Tien-Min Lin

发表

Nanogel-DFO conjugates as a model to investigate pharmacokinetics, biodistribution, and iron chelation in vivo.

May P. Xiong, Zhi Liu, Yan Wang, 2018, International journal of pharmaceutics.

Evaluating the Anticancer Properties of Liposomal Copper in a Nude Xenograft Mouse Model of Human Prostate Cancer: Formulation, In Vitro, In Vivo, Histology and Tissue Distribution Studies

L. Krugner-Higby, May P. Xiong, Yan Wang, 2014, Pharmaceutical Research.

AHR signaling in prostate growth, morphogenesis, and disease.

R. Peterson, C. Vezina, Chad M. Vezina, 2009, Biochemical pharmacology.

In utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure: effects on the prostate and its response to castration in senescent C57BL/6J mice.

Robert W. Moore, R. Peterson, P. Cooke, 2005, Toxicological sciences : an official journal of the Society of Toxicology.

2,3,7,8-tetrachlorodibenzo-p-dioxin inhibits prostatic epithelial bud formation by acting directly on the urogenital sinus.

Robert W. Moore, R. Peterson, R. Albrecht, 2004, The Journal of urology.

Region-specific inhibition of prostatic epithelial bud formation in the urogenital sinus of C57BL/6 mice exposed in utero to 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Robert W. Moore, R. Peterson, R. Albrecht, 2003, Toxicological sciences : an official journal of the Society of Toxicology.

Organic Chemicals Adsorbed onto Diesel Exhaust Particles Directly Alter the Differentiation of Fetal Thymocytes Through Arylhydrocarbon Receptor but Not Oxidative Stress Responses

C. Tohyama, R. Peterson, H. Nagai, 2006, Journal of immunotoxicology.

Differences in gene expression and benzo[a]pyrene‐induced DNA adduct formation in the liver of three strains of female mice with identical AhRb2 genotype treated with 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin and/or benzo[a]pyrene

C. Tohyama, R. Peterson, S. Ohsako, 2008, Journal of applied toxicology : JAT.

Behavioral Rhythmicity of Mice Lacking AhR and Attenuation of Light-Induced Phase Shift by 2,3,7,8-Tetrachlorodibenzo-p-Dioxin

R. Peterson, P. Cooke, M. Mukai, 2008, Journal of biological rhythms.

Expression of novel genes linked to the androgen-induced, proliferative shutoff in prostate cancer cells

C. Sonnenschein, A. Soto, J. Szelei, 1997, The Journal of Steroid Biochemistry and Molecular Biology.

The aryl hydrocarbon receptor inhibits prostate carcinogenesis in TRAMP mice.

R. Cardiff, R. Peterson, Tien-Min Lin, 2006, Carcinogenesis.

Critical windows of vulnerability for effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on prostate and seminal vesicle development in C57BL/6 mice.

Robert W. Moore, R. Peterson, U. Simanainen, 2002, Toxicological sciences : an official journal of the Society of Toxicology.

Effects of aryl hydrocarbon receptor null mutation and in utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on prostate and seminal vesicle development in C57BL/6 mice.

Robert W. Moore, R. Peterson, K. Ko, 2002, Toxicological sciences : an official journal of the Society of Toxicology.

Beta-catenin (CTNNB1) induces Bmp expression in urogenital sinus epithelium and participates in prostatic bud initiation and patterning.

Kimberly P Keil, M. Taketo, Xin Sun, 2013, Developmental biology.

Androgenic regulation of ventral epithelial bud number and pattern in mouse urogenital sinus

Robert W. Moore, R. Peterson, Lisa L. Abler, 2010, Developmental dynamics : an official publication of the American Association of Anatomists.

WNT5A selectively inhibits mouse ventral prostate development.

Robert W. Moore, S. Chiu, R. Peterson, 2008, Developmental biology.

Enzymatically Biodegradable Polyrotaxane-Deferoxamine Conjugates for Iron Chelation.

May P. Xiong, Zhi Liu, Max Purro, 2016, ACS applied materials & interfaces.

Evaluating the Anticancer Properties of Liposomal Copper in a Nude Xenograft Mouse Model of Human Prostate Cancer: Formulation, In Vitro, In Vivo, Histology and Tissue Distribution Studies

L. Krugner-Higby, May P. Xiong, Yan Wang, 2014, Pharmaceutical Research.

In utero exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin causes accelerated terminal differentiation in fetal mouse skin.

R. Peterson, J. Loertscher, B. Allen-Hoffmann, 2002, Toxicological sciences : an official journal of the Society of Toxicology.

Dioxin causes ventral prostate agenesis by disrupting dorsoventral patterning in developing mouse prostate.

Robert W. Moore, R. Peterson, J. Bemis, 2008, Toxicological sciences : an official journal of the Society of Toxicology.

A Constitutively Active Arylhydrocarbon Receptor Induces Growth Inhibition of Jurkat T Cells through Changes in the Expression of Genes Related to Apoptosis and Cell Cycle Arrest*

C. Tohyama, Y. Fujii‐Kuriyama, R. Peterson, 2004, Journal of Biological Chemistry.

The aryl hydrocarbon receptor (AhR) inhibits vanadate-induced vascular endothelial growth factor (VEGF) production in TRAMP prostates.

Richard E Peterson, R. Peterson, Wayne A Fritz, 2008, Carcinogenesis.

Multiple Functions of the TR2-11 Orphan Receptor in Modulating Activation of Two Key Cis-acting Elements Involved in the Retinoic Acid Signal Transduction System (*)

Chawnshang Chang, W. Young, Tien-Min Lin, 1995, The Journal of Biological Chemistry.

Aryl Hydrocarbon Receptor Regulates Growth, But Not Atresia, of Mouse Preantral and Antral Follicles1

R. Peterson, J. Flaws, C. Greenfeld, 2003, Biology of reproduction.

ROLE OF THE ARYL HYDROCARBON RECEPTOR IN THE DEVELOPMENT OF CONTROL AND 2,3,7,8-TETRACHLORODIBENZO-p-DIOXIN-EXPOSED MALE MICE

Robert W. Moore, R. Peterson, P. Cooke, 2001, Journal of toxicology and environmental health. Part A.

2,3,7,8-Tetrachlorodibenzo-p-dioxin has both pro-carcinogenic and anti-carcinogenic effects on neuroendocrine prostate carcinoma formation in TRAMP mice.

Robert W. Moore, S. Safe, R. Peterson, 2016, Toxicology and applied pharmacology.

The selective aryl hydrocarbon receptor modulator 6-methyl-1,3,8-trichlorodibenzofuran inhibits prostate tumor metastasis in TRAMP mice.

Richard E. Peterson, Stephen Safe, Robert W. Moore, 2009, Biochemical pharmacology.

Tetrachlorodibenzo‐p‐dioxin exposure alters radial arm maze performance and hippocampal morphology in female AhR +/– mice

R. Peterson, S. Schantz, B. Powers, 2004, Genes, brain, and behavior.

Estrogen signaling is not required for prostatic bud patterning or for its disruption by 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Robert W. Moore, R. Peterson, P. Cooke, 2009, Toxicology and applied pharmacology.

In utero and lactational exposure of male rats to 2,3,7,8-tetrachlorodibenzo-P-dioxin decreases androgen responsiveness of the dorsolateral prostate without inhibiting dihydrotestosterone formation

R. Peterson, Tien-Min Lin, H. M. Theobald, 2000 .

Lack of expression of EGF and TGF-alpha in the fetal mouse alters formation of prostatic epithelial buds and influences the response to TCDD.

R. Peterson, R. Albrecht, B. Abbott, 2003, Toxicological sciences : an official journal of the Society of Toxicology.