Du R - Search Results

1

HSF4 is involved in DNA damage repair through regulation of Rad51.

Cui X, Zhang J, Du R, Wang L, Archacki S, Zhang Y, Yuan M, Ke T, Li H, Li D, Li C, Li DW, Tang Z, Yin Z, Liu M. Cui X, et al. Among authors: du r. Biochim Biophys Acta. 2012 Aug;1822(8):1308-15. doi: 10.1016/j.bbadis.2012.05.005. Epub 2012 May 14. Biochim Biophys Acta. 2012. PMID: 22587838 Free article.

2

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J. Wang Q, et al. Among authors: du r. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. J Mol Med (Berl). 2005. PMID: 15726306 Free PMC article.

3

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.

Cui X, Zeng F, Liu Y, Zhang J, Archacki S, Zhan T, Du R, Tang Z, Liu J, Wang QK, Liu M. Cui X, et al. Among authors: du r. Neurosci Lett. 2011 Sep 26;503(1):27-30. doi: 10.1016/j.neulet.2011.08.001. Epub 2011 Aug 6. Neurosci Lett. 2011. PMID: 21843600

4

HSF4 regulates DLAD expression and promotes lens de-nucleation.

Cui X, Wang L, Zhang J, Du R, Liao S, Li D, Li C, Ke T, Li DW, Huang H, Yin Z, Tang Z, Liu M. Cui X, et al. Among authors: du r. Biochim Biophys Acta. 2013 Aug;1832(8):1167-72. doi: 10.1016/j.bbadis.2013.03.007. Epub 2013 Mar 16. Biochim Biophys Acta. 2013. PMID: 23507146 Free article.

5

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.

Liu F, Li P, Liu Y, Li W, Wong F, Du R, Wang L, Li C, Jiang F, Tang Z, Liu M. Liu F, et al. Among authors: du r. Mol Vis. 2013;19:695-701. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559863 Free PMC article.

6

BCAS2 interacts with HSF4 and negatively regulates its protein stability via ubiquitination.

Liao S, Du R, Wang L, Qu Z, Cui X, Li C, Liu F, Huang M, Wang J, Chen J, Gao M, Yu S, Tang Z, Li DW, Jiang T, Liu M. Liao S, et al. Among authors: du r. Int J Biochem Cell Biol. 2015 Nov;68:78-86. doi: 10.1016/j.biocel.2015.08.016. Epub 2015 Aug 28. Int J Biochem Cell Biol. 2015. PMID: 26319152

7

Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.

Wu X, Wang QK, Gui L, Liu M, Zhang X, Jin R, Li W, Yan L, Du R, Wang Q, Zhu J, Yang J. Wu X, et al. Among authors: du r. J Huazhong Univ Sci Technolog Med Sci. 2010 Feb;30(1):103-7. doi: 10.1007/s11596-010-0119-z. Epub 2010 Feb 14. J Huazhong Univ Sci Technolog Med Sci. 2010. PMID: 20155465

8

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].

Li J, Yang JG, Li W, Du R, Gui L, Tian L, Guo QH. Li J, et al. Among authors: du r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):265-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767660 Chinese.

9

[Gene mutation in secundum atrial septal defect: analysis of a Chinese family with 3 patients].

Tian L, Zhu JF, Yang JG, Zhu QH, Du R, Li J, Li W. Tian L, et al. Among authors: du r. Zhonghua Yi Xue Za Zhi. 2008 Jan 22;88(4):250-3. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18361836 Chinese.

10

Protective effect of allograft inflammatory factor-1 on the apoptosis of fibroblast-like synoviocytes in patients with rheumatic arthritis induced by nitro oxide donor sodium nitroprusside.

Liu Y, Mei C, Du R, Shen L. Liu Y, et al. Among authors: du r. Scand J Rheumatol. 2013;42(5):349-55. doi: 10.3109/03009742.2013.772233. Epub 2013 Apr 2. Scand J Rheumatol. 2013. PMID: 23547889

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