
artikel
32 Binding to complement receptor 1 affects the growth of Staphylococcus aureus in fresh human whole blood Dahl, J.A.
2017
89 C p. 170-
1 p.
artikel
33 Blood levels of glycated CD59 (GCD59), a novel biomarker in diabetes, predict pregnancy-induced glucose intolerance Halperin, Jose
2017
89 C p. 188-
1 p.
artikel
34 Candida albicans battles the Dectin-1 and Dectin-2 mediated host-immune response Reiher, Nadine
2017
89 C p. 157-
1 p.
artikel
35 CD40 ligation on antigen presenting cells (APCs) enhances properdin production van Essen, Mieke
2017
89 C p. 132-
1 p.
artikel
36 Cell-type specific complement expression in aging, albino mice Pauly, Diana
2017
89 C p. 190-
1 p.
artikel
37 Cell type-specific phosphokinetics for central intracellular signal transducers downstream of pattern recognition signaling by E. coli-induced inflammation in human whole blood Lau, Corinna
2017
89 C p. 168-
1 p.
artikel
38 CFHR5 binds to MAA-epitopes exposed on the surface of modified human endothelial cells Rudnick, Ramona B.
2017
89 C p. 196-
1 p.
artikel
39 Characterization of a novel whole blood model for the study of thrombin in complement activation and inflammation Nilsson, Per H.
2017
89 C p. 136-137
2 p.
artikel
40 Characterization of collectin LK, CL-LK Hansen, Soren W.K.
2017
89 C p. 190-191
2 p.
artikel
41 Characterization of complement components in a Spanish cohort of ANCA-associated vasculitis Gutierrez-Tenorio, Josue
2017
89 C p. 116-
1 p.
artikel
42 C1-inhibitor treatment decreases renal injury in an established brain-dead rat model Jager, N.M.
2017
89 C p. 211-
1 p.
artikel
43 CL-11 in systemic inflammatory response syndrome Bayarri-Olmos, Rafael
2017
89 C p. 169-
1 p.
artikel
44 Clot formation is enhanced by complement activation in a microvascular flow model Jenny, Lorenz
2017
89 C p. 133-
1 p.
artikel
45 Combined C5aR1 and CD14 inhibition significantly reduced cytokine release induced by both viable and heat inactivated bacteria in human whole blood Christiansen, Dorte
2017
89 C p. 169-170
2 p.
artikel
46 Combined inhibition of C5 and CD14 attenuates systemic inflammation in a newborn pig-model of meconium aspiration syndrome Thomas, Anub Mathew
2017
89 C p. 166-167
2 p.
artikel
47 Complement activation fragment C4a acts as effector molecule by signaling via protease-activated receptors 1 and 4 Ricklin, Daniel
2017
89 C p. 130-
1 p.
artikel
48 Complement anaphylatoxin receptors have critical physiological functions in the developing mammalian brain Woodruff, Trent M.
2017
89 C p. 185-186
2 p.
artikel
49 Complement and coagulation is activated in periodontitis in acute intermittent porphyria Storjord, Elin
2017
89 C p. 131-132
2 p.
artikel
50 Complement biomarkers in Alzheimer's disease Morgan, Angharad R.
2017
89 C p. 187-
1 p.
artikel
51 Complement component C3 is highly expressed in human pancreatic islets and promotes β-cell survival Kulak, Klaudia
2017
89 C p. 137-
1 p.
artikel
52 Complement C5, phagocytosis and Toll-like receptor 4 play key roles in Escherichia coli-induced surface expression of tissue factor on human monocytes Landsem, Anne
2017
89 C p. 138-
1 p.
artikel
53 Complement endorse the pathogenesis in autoinflammation Brunner, Jürgen
2017
89 C p. 119-
1 p.
artikel
54 Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, Sub-Saharan Africa: Implications for the susceptibility to meningococcal disease Franco-Jarava, Clara
2017
89 C p. 158-159
2 p.
artikel
55 Complement factor H and the long pentraxin PTX3 cooperate in the immune response to Aspergillus fumigatus Inforzato, Antonio
2017
89 C p. 156-
1 p.
artikel
56 Complement factor H-related (CFHR) proteins 2 and 5 as well as iC3b and properdin are deposited in different glomerular diseases Person, Fermin
2017
89 C p. 183-
1 p.
artikel
57 Complement factors C4 and C3 are down regulated in response to short term overfeeding in healthy young men Foghmar, Caroline
2017
89 C p. 136-
1 p.
artikel
58 Complement in clinical medicine: Clinical trials, case reports and therapy monitoring Ricklin, Daniel
2017
89 C p. 10-21
12 p.
artikel
59 Complement inhibition during brain death to improve the quality of thoracic organs: Which pathway(s) has potential? van Zanden, J.E.
2017
89 C p. 211-
1 p.
artikel
60 Complement inhibitor CSMD1 acts as a tumor suppressor in breast cancer by interacting with EGF receptor Gialeli, Chrysostomi
2017
89 C p. 123-
1 p.
artikel
61 Complement in renal transplantation: The road to translation Jager, Neeltina M.
2017
89 C p. 22-35
14 p.
artikel
62 Complement interaction with cells undergoing immunogenic cell death Noe, Remi
2017
89 C p. 122-
1 p.
artikel
63 Complement markers in immunoadsorption combined with membrane filtration for antibody-mediated rejection kidney transplantation Defendi, Federica
2017
89 C p. 210-
1 p.
artikel
64 Complement MASP-1 induced transcriptomic changes in the inflammation-related gene expression in endothelial cells Németh, Zsuzsanna
2017
89 C p. 165-
1 p.
artikel
65 Complement profile and autoantibodies against adipocytes on acquired lipodystrophies Corvillo, Fernando
2017
89 C p. 120-
1 p.
artikel
66 Complement receptor 3 mediates TGFβ-1 comprising extracellular vesicles in human monocytes Halder, Luke D.
2017
89 C p. 162-
1 p.
artikel
67 Complement receptor 1 polymorphism is associated with cerebral malaria in two discrete populations, but no evidence that human brain endothelial cells express the molecule Swann, Olivia
2017
89 C p. 157-
1 p.
artikel
68 Complement regulator factor H and its proposed antagonists in invasive bacterial infections van Beek, Anna E.
2017
89 C p. 158-
1 p.
artikel
69 Complement system biomarkers in first episode psychosis Morgan, B. Paul
2017
89 C p. 187-
1 p.
artikel
70 Complement system proteins in human embryonic stem cell-derived retinal pigment epithelial cells co-cultured with or without porcine retina Mohlin, C.
2017
89 C p. 162-163
2 p.
artikel
71 Contribution of adipose-derived factor D/adipsin to alternative pathway complement activation: Lessons from lipodystrophy Wu, Xiaobo
2017
89 C p. 143-
1 p.
artikel
72 CORVOS – A model for a European Complement PhD (EC-PhD) Würzner, Reinhard
2017
89 C p. 192-
1 p.
artikel
73 C1q: A fresh look upon an old molecule Thielens, Nicole M.
2017
89 C p. 73-83
11 p.
artikel
74 C1QA gene mutations in a pediatric SLE cohort from North India Rawat, Amit
2017
89 C p. 117-
1 p.
artikel
75 Creating model systems to study molecular mechanisms of C5 convertase-induced Membrane Attack Complex assembly Doorduijn, D.J.
2017
89 C p. 160-
1 p.
artikel
76 Crohn's disease patients in remission display enhanced intestinal infiltration of CR2 expressing cells in concert with strong induction of the classical complement pathway Derer, Stefanie
2017
89 C p. 164-165
2 p.
artikel
77 Cyclodextrin inhibits CC-induced complement activation Bakke, Siril S.
2017
89 C p. 167-168
2 p.
artikel
78 Cysteine cathepsins L and S diminish complement activation on the surface of tumour cells Hočevar, Katarina
2017
89 C p. 122-123
2 p.
artikel
79 Deficiency of C4 from brain death mice protects against renal injury Poppelaars, F.
2017
89 C p. 207-208
2 p.
artikel
80 Defining the molecular interplay between antibodies and complement in bacterial infections Zwarthoff, Seline A.
2017
89 C p. 154-155
2 p.
artikel
81 Delivery of CR2-fH using AAV vector therapy and encapsulated cell technology as treatment strategies in mouse model of neovascularization Rohrer, Bärbel
2017
89 C p. 202-
1 p.
artikel
82 Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutations Tabib, Adi
2017
89 C p. 69-72
4 p.
artikel
83 Design, expression, and function of chimeric bispecific complement inhibitors containing MAP-1 and functional domains of C4b-binding protein Hertz, Cecilie Elkjær
2017
89 C p. 165-
1 p.
artikel
84 Detection of convertase-stabilizing factors in patients with complement-mediated renal diseases: Translation to a diagnostic approach Michels, Marloes
2017
89 C p. 174-175
2 p.
artikel
85 Development of an automated assay for the measurement of C2 Tange, Clare
2017
89 C p. 191-
1 p.
artikel
86 Development of an automated assay for the measurement of C1 inhibitor Parker, Antony
2017
89 C p. 191-
1 p.
artikel
87 Discovery of microRNAs regulating complement-dependent cytotoxicity Hillman, Yaron
2017
89 C p. 150-
1 p.
artikel
88 Distribution and function of the complement protein C1q in malignant pleural mesothelioma microenvironment Roberta, Bulla
2017
89 C p. 121-
1 p.
artikel
89 Dual inhibition of the lectin and alternative complement pathways efficiently protects from myocardial ischemic reperfusion related injuries Skjoedt, Mikkel-Ole
2017
89 C p. 125-
1 p.
artikel
90 Early increase of complement terminal pathway activation marker sC5b-9 is predictive for the development of thrombotic microangiopathy after stem cell transplantation Horváth, Orsolya
2017
89 C p. 210-
1 p.
artikel
91 Eculizumab-C5 complexes express a C5a neoepitope in vivo: Consequences for interpretation of patient complement analyses Nilsson, Per H.
2017
89 C p. 111-114
4 p.
artikel
92 Editorial Board/ Publication Information 2017
89 C p. IFC-
1 p.
artikel
93 Establishment of a complement examination system for complement-related diseases by the Japanese Association for Complement Research (JACR) Hidaka, Yoshihiko
2017
89 C p. 192-
1 p.
artikel
94 Establishment of a method for the detection of C4-nephritic factor Garam, Nóra
2017
89 C p. 182-
1 p.
artikel
95 Evaluation of mechanisms of paroxysm in paroxysmal nocturnal hemoglobinuria: In vitro explorations of “bystander” hemolysis and of perturbations of soluble regulators Thanassi, Jane A.
2017
89 C p. 204-
1 p.
artikel
96 Evaluation of risk of bacteria-mediated putative “bystander” hemolysis of PNH red blood cells in vitro: No evidence of significant complement-mediated hemolysis induced by microorganisms Yang, Guangwei
2017
89 C p. 205-
1 p.
artikel
97 Extracellular histones inhibit complement activation through interactions with complement component C4b Qaddoori, Yasir
2017
89 C p. 132-
1 p.
artikel
98 Factor H-mediated complement evasion by the infective sporozoite stages of the malaria parasite Plasmodium falciparum de Araujo Rosa, Thiago Ferreira
2017
89 C p. 153-
1 p.
artikel
99 Factor I deficiency due to homozygosity for a novel mutation in the CFI gene Skattum, Lillemor
2017
89 C p. 149-
1 p.
artikel
100 Families presenting with Carboxypeptidase N deficiency, 37 years after the single description Vincent, Denis
2017
89 C p. 194-
1 p.
artikel
101 FHR-3 drives RPE cells towards pro-inflammation Schäfer, Nicole
2017
89 C p. 143-
1 p.
artikel
102 Ficolin-2 circulating levels and intraplaque presence are associated with vulnerable atherosclerotic lesions Fumagalli, Stefano
2017
89 C p. 126-
1 p.
artikel
103 Ficolin-2 from the lectin pathway of complement recognizes enteroaggregative Escherichia coli and contributes to innate complement dependent immune protection Sørensen, Camilla Adler
2017
89 C p. 160-
1 p.
artikel
104 Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo Genster, Ninette
2017
89 C p. 163-164
2 p.
artikel
105 Forms of contact-activated C3 associated with AP convertase formation Fromell, Karin
2017
89 C p. 141-
1 p.
artikel
106 Functional analysis of AMD-associated rare genetic variants in C9 Kremlitzka, Mariann
2017
89 C p. 150-
1 p.
artikel
107 Functional characterization of alternative pathway C3 and C5 convertase inhibitors Gorham Jr., Ronald D.
2017
89 C p. 141-
1 p.
artikel
108 Functional studies of chronic lymphocytic leukemia B cells expressing β2-integrin type complement receptors CR3 and CR4 Mácsik-Valent, Bernadett
2017
89 C p. 123-
1 p.
artikel
109 Gain-of-function mutants of complement factor B as standards in functional assay measuring the activity of complement convertases Urban, Aleksandra
2017
89 C p. 118-
1 p.
artikel
110 Gas embolism during surgery. A complement mediated condition? Storm, Benjamin Stage
2017
89 C p. 193-
1 p.
artikel
111 Generation of CD46, CD55 and CD59 CRISPR/Cas9 knockout cell lines Gormley, Darren
2017
89 C p. 169-
1 p.
artikel
112 Genetic association of complement receptors to preeclampsia revealed by targeted exomic sequencing Lokki, A. Inkeri
2017
89 C p. 147-148
2 p.
artikel
113 Genetic rearrangements in CFH and CFH-Related genes in atypical Hemolytic Uremic Syndrome, C3 glomerulopathy and Immuno-Complex mediated MPGN Piras, Rossella
2017
89 C p. 148-
1 p.
artikel
114 Hemodialysis patients with cardiovascular event have unfavorable complement profile Costa, M. Gaya da
2017
89 C p. 128-
1 p.
artikel
115 Heparan sulfate-modifying enzymes differentially determine complement factor H/factor H-related protein binding to glomerular endothelial cells Loeven, Markus A.
2017
89 C p. 177-
1 p.
artikel
116 High levels of soluble CD59 in CSF compared to plasma suggests intrathecal source of soluble CD59 Zelek, Wioleta
2017
89 C p. 186-
1 p.
artikel
117 HLA study in anti-complement factor H antibody-associated atypical hemolytic uremic syndrome Dragon-Durey, M.-A.
2017
89 C p. 175-
1 p.
artikel
118 How clinical laboratory standard capillary protein electrophoresis alerted to a low C3 state Hernández-González, Manuel
2017
89 C p. 152-
1 p.
artikel
119 Human c1q induces apoptosis in an ovarian cancer cell line via tumor necrosis factor pathway Kaur, Anuvinder
2017
89 C p. 124-
1 p.
artikel
120 Human epithelial C5aR1 signalling enhances bacterial adhesion to renal tubular epithelial cells through upregulation of the expression of mannosyle residues (the ligand for type I fimbrae) Song, Yun
2017
89 C p. 173-174
2 p.
artikel
121 Impact of carbamylation on IgG mediated complement activation Lubbers, Rosalie
2017
89 C p. 142-
1 p.
artikel
122 Improved function and in vivo half-life of new homo-dimeric mini-FH constructs in experimental kidney disease Yang, Yi
2017
89 C p. 202-
1 p.
artikel
123 Increasing endothelial permeability: A novel function of complement MASP-1 Debreczeni, Márta Lídia
2017
89 C p. 134-
1 p.
artikel
124 Independent role of C5aR1 and C5aR2 during acute Toxoplasma gondii infection Mey, Fabian T.
2017
89 C p. 161-162
2 p.
artikel
125 Inhibiting and activating effects of antimicrobial peptides on complement Berlov, Mikhail N.
2017
89 C p. 195-196
2 p.
artikel
126 Inhibition of complement alternative pathway by ACH-4471, the first clinical investigational orally-administered inhibitor of complement factor D Huang, Mingjun
2017
89 C p. 200-201
2 p.
artikel
127 Interaction between multimeric VWF and complement: A fresh look to the pathophysiology of microvascular thrombosis Noris, Marina
2017
89 C p. 133-
1 p.
artikel
128 Interaction of complement defence collagens C1q and MBL with BMP-1/tolloid-like proteinases Lacroix, Monique
2017
89 C p. 130-131
2 p.
artikel
129 Interaction of factor H family proteins with DNA and dead cells: Implications for the regulation of opsonization Kárpáti, Éva
2017
89 C p. 140-141
2 p.
artikel
130 Intracellular complement − the complosome − in immune cell regulation Arbore, Giuseppina
2017
89 C p. 2-9
8 p.
artikel
131 Intravascular hemolysis induces complement system activation Merle, Nicolas S.
2017
89 C p. 164-
1 p.
artikel
132 In vitro assessment of xenogeneic complement and endothelial cell activation using a microvascular flow model Sfriso, Riccardo
2017
89 C p. 209-
1 p.
artikel
133 Kallikrein represents an independent complement activator Irmscher, Sarah
2017
89 C p. 140-
1 p.
artikel
134 Lectin pathway proteins and association with complement activation and disease activity in patients with Systemic Lupus Erythematosus Troldborg, Anne
2017
89 C p. 117-
1 p.
artikel
135 Local complement activation in aqueous humor in patients with age-related macular degeneration Kirschfink, Michael
2017
89 C p. 163-
1 p.
artikel
136 Malaria parasite evasion of classical complement pathway attack Larsen, Mads Delbo
2017
89 C p. 159-
1 p.
artikel
137 Mannose-binding lectin drives vascular damage and interacts with platelet-derived IL-1α after cerebral ischemia in mice De Simoni, Maria-Grazia
2017
89 C p. 185-
1 p.
artikel
138 Mapping of ligand binding sites provides insight into the function of factor H-related protein 5 Papp, Alexandra
2017
89 C p. 145-
1 p.
artikel
139 Markers of the lectin-complement pathway in patients with aneurysmal subarachnoid haemorrhage Krogh, Charlotte Loumann
2017
89 C p. 170-171
2 p.
artikel
140 MASP-3 specifically recognizes different Aspergillus species Rosbjerg, Anne
2017
89 C p. 154-
1 p.
artikel
141 Monitoring of hemolytic activity of serum during alemtuzumab/ofatumumab therapy of chronic lymphocytic leukemia Stasiłojć, Grzegorz
2017
89 C p. 203-
1 p.
artikel
142 Monoclonal gammopathy-associated atypical hemolytic uremic syndrome: A relevant concept? Fremeaux-Bacchi, Veronique
2017
89 C p. 172-
1 p.
artikel
143 Motor neuron disease proteins activate complement and generate C5a Deora, Vandana
2017
89 C p. 168-
1 p.
artikel
144 Mouse FHRB interacts with renal-bound C3 in vivo: Implications for C3 glomerulopathy Malik, Talat H.
2017
89 C p. 176-
1 p.
artikel
145 Multimeric FHR4 immunoconjugates promote efficient activation of CAP on Her2 tumour cells, further controlled by overexpressed mCRPs, limiting MAC formation and CDC Plesseria, Jean-Marc
2017
89 C p. 206-
1 p.
artikel
146 Natural history study of C3 glomerulopathy Lomax-Browne, Hannah J.
2017
89 C p. 176-
1 p.
artikel
147 Neoepitope based assays to detect C5a – Pitfalls and interpretations Bergseth, Grethe
2017
89 C p. 201-
1 p.
artikel
148 Neutralization of the potent neurotropic Chandipura virus via classical pathway is dependent on C1q Kunnakkadan, Umerali
2017
89 C p. 153-
1 p.
artikel
149 New concepts on the therapeutic control of complement anaphylatoxin receptors Hawksworth, Owen A.
2017
89 C p. 36-43
8 p.
artikel
150 Novel CFHR2 variants: Another nuance in the complex spectrum of kidney disease aHUS and C3GN Stea, Emma D.
2017
89 C p. 179-
1 p.
artikel
151 Novel duplication of the FHRs dimerization domain associated with C3G Tortajada, Agustín
2017
89 C p. 181-
1 p.
artikel
152 Novel insights into the expression pattern of anaphylatoxin receptors in mice and men Laumonnier, Yves
2017
89 C p. 44-58
15 p.
artikel
153 Pathogenic mutations in C1R and C1S: In quest for molecular mechanisms Christine, Gaboriaud
2017
89 C p. 188-189
2 p.
artikel
154 Pentraxins PTX3 and CRP recruit C1q to cholesterol crystals and co-localize with the terminal complement complex in human atherosclerotic plaques Pilely, Katrine
2017
89 C p. 126-127
2 p.
artikel
155 Peritoneal eosinophils increase during induction of peritoneal dialysis and may be related to production of C3a in peritoneal dialysate Mizuno, Masashi
2017
89 C p. 193-
1 p.
artikel
156 Permeability of Bruch's membrane to complement proteins: Implications for translational medicine in AMD Clark, Simon J.
2017
89 C p. 200-
1 p.
artikel
157 Phenotypic studies of a novel factor B mutation in familial atypical hemolytic uremic syndrome Aradottir, Sigridur Sunna
2017
89 C p. 182-
1 p.
artikel
158 Plasma C4d as marker for lupus nephritis in Systemic Lupus Erythematosus Martin, Myriam
2017
89 C p. 115-116
2 p.
artikel
159 Plasma levels of lectin pathway components in IgA nephropathy Medjeral-Thomas, Nicholas R.
2017
89 C p. 178-
1 p.
artikel
160 Post-translational modification of complement anaphylatoxins during chronic neutrophilic inflammation Stott, Matthew
2017
89 C p. 167-
1 p.
artikel
161 Preface 16th European Meeting of Complement in Human Disease, Copenhagen, Denmark, September 8th-12th 2017 2017
89 C p. 1-
1 p.
artikel
162 Quantitative Western-blot profiles of factor H and factor H-related proteins in atypical haemolytic uraemic syndrome and C3 glomerulopathy Gómez, Irene
2017
89 C p. 181-
1 p.
artikel
163 RA101495 abolishes residual complement activity observed in the presence of eculizumab Ricardo, Alonso
2017
89 C p. 189-
1 p.
artikel
164 Reduction of myocardial ischemia reperfusion injury in pigs by (over) expression of human membrane co-factor protein Abdelhafez, Mai
2017
89 C p. 129-
1 p.
artikel
165 Relationship between CFHR5 and complement parameters in patients suffering from complement-mediated kidney disorders, with or without CFHR5 mutations Csuka, Dorottya
2017
89 C p. 177-
1 p.
artikel
166 Role of complement in cancer-related inflammation Di Marco, Sabrina
2017
89 C p. 124-
1 p.
artikel
167 Role of complement in cancer-related inflammation Magrini, Elena
2017
89 C p. 121-122
2 p.
artikel
168 Role of monoclonal and polyclonal immunoglobulins in AP dysregulation in C3 glomerulopathy associated with monoclonal gammopathy Chauvet, Sophie
2017
89 C p. 174-
1 p.
artikel
169 Role of the complement system in the inflammatory process caused by a class P1 metalloproteinase from Bothrops pirajai venom: Analysis in the ex vivo model of human whole blood Luchini, Lygia S.G.
2017
89 C p. 166-
1 p.
artikel
170 SALSA—A dance on a slippery floor with changing partners Reichhardt, M.P.
2017
89 C p. 100-110
11 p.
artikel
171 SALSA – Step by step Reichhardt, Martin Parnov
2017
89 C p. 197-
1 p.
artikel
172 Simultaneous determination of C1-INH-containing activation complexes in human plasma Kajdácsi, Erika
2017
89 C p. 137-138
2 p.
artikel
173 siRNA-mediated targeting of hepatocyte mannan-binding lectin-associated serine protease-3 for the treatment of murine collagen-antibody-inducsed arthritis (CAIA), a model for human rheumatoid arthritis Banda, Nirmal K.
2017
89 C p. 161-
1 p.
artikel
174 Structural and functional studies of human complement factor P Pedersen, Dennis V.
2017
89 C p. 197-198
2 p.
artikel
175 Structural studies of convertases in the complement system. The properdin-stabilised proconvertase, and the C5 convertase Gadeberg, Trine A.F.
2017
89 C p. 198-
1 p.
artikel
176 Systemic- and local complement activation controls the NLRP3 inflammasome pathway in patients with atherosclerosis Espevik, Terje
2017
89 C p. 125-126
2 p.
artikel
177 Systemic complement activation 3–6h after trauma predicts patient outcome Pischke, Soeren E.
2017
89 C p. 212-
1 p.
artikel
178 Targeted C4 inhibition by affinity purified immunoglobulins Volokhina, Elena
2017
89 C p. 201-202
2 p.
artikel
179 Targeted nanoparticles and complement activation Macor, Paolo
2017
89 C p. 204-
1 p.
artikel
180 The activated form of complement MASP-3 is the major variant in resting blood Dobó, József
2017
89 C p. 194-195
2 p.
artikel
181 The alternative complement pathway is dysregulated in patients with chronic heart failure Shahini, Negar
2017
89 C p. 127-
1 p.
artikel
182 The C5a/C5aR1 axis controls the development of Epidermolysis bullosa acquisita through its impact on IgG autoantibody formation and glycosylation Kovács, Bálint
2017
89 C p. 134-
1 p.
artikel
183 The effect of complement inhibition on erythrocyte destruction in AIHA Baas, Inge
2017
89 C p. 203-
1 p.
artikel
184 The Factor H splice variant FHL-1 contributes substantially to alternative pathway regulation, but is not specific for the host marker sialic acid Schmidt, Christoph Q.
2017
89 C p. 195-
1 p.
artikel
185 The human complement system sensitizes Gram-negative bacteria for Gram-positive-specific antibiotics via pore formation in the outer membrane Bardoel, B.W.
2017
89 C p. 155-
1 p.
artikel
186 The IL-6 receptor inhibitor tocilizumab attenuated expression of C5a receptor 1 and 2 in patients with myocardial infarction Orrem, Hilde L.
2017
89 C p. 128-
1 p.
artikel
187 The intracellular C5 system is critical to DAMP sensing and cellular responses in human monocytes Niyonzima, Nathalie
2017
89 C p. 131-
1 p.
artikel
188 The link between morphology and complement in ocular disease Mohlin, Camilla
2017
89 C p. 84-99
16 p.
artikel
189 The murine factor H-related protein FHR-B promotes complement activation Cserhalmi, Marcell
2017
89 C p. 142-143
2 p.
artikel
190 Therapy with eculizumab for patients with primary p.Cys89Tyr mutation in the CD59 gene avoids recurrent arterial thrombosis Mevorach, Dror
2017
89 C p. 186-
1 p.
artikel
191 Thermodynamics of the complex formation between Mannan-binding lectin and MASPs Schatz-Jakobsen, Janus A.
2017
89 C p. 144-
1 p.
artikel
192 The role of C5 convertases in membrane attack complex dependent killing of Gram-negative bacteria Heesterbeek, D.A.C.
2017
89 C p. 154-
1 p.
artikel
193 The role of CR3 (CD11b/CD18) and CR4 (CD11c/CD18) in complement-mediated phagocytosis and podosome formation by human phagocytes Lukácsi, Szilvia
2017
89 C p. 144-145
2 p.
artikel
194 The role of the complement system in hereditary angioedema Csuka, Dorottya
2017
89 C p. 59-68
10 p.
artikel
195 The spectrum of complement C9 staining in lupus nephritis Wilson, Hannah R.
2017
89 C p. 179-
1 p.
artikel
196 Treating C3G murine models by mini-Factor H Keenan, Adam
2017
89 C p. 205-
1 p.
artikel
197 Treatment of experimental C3 Glomerulopathy by human complement factor H produced in glycosylation-optimized Physcomitrella patens Häffner, Karsten
2017
89 C p. 120-
1 p.
artikel
198 Treatment of the C3 gain-of-function mouse model of aHUS with BB5.1, TT30 or genetic deletion of C5 Smith-Jackson, Kate
2017
89 C p. 180-
1 p.
artikel
199 Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype Leonhardt, Alexandria
2017
89 C p. 175-176
2 p.
artikel
200 Unraveling the role of the glomerular glycomatrix in C3 glomerulopathy Hauer, Jill
2017
89 C p. 183-
1 p.
artikel
201 Unravelling the pathophysiology of C3G/IC-MPGN and how to predict disease progression and orient therapies Iatropoulos, Paraskevas
2017
89 C p. 178-
1 p.
artikel
202 Utilising Staphylococcus aureus immune evasion protein Sbi as a novel vaccine conjugate Back, Catherine R.
2017
89 C p. 199-
1 p.
artikel
203 Validation of complement Factor H function assay and assessment of patients diagnosed with aHUS Dennis, Jaclyn
2017
89 C p. 145-146
2 p.
artikel
204 Variable biological properties of two different preparations of Shiga toxins yielding new insights into eHUS pathogenesis Chatterjee, Sneha
2017
89 C p. 159-
1 p.
artikel
205 Whole exome sequencing in diagnostics of atypical hemolytic uremic syndrome Koskinen, Aino R.
2017
89 C p. 148-149
2 p.
artikel
                             205 gevonden resultaten
 
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