Yhun Yhong Sheen - Concepedia

Author

Yhun Yhong Sheen

Also Known As

Masanobu Oshima, Y SHEEN, Y Y Sheen, Y. Y. Sheen, Y. Yhong Sheen, Y.Y. Sheen, YHUN YHONG SHEEN, Yhun Sheen, Yhun Y Sheen, Yhun Y. SHEEN

145

Publications

3.2K

Citations

H-Index

104

Concepts

All Affiliations

Ewha Womans University Gachon University Ministry of Food and Drug Safety Sungkyunkwan University National Institute of Food and Drug Safety Evaluation

About

Yhun Yhong Sheen is an author at Ewha Womans University specializing in medicine, pharmacology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	29	1.6K
2	Natural Sciences	8	8	485
3	Engineering	3	3	350
4	Health Sciences	2	2	88
5	Allergy	1	1	50

Yhun Yhong Sheen

Publications

Citations

H-Index

Page 1

	Year	Citations
A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini. Joseph K. Ritter, Fei Chen, Yhun Yhong Sheen, Journal of Biological Chemistry	1992	478
The impact of size on tissue distribution and elimination by single intravenous injection of silica nanoparticles Minjung Cho, Wan‐Seob Cho, Mina Choi, Toxicology Letters NanoparticlesNanomedicineSingle Intravenous InjectionEngineeringNanomaterials	2009	294
IN-1130, a novel transforming growth factor-β type I receptor kinase (ALK5) inhibitor, suppresses renal fibrosis in obstructive nephropathy J.-A. Moon, Hongduk Kim, I.-S. Cho, Kidney International GlomerulonephritisUrologyRenal DiseaseRenal FunctionMedicine	2006	197
Cloning and expression of human liver UDP-glucuronosyltransferase in COS-1 cells. 3,4-catechol estrogens and estriol as primary substrates. Joseph K. Ritter, Yhun Yhong Sheen, I S Owens Journal of Biological Chemistry Human Liver Udp-glucuronosyltransferaseGlycobiologyMolecular BiologyLiver Udp-glucuronosyltransferaseProtein Expression	1990	155
Discovery of <i>N</i>-((4-([1,2,4]Triazolo[1,5-<i>a</i>]pyridin-6-yl)-5-(6-methylpyridin-2-yl)-1<i>H</i>-imidazol-2-yl)methyl)-2-fluoroaniline (EW-7197): A Highly Potent, Selective, and Orally Bioavailable Inhibitor of TGF-β Type I Receptor Kinase as Cancer Immunotherapeutic/Antifibrotic Agent Cheng Hua Jin, Maddeboina Krishnaiah, D. Sreenu, Journal of Medicinal Chemistry Oral BioavailabilityImmunologyPharmacotherapyPharmaceutical ChemistryTgf-β Type	2014	155
EW-7197 inhibits hepatic, renal, and pulmonary fibrosis by blocking TGF-β/Smad and ROS signaling Sang-A Park, Min-Jin Kim, So-Yeon Park, Cellular and Molecular Life Sciences FibrosisHepatologyLung InflammationLiver PhysiologyImmunology	2014	150
Antiestrogen action in breast cancer cells: Modulation of proliferation and protein synthesis, and interaction with estrogen receptors and additional antiestrogen binding sites Benita S. Katzenellenbogen, Margaret A. Miller, Alaka Mullick, Breast Cancer Research and Treatment Breast OncologyAntiestrogen ActionMedicineHormonal ReceptorBreast Cancer Cells	1985	113
EW-7197, a Novel ALK-5 Kinase Inhibitor, Potently Inhibits Breast to Lung Metastasis Ji Yeon Son, So-Yeon Park, Sol‐Ji Kim, Molecular Cancer Therapeutics	2014	110
Two human liver cDNAs encode UDP-glucuronosyltransferases with 2 log differences in activity toward parallel substrates including hyodeoxycholic acid and certain estrogen derivatives Joseph K. Ritter, Fan Chen, Yhun Yhong Sheen, Biochemistry	1992	100
High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2α Ran‐Ju Kim, Jeong-Ran Park, Kyung‐Jin Roh, Cancer Letters Tumor BiologyAldehyde DehydrogenaseBiochemistryHypoxia-inducible Factor-2αMedicine	2012	90

Page 1