Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1045 to 1050 of 1050 entries
Sorted by: Best Match Show Resources per page
Effect of the Characteristic Properties of Membrane on Long-Term Stability in the Vacuum Membrane Distillation Process.

Membranes

Suga Y, Takagi R, Matsuyama H.
PMID: 33807154
Membranes (Basel). 2021 Mar 31;11(4). doi: 10.3390/membranes11040252.

Membrane distillation (MD) is a technology that can treat feed solutions with higher osmotic pressure, as well as produce high-purity water. However, the water production cost of the MD process is expensive. In this study, to decrease the water...

Cite
Suga Y, Takagi R, Matsuyama H. Effect of the Characteristic Properties of Membrane on Long-Term Stability in the Vacuum Membrane Distillation Process. Membranes (Basel). 2021;11(4)doi: 10.3390/membranes11040252.
Suga, Y., Takagi, R., & Matsuyama, H. (2021). Effect of the Characteristic Properties of Membrane on Long-Term Stability in the Vacuum Membrane Distillation Process. Membranes, 11(4), . https://doi.org/10.3390/membranes11040252
Suga, Yuki, et al. "Effect of the Characteristic Properties of Membrane on Long-Term Stability in the Vacuum Membrane Distillation Process." Membranes vol. 11,4 (2021). doi: https://doi.org/10.3390/membranes11040252
Suga Y, Takagi R, Matsuyama H. Effect of the Characteristic Properties of Membrane on Long-Term Stability in the Vacuum Membrane Distillation Process. Membranes (Basel). 2021 Mar 31;11(4). doi: 10.3390/membranes11040252. PMID: 33807154; PMCID: PMC8066549.
Copy Download .nbib Format: NLM
Association between procrastination in childhood and the number of remaining teeth in Japanese older adults.

Journal of epidemiology

Shimamura M, Matsuyama Y, Morita A, Fujiwara T.
PMID: 33840649
J Epidemiol. 2021 Apr 10; doi: 10.2188/jea.JE20200366. Epub 2021 Apr 10.

BACKGROUND: Procrastination is associated with stress and unhealthy behaviors. The oral condition reflects the long-term history of an individual's stress exposure and oral health behaviors; however, empirical studies on the association of procrastination in childhood with remaining teeth in...

Cite
Shimamura M, Matsuyama Y, Morita A, et al. Association between procrastination in childhood and the number of remaining teeth in Japanese older adults. J Epidemiol. 2021;doi: 10.2188/jea.JE20200366.
Shimamura, M., Matsuyama, Y., Morita, A., & Fujiwara, T. (2021). Association between procrastination in childhood and the number of remaining teeth in Japanese older adults. Journal of epidemiology, . https://doi.org/10.2188/jea.JE20200366
Shimamura, Moemi, et al. "Association between procrastination in childhood and the number of remaining teeth in Japanese older adults." Journal of epidemiology vol. (2021). doi: https://doi.org/10.2188/jea.JE20200366
Shimamura M, Matsuyama Y, Morita A, Fujiwara T. Association between procrastination in childhood and the number of remaining teeth in Japanese older adults. J Epidemiol. 2021 Apr 10; doi: 10.2188/jea.JE20200366. Epub 2021 Apr 10. PMID: 33840649.
Copy Download .nbib Format: NLM
Role of active site arginine residues in substrate recognition by PPM1A.

Biochemical and biophysical research communications

Tani I, Ito S, Shirahata Y, Matsuyama Y, Omichinski JG, Shimohigashi Y, Kamada R, Sakaguchi K.
PMID: 34637963
Biochem Biophys Res Commun. 2021 Dec 03;581:1-5. doi: 10.1016/j.bbrc.2021.10.001. Epub 2021 Oct 06.

Reversible protein phosphorylation is a key mechanism for regulating numerous cellular events. The metal-dependent protein phosphatases (PPM) are a family of Ser/Thr phosphatases, which uniquely recognize their substrate as a monomeric enzyme. In the case of PPM1A, it has...

Cite
Tani I, Ito S, Shirahata Y, et al. Role of active site arginine residues in substrate recognition by PPM1A. Biochem Biophys Res Commun. 2021;581:1-5doi: 10.1016/j.bbrc.2021.10.001.
Tani, I., Ito, S., Shirahata, Y., Matsuyama, Y., Omichinski, J. G., Shimohigashi, Y., Kamada, R., & Sakaguchi, K. (2021). Role of active site arginine residues in substrate recognition by PPM1A. Biochemical and biophysical research communications, 5811-5. https://doi.org/10.1016/j.bbrc.2021.10.001
Tani, Itsumi, et al. "Role of active site arginine residues in substrate recognition by PPM1A." Biochemical and biophysical research communications vol. 581 (2021): 1-5. doi: https://doi.org/10.1016/j.bbrc.2021.10.001
Tani I, Ito S, Shirahata Y, Matsuyama Y, Omichinski JG, Shimohigashi Y, Kamada R, Sakaguchi K. Role of active site arginine residues in substrate recognition by PPM1A. Biochem Biophys Res Commun. 2021 Dec 03;581:1-5. doi: 10.1016/j.bbrc.2021.10.001. Epub 2021 Oct 06. PMID: 34637963.
Copy Download .nbib Format: NLM
Effects of LPXRFamide peptides on chub mackerel gonadotropin secretion†.

Biology of reproduction

Ohga H, Matsuyama M.
PMID: 34198332
Biol Reprod. 2021 Nov 15;105(5):1179-1188. doi: 10.1093/biolre/ioab130.

Gonadotropin-inhibitory hormone (GnIH), a neuropeptide, suppresses gonadotropin (GTH) secretion in birds and mammals. In fish, the GnIH homolog LPXRFamide (LPXRFa) produces mature peptides with species-dependent effects on sexual reproduction. Here, we investigated the effects of LPXRFa on GTH secretion...

Cite
Ohga H, Matsuyama M. Effects of LPXRFamide peptides on chub mackerel gonadotropin secretion†. Biol Reprod. 2021;105(5):1179-1188doi: 10.1093/biolre/ioab130.
Ohga, H., & Matsuyama, M. (2021). Effects of LPXRFamide peptides on chub mackerel gonadotropin secretion†. Biology of reproduction, 105(5), 1179-1188. https://doi.org/10.1093/biolre/ioab130
Ohga, Hirofumi, and Matsuyama, Michiya. "Effects of LPXRFamide peptides on chub mackerel gonadotropin secretion†." Biology of reproduction vol. 105,5 (2021): 1179-1188. doi: https://doi.org/10.1093/biolre/ioab130
Ohga H, Matsuyama M. Effects of LPXRFamide peptides on chub mackerel gonadotropin secretion†. Biol Reprod. 2021 Nov 15;105(5):1179-1188. doi: 10.1093/biolre/ioab130. PMID: 34198332.
Copy Download .nbib Format: NLM
Formation Mechanism and Toxicological Significance of Biogenic Mercury Selenide Nanoparticles in Human Hepatoma HepG2 Cells.

Chemical research in toxicology

Tanaka YK, Usuzawa H, Yoshida M, Kumagai K, Kobayashi K, Matsuyama S, Inoue T, Matsunaga A, Shimura M, Ruiz Encinar J, Costa-Fernández JM, Fukumoto Y, Suzuki N, Ogra Y.
PMID: 34841876
Chem Res Toxicol. 2021 Dec 20;34(12):2471-2484. doi: 10.1021/acs.chemrestox.1c00231. Epub 2021 Nov 29.

It is widely recognized that the toxicity of mercury (Hg) is attenuated by the simultaneous administration of selenium (Se) compounds in various organisms. In this study, we revealed the mechanisms underlying the antagonistic effect of sodium selenite (Na

Cite
Tanaka YK, Usuzawa H, Yoshida M, et al. Formation Mechanism and Toxicological Significance of Biogenic Mercury Selenide Nanoparticles in Human Hepatoma HepG2 Cells. Chem Res Toxicol. 2021;34(12):2471-2484doi: 10.1021/acs.chemrestox.1c00231.
Tanaka, Y. K., Usuzawa, H., Yoshida, M., Kumagai, K., Kobayashi, K., Matsuyama, S., Inoue, T., Matsunaga, A., Shimura, M., Ruiz Encinar, J., Costa-Fernández, J. M., Fukumoto, Y., Suzuki, N., & Ogra, Y. (2021). Formation Mechanism and Toxicological Significance of Biogenic Mercury Selenide Nanoparticles in Human Hepatoma HepG2 Cells. Chemical research in toxicology, 34(12), 2471-2484. https://doi.org/10.1021/acs.chemrestox.1c00231
Tanaka, Yu-Ki, et al. "Formation Mechanism and Toxicological Significance of Biogenic Mercury Selenide Nanoparticles in Human Hepatoma HepG2 Cells." Chemical research in toxicology vol. 34,12 (2021): 2471-2484. doi: https://doi.org/10.1021/acs.chemrestox.1c00231
Tanaka YK, Usuzawa H, Yoshida M, Kumagai K, Kobayashi K, Matsuyama S, Inoue T, Matsunaga A, Shimura M, Ruiz Encinar J, Costa-Fernández JM, Fukumoto Y, Suzuki N, Ogra Y. Formation Mechanism and Toxicological Significance of Biogenic Mercury Selenide Nanoparticles in Human Hepatoma HepG2 Cells. Chem Res Toxicol. 2021 Dec 20;34(12):2471-2484. doi: 10.1021/acs.chemrestox.1c00231. Epub 2021 Nov 29. PMID: 34841876.
Copy Download .nbib Format: NLM
Plasmacytoid Dendritic Cell (pDC) Infiltration Correlate with Tumor Infiltrating Lymphocytes, Cancer Immunity, and Better Survival in Triple Negative Breast Cancer (TNBC) More Strongly than Conventional Dendritic Cell (cDC).

Cancers

Oshi M, Newman S, Tokumaru Y, Yan L, Matsuyama R, Kalinski P, Endo I, Takabe K.
PMID: 33198125
Cancers (Basel). 2020 Nov 12;12(11). doi: 10.3390/cancers12113342.

Dendritic cells (DC) represent a major antigen-presenting cell type in the tumor immune microenvironment (TIME) and play an essential role in cancer immunity. Conventional DC (cDC) and plasmacytoid DC (pDC) were defined by the xCell algorithm and a total...

Cite
Oshi M, Newman S, Tokumaru Y, et al. Plasmacytoid Dendritic Cell (pDC) Infiltration Correlate with Tumor Infiltrating Lymphocytes, Cancer Immunity, and Better Survival in Triple Negative Breast Cancer (TNBC) More Strongly than Conventional Dendritic Cell (cDC). Cancers (Basel). 2020;12(11)doi: 10.3390/cancers12113342.
Oshi, M., Newman, S., Tokumaru, Y., Yan, L., Matsuyama, R., Kalinski, P., Endo, I., & Takabe, K. (2020). Plasmacytoid Dendritic Cell (pDC) Infiltration Correlate with Tumor Infiltrating Lymphocytes, Cancer Immunity, and Better Survival in Triple Negative Breast Cancer (TNBC) More Strongly than Conventional Dendritic Cell (cDC). Cancers, 12(11), . https://doi.org/10.3390/cancers12113342
Oshi, Masanori, et al. "Plasmacytoid Dendritic Cell (pDC) Infiltration Correlate with Tumor Infiltrating Lymphocytes, Cancer Immunity, and Better Survival in Triple Negative Breast Cancer (TNBC) More Strongly than Conventional Dendritic Cell (cDC)." Cancers vol. 12,11 (2020). doi: https://doi.org/10.3390/cancers12113342
Oshi M, Newman S, Tokumaru Y, Yan L, Matsuyama R, Kalinski P, Endo I, Takabe K. Plasmacytoid Dendritic Cell (pDC) Infiltration Correlate with Tumor Infiltrating Lymphocytes, Cancer Immunity, and Better Survival in Triple Negative Breast Cancer (TNBC) More Strongly than Conventional Dendritic Cell (cDC). Cancers (Basel). 2020 Nov 12;12(11). doi: 10.3390/cancers12113342. PMID: 33198125; PMCID: PMC7697894.
Copy Download .nbib Format: NLM
Showing 1045 to 1050 of 1050 entries