Year |
Citation |
Score |
2023 |
Kim KH, Wooton-Kee CR. Editorial for the MCE special issue on "FXR and metabolism". Molecular and Cellular Endocrinology. 565: 111889. PMID 36804839 DOI: 10.1016/j.mce.2023.111889 |
0.398 |
|
2020 |
Wooton-Kee CR, Robertson M, Zhou Y, Dong B, Sun Z, Kim KH, Liu H, Xu Y, Putluri N, Saha P, Coarfa C, Moore DD, Nuotio-Antar AM. Metabolic dysregulation in the Wilson's disease mouse model. Proceedings of the National Academy of Sciences of the United States of America. PMID 31924743 DOI: 10.1073/Pnas.1914267117 |
0.756 |
|
2019 |
Kim KH, Choi JM, Li F, Dong B, Wooton-Kee CR, Arizpe A, Anakk S, Jung SY, Hartig SM, Moore DD. Constitutive Androstane Receptor Differentially Regulates Bile Acid Homeostasis in Mouse Models of Intrahepatic Cholestasis. Hepatology Communications. 3: 147-159. PMID 30620001 DOI: 10.1002/hep4.1274 |
0.761 |
|
2018 |
Pankowicz FP, Barzi M, Kim KH, Legras X, Martins CS, Wooton-Kee CR, Lagor WR, Marini JC, Elsea SH, Bissig-Choisat B, Moore DD, Bissig KD. Rapid Disruption of Genes Specifically in Livers of Mice Using Multiplex CRISPR/Cas9 Editing. Gastroenterology. PMID 30170115 DOI: 10.1053/J.Gastro.2018.08.037 |
0.65 |
|
2018 |
Kim KH, Choi JM, Li F, Arizpe A, Wooton-Kee CR, Anakk S, Jung SY, Finegold MJ, Moore DD. Xenobiotic Nuclear Receptor Signaling Determines Molecular Pathogenesis of Progressive Familial Intrahepatic Cholestasis. Endocrinology. PMID 29718219 DOI: 10.1210/En.2018-00110 |
0.662 |
|
2017 |
Muchenditsi A, Yang H, Hamilton JP, Koganti L, Housseau F, Aronov L, Fan H, Pierson H, Bhattacharjee A, Murphy RC, Sears CL, Potter JJ, Wooton-Kee CR, Lutsenko S. TARGETED INACTIVATION OF COPPER-TRANSPORTER ATP7B IN HEPATOCYTES CAUSES LIVER STEATOSIS AND OBESITY IN MICE. American Journal of Physiology. Gastrointestinal and Liver Physiology. ajpgi.00312.2016. PMID 28428350 DOI: 10.1152/Ajpgi.00312.2016 |
0.433 |
|
2015 |
Wooton-Kee CR, Jain AK, Wagner M, Grusak MA, Finegold MJ, Lutsenko S, Moore DD. Elevated copper impairs hepatic nuclear receptor function in Wilson's disease. The Journal of Clinical Investigation. PMID 26241054 DOI: 10.1172/Jci78991 |
0.55 |
|
2011 |
Athippozhy A, Huang L, Wooton-Kee CR, Zhao T, Jungsuwadee P, Stromberg AJ, Vore M. Differential gene expression in liver and small intestine from lactating rats compared to age-matched virgin controls detects increased mRNA of cholesterol biosynthetic genes. Bmc Genomics. 12: 95. PMID 21291544 DOI: 10.1186/1471-2164-12-95 |
0.751 |
|
2010 |
Coy DJ, Wooton-Kee CR, Yan B, Sabeva N, Su K, Graf G, Vore M. ABCG5/ABCG8-independent biliary cholesterol excretion in lactating rats. American Journal of Physiology. Gastrointestinal and Liver Physiology. 299: G228-35. PMID 20413720 DOI: 10.1152/Ajpgi.00502.2009 |
0.693 |
|
2010 |
Wooton-Kee CR, Coy DJ, Athippozhy AT, Zhao T, Jones BR, Vore M. Mechanisms for increased expression of cholesterol 7alpha-hydroxylase (Cyp7a1) in lactating rats. Hepatology (Baltimore, Md.). 51: 277-85. PMID 19957370 DOI: 10.1002/Hep.23289 |
0.61 |
|
2009 |
Athippozhy AT, Huang L, Zhao T, Wooton-Kee CR, Jungsuwadee P, Stromberg AJ, Vore M. Utilizing a mixed model approach to compare the lactating rat transcriptome against age-matched control virgins Bmc Bioinformatics. 10. DOI: 10.1186/1471-2105-10-S7-A16 |
0.706 |
|
2008 |
Wooton-Kee CR, Cohen DE, Vore M. Increased cholesterol 7alpha-hydroxylase expression and size of the bile acid pool in the lactating rat. American Journal of Physiology. Gastrointestinal and Liver Physiology. 294: G1009-16. PMID 18292185 DOI: 10.1152/ajpgi.00017.2008 |
0.681 |
|
2008 |
Wooton-Kee CR, Cohen DE, Vore M. Increased cholesterol 7α-hydroxylase expression and size of the bile acid pool in the lactating rat American Journal of Physiology - Gastrointestinal and Liver Physiology. 294: G1009-G1016. DOI: 10.1152/Ajpgi.00017.2008 |
0.695 |
|
2000 |
Wooton-Kee CR, Clark BJ. Steroidogenic Factor-1 Influences Protein-Deoxyribonucleic Acid Interactions within the Cyclic Adenosine 3',5'-Monophosphate-Responsive Regions of the Murine Steroidogenic Acute Regulatory Protein Gene. Endocrinology. 141: 1345-1355. PMID 28200872 DOI: 10.1210/Endo.141.4.7412 |
0.582 |
|
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