Yuichiro Kanno

发表

Biological Evaluation of the Pollution of the Tsurumi River with 7-Ethoxycoumarin O-Deethylase Activity Induced by River Sediment Extracts in HepG2 Cells

S. Nito, Yuichiro Kanno, A. Muto, 2003 .

Nigramide C Is a Natural Agonist of Human Pregnane X Receptor

Wei Li, K. Koike, Yuichiro Kanno, 2014, Drug Metabolism and Disposition.

A consecutive three alanine residue insertion mutant of human CAR: a novel CAR ligand screening system in HepG2 cells.

Yuichiro Kanno, Y. Inouye, 2010, The Journal of toxicological sciences.

BPB Reports

K. Nemoto, Yuichiro Kanno, T. Ishii, 2018 .

Comparative Study of Different Epidermal Growth Factor Receptor (EGFR)-Tyrosine Kinase Inhibitors Affecting Lung Cancer Cell Lines Stably Overexpressing EGFR Mutations

K. Nemoto, Yuichiro Kanno, T. Ishii, 2021, BPB Reports.

The nuclear import of the constitutive androstane receptor by importin/Ran-GTP systems.

Yuichiro Kanno, Y. Inouye, Yukari Miyazaki, 2010, Biochimica et biophysica acta.

Primary structure and organ-specific expression of the rat aryl hydrocarbon receptor repressor gene.

Yuichiro Kanno, T. Nakahama, Y. Inouye, 2006, Biological & pharmaceutical bulletin.

Antiepileptic Drug–Activated Constitutive Androstane Receptor Inhibits Peroxisome Proliferator–Activated Receptor α and Peroxisome Proliferator–Activated Receptor γ Coactivator 1α–Dependent Gene Expression to Increase Blood Triglyceride Levels

T. Hosaka, K. Yoshinari, M. Miyata, 2020, Molecular Pharmacology.

The Differential Selectivity of Aryl Hydrocarbon Receptor (AHR) Agonists towards AHR-Dependent Suppression of Mammosphere Formation and Gene Transcription in Human Breast Cancer Cells.

K. Yoshinari, K. Nemoto, Yuichiro Kanno, 2021, Biological & pharmaceutical bulletin.

The inhibitory effect of aryl hydrocarbon receptor repressor (AhRR) on the growth of human breast cancer MCF-7 cells.

Yuichiro Kanno, T. Nakahama, Y. Inouye, 2006, Biological & pharmaceutical bulletin.

5-aminoimidazole-4-carboxamide-1-beta-ribofuranoside (AICAR) prevents nuclear translocation of constitutive androstane receptor by AMP-activated protein kinase (AMPK) independent manner.

Yuichiro Kanno, Y. Inouye, Y. Inoue, 2010, The Journal of toxicological sciences.

Identification of intracellular localization signals and of mechanisms underlining the nucleocytoplasmic shuttling of human aryl hydrocarbon receptor repressor.

Yuichiro Kanno, T. Nakahama, Y. Inouye, 2007, Biochemical and biophysical research communications.

Characterization of nuclear localization signals and cytoplasmic retention region in the nuclear receptor CAR.

Yuichiro Kanno, T. Nakahama, Y. Inouye, 2005, Biochimica et biophysica acta.

Camalexin, an indole phytoalexin, inhibits cell proliferation, migration, and mammosphere formation in breast cancer cells via the aryl hydrocarbon receptor

R. Kizu, Yuichiro Kanno, C. Taga, 2021, Journal of Natural Medicines.

Protein arginine methyltransferase 5 (PRMT5) is a novel coactivator of constitutive androstane receptor (CAR).

Sayaka Kato, Yuichiro Kanno, Y. Inouye, 2015, Biochemical and biophysical research communications.

Euphorins A–H: bioactive diterpenoids from Euphorbia fischeriana

Wei Li, K. Koike, Shoko Kikkawa, 2016, Journal of Natural Medicines.

TO901317, a potent LXR agonist, is an inverse agonist of CAR.

Ami Takahashi, Yuichiro Kanno, Y. Inouye, 2013, The Journal of toxicological sciences.

Differential DNA-binding and cofactor recruitment are possible determinants of the synthetic steroid YK11-dependent gene expression by androgen receptor in breast cancer MDA-MB 453 cells.

T. Hosaka, K. Yoshinari, K. Nemoto, 2022, Experimental cell research.

Androgen receptor functions as a negative transcriptional regulator of DEPTOR, mTOR inhibitor.

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2015, The Journal of toxicological sciences.

Cell Cycle and Apoptosis Regulator 1, CCAR1, Regulates Enhancer-Dependent Nuclear Receptor CAR Transactivation

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2018, Molecular Pharmacology.

DP97, a DEAD box DNA/RNA helicase, is a target gene-selective co-regulator of the constitutive androstane receptor.

Yuichiro Kanno, Y. Inouye, T. Serikawa, 2012, Biochemical and biophysical research communications.

Dependence on the Microtubule Network and 90-kDa Heat Shock Protein of Phenobarbital-Induced Nuclear Translocation of the Rat Constitutive Androstane Receptor

M. Ando, Yuichiro Kanno, Y. Inouye, 2010, Molecular Pharmacology.

Dependence on the microtubule network and heat shock protein 90 of phenobarbital-induced nuclear translocation of the rat constitutive androstane receptor

M. Ando, Yuichiro Kanno, Y. Inouye, 2009 .

Possible Involvement of the Upregulation of ΔNp63 Expression Mediated by HER2-Activated Aryl Hydrocarbon Receptor in Mammosphere Maintenance

T. Hosaka, K. Yoshinari, K. Nemoto, 2022, International journal of molecular sciences.

FDI-6, a FOXM1 inhibitor, activates the aryl hydrocarbon receptor and suppresses tumorsphere formation.

R. Kizu, Yuichiro Kanno, Noriko Sanada, 2022, Biochemical and biophysical research communications.

Differences in Gene Regulation by Dual Ligands of Nuclear Receptors Constitutive Androstane Receptor (CAR) and Pregnane X Receptor (PXR) in HepG2 Cells Stably Expressing CAR/PXR

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2016, Drug Metabolism and Disposition.

Molecular Basis of the Intracellular Localization of the Constitutive Androstane Receptor (CAR)

Yuichiro Kanno, Y. Inouye, 2008 .

Transcriptional Determination of Sexually Dimorphic Expression of Nuclear Receptor Constitutively Active Receptor (CAR) in Wistar Rats

Yuichiro Kanno, T. Nakahama, Y. Inouye, 2004 .

Improved Synthesis and Determination of the Biologically Active Diastereomer of YK11

Shoko Kikkawa, I. Azumaya, K. Nemoto, 2020, Molbank.

Pd(II)-catalyzed ligand controlled synthesis of pyrazole-4-carboxylates and benzo[b]thiophene-3-carboxylates.

Yuichiro Kanno, Y. Inouye, Keisuke Kato, 2014, Organic & biomolecular chemistry.

Selective Androgen Receptor Modulator, YK11, Up-Regulates Osteoblastic Proliferation and Differentiation in MC3T3-E1 Cells.

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2018, Biological & pharmaceutical bulletin.

(17α,20E)-17,20-[(1-methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna-4,20-diene-21-carboxylic acid methyl ester (YK11) is a partial agonist of the androgen receptor.

A. Yamaguchi, K. Arizono, N. Tominaga, 2011, Biological & pharmaceutical bulletin.

Chemical characterization of anemia-inducing aniline-related substances and their application to the construction of a decision tree-based anemia prediction model.

T. Hosaka, K. Yoshinari, Ryota Shizu, 2021, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Aryl hydrocarbon receptor counteracts pharmacological efficacy of doxorubicin via enhanced AKR1C3 expression in triple negative breast cancer cells.

N. Hiruta, H. Bujo, K. Nemoto, 2019, Biochemical and biophysical research communications.

Identification of Picrasidine C as a Subtype-Selective PPARα Agonist.

Xiangyu Zhang, Wei Li, Yuichiro Kanno, 2016, Journal of natural products.

Euphorins A–H: bioactive diterpenoids from Euphorbia fischeriana

Wei Li, K. Koike, Shoko Kikkawa, 2016, Journal of Natural Medicines.

Diurnal difference in CAR mRNA expression

Satoshi Otsuka, Yuichiro Kanno, T. Nakahama, 2004, Nuclear receptor.

Development of a strategy to identify and evaluate direct and indirect activators of constitutive androstane receptor in rats.

T. Hosaka, K. Yoshinari, Takamitsu Sasaki, 2022, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Suppressive effect of aryl hydrocarbon receptor repressor on transcriptional activity of estrogen receptor alpha by protein–protein interaction in stably and transiently expressing cell lines

Yuichiro Kanno, Y. Inouye, Yusuke Takane, 2008, Molecular and Cellular Endocrinology.

ent-Atisane diterpenoids from Euphorbia fischeriana inhibit mammosphere formation in MCF-7 cells

Wei Li, K. Koike, K. Nemoto, 2015, Journal of Natural Medicines.

Tripartite Motif Containing 24 Acts as a Novel Coactivator of the Constitutive Active/Androstane Receptor

Saori Kobayashi, K. Nemoto, Yuichiro Kanno, 2018, Drug Metabolism and Disposition.

Selective androgen receptor modulator, YK11, regulates myogenic differentiation of C2C12 myoblasts by follistatin expression.

Yuichiro Kanno, Y. Inouye, Keisuke Kato, 2013, Biological & pharmaceutical bulletin.

Identification of CAR/RXRα Hetero-dimer Binding Sites in the Human Genome by a Modified Yeast One-Hybrid Assay

Yuichiro Kanno, Y. Inouye, K. Yanai, 2015 .

Difference in nucleocytoplasmic shuttling sequences of rat and human constitutive active/androstane receptor.

J. Sawada, K. Kurose, Yuichiro Kanno, 2007, Biochimica et biophysica acta.

Molecular Mechanism of the Effect of Gegen Qinlian Decoction on Type 2 Diabetes Mellitus Based on Network Pharmacology and Molecular Docking

Yuichiro Kanno, Shuai Zhao, 2022, SSRN Electronic Journal.

Picrasidine G decreases viability of MDA-MB 468 EGFR-overexpressing triple-negative breast cancer cells through inhibition of EGFR/STAT3 signaling pathway.

Wei Li, K. Koike, K. Nemoto, 2017, Bioorganic & medicinal chemistry letters.

Identification of 10-dehydrooxyglycyuralin E as a selective human estrogen receptor alpha partial agonist.

Wei Li, K. Koike, Jian Wang, 2019, Bioorganic chemistry.

Helix 12 stabilization contributes to basal transcriptional activity of PXR

T. Hosaka, K. Yoshinari, Ayaka Sugawara, 2021, The Journal of biological chemistry.

Activation of the aryl hydrocarbon receptor represses mammosphere formation in MCF-7 cells.

Yuichiro Kanno, Y. Inouye, Shuai Zhao, 2012, Cancer letters.

A dihydrochalcone and several homoisoflavonoids from Polygonatum odoratum are activators of adenosine monophosphate-activated protein kinase.

Wei Li, K. Koike, Haipeng Jiang, 2013, Bioorganic & medicinal chemistry letters.

Picrasidine N Is a Subtype-Selective PPARβ/δ Agonist.

Wei Li, K. Koike, Huicheng Li, 2016, Journal of natural products.

Alisol B 23-acetate from the rhizomes of Alisma orientale is a natural agonist of the human pregnane X receptor.

Wei Li, K. Koike, K. Nemoto, 2017, Phytomedicine : international journal of phytotherapy and phytopharmacology.

Activation of the aryl hydrocarbon receptor by 3-methylcholanthrene, but not by indirubin, suppresses mammosphere formation via downregulation of CDC20 expression in breast cancer cells.

K. Nemoto, R. Kizu, Yuichiro Kanno, 2021, Biochemical and Biophysical Research Communications - BBRC.

Camalexin, an indole phytoalexin, inhibits cell proliferation, migration, and mammosphere formation in breast cancer cells via the aryl hydrocarbon receptor

R. Kizu, Yuichiro Kanno, C. Taga, 2021, Journal of Natural Medicines.

HER2 overexpression-mediated inflammatory signaling enhances mammosphere formation through up-regulation of aryl hydrocarbon receptor transcription.

Yuichiro Kanno, Y. Inouye, Youngjin Park, 2013, Cancer letters.

Palladium(II) Catalyzed Cyclization-Carbonylation-Cyclization Coupling Reaction of (ortho-Alkynyl Phenyl) (Methoxymethyl) Sulfides Using Molecular Oxygen as the Terminal Oxidant

R. Shen, K. Nemoto, Yuichiro Kanno, 2016, Molecules.

Nigramide J is a novel potent inverse agonist of the human constitutive androstane receptor

Wei Li, K. Koike, Yuichiro Kanno, 2014, Pharmacology research & perspectives.