Yakabe Y - Search Results

1

Biodegradation of poly(tetramethylene succinate-co-tetramethylene adipate) and poly(tetramethylene succinate) through water-soluble products.

Kitakuni E, Yoshikawa K, Nakano K, Sasuga J, Nobiki M, Naoi H, Yokota Y, Ishioka R, Yakabe Y. Kitakuni E, et al. Among authors: yakabe y. Environ Toxicol Chem. 2001 May;20(5):941-6. Environ Toxicol Chem. 2001. PMID: 11337881

2

Comparison of reporter gene assay and immature rat uterotrophic assay of twenty-three chemicals.

Yamasaki K, Takeyoshi M, Yakabe Y, Sawaki M, Imatanaka N, Takatsuki M. Yamasaki K, et al. Among authors: yakabe y. Toxicology. 2002 Jan 15;170(1-2):21-30. doi: 10.1016/s0300-483x(01)00505-4. Toxicology. 2002. PMID: 11750080

3

Comparison of the Hershberger assay and androgen receptor binding assay of twelve chemicals.

Yamasaki K, Sawaki M, Noda S, Muroi T, Takakura S, Mitoma H, Sakamoto S, Nakai M, Yakabe Y. Yamasaki K, et al. Among authors: yakabe y. Toxicology. 2004 Feb 15;195(2-3):177-86. doi: 10.1016/j.tox.2003.09.012. Toxicology. 2004. PMID: 14751673

4

Comparison of the reporter gene assay for ER-alpha antagonists with the immature rat uterotrophic assay of 10 chemicals.

Yamasaki K, Takeyoshi M, Yakabe Y, Sawaki M, Takatsuki M. Yamasaki K, et al. Among authors: yakabe y. Toxicol Lett. 2003 Apr 30;142(1-2):119-31. doi: 10.1016/s0378-4274(03)00019-5. Toxicol Lett. 2003. PMID: 12765246

5

Comparative study of the uterotrophic potency of 14 chemicals in a uterotrophic assay and their receptor-binding affinity.

Yamasaki K, Noda S, Imatanaka N, Yakabe Y. Yamasaki K, et al. Among authors: yakabe y. Toxicol Lett. 2004 Jan 15;146(2):111-20. doi: 10.1016/j.toxlet.2003.07.003. Toxicol Lett. 2004. PMID: 14643963

6

Development of non-radio isotopic endpoint of murine local lymph node assay based on 5-bromo-2'-deoxyuridine (BrdU) incorporation.

Takeyoshi M, Yamasaki K, Yakabe Y, Takatsuki M, Kimber I. Takeyoshi M, et al. Among authors: yakabe y. Toxicol Lett. 2001 Mar 8;119(3):203-8. doi: 10.1016/s0378-4274(00)00315-5. Toxicol Lett. 2001. PMID: 11246173

7

Comprehensive identification of cytochrome p450 isoforms from solubility-based fractionated rat liver microsomes.

Yamanaka H, Takeyoshi M, Minobe Y, Yakabe Y, Takatsuki M, Sato H. Yamanaka H, et al. Among authors: yakabe y. Drug Metab Lett. 2007 Dec;1(4):281-6. doi: 10.2174/187231207783221394. Drug Metab Lett. 2007. PMID: 19356056

8

Structural essentials of xenoestrogen dialkyl phthalates to bind to the estrogen receptors.

Asai D, Tahara Y, Nakai M, Yakabe Y, Takatsuki M, Nose T, Shinmyozu T, Shimohigashi Y. Asai D, et al. Among authors: yakabe y. Toxicol Lett. 2000 Dec 20;118(1-2):1-8. doi: 10.1016/s0378-4274(00)00253-8. Toxicol Lett. 2000. PMID: 11137303

9

Two-step models to predict binding affinity of chemicals to the human estrogen receptor alpha by three-dimensional quantitative structure-activity relationships (3D-QSARs) using receptor-ligand docking simulation.

Akahori Y, Nakai M, Yakabe Y, Takatsuki M, Mizutani M, Matsuo M, Shimohigashi Y. Akahori Y, et al. Among authors: yakabe y. SAR QSAR Environ Res. 2005 Aug;16(4):323-37. doi: 10.1080/10659360500204442. SAR QSAR Environ Res. 2005. PMID: 16234174

10

Binding characteristics of dialkyl phthalates for the estrogen receptor.

Nakai M, Tabira Y, Asai D, Yakabe Y, Shimyozu T, Noguchi M, Takatsuki M, Shimohigashi Y. Nakai M, et al. Among authors: yakabe y. Biochem Biophys Res Commun. 1999 Jan 19;254(2):311-4. doi: 10.1006/bbrc.1998.9928. Biochem Biophys Res Commun. 1999. PMID: 9918834

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