Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bunpei Kakinoki"'
Publikováno v:
Journal of Pharmacological Sciences, Vol 108, Iss 1, Pp 131-134 (2008)
The cholestane amide conjugate MCC-257 has been shown to augment the effects of nerve growth factor (NGF) on cell survival and on tyrosine phosphorylation of the TrkA receptor in PC12 cells. Recent findings suggest that signaling pathways downstream
Externí odkaz:
https://doaj.org/article/a4adc1c5770343df865d0d12fff2b1bd
Publikováno v:
Journal of Pharmacological Sciences, Vol 108, Iss 1, Pp 131-134 (2008)
The cholestane amide conjugate MCC-257 has been shown to augment the effects of nerve growth factor (NGF) on cell survival and on tyrosine phosphorylation of the TrkA receptor in PC12 cells. Recent findings suggest that signaling pathways downstream
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be71a85482bd8936380feb84f7356c9c
http://www.sciencedirect.com/science/article/pii/S1347861319313830
http://www.sciencedirect.com/science/article/pii/S1347861319313830
Autor:
Sumito Sekimoto, Kenichi Saito, Keiji Yamagami, Tetsuya Ohgami, Satoshi Yuki, Bunpei Kakinoki, Mikiko Sejima
Publikováno v:
Diabetes. 55:616-621
Biological substances with neurotrophic activities, such as nerve growth factor (NGF) and monosialoganglioside GM1, have been considered as agents for diabetic peripheral neuropathy. Because recent studies have suggested that decreased availability o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131ad5d9294125693e62d440b952165d
https://doi.org/10.2337/diabetes.55.03.06.db05-1091
https://doi.org/10.2337/diabetes.55.03.06.db05-1091
Publikováno v:
The Japanese Journal of Physiology. 46:311-318
Properties of hypotonically-activated Cl- channels in isolated rat hepatocytes were studied by the patch-clamp whole-cell technique. Hypotonic stress (140-150 mosmol kg 1 H2O) induced a hyperpolarization of the membrane of hepatocytes in the presence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d5de3f6548dbdec61b143695dd638e6
https://doi.org/10.2170/jjphysiol.46.311
https://doi.org/10.2170/jjphysiol.46.311
Autor:
Hisayuki Seike, Chika Matsumoto, Hideki Sakai, Bunpei Kakinoki, Yoshiaki Tabuchi, Shigeyo Kumagai, Noriaki Takeguchi
Publikováno v:
European Journal of Pharmacology: Molecular Pharmacology. 291:153-158
Gastric enterochromaffin-like (ECL) cells were isolated from rat gastric fundic mucosa by Percoll density-gradient centrifugation and counter-flow elutriation. About 67% of cells in the purified cell suspension were ECL cells, which were reacted with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::710cebe9cd3db50ca6cc4d78067c4597
https://doi.org/10.1016/0922-4106(95)90137-x
https://doi.org/10.1016/0922-4106(95)90137-x
Autor:
Yasuhiro Morinaka, Yoshishige Takeuchi, Bunpei Kakinoki, Tsutomu Araki, Daisuke Wakatsuki, Kazuyuki Uchiyama
Publikováno v:
The Journal of pharmacy and pharmacology. 51(4)
We have used Heidenhain-pouch dogs to investigate the effects of (±)-5-methoxy-2-{[(4-methoxy-3,5-dimethylpyrid-2-yl)methyl]sulphinyl}-1H-imidazo[4,5-b]pyridine (TU-199), an imidazopyridine derivative, on gastric acid secretion stimulated by histami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b08e766852687368595c0d9388f59250
https://pubmed.ncbi.nlm.nih.gov/10385219
https://pubmed.ncbi.nlm.nih.gov/10385219
Autor:
Akira Ikari, Takahiro Sato, Miyuki Yasue, Noriko Hamada, Bunpei Kakinoki, Noriaki Takeguchi, Hideki Sakai
1. A camptothecin derivative, irinotecan (Cpt-11), is a topoisomerase I inhibitor and has a strong activity against a broad range of human cancer. One of the side-effects of this drug is diarrhoea. Here, we tried to determine the mediator of the irin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0bd84f99d80c300f976687f49afc5ad
https://europepmc.org/articles/PMC1160099/
https://europepmc.org/articles/PMC1160099/
Publikováno v:
Japanese Journal of Pharmacology. 79:206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b36cfb7cb04301f1a1078deccd1721c9
https://doi.org/10.1016/s0021-5198(19)34837-1
https://doi.org/10.1016/s0021-5198(19)34837-1