Year |
Citation |
Score |
2023 |
Catalano F, O'Brien TJ, Mekhova AA, Sepe LV, Elia M, De Cegli R, Gallotta I, Santonicola P, Zampi G, Ilyechova EY, Romanov AA, Samuseva PD, Salzano J, Petruzzelli R, Polishchuk EV, ... ... Kim BE, et al. A new Caenorhabditis elegans model to study copper toxicity in Wilson disease. Traffic (Copenhagen, Denmark). PMID 37886910 DOI: 10.1111/tra.12920 |
0.463 |
|
2022 |
Yuan S, Korolnek T, Kim BE. Oral Elesclomol Treatment Alleviates Copper Deficiency in Animal Models. Frontiers in Cell and Developmental Biology. 10: 856300. PMID 35433682 DOI: 10.3389/fcell.2022.856300 |
0.549 |
|
2020 |
Guthrie LM, Soma S, Yuan S, Silva A, Zulkifli M, Snavely TC, Greene HF, Nunez E, Lynch B, De Ville C, Shanbhag V, Lopez FR, Acharya A, Petris MJ, Kim BE, et al. Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice. Science (New York, N.Y.). 368: 620-625. PMID 32381719 DOI: 10.1126/Science.Aaz8899 |
0.719 |
|
2018 |
Chun H, Korolnek T, Lee CJ, Coyne HJ, Winge DR, Kim BE, Petris MJ. An extracellular histidine-containing motif in the zinc transporter ZIP4 plays a role in zinc sensing and zinc-induced endocytosis in mammalian cells. The Journal of Biological Chemistry. PMID 30593504 DOI: 10.1074/Jbc.Ra118.005203 |
0.738 |
|
2018 |
Soma S, Latimer AJ, Chun H, Vicary AC, Timbalia SA, Boulet A, Rahn JJ, Chan SSL, Leary SC, Kim BE, Gitlin JD, Gohil VM. Elesclomol restores mitochondrial function in genetic models of copper deficiency. Proceedings of the National Academy of Sciences of the United States of America. PMID 30038027 DOI: 10.1073/Pnas.1806296115 |
0.627 |
|
2018 |
Yuan S, Sharma AK, Richart A, Lee J, Kim BE. CHCA-1 is a copper-regulated Ctr1 homolog required for normal development, copper accumulation, and copper-sensing behavior in . The Journal of Biological Chemistry. PMID 29784876 DOI: 10.1074/jbc.RA118.003503 |
0.612 |
|
2017 |
Baker ZN, Jett K, Boulet A, Hossain A, Cobine PA, Kim BE, El Zawily AM, Lee L, Tibbits GF, Petris MJ, Leary SC. The mitochondrial metallochaperone SCO1 maintains CTR1 at the plasma membrane to preserve copper homeostasis in the murine heart. Human Molecular Genetics. PMID 28973536 DOI: 10.1093/Hmg/Ddx344 |
0.712 |
|
2017 |
Pierson H, Muchenditsi A, Kim BE, Ralle M, Zachos N, Huster D, Lutsenko S. The Function of ATPase Copper Transporter ATP7B in Intestine. Gastroenterology. PMID 28958857 DOI: 10.1053/j.gastro.2017.09.019 |
0.513 |
|
2017 |
Chun H, Catterton T, Kim H, Lee J, Kim BE. Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis. Scientific Reports. 7: 12001. PMID 28931909 DOI: 10.1038/s41598-017-11961-z |
0.44 |
|
2016 |
Chun H, Sharma AK, Lee J, Chan J, Jia S, Kim BE. The Intestinal Copper Exporter CUA-1 is required for Systemic Copper Homeostasis in Caenorhabditis elegans. The Journal of Biological Chemistry. PMID 27881675 DOI: 10.1074/Jbc.M116.760876 |
0.614 |
|
2013 |
Öhrvik H, Nose Y, Wood LK, Kim BE, Gleber SC, Ralle M, Thiele DJ. Ctr2 regulates biogenesis of a cleaved form of mammalian Ctr1 metal transporter lacking the copper- and cisplatin-binding ecto-domain. Proceedings of the National Academy of Sciences of the United States of America. 110: E4279-88. PMID 24167251 DOI: 10.1073/Pnas.1311749110 |
0.556 |
|
2012 |
Turski ML, Brady DC, Kim HJ, Kim BE, Nose Y, Counter CM, Winge DR, Thiele DJ. A novel role for copper in Ras/mitogen-activated protein kinase signaling. Molecular and Cellular Biology. 32: 1284-95. PMID 22290441 DOI: 10.1128/Mcb.05722-11 |
0.38 |
|
2010 |
Nose Y, Wood LK, Kim BE, Prohaska JR, Fry RS, Spears JW, Thiele DJ. Ctr1 is an apical copper transporter in mammalian intestinal epithelial cells in vivo that is controlled at the level of protein stability. The Journal of Biological Chemistry. 285: 32385-92. PMID 20699218 DOI: 10.1074/Jbc.M110.143826 |
0.619 |
|
2010 |
Kim BE, Turski ML, Nose Y, Casad M, Rockman HA, Thiele DJ. Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs. Cell Metabolism. 11: 353-63. PMID 20444417 DOI: 10.1016/J.Cmet.2010.04.003 |
0.493 |
|
2008 |
Kim BE, Nevitt T, Thiele DJ. Mechanisms for copper acquisition, distribution and regulation. Nature Chemical Biology. 4: 176-85. PMID 18277979 DOI: 10.1038/Nchembio.72 |
0.521 |
|
2007 |
Kim BE, Petris MJ. Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein. Journal of Medical Genetics. 44: 641-6. PMID 17483305 DOI: 10.1136/Jmg.2007.049627 |
0.77 |
|
2007 |
Mao X, Kim BE, Wang F, Eide DJ, Petris MJ. A histidine-rich cluster mediates the ubiquitination and degradation of the human zinc transporter, hZIP4, and protects against zinc cytotoxicity. The Journal of Biological Chemistry. 282: 6992-7000. PMID 17202136 DOI: 10.1074/Jbc.M610552200 |
0.756 |
|
2006 |
Nose Y, Kim BE, Thiele DJ. Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function. Cell Metabolism. 4: 235-44. PMID 16950140 DOI: 10.1016/J.Cmet.2006.08.009 |
0.538 |
|
2004 |
Wang F, Kim BE, Petris MJ, Eide DJ. The mammalian Zip5 protein is a zinc transporter that localizes to the basolateral surface of polarized cells. The Journal of Biological Chemistry. 279: 51433-41. PMID 15322118 DOI: 10.1074/Jbc.M408361200 |
0.715 |
|
2004 |
Wang F, Dufner-Beattie J, Kim BE, Petris MJ, Andrews G, Eide DJ. Zinc-stimulated endocytosis controls activity of the mouse ZIP1 and ZIP3 zinc uptake transporters. The Journal of Biological Chemistry. 279: 24631-9. PMID 15054103 DOI: 10.1074/Jbc.M400680200 |
0.735 |
|
2004 |
Wang F, Kim BE, Dufner-Beattie J, Petris MJ, Andrews G, Eide DJ. Acrodermatitis enteropathica mutations affect transport activity, localization and zinc-responsive trafficking of the mouse ZIP4 zinc transporter. Human Molecular Genetics. 13: 563-71. PMID 14709598 DOI: 10.1093/Hmg/Ddh049 |
0.746 |
|
2004 |
Kim BE, Wang F, Dufner-Beattie J, Andrews GK, Eide DJ, Petris MJ. Zn2+-stimulated endocytosis of the mZIP4 zinc transporter regulates its location at the plasma membrane. The Journal of Biological Chemistry. 279: 4523-30. PMID 14612438 DOI: 10.1074/Jbc.M310799200 |
0.741 |
|
2003 |
Kim BE, Smith K, Petris MJ. A copper treatable Menkes disease mutation associated with defective trafficking of a functional Menkes copper ATPase. Journal of Medical Genetics. 40: 290-5. PMID 12676902 |
0.713 |
|
2002 |
Petris MJ, Voskoboinik I, Cater M, Smith K, Kim BE, Llanos RM, Strausak D, Camakaris J, Mercer JF. Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate. The Journal of Biological Chemistry. 277: 46736-42. PMID 12228238 DOI: 10.1074/Jbc.M208864200 |
0.77 |
|
2002 |
Kim BE, Smith K, Meagher CK, Petris MJ. A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation. The Journal of Biological Chemistry. 277: 44079-84. PMID 12221109 DOI: 10.1074/Jbc.M208737200 |
0.773 |
|
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