| Year |
Citation |
Score |
| 2020 |
Surface LE, Burrow DT, Li J, Park J, Kumar S, Lyu C, Song N, Yu Z, Rajagopal A, Bae Y, Lee BH, Mumm S, Gu CC, Baker JC, Mohseni M, et al. regulates the action of nitrogen-containing bisphosphonates on bone. Science Translational Medicine. 12. PMID 32434850 DOI: 10.1126/Scitranslmed.Aav9166 |
0.319 |
|
| 2017 |
Zheng H, Bae Y, Kasimir-Bauer S, Tang R, Chen J, Ren G, Yuan M, Esposito M, Li W, Wei Y, Shen M, Zhang L, Tupitsyn N, Pantel K, King C, et al. Therapeutic Antibody Targeting Tumor- and Osteoblastic Niche-Derived Jagged1 Sensitizes Bone Metastasis to Chemotherapy. Cancer Cell. 32: 731-747.e6. PMID 29232552 DOI: 10.1016/J.Ccell.2017.11.002 |
0.301 |
|
| 2017 |
Marom R, Jain M, Burrage LC, Song IW, Graham BH, Brown CW, Stevens SJC, Stegmann APA, Gunter AT, Kaplan JD, Gavrilova RH, Shinawi M, Rosenfeld JA, Bae Y, Tran AA, et al. Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Human Mutation. PMID 28649782 DOI: 10.1002/Humu.23282 |
0.319 |
|
| 2017 |
Egunsola AT, Bae Y, Jiang MM, Liu DS, Chen-Evenson Y, Bertin T, Chen S, Lu JT, Nevarez L, Magal N, Raas-Rothschild A, Swindell EC, Cohn DH, Gibbs RA, Campeau PM, et al. Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia. The Journal of Clinical Investigation. PMID 28263186 DOI: 10.1172/Jci90193 |
0.401 |
|
| 2015 |
Chen S, Grover M, Sibai T, Black J, Rianon N, Rajagopal A, Munivez E, Bertin T, Dawson B, Chen Y, Jiang MM, Lee B, Yang T, Bae Y. Losartan increases bone mass and accelerates chondrocyte hypertrophy in developing skeleton. Molecular Genetics and Metabolism. 115: 53-60. PMID 25779879 DOI: 10.1016/J.Ymgme.2015.02.006 |
0.347 |
|
| 2015 |
Lu L, Harutyunyan K, Jin W, Wu J, Yang T, Chen Y, Joeng KS, Bae Y, Tao J, Dawson BC, Jiang MM, Lee B, Wang LL. RECQL4 Regulates p53 Function In Vivo During Skeletogenesis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 30: 1077-89. PMID 25556649 DOI: 10.1002/Jbmr.2436 |
0.364 |
|
| 2014 |
Chen S, Lee BH, Bae Y. Notch signaling in skeletal stem cells. Calcified Tissue International. 94: 68-77. PMID 23963632 DOI: 10.1007/S00223-013-9773-Z |
0.326 |
|
| 2013 |
Campeau PM, Lenk GM, Lu JT, Bae Y, Burrage L, Turnpenny P, Román Corona-Rivera J, Morandi L, Mora M, Reutter H, Vulto-van Silfhout AT, Faivre L, Haan E, Gibbs RA, Meisler MH, et al. Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase. American Journal of Human Genetics. 92: 781-91. PMID 23623387 DOI: 10.1016/J.Ajhg.2013.03.020 |
0.334 |
|
| 2013 |
Yang T, Grafe I, Bae Y, Chen S, Chen Y, Bertin TK, Jiang MM, Ambrose CG, Lee B. E-selectin ligand 1 regulates bone remodeling by limiting bioactive TGF-β in the bone microenvironment. Proceedings of the National Academy of Sciences of the United States of America. 110: 7336-41. PMID 23589896 DOI: 10.1073/Pnas.1219748110 |
0.309 |
|
| 2013 |
Chen S, Tao J, Bae Y, Jiang MM, Bertin T, Chen Y, Yang T, Lee B. Notch gain of function inhibits chondrocyte differentiation via Rbpj-dependent suppression of Sox9. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 649-59. PMID 22991339 DOI: 10.1002/Jbmr.1770 |
0.405 |
|
| 2012 |
Campeau PM, Lu JT, Sule G, Jiang MM, Bae Y, Madan S, Högler W, Shaw NJ, Mumm S, Gibbs RA, Whyte MP, Lee BH. Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis. Human Molecular Genetics. 21: 4904-9. PMID 22875837 DOI: 10.1093/Hmg/Dds326 |
0.329 |
|
| 2012 |
Bae Y, Yang T, Zeng HC, Campeau PM, Chen Y, Bertin T, Dawson BC, Munivez E, Tao J, Lee BH. miRNA-34c regulates Notch signaling during bone development. Human Molecular Genetics. 21: 2991-3000. PMID 22498974 DOI: 10.1093/Hmg/Dds129 |
0.327 |
|
| 2006 |
Zhang Q, Bae Y, Kemper JK, Kemper B. Analysis of multiple nuclear receptor binding sites for CAR/RXR in the phenobarbital responsive unit of CYP2B2. Archives of Biochemistry and Biophysics. 451: 119-27. PMID 16725103 DOI: 10.1016/J.Abb.2006.04.016 |
0.494 |
|
| 2006 |
Miao J, Fang S, Bae Y, Kemper JK. Functional inhibitory cross-talk between constitutive androstane receptor and hepatic nuclear factor-4 in hepatic lipid/glucose metabolism is mediated by competition for binding to the DR1 motif and to the common coactivators, GRIP-1 and PGC-1alpha. The Journal of Biological Chemistry. 281: 14537-46. PMID 16492670 DOI: 10.1074/Jbc.M510713200 |
0.377 |
|
| 2004 |
Kemper JK, Kim H, Miao J, Bhalla S, Bae Y. Role of an mSin3A-Swi/Snf chromatin remodeling complex in the feedback repression of bile acid biosynthesis by SHP. Molecular and Cellular Biology. 24: 7707-19. PMID 15314177 DOI: 10.1128/Mcb.24.17.7707-7719.2004 |
0.422 |
|
| 2004 |
Bae Y, Kemper JK, Kemper B. Repression of CAR-mediated transactivation of CYP2B genes by the orphan nuclear receptor, short heterodimer partner (SHP). Dna and Cell Biology. 23: 81-91. PMID 15000748 DOI: 10.1089/104454904322759894 |
0.515 |
|
| 2002 |
Min G, Kim H, Bae Y, Petz L, Kemper JK. Inhibitory cross-talk between estrogen receptor (ER) and constitutively activated androstane receptor (CAR). CAR inhibits ER-mediated signaling pathway by squelching p160 coactivators. The Journal of Biological Chemistry. 277: 34626-33. PMID 12114525 DOI: 10.1074/Jbc.M205239200 |
0.352 |
|
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