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  1. Article ; Online: Association between albumin-bilirubin grade and plasma trough concentrations of regorafenib and its metabolites M-2 and M-5 at steady-state in Japanese patients.

    Fujita, Kazuma / Taguchi, Daiki / Fukuda, Koji / Yoshida, Taichi / Shimazu, Kazuhiro / Shinozaki, Hanae / Shibata, Hiroyuki / Miura, Masatomo

    Investigational new drugs

    2024  

    Abstract: The aim of the present study was to determine whether the trough plasma concentrations ( ... ...

    Abstract The aim of the present study was to determine whether the trough plasma concentrations (C
    Language English
    Publishing date 2024-03-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604895-x
    ISSN 1573-0646 ; 0167-6997
    ISSN (online) 1573-0646
    ISSN 0167-6997
    DOI 10.1007/s10637-024-01429-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Spatiotemporal Design of the Metal-Organic Framework DUT-8(M).

    Miura, Hiroki / Bon, Volodymyr / Senkovska, Irena / Ehrling, Sebastian / Bönisch, Nadine / Mäder, Gerrit / Grünzner, Stefan / Khadiev, Azat / Novikov, Dmitri / Maity, Kartik / Richter, Andreas / Kaskel, Stefan

    Advanced materials (Deerfield Beach, Fla.)

    2022  Volume 35, Issue 8, Page(s) e2207741

    Abstract: ... the first example in which an explicit temporal engineering of a switchable MOF (DUT-8, [M ...

    Abstract Switchable metal-organic frameworks (MOFs) change their structure in time and selectively open their pores adsorbing guest molecules, leading to highly selective separation, pressure amplification, sensing, and actuation applications. The 3D engineering of MOFs has reached a high level of maturity, but spatiotemporal evolution opens a new perspective toward engineering materials in the 4th dimension (time) by t-axis design, in essence exploiting the deliberate tuning of activation barriers. This work demonstrates the first example in which an explicit temporal engineering of a switchable MOF (DUT-8, [M
    Language English
    Publishing date 2022-12-27
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1474949-X
    ISSN 1521-4095 ; 0935-9648
    ISSN (online) 1521-4095
    ISSN 0935-9648
    DOI 10.1002/adma.202207741
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Rapid and efficient synthesis of a novel cholinergic muscarinic M

    Miura, Shotaro / Fukuda, Koichiro / Masada, Shinichi / Usutani, Hirotsugu / Kanematsu, Makoto / Cork, David G / Kawamoto, Tetsuji

    Organic & biomolecular chemistry

    2019  Volume 17, Issue 35, Page(s) 8166–8174

    Abstract: ... of a novel cholinergic muscarinic M ...

    Abstract Continuous flow-flash synthesis of a 2-bromobenzaldehyde derivative 18 as a key intermediate of a novel cholinergic muscarinic M
    MeSH term(s) Allosteric Regulation/drug effects ; Benzaldehydes/chemical synthesis ; Benzaldehydes/chemistry ; Benzaldehydes/pharmacology ; Cholinergic Agents/chemical synthesis ; Cholinergic Agents/chemistry ; Cholinergic Agents/pharmacology ; Humans ; Molecular Structure ; Receptor, Muscarinic M1/metabolism
    Chemical Substances 2-bromobenzaldehyde ; Benzaldehydes ; CHRM1 protein, human ; Cholinergic Agents ; Receptor, Muscarinic M1
    Language English
    Publishing date 2019-08-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 2097583-1
    ISSN 1477-0539 ; 1477-0520
    ISSN (online) 1477-0539
    ISSN 1477-0520
    DOI 10.1039/c9ob01718f
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Spiro[3.5]nonenyl Meroterpenoid Lactones, Cryptolaevilactones G-L, an Ionone Derivative, and Total Synthesis of Cryptolaevilactone M from

    Tsurumi, Fumika / Miura, Yuta / Nakano, Misaki / Saito, Yohei / Fukuyoshi, Shuichi / Miyake, Katsunori / Newman, David J / O'Keefe, Barry R / Lee, Kuo-Hsiung / Nakagawa-Goto, Kyoko

    Journal of natural products

    2019  Volume 82, Issue 9, Page(s) 2368–2378

    Abstract: ... A ... ...

    Abstract A CH
    MeSH term(s) Antineoplastic Agents, Phytogenic/chemistry ; Cell Line, Tumor ; Cryptocarya/chemistry ; Humans ; Lactones/chemistry ; Molecular Structure ; Monoterpenes/chemistry ; Plant Leaves/chemistry ; Spectrum Analysis/methods ; Spiro Compounds/chemistry
    Chemical Substances Antineoplastic Agents, Phytogenic ; Lactones ; Monoterpenes ; Spiro Compounds
    Language English
    Publishing date 2019-08-23
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 304325-3
    ISSN 1520-6025 ; 0163-3864
    ISSN (online) 1520-6025
    ISSN 0163-3864
    DOI 10.1021/acs.jnatprod.8b00732
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Insulin-like growth factor I receptor regulates the radiation-induced G2/M checkpoint in HeLa cells.

    Manila, Nisha Gowri / Kaida, Atsushi / Nakahama, Ken-Ichi / Miura, Masahiko

    Biochemical and biophysical research communications

    2018  Volume 503, Issue 4, Page(s) 2977–2983

    Abstract: ... with release from G2 arrest. We conclude that IGF-IR directly regulates the G2/M checkpoint via the PI3K/AKT ...

    Abstract Insulin-like growth factor I receptor (IGF-IR) plays pivotal roles in various biological events, including cell growth, transformation, survival, and DNA repair. In this study, we explored its possible involvement in cell cycle checkpoints, using HeLa cells expressing the fluorescent ubiquitination-based cell cycle indicator (Fucci). We found that IGF-IR inhibitor delayed release from radiation-induced G2 arrest, as demonstrated by FACS and pedigree analysis of Fucci fluorescence. Elongated G2 arrest was also induced by inhibitors of phosphatidylinositol-3 kinase (PI3K) and AKT, but not by inhibitor of MEK, which are two major IGF-IR downstream signaling pathways. Double-strand break (DSB) repair kinetics were not affected by IGF-IR inhibitor. CHK1 inhibitor abrogated radiation-induced G2 arrest, whereas radiation-induced phosphorylation of CHK1 at Ser 345 or Ser 296 was decreased by the IGF-IR inhibitor. However, radiation-induced nuclear localization of CHK1 was prolonged in IGF-IR inhibitor-treated cells in comparison with cells that received radiation alone; in the latter, CHK1 returned to the original diffuse distribution in conjunction with release from G2 arrest. We conclude that IGF-IR directly regulates the G2/M checkpoint via the PI3K/AKT pathway without influencing DSB repair, in part by controlling CHK1 localization between the nucleus and cytoplasm.
    MeSH term(s) Cell Cycle Checkpoints/radiation effects ; Checkpoint Kinase 1/metabolism ; Fluorescence ; G2 Phase Cell Cycle Checkpoints/radiation effects ; HeLa Cells ; Humans ; Phosphatidylinositol 3-Kinases/metabolism ; Proto-Oncogene Proteins c-akt/metabolism ; Receptor, IGF Type 1/physiology
    Chemical Substances Phosphatidylinositol 3-Kinases (EC 2.7.1.-) ; Receptor, IGF Type 1 (EC 2.7.10.1) ; Checkpoint Kinase 1 (EC 2.7.11.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2018-08-16
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 205723-2
    ISSN 1090-2104 ; 0006-291X ; 0006-291X
    ISSN (online) 1090-2104 ; 0006-291X
    ISSN 0006-291X
    DOI 10.1016/j.bbrc.2018.08.080
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The discovery of (1R, 3R)-1-(3-chloro-5-fluorophenyl)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-6-carbonitrile, a potent and selective agonist of human transient receptor potential cation channel subfamily m member 5 (TRPM5) and evaluation of as a potential gastrointestinal prokinetic agent.

    Sabat, M / Raveglia, L F / Aldegheri, L / Barilli, A / Bianchi, F / Brault, L / Brodbeck, D / Feriani, A / Lingard, I / Miura, J / Myers, R / Piccoli, L / Tassini, S / Tyhonas, J / Ton-Nu, T / Wang, H / Virginio, C

    Bioorganic & medicinal chemistry

    2022  Volume 76, Page(s) 117084

    Abstract: ... channel subfamily M member 5 (TRPM5) agonists culminating with the identification of the lead compound (1R ...

    Abstract This publication details the discovery of a series of selective transient receptor potential cation channel subfamily M member 5 (TRPM5) agonists culminating with the identification of the lead compound (1R, 3R)-1-(3-chloro-5-fluorophenyl)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-6-carbonitrile (39). We describe herein our biological rationale for agonism of the target, the examination of the then current literature tool molecules, and finally the process of our discovery starting with a high throughput screening hit through lead development. We also detail the selectivity of the lead compound 39 versus related family members TRPA1, TRPV1, TRPV4, TRPM4 and TRPM8, the drug metabolism and pharmacokinetics (DMPK) profile and in vivo efficacy in a mouse model of gastrointestinal motility.
    MeSH term(s) Animals ; Mice ; Humans ; Transient Receptor Potential Channels ; TRPM Cation Channels ; TRPV Cation Channels
    Chemical Substances 1,2,3,4-tetrahydroisoquinoline (56W89FBX3E) ; Transient Receptor Potential Channels ; TRPM4 protein, mouse ; TRPM Cation Channels ; Trpv4 protein, mouse ; TRPV Cation Channels ; Trpm5 protein, mouse
    Language English
    Publishing date 2022-11-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 1161284-8
    ISSN 1464-3391 ; 0968-0896
    ISSN (online) 1464-3391
    ISSN 0968-0896
    DOI 10.1016/j.bmc.2022.117084
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: On-chip light-sheet fluorescence imaging flow cytometry at a high flow speed of 1 m/s.

    Miura, Taichi / Mikami, Hideharu / Isozaki, Akihiro / Ito, Takuro / Ozeki, Yasuyuki / Goda, Keisuke

    Biomedical optics express

    2018  Volume 9, Issue 7, Page(s) 3424–3433

    Abstract: ... flowing at a high speed of 1 m/s, which is comparable to the flow speed of conventional non-imaging flow ...

    Abstract We present on-chip fluorescence imaging flow cytometry by light-sheet excitation on a mirror-embedded microfluidic chip. The method allows us to obtain microscopy-grade fluorescence images of cells flowing at a high speed of 1 m/s, which is comparable to the flow speed of conventional non-imaging flow cytometers. To implement the light-sheet excitation of flowing cells in a microchannel, we designed and fabricated a mirror-embedded PDMS-based microfluidic chip. To show its broad utility, we used the method to classify large populations of microalgal cells (
    Language English
    Publishing date 2018-06-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2572216-5
    ISSN 2156-7085
    ISSN 2156-7085
    DOI 10.1364/BOE.9.003424
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Book ; Online: Perpendicular magnetic anisotropy at Fe/Au(111) interface studied by M\"{o}ssbauer, x-ray absorption, and photoemission spectroscopies

    Okabayashi, Jun / Li, Songtian / Sakai, Seiji / Kobayashi, Yasuhiro / Mitsui, Takaya / Tanaka, Kiyohisa / Miura, Yoshio / Mitani, Seiji

    2021  

    Abstract: ... layer on the Au(111) surface was examined using synchrotron-radiation-based M\"{o}ssbauer spectroscopy ...

    Abstract The origin of the interfacial perpendicular magnetic anisotropy (PMA) induced in the ultrathin Fe layer on the Au(111) surface was examined using synchrotron-radiation-based M\"{o}ssbauer spectroscopy (MS), X-ray magnetic circular dichroism (XMCD), and angle-resolved photoemission spectroscopy (ARPES). To probe the detailed interfacial electronic structure of orbital hybridization between the Fe 3$d$ and Au 6$p$ bands, we detected the interfacial proximity effect, which modulates the valence-band electronic structure of Fe, resulting in PMA. MS and XMCD measurements were used to detect the interfacial magnetic structure and anisotropy in orbital magnetic moments, respectively. $In$-$situ$ ARPES also confirms the initial growth of Fe on large spin-orbit coupled surface Shockley states under Au(111) modulated electronic states in the vicinity of the Fermi level. This suggests that PMA in the Fe/Au(111) interface originates from the cooperation effects among the spin, orbital magnetic moments in Fe, and large spin-orbit coupling in Au. These findings pave the way to develop interfacial PMA using $p$-$d$ hybridization with a large spin-orbit interaction.
    Keywords Condensed Matter - Materials Science
    Subject code 530
    Publishing date 2021-03-11
    Publishing country us
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: The complexity of DNA double strand break is a crucial factor for activating ATR signaling pathway for G2/M checkpoint regulation regardless of ATM function.

    Xue, Lian / Furusawa, Yoshiya / Okayasu, Ryuichi / Miura, Masahiko / Cui, Xing / Liu, Cuihua / Hirayama, Ryoichi / Matsumoto, Yoshitaka / Yajima, Hirohiko / Yu, Dong

    DNA repair

    2015  Volume 25, Page(s) 72–83

    Abstract: ... we investigated how the complexity of DSB influences the function of ATR pathway on the G2/M checkpoint regulation ... played a pivotal role and functioned in a dose- and LET-dependent way to regulate the early G2/M arrest ... Furthermore, ATR pathway also functioned more efficiently in ATM-proficient cells to block G2 to M transition ...

    Abstract DNA double strand break (DSB) repair pathway choice following ionizing radiation (IR) is currently an appealing research topic, which is still largely unclear. Our recent paper indicated that the complexity of DSBs is a critical factor that enhances DNA end resection. It has been well accepted that the RPA-coated single strand DNA produced by resection is a signaling structure for ATR activation. Therefore, taking advantage of high linear energy transfer (LET) radiation to effectively produce complex DSBs, we investigated how the complexity of DSB influences the function of ATR pathway on the G2/M checkpoint regulation. Human skin fibroblast cells with or without ATM were irradiated with X rays or heavy ion particles, and dual-parameter flow cytometry was used to quantitatively assess the mitotic entry at early period post radiation by detecting the cells positive for phosphor histone H3. In ATM-deficient cells, ATR pathway played a pivotal role and functioned in a dose- and LET-dependent way to regulate the early G2/M arrest even as low as 0.2Gy for heavy ion radiation, which indicated that ATR pathway could be rapidly activated and functioned in an ATM-independent, but DSB complexity-dependent manner following exposure to IR. Furthermore, ATR pathway also functioned more efficiently in ATM-proficient cells to block G2 to M transition at early period of particle radiation exposure. Accordingly, in contrast to ATM inhibitor, ATR inhibitor had a more effective radiosensitizing effect on survival fraction following heavy ion beams as compared with X ray radiation. Taken together, our results reveal that the complexity of DSBs is a crucial factor for the activation of ATR pathway for G2/M checkpoint regulation, and ATM-dependent end resection is not essential for the activation.
    MeSH term(s) Ataxia Telangiectasia Mutated Proteins/genetics ; Ataxia Telangiectasia Mutated Proteins/metabolism ; Cells, Cultured ; DNA/metabolism ; DNA/radiation effects ; DNA Breaks, Double-Stranded ; DNA End-Joining Repair ; G2 Phase/radiation effects ; G2 Phase Cell Cycle Checkpoints/genetics ; Humans ; Linear Energy Transfer ; Phosphorylation ; Radiation, Ionizing ; Recombinational DNA Repair ; Signal Transduction
    Chemical Substances DNA (9007-49-2) ; ATM protein, human (EC 2.7.11.1) ; ATR protein, human (EC 2.7.11.1) ; Ataxia Telangiectasia Mutated Proteins (EC 2.7.11.1)
    Language English
    Publishing date 2015-01
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2071608-4
    ISSN 1568-7856 ; 1568-7864
    ISSN (online) 1568-7856
    ISSN 1568-7864
    DOI 10.1016/j.dnarep.2014.11.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Complete nucleotide sequence of the IncN plasmid encoding IMP-6 and CTX-M-2 from emerging carbapenem-resistant Enterobacteriaceae in Japan.

    Kayama, Shizuo / Shigemoto, Norifumi / Kuwahara, Ryuichi / Oshima, Kenshiro / Hirakawa, Hideki / Hisatsune, Junzo / Jové, Thomas / Nishio, Hisaaki / Yamasaki, Katsutoshi / Wada, Yasunao / Ueshimo, Takeshi / Miura, Tetsuya / Sueda, Taijiro / Onodera, Makoto / Yokozaki, Michiya / Hattori, Masahira / Ohge, Hiroki / Sugai, Motoyuki

    Antimicrobial agents and chemotherapy

    2015  Volume 59, Issue 2, Page(s) 1356–1359

    Abstract: ... which is a self-transmissible IncN-type plasmid. pKPI-6 harboring blaIMP-6 and blaCTX-M-2 confers a stealth ... with imipenem. pKPI-6 is already epidemic in Japan, favoring the dissemination of IMP-6 and CTX-M-2 in members ...

    Abstract We have determined the DNA sequence of Klebsiella pneumoniae multidrug resistance plasmid pKPI-6, which is a self-transmissible IncN-type plasmid. pKPI-6 harboring blaIMP-6 and blaCTX-M-2 confers a stealth-type carbapenem resistance phenotype on members of the family Enterobacteriaceae that is not detectable with imipenem. pKPI-6 is already epidemic in Japan, favoring the dissemination of IMP-6 and CTX-M-2 in members of the family Enterobacteriaceae.
    MeSH term(s) Enterobacteriaceae/drug effects ; Enterobacteriaceae/enzymology ; Imipenem/pharmacology ; Japan ; Microbial Sensitivity Tests ; Molecular Sequence Data ; Plasmids/genetics ; beta-Lactamases/metabolism
    Chemical Substances Imipenem (71OTZ9ZE0A) ; beta-lactamase CTX-2 (EC 3.5.2.-) ; beta-Lactamases (EC 3.5.2.6)
    Language English
    Publishing date 2015-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/AAC.04759-14
    Database MEDical Literature Analysis and Retrieval System OnLINE

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