Mètres 1 m est égal à 1,0936 verges ou à 39,370 pouces. Depuis 1983, le mètre a été officiellement défini comme étant la longueur du trajet parcouru par la lumière dans le vide pendant un intervalle de temps de de seconde.
Lenuméro de téléphone +33 01 87 64 13 46 est un numéro valide et a un notation neutre . Le numéro de téléphone appartient la Louche . Nous n'enregistrons aucune évaluation pour ce
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Webcam de UshuaiaArgentine - Terre de Feu - 6 mUshuaia METEOVous visualisez en direct la webcam de Ushuaia, localisée dans la région Terre de Feu, Argentine. Cette webcam se situe à une altitude de 6 mètres, la température indique au dernier relevé degrés et le vent moyen souffle à km/ nombre de visites de ce spot est de 9 939, en cliquant sur Gaston Zajaczkowski, vous pouvez visiter le site du propriétaire de la webcam où il fait actuellement le plus chaud se trouve à Palm Springs et atteint une température de °.Celle où il fait le plus froid est située à Namcha Barwa avec °.Voici la liste des 15 webcams les plus proches de Ushuaia, cliquez sur les liens ci-dessous pour visiter ces autres webcams - Ushuaia km- Comodoro Rivadaria km- San Carlos de Bariloche km- Osorno km- Corralco km- Miramar km- Mar Chiquita km- Pinamar km- Buenos Aires km- Santiago de Chili km- Santiago de Chili km- Montevideo km- Portillo km- Colola km- Jaguelito km- Porto Alegre kmEt la liste des 15 webcams les plus éloignées de Ushuaia - Severobaikalsk km- Tchita km- Oust-Kout km- Listvianka km- Irkoutsk km- Baikalsk - Sobolinaya km- Bratsk km- Lensk km- Olekminsk km- Krasnoyarsk km- Bulgunnyakhtakh km- Bestyakh km- Oudatchny km- Abakan km- Yakutsk km- Sangar kmDécouvrez toutes les webcams touristiques de toutes les webcams touristiques de Terre de toutes les webcams touristiques du site & Météorologie Dernière image et timelapse
Single-nucleus and spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment. Hwang WL, Jagadeesh KA, Guo JA, Hoffman HI, Yadollahpour P, Reeves JW, Mohan R, Drokhlyansky E, Van Wittenberghe N, Ashenberg O, Farhi SL, Schapiro D, Divakar P, Miller E, Zollinger DR, Eng G, Schenkel JM, Su J, Shiau C, Yu P, Freed-Pastor WA, Abbondanza D, Mehta A, Gould J, Lambden C, Porter CBM, Tsankov A, Dionne D, Waldman J, Cuoco MS, Nguyen L, Delorey T, Phillips D, Barth JL, Kem M, Rodrigues C, Ciprani D, Roldan J, Zelga P, Jorgji V, Chen JH, Ely Z, Zhao D, Fuhrman K, Fropf R, Beechem JM, Loeffler JS, Ryan DP, Weekes CD, Ferrone CR, Qadan M, Aryee MJ, Jain RK, Neuberg DS, Wo JY, Hong TS, Xavier R, Aguirre AJ, Rozenblatt-Rosen O, Mino-Kenudson M, Castillo CF, Liss AS, Ting DT, Jacks T, Regev A. Hwang WL, et al. Nat Genet. 2022 Aug;5481178-1191. doi Epub 2022 Jul 28. Nat Genet. 2022. PMID 35902743 Genome-wide bidirectional CRISPR screens identify mucins as host factors modulating SARS-CoV-2 infection. Biering SB, Sarnik SA, Wang E, Zengel JR, Leist SR, Schäfer A, Sathyan V, Hawkins P, Okuda K, Tau C, Jangid AR, Duffy CV, Wei J, Gilmore RC, Alfajaro MM, Strine MS, Nguyenla X, Van Dis E, Catamura C, Yamashiro LH, Belk JA, Begeman A, Stark JC, Shon DJ, Fox DM, Ezzatpour S, Huang E, Olegario N, Rustagi A, Volmer AS, Livraghi-Butrico A, Wehri E, Behringer RR, Cheon DJ, Schaletzky J, Aguilar HC, Puschnik AS, Button B, Pinsky BA, Blish CA, Baric RS, O'Neal WK, Bertozzi CR, Wilen CB, Boucher RC, Carette JE, Stanley SA, Harris E, Konermann S, Hsu PD. Biering SB, et al. Nat Genet. 2022 Aug;5481078-1089. doi Epub 2022 Jul 25. Nat Genet. 2022. PMID 35879412 Free PMC article.
Review . 2022 Jan;431300-328. doi Epub 2021 Feb 21. Ida E Sønderby 1 2 3 , Sophia I Thomopoulos 4 , Dennis van der Meer 2 5 , Daqiang Sun 6 7 , Julio E Villalon-Reina 4 , Ingrid Agartz 8 9 10 , Katrin Amunts 11 12 , Celso Arango 13 14 , Nicola J Armstrong 15 , Rosa Ayesa-Arriola 14 16 , Geor Bakker 17 18 , Anne S Bassett 19 20 21 , Dorret I Boomsma 22 23 , Robin Bülow 24 , Nancy J Butcher 21 25 , Vince D Calhoun 26 , Svenja Caspers 11 27 , Eva W C Chow 19 21 , Sven Cichon 11 28 29 , Simone Ciufolini 30 , Michael C Craig 31 , Benedicto Crespo-Facorro 32 , Adam C Cunningham 33 , Anders M Dale 34 35 , Paola Dazzan 36 , Greig I de Zubicaray 37 , Srdjan Djurovic 1 38 , Joanne L Doherty 33 39 , Gary Donohoe 40 , Bogdan Draganski 41 42 , Courtney A Durdle 43 , Stefan Ehrlich 44 , Beverly S Emanuel 45 , Thomas Espeseth 46 47 , Simon E Fisher 48 49 , Tian Ge 50 51 , David C Glahn 52 53 , Hans J Grabe 54 55 , Raquel E Gur 56 57 , Boris A Gutman 58 , Jan Haavik 59 60 , Asta K Håberg 61 62 , Laura A Hansen 63 , Ryota Hashimoto 64 65 , Derrek P Hibar 66 , Avram J Holmes 67 68 , Jouke-Jan Hottenga 22 , Hilleke E Hulshoff Pol 69 , Maria Jalbrzikowski 70 , Emma E M Knowles 51 71 , Leila Kushan 72 , David E J Linden 73 74 , Jingyu Liu 26 75 , Astri J Lundervold 76 , Sandra Martin-Brevet 41 , Kenia Martínez 13 14 77 , Karen A Mather 78 79 , Samuel R Mathias 53 71 , Donna M McDonald-McGinn 45 80 81 , Allan F McRae 82 , Sarah E Medland 83 , Torgeir Moberget 84 , Claudia Modenato 41 85 , Jennifer Monereo Sánchez 73 86 87 , Clara A Moreau 88 , Thomas W Mühleisen 11 12 29 , Tomas Paus 89 90 , Zdenka Pausova 91 , Carlos Prieto 92 , Anjanibhargavi Ragothaman 93 , Céline S Reinbold 29 94 , Tiago Reis Marques 30 95 , Gabriela M Repetto 96 , Alexandre Reymond 97 , David R Roalf 56 , Borja Rodriguez-Herreros 98 , James J Rucker 36 , Perminder S Sachdev 78 99 , James E Schmitt 100 , Peter R Schofield 79 101 , Ana I Silva 74 102 , Hreinn Stefansson 103 , Dan J Stein 104 , Christian K Tamnes 2 9 105 , Diana Tordesillas-Gutiérrez 14 106 , Magnus O Ulfarsson 103 107 , Ariana Vajdi 72 , Dennis van 't Ent 22 , Marianne B M van den Bree 33 , Evangelos Vassos 108 , Javier Vázquez-Bourgon 14 16 109 , Fidel Vila-Rodriguez 110 , G Bragi Walters 103 111 , Wei Wen 78 , Lars T Westlye 3 46 112 , Katharina Wittfeld 54 55 , Elaine H Zackai 45 80 , Kári Stefánsson 103 111 , Sebastien Jacquemont 88 113 , Paul M Thompson 4 , Carrie E Bearden 6 114 , Ole A Andreassen 2 , ENIGMA-CNV Working Group; ENIGMA Deletion Syndrome Working Group Collaborators, Affiliations PMID 33615640 PMCID PMC8675420 DOI Free PMC article Review Effects of copy number variations on brain structure and risk for psychiatric illness Large-scale studies from the ENIGMA working groups on CNVs Ida E Sønderby et al. Hum Brain Mapp. 2022 Jan. Free PMC article Abstract The Enhancing NeuroImaging Genetics through Meta-Analysis copy number variant ENIGMA-CNV and Deletion Syndrome Working Groups 22q-ENIGMA WGs were created to gain insight into the involvement of genetic factors in human brain development and related cognitive, psychiatric and behavioral manifestations. To that end, the ENIGMA-CNV WG has collated CNV and magnetic resonance imaging MRI data from ~49,000 individuals across 38 global research sites, yielding one of the largest studies to date on the effects of CNVs on brain structures in the general population. The 22q-ENIGMA WG includes 12 international research centers that assessed over 533 individuals with a confirmed deletion syndrome, 40 with duplications, and 333 typically developing controls, creating the largest-ever CNV neuroimaging data set. In this review, we outline the ENIGMA infrastructure and procedures for multi-site analysis of CNVs and MRI data. So far, ENIGMA has identified effects of the distal, and distal CNVs on subcortical and cortical brain structures. Each CNV is associated with differences in cognitive, neurodevelopmental and neuropsychiatric traits, with characteristic patterns of brain structural abnormalities. Evidence of gene-dosage effects on distinct brain regions also emerged, providing further insight into genotype-phenotype relationships. Taken together, these results offer a more comprehensive picture of molecular mechanisms involved in typical and atypical brain development. This "genotype-first" approach also contributes to our understanding of the etiopathogenesis of brain disorders. Finally, we outline future directions to better understand effects of CNVs on brain structure and behavior. Keywords brain structural imaging; copy number variant; diffusion tensor imaging; evolution; genetics-first approach; neurodevelopmental disorders; psychiatric disorders. © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. Figures FIGURE 1 Copy number variants. CNV carriers may have a deletion one copy of region D, red or duplication three copies of region D, blue compared with the normal copy number two copies of region D, black. Reciprocal CNVs are a deletion and duplication occurring at the same locus FIGURE 2 World map of the ENIGMA‐CNV and 22q‐ENIGMA WG study sites. A full list of participating cohorts and members for ENIGMA‐CNV and 22q‐ENIGMA may be found at the respective webpages and Both working groups consist of international teams of clinicians, neuroscientists, engineers, bioinformaticians, statisticians, computer scientists, and geneticists who pool their resources to conduct large‐scale neuroimaging studies of CNVs FIGURE 3 The overall procedure for participation in ENIGMA‐CNV and 22q‐ENIGMA FIGURE 4 The subcortical findings from ENIGMA‐CNV, 22q‐ENIGMA and selected ENIGMA psychiatric working groups. Averaged left and right subcortical volume case versus non‐carriers NC Cohen's d effect size estimates for the ENIGMA SCZ van Erp et al., 2016, ADHD Hoogman et al., 2017, ASD van Rooij et al., 2018, 22q11DS Ching et al., 2020, CNV van der Meer, 2019, distal CNV Sønderby et al., 2018, and the distal CNV in review studies. 22q+Psy vs. 22q‐Psy indicates a comparison from Ching et al. 2020 where a subset of individuals with deletion syndrome with a history of psychosis were compared to a matched group of individuals with deletion without a history of psychosis. Significant group differences are indicated by an asterisk *; the plot includes vertical 95% confidence intervals FIGURE 5 Cortical findings from the ENIGMA‐CNV, 22q‐ENIGMA, and selected ENIGMA psychiatric working groups. Copy number variant CNV analyses for deletion or duplication carriers vs non‐carriers for the CNVs ICV‐corrected; van der Meer et al., 2019, distal CNVs ICV‐corrected; in review and 22q11DS Sun et al., 2018. 22q11DS results include 22q11DS psychosis deletion Del+Psy vs non psychosis deletion Del‐Psy; left hemisphere shown. Behaviorally defined disorders analyses Results are shown from case‐control studies from ASD's mega‐analysis left hemisphere shown; van Rooij et al., 2018, all ages in ADHD combined children, adolescents and adults; Hoogman et al., 2017, all types of epilepsies combined left hemisphere shown; Whelan et al., 2018, and schizophrenia SCZ; left hemisphere shown; van Erp et al., 2018. Only significant results are shown Similar articles Quantifying the Effects of Copy Number Variants on Brain Structure A Multisite Genetic-First Study. Martin-Brevet S, Rodríguez-Herreros B, Nielsen JA, Moreau C, Modenato C, Maillard AM, Pain A, Richetin S, Jønch AE, Qureshi AY, Zürcher NR, Conus P; European Consortium; Simons Variation in Individuals Project VIP Consortium, Chung WK, Sherr EH, Spiro JE, Kherif F, Beckmann JS, Hadjikhani N, Reymond A, Buckner RL, Draganski B, Jacquemont S. Martin-Brevet S, et al. Biol Psychiatry. 2018 Aug 15;844253-264. doi Epub 2018 Mar 27. Biol Psychiatry. 2018. PMID 29778275 Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK IMAGINE-ID a case-control cohort study. Chawner SJRA, Owen MJ, Holmans P, Raymond FL, Skuse D, Hall J, van den Bree MBM. Chawner SJRA, et al. Lancet Psychiatry. 2019 Jun;66493-505. doi Epub 2019 May 2. Lancet Psychiatry. 2019. PMID 31056457 Effects of eight neuropsychiatric copy number variants on human brain structure. Modenato C, Kumar K, Moreau C, Martin-Brevet S, Huguet G, Schramm C, Jean-Louis M, Martin CO, Younis N, Tamer P, Douard E, Thébault-Dagher F, Côté V, Charlebois AR, Deguire F, Maillard AM, Rodriguez-Herreros B, Pain A, Richetin S; European Consortium; Simons Searchlight Consortium, Melie-Garcia L, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Chakravarty M, Bzdok D, Bearden CE, Draganski B, Jacquemont S. Modenato C, et al. Transl Psychiatry. 2021 Jul 20;111399. doi Transl Psychiatry. 2021. PMID 34285187 Free PMC article. Lessons Learned From Neuroimaging Studies of Copy Number Variants A Systematic Review. Modenato C, Martin-Brevet S, Moreau CA, Rodriguez-Herreros B, Kumar K, Draganski B, Sønderby IE, Jacquemont S. Modenato C, et al. Biol Psychiatry. 2021 Nov 1;909596-610. doi Epub 2021 Jun 15. Biol Psychiatry. 2021. PMID 34509290 Review. Animal models of psychiatric disorders that reflect human copy number variation. Nomura J, Takumi T. Nomura J, et al. Neural Plast. 2012;2012589524. doi Epub 2012 Jul 30. Neural Plast. 2012. PMID 22900207 Free PMC article. Review. Cited by Cross disorder comparisons of brain structure in schizophrenia, bipolar disorder, major depressive disorder, and deletion syndrome A review of ENIGMA findings. Cheon EJ, Bearden CE, Sun D, Ching CRK, Andreassen OA, Schmaal L, Veltman DJ, Thomopoulos SI, Kochunov P, Jahanshad N, Thompson PM, Turner JA, van Erp TGM. Cheon EJ, et al. Psychiatry Clin Neurosci. 2022 May;765140-161. doi Epub 2022 Feb 26. Psychiatry Clin Neurosci. 2022. PMID 35119167 Review. Translational Study of Copy Number Variations in Schizophrenia. Cheng MC, Chien WH, Huang YS, Fang TH, Chen CH. Cheng MC, et al. Int J Mol Sci. 2021 Dec 31;231457. doi Int J Mol Sci. 2021. PMID 35008879 Free PMC article. Primary Psychosis Risk and Protective Factors and Early Detection of the Onset. Brasso C, Giordano B, Badino C, Bellino S, Bozzatello P, Montemagni C, Rocca P. Brasso C, et al. Diagnostics Basel. 2021 Nov 19;11112146. doi Diagnostics Basel. 2021. PMID 34829493 Free PMC article. Review. The Enhancing NeuroImaging Genetics through Meta-Analysis Consortium 10 Years of Global Collaborations in Human Brain Mapping. Thompson PM, Jahanshad N, Schmaal L, Turner JA, Winkler AM, Thomopoulos SI, Egan GF, Kochunov P. Thompson PM, et al. Hum Brain Mapp. 2022 Jan;43115-22. doi Epub 2021 Oct 6. Hum Brain Mapp. 2022. PMID 34612558 Free PMC article. References Abdellaoui, A. , Ehli, E. A. , Hottenga, J. J. , Weber, Z. , Mbarek, H. , Willemsen, G. , … Boomsma, D. I. 2015. CNV concordance in 1,097 MZ twin pairs. Twin Research and Human Genetics, 181, 1–12. - DOI - PubMed Adams, H. H. , Hibar, D. P. , Chouraki, V. , Stein, J. L. , Nyquist, P. A. , Renteria, M. E. , … Thompson, P. M. 2016. Novel genetic loci underlying human intracranial volume identified through genome‐wide association. Nature Neuroscience, 1912, 1569–1582. - DOI - PMC - PubMed Adhikari, B. M. , Jahanshad, N. , Shukla, D. , Glahn, D. C. , Blangero, J. , Fox, P. T. , … Kochunov, P. 2018. Comparison of heritability estimates on resting state fMRI connectivity phenotypes using the ENIGMA analysis pipeline. Human Brain Mapping, 3912, 4893–4902. - DOI - PMC - PubMed Alexander‐Bloch, A. , Raznahan, A. , Bullmore, E. , & Giedd, J. 2013. The convergence of maturational change and structural covariance in human cortical networks. The Journal of Neuroscience, 337, 2889–2899. - DOI - PMC - PubMed Alfaro‐Almagro, F. , Jenkinson, M. , Bangerter, N. K. , Andersson, J. L. , Griffanti, L. , Douaud, G. , … Vallee, E. 2018. Image processing and quality control for the first 10,000 brain imaging datasets from UKbiobank. 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