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Institution

Hokkaido University

EducationSapporo, Hokkaidô, Japan
About: Hokkaido University is a education organization based out in Sapporo, Hokkaidô, Japan. It is known for research contribution in the topics: Population & Catalysis. The organization has 53925 authors who have published 115403 publications receiving 2651647 citations. The organization is also known as: Hokudai & Hokkaidō daigaku.
Topics: Population, Catalysis, Gene, Transplantation, Virus


Papers
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Journal ArticleDOI
Liping Hou1, Urs Heilbronner2, Urs Heilbronner3, Franziska Degenhardt4, Mazda Adli5, Kazufumi Akiyama6, Nirmala Akula1, Raffaella Ardau, Bárbara Arias7, Lena Backlund8, Claudio E. M. Banzato9, Antoni Benabarre7, Susanne Bengesser10, Abesh Kumar Bhattacharjee11, Joanna M. Biernacka12, Armin Birner10, Clara Brichant-Petitjean13, Elise T. Bui1, Pablo Cervantes14, Guo-Bo Chen15, Hsi-Chung Chen16, Caterina Chillotti, Sven Cichon4, Sven Cichon17, Scott R. Clark18, Francesc Colom7, David A. Cousins19, Cristiana Cruceanu20, Piotr M. Czerski21, Clarissa de Rosalmeida Dantas9, Alexandre Dayer22, Bruno Etain23, Peter Falkai2, Andreas J. Forstner4, Louise Frisén8, Janice M. Fullerton24, Janice M. Fullerton25, Sébastien Gard, Julie Garnham26, Fernando S. Goes27, Paul Grof, Oliver Gruber3, Ryota Hashimoto28, Joanna Hauser21, Stefan Herms17, Stefan Herms4, Per Hoffmann4, Per Hoffmann17, Andrea Hofmann4, Stéphane Jamain23, Esther Jiménez7, Jean-Pierre Kahn29, Layla Kassem1, Sarah Kittel-Schneider30, Sebastian Kliwicki21, Barbara König, Ichiro Kusumi31, N. Lackner10, Gonzalo Laje1, Mikael Landén32, Mikael Landén33, Catharina Lavebratt8, Marion Leboyer, Susan G. Leckband34, Susan G. Leckband8, Carlos Jaramillo35, Glenda MacQueen36, Mirko Manchia37, Mirko Manchia26, Lina Martinsson32, Manuel Mattheisen38, Michael McCarthy34, Susan L. McElroy39, Marina Mitjans7, Francis M. Mondimore27, Palmiero Monteleone40, Palmiero Monteleone41, Caroline M. Nievergelt11, Markus M. Nöthen4, Urban Ösby8, Norio Ozaki42, Roy H. Perlis43, Andrea Pfennig44, Daniela Reich-Erkelenz2, Guy A. Rouleau45, Peter R. Schofield24, Peter R. Schofield25, K Oliver Schubert18, Barbara W. Schweizer27, Florian Seemüller2, Giovanni Severino37, Tatyana Shekhtman11, Tatyana Shekhtman46, Paul D. Shilling11, Kazutaka Shimoda6, Christian Simhandl, Claire Slaney26, Jordan W. Smoller43, Alessio Squassina37, Thomas Stamm5, Pavla Stopkova47, Sarah K. Tighe48, Sarah K. Tighe49, Alfonso Tortorella40, Gustavo Turecki20, Julia Volkert30, Stephanie H. Witt50, Adam Wright24, L. Trevor Young51, Peter P. Zandi27, James B. Potash49, J. Raymond DePaulo27, Michael Bauer44, Eva Z. Reininghaus10, Tomas Novak47, Jean-Michel Aubry22, Mario Maj40, Bernhard T. Baune18, Philip B. Mitchell24, Eduard Vieta7, Mark A. Frye12, Janusz K. Rybakowski21, Po-Hsiu Kuo16, Tadafumi Kato52, Maria Grigoroiu-Serbanescu, Andreas Reif30, Maria Del Zompo37, Frank Bellivier13, Martin Schalling8, Naomi R. Wray15, John R. Kelsoe11, John R. Kelsoe46, Martin Alda26, Martin Alda47, Marcella Rietschel50, Francis J. McMahon1, Thomas G. Schulze 
United States Department of Health and Human Services1, Ludwig Maximilian University of Munich2, University of Göttingen3, University of Bonn4, Charité5, Dokkyo Medical University6, University of Barcelona7, Karolinska University Hospital8, State University of Campinas9, Medical University of Graz10, University of California, San Diego11, Mayo Clinic12, Paris Diderot University13, McGill University Health Centre14, University of Queensland15, National Taiwan University16, University Hospital of Basel17, University of Adelaide18, Newcastle University19, Douglas Mental Health University Institute20, Poznan University of Medical Sciences21, Geneva College22, French Institute of Health and Medical Research23, University of New South Wales24, Neuroscience Research Australia25, Dalhousie University26, Johns Hopkins University27, Osaka University28, University of Lorraine29, Goethe University Frankfurt30, Hokkaido University31, Karolinska Institutet32, University of Gothenburg33, Veterans Health Administration34, University of Antioquia35, University of Calgary36, University of Cagliari37, Aarhus University38, University of Cincinnati39, University of Naples Federico II40, University of Salerno41, Nagoya University42, Harvard University43, Dresden University of Technology44, Montreal Neurological Institute and Hospital45, United States Department of Veterans Affairs46, National Institutes of Health47, Roy J. and Lucille A. Carver College of Medicine48, University of Iowa49, Heidelberg University50, University of Toronto51, RIKEN Brain Science Institute52
TL;DR: A genome-wide association study of lithium response in 2,563 patients collected by 22 participating sites from the International Consortium on Lithium Genetics (ConLiGen); the largest attempted so far finds a single locus of four linked SNPs on chromosome 21 met genome- wide significance criteria for association with lithium response.

258 citations

Journal ArticleDOI
TL;DR: In this article, a ring-opening polymerization of δ-valerolactone and e-caprolactone (e-CL) using 3-phenyl-1-propanol (PPA) as initiator and diphenyl phosphate (DPP) as the catalyst in toluene at room temperature with the [δ-VL or e-CL] 0/[PPA]0/[DPP] ratio of 50/1/1 homogeneously proceeded to afford poly(α-βαβββ ββ
Abstract: The ring-opening polymerization of δ-valerolactone (δ-VL) and e-caprolactone (e-CL) using 3-phenyl-1-propanol (PPA) as the initiator and diphenyl phosphate (DPP) as the catalyst in toluene at room temperature with the [δ-VL or e-CL]0/[PPA]0/[DPP] ratio of 50/1/1 homogeneously proceeded to afford poly(δ-valerolactone) (PVL) and poly(e-caprolactone) (PCL) with narrow polydispersity indices. The molecular weights determined from a 1H NMR analysis (PVL, Mn,NMR = 5170 g mol−1 and PCL, Mn,NMR = 5920 g mol−1) showed good agreement with those estimated from the initial ratio of [δ-VL or e-CL]0/[PPA]0 and monomer conversions (PVL, Mn,theo = 4890 g mol−1 and PCL, Mn,theo = 5680 g mol−1). The 1H NMR, SEC, and MALDI-TOF MS measurements of the obtained PVL and PCL clearly indicated the presence of the initiator residue at the chain end, confirming that the DPP-catalyzed ROP of lactones proceeded through an activated monomer mechanism. The kinetic and chain extension experiments confirmed the controlled/living nature f...

258 citations

Journal ArticleDOI
TL;DR: The muscarinic system can influence hippocampal functions by controlling different subsets of inhibitory synapses through the two distinct mechanisms, namely a cannabinoid‐dependent and cannabinoid‐independent mechanism.
Abstract: The cholinergic system in the CNS plays important roles in higher brain functions, primarily through muscarinic acetylcholine receptors. At cellular levels, muscarinic activation produces various effects including modulation of synaptic transmission. Here we report that muscarinic activation suppresses hippocampal inhibitory transmission through two distinct mechanisms, namely a cannabinoid-dependent and cannabinoid-independent mechanism. We made paired whole-cell recordings from cultured hippocampal neurons of rats and mice, and monitored inhibitory postsynaptic currents (IPSCs). When cannabinoid receptor type 1 (CB1) was blocked, oxotremorine M (oxo-M), a muscarinic agonist, suppressed IPSCs in a subset of neuron pairs. This suppression was associated with an increase in paired-pulse ratio, blocked by the M(2)-preferring antagonist gallamine, and was totally absent in neuron pairs from M(2)-knockout mice. When CB1 receptors were not blocked, oxo-M suppressed IPSCs in a gallamine-resistant manner in cannabinoid-sensitive pairs. This suppression was associated with an increase in paired-pulse ratio, blocked by the CB1 antagonist AM281, and was completely eliminated in neuron pairs from M(1)/M(3)-compound-knockout mice. Our immunohistochemical examination showed that M(2) and CB1 receptors were present at inhibitory presynaptic terminals of mostly different origins. These results indicate that two distinct mechanisms mediate the muscarinic suppression. In a subset of synapses, activation of M(2) receptors at presynaptic terminals suppresses GABA release directly. In contrast, in a different subset of synapses, activation of M(1)/M(3) receptors causes endocannabinoid production and subsequent suppression of GABA release by activating presynaptic CB1 receptors. Thus, the muscarinic system can influence hippocampal functions by controlling different subsets of inhibitory synapses through the two distinct mechanisms.

258 citations

Journal ArticleDOI
16 Mar 2001-Science
TL;DR: New methods for retrieving tropospheric ozone column depth and absorbing aerosol from the Earth Probe-Total Ozone Mapping Spectrometer (EP/TOMS) are used to follow pollution and to determine interannual variability and trends.
Abstract: New methods for retrieving tropospheric ozone column depth and absorbing aerosol (smoke and dust) from the Earth Probe–Total Ozone Mapping Spectrometer (EP/TOMS) are used to follow pollution and to determine interannual variability and trends. During intense fires over Indonesia (August to November 1997), ozone plumes, decoupled from the smoke below, extended as far as India. This ozone overlay a regional ozone increase triggered by atmospheric responses to the El Nino and Indian Ocean Dipole. Tropospheric ozone and smoke aerosol measurements from the Nimbus 7 TOMS instrument show El Nino signals but no tropospheric ozone trend in the 1980s. Offsets between smoke and ozone seasonal maxima point to multiple factors determining tropical tropospheric ozone variability.

258 citations

Journal ArticleDOI
TL;DR: Members of the highly diverse Miscellaneous Crenarchaeotal Group (MCG) are globally distributed in various marine and continental habitats and their high diversity and widespread distribution in subsurface sediments indicates that this group is globally important in sedimentary processes.
Abstract: Members of the highly diverse Miscellaneous Crenarchaeotal Group (MCG) are globally distributed in various marine and continental habitats In this study, we applied a polyphasic approach (rRNA slot blot hybridization, quantitative PCR (qPCR) and catalyzed reporter deposition FISH) using newly developed probes and primers for the in situ detection and quantification of MCG crenarchaeota in diverse types of marine sediments and microbial mats In general, abundance of MCG (cocci, 04 μm) relative to other archaea was highest (12–100%) in anoxic, low-energy environments characterized by deeper sulfate depletion and lower microbial respiration rates (P=006 for slot blot and P=005 for qPCR) When studied in high depth resolution in the White Oak River estuary and Hydrate Ridge methane seeps, changes in MCG abundance relative to total archaea and MCG phylogenetic composition did not correlate with changes in sulfate reduction or methane oxidation with depth In addition, MCG abundance did not vary significantly (P>01) between seep sites (with high rates of methanotrophy) and non-seep sites (with low rates of methanotrophy) This suggests that MCG are likely not methanotrophs MCG crenarchaeota are highly diverse and contain 17 subgroups, with a range of intragroup similarity of 82 to 94% This high diversity and widespread distribution in subsurface sediments indicates that this group is globally important in sedimentary processes

258 citations


Authors

Showing all 54156 results

NameH-indexPapersCitations
Shizuo Akira2611308320561
Yi Cui2201015199725
John F. Hartwig14571466472
Yoshihiro Kawaoka13988375087
David Y. Graham138104780886
Takashi Kadowaki13787389729
Kazunari Domen13090877964
Susumu Kitagawa12580969594
Toshikazu Nakamura12173251374
Toshio Hirano12040155721
Li-Jun Wan11363952128
Wenbin Lin11347456786
Xiaoming Li113193272445
Jinhua Ye11265849496
Terence Tao11160694316
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023127
2022427
20214,743
20204,805
20194,363
20184,112