Results 101 to 110 of about 22,609,963 (202)

Measurement of antiphospholipid antibody by ELISA using purified β2-glycoprotein I in preeclampsia

, 1993
SUMMARY It has been reported that the binding of some antiphospholipid antibodies (APA) to phospholipids requires the presence of β2-glycoprotein 1 (β2-GPI).
T KOBAYASHI, Y GESHI, T YAMAMOTO, H MORI, Y SASAMORI, S OKINAGA, S YOSHIMURA   +6 more
core   +1 more source

Proatherogenic Oxidized Low-Density Lipoprotein/β2-Glycoprotein I Complexes in Arterial and Venous Disease

Journal of Immunology Research, 2014
OxLDL/β2GPI complexes have been implicated in the initiation and progression of atherosclerosis and associated with disease severity and adverse outcomes.
Jeffrey S. Berger, Caron B. Rockman, Kirk E. Guyer, Luis R. Lopez   +3 more
doaj   +1 more source

Alarmin HMGB1 and Soluble RAGE as New Tools to Evaluate the Risk Stratification in Patients With the Antiphospholipid Syndrome

Frontiers in Immunology, 2019
Antiphospholipid antibody syndrome (APS) is a systemic autoimmune disease characterized by arterial and/or venous thrombosis, pregnancy morbidity in the presence of circulating “anti-phospholipid antibodies” (aPL).
Valeria Manganelli, Simona Truglia, Antonella Capozzi, Cristiano Alessandri, Gloria Riitano, Francesca Romana Spinelli, Fulvia Ceccarelli, Silvia Mancuso, Tina Garofalo, Agostina Longo, Guido Valesini, Maurizio Sorice, Fabrizio Conti, Roberta Misasi   +13 more
doaj   +1 more source

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult‐Onset Primary Lateral Sclerosis‐Like Syndrome

Clinical Genetics, EarlyView.
A 43‐year‐old woman developed a progressive adult‐onset upper motor neuron syndrome fulfilling the clinical criteria for primary lateral sclerosis (PLS), with mild cerebellar involvement. Genetic testing identified a de novo ATP1A3 p.Arg995His variant affecting a highly conserved residue within the transmembrane M8 domain.
Pablo Hernandez‐Vitorique, Marta García de Burgos, Ana Campos Villegas, María José Gómez Heredia, Pilar Carbonell Corvillo   +4 more
wiley   +1 more source

β2-Gp1 binding to mitochondria.

Panel A, wells of microtiter plates were coated with mitochondria (100 μg per well) and various concentrations of β2-Gp1 were added. Bound β2-Gp1 was quantified by an antibody to β2-glycoprotein I by ELISA.
Perumal Thiagarajan (498147), Swapan Kumar Dasgupta (17846842), Rolando E. Rumbaut (7860977), Stefanie Rivera (17846848), Jahnavi Gollamudi (17846845), Ross A. Poche (17846851)   +5 more
core   +1 more source

Unmasking Iododerma: A Distinctive Histopathologic Pattern of Neutrophil‐Rich Dermatosis With Haloed Cryptococcoid Bodies in the Setting of Hydralazine Exposure and Autoimmune Serologic Abnormalities

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Cutaneous iododerma is a rare adverse reaction to iodine‐containing compounds that may clinically and histopathologically mimic infection, vasculitis, malignancy, and other neutrophilic dermatoses. Although most commonly associated with iodinated contrast exposure, a variety of predisposing factors and potential associations have been reported,
Volha Lenskaya, Ana M. Ciurea, Mika Tabata, Teny M. John, Woo Cheal Cho   +4 more
wiley   +1 more source

News and meta-analysis regarding anti-Beta 2 glycoprotein I antibodies and their determination

, 2019
International audienceRecent advances allow us to propose antibodies targeting beta-2-glycoprotein I (β2-GPI) as the most specific antibodies associated with anti-phospholipid syndrome (APS). Therefore, there is now a crucial need for powerful biological
Nafai, Salma, Yves, Renaudineau, Bettacchioli, Eléonore, Eléonore Bettacchioli, Salma Nafai, Yves Renaudineau   +5 more
core   +1 more source

CD68 and F4/80 Markers Demonstrate Inflammatory Synergism Between Apical Periodontitis and Liver Fibrosis in Wistar Rats

International Endodontic Journal, EarlyView.
ABSTRACT Aim To evaluate CD68 and F4/80 glycoproteins in the worsening of apical periodontitis (AP) and liver fibrosis (LF) in Wistar rats. Methodology Thirty‐two Wistar rats were distributed in the following groups (n = 8): C—control; AP—apical periodontitis; LF—liver fibrosis; APLF—AP and LF.
L. V. Barroti, C. Cantiga‐Silva, M. P. Justo, P. H. C. Oliveira, F. D. Faria, J. Goto, E. Ervolino, G. Sivieri‐Araújo, T. N. Pinheiro, L. T. A. Cintra   +9 more
wiley   +1 more source

Optimization of simulated physiological binding conditions of antibodies against β2-glycoprotein I to crystallized annexin A5 on a phospholipid bilayer [PDF]

, 2020
Antifosfolipidni sindrom je sistemska avtoimunska bolezen, ki se kaže v obliki tromboz in zapletov v nosečnosti, in pri kateri so prisotna antifosfolipidna protitelesa v plazmi bolnikov.
Tahirović, Aneja
core  

Performance Assessment of Staclot‐LA Assay on Fully Automated Coagulation Analyser for Lupus Anticoagulant Testing Using Internal and External Quality Controls

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction It is recommended to detect lupus anticoagulant (LA) using two phospholipid‐dependent clotting assays, including a LA‐sensitive activated partial‐thromboplastin‐time (aPTT). Among these reagents, Staclot‐LA assay is performed on a mixture of test and normal plasma with and without hexagonal phase phospholipids.
V. Siguret, G. Jourdi, S. Melicine, L. Goubeau, Q. Pomorski, B. Joly‐Laffargue, A. Stepanian, M. Delrue, C. Bon, P. Meijer, E. Curis   +10 more
wiley   +1 more source