Qu J - Search Results

1

cTFbase: a database for comparative genomics of transcription factors in cyanobacteria.

Wu J, Zhao F, Wang S, Deng G, Wang J, Bai J, Lu J, Qu J, Bao Q. Wu J, et al. Among authors: qu j. BMC Genomics. 2007 Apr 18;8:104. doi: 10.1186/1471-2164-8-104. BMC Genomics. 2007. PMID: 17439663 Free PMC article.

2

CSCDB: the cAMP and cGMP signaling components database.

Lu J, Bao Q, Wu J, Wang H, Li D, Xi Y, Wang S, Yu S, Qu J. Lu J, et al. Among authors: qu j. Genomics. 2008 Jul;92(1):60-4. doi: 10.1016/j.ygeno.2008.03.012. Epub 2008 May 8. Genomics. 2008. PMID: 18472393 Free article.

3

Exome sequencing reveals CCDC111 mutation associated with high myopia.

Zhao F, Wu J, Xue A, Su Y, Wang X, Lu X, Zhou Z, Qu J, Zhou X. Zhao F, et al. Among authors: qu j. Hum Genet. 2013 Aug;132(8):913-21. doi: 10.1007/s00439-013-1303-6. Epub 2013 Apr 12. Hum Genet. 2013. PMID: 23579484

4

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Jin ZB, Huang XF, Lv JN, Xiang L, Li DQ, Chen J, Huang C, Wu J, Lu F, Qu J. Jin ZB, et al. Among authors: qu j. Nat Commun. 2014 Mar 27;5:3517. doi: 10.1038/ncomms4517. Nat Commun. 2014. PMID: 24670872 Free PMC article.

5

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.

Ran X, Cai WJ, Huang XF, Liu Q, Lu F, Qu J, Wu J, Jin ZB. Ran X, et al. Among authors: qu j. Database (Oxford). 2014 Jun 17;2014:bau047. doi: 10.1093/database/bau047. Print 2014. Database (Oxford). 2014. PMID: 24939193 Free PMC article.

6

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.

Jin ZB, Wu J, Huang XF, Feng CY, Cai XB, Mao JY, Xiang L, Wu KC, Xiao X, Kloss BA, Li Z, Liu Z, Huang S, Shen M, Cheng FF, Cheng XW, Zheng ZL, Chen X, Zhuang W, Zhang Q, Young TL, Xie T, Lu F, Qu J. Jin ZB, et al. Among authors: qu j. Proc Natl Acad Sci U S A. 2017 Apr 18;114(16):4219-4224. doi: 10.1073/pnas.1615970114. Epub 2017 Apr 3. Proc Natl Acad Sci U S A. 2017. PMID: 28373534 Free PMC article.

7

A comparative gene expression profile of the whole eye from human, mouse, and guinea pig.

Zhou X, Wang W, Lu F, Hu S, Jiang L, Yan D, Zhang X, Yu X, Yu J, Qu J. Zhou X, et al. Among authors: qu j. Mol Vis. 2007 Nov 28;13:2214-21. Mol Vis. 2007. PMID: 18087242

8

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.

Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX. Cai W, et al. Among authors: qu j. J Genet Genomics. 2008 Nov;35(11):649-55. doi: 10.1016/S1673-8527(08)60086-7. J Genet Genomics. 2008. PMID: 19022198

9

Preparation of C-23 esterified silybin derivatives and evaluation of their lipid peroxidation inhibitory and DNA protective properties.

Wang F, Huang K, Yang L, Gong J, Tao Q, Li H, Zhao Y, Zeng S, Wu X, Stöckigt J, Li X, Qu J. Wang F, et al. Among authors: qu j. Bioorg Med Chem. 2009 Sep 1;17(17):6380-9. doi: 10.1016/j.bmc.2009.07.023. Epub 2009 Jul 18. Bioorg Med Chem. 2009. PMID: 19660956

10

[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation].

Liu Y, Zhuang SL, Tong Y, Qu J, Zhou XT, Zhao FX, Zhang JJ, Zhang YM, Zhang Y, Guan MX. Liu Y, et al. Among authors: qu j. Yi Chuan. 2010 Feb;32(2):141-7. doi: 10.3724/sp.j.1005.2010.00141. Yi Chuan. 2010. PMID: 20176558 Chinese.

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