56 research outputs found

    Fluorescent carbon dioxide indicators

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    Over the last decade, fluorescence has become the dominant tool in biotechnology and medical imaging. These exciting advances have been underpinned by the advances in time-resolved techniques and instrumentation, probe design, chemical / biochemical sensing, coupled with our furthered knowledge in biology. Complementary volumes 9 and 10, Advanced Concepts of Fluorescence Sensing: Small Molecule Sensing and Advanced Concepts of Fluorescence Sensing: Macromolecular Sensing, aim to summarize the current state of the art in fluorescent sensing. For this reason, Drs. Geddes and Lakowicz have invited chapters, encompassing a broad range of fluorescence sensing techniques. Some chapters deal with small molecule sensors, such as for anions, cations, and CO2, while others summarize recent advances in protein-based and macromolecular sensors. The Editors have, however, not included DNA or RNA based sensing in this volume, as this were reviewed in Volume 7 and is to be the subject of a more detailed volume in the near future

    A Historiometric Examination of Machiavellianism and a New Taxonomy of Leadership

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    Although researchers have extensively examined the relationship between charismatic leadership and Machiavellianism (Deluga, 2001; Gardner & Avolio, 1995; House & Howell, 1992), there has been a lack of investigation of Machiavellianism in relation to alternative forms of outstanding leadership. Thus, the purpose of this investigation was to examine the relationship between Machiavellianism and a new taxonomy of outstanding leadership comprised of charismatic, ideological, and pragmatic leaders. Using an historiometric approach, raters assessed Machiavellianism via the communications of 120 outstanding leaders in organizations across the domains of business, political, military, and religious institutions. Academic biographies were used to assess twelve general performance measures as well as twelve general controls and five communication specific controls. The results indicated that differing levels of Machiavellianism is evidenced across the differing leader types as well as differing leader orientation. Additionally, Machiavellianism appears negatively related to performance, though less so when type and orientation are taken into account.Yeshttps://us.sagepub.com/en-us/nam/manuscript-submission-guideline

    Whole-genome sequencing reveals host factors underlying critical COVID-19

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    Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease

    Cross‐linking of surface IgM activates NF‐xB in B lymphocyte

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    In B lymphocytes, cross‐linking of surface IgM activates changes in both the cell cycle and differentiation. In normal B cells and B cell tumors, many stimuli induce the activation of NF‐xB and its translocation from the cytoplasm to the nucleus. In this study we sought to determine if cross‐linking of surface IgM led to the activation of NF‐xB. Our results show that activation of B cells by cross‐linking anti‐IgM antibodies activated NF‐xB in the murine B lymphoid cell lines 70Z/3 and M12, and in the dense fraction of splenic cells. The activation of NF‐xB required optimal doses of anti‐IgM antibodies and took 5 to 10 min to reach maximal levels. Cross‐linking of IgM has also been shown to activate protein kinases including protein kinase C (PKC). To test wether PKC activation was required for NF‐xB translocation, we treated 70Z/3 cells for 18 h with phorbol 12‐myristate 13‐acetate, a procedure which depletes these cells of functional PKC. This treatment did not abrogate the nuclear translocation of NF‐xB following anti‐IgM cross‐linking. These results indicate that the nuclear translocation of NF‐xB is rapidly induced by surface IgM cross‐linking and that this activation appears to use a pathway which does not require PKC. Copyright © 1991 WILEY‐VCH Verlag GmbH & Co. KGaA, WeinheimSCOPUS: ar.jFLWNAinfo:eu-repo/semantics/publishe

    Cladosporium Avr2 inhibits tomato Rcr3 protease required for Cf-2-dependent disease resistance

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    How plants recognize pathogens and activate defense is still mysterious. Direct interaction between pathogen avirulence (Avr) proteins and plant disease resistance proteins is the exception rather than the rule. During infection, Cladosporium fulvum secretes Avr2 protein into the apoplast of tomato leaves and, in the presence of the extracellular leucine-rich repeat receptor-like Cf-2 protein, triggers a hypersensitive response (HR) that also requires the extracellular tomato cysteine protease Rcr3. We show here that Avr2 binds and inhibits Rcr3 and propose that the Rcr3-Avr2 complex enables the Cf-2 protein to activate an H

    Wild red deer [Cervus elaphus

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    This study aimed at estimating the impact of red deer grazing on the productivity of meadows located in Pian Cansiglio, north-eastern Italian Pre-Alps. These meadows (383 ha; average elevation 1000 m asl are managed for hay/silage production (1-2 cuts per season) and are included in a protected area that hosts a high density of deer (around 30 heads/100 ha). In 2008 and 2010, dry matter (DM) production and loss due to deer grazing were estimated with exclusion cages (1 m2; 48 exclusion cages in 2008 and 52 in 2010). Night counts with spotlights were conducted to index deer use of meadows plots. DM production inside the cages was fairly good for the area (first and second cut: 5079 - 2193 Kg DM/ha in 2008, and 4200 - 2615 Kg DM/ha in 2010). DM production outside the cages was significantly lower (first and second cut in 2008: 4314-1389 Kg DM/ha, and in 2010: 3376-2052 Kg DM/ha). Therefore, the magnitude of losses was of 15-20% in the first and 25-40% in the second cut. DM losses in the different meadow plots were positively correlated with index of deer use, which in some plots was as high as 7-8 heads/ha. Deer grazing reduced also crude protein (CP) content of forage (15.6±4.4% DM inside exclusion cages and 13.8±3.5% DM outside), with losses being greater where CP content was higher. This study demonstrates that high densities of grazing deer may seriously impact on forage production and quality

    Calcium Domains around Single and Clustered IP3 Receptors and Their Modulation by Buffers

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    We study Ca2+ release through single and clustered IP3 receptor channels on the ER membrane under presence of buffer proteins. Our computational scheme couples reaction-diffusion equations and a Markovian channel model and allows our investigating the effects of buffer proteins on local calcium concentrations and channel gating. We find transient and stationary elevations of calcium concentrations around active channels and show how they determine release amplitude. Transient calcium domains occur after closing of isolated channels and constitute an important part of the channel's feedback. They cause repeated openings (bursts) and mediate increased release due to Ca2+ buffering by immobile proteins. Stationary domains occur during prolonged activity of clustered channels, where the spatial proximity of IP3Rs produces a distinct [Ca2+] scale (0.5–10 ÎŒM), which is smaller than channel pore concentrations (>100 ÎŒM) but larger than transient levels. While immobile buffer affects transient levels only, mobile buffers in general reduce both transient and stationary domains, giving rise to Ca2+ evacuation and biphasic modulation of release amplitude. Our findings explain recent experiments in oocytes and provide a general framework for the understanding of calcium signals
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