| Year |
Citation |
Score |
| 2018 |
Gurzau AD, Chen K, Xue S, Dai W, Lucet IS, Ly TTN, Reversade B, Blewitt ME, Murphy JM. FSHD2- and BAMS-associated mutations confer opposing effects on SMCHD1 function. The Journal of Biological Chemistry. PMID 29748383 DOI: 10.1074/Jbc.Ra118.003104 |
0.304 |
|
| 2017 |
Gordon CT, Xue S, Yigit G, Filali H, Chen K, Rosin N, Yoshiura KI, Oufadem M, Beck TJ, McGowan R, Magee AC, Altmüller J, Dion C, Thiele H, Gurzau AD, et al. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature Genetics. PMID 28067911 DOI: 10.1038/Ng.3765 |
0.318 |
|
| 2017 |
Xue S, Reversade B. Building a nose: Mutations in an epigenetic regulator cause congenital arhinia Mechanisms of Development. 145: S38. DOI: 10.1016/J.Mod.2017.04.053 |
0.3 |
|
| 2015 |
Xue S, Barna M. Cis-regulatory RNA elements that regulate specialized ribosome activity. Rna Biology. 1-5. PMID 26327194 DOI: 10.1080/15476286.2015.1085149 |
0.33 |
|
| 2015 |
Xue S, Tian S, Fujii K, Kladwang W, Das R, Barna M. RNA regulons in Hox 5' UTRs confer ribosome specificity to gene regulation. Nature. 517: 33-8. PMID 25409156 DOI: 10.1038/Nature14010 |
0.326 |
|
| 2012 |
Xue S, Barna M. Specialized ribosomes: A new frontier in gene regulation and organismal biology Nature Reviews Molecular Cell Biology. 13: 355-369. PMID 22617470 DOI: 10.1038/Nrm3359 |
0.336 |
|
| 2011 |
Kondrashov N, Pusic A, Stumpf CR, Shimizu K, Hsieh AC, Xue S, Ishijima J, Shiroishi T, Barna M. Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning. Cell. 145: 383-97. PMID 21529712 DOI: 10.1016/J.Cell.2011.03.028 |
0.357 |
|
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