نتایج جستجو برای: رگرسیون m5

تعداد نتایج: 39593  

1997
I. Chepelev

We discuss long-distance, low-velocity interaction potentials for processes involving longitudinal M5-brane (corresponding in type IIA theory language to the 1/4 supersymmetric bound state of 4-brane and 0-brane). We consider the following scattering configurations: (a) D = 11 graviton off longitudinal M5-brane, or, equivalently, 0-branes off marginal 4‖0 bound state; (b) M2-brane off longitudi...

Journal: :Journal of immunology 2006
Kellen C Faé Danielle Diefenbach da Silva Sandra E Oshiro Ana C Tanaka Pablo M A Pomerantzeff Corinne Douay Dominique Charron Antoine Toubert Madeleine W Cunningham Jorge Kalil Luiza Guilherme

Molecular mimicry between Streptococcus pyogenes Ags and human proteins has been considered as a mechanism leading to autoimmune reactions in rheumatic fever and rheumatic heart disease (RHD). Cardiac myosin has been shown as a putative autoantigen recognized by autoantibodies of rheumatic fever patients. We assessed the human heart-intralesional T cell response against human light meromyosin (...

2014
Vivien Kauschke Katrin Susanne Lips Christian Heiss Reinhard Schnettler

BACKGROUND Cholinergic signaling via muscarinic acetylcholine receptors (mAChR) is known to influence various physiological functions. In bone, M3 mAChR and M5 mAChR were identified on the membrane of osteoblast-like cells. M3 mAChR seems to be particularly relevant for bone physiology, as signaling via this receptor was reported to increase bone formation and decrease bone resorption. Thus, in...

2009
Johan Waldemarsson Margaretha Stålhammar-Carlemalm Charlotta Sandin Francis J. Castellino Gunnar Lindahl

The surface-localized M protein of Streptococcus pyogenes is a major virulence factor that inhibits phagocytosis, as determined ex vivo. Because little is known about the role of M protein in vivo we analyzed the contribution of different M protein regions to virulence, using the fibrinogen (Fg)-binding M5 protein and a mouse model of acute invasive infection. This model was suitable, because M...

2016
Alexandre Rouette Assya Trofimov David Haberl Geneviève Boucher Vincent-Philippe Lavallée Giovanni D’Angelo Josée Hébert Guy Sauvageau Sébastien Lemieux Claude Perreault

Based on transcriptomic analyses of thousands of samples from The Cancer Genome Atlas, we report that expression of constitutive proteasome (CP) genes (PSMB5, PSMB6, PSMB7) and immunoproteasome (IP) genes (PSMB8, PSMB9, PSMB10) is increased in most cancer types. In breast cancer, expression of IP genes was determined by the abundance of tumor infiltrating lymphocytes and high expression of IP g...

Journal: :The Journal of pharmacology and experimental therapeutics 2002
Diane J Ford Anthony Essex Tracy A Spalding Ethan S Burstein John Ellis

Previous studies have found that a mutation near the junction of the sixth transmembrane domain (TM6) and the third extracellular loop of the M5 muscarinic receptor leads to constitutive activation and enhanced agonist affinity for the mutated receptor. These results were consistent with the extended ternary complex model, which predicts a correlation between agonist affinity and constitutive a...

2005
Katrin Becker Melanie Becker

We derive inflation from M-theory on S/Z2 via the non-perturbative dynamics of N M5-branes. The open membrane instanton interactions between the M5-branes give rise to exponential potentials which are too steep for inflation individually but lead to inflation when combined together. The resulting type of inflation, known as assisted inflation, facilitates considerably the requirement of having ...

2014
Rao N. V. S. Mamidi Filip Cuyckens Jie Chen Ellen Scheers Dennis Kalamaridis Ronghui Lin Jose Silva Sue Sha David C. Evans Michael F. Kelley Damayanthi Devineni Mark D. Johnson Heng Keang Lim

Canagliflozin is an oral antihyperglycemic agent used for the treatment of type 2 diabetes mellitus. It blocks the reabsorption of glucose in the proximal renal tubule by inhibiting the sodium-glucose cotransporter 2. This article describes the in vivo biotransformation and disposition of canagliflozin after a single oral dose of [C]canagliflozin to intact and bile duct-cannulated (BDC) mice an...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Wei Tang Ralph A Stearns Randall R Miller Jason S Ngui Robert J Mathvink Ann E Weber Gloria Y Kwei John R Strauss Carol A Keohane George A Doss Shuet-Hing L Chiu Thomas A Baillie

(R)-N-[4-[2-[[2-Hydroxy-2-(pyridin-3-yl)ethyl]amino]ethyl]phenyl]- 4-[4-(4-trifluoro-methylphenyl)thiazol-2-yl]benzenesulfonamide (1) is a potent and selective agonist of the human beta3-adrenergic receptor. We report herein the data from studies of the metabolism and excretion of 1 in rats. Five metabolites were identified in the bile of male Sprague-Dawley rats administered 3H-labeled 1 by ei...

Journal: :Blood 2000
C M Zwaan G J Kaspers R Pieters N L Ramakers-Van Woerden M L den Boer R Wünsche M M Rottier K Hählen E R van Wering G E Janka-Schaub U Creutzig A J Veerman

Determining in vitro drug resistance may reveal clinically relevant information in childhood leukemia. Using the methyl-thiazol-tetrazolium assay, the resistance of untreated leukemic cells to 21 drugs was compared in 128 children with acute myeloid leukemia (AML) and 536 children with acute lymphoblastic leukemia (ALL). The differences between 3 French-American-British (FAB) types (M1/M2, M4, ...

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