@article{HierroBurgosFonsecaRamezaniZiaranietal.2019,
  author    = {Hierro, Rodrigo and Burgos Fonseca, Y. and Ramezani Ziarani, Maryam and Llamedo, P. and Schmidt, Torsten and de la Torre, Alejandro and Alexander, P.},
  title     = {On the behavior of rainfall maxima at the eastern Andes},
  series = {Atmospheric Research},
  volume    = {234},
  journal   = {Atmospheric Research},
  publisher = {Elsevier},
  address   = {Amsterdam [u.a.]},
  issn      = {0169-8095},
  doi       = {10.1016/j.atmosres.2019.104792},
  year      = {2019},
  abstract  = {In this study, we detect high percentile rainfall events in the eastern central Andes, based on Tropical Rainfall Measuring Mission (TRMM) with a spatial resolution of 0.25 × 0.25°, a temporal resolution of 3 h, and for the duration from 2001 to 2018. We identify three areas with high mean accumulated rainfall and analyze their atmospheric behaviour and rainfall characteristics with specific focus on extreme events. Extreme events are defined by events above the 95th percentile of their daily mean accumulated rainfall. Austral summer (DJF) is the period of the year presenting the most frequent extreme events over these three regions. Daily statistics show that the spatial maxima, as well as their associated extreme events, are produced during the night. For the considered period, ERA-Interim reanalysis data, provided by the European Centre for Medium-Range Weather Forecasts (ECMWF) with 0.75° x0.75° spatial and 6-hourly temporal resolutions, were used for the analysis of the meso- and synoptic-scale atmospheric patterns. Night- and day-time differences indicate a nocturnal overload of northerly and northeasterly low-level humidity flows arriving from tropical South America. Under these conditions, cooling descending air from the mountains may find unstable air at the surface, giving place to the development of strong local convection. Another possible mechanism is presented here: a forced ascent of the low-level flow due to the mountains, disrupting the atmospheric stratification and generating vertical displacement of air trajectories. A Principal Component Analysis (PCA) in T-mode is applied to day- and night-time data during the maximum and extreme events. The results show strong correlation areas over each subregion under study during night-time, whereas during day-time no defined patterns are found. This confirms the observed nocturnal behavior of rainfall within these three hotspots.},
  language  = {en}
}
@article{SicKrausMadletal.2014,
  author    = {Sic, Heiko and Kraus, Helene and Madl, Josef and Flittner, Karl-Andreas and von Muenchow, Audrey Lilly and Pieper, Kathrin and Rizzi, Marta and Kienzler, Anne-Kathrin and Ayata, Korcan and Rauer, Sebastian and Kleuser, Burkhard and Salzer, Ulrich and Burger, Meike and Zirlik, Katja and Lougaris, Vassilios and Plebani, Alessandro and Roemer, Winfried and Loeffler, Christoph and Scaramuzza, Samantha and Villa, Anna and Noguchi, Emiko and Grimbacher, Bodo and Eibel, Hermann},
  title     = {Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis},
  series = {The journal of allergy and clinical immunology},
  volume    = {134},
  journal   = {The journal of allergy and clinical immunology},
  number    = {2},
  publisher = {Elsevier},
  address   = {New York},
  issn      = {0091-6749},
  doi       = {10.1016/j.jaci.2014.01.037},
  pages     = {420 -- +},
  year      = {2014},
  abstract  = {Background: Five different G protein-coupled sphingosine-1-phosphate (S1P) receptors (S1P1-S1P5) regulate a variety of physiologic and pathophysiologic processes, including lymphocyte circulation, multiple sclerosis (MS), and cancer. Although B-lymphocyte circulation plays an important role in these processes and is essential for normal immune responses, little is known about S1P receptors in human B cells. Objective: To explore their function and signaling, we studied B-cell lines and primary B cells from control subjects, patients with leukemia, patients with S1P receptor inhibitor-treated MS, and patients with primary immunodeficiencies. Methods: S1P receptor expression was analyzed by using multicolor immunofluorescence microscopy and quantitative PCR. Transwell assays were used to study cell migration. S1P receptor internalization was visualized by means of time-lapse imaging with fluorescent S1P receptor fusion proteins expressed by using lentiviral gene transfer. B-lymphocyte subsets were characterized by means of flow cytometry and immunofluorescence microscopy. Results: Showing that different B-cell populations express different combinations of S1P receptors, we found that S1P1 promotes migration, whereas S1P4 modulates and S1P2 inhibits S1P1 signals. Expression of CD69 in activated B lymphocytes and B cells from patients with chronic lymphocytic leukemia inhibited S1P-induced migration. Studying B-cell lines, normal B lymphocytes, and B cells from patients with primary immunodeficiencies, we identified Bruton tyrosine kinase, beta-arrestin 2, LPS-responsive beige-like anchor protein, dedicator of cytokinesis 8, and Wiskott-Aldrich syndrome protein as critical signaling components downstream of S1P1. Conclusion: Thus S1P receptor signaling regulates human B-cell circulation and might be a factor contributing to the pathology of MS, chronic lymphocytic leukemia, and primary immunodeficiencies.},
  language  = {en}
}