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- Publication . Conference object . 2018Authors:Masen Lamb; Andrew Norton; Bruce Macintosh; Carlos Correia; Jean-Pierre Véran; Christian Marois; Suresh Sivanandam;Masen Lamb; Andrew Norton; Bruce Macintosh; Carlos Correia; Jean-Pierre Véran; Christian Marois; Suresh Sivanandam;
doi: 10.1117/12.2313458
Publisher: SPIEWe explore the application of phase diversity to calibrate the non common path aberrations (NCPA) in the Gemini Planet Imager (GPI). This is first investigated in simulation in order to characterize the ideal technique parameters with simulated GPI calibration source data. The best working simulation parameters are derived and we establish the algorithm's capability to recover an injected astigmatism. Furthermore, the real data appear to exhibit signs of de-centering between the in and out of focus images that are required by phase diversity; this effect can arise when the diverse images are acquired in closed loop and are close to the non-linear regime of the wavefront sensor. We show in simulation that this effect can inhibit our algorithm, which does not take into account the impact of de-centering between images. To mitigate this effect, we validate the technique of using a single diverse image with our algorithm; this is first demonstrated in simulation and then applied to the real GPI data. Following this approach, we find that we can successfully recover a known astigmatism injection using the real GPI data and subsequently apply an NCPA correction to GPI (in the format of offset reference slopes) to improve the relative Strehl ratio by 5%; we note this NCPA correction application is rudimentary and a more thorough application will be investigated in the near future. Finally, the estimated NCPA in the form of astigmatism and coma agree well with the magnitude of the same modes reported by Poyneer et al. 2016.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Open Access EnglishAuthors:Mark Haas; Alexandre Loupy; Carmen Lefaucheur; Candice Roufosse; Denis Glotz; Daniel Serón; Brian J. Nankivell; Philip F. Halloran; Robert B. Colvin; Enver Akalin; +19 moreMark Haas; Alexandre Loupy; Carmen Lefaucheur; Candice Roufosse; Denis Glotz; Daniel Serón; Brian J. Nankivell; Philip F. Halloran; Robert B. Colvin; Enver Akalin; Nada Alachkar; Serena M. Bagnasco; Yassine Bouatou; Jan U. Becker; Lynn D. Cornell; J.-P. Duong Van Huyen; Ian W. Gibson; Edward S. Kraus; Roslyn B. Mannon; Maarten Naesens; Volker Nickeleit; Peter Nickerson; Dorry L. Segev; Harsharan K. Singh; Mark D. Stegall; P. Randhawa; Lorraine C. Racusen; Kim Solez; Michael Mengel;Countries: Spain, United States, United Kingdom
The kidney sessions of the 2017 Banff Conference focused on 2 areas: clinical implications of inflammation in areas of interstitial fibrosis and tubular atrophy (i‐IFTA) and its relationship to T cell–mediated rejection (TCMR), and the continued evolution of molecular diagnostics, particularly in the diagnosis of antibody‐mediated rejection (ABMR). In confirmation of previous studies, it was independently demonstrated by 2 groups that i‐IFTA is associated with reduced graft survival. Furthermore, these groups presented that i‐IFTA, particularly when involving >25% of sclerotic cortex in association with tubulitis, is often a sequela of acute TCMR in association with underimmunosuppression. The classification was thus revised to include moderate i‐IFTA plus moderate or severe tubulitis as diagnostic of chronic active TCMR. Other studies demonstrated that certain molecular classifiers improve diagnosis of ABMR beyond what is possible with histology, C4d, and detection of donor‐specific antibodies (DSAs) and that both C4d and validated molecular assays can serve as potential alternatives and/or complements to DSAs in the diagnosis of ABMR. The Banff ABMR criteria are thus updated to include these alternatives. Finally, the present report paves the way for the Banff scheme to be part of an integrative approach for defining surrogate endpoints in next‐generation clinical trials. The Banff consortium presents revisions to the diagnostic criteria for T cell– and antibody‐mediated kidney transplant rejection, including specific criteria for chronic active T cell–mediated rejection, plus prospects for integrative endpoints in clinical trials. See related articles on pages 321, 364, and 377.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2020 . Embargo End Date: 04 Feb 2021Open AccessAuthors:Carlevaro-Fita J.; Lanzos A.; Feuerbach L.; Hong C.; Mas-Ponte D.; Pedersen J. S.; Abascal F.; Amin S. B.; Bader G. D.; Barenboim J.; +127 moreCarlevaro-Fita J.; Lanzos A.; Feuerbach L.; Hong C.; Mas-Ponte D.; Pedersen J. S.; Abascal F.; Amin S. B.; Bader G. D.; Barenboim J.; Beroukhim R.; Bertl J.; Boroevich K. A.; Brunak S.; Campbell P. J.; Carlevaro-Fita J.; Chakravarty D.; Chan C. W. Y.; Chen K.; Choi J. K.; Deu-Pons J.; Dhingra P.; Diamanti K.; Feuerbach L.; Fink J. L.; Fonseca N. A.; Frigola J.; Gambacorti Passerini C.; Garsed D. W.; Gerstein M.; Getz G.; Gonzalez-Perez A.; Guo Q.; Gut I. G.; Haan D.; Hamilton M. P.; Haradhvala N. J.; Harmanci A. O.; Helmy M.; Herrmann C.; Hess J. M.; Hobolth A.; Hodzic E.; Hong C.; Hornshoj H.; Isaev K.; Izarzugaza J. M. G.; Johnson R.; Johnson T. A.; Juul M.; Juul R. I.; Kahles A.; Kahraman A.; Kellis M.; Khurana E.; Kim J.; Kim J. K.; Kim Y.; Komorowski J.; Korbel J. O.; Kumar S.; Lanzos A.; Larsson E.; Lawrence M. S.; Lee D.; Lehmann K. -V.; Li S.; Li X.; Lin Z.; Liu E. M.; Lochovsky L.; Lou S.; Madsen T.; Marchal K.; Martincorena I.; Martinez-Fundichely A.; Maruvka Y. E.; McGillivray P. D.; Meyerson W.; Muinos F.; Mularoni L.; Nakagawa H.; Nielsen M. M.; Paczkowska M.; Park K.; Park K.; Pedersen J. S.; Pich O.; Pons T.; Pulido-Tamayo S.; Raphael B. J.; Reimand J.; Reyes-Salazar I.; Reyna M. A.; Rheinbay E.; Rubin M. A.; Rubio-Perez C.; Sabarinathan R.; Sahinalp S. C.; Saksena G.; Salichos L.; Sander C.; Schumacher S. E.; Shackleton M.; Shapira O.; Shen C.; Shrestha R.; Shuai S.; Sidiropoulos N.; Sieverling L.; Sinnott-Armstrong N.; Stein L. D.; Stuart J. M.; Tamborero D.; Tiao G.; Tsunoda T.; Umer H. M.; Uuskula-Reimand L.; Valencia A.; Vazquez M.; Verbeke L. P. C.; Wadelius C.; Wadi L.; Wang J.; Warrell J.; Waszak S. M.; Weischenfeldt J.; Wheeler D. A.; Wu G.; Yu J.; Zhang J.; Zhang X.; Zhang Y.; Zhao Z.; Zou L.; von Mering C.; Johnson R.;
doi: 10.17863/cam.64282 , 10.3929/ethz-b-000399368 , 10.17863/cam.64917 , 10.7892/boris.143033 , 10.1038/s42003-019-0741-7
pmc: PMC7002399
handle: 2066/288696 , 20.500.11850/399368 , 1854/LU-8658728
Publisher: Apollo - University of Cambridge RepositoryCountries: Netherlands, Switzerland, Italy, Belgium, Switzerland, Sweden, Spain, Denmark, United KingdomLong non-coding RNAs (lncRNAs) are a growing focus of cancer genomics studies, creating the need for a resource of lncRNAs with validated cancer roles. Furthermore, it remains debated whether mutated lncRNAs can drive tumorigenesis, and whether such functions could be conserved during evolution. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, we introduce the Cancer LncRNA Census (CLC), a compilation of 122 GENCODE lncRNAs with causal roles in cancer phenotypes. In contrast to existing databases, CLC requires strong functional or genetic evidence. CLC genes are enriched amongst driver genes predicted from somatic mutations, and display characteristic genomic features. Strikingly, CLC genes are enriched for driver mutations from unbiased, genome-wide transposon-mutagenesis screens in mice. We identified 10 tumour-causing mutations in orthologues of 8 lncRNAs, including LINC-PINT and NEAT1, but not MALAT1. Thus CLC represents a dataset of high-confidence cancer lncRNAs. Mutagenesis maps are a novel means for identifying deeply-conserved roles of lncRNAs in tumorigenesis. Communications Biology, 3 (1) ISSN:2399-3642
Substantial popularitySubstantial popularity In top 1%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open AccessAuthors:Gordon Pennycook; Jonathon McPhetres; Bence Bago; David G. Rand;Gordon Pennycook; Jonathon McPhetres; Bence Bago; David G. Rand;Publisher: SAGE PublicationsCountries: United Kingdom, FranceProject: CIHR , SSHRC
What are the psychological consequences of the increasingly politicized nature of the COVID-19 pandemic in the United States relative to similar Western countries? In a two-wave study completed early (March) and later (December) in the pandemic, we found that polarization was greater in the United States ( N = 1,339) than in Canada ( N = 644) and the United Kingdom. ( N = 1,283). Political conservatism in the United States was strongly associated with engaging in weaker mitigation behaviors, lower COVID-19 risk perceptions, greater misperceptions, and stronger vaccination hesitancy. Although there was some evidence that cognitive sophistication was associated with increased polarization in the United States in December (but not March), cognitive sophistication was nonetheless consistently negatively correlated with misperceptions and vaccination hesitancy across time, countries, and party lines. Furthermore, COVID-19 skepticism in the United States was strongly correlated with distrust in liberal-leaning mainstream news outlets and trust in conservative-leaning news outlets, suggesting that polarization may be driven by differences in information environments.
Substantial popularitySubstantial popularity In top 1%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Closed AccessAuthors:Romain Jouffroy; Xavier Bobbia; Tobias Gauss; Pierre Bouzat; Michelet Pierre;Romain Jouffroy; Xavier Bobbia; Tobias Gauss; Pierre Bouzat; Michelet Pierre;
pmid: 30308243
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:Hanns Lochmüller; Anthony Behin; Ivailo Tournev; Mark A. Tarnopolsky; Rita Horvath; Oksana Pogoryelova; J. Shah; Tony Koutsoukos; Alison Skrinar; Emil D. Kakkis; +2 moreHanns Lochmüller; Anthony Behin; Ivailo Tournev; Mark A. Tarnopolsky; Rita Horvath; Oksana Pogoryelova; J. Shah; Tony Koutsoukos; Alison Skrinar; Emil D. Kakkis; Camille L Bedrosian; Tahseen Mozaffar;Publisher: HAL CCSDCountries: France, United States, United Kingdom
Author(s): Lochmuller, Hanns; Behin, Anthony; Tournev, Ivailo; Tarnopolsky, Mark; Horvath, Rita; Pogoryelova, Oksana; Shah, Jinay; Koutsoukos, Tony; Skrinar, Alison; Kakkis, Emil; Bedrosian, Camille L; Mozaffar, Tahseen | Abstract: BackgroundGNE myopathy is a rare, autosomal recessive, muscle disease caused by mutations in GNE and is characterized by rimmed vacuoles on muscle biopsy and progressive distal to proximal muscle weakness.ObjectiveInvestigate the clinical presentation and progression of GNE myopathy.MethodsThe GNE Myopathy Disease Monitoring Program was an international, prospective, observational study in subjects with GNE myopathy. Muscle strength was assessed with hand-held dynamometry (HHD), with upper extremity (UE) and lower extremity (LE) composite scores reflecting upper and lower extremity muscle groups, respectively. The GNE myopathy-Functional Activity Scale (GNEM-FAS) was used to further assess impairment in mobility, upper extremity function, and self-care.ResultsEighty-seven of 101 enrolled subjects completed the trial until study closure by the sponsor; 60 completed 36 months. Mean (SD) HHD UE composite score decreased from 34.3 kg (32.0) at baseline to 29.4 kg (32.6) kg at month 36 (LS mean change [95%CI]: -3.8 kg [-5.9, -1.7]; P = 0.0005). Mean (SD) HHD LE composite score decreased from 32.0 kg (34.1) at baseline to 25.5 kg (31.2) at month 36 (LS mean change [95%CI]: -4.9 [-7.7, -2.2]; P = 0.0005). GNEM-FAS scores were more severe at baseline in subjects who walked l200 meters versus ≥200 meters in 6 minutes; in both groups, GNEM-FAS total, mobility, UE, and self-care scores decreased from baseline through month 36.ConclusionsThese findings demonstrate progressive decline in muscle strength in GNE myopathy and provide insight into the appropriate tools to detect clinically meaningful changes in future GNE myopathy interventional trials.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open Access EnglishAuthors:Uwe John; Yameng Lu; Sylke Wohlrab; Marco Groth; Jan Janouškovec; Gurjeet S. Kohli; Felix Christopher Mark; Ulf Bickmeyer; Sarah Farhat; Marius Felder; +7 moreUwe John; Yameng Lu; Sylke Wohlrab; Marco Groth; Jan Janouškovec; Gurjeet S. Kohli; Felix Christopher Mark; Ulf Bickmeyer; Sarah Farhat; Marius Felder; Stephan Frickenhaus; Laure Guillou; Patrick J. Keeling; Ahmed A. Moustafa; Betina M. Porcel; Klaus-Ulrich Valentin; Gernot Glöckner;Countries: Germany, Singapore, FranceProject: EC | MICRO B3 (287589)
Dinoflagellates are microbial eukaryotes that have exceptionally large nuclear genomes; however, their organelle genomes are small and fragmented and contain fewer genes than those of other eukaryotes. The genus Amoebophrya (Syndiniales) comprises endoparasites with high genetic diversity that can infect other dinoflagellates, such as those forming harmful algal blooms (e.g., Alexandrium). We sequenced the genome (~100 Mb) of Amoebophrya ceratii to investigate the early evolution of genomic characters in dinoflagellates. The A. ceratii genome encodes almost all essential biosynthetic pathways for self-sustaining cellular metabolism, suggesting a limited dependency on its host. Although dinoflagellates are thought to have descended from a photosynthetic ancestor, A. ceratii appears to have completely lost its plastid and nearly all genes of plastid origin. Functional mitochondria persist in all life stages of A. ceratii, but we found no evidence for the presence of a mitochondrial genome. Instead, all mitochondrial proteins appear to be lost or encoded in the A. ceratii nucleus. The parasitic marine dinoflagellate Amoebophrya is the first known eukaryote with aerobic mitochondria without a genome.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open AccessAuthors:Hendrik Bartolomaeus; András Balogh; Mina Yakoub; Susanne Homann; Lajos Markó; Sascha Höges; D. Tsvetkov; Alexander Krannich; Sebastian Wundersitz; Ellen G. Avery; +19 moreHendrik Bartolomaeus; András Balogh; Mina Yakoub; Susanne Homann; Lajos Markó; Sascha Höges; D. Tsvetkov; Alexander Krannich; Sebastian Wundersitz; Ellen G. Avery; Nadine Haase; Kristin Kräker; Lydia Hering; Martina Maase; Kristina Kusche-Vihrog; Maria Grandoch; Jens Fielitz; Stefan Kempa; Maik Gollasch; Zhaxybay Zhumadilov; Samat Kozhakhmetov; Almagul Kushugulova; Kai-Uwe Eckardt; Ralf Dechend; Lars Christian Rump; Sofia K. Forslund; Dominik N. Müller; Johannes Stegbauer; Nicola Wilck;Publisher: Ovid Technologies (Wolters Kluwer Health)
Background: Arterial hypertension and its organ sequelae show characteristics of T cell–mediated inflammatory diseases. Experimental anti-inflammatory therapies have been shown to ameliorate hypertensive end-organ damage. Recently, the CANTOS study (Canakinumab Antiinflammatory Thrombosis Outcome Study) targeting interleukin-1β demonstrated that anti-inflammatory therapy reduces cardiovascular risk. The gut microbiome plays a pivotal role in immune homeostasis and cardiovascular health. Short-chain fatty acids (SCFAs) are produced from dietary fiber by gut bacteria and affect host immune homeostasis. Here, we investigated effects of the SCFA propionate in 2 different mouse models of hypertensive cardiovascular damage. Methods: To investigate the effect of SCFAs on hypertensive cardiac damage and atherosclerosis, wild-type NMRI or apolipoprotein E knockout–deficient mice received propionate (200 mmol/L) or control in the drinking water. To induce hypertension, wild-type NMRI mice were infused with angiotensin II (1.44 mg·kg–1·d–1 subcutaneous) for 14 days. To accelerate the development of atherosclerosis, apolipoprotein E knockout mice were infused with angiotensin II (0.72 mg·kg–1·d–1 subcutaneous) for 28 days. Cardiac damage and atherosclerosis were assessed using histology, echocardiography, in vivo electrophysiology, immunofluorescence, and flow cytometry. Blood pressure was measured by radiotelemetry. Regulatory T cell depletion using PC61 antibody was used to examine the mode of action of propionate. Results: Propionate significantly attenuated cardiac hypertrophy, fibrosis, vascular dysfunction, and hypertension in both models. Susceptibility to cardiac ventricular arrhythmias was significantly reduced in propionate-treated angiotensin II–infused wild-type NMRI mice. Aortic atherosclerotic lesion area was significantly decreased in propionate-treated apolipoprotein E knockout–deficient mice. Systemic inflammation was mitigated by propionate treatment, quantified as a reduction in splenic effector memory T cell frequencies and splenic T helper 17 cells in both models, and a decrease in local cardiac immune cell infiltration in wild-type NMRI mice. Cardioprotective effects of propionate were abrogated in regulatory T cell–depleted angiotensin II–infused mice, suggesting the effect is regulatory T cell–dependent. Conclusions: Our data emphasize an immune-modulatory role of SCFAs and their importance for cardiovascular health. The data suggest that lifestyle modifications leading to augmented SCFA production could be a beneficial nonpharmacological preventive strategy for patients with hypertensive cardiovascular disease. Supplemental Digital Content is available in the text.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Other literature type . Preprint . 2021Open Access EnglishAuthors:Francesco Petrelli; Tamara Zehnder; Luca Pucci; Corrado Calì; Bianca Maria Bondiolotti; Alicia Molinero Perez; Glenn Dallérac; Nicole Déglon; Bruno Giros; Fulvio Magara; +4 moreFrancesco Petrelli; Tamara Zehnder; Luca Pucci; Corrado Calì; Bianca Maria Bondiolotti; Alicia Molinero Perez; Glenn Dallérac; Nicole Déglon; Bruno Giros; Fulvio Magara; Lorenzo Magrassi; Jean-Pierre Mothet; Linda D. Simmler; P. Bezzi;Publisher: HAL CCSDCountry: France
AbstractAstrocytes control synaptic activity by modulating peri-synaptic concentrations of ion and neurotransmitters including dopamine and, as such, can be critically involved in the modulation of some aspect of mammalian behavior. Here we report that genetic mouse model with a reduced medial prefrontal cortex (mPFC) dopamine levels, arising from astrocyte-specific conditional deletion of vesicular monoamine transporter 2 (VMAT2; aVMTA2cKO mice) shows excessive grooming and anxiety-like behaviour. The VMAT2cKO mice also develop a synaptic pathology, expressed through increased relative AMPA vs. NMDA receptor currents in synapses of the dorsal striatum receiving inputs from the mPFC. Importantly, behavioural and synaptic phenotypes are prevented by reexpression of mPFC VMAT2, showing that the deficits are driven by mPFC astrocytes. By analysing human tissue samples, we found that VMAT2 is expressed in human mPFC astrocytes, corroborating the potential translational relevance of our observations in mice. Our study shows that impairments of the astrocytic-control of dopamine in the mPFC has a profound impact on circuit function and behaviours, which resemble symptoms of anxiety disorders and obsessive compulsive disorder (OCD).
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:Huan Liu; Guangji Hu; İbrahim Alper Başar; Jianbing Li; Nathalie Lyczko; Ange Nzihou; Cigdem Eskicioglu;Huan Liu; Guangji Hu; İbrahim Alper Başar; Jianbing Li; Nathalie Lyczko; Ange Nzihou; Cigdem Eskicioglu;Publisher: ElsevierCountry: FranceProject: NSERC
International audience; Phosphorus (P) is a non-renewable resource, and its recovery and recycling are necessary for meeting future P demands and environmental conservation. Ash and hydrochar from incineration and hydrothermal liquefaction (HTL) of municipal sludge, respectively, represent promising sources for efficient P recovery. The full-scale application of wet-chemical techniques has proven their technical feasibility for P recovery from sludge-derived ash. HTL for sludge treatment has received significant attention for producing biocrude with net-positive energy recovery. P recovery from the solid by-product of sludge HTL, hydrochar, is a critical step in holistic sustainable sludge management. This review aims to guide P recovery from sludge-derived ash and hydrochar by presenting recent advances in wet-chemical extraction and precipitation. By comparing their characteristics, ash and hydrochar derived from municipal sludge exhibit similar feasibilities and challenges for P recovery. Extraction is recognized as the critical step for P recovery. The advantages and disadvantages of various P extraction approaches are provided. Acidic extraction achieves high efficiency (up to 100%) but requires removal of co-extracted heavy metals. Alkaline extraction prevents metals contamination but shows low efficiency (<70%). Sequential extraction is first identified as an important advance in this review, with promising P extraction efficiencies (70–91%) and low metal interferences. Three possible fertilizers (struvite, calcium phosphates, and vivianite) are recommended through the final precipitation, given their pros and cons of recovery. Ultimately, this review highlights the need for a wastewater biorefinery integrating wastewater treatment, HTL (energy recovery), and nutrient recovery for sustainable sludge management.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.
26,166 Research products, page 1 of 2,617
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- Publication . Conference object . 2018Authors:Masen Lamb; Andrew Norton; Bruce Macintosh; Carlos Correia; Jean-Pierre Véran; Christian Marois; Suresh Sivanandam;Masen Lamb; Andrew Norton; Bruce Macintosh; Carlos Correia; Jean-Pierre Véran; Christian Marois; Suresh Sivanandam;
doi: 10.1117/12.2313458
Publisher: SPIEWe explore the application of phase diversity to calibrate the non common path aberrations (NCPA) in the Gemini Planet Imager (GPI). This is first investigated in simulation in order to characterize the ideal technique parameters with simulated GPI calibration source data. The best working simulation parameters are derived and we establish the algorithm's capability to recover an injected astigmatism. Furthermore, the real data appear to exhibit signs of de-centering between the in and out of focus images that are required by phase diversity; this effect can arise when the diverse images are acquired in closed loop and are close to the non-linear regime of the wavefront sensor. We show in simulation that this effect can inhibit our algorithm, which does not take into account the impact of de-centering between images. To mitigate this effect, we validate the technique of using a single diverse image with our algorithm; this is first demonstrated in simulation and then applied to the real GPI data. Following this approach, we find that we can successfully recover a known astigmatism injection using the real GPI data and subsequently apply an NCPA correction to GPI (in the format of offset reference slopes) to improve the relative Strehl ratio by 5%; we note this NCPA correction application is rudimentary and a more thorough application will be investigated in the near future. Finally, the estimated NCPA in the form of astigmatism and coma agree well with the magnitude of the same modes reported by Poyneer et al. 2016.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Open Access EnglishAuthors:Mark Haas; Alexandre Loupy; Carmen Lefaucheur; Candice Roufosse; Denis Glotz; Daniel Serón; Brian J. Nankivell; Philip F. Halloran; Robert B. Colvin; Enver Akalin; +19 moreMark Haas; Alexandre Loupy; Carmen Lefaucheur; Candice Roufosse; Denis Glotz; Daniel Serón; Brian J. Nankivell; Philip F. Halloran; Robert B. Colvin; Enver Akalin; Nada Alachkar; Serena M. Bagnasco; Yassine Bouatou; Jan U. Becker; Lynn D. Cornell; J.-P. Duong Van Huyen; Ian W. Gibson; Edward S. Kraus; Roslyn B. Mannon; Maarten Naesens; Volker Nickeleit; Peter Nickerson; Dorry L. Segev; Harsharan K. Singh; Mark D. Stegall; P. Randhawa; Lorraine C. Racusen; Kim Solez; Michael Mengel;Countries: Spain, United States, United Kingdom
The kidney sessions of the 2017 Banff Conference focused on 2 areas: clinical implications of inflammation in areas of interstitial fibrosis and tubular atrophy (i‐IFTA) and its relationship to T cell–mediated rejection (TCMR), and the continued evolution of molecular diagnostics, particularly in the diagnosis of antibody‐mediated rejection (ABMR). In confirmation of previous studies, it was independently demonstrated by 2 groups that i‐IFTA is associated with reduced graft survival. Furthermore, these groups presented that i‐IFTA, particularly when involving >25% of sclerotic cortex in association with tubulitis, is often a sequela of acute TCMR in association with underimmunosuppression. The classification was thus revised to include moderate i‐IFTA plus moderate or severe tubulitis as diagnostic of chronic active TCMR. Other studies demonstrated that certain molecular classifiers improve diagnosis of ABMR beyond what is possible with histology, C4d, and detection of donor‐specific antibodies (DSAs) and that both C4d and validated molecular assays can serve as potential alternatives and/or complements to DSAs in the diagnosis of ABMR. The Banff ABMR criteria are thus updated to include these alternatives. Finally, the present report paves the way for the Banff scheme to be part of an integrative approach for defining surrogate endpoints in next‐generation clinical trials. The Banff consortium presents revisions to the diagnostic criteria for T cell– and antibody‐mediated kidney transplant rejection, including specific criteria for chronic active T cell–mediated rejection, plus prospects for integrative endpoints in clinical trials. See related articles on pages 321, 364, and 377.
Substantial popularitySubstantial popularity In top 1%Substantial influencePopularity: Citation-based measure reflecting the current impact.Substantial influence In top 1%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2020 . Embargo End Date: 04 Feb 2021Open AccessAuthors:Carlevaro-Fita J.; Lanzos A.; Feuerbach L.; Hong C.; Mas-Ponte D.; Pedersen J. S.; Abascal F.; Amin S. B.; Bader G. D.; Barenboim J.; +127 moreCarlevaro-Fita J.; Lanzos A.; Feuerbach L.; Hong C.; Mas-Ponte D.; Pedersen J. S.; Abascal F.; Amin S. B.; Bader G. D.; Barenboim J.; Beroukhim R.; Bertl J.; Boroevich K. A.; Brunak S.; Campbell P. J.; Carlevaro-Fita J.; Chakravarty D.; Chan C. W. Y.; Chen K.; Choi J. K.; Deu-Pons J.; Dhingra P.; Diamanti K.; Feuerbach L.; Fink J. L.; Fonseca N. A.; Frigola J.; Gambacorti Passerini C.; Garsed D. W.; Gerstein M.; Getz G.; Gonzalez-Perez A.; Guo Q.; Gut I. G.; Haan D.; Hamilton M. P.; Haradhvala N. J.; Harmanci A. O.; Helmy M.; Herrmann C.; Hess J. M.; Hobolth A.; Hodzic E.; Hong C.; Hornshoj H.; Isaev K.; Izarzugaza J. M. G.; Johnson R.; Johnson T. A.; Juul M.; Juul R. I.; Kahles A.; Kahraman A.; Kellis M.; Khurana E.; Kim J.; Kim J. K.; Kim Y.; Komorowski J.; Korbel J. O.; Kumar S.; Lanzos A.; Larsson E.; Lawrence M. S.; Lee D.; Lehmann K. -V.; Li S.; Li X.; Lin Z.; Liu E. M.; Lochovsky L.; Lou S.; Madsen T.; Marchal K.; Martincorena I.; Martinez-Fundichely A.; Maruvka Y. E.; McGillivray P. D.; Meyerson W.; Muinos F.; Mularoni L.; Nakagawa H.; Nielsen M. M.; Paczkowska M.; Park K.; Park K.; Pedersen J. S.; Pich O.; Pons T.; Pulido-Tamayo S.; Raphael B. J.; Reimand J.; Reyes-Salazar I.; Reyna M. A.; Rheinbay E.; Rubin M. A.; Rubio-Perez C.; Sabarinathan R.; Sahinalp S. C.; Saksena G.; Salichos L.; Sander C.; Schumacher S. E.; Shackleton M.; Shapira O.; Shen C.; Shrestha R.; Shuai S.; Sidiropoulos N.; Sieverling L.; Sinnott-Armstrong N.; Stein L. D.; Stuart J. M.; Tamborero D.; Tiao G.; Tsunoda T.; Umer H. M.; Uuskula-Reimand L.; Valencia A.; Vazquez M.; Verbeke L. P. C.; Wadelius C.; Wadi L.; Wang J.; Warrell J.; Waszak S. M.; Weischenfeldt J.; Wheeler D. A.; Wu G.; Yu J.; Zhang J.; Zhang X.; Zhang Y.; Zhao Z.; Zou L.; von Mering C.; Johnson R.;
doi: 10.17863/cam.64282 , 10.3929/ethz-b-000399368 , 10.17863/cam.64917 , 10.7892/boris.143033 , 10.1038/s42003-019-0741-7
pmc: PMC7002399
handle: 2066/288696 , 20.500.11850/399368 , 1854/LU-8658728
Publisher: Apollo - University of Cambridge RepositoryCountries: Netherlands, Switzerland, Italy, Belgium, Switzerland, Sweden, Spain, Denmark, United KingdomLong non-coding RNAs (lncRNAs) are a growing focus of cancer genomics studies, creating the need for a resource of lncRNAs with validated cancer roles. Furthermore, it remains debated whether mutated lncRNAs can drive tumorigenesis, and whether such functions could be conserved during evolution. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, we introduce the Cancer LncRNA Census (CLC), a compilation of 122 GENCODE lncRNAs with causal roles in cancer phenotypes. In contrast to existing databases, CLC requires strong functional or genetic evidence. CLC genes are enriched amongst driver genes predicted from somatic mutations, and display characteristic genomic features. Strikingly, CLC genes are enriched for driver mutations from unbiased, genome-wide transposon-mutagenesis screens in mice. We identified 10 tumour-causing mutations in orthologues of 8 lncRNAs, including LINC-PINT and NEAT1, but not MALAT1. Thus CLC represents a dataset of high-confidence cancer lncRNAs. Mutagenesis maps are a novel means for identifying deeply-conserved roles of lncRNAs in tumorigenesis. Communications Biology, 3 (1) ISSN:2399-3642
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open AccessAuthors:Gordon Pennycook; Jonathon McPhetres; Bence Bago; David G. Rand;Gordon Pennycook; Jonathon McPhetres; Bence Bago; David G. Rand;Publisher: SAGE PublicationsCountries: United Kingdom, FranceProject: CIHR , SSHRC
What are the psychological consequences of the increasingly politicized nature of the COVID-19 pandemic in the United States relative to similar Western countries? In a two-wave study completed early (March) and later (December) in the pandemic, we found that polarization was greater in the United States ( N = 1,339) than in Canada ( N = 644) and the United Kingdom. ( N = 1,283). Political conservatism in the United States was strongly associated with engaging in weaker mitigation behaviors, lower COVID-19 risk perceptions, greater misperceptions, and stronger vaccination hesitancy. Although there was some evidence that cognitive sophistication was associated with increased polarization in the United States in December (but not March), cognitive sophistication was nonetheless consistently negatively correlated with misperceptions and vaccination hesitancy across time, countries, and party lines. Furthermore, COVID-19 skepticism in the United States was strongly correlated with distrust in liberal-leaning mainstream news outlets and trust in conservative-leaning news outlets, suggesting that polarization may be driven by differences in information environments.
Substantial popularitySubstantial popularity In top 1%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Closed AccessAuthors:Romain Jouffroy; Xavier Bobbia; Tobias Gauss; Pierre Bouzat; Michelet Pierre;Romain Jouffroy; Xavier Bobbia; Tobias Gauss; Pierre Bouzat; Michelet Pierre;
pmid: 30308243
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:Hanns Lochmüller; Anthony Behin; Ivailo Tournev; Mark A. Tarnopolsky; Rita Horvath; Oksana Pogoryelova; J. Shah; Tony Koutsoukos; Alison Skrinar; Emil D. Kakkis; +2 moreHanns Lochmüller; Anthony Behin; Ivailo Tournev; Mark A. Tarnopolsky; Rita Horvath; Oksana Pogoryelova; J. Shah; Tony Koutsoukos; Alison Skrinar; Emil D. Kakkis; Camille L Bedrosian; Tahseen Mozaffar;Publisher: HAL CCSDCountries: France, United States, United Kingdom
Author(s): Lochmuller, Hanns; Behin, Anthony; Tournev, Ivailo; Tarnopolsky, Mark; Horvath, Rita; Pogoryelova, Oksana; Shah, Jinay; Koutsoukos, Tony; Skrinar, Alison; Kakkis, Emil; Bedrosian, Camille L; Mozaffar, Tahseen | Abstract: BackgroundGNE myopathy is a rare, autosomal recessive, muscle disease caused by mutations in GNE and is characterized by rimmed vacuoles on muscle biopsy and progressive distal to proximal muscle weakness.ObjectiveInvestigate the clinical presentation and progression of GNE myopathy.MethodsThe GNE Myopathy Disease Monitoring Program was an international, prospective, observational study in subjects with GNE myopathy. Muscle strength was assessed with hand-held dynamometry (HHD), with upper extremity (UE) and lower extremity (LE) composite scores reflecting upper and lower extremity muscle groups, respectively. The GNE myopathy-Functional Activity Scale (GNEM-FAS) was used to further assess impairment in mobility, upper extremity function, and self-care.ResultsEighty-seven of 101 enrolled subjects completed the trial until study closure by the sponsor; 60 completed 36 months. Mean (SD) HHD UE composite score decreased from 34.3 kg (32.0) at baseline to 29.4 kg (32.6) kg at month 36 (LS mean change [95%CI]: -3.8 kg [-5.9, -1.7]; P = 0.0005). Mean (SD) HHD LE composite score decreased from 32.0 kg (34.1) at baseline to 25.5 kg (31.2) at month 36 (LS mean change [95%CI]: -4.9 [-7.7, -2.2]; P = 0.0005). GNEM-FAS scores were more severe at baseline in subjects who walked l200 meters versus ≥200 meters in 6 minutes; in both groups, GNEM-FAS total, mobility, UE, and self-care scores decreased from baseline through month 36.ConclusionsThese findings demonstrate progressive decline in muscle strength in GNE myopathy and provide insight into the appropriate tools to detect clinically meaningful changes in future GNE myopathy interventional trials.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open Access EnglishAuthors:Uwe John; Yameng Lu; Sylke Wohlrab; Marco Groth; Jan Janouškovec; Gurjeet S. Kohli; Felix Christopher Mark; Ulf Bickmeyer; Sarah Farhat; Marius Felder; +7 moreUwe John; Yameng Lu; Sylke Wohlrab; Marco Groth; Jan Janouškovec; Gurjeet S. Kohli; Felix Christopher Mark; Ulf Bickmeyer; Sarah Farhat; Marius Felder; Stephan Frickenhaus; Laure Guillou; Patrick J. Keeling; Ahmed A. Moustafa; Betina M. Porcel; Klaus-Ulrich Valentin; Gernot Glöckner;Countries: Germany, Singapore, FranceProject: EC | MICRO B3 (287589)
Dinoflagellates are microbial eukaryotes that have exceptionally large nuclear genomes; however, their organelle genomes are small and fragmented and contain fewer genes than those of other eukaryotes. The genus Amoebophrya (Syndiniales) comprises endoparasites with high genetic diversity that can infect other dinoflagellates, such as those forming harmful algal blooms (e.g., Alexandrium). We sequenced the genome (~100 Mb) of Amoebophrya ceratii to investigate the early evolution of genomic characters in dinoflagellates. The A. ceratii genome encodes almost all essential biosynthetic pathways for self-sustaining cellular metabolism, suggesting a limited dependency on its host. Although dinoflagellates are thought to have descended from a photosynthetic ancestor, A. ceratii appears to have completely lost its plastid and nearly all genes of plastid origin. Functional mitochondria persist in all life stages of A. ceratii, but we found no evidence for the presence of a mitochondrial genome. Instead, all mitochondrial proteins appear to be lost or encoded in the A. ceratii nucleus. The parasitic marine dinoflagellate Amoebophrya is the first known eukaryote with aerobic mitochondria without a genome.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open AccessAuthors:Hendrik Bartolomaeus; András Balogh; Mina Yakoub; Susanne Homann; Lajos Markó; Sascha Höges; D. Tsvetkov; Alexander Krannich; Sebastian Wundersitz; Ellen G. Avery; +19 moreHendrik Bartolomaeus; András Balogh; Mina Yakoub; Susanne Homann; Lajos Markó; Sascha Höges; D. Tsvetkov; Alexander Krannich; Sebastian Wundersitz; Ellen G. Avery; Nadine Haase; Kristin Kräker; Lydia Hering; Martina Maase; Kristina Kusche-Vihrog; Maria Grandoch; Jens Fielitz; Stefan Kempa; Maik Gollasch; Zhaxybay Zhumadilov; Samat Kozhakhmetov; Almagul Kushugulova; Kai-Uwe Eckardt; Ralf Dechend; Lars Christian Rump; Sofia K. Forslund; Dominik N. Müller; Johannes Stegbauer; Nicola Wilck;Publisher: Ovid Technologies (Wolters Kluwer Health)
Background: Arterial hypertension and its organ sequelae show characteristics of T cell–mediated inflammatory diseases. Experimental anti-inflammatory therapies have been shown to ameliorate hypertensive end-organ damage. Recently, the CANTOS study (Canakinumab Antiinflammatory Thrombosis Outcome Study) targeting interleukin-1β demonstrated that anti-inflammatory therapy reduces cardiovascular risk. The gut microbiome plays a pivotal role in immune homeostasis and cardiovascular health. Short-chain fatty acids (SCFAs) are produced from dietary fiber by gut bacteria and affect host immune homeostasis. Here, we investigated effects of the SCFA propionate in 2 different mouse models of hypertensive cardiovascular damage. Methods: To investigate the effect of SCFAs on hypertensive cardiac damage and atherosclerosis, wild-type NMRI or apolipoprotein E knockout–deficient mice received propionate (200 mmol/L) or control in the drinking water. To induce hypertension, wild-type NMRI mice were infused with angiotensin II (1.44 mg·kg–1·d–1 subcutaneous) for 14 days. To accelerate the development of atherosclerosis, apolipoprotein E knockout mice were infused with angiotensin II (0.72 mg·kg–1·d–1 subcutaneous) for 28 days. Cardiac damage and atherosclerosis were assessed using histology, echocardiography, in vivo electrophysiology, immunofluorescence, and flow cytometry. Blood pressure was measured by radiotelemetry. Regulatory T cell depletion using PC61 antibody was used to examine the mode of action of propionate. Results: Propionate significantly attenuated cardiac hypertrophy, fibrosis, vascular dysfunction, and hypertension in both models. Susceptibility to cardiac ventricular arrhythmias was significantly reduced in propionate-treated angiotensin II–infused wild-type NMRI mice. Aortic atherosclerotic lesion area was significantly decreased in propionate-treated apolipoprotein E knockout–deficient mice. Systemic inflammation was mitigated by propionate treatment, quantified as a reduction in splenic effector memory T cell frequencies and splenic T helper 17 cells in both models, and a decrease in local cardiac immune cell infiltration in wild-type NMRI mice. Cardioprotective effects of propionate were abrogated in regulatory T cell–depleted angiotensin II–infused mice, suggesting the effect is regulatory T cell–dependent. Conclusions: Our data emphasize an immune-modulatory role of SCFAs and their importance for cardiovascular health. The data suggest that lifestyle modifications leading to augmented SCFA production could be a beneficial nonpharmacological preventive strategy for patients with hypertensive cardiovascular disease. Supplemental Digital Content is available in the text.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Other literature type . Preprint . 2021Open Access EnglishAuthors:Francesco Petrelli; Tamara Zehnder; Luca Pucci; Corrado Calì; Bianca Maria Bondiolotti; Alicia Molinero Perez; Glenn Dallérac; Nicole Déglon; Bruno Giros; Fulvio Magara; +4 moreFrancesco Petrelli; Tamara Zehnder; Luca Pucci; Corrado Calì; Bianca Maria Bondiolotti; Alicia Molinero Perez; Glenn Dallérac; Nicole Déglon; Bruno Giros; Fulvio Magara; Lorenzo Magrassi; Jean-Pierre Mothet; Linda D. Simmler; P. Bezzi;Publisher: HAL CCSDCountry: France
AbstractAstrocytes control synaptic activity by modulating peri-synaptic concentrations of ion and neurotransmitters including dopamine and, as such, can be critically involved in the modulation of some aspect of mammalian behavior. Here we report that genetic mouse model with a reduced medial prefrontal cortex (mPFC) dopamine levels, arising from astrocyte-specific conditional deletion of vesicular monoamine transporter 2 (VMAT2; aVMTA2cKO mice) shows excessive grooming and anxiety-like behaviour. The VMAT2cKO mice also develop a synaptic pathology, expressed through increased relative AMPA vs. NMDA receptor currents in synapses of the dorsal striatum receiving inputs from the mPFC. Importantly, behavioural and synaptic phenotypes are prevented by reexpression of mPFC VMAT2, showing that the deficits are driven by mPFC astrocytes. By analysing human tissue samples, we found that VMAT2 is expressed in human mPFC astrocytes, corroborating the potential translational relevance of our observations in mice. Our study shows that impairments of the astrocytic-control of dopamine in the mPFC has a profound impact on circuit function and behaviours, which resemble symptoms of anxiety disorders and obsessive compulsive disorder (OCD).
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:Huan Liu; Guangji Hu; İbrahim Alper Başar; Jianbing Li; Nathalie Lyczko; Ange Nzihou; Cigdem Eskicioglu;Huan Liu; Guangji Hu; İbrahim Alper Başar; Jianbing Li; Nathalie Lyczko; Ange Nzihou; Cigdem Eskicioglu;Publisher: ElsevierCountry: FranceProject: NSERC
International audience; Phosphorus (P) is a non-renewable resource, and its recovery and recycling are necessary for meeting future P demands and environmental conservation. Ash and hydrochar from incineration and hydrothermal liquefaction (HTL) of municipal sludge, respectively, represent promising sources for efficient P recovery. The full-scale application of wet-chemical techniques has proven their technical feasibility for P recovery from sludge-derived ash. HTL for sludge treatment has received significant attention for producing biocrude with net-positive energy recovery. P recovery from the solid by-product of sludge HTL, hydrochar, is a critical step in holistic sustainable sludge management. This review aims to guide P recovery from sludge-derived ash and hydrochar by presenting recent advances in wet-chemical extraction and precipitation. By comparing their characteristics, ash and hydrochar derived from municipal sludge exhibit similar feasibilities and challenges for P recovery. Extraction is recognized as the critical step for P recovery. The advantages and disadvantages of various P extraction approaches are provided. Acidic extraction achieves high efficiency (up to 100%) but requires removal of co-extracted heavy metals. Alkaline extraction prevents metals contamination but shows low efficiency (<70%). Sequential extraction is first identified as an important advance in this review, with promising P extraction efficiencies (70–91%) and low metal interferences. Three possible fertilizers (struvite, calcium phosphates, and vivianite) are recommended through the final precipitation, given their pros and cons of recovery. Ultimately, this review highlights the need for a wastewater biorefinery integrating wastewater treatment, HTL (energy recovery), and nutrient recovery for sustainable sludge management.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.