Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 13 to 24 of 870 entries
Sorted by: Best Match Show Resources per page
Ultraviolet-induced alloantigen-specific immunosuppression in transplant immunity.

World journal of transplantation

Hori T, Kuribayashi K, Saito K, Wang L, Torii M, Uemoto S, Iida T, Yagi S, Kato T.
PMID: 25815267
World J Transplant. 2015 Mar 24;5(1):11-8. doi: 10.5500/wjt.v5.i1.11.

After the first observation of the immunosuppressive effects of ultraviolet (UV) irradiation was reported in 1974, therapeutic modification of immune responses by UV irradiation began to be investigated in the context immunization. UV-induced immunosuppression is via the action of...

Cite
Hori T, Kuribayashi K, Saito K, et al. Ultraviolet-induced alloantigen-specific immunosuppression in transplant immunity. World J Transplant. 2015;5(1):11-8doi: 10.5500/wjt.v5.i1.11.
Hori, T., Kuribayashi, K., Saito, K., Wang, L., Torii, M., Uemoto, S., Iida, T., Yagi, S., & Kato, T. (2015). Ultraviolet-induced alloantigen-specific immunosuppression in transplant immunity. World journal of transplantation, 5(1), 11-8. https://doi.org/10.5500/wjt.v5.i1.11
Hori, Tomohide, et al. "Ultraviolet-induced alloantigen-specific immunosuppression in transplant immunity." World journal of transplantation vol. 5,1 (2015): 11-8. doi: https://doi.org/10.5500/wjt.v5.i1.11
Hori T, Kuribayashi K, Saito K, Wang L, Torii M, Uemoto S, Iida T, Yagi S, Kato T. Ultraviolet-induced alloantigen-specific immunosuppression in transplant immunity. World J Transplant. 2015 Mar 24;5(1):11-8. doi: 10.5500/wjt.v5.i1.11. PMID: 25815267; PMCID: PMC4371157.
Copy Download .nbib Format: NLM
Effect of different mattress designs on promoting sleep quality, pain reduction, and spinal alignment in adults with or without back pain; systematic review of controlled trials.

Sleep health

Radwan A, Fess P, James D, Murphy J, Myers J, Rooney M, Taylor J, Torii A.
PMID: 29073401
Sleep Health. 2015 Dec;1(4):257-267. doi: 10.1016/j.sleh.2015.08.001. Epub 2015 Oct 19.

A significant number of US citizens lack appropriate sleep for several reasons. Back pain has been identified as possible cause for inappropriate sleep in adults. Previously, the quality of mattresses and bedding systems has been correlated to the pain...

Cite
Radwan A, Fess P, James D, et al. Effect of different mattress designs on promoting sleep quality, pain reduction, and spinal alignment in adults with or without back pain; systematic review of controlled trials. Sleep Health. 2015;1(4):257-267doi: 10.1016/j.sleh.2015.08.001.
Radwan, A., Fess, P., James, D., Murphy, J., Myers, J., Rooney, M., Taylor, J., & Torii, A. (2015). Effect of different mattress designs on promoting sleep quality, pain reduction, and spinal alignment in adults with or without back pain; systematic review of controlled trials. Sleep health, 1(4), 257-267. https://doi.org/10.1016/j.sleh.2015.08.001
Radwan, Ahmed, et al. "Effect of different mattress designs on promoting sleep quality, pain reduction, and spinal alignment in adults with or without back pain; systematic review of controlled trials." Sleep health vol. 1,4 (2015): 257-267. doi: https://doi.org/10.1016/j.sleh.2015.08.001
Radwan A, Fess P, James D, Murphy J, Myers J, Rooney M, Taylor J, Torii A. Effect of different mattress designs on promoting sleep quality, pain reduction, and spinal alignment in adults with or without back pain; systematic review of controlled trials. Sleep Health. 2015 Dec;1(4):257-267. doi: 10.1016/j.sleh.2015.08.001. Epub 2015 Oct 19. PMID: 29073401.
Copy Download .nbib Format: NLM
Highlights from the latest articles in epigenomics.

Epigenomics

Fukushige S, Horii A.
PMID: 24811785
Epigenomics. 2014 Apr;6(2):171-3. doi: 10.2217/epi.14.2.

No abstract available.

Cite
Fukushige S, Horii A. Highlights from the latest articles in epigenomics. Epigenomics. 2014;6(2):171-3doi: 10.2217/epi.14.2.
Fukushige, S., & Horii, A. (2014). Highlights from the latest articles in epigenomics. Epigenomics, 6(2), 171-3. https://doi.org/10.2217/epi.14.2
Fukushige, Shinichi, and Horii, Akira. "Highlights from the latest articles in epigenomics." Epigenomics vol. 6,2 (2014): 171-3. doi: https://doi.org/10.2217/epi.14.2
Fukushige S, Horii A. Highlights from the latest articles in epigenomics. Epigenomics. 2014 Apr;6(2):171-3. doi: 10.2217/epi.14.2. PMID: 24811785.
Copy Download .nbib Format: NLM
Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2.

Frontiers in neurology

Koizumi H, Goto S, Okita S, Morigaki R, Akaike N, Torii Y, Harakawa T, Ginnaga A, Kaji R.
PMID: 25002857
Front Neurol. 2014 Jun 23;5:98. doi: 10.3389/fneur.2014.00098. eCollection 2014.

Because of its unique ability to exert long-lasting synaptic transmission blockade, botulinum neurotoxin A (BoNT/A) is used to treat a wide variety of disorders involving peripheral nerve terminal hyperexcitability. However, it has been a matter of debate whether this...

Cite
Koizumi H, Goto S, Okita S, et al. Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2. Front Neurol. 2014;5:98doi: 10.3389/fneur.2014.00098.
Koizumi, H., Goto, S., Okita, S., Morigaki, R., Akaike, N., Torii, Y., Harakawa, T., Ginnaga, A., & Kaji, R. (2014). Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2. Frontiers in neurology, 598. https://doi.org/10.3389/fneur.2014.00098
Koizumi, Hidetaka, et al. "Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2." Frontiers in neurology vol. 5 (2014): 98. doi: https://doi.org/10.3389/fneur.2014.00098
Koizumi H, Goto S, Okita S, Morigaki R, Akaike N, Torii Y, Harakawa T, Ginnaga A, Kaji R. Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2. Front Neurol. 2014 Jun 23;5:98. doi: 10.3389/fneur.2014.00098. eCollection 2014. PMID: 25002857; PMCID: PMC4066301.
Copy Download .nbib Format: NLM
Dock8 interacts with Nck1 in mediating Schwann cell precursor migration.

Biochemistry and biophysics reports

Miyamoto Y, Torii T, Kawahara K, Tanoue A, Yamauchi J.
PMID: 28955869
Biochem Biophys Rep. 2016 Mar 24;6:113-123. doi: 10.1016/j.bbrep.2016.03.013. eCollection 2016 Jul.

During embryonic development of the peripheral nervous system (PNS), Schwann cell precursors migrate along neuronal axons to their final destinations, where they will myelinate the axons after birth. While the intercellular signals controlling Schwann cell precursor migration are well...

Cite
Miyamoto Y, Torii T, Kawahara K, et al. Dock8 interacts with Nck1 in mediating Schwann cell precursor migration. Biochem Biophys Rep. 2016;6:113-123doi: 10.1016/j.bbrep.2016.03.013.
Miyamoto, Y., Torii, T., Kawahara, K., Tanoue, A., & Yamauchi, J. (2016). Dock8 interacts with Nck1 in mediating Schwann cell precursor migration. Biochemistry and biophysics reports, 6113-123. https://doi.org/10.1016/j.bbrep.2016.03.013
Miyamoto, Yuki, et al. "Dock8 interacts with Nck1 in mediating Schwann cell precursor migration." Biochemistry and biophysics reports vol. 6 (2016): 113-123. doi: https://doi.org/10.1016/j.bbrep.2016.03.013
Miyamoto Y, Torii T, Kawahara K, Tanoue A, Yamauchi J. Dock8 interacts with Nck1 in mediating Schwann cell precursor migration. Biochem Biophys Rep. 2016 Mar 24;6:113-123. doi: 10.1016/j.bbrep.2016.03.013. eCollection 2016 Jul. PMID: 28955869; PMCID: PMC5600352.
Copy Download .nbib Format: NLM
Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery.

Biochemistry and biophysics reports

Kizawa H, Nagao E, Shimamura M, Zhang G, Torii H.
PMID: 28955746
Biochem Biophys Rep. 2017 Apr 14;10:186-191. doi: 10.1016/j.bbrep.2017.04.004. eCollection 2017 Jul.

The liver plays a central role in metabolism. Although many studies have described

Cite
Kizawa H, Nagao E, Shimamura M, et al. Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery. Biochem Biophys Rep. 2017;10:186-191doi: 10.1016/j.bbrep.2017.04.004.
Kizawa, H., Nagao, E., Shimamura, M., Zhang, G., & Torii, H. (2017). Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery. Biochemistry and biophysics reports, 10186-191. https://doi.org/10.1016/j.bbrep.2017.04.004
Kizawa, Hideki, et al. "Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery." Biochemistry and biophysics reports vol. 10 (2017): 186-191. doi: https://doi.org/10.1016/j.bbrep.2017.04.004
Kizawa H, Nagao E, Shimamura M, Zhang G, Torii H. Scaffold-free 3D bio-printed human liver tissue stably maintains metabolic functions useful for drug discovery. Biochem Biophys Rep. 2017 Apr 14;10:186-191. doi: 10.1016/j.bbrep.2017.04.004. eCollection 2017 Jul. PMID: 28955746; PMCID: PMC5614670.
Copy Download .nbib Format: NLM
Gas6-Tyro3 signaling is required for Schwann cell myelination and possible remyelination.

Neural regeneration research

Torii T, Yamauchi J.
PMID: 27073361
Neural Regen Res. 2016 Feb;11(2):215-6. doi: 10.4103/1673-5374.177714.

No abstract available.

Cite
Torii T, Yamauchi J. Gas6-Tyro3 signaling is required for Schwann cell myelination and possible remyelination. Neural Regen Res. 2016;11(2):215-6doi: 10.4103/1673-5374.177714.
Torii, T., & Yamauchi, J. (2016). Gas6-Tyro3 signaling is required for Schwann cell myelination and possible remyelination. Neural regeneration research, 11(2), 215-6. https://doi.org/10.4103/1673-5374.177714
Torii, Tomohiro, and Yamauchi, Junji. "Gas6-Tyro3 signaling is required for Schwann cell myelination and possible remyelination." Neural regeneration research vol. 11,2 (2016): 215-6. doi: https://doi.org/10.4103/1673-5374.177714
Torii T, Yamauchi J. Gas6-Tyro3 signaling is required for Schwann cell myelination and possible remyelination. Neural Regen Res. 2016 Feb;11(2):215-6. doi: 10.4103/1673-5374.177714. PMID: 27073361; PMCID: PMC4810972.
Copy Download .nbib Format: NLM
Involvement of inhibitory PAS domain protein in neuronal cell death in Parkinson's disease.

Cell death discovery

Torii S, Kasai S, Suzuki A, Todoroki Y, Yokozawa K, Yasumoto KI, Seike N, Kiyonari H, Mukumoto Y, Kakita A, Sogawa K.
PMID: 27551449
Cell Death Discov. 2015 Aug 17;1:15015. doi: 10.1038/cddiscovery.2015.15. eCollection 2015.

Inhibitory PAS domain protein (IPAS), a repressor of hypoxia-inducible factor-dependent transcription under hypoxia, was found to exert pro-apoptotic activity in oxidative stress-induced cell death. However, physiological and pathological processes associated with this activity are not known. Here we show...

Cite
Torii S, Kasai S, Suzuki A, et al. Involvement of inhibitory PAS domain protein in neuronal cell death in Parkinson's disease. Cell Death Discov. 2015;1:15015doi: 10.1038/cddiscovery.2015.15.
Torii, S., Kasai, S., Suzuki, A., Todoroki, Y., Yokozawa, K., Yasumoto, K. I., Seike, N., Kiyonari, H., Mukumoto, Y., Kakita, A., & Sogawa, K. (2015). Involvement of inhibitory PAS domain protein in neuronal cell death in Parkinson's disease. Cell death discovery, 115015. https://doi.org/10.1038/cddiscovery.2015.15
Torii, S, et al. "Involvement of inhibitory PAS domain protein in neuronal cell death in Parkinson's disease." Cell death discovery vol. 1 (2015): 15015. doi: https://doi.org/10.1038/cddiscovery.2015.15
Torii S, Kasai S, Suzuki A, Todoroki Y, Yokozawa K, Yasumoto KI, Seike N, Kiyonari H, Mukumoto Y, Kakita A, Sogawa K. Involvement of inhibitory PAS domain protein in neuronal cell death in Parkinson's disease. Cell Death Discov. 2015 Aug 17;1:15015. doi: 10.1038/cddiscovery.2015.15. eCollection 2015. PMID: 27551449; PMCID: PMC4981001.
Copy Download .nbib Format: NLM
Prevalence and Intensity of Paramphistomum Spp. In Cattle from South-Eastern Iran.

Iranian journal of parasitology

Khedri J, Radfar MH, Borji H, Mirzaei M.
PMID: 26246825
Iran J Parasitol. 2015 Apr-Jun;10(2):268-72.

BACKGROUND: Parasitological investigations on paramphistomosis were carried out over a 12-month period in the southeast of Iran to determine the prevalence and intensity of this disease.METHODS: A total of 1000 cattle, Sistani breed (n= 450) and Brahman breed (n=...

Cite
Khedri J, Radfar MH, Borji H, et al. Prevalence and Intensity of Paramphistomum Spp. In Cattle from South-Eastern Iran. Iran J Parasitol. 2015;10(2):268-72
Khedri, J., Radfar, M. H., Borji, H., & Mirzaei, M. (2015). Prevalence and Intensity of Paramphistomum Spp. In Cattle from South-Eastern Iran. Iranian journal of parasitology, 10(2), 268-72.
Khedri, Javad, et al. "Prevalence and Intensity of Paramphistomum Spp. In Cattle from South-Eastern Iran." Iranian journal of parasitology vol. 10,2 (2015): 268-72.
Khedri J, Radfar MH, Borji H, Mirzaei M. Prevalence and Intensity of Paramphistomum Spp. In Cattle from South-Eastern Iran. Iran J Parasitol. 2015 Apr-Jun;10(2):268-72. PMID: 26246825; PMCID: PMC4522303.
Copy Download .nbib Format: NLM
Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus).

Iranian journal of parasitology

Borji H, Moosavi Z, Ahmadi F.
PMID: 25678931
Iran J Parasitol. 2014 Sep;9(3):441-4.

Arteritis due to Strongylus vulgaris is a well-known cause of colic in horses and donkeys. The current report describes a fatal incidence of arterial obstruction in cranial mesenteric artery caused by S. vulgaris infection in an adult donkey in...

Cite
Borji H, Moosavi Z, Ahmadi F. Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus). Iran J Parasitol. 2014;9(3):441-4
Borji, H., Moosavi, Z., & Ahmadi, F. (2014). Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus). Iranian journal of parasitology, 9(3), 441-4.
Borji, Hassan, et al. "Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus)." Iranian journal of parasitology vol. 9,3 (2014): 441-4.
Borji H, Moosavi Z, Ahmadi F. Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus). Iran J Parasitol. 2014 Sep;9(3):441-4. PMID: 25678931; PMCID: PMC4316578.
Copy Download .nbib Format: NLM
Complications after implantation of subcutaneous central venous ports (PowerPort.

Annals of medicine and surgery (2012)

Nakamura T, Sasaki J, Asari Y, Sato T, Torii S, Watanabe M.
PMID: 28348733
Ann Med Surg (Lond). 2017 Mar 10;17:1-6. doi: 10.1016/j.amsu.2017.03.014. eCollection 2017 May.

BACKGROUND: The aim of our study was revised as follows: to clarify the postoperative complications of multifunctional central venous ports and the risk factors for such complications to promote the safe use of the PowerPort system in the hospital.METHODS:...

Cite
Nakamura T, Sasaki J, Asari Y, et al. Complications after implantation of subcutaneous central venous ports (PowerPort. Ann Med Surg (Lond). 2017;17:1-6doi: 10.1016/j.amsu.2017.03.014.
Nakamura, T., Sasaki, J., Asari, Y., Sato, T., Torii, S., & Watanabe, M. (2017). Complications after implantation of subcutaneous central venous ports (PowerPort. Annals of medicine and surgery (2012), 171-6. https://doi.org/10.1016/j.amsu.2017.03.014
Nakamura, Takatoshi, et al. "Complications after implantation of subcutaneous central venous ports (PowerPort." Annals of medicine and surgery (2012) vol. 17 (2017): 1-6. doi: https://doi.org/10.1016/j.amsu.2017.03.014
Nakamura T, Sasaki J, Asari Y, Sato T, Torii S, Watanabe M. Complications after implantation of subcutaneous central venous ports (PowerPort. Ann Med Surg (Lond). 2017 Mar 10;17:1-6. doi: 10.1016/j.amsu.2017.03.014. eCollection 2017 May. PMID: 28348733; PMCID: PMC5358939.
Copy Download .nbib Format: NLM
Effects of a custom-made hinged knee brace with knee flexion support for patients with knee osteoarthritis:a preliminary study.

Nagoya journal of medical science

Ota S, Kanai A, Torii Y, Taniyama H, Imaizumi F, Matsui Y.
PMID: 25797974
Nagoya J Med Sci. 2015 Feb;77(1):95-101.

A knee brace for medial knee osteoarthritis (OA) is required to restrict knee adduction moment (KAM), but must not restrict knee flexion during swing phase. There is no report of a knee brace with both functions. The purpose of...

Cite
Ota S, Kanai A, Torii Y, et al. Effects of a custom-made hinged knee brace with knee flexion support for patients with knee osteoarthritis:a preliminary study. Nagoya J Med Sci. 2015;77(1):95-101
Ota, S., Kanai, A., Torii, Y., Taniyama, H., Imaizumi, F., & Matsui, Y. (2015). Effects of a custom-made hinged knee brace with knee flexion support for patients with knee osteoarthritis:a preliminary study. Nagoya journal of medical science, 77(1), 95-101.
Ota, Susumu, et al. "Effects of a custom-made hinged knee brace with knee flexion support for patients with knee osteoarthritis:a preliminary study." Nagoya journal of medical science vol. 77,1 (2015): 95-101.
Ota S, Kanai A, Torii Y, Taniyama H, Imaizumi F, Matsui Y. Effects of a custom-made hinged knee brace with knee flexion support for patients with knee osteoarthritis:a preliminary study. Nagoya J Med Sci. 2015 Feb;77(1):95-101. PMID: 25797974; PMCID: PMC4361511.
Copy Download .nbib Format: NLM
Showing 13 to 24 of 870 entries