10,238 research outputs found

    Mechanical properties of freely suspended atomically thin dielectric layers of mica

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    We have studied the elastic deformation of freely suspended atomically thin sheets of muscovite mica, a widely used electrical insulator in its bulk form. Using an atomic force microscope, we carried out bending test experiments to determine the Young's modulus and the initial pre-tension of mica nanosheets with thicknesses ranging from 14 layers down to just one bilayer. We found that their Young's modulus is high (190 GPa), in agreement with the bulk value, which indicates that the exfoliation procedure employed to fabricate these nanolayers does not introduce a noticeable amount of defects. Additionally, ultrathin mica shows low pre-strain and can withstand reversible deformations up to tens of nanometers without breaking. The low pre-tension and high Young's modulus and breaking force found in these ultrathin mica layers demonstrates their prospective use as a complement for graphene in applications requiring flexible insulating materials or as reinforcement in nanocomposites.Comment: 9 pages, 5 figures, selected as cover of Nano Research, Volume 5, Number 8 (2012

    New observations of upper tropospheric NO2 from TROPOMI

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    Nitrogen oxides (NOx ≡ NO + NO2) in the NOx-limited upper troposphere (UT) are long-lived and so have a large influence on the oxidizing capacity of the troposphere and formation of the greenhouse gas ozone. Models misrepresent NOx in the UT and observations to address deficiencies in models are sparse. Here we obtain a year of near-global seasonal mean mixing ratios of NO2 in the UT (450–180 hPa) at 1 ° x 1° by applying cloud-slicing to partial columns of NO2 from TROPOMI. This follows refinement of the cloud-slicing algorithm with synthetic partial columns from the GEOS-Chem chemical transport model. We find that synthetic cloud-sliced UT NO2 are spatially consistent (R = 0.64) with UT NO2 calculated across the same cloud pressure range and scenes as are cloud-sliced (“true” UT NO2), but the cloud-sliced UT NO2 is 11–22 % more than the "true" all-sky seasonal mean. The largest contributors to differences between synthetic cloud-sliced and “true” UT NO2 are target resolution of the cloud-sliced product and uniformity of overlying stratospheric NO2. TROPOMI, prior to cloud-slicing, is corrected for a 13 % underestimate in stratospheric NO2 variance and a 50 % overestimate in free tropospheric NO2 determined by comparison to Pandora total columns at high-altitude sites in Mauna Loa, Izaña and Altzomoni, and MAX-DOAS and Pandora tropospheric columns at Izaña. Two cloud-sliced seasonal mean UT NO2 products for June 2019 to May 2020 are retrieved from corrected TROPOMI total columns using distinct TROPOMI cloud products that assume clouds are reflective boundaries (FRESCO-S) or water droplet layers (ROCINN-CAL). TROPOMI UT NO2 typically ranges from 20-30 pptv over remote oceans to > 80 pptv over locations with intense seasonal lightning. Spatial coverage is mostly in the tropics and subtropics with FRESCO-S and extends to the midlatitudes and polar regions with ROCINN-CAL, due to its greater abundance of optically thick clouds and wider cloud top altitude range. TROPOMI UT NO2 seasonal means are spatially consistent (R = 0.6–0.8) with an existing coarser spatial resolution (5° latitude x 8° longitude) UT NO2 product from the Ozone Monitoring Instrument (OMI). UT NO2 from TROPOMI is 12–26 pptv more than that from OMI due to increase in NO2 with altitude from the OMI pressure ceiling (280 hPa) to that for TROPOMI (180 hPa), but possibly also systematic altitude differences between the TROPOMI and OMI cloud products. The TROPOMI UT NO2 product offers potential to evaluate and improve representation of UT NOx in models and supplement aircraft observations that are sporadic and susceptible to large biases in the UT

    Epigenetic regulation of human cancer/testis antigen gene, HAGE, in chronic myeloid leukemia

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    Cancer testis antigens (CTA) provide attractive targets for cancer-specific immunotherapy. Although CTA genes are expressed in some normal tissues, such as the testis, this immunologically protected site lacks MHC I expression and as such, does not present self antigens to T cells. To date, CTA genes have been shown to be expressed in a range of solid tumors via demethylation of their promoter CpG islands, but rarely in chronic myeloid leukemia (CML) or other hematologic malignancies

    The Calcineurin Variant CnAβ1 Controls Mouse Embryonic Stem Cell Differentiation by Directing mTORC2 Membrane Localization and Activation

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    Embryonic stem cells (ESC) have the potential to generate all the cell lineages that form the body. However, the molecular mechanisms underlying ESC differentiation and especially the role of alternative splicing in this process remain poorly understood. Here, we show that the alternative splicing regulator MBNL1 promotes generation of the atypical calcineurin Aβ variant CnAβ1 in mouse ESCs (mESC). CnAβ1 has a unique C-terminal domain that drives its localization mainly to the Golgi apparatus by interacting with Cog8. CnAβ1 regulates the intracellular localization and activation of the mTORC2 complex. CnAβ1 knockdown results in delocalization of mTORC2 from the membrane to the cytoplasm, inactivation of the AKT/GSK3β/β-catenin signaling pathway, and defective mesoderm specification. In summary, here we unveil the structural basis for the mechanism of action of CnAβ1 and its role in the differentiation of mESCs to the mesodermal lineage.European Union's FP7 [CardioNext-ITN-608027, Cardio-NeT-ITN-289600]; Spanish Ministry of Science and Innovation [SAF2012-31451, CP08/00144]; Regional Government of Madrid [2010-BMD-2321]; Spanish Ministry of Economy and Competitiveness; Pro-CNIC Foundation; Severo Ochoa Center of Excellence (MINECO award) [SEV-2015-0505]S

    Glomerulonefritis membranoproliferativa paraneoplásica en leucemia linfática crónica: a propósito de un caso

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    PB-070 Introducción: La leucemia linfática crónica (LLC) es una neoplasia hematológica con alta incidencia en la población general. Sin embargo, la incidencia de afectación extranodal o extramedular secundaria a procesos paraneoplásicos es rara. En las series de casos encontradas en la literatura, la incidencia de afectación sintomática a nivel genitourinario o ginecológico es inferior al 10%, pero en autopsias se ha encontrado infiltración asintomática hasta en un 90% de los casos. La glomerulonefritis membranoproliferativa (GNMP) es la afectación paraneoplásica más frecuentemente encontrada a nivel renal y se presenta generalmente con insuficiencia renal o síndrome nefrótico. Caso clínico: Paciente de 81 años con antecedentes de HTA, dislipemia, fibrilación auricular, HBP e hipoacusia crónica. Ingresa en Nefrología en septiembre de 2018 por insuficiencia renal progresiva desde una creatinina basal de 1.26 mg/dL hasta 2.54 mg/dL, asociado a microhematuria y proteinuria; sin proceso intercurrente ni exposición a nefrotóxicos. Se encuentra asintomático, sin hallazgos patológicos a la exploración física. Se objetiva proteinuria de 7.7 gramos en orina de 24 horas, proteinuria de Bence Jones negativa y hematuria persistente. Así mismo, se objetiva una linfocitosis de 5.8x103/microL. Se completa el estudio etiológico mediante biopsia renal, con el diagnóstico de GNMP. En las pruebas de inmunohistoquímica, se objetiva un infiltrado linfocítico en cápsula renal CD20 positivo, CD23 y CD5 focalmente positivos; compatible con infiltración por LLC. En la citometría de flujo de sangre periférica, se halla un 38, 1% de linfocitos B maduros, siendo un 96% elementos clonales con inmunofenotipo de LLC con coexpresión de CD20, CD19, CD23, CD200 y CD5. En la citogenética se obtiene trisomía del cromosoma 12. Presenta biología molecular no mutada para TP53 y VH. En la serie ósea no se objetivan imágenes osteolíticas. En diciembre de 2018, Nefrología inicia tratamiento con ..
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