Guo L - Search Results

1

The effect of microRNAs in the regulation of human CYP3A4: a systematic study using a mathematical model.

Wei Z, Jiang S, Zhang Y, Wang X, Peng X, Meng C, Liu Y, Wang H, Guo L, Qin S, He L, Shao F, Zhang L, Xing Q. Wei Z, et al. Among authors: guo l. Sci Rep. 2014 Mar 5;4:4283. doi: 10.1038/srep04283. Sci Rep. 2014. PMID: 24594634 Free PMC article.

2

Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants.

Cheng X, Li T, Wang H, Zhu D, Ma C, Ma B, Wang Y, Zhang J, Guo L, Wang L, Yun L, Chen S, Jiang Z, He L, Zhu C, Xing Q. Cheng X, et al. Among authors: guo l. J Hum Genet. 2011 Jan;56(1):17-21. doi: 10.1038/jhg.2010.127. Epub 2010 Oct 21. J Hum Genet. 2011. PMID: 20962791

3

SASH1 regulates melanocyte transepithelial migration through a novel Gαs-SASH1-IQGAP1-E-Cadherin dependent pathway.

Zhou D, Wei Z, Deng S, Wang T, Zai M, Wang H, Guo L, Zhang J, Zhong H, He L, Xing Q. Zhou D, et al. Among authors: guo l. Cell Signal. 2013 Jun;25(6):1526-38. doi: 10.1016/j.cellsig.2012.12.025. Epub 2013 Jan 16. Cell Signal. 2013. PMID: 23333244

4

A functional alternative splicing mutation in AIRE gene causes autoimmune polyendocrine syndrome type 1.

Zhang J, Liu H, Liu Z, Liao Y, Guo L, Wang H, He L, Zhang X, Xing Q. Zhang J, et al. Among authors: guo l. PLoS One. 2013;8(1):e53981. doi: 10.1371/journal.pone.0053981. Epub 2013 Jan 8. PLoS One. 2013. PMID: 23342054 Free PMC article.

5

A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family.

Zhou D, Ji H, Wei Z, Guo L, Li Y, Wang T, Zhu Y, Dong X, Wang Y, He L, Xing Q, Zhang L. Zhou D, et al. Among authors: guo l. Mol Vis. 2013 Apr 5;19:789-95. Print 2013. Mol Vis. 2013. PMID: 23592915 Free PMC article.

6

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment.

Sang Q, Mei H, Kuermanhan A, Feng R, Guo L, Qu R, Xu Y, Li H, Jin L, He L, Wang L. Sang Q, et al. Among authors: guo l. Mol Genet Genomics. 2015 Jun;290(3):1135-9. doi: 10.1007/s00438-014-0979-1. Epub 2015 Jan 4. Mol Genet Genomics. 2015. PMID: 25557914

7

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

Feng R, Sang Q, Kuang Y, Sun X, Yan Z, Zhang S, Shi J, Tian G, Luchniak A, Fukuda Y, Li B, Yu M, Chen J, Xu Y, Guo L, Qu R, Wang X, Sun Z, Liu M, Shi H, Wang H, Feng Y, Shao R, Chai R, Li Q, Xing Q, Zhang R, Nogales E, Jin L, He L, Gupta ML Jr, Cowan NJ, Wang L. Feng R, et al. Among authors: guo l. N Engl J Med. 2016 Jan 21;374(3):223-32. doi: 10.1056/NEJMoa1510791. N Engl J Med. 2016. PMID: 26789871 Free PMC article.

8

Spectrum of ATP7B mutations and genotype-phenotype correlation in large-scale Chinese patients with Wilson Disease.

Cheng N, Wang H, Wu W, Yang R, Liu L, Han Y, Guo L, Hu J, Xu L, Zhao J, Han Y, Liu Q, Li K, Wang X, Chen W. Cheng N, et al. Among authors: guo l. Clin Genet. 2017 Jul;92(1):69-79. doi: 10.1111/cge.12951. Epub 2017 Feb 16. Clin Genet. 2017. PMID: 27982432

9

Characterization of Lgr5+ progenitor cell transcriptomes in the apical and basal turns of the mouse cochlea.

Waqas M, Guo L, Zhang S, Chen Y, Zhang X, Wang L, Tang M, Shi H, Bird PI, Li H, Chai R. Waqas M, et al. Among authors: guo l. Oncotarget. 2016 Jul 5;7(27):41123-41141. doi: 10.18632/oncotarget.8636. Oncotarget. 2016. PMID: 27070092 Free PMC article.

10

Extensive Supporting Cell Proliferation and Mitotic Hair Cell Generation by In Vivo Genetic Reprogramming in the Neonatal Mouse Cochlea.

Ni W, Lin C, Guo L, Wu J, Chen Y, Chai R, Li W, Li H. Ni W, et al. Among authors: guo l. J Neurosci. 2016 Aug 17;36(33):8734-45. doi: 10.1523/JNEUROSCI.0060-16.2016. J Neurosci. 2016. PMID: 27535918 Free PMC article.

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