Year |
Citation |
Score |
2013 |
Aron R, Tsvetkov A, Finkbeiner S. NUB1 snubs huntingtin toxicity. Nature Neuroscience. 16: 523-5. PMID 23619755 DOI: 10.1038/Nn.3380 |
0.477 |
|
2012 |
Sontag EM, Lotz GP, Agrawal N, Tran A, Aron R, Yang G, Necula M, Lau A, Finkbeiner S, Glabe C, Marsh JL, Muchowski PJ, Thompson LM. Methylene blue modulates huntingtin aggregation intermediates and is protective in Huntington's disease models. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 11109-19. PMID 22875942 DOI: 10.1523/JNEUROSCI.0895-12.2012 |
0.381 |
|
2010 |
Lotz GP, Legleiter J, Aron R, Mitchell EJ, Huang SY, Ng C, Glabe C, Thompson LM, Muchowski PJ. Hsp70 and Hsp40 functionally interact with soluble mutant huntingtin oligomers in a classic ATP-dependent reaction cycle. The Journal of Biological Chemistry. 285: 38183-93. PMID 20864533 DOI: 10.1074/Jbc.M110.160218 |
0.467 |
|
2009 |
Wacker JL, Huang SY, Steele AD, Aron R, Lotz GP, Nguyen Q, Giorgini F, Roberson ED, Lindquist S, Masliah E, Muchowski PJ. Loss of Hsp70 exacerbates pathogenesis but not levels of fibrillar aggregates in a mouse model of Huntington's disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 9104-14. PMID 19605647 DOI: 10.1523/Jneurosci.2250-09.2009 |
0.563 |
|
2008 |
Higurashi T, Hines JK, Sahi C, Aron R, Craig EA. Specificity of the J-protein Sis1 in the propagation of 3 yeast prions. Proceedings of the National Academy of Sciences of the United States of America. 105: 16596-601. PMID 18955697 DOI: 10.1073/Pnas.0808934105 |
0.692 |
|
2007 |
Aron R, Higurashi T, Sahi C, Craig EA. J-protein co-chaperone Sis1 required for generation of [RNQ+] seeds necessary for prion propagation Embo Journal. 26: 3794-3803. PMID 17673909 DOI: 10.1038/Sj.Emboj.7601811 |
0.658 |
|
2006 |
Craig EA, Huang P, Aron R, Andrew A. The diverse roles of J-proteins, the obligate Hsp70 co-chaperone Reviews of Physiology, Biochemistry and Pharmacology. 156: 1-21. PMID 16634144 DOI: 10.1007/S10254-005-0001-0 |
0.526 |
|
2005 |
Aron R, Lopez N, Walter W, Craig EA, Johnson J. In vivo bipartite interaction between the Hsp40 Sis1 and Hsp70 in Saccharomyces cerevisiae Genetics. 169: 1873-1882. PMID 15687271 DOI: 10.1534/Genetics.104.037242 |
0.569 |
|
2003 |
Lopez N, Aron R, Craig EA. Specificity of class II Hsp40 Sis1 in maintenance of yeast prion [RNQ+] Molecular Biology of the Cell. 14: 1172-1181. PMID 12631732 DOI: 10.1091/Mbc.E02-09-0593 |
0.585 |
|
2001 |
Halaban R, Cheng E, Svedine S, Aron R, Hebert DN. Proper folding and endoplasmic reticulum to golgi transport of tyrosinase are induced by its substrates, DOPA and tyrosine. The Journal of Biological Chemistry. 276: 11933-8. PMID 11124258 DOI: 10.1074/Jbc.M008703200 |
0.4 |
|
2001 |
Ujvari A, Aron R, Eisenhaure T, Cheng E, Parag HA, Smicun Y, Halaban R, Hebert DN. Translation rate of human tyrosinase determines its N-linked glycosylation level. The Journal of Biological Chemistry. 276: 5924-31. PMID 11069924 DOI: 10.1074/Jbc.M009203200 |
0.437 |
|
2000 |
Halaban R, Svedine S, Cheng E, Smicun Y, Aron R, Hebert DN. Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism. Proceedings of the National Academy of Sciences of the United States of America. 97: 5889-94. PMID 10823941 DOI: 10.1073/Pnas.97.11.5889 |
0.416 |
|
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