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Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice.

Journal of oral & facial pain and headache

Maruno M, Shinoda M, Honda K, Ito R, Urata K, Watanabe M, Okada S, Lee J, Gionhaku N, Iwata K.
PMID: 28973050
J Oral Facial Pain Headache. 2017;31(4):372–380. doi: 10.11607/ofph.1849. Epub 2017 Oct 03.

AIMS: To develop a tongue pain model with no mucosal pathologic changes and to examine whether phosphorylation of p38 in trigeminal ganglion (TG) neurons innervating the tongue is associated with tongue heat hypersensitivity in mice.METHODS: Tongue heat sensitivity in...

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Maruno M, Shinoda M, Honda K, et al. Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. J Oral Facial Pain Headache. 2017;31(4):372–380doi: 10.11607/ofph.1849.
Maruno, M., Shinoda, M., Honda, K., Ito, R., Urata, K., Watanabe, M., Okada, S., Lee, J., Gionhaku, N., & Iwata, K. (2017). Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. Journal of oral & facial pain and headache, 31(4), 372–380. https://doi.org/10.11607/ofph.1849
Maruno, Mitsuru, et al. "Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice." Journal of oral & facial pain and headache vol. 31,4 (2017): 372–380. doi: https://doi.org/10.11607/ofph.1849
Maruno M, Shinoda M, Honda K, Ito R, Urata K, Watanabe M, Okada S, Lee J, Gionhaku N, Iwata K. Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. J Oral Facial Pain Headache. 2017;31(4):372–380. doi: 10.11607/ofph.1849. Epub 2017 Oct 03. PMID: 28973050.
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Observation of coherent phonon-plasma coupled modes in wide gap semiconductors by transmission pump-probe measurements.

Optics express

Kunugita H, Hatashita K, Ohkubo Y, Okada T, Ema K.
PMID: 26367628
Opt Express. 2015 Jul 27;23(15):19705-14. doi: 10.1364/OE.23.019705.

We have investigated coherent LO phonon properties in zinc-based II-VI widegap semiconductors, focusing on phonon-plasma coupled modes. By a careful treatment of the time evolution of the signals in ZnS, ZnSe, and ZnTe, we found a frequency upshift as...

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Kunugita H, Hatashita K, Ohkubo Y, et al. Observation of coherent phonon-plasma coupled modes in wide gap semiconductors by transmission pump-probe measurements. Opt Express. 2015;23(15):19705-14doi: 10.1364/OE.23.019705.
Kunugita, H., Hatashita, K., Ohkubo, Y., Okada, T., & Ema, K. (2015). Observation of coherent phonon-plasma coupled modes in wide gap semiconductors by transmission pump-probe measurements. Optics express, 23(15), 19705-14. https://doi.org/10.1364/OE.23.019705
Kunugita, Hideyuki, et al. "Observation of coherent phonon-plasma coupled modes in wide gap semiconductors by transmission pump-probe measurements." Optics express vol. 23,15 (2015): 19705-14. doi: https://doi.org/10.1364/OE.23.019705
Kunugita H, Hatashita K, Ohkubo Y, Okada T, Ema K. Observation of coherent phonon-plasma coupled modes in wide gap semiconductors by transmission pump-probe measurements. Opt Express. 2015 Jul 27;23(15):19705-14. doi: 10.1364/OE.23.019705. PMID: 26367628.
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Hepatitis C and hepatocellular carcinoma.

Journal of gastroenterology and hepatology

Okuda K.
PMID: 28976662
J Gastroenterol Hepatol. 1998 Nov;13:S294-S297. doi: 10.1111/j.1440-1746.1998.tb01896.x.

Hepatitis C virus (HCV) infection is aetiologically very closely associated with hepatocellular carcinoma (HCC). World-wide, hepatitis B virus infection is the predominant aetiological factor in developing countries, whereas in industrialized countries, HCV has a far more important role in...

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Okuda K. Hepatitis C and hepatocellular carcinoma. J Gastroenterol Hepatol. 1998;13:S294-S297doi: 10.1111/j.1440-1746.1998.tb01896.x.
Okuda, K. (1998). Hepatitis C and hepatocellular carcinoma. Journal of gastroenterology and hepatology, 13S294-S297. https://doi.org/10.1111/j.1440-1746.1998.tb01896.x
Okuda, Kunio. "Hepatitis C and hepatocellular carcinoma." Journal of gastroenterology and hepatology vol. 13 (1998): S294-S297. doi: https://doi.org/10.1111/j.1440-1746.1998.tb01896.x
Okuda K. Hepatitis C and hepatocellular carcinoma. J Gastroenterol Hepatol. 1998 Nov;13:S294-S297. doi: 10.1111/j.1440-1746.1998.tb01896.x. PMID: 28976662.
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X-Ray-Induced Damage to the Submandibular Salivary Glands in Mice: An Analysis of Strain-Specific Responses.

BioResearch open access

Kamiya M, Kawase T, Hayama K, Tsuchimochi M, Okuda K, Yoshie H.
PMID: 26309806
Biores Open Access. 2015 Jun 01;4(1):307-18. doi: 10.1089/biores.2015.0017. eCollection 2015.

Radiation therapy for head and neck cancers often causes xerostomia (dry mouth) by acutely damaging the salivary glands through the induction of severe acute inflammation. By contrast, the mechanism underlying the X-ray-induced delayed salivary dysfunction is unknown and has...

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Kamiya M, Kawase T, Hayama K, et al. X-Ray-Induced Damage to the Submandibular Salivary Glands in Mice: An Analysis of Strain-Specific Responses. Biores Open Access. 2015;4(1):307-18doi: 10.1089/biores.2015.0017.
Kamiya, M., Kawase, T., Hayama, K., Tsuchimochi, M., Okuda, K., & Yoshie, H. (2015). X-Ray-Induced Damage to the Submandibular Salivary Glands in Mice: An Analysis of Strain-Specific Responses. BioResearch open access, 4(1), 307-18. https://doi.org/10.1089/biores.2015.0017
Kamiya, Mana, et al. "X-Ray-Induced Damage to the Submandibular Salivary Glands in Mice: An Analysis of Strain-Specific Responses." BioResearch open access vol. 4,1 (2015): 307-18. doi: https://doi.org/10.1089/biores.2015.0017
Kamiya M, Kawase T, Hayama K, Tsuchimochi M, Okuda K, Yoshie H. X-Ray-Induced Damage to the Submandibular Salivary Glands in Mice: An Analysis of Strain-Specific Responses. Biores Open Access. 2015 Jun 01;4(1):307-18. doi: 10.1089/biores.2015.0017. eCollection 2015. PMID: 26309806; PMCID: PMC4497710.
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Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes.

Chemical science

Okada K, Yagi A, Segawa Y, Itami K.
PMID: 28451214
Chem Sci. 2017 Jan 01;8(1):661-667. doi: 10.1039/c6sc04048a. Epub 2016 Sep 12.

The synthesis and properties of various [

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Okada K, Yagi A, Segawa Y, et al. Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes. Chem Sci. 2016;8(1):661-667doi: 10.1039/c6sc04048a.
Okada, K., Yagi, A., Segawa, Y., & Itami, K. (2017). Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes. Chemical science, 8(1), 661-667. https://doi.org/10.1039/c6sc04048a
Okada, Keishu, et al. "Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes." Chemical science vol. 8,1 (2017): 661-667. doi: https://doi.org/10.1039/c6sc04048a
Okada K, Yagi A, Segawa Y, Itami K. Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes. Chem Sci. 2017 Jan 01;8(1):661-667. doi: 10.1039/c6sc04048a. Epub 2016 Sep 12. PMID: 28451214; PMCID: PMC5297897.
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Quality Assessment of Platelet-Rich Fibrin-Like Matrix Prepared from Whole Blood Samples after Extended Storage.

Biomedicines

Kawabata H, Isobe K, Watanabe T, Okudera T, Nakamura M, Suzuki M, Ryu J, Kitamura Y, Okudera H, Okuda K, Nakata K, Kawase T.
PMID: 28926988
Biomedicines. 2017 Sep 18;5(3). doi: 10.3390/biomedicines5030057.

The platelet-rich fibrin-like matrix (PRFM) is usually prepared onsite and immediately used for regenerative therapy. Nonetheless, to meet the clinical necessity of preserving the PRFM without quality deterioration, we developed a method for preparation of PRFMs from short-term-stored whole...

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Kawabata H, Isobe K, Watanabe T, et al. Quality Assessment of Platelet-Rich Fibrin-Like Matrix Prepared from Whole Blood Samples after Extended Storage. Biomedicines. 2017;5(3)doi: 10.3390/biomedicines5030057.
Kawabata, H., Isobe, K., Watanabe, T., Okudera, T., Nakamura, M., Suzuki, M., Ryu, J., Kitamura, Y., Okudera, H., Okuda, K., Nakata, K., & Kawase, T. (2017). Quality Assessment of Platelet-Rich Fibrin-Like Matrix Prepared from Whole Blood Samples after Extended Storage. Biomedicines, 5(3), . https://doi.org/10.3390/biomedicines5030057
Kawabata, Hideo, et al. "Quality Assessment of Platelet-Rich Fibrin-Like Matrix Prepared from Whole Blood Samples after Extended Storage." Biomedicines vol. 5,3 (2017). doi: https://doi.org/10.3390/biomedicines5030057
Kawabata H, Isobe K, Watanabe T, Okudera T, Nakamura M, Suzuki M, Ryu J, Kitamura Y, Okudera H, Okuda K, Nakata K, Kawase T. Quality Assessment of Platelet-Rich Fibrin-Like Matrix Prepared from Whole Blood Samples after Extended Storage. Biomedicines. 2017 Sep 18;5(3). doi: 10.3390/biomedicines5030057. PMID: 28926988; PMCID: PMC5618315.
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Dexmedetomidine sedation during the nighttime reduced the incidence of postoperative atrial fibrillation in cardiovascular surgery patients after tracheal extubation.

Journal of intensive care

Narisawa A, Nakane M, Kano T, Momose N, Onodera Y, Akimoto R, Kobayashi T, Iwabuchi M, Okada M, Miura Y, Kawamae K.
PMID: 26060574
J Intensive Care. 2015 May 30;3(1):26. doi: 10.1186/s40560-015-0092-5. eCollection 2015.

BACKGROUND: Dexmedetomidine (Dex) provides sedation and analgesia by acting on central alpha-2 receptors and is suitable for use after extubation because it has little respiratory depression. Considering the sympathoinhibitory and anxiolytic action of Dex, there is the possibility that...

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Narisawa A, Nakane M, Kano T, et al. Dexmedetomidine sedation during the nighttime reduced the incidence of postoperative atrial fibrillation in cardiovascular surgery patients after tracheal extubation. J Intensive Care. 2015;3(1):26doi: 10.1186/s40560-015-0092-5.
Narisawa, A., Nakane, M., Kano, T., Momose, N., Onodera, Y., Akimoto, R., Kobayashi, T., Iwabuchi, M., Okada, M., Miura, Y., & Kawamae, K. (2015). Dexmedetomidine sedation during the nighttime reduced the incidence of postoperative atrial fibrillation in cardiovascular surgery patients after tracheal extubation. Journal of intensive care, 3(1), 26. https://doi.org/10.1186/s40560-015-0092-5
Narisawa, Ayuka, et al. "Dexmedetomidine sedation during the nighttime reduced the incidence of postoperative atrial fibrillation in cardiovascular surgery patients after tracheal extubation." Journal of intensive care vol. 3,1 (2015): 26. doi: https://doi.org/10.1186/s40560-015-0092-5
Narisawa A, Nakane M, Kano T, Momose N, Onodera Y, Akimoto R, Kobayashi T, Iwabuchi M, Okada M, Miura Y, Kawamae K. Dexmedetomidine sedation during the nighttime reduced the incidence of postoperative atrial fibrillation in cardiovascular surgery patients after tracheal extubation. J Intensive Care. 2015 May 30;3(1):26. doi: 10.1186/s40560-015-0092-5. eCollection 2015. PMID: 26060574; PMCID: PMC4460695.
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Comparison of 3 body size descriptors in critically ill obese children and adolescents: implications for medication dosing.

The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG

Ross EL, Jorgensen J, DeWitt PE, Okada C, Porter R, Haemer M, Reiter PD.
PMID: 25024670
J Pediatr Pharmacol Ther. 2014 Apr;19(2):103-10. doi: 10.5863/1551-6776-19.2.103.

OBJECTIVE: To compare 3 methods of weight determination for medication dose calculations in obese children and to discuss feasibility for use in routine care.METHODS: This was a patient safety and quality improvement study evaluating patients (2-19 years old) admitted...

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Ross EL, Jorgensen J, DeWitt PE, et al. Comparison of 3 body size descriptors in critically ill obese children and adolescents: implications for medication dosing. J Pediatr Pharmacol Ther. 2014;19(2):103-10doi: 10.5863/1551-6776-19.2.103.
Ross, E. L., Jorgensen, J., DeWitt, P. E., Okada, C., Porter, R., Haemer, M., & Reiter, P. D. (2014). Comparison of 3 body size descriptors in critically ill obese children and adolescents: implications for medication dosing. The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 19(2), 103-10. https://doi.org/10.5863/1551-6776-19.2.103
Ross, Emma L, et al. "Comparison of 3 body size descriptors in critically ill obese children and adolescents: implications for medication dosing." The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG vol. 19,2 (2014): 103-10. doi: https://doi.org/10.5863/1551-6776-19.2.103
Ross EL, Jorgensen J, DeWitt PE, Okada C, Porter R, Haemer M, Reiter PD. Comparison of 3 body size descriptors in critically ill obese children and adolescents: implications for medication dosing. J Pediatr Pharmacol Ther. 2014 Apr;19(2):103-10. doi: 10.5863/1551-6776-19.2.103. PMID: 25024670; PMCID: PMC4093662.
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Exosomes isolated from plasma of glioma patients enrolled in a vaccination trial reflect antitumor immune activity and might predict survival.

Oncoimmunology

Muller L, Muller-Haegele S, Mitsuhashi M, Gooding W, Okada H, Whiteside TL.
PMID: 26155415
Oncoimmunology. 2015 Mar 02;4(6):e1008347. doi: 10.1080/2162402X.2015.1008347. eCollection 2015 Jun.

Exosomes in plasma of glioma patients hold promise as biomarkers of prognosis. We aimed to determine whether changes in total exosomal protein and mRNA expression levels could serve as surrogate markers of immunological and clinical responses in glioma patients...

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Muller L, Muller-Haegele S, Mitsuhashi M, et al. Exosomes isolated from plasma of glioma patients enrolled in a vaccination trial reflect antitumor immune activity and might predict survival. Oncoimmunology. 2015;4(6):e1008347doi: 10.1080/2162402X.2015.1008347.
Muller, L., Muller-Haegele, S., Mitsuhashi, M., Gooding, W., Okada, H., & Whiteside, T. L. (2015). Exosomes isolated from plasma of glioma patients enrolled in a vaccination trial reflect antitumor immune activity and might predict survival. Oncoimmunology, 4(6), e1008347. https://doi.org/10.1080/2162402X.2015.1008347
Muller, Laurent, et al. "Exosomes isolated from plasma of glioma patients enrolled in a vaccination trial reflect antitumor immune activity and might predict survival." Oncoimmunology vol. 4,6 (2015): e1008347. doi: https://doi.org/10.1080/2162402X.2015.1008347
Muller L, Muller-Haegele S, Mitsuhashi M, Gooding W, Okada H, Whiteside TL. Exosomes isolated from plasma of glioma patients enrolled in a vaccination trial reflect antitumor immune activity and might predict survival. Oncoimmunology. 2015 Mar 02;4(6):e1008347. doi: 10.1080/2162402X.2015.1008347. eCollection 2015 Jun. PMID: 26155415; PMCID: PMC4485717.
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A Case of Metastatic Urothelial Carcinoma Treated with Pemetrexed as Third-Line Chemotherapy with Discussion and Literature Review.

Case reports in oncology

Iida K, Kawai N, Naiki T, Etani T, Ando R, Nagai T, Sugiyama Y, Naiki-Ito A, Nishio H, Okada A, Kohri K, Yasui T.
PMID: 26668577
Case Rep Oncol. 2015 Nov 01;8(3):530-5. doi: 10.1159/000442347. eCollection 2015.

Pemetrexed is an antifolate agent that is regarded as an alternative second-line chemotherapy against advanced or metastatic urothelial carcinoma (UC). However, there is limited information on pemetrexed in a third-line setting. We report a case of metastatic UC treated...

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Iida K, Kawai N, Naiki T, et al. A Case of Metastatic Urothelial Carcinoma Treated with Pemetrexed as Third-Line Chemotherapy with Discussion and Literature Review. Case Rep Oncol. 2015;8(3):530-5doi: 10.1159/000442347.
Iida, K., Kawai, N., Naiki, T., Etani, T., Ando, R., Nagai, T., Sugiyama, Y., Naiki-Ito, A., Nishio, H., Okada, A., Kohri, K., & Yasui, T. (2015). A Case of Metastatic Urothelial Carcinoma Treated with Pemetrexed as Third-Line Chemotherapy with Discussion and Literature Review. Case reports in oncology, 8(3), 530-5. https://doi.org/10.1159/000442347
Iida, Keitaro, et al. "A Case of Metastatic Urothelial Carcinoma Treated with Pemetrexed as Third-Line Chemotherapy with Discussion and Literature Review." Case reports in oncology vol. 8,3 (2015): 530-5. doi: https://doi.org/10.1159/000442347
Iida K, Kawai N, Naiki T, Etani T, Ando R, Nagai T, Sugiyama Y, Naiki-Ito A, Nishio H, Okada A, Kohri K, Yasui T. A Case of Metastatic Urothelial Carcinoma Treated with Pemetrexed as Third-Line Chemotherapy with Discussion and Literature Review. Case Rep Oncol. 2015 Nov 01;8(3):530-5. doi: 10.1159/000442347. eCollection 2015. PMID: 26668577; PMCID: PMC4677708.
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Eicosapentaenoic acid/arachidonic acid ratio and smoking status in elderly patients with type 2 diabetes mellitus.

Diabetology & metabolic syndrome

Okada K, Kotani K, Yagyu H, Ishibashi S.
PMID: 25143787
Diabetol Metab Syndr. 2014 Aug 13;6(1):85. doi: 10.1186/1758-5996-6-85. eCollection 2014.

BACKGROUND: A low ratio of eicosapentaenoic acid (EPA)/arachidonic acid (AA) is considered a risk factor for cardiovascular disease. Smoking is also a risk factor for cardiovascular disease even in an elderly population. This study investigated the relationship between EPA/AA...

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Okada K, Kotani K, Yagyu H, et al. Eicosapentaenoic acid/arachidonic acid ratio and smoking status in elderly patients with type 2 diabetes mellitus. Diabetol Metab Syndr. 2014;6(1):85doi: 10.1186/1758-5996-6-85.
Okada, K., Kotani, K., Yagyu, H., & Ishibashi, S. (2014). Eicosapentaenoic acid/arachidonic acid ratio and smoking status in elderly patients with type 2 diabetes mellitus. Diabetology & metabolic syndrome, 6(1), 85. https://doi.org/10.1186/1758-5996-6-85
Okada, Kenta, et al. "Eicosapentaenoic acid/arachidonic acid ratio and smoking status in elderly patients with type 2 diabetes mellitus." Diabetology & metabolic syndrome vol. 6,1 (2014): 85. doi: https://doi.org/10.1186/1758-5996-6-85
Okada K, Kotani K, Yagyu H, Ishibashi S. Eicosapentaenoic acid/arachidonic acid ratio and smoking status in elderly patients with type 2 diabetes mellitus. Diabetol Metab Syndr. 2014 Aug 13;6(1):85. doi: 10.1186/1758-5996-6-85. eCollection 2014. PMID: 25143787; PMCID: PMC4138366.
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Fournier's gangrene caused by Listeria monocytogenes as the primary organism.

The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale

Asahata S, Hirai Y, Ainoda Y, Fujita T, Okada Y, Kikuchi K.
PMID: 25798155
Can J Infect Dis Med Microbiol. 2015 Jan-Feb;26(1):44-6. doi: 10.1155/2015/501386.

A 70-year-old man with a history of tongue cancer presented with Fournier's gangrene caused by Listeria monocytogenes serotype 4b. Surgical debridement revealed undiagnosed rectal adenocarcinoma. The patient did not have an apparent dietary or travel history but reported daily...

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Asahata S, Hirai Y, Ainoda Y, et al. Fournier's gangrene caused by Listeria monocytogenes as the primary organism. Can J Infect Dis Med Microbiol. 2015;26(1):44-6doi: 10.1155/2015/501386.
Asahata, S., Hirai, Y., Ainoda, Y., Fujita, T., Okada, Y., & Kikuchi, K. (2015). Fournier's gangrene caused by Listeria monocytogenes as the primary organism. The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 26(1), 44-6. https://doi.org/10.1155/2015/501386
Asahata, Sayaka, et al. "Fournier's gangrene caused by Listeria monocytogenes as the primary organism." The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale vol. 26,1 (2015): 44-6. doi: https://doi.org/10.1155/2015/501386
Asahata S, Hirai Y, Ainoda Y, Fujita T, Okada Y, Kikuchi K. Fournier's gangrene caused by Listeria monocytogenes as the primary organism. Can J Infect Dis Med Microbiol. 2015 Jan-Feb;26(1):44-6. doi: 10.1155/2015/501386. PMID: 25798155; PMCID: PMC4353270.
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Showing 13 to 24 of 4843 entries