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Kiyotoshi Mori
Institution:
Kyowa Kirin (Japan)
Observed institutions:
Kyowa Kirin (Japan),
Biosignal Research Center, Kobe University,
Research Institute for Microbial Diseases, The University of Osaka,
Kobe University,
The University of Osaka
OpenAlex ID:
A5113929282
Cutting Edge: A Novel Toll/IL-1 Receptor Domain-Containing Adapter That Preferentially Activates the IFN-β Promoter in the Toll-Like Receptor Signaling
2002
·
Masahiro Yamamoto
, Shintaro Sato
, et al.
·
The Journal of Immunology
·
1,251
PDF
The novel potent TEAD inhibitor, K-975, inhibits YAP1/TAZ-TEAD protein-protein interactions and exerts an anti-tumor effect on malignant pleural mesothelioma.
2020
·
Ayumi Kaneda
, Toshihiro Seike
, et al.
·
American Journal of Cancer Research
·
136
Purification and Characterization of a Src-related p57 Protein-tyrosine Kinase from Xenopus Oocytes
1996
·
Ken-ichi Sato
, Mamoru Aoto
, et al.
·
Journal of Biological Chemistry
·
77
PDF
The Noncompetitive Antagonism of Histamine H1 Receptors Expressed in Chinese Hamster Ovary Cells by Olopatadine Hydrochloride: Its Potency and Molecular Mechanism
2008
·
Yuichi Matsumoto
, Jun Funahashi
, et al.
·
Pharmacology
·
16
Biochemical evidence for the interaction of regulatory subunit of cAMP‐dependent protein kinase with IDA (Inter‐DFG‐APE) region of catalytic subunit
1996
·
Setsuko Sahara
, Ken-ichi Sato
, et al.
·
FEBS Letters
·
14
PDF
K-685, a TRPV1 Antagonist, Blocks PKC-Sensitized TRPV1 Activation and Improves the Inflammatory Pain in a Rat Complete Freund’s Adjuvant Model
2013
·
Yoshiyuki Sugimoto
, Yozo Kojima
, et al.
·
Journal of Pharmacological Sciences
·
12
PDF
A novel mouse model of cutaneous T‐cell lymphoma revealed the combined effect of mogamulizumab with psoralen and ultraviolet a therapy
2022
·
Keiko Nakahashi
, Kaito Nihira
, et al.
·
Experimental Dermatology
·
4
PDF
The novel and potent CD40 agonist KHK2840 augments the antitumor efficacy of anti‐ PD ‐1 antibody and paclitaxel
2024
·
Chiaki Kobayashi
, Minami Suzuki‐Imaizumi
, et al.
·
Cancer Science
·
3
PDF
Development and Efficacy of a Novel Bromodomain and Extraterminal Domain Degrader K-256 in MYC/BCL2-Related Lymphoma
2023
·
Kastuya Furukawa
, Kazuyuki Shimada
, et al.
·
Blood
·
3
PDF
Glucose concentration-dependent potentiation of insulin secretion by a new chemical entity, KCP256
2005
·
Kiyotoshi Mori
, Kotaro Takasaki
, et al.
·
European Journal of Pharmacology
·
1
Abstract 2913: Entinostat (KHK2375), class I histone deacetylase inhibitor, regulates human Treg function by decreasing Foxp3 expression and effector Treg population
2020
·
Hiromichi Kosaka
, Yozo Nishimura
, et al.
·
Cancer Research
In Vitro and In Vivo Characterization of KHK2455, a novel, Highly Potent and Selective Indoleamine 2,3-dioxygenase 1 (IDO1) Inhibitor
2018
·
Motoya Mie
, Kunieda Kana
, et al.
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Works count:
12
Citation count:
1,517
H-index:
6
I10-index:
6
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