研究者を探す
中岡 秀憲
徳島大学
2025年7月2日更新
- 職名
- 助教
- 電話
- 研究者総覧に該当データはありませんでした。
- 電子メール
- nakaoka.hidenori@tokushima-u.ac.jp
- 学歴
- 2000/: 京都大学 理学部 化学科 ( - 2004.)
2004/: 京都大学 大学院生命科学研究科 修士課程 ( - 2006.)
2006/: 京都大学 大学院生命科学研究科 博士課程 ( - 2011.) - 学位
- 博士 / 博士(生命科学) (京都大学) (2012年3月)
- 職歴・経歴
- 2024/4: 徳島大学 助教, 先端研究推進センター
- 専門分野・研究分野
- ライフサイエンス (Life sciences) [分子生物学 (Molecular biology)]
ライフサイエンス (Life sciences) [細胞生物学 (Cell biology)]
ライフサイエンス (Life sciences) [生物物理学 (Biophysics)]
2025年7月2日更新
- 専門分野・研究分野
- ライフサイエンス (Life sciences) [分子生物学 (Molecular biology)]
ライフサイエンス (Life sciences) [細胞生物学 (Cell biology)]
ライフサイエンス (Life sciences) [生物物理学 (Biophysics)] - 担当経験のある授業科目
- 研究者総覧に該当データはありませんでした。
- 指導経験
- 研究者総覧に該当データはありませんでした。
2025年7月2日更新
- 専門分野・研究分野
- ライフサイエンス (Life sciences) [分子生物学 (Molecular biology)]
ライフサイエンス (Life sciences) [細胞生物学 (Cell biology)]
ライフサイエンス (Life sciences) [生物物理学 (Biophysics)]
- 研究テーマ
- 研究者総覧に該当データはありませんでした。
- 著書
- Hidenori Nakaoka :
Live Imaging of Fission Yeast Single-Cell Lineages Using a Microfluidic Device,
2025.- (要約)
- Mother machine (MM) is a microfluidic device originally developed for long-term live imaging of Escherichia coli bacterial cells under a microscope. The simple yet sophisticated design has enabled microbiologists to track multiple single-cell lineages cultured under highly controlled external environments. Here, I describe how to fabricate a fission yeast version of MM with photolithography and soft lithography. Procedures for setting up the microfluidic device for long-term live microscopy are also explained.
- (キーワード)
- Aging / Cell growth / Live imaging / Microfluidics / Mother machine / Photolithography / Single cell / Soft lithography
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1007/978-1-0716-4168-2_5
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39527193
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85209484110
(DOI: 10.1007/978-1-0716-4168-2_5, PubMed: 39527193, Elsevier: Scopus) - 論文
- Taishi Kakizuka, Hidenori Nakaoka, Yusuke Hara, Aya Ichiraku, Yoshiyuki Arai, Hiroya Itoga, Shuichi Onami, Taro Ichimura, Takeharu Nagai and Kazuki Horikawa :
Mesoscale heterogeneity is a critical determinant for spiral pattern formation in developing social amoeba,
Scientific Reports, 15, 1, 1422, 2025.- (要約)
- Heterogeneity is a critical determinant for multicellular pattern formation. Although the importance of microscale and macroscale heterogeneity at the single-cell and whole-system levels, respectively, has been well accepted, the presence and functions of mesoscale heterogeneity, such as cell clusters with distinct properties, have been poorly recognized. We investigated the biological importance of mesoscale heterogeneity in signal-relaying abilities (excitability) in the self-organization of spiral waves of intercellular communications by studying the self-organized pattern formation in a population of Dictyostelium discoideum cells, a classical signal-relaying system model. By utilizing pulse-count analysis to evaluate cellular excitability, we successfully visualized the development of mesoscale heterogeneity in excitability, whose spatial scale was comparably large to that of the traveling waves of intercellular communication. Together with perturbation experiments, our detailed analysis of the structural change in mesoscale heterogeneity and associated wave dynamics demonstrated the functional importance of mesoscale heterogeneity in generating the spiral wave pattern, whose experimental observations were first realized. We propose that mesoscale heterogeneity, in addition to microscale and macroscale heterogeneities, is a critical determinant of diverse multicellular pattern formations.
- (キーワード)
- Dictyostelium / Cell Communication / Models, Biological / Signal Transduction
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1038/s41598-025-85759-9
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39789232
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85214891989
(DOI: 10.1038/s41598-025-85759-9, PubMed: 39789232, Elsevier: Scopus) Sotaro Takano, Miki Umetani, Hidenori Nakaoka and Ryo Miyazaki :
Diversification of single-cell growth dynamics under starvation influences subsequent reproduction in a clonal bacterial population,
The ISME Journal, 19, 1, 2025.- (要約)
- Most of the microbes in nature infrequently receive nutrients and are thus in slow- or non-growing states. How quickly they can resume their growth upon an influx of new resources is crucial to occupy environmental niches. Isogenic microbial populations are known to harbor only a fraction of cells with rapid growth resumption, yet little is known about the physiological characteristics of those cells and their emergence in the population. Here, we tracked growth of individual Escherichia coli cells in populations under fluctuating nutrient conditions. We found that shifting from high- to low-nutrient conditions caused stalling of cell growth with few cells continuing to divide extremely slowly, a process which was dependent on lipid turnover. Resuming high-nutrient inflow after low-nutrient conditions resulted in cells resuming growth and division, but with different lag times and leading to varying progeny. The history of cell growth during low-nutrient but not high-nutrient conditions was determinant for resumption of growth, which cellular genealogy analysis suggested to originate from inherited physiological differences. Our results demonstrate that cellular growth dynamics become diverse by nutrient limitations, under which a fraction of cells experienced a particular growth history can reproduce progeny with new resources in the future.
- (キーワード)
- growth dynamics / single cell / starvation / time-lapse imaging
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1093/ismejo/wrae257
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 39714219
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85216941984
(DOI: 10.1093/ismejo/wrae257, PubMed: 39714219, Elsevier: Scopus) Tomohiko Hara, Hidenori Nakaoka, Tomoicihiro Miyoshi and Fuyuki Ishikawa :
The CST complex facilitates cell survival under oxidative genotoxic stress,
PLoS ONE, 18, 8 AUGUST, e0289304, 2023.- (要約)
- Genomic DNA is constantly exposed to a variety of genotoxic stresses, and it is crucial for organisms to be equipped with mechanisms for repairing the damaged genome. Previously, it was demonstrated that the mammalian CST (CTC1-STN1-TEN1) complex, which was originally identified as a single-stranded DNA-binding trimeric protein complex essential for telomere maintenance, is required for survival in response to hydroxyurea (HU), which induces DNA replication fork stalling. It is still unclear, however, how the CST complex is involved in the repair of diverse types of DNA damage induced by oxidizing agents such as H2O2. STN1 knockdown (KD) sensitized HeLa cells to high doses of H2O2. While H2O2 induced DNA strand breaks throughout the cell cycle, STN1 KD cells were as resistant as control cells to H2O2 treatment when challenged in the G1 phase of the cell cycle, but they were sensitive when exposed to H2O2 in S/G2/M phase. STN1 KD cells showed a failure of DNA synthesis and RAD51 foci formation upon H2O2 treatment. Chemical inhibition of RAD51 in shSTN1 cells did not exacerbate the sensitivity to H2O2, implying that the CST complex and RAD51 act in the same pathway. Collectively, our results suggest that the CST complex is required for maintaining genomic stability in response to oxidative DNA damage, possibly through RAD51-dependent DNA repair/protection mechanisms.
- (キーワード)
- Humans / Animals / Shelterin Complex / Cell Survival / HeLa Cells / Hydrogen Peroxide / Telomere / DNA Damage / Mammals
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1371/journal.pone.0289304
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 37590191
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85168286412
(DOI: 10.1371/journal.pone.0289304, PubMed: 37590191, Elsevier: Scopus) Io Yamamoto, Hidenori Nakaoka, Masahiro Takikawa, Sanki Tashiro, Junko Kanoh, Tomoichiro Miyoshi and Fuyuki Ishikawa :
Fission yeast Stn1 maintains stability of repetitive DNA at subtelomere and ribosomal DNA regions,
Nucleic Acids Research, 49, 18, 10465-10476, 2021.- (要約)
- Telomere binding protein Stn1 forms the CST (Cdc13/CTC1-STN1-TEN1) complex in budding yeast and mammals. Likewise, fission yeast Stn1 and Ten1 form a complex indispensable for telomere protection. We have previously reported that stn1-1, a high-temperature sensitive mutant, rapidly loses telomere DNA at the restrictive temperature due to frequent failure of replication fork progression at telomeres and subtelomeres, both containing repetitive sequences. It is unclear, however, whether Stn1 is required for maintaining other repetitive DNAs such as ribosomal DNA. In this study, we have demonstrated that stn1-1 cells, even when grown at the permissive temperature, exhibited dynamic rearrangements in the telomere-proximal regions of subtelomere and ribosomal DNA repeats. Furthermore, Rad52 and γH2A accumulation was observed at ribosomal DNA repeats in the stn1-1 mutant. The phenotypes exhibited by the stn1-1 allele were largely suppressed in the absence of Reb1, a replication fork barrier-forming protein, suggesting that Stn1 is involved in the maintenance of the arrested replication forks. Collectively, we propose that Stn1 maintains the stability of repetitive DNAs at subtelomeres and rDNA regions.
- (キーワード)
- DNA, Fungal / DNA, Ribosomal / DNA-Binding Proteins / Microbial Viability / Mutation / Recombination, Genetic / Recombinational DNA Repair / Repetitive Sequences, Nucleic Acid / Schizosaccharomyces / Schizosaccharomyces pombe Proteins / Telomere / Telomere-Binding Proteins / Transcription Factors
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1093/nar/gkab767
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 34520548
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85118286518
(DOI: 10.1093/nar/gkab767, PubMed: 34520548, Elsevier: Scopus) Akihisa Seita, Hidenori Nakaoka, Reiko Okura and Yuichi Wakamoto :
Intrinsic growth heterogeneity of mouse leukemia cells underlies differential susceptibility to a growth-inhibiting anticancer drug,
PLoS ONE, 16, 2 February, e0236534, 2021.- (要約)
- Cancer cell populations consist of phenotypically heterogeneous cells. Growing evidence suggests that pre-existing phenotypic differences among cancer cells correlate with differential susceptibility to anticancer drugs and eventually lead to a relapse. Such phenotypic differences can arise not only externally driven by the environmental heterogeneity around individual cells but also internally by the intrinsic fluctuation of cells. However, the quantitative characteristics of intrinsic phenotypic heterogeneity emerging even under constant environments and their relevance to drug susceptibility remain elusive. Here we employed a microfluidic device, mammalian mother machine, for studying the intrinsic heterogeneity of growth dynamics of mouse lymphocytic leukemia cells (L1210) across tens of generations. The generation time of this cancer cell line had a distribution with a long tail and a heritability across generations. We determined that a minority of cell lineages exist in a slow-cycling state for multiple generations. These slow-cycling cell lineages had a higher chance of survival than the fast-cycling lineages under continuous exposure to the anticancer drug Mitomycin C. This result suggests that heritable heterogeneity in cancer cells' growth in a population influences their susceptibility to anticancer drugs.
- (キーワード)
- Animals / Antineoplastic Agents / Cell Line, Tumor / Cell Proliferation / Drug Resistance, Neoplasm / Leukemia / Leukemia, Lymphoid / Mice / Microfluidic Analytical Techniques / Mitomycin / Neoplasms / Phenotype
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1371/journal.pone.0236534
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 33524064
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85100558224
(DOI: 10.1371/journal.pone.0236534, PubMed: 33524064, Elsevier: Scopus) J. Koseki Kobayashi-Kirschvink, Hidenori Nakaoka, Arisa Oda, F. Ken ichiro Kamei, Kazuki Nosho, Hiroko Fukushima, Yu Kanesaki, Shunsuke Yajima, Haruhiko Masaki, Kunihiro Ohta and Yuichi Wakamoto :
Linear Regression Links Transcriptomic Data and Cellular Raman Spectra,
Cell Systems, 7, 1, 104-117.e4, 2018.- (要約)
- Raman microscopy is an imaging technique that has been applied to assess molecular compositions of living cells to characterize cell types and states. However, owing to the diverse molecular species in cells and challenges of assigning peaks to specific molecules, it has not been clear how to interpret cellular Raman spectra. Here, we provide firm evidence that cellular Raman spectra and transcriptomic profiles of Schizosaccharomyces pombe and Escherichia coli can be computationally connected and thus interpreted. We find that the dimensions of high-dimensional Raman spectra and transcriptomes measured by RNA sequencing can be reduced and connected linearly through a shared low-dimensional subspace. Accordingly, we were able to predict global gene expression profiles by applying the calculated transformation matrix to Raman spectra, and vice versa. Highly expressed non-coding RNAs contributed to the Raman-transcriptome linear correspondence more significantly than mRNAs in S. pombe. This demonstration of correspondence between cellular Raman spectra and transcriptomes is a promising step toward establishing spectroscopic live-cell omics studies.
- (キーワード)
- high-dimensional biological data analysis / live-cell omics / Raman microscopy / single-cell analysis / transcriptome
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1016/j.cels.2018.05.015
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 29936183
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85048535161
(DOI: 10.1016/j.cels.2018.05.015, PubMed: 29936183, Elsevier: Scopus) Hidenori Nakaoka and Yuichi Wakamoto :
Aging, mortality, and the fast growth trade-off of Schizosaccharomyces pombe,
PLoS Biology, 15, 6, e2001109, 2017.- (要約)
- Replicative aging has been demonstrated in asymmetrically dividing unicellular organisms, seemingly caused by unequal damage partitioning. Although asymmetric segregation and inheritance of potential aging factors also occur in symmetrically dividing species, it nevertheless remains controversial whether this results in aging. Based on large-scale single-cell lineage data obtained by time-lapse microscopy with a microfluidic device, in this report, we demonstrate the absence of replicative aging in old-pole cell lineages of Schizosaccharomyces pombe cultured under constant favorable conditions. By monitoring more than 1,500 cell lineages in 7 different culture conditions, we showed that both cell division and death rates are remarkably constant for at least 50-80 generations. Our measurements revealed that the death rate per cellular generation increases with the division rate, pointing to a physiological trade-off with fast growth under balanced growth conditions. We also observed the formation and inheritance of Hsp104-associated protein aggregates, which are a potential aging factor in old-pole cell lineages, and found that these aggregates exhibited a tendency to preferentially remain at the old poles for several generations. However, the aggregates were eventually segregated from old-pole cells upon cell division and probabilistically allocated to new-pole cells. We found that cell deaths were typically preceded by sudden acceleration of protein aggregation; thus, a relatively large amount of protein aggregates existed at the very ends of the dead cell lineages. Our lineage tracking analyses, however, revealed that the quantity and inheritance of protein aggregates increased neither cellular generation time nor cell death initiation rates. Furthermore, our results demonstrated that unusually large amounts of protein aggregates induced by oxidative stress exposure did not result in aging; old-pole cells resumed normal growth upon stress removal, despite the fact that most of them inherited significant quantities of aggregates. These results collectively indicate that protein aggregates are not a major determinant of triggering cell death in S. pombe and thus cannot be an appropriate molecular marker or index for replicative aging under both favorable and stressful environmental conditions.
- (キーワード)
- Adenosine Triphosphatases / Asymmetric Cell Division / Biomarkers / Cell Tracking / DNA Replication / Gene Deletion / Heat-Shock Proteins / Luminescent Proteins / Microbial Viability / Microfluidics / Microscopy, Confocal / Microscopy, Fluorescence / Orthoreovirus / Oxidative Stress / Peptide Fragments / Protein Aggregates / Recombinant Fusion Proteins / Schizosaccharomyces / Schizosaccharomyces pombe Proteins / Single-Cell Analysis / Spindle Poles / Stress, Physiological / Time-Lapse Imaging / Viral Nonstructural Proteins
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1371/journal.pbio.2001109
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 28632741
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85021627558
(DOI: 10.1371/journal.pbio.2001109, PubMed: 28632741, Elsevier: Scopus) Mikihiro Hashimoto, Takashi Nozoe, Hidenori Nakaoka, Reiko Okura, Sayo Akiyoshi, Kunihiko Kaneko, Edo Kussell and Yuichi Wakamoto :
Noise-driven growth rate gain in clonal cellular populations,
Proceedings of the National Academy of Sciences of the United States of America, 113, 12, 3151-3156, 2016.- (要約)
- Cellular populations in both nature and the laboratory are composed of phenotypically heterogeneous individuals that compete with each other resulting in complex population dynamics. Predicting population growth characteristics based on knowledge of heterogeneous single-cell dynamics remains challenging. By observing groups of cells for hundreds of generations at single-cell resolution, we reveal that growth noise causes clonal populations of Escherichia coli to double faster than the mean doubling time of their constituent single cells across a broad set of balanced-growth conditions. We show that the population-level growth rate gain as well as age structures of populations and of cell lineages in competition are predictable. Furthermore, we theoretically reveal that the growth rate gain can be linked with the relative entropy of lineage generation time distributions. Unexpectedly, we find an empirical linear relation between the means and the variances of generation times across conditions, which provides a general constraint on maximal growth rates. Together, these results demonstrate a fundamental benefit of noise for population growth, and identify a growth law that sets a "speed limit" for proliferation.
- (キーワード)
- Age-structured population model / Cell lineage analysis / Growth law / Growth noise / Microfluidics
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1073/pnas.1519412113
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 26951676
- ● Summary page in Scopus @ Elsevier: 2-s2.0-84962236530
(DOI: 10.1073/pnas.1519412113, PubMed: 26951676, Elsevier: Scopus) Noriko Satoh-Asahara, Akira Shimatsu, Yousuke Sasaki, Hidenori Nakaoka, Akihiro Himeno, Mayu Tochiya, Shigeo Kono, Tomohide Takaya, Koh Ono, Hiromichi Wada, Takayoshi Suganami, Koji Hasegawa and Yoshihiro Ogawa :
Highly purified eicosapentaenoic acid increases interleukin-10 levels of peripheral blood monocytes in obese patients with dyslipidemia,
Diabetes Care, 35, 12, 2631-2639, 2012.- (要約)
- It has recently been highlighted that proinflammatory (M1) macrophages predominate over anti-inflammatory (M2) macrophages in obesity, thereby contributing to obesity-induced adipose inflammation and insulin resistance. A recent clinical trial revealed that highly purified eicosapentaenoic acid (EPA) reduces the incidence of major coronary events. In this study, we examined the effect of EPA on M1/M2-like phenotypes of peripheral blood monocytes in obese dyslipidemic patients. Peripheral blood monocytes were prepared from 26 obese patients without and 90 obese patients with dyslipidemia. Of the latter 90 obese patients with dyslipidemia, 82 patients were treated with or without EPA treatment (1.8 g daily) for 3 months. Monocytes in obese patients with dyslipidemia showed a significantly lower expression of interleukin-10 (IL-10), an M2 marker, than those without dyslipidemia. EPA significantly increased serum IL-10 and EPA levels, the EPA/arachidonic acid (AA) ratio, and monocyte IL-10 expression and decreased the pulse wave velocity (PWV), an index of arterial stiffness, compared with the control group. After EPA treatment, the serum EPA/AA ratio was significantly correlated with monocyte IL-10 expression. Only increases in monocyte IL-10 expression and serum adiponectin were independent determinants of a decreased PWV by EPA. Furthermore, EPA significantly increased the expression and secretion of IL-10 in human monocytic THP-1 cells through a peroxisome proliferator-activated receptor (PPAR)γ-dependent pathway. This study is the first to show that EPA increases the monocyte IL-10 expression in parallel with decrease of arterial stiffness, which may contribute to the antiatherogenic effect of EPA in obese dyslipidemic patients.
- (キーワード)
- Dyslipidemias / Eicosapentaenoic Acid / Female / Humans / Interleukin-10 / Leukocytes, Mononuclear / Male / Middle Aged / Obesity
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.2337/dc12-0269
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 22912426
- ● Summary page in Scopus @ Elsevier: 2-s2.0-84869780896
(DOI: 10.2337/dc12-0269, PubMed: 22912426, Elsevier: Scopus) Hidenori Nakaoka, Atsuya Nishiyama, Motoki Saito and Fuyuki Ishikawa :
Xenopus laevis Ctc1-Stn1-Ten1 (xCST) protein complex is involved in priming DNA synthesis on single-stranded DNA template in Xenopus egg extract,
The Journal of Biological Chemistry, 287, 1, 619-627, 2011.- (要約)
- The Ctc1-Stn1-Ten1 (CST) complex is an RPA (replication protein A)-like protein complex that binds to single-stranded (ss) DNA. It localizes at telomeres and is involved in telomere end protection in mammals and plants. It is also known to stimulate DNA polymerase α-primase in vitro. However, it is not known how CST accomplishes these functions in vivo. Here, we report the identification and characterization of Xenopus laevis CST complex (xCST). xCST showed ssDNA binding activity with moderate preference for G (guanine)-rich sequences. xStn1-immunodepleted Xenopus egg extracts supported chromosomal DNA replication in in vitro reconstituted sperm nuclei, suggesting that xCST is not a general replication factor. However, the immunodepletion or neutralization of xStn1 compromised DNA synthesis on ssDNA template. Because primed ssDNA template was replicated in xStn1-immunodepleted extracts as efficiently as in control ones, we conclude that xCST is involved in the priming step on ssDNA template. These results are consistent with the current model that CST is involved in telomeric C-strand synthesis through the regulation of DNA polymerase α-primase.
- (キーワード)
- Animals / Base Sequence / Cell Nucleus / Chromatin / Cloning, Molecular / DNA Replication / DNA, Single-Stranded / GC Rich Sequence / Humans / Male / Ovum / Protein Transport / Spermatozoa / Substrate Specificity / Telomere / Xenopus Proteins / Xenopus laevis
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.1074/jbc.M111.263723
- (文献検索サイトへのリンク)
- ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 22086929
- ● Summary page in Scopus @ Elsevier: 2-s2.0-84855295468
(DOI: 10.1074/jbc.M111.263723, PubMed: 22086929, Elsevier: Scopus) - MISC
- 研究者総覧に該当データはありませんでした。
- 総説・解説
- Hidenori Nakaoka :
Live fast, die fast principle in a single cell of fission yeast,
Microbial Cell, 4, 9, 308-310, Sep. 2017.- (キーワード)
- Aging / Death / Fission yeast / Growth / Macroscopic phenomenology / Microfluidics / Protein aggregation
- (出版サイトへのリンク)
- ● Publication site (DOI): 10.15698/mic2017.09.591
- (文献検索サイトへのリンク)
- ● Summary page in Scopus @ Elsevier: 2-s2.0-85068472827
(DOI: 10.15698/mic2017.09.591, Elsevier: Scopus) - 講演・発表
- 研究者総覧に該当データはありませんでした。
- 研究会・報告書
- 研究者総覧に該当データはありませんでした。
- 特許
- 研究者総覧に該当データはありませんでした。
- 作品
- 研究者総覧に該当データはありませんでした。
- 補助金・競争的資金
- 『生命-非生命転移境界』の in vivo 定量解析 (研究課題/領域番号: 25H01389 )
『生命-非生命転移』学の創出 (研究課題/領域番号: 25H01388 )
低栄養環境によって誘導される細胞の休眠状態を理解する (研究課題/領域番号: 23K05010 )
研究者番号（50724423）による検索
- その他
- 研究者総覧に該当データはありませんでした。
2025年7月2日更新
- 専門分野・研究分野
- ライフサイエンス (Life sciences) [分子生物学 (Molecular biology)]
ライフサイエンス (Life sciences) [細胞生物学 (Cell biology)]
ライフサイエンス (Life sciences) [生物物理学 (Biophysics)] - 所属学会・所属協会
- 研究者総覧に該当データはありませんでした。
- 委員歴・役員歴
- 研究者総覧に該当データはありませんでした。
- 受賞
- 研究者総覧に該当データはありませんでした。
- 活動
- 研究者総覧に該当データはありませんでした。
2025年6月29日更新
2025年6月28日更新
Ｊグローバル
- Jグローバル最終確認日
- 2025/6/28 01:20
- 氏名（漢字）
- 中岡 秀憲
- 氏名（フリガナ）
- ナカオカ ヒデノリ
- 氏名（英字）
- Nakaoka Hidenori
- 所属機関
- 徳島大学 助教
リサーチマップ
- researchmap最終確認日
- 2025/6/29 02:05
- 氏名（漢字）
- 中岡 秀憲
- 氏名（フリガナ）
- ナカオカ ヒデノリ
- 氏名（英字）
- Nakaoka Hidenori
- プロフィール
- リサーチマップAPIで取得できませんでした。
- 登録日時
- 2018/10/16 00:18
- 更新日時
- 2025/5/14 09:24
- アバター画像URI
- https://researchmap.jp/hidenorinakaoka/avatar.jpg
- ハンドル
- リサーチマップAPIで取得できませんでした。
- eメール
- リサーチマップAPIで取得できませんでした。
- eメール（その他）
- リサーチマップAPIで取得できませんでした。
- 携帯メール
- リサーチマップAPIで取得できませんでした。
- 性別
- リサーチマップAPIで取得できませんでした。
- 没年月日
- リサーチマップAPIで取得できませんでした。
- 所属ID
- 0344000000
- 所属
- 徳島大学
- 部署
- 先端研究推進センター
- 職名
- 助教
- 学位
- 生命科学博士
- 学位授与機関
- 京都大学
- URL
- リサーチマップAPIで取得できませんでした。
- 科研費研究者番号
- リサーチマップAPIで取得できませんでした。
- Google Analytics ID
- リサーチマップAPIで取得できませんでした。
- ORCID ID
- リサーチマップAPIで取得できませんでした。
- その他の所属ID
- リサーチマップAPIで取得できませんでした。
- その他の所属名
- リサーチマップAPIで取得できませんでした。
- その他の所属 部署
- リサーチマップAPIで取得できませんでした。
- その他の所属 職名
- リサーチマップAPIで取得できませんでした。
- 最近のエントリー
- リサーチマップAPIで取得できませんでした。
- Read会員ID
- リサーチマップAPIで取得できませんでした。
- 経歴
- 受賞
- Misc
- 論文
- 講演・口頭発表等
- 書籍等出版物
- 研究キーワード
- 研究分野
- 所属学協会
- 担当経験のある科目
- その他
- Works
- リサーチマップAPIで取得できませんでした。
- 特許
- リサーチマップAPIで取得できませんでした。
- 学歴
- 委員歴
- リサーチマップAPIで取得できませんでした。
- 社会貢献活動
2025年6月28日更新
- 研究者番号
- 50724423
- 所属（現在）
- 2025/4/1 : 徳島大学, 先端研究推進センター, 助教
- 所属（過去の研究課題
情報に基づく）*注記 - 2025/4/1 : 徳島大学, 先端研究推進センター, 助教
2023/4/1 : 京都大学, 生命科学研究科, 助教
- 審査区分/研究分野
-
研究代表者
小区分38020:応用微生物学関連
学術変革領域研究区分(Ⅱ)研究代表者以外
学術変革領域研究区分(Ⅱ)
- キーワード
-
研究代表者
栄養飢餓 / 細胞内pH / 環境ストレス応答 / 分子生物学 / イメージング / マイクロデバイス / 分裂酵母 / cell death / metabolome / imaging / miccrofluidics
研究代表者以外
細胞死 / 微生物学 / 一細胞計測 / 代謝 / 数理モデル
研究課題
研究成果
共同研究者
注目研究はありません。