Zobrazeno 1 - 10
of 144
pro vyhledávání: '"J. Caride"'
Autor:
George Vasmatzis, Yan W. Asmann, Ariel J. Caride, Jaime I. Davila, Andrew L. Feldman, Julie C. Porcher, Stephen M. Ansell, Sarah H. Johnson, Bruce W. Eckloff, Sumit Middha
Publikováno v:
Genes, Chromosomes and Cancer. 52:1097-1102
Chromosomal translocations leading to expression of abnormal fusion proteins play a major role in the pathogenesis of various hematologic malignancies. The recent development of high-throughput, "deep" sequencing has allowed discovery of novel transl
Autor:
L. Malina, Robert Richter, Jelena Ninkovic, A. Frey, J. Knopf, Carlos Lacasta, C. Geisler, Hans Krüger, Peter Kodys, Carlos A. Iglesias, S. Rummel, Z. Doležal, J. Scheirich, T. Weiler, J. Caride, L. Reuen, Christian Koffmane, Norbert Wermes, Benjamin Schwenker, S. Heindl, C. Kreidl, Ladislav Andricek, Marcel Vos, Sergey Furletov, M. Koch, J. Schneider, Z. Drásal, P. Vazquez, Peter Kvasnicka, Julia Furletova, S. Esch, Carlos Marinas
Publikováno v:
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 638:24-32
The paper is based on the data of the 2009 DEPFET beam test at CERN SPS. The beam test used beams of pions and electrons with energies between 40 and 120 GeV, and the sensors tested were prototypes with thickness of 450 μ m and pixel pitch between 2
Autor:
Rolando C. Rossi, Emanuel E. Strehler, Ariel J. Caride, Juan Pablo F.C. Rossi, Irene C. Mangialavori
Publikováno v:
Current Chemical Biology. 5:118-129
Although membrane proteins constitute more than 20% of the total proteins, the structures of only a few are known in detail. An important group of integral membrane proteins are ion-transporting ATPases of the P-type family, which share the formation
Autor:
Ariel J. Caride, Jordan D. Miller, Kyaw Zaw Hein, Jay L. Zweier, João F. Passos, Mariana G. Tarragó, Diana Jurk, Dong Seong Cho, Adrienne Samani, Guilherme C. de Oliveira, Runqing Huang, James Boslett, Micaela Rud, Gina M. Warner, Jason D. Doles, Karina S. Kanamori, David J. Becherer, Claudia C.S. Chini, Eduardo N. Chini
Publikováno v:
Cell Metabolism. 27:1081-1095.e10
Aging is characterized by the development of metabolic dysfunction and frailty. Recent studies show that a reduction in nicotinamide adenine dinucleotide (NAD(+)) is a key factor for the development of age-associated metabolic decline. We recently de
Publikováno v:
Journal of Biological Chemistry. 282:25640-25648
The inhibition by the regulatory domain and the interaction with calmodulin (CaM) vary among plasma membrane calcium pump (PMCA) isoforms. To explore these differences, the kinetics of CaM effects on PMCA4a were investigated and compared with those o
Autor:
Ariel J. Caride, Ágnes Enyedi, Adelaida G. Filoteo, Emanuel E. Strehler, John T. Penniston, Yuning Xiong
Publikováno v:
Annals of the New York Academy of Sciences. 1099:226-236
Plasma membrane Ca2+ ATPases (PMCAs) are essential components of the cellular toolkit to regulate and fine-tune cytosolic Ca2+ concentrations. Historically, the PMCAs have been assigned a housekeeping role in the maintenance of intracellular Ca2+ hom
Autor:
Katalin, Pászty, Ariel J, Caride, Željko, Bajzer, Chetan P, Offord, Rita, Padányi, Luca, Hegedűs, Karolina, Varga, Emanuel E, Strehler, Agnes, Enyedi
Publikováno v:
Science signaling. 8(364)
Calcium (Ca(2+)) is a critical cofactor and signaling mediator in cells, and the concentration of cytosolic Ca(2+) is regulated by multiple proteins, including the plasma membrane Ca(2+)-ATPases (adenosine triphosphatases) (PMCAs), which use ATP to t
Autor:
Željko Bajzer, Katalin Pászty, Chetan P. Offord, Luca Hegedűs, Karolina Varga, Ariel J. Caride, Ágnes Enyedi, Rita Padányi, Emanuel E. Strehler
Publikováno v:
Science Signaling. 8
Calcium (Ca 2+ ) is a critical cofactor and signaling mediator in cells, and the concentration of cytosolic Ca 2+ is regulated by multiple proteins, including the plasma membrane Ca 2+ –ATPases (adenosine triphosphatases) (PMCAs), which use ATP to
Autor:
Yandan Yang, Julie M. Schultz, Anne C. Madeo, Lameh Fananapazir, Robert J. Morell, Ariel J. Caride, Adelaida G. Filoteo, Andrew J. Griffith, Ayala Lagziel, John T. Penniston, Saidi A Mohiddin, Alan R. Penheiter
Publikováno v:
New England Journal of Medicine. 352:1557-1564
Five adult siblings presented with autosomal recessive sensorineural hearing loss: two had high-frequency loss, whereas the other three had severe-to-profound loss affecting all frequencies. Genetic evaluation revealed that a homozygous mutation in C