Qu N - Search Results

1

Depth-Resolved Enhanced Spectral-Domain OCT Imaging of Live Mammalian Embryos Using Gold Nanoparticles as Contrast Agent.

Huang Y, Li M, Huang D, Qiu Q, Lin W, Liu J, Yang W, Yao Y, Yan G, Qu N, Tuchin VV, Fan S, Liu G, Zhao Q, Chen X. Huang Y, et al. Among authors: qu n. Small. 2019 Aug;15(35):e1902346. doi: 10.1002/smll.201902346. Epub 2019 Jul 15. Small. 2019. PMID: 31304667

2

Noninvasive Dual-Modality Photoacoustic-Ultrasonic Imaging to Detect Mammalian Embryo Abnormalities after Prenatal Exposure to Methylmercury Chloride (MMC): A Mouse Study.

Qiu Q, Huang Y, Zhang B, Huang D, Chen X, Fan Z, Lin J, Yang W, Wang K, Qu N, Li J, Li Z, Huang J, Li S, Zhang J, Liu G, Rui G, Chen X, Zhao Q. Qiu Q, et al. Among authors: qu n. Environ Health Perspect. 2022 Feb;130(2):27002. doi: 10.1289/EHP8907. Epub 2022 Feb 2. Environ Health Perspect. 2022. PMID: 35108087 Free PMC article.

3

A novel mutation of the SLC25A13 gene in a Chinese patient with citrin deficiency detected by target next-generation sequencing.

Liu G, Wei X, Chen R, Zhou H, Li X, Sun Y, Xie S, Zhu Q, Qu N, Yang G, Chu Y, Wu H, Lan Z, Wang J, Yang Y, Yi X. Liu G, et al. Among authors: qu n. Gene. 2014 Jan 10;533(2):547-53. doi: 10.1016/j.gene.2013.10.021. Epub 2013 Oct 23. Gene. 2014. PMID: 24161253

4

A novel mutation of IDS gene in a Chinese patient with mucopolysaccharidosis II by next-generation sequencing.

Wei X, Jin F, Ye Y, Xu C, Qu N, Ju X, Yi X. Wei X, et al. Among authors: qu n. Clin Chim Acta. 2011 Nov 20;412(23-24):2340-2. doi: 10.1016/j.cca.2011.08.031. Epub 2011 Sep 3. Clin Chim Acta. 2011. PMID: 21910981

5

Identification of sequence variants in genetic disease-causing genes using targeted next-generation sequencing.

Wei X, Ju X, Yi X, Zhu Q, Qu N, Liu T, Chen Y, Jiang H, Yang G, Zhen R, Lan Z, Qi M, Wang J, Yang Y, Chu Y, Li X, Guang Y, Huang J. Wei X, et al. Among authors: qu n. PLoS One. 2011;6(12):e29500. doi: 10.1371/journal.pone.0029500. Epub 2011 Dec 21. PLoS One. 2011. PMID: 22216297 Free PMC article.

6

Detection of truncated dystrophin lacking the C-terminal domain in a Chinese pedigree by next-generation sequencing.

Xie S, Lan Z, Qu N, Wei X, Yu P, Zhu Q, Yang G, Wang J, Shi Q, Wang W, Yang L, Yi X. Xie S, et al. Among authors: qu n. Gene. 2012 May 10;499(1):139-42. doi: 10.1016/j.gene.2012.03.029. Epub 2012 Mar 9. Gene. 2012. PMID: 22425969

7

Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B.

Wei X, Sun Y, Xie J, Shi Q, Qu N, Yang G, Cai J, Yang Y, Liang Y, Wang W, Yi X. Wei X, et al. Among authors: qu n. Clin Chim Acta. 2012 Nov 20;413(23-24):1866-71. doi: 10.1016/j.cca.2012.07.022. Epub 2012 Aug 8. Clin Chim Acta. 2012. PMID: 22898263

8

Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing.

Sun Y, Wang L, Wei X, Zhu Q, Yang Y, Lan Z, Qu N, Chu Y, Wang Y, Yang S, Liang Y, Wang W, Yi X. Sun Y, et al. Among authors: qu n. Clin Chim Acta. 2013 Feb 18;417:57-61. doi: 10.1016/j.cca.2012.12.005. Epub 2012 Dec 13. Clin Chim Acta. 2013. PMID: 23247051

9

Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study.

Wei X, Dai Y, Yu P, Qu N, Lan Z, Hong X, Sun Y, Yang G, Xie S, Shi Q, Zhou H, Zhu Q, Chu Y, Yao F, Wang J, He J, Yang Y, Liang Y, Yang Y, Qi M, Yang L, Wang W, Wu H, Duan J, Shen C, Wang J, Cui L, Yi X. Wei X, et al. Among authors: qu n. Eur J Hum Genet. 2014 Jan;22(1):110-8. doi: 10.1038/ejhg.2013.82. Epub 2013 Jun 12. Eur J Hum Genet. 2014. PMID: 23756440 Free PMC article.

10

Transcriptome and network changes in climbers at extreme altitudes.

Chen F, Zhang W, Liang Y, Huang J, Li K, Green CD, Liu J, Zhang G, Zhou B, Yi X, Wang W, Liu H, Xu X, Shen F, Qu N, Wang Y, Gao G, San A, JiangBai L, Sang H, Fang X, Kristiansen K, Yang H, Wang J, Han JD, Wang J. Chen F, et al. Among authors: qu n. PLoS One. 2012;7(2):e31645. doi: 10.1371/journal.pone.0031645. Epub 2012 Feb 29. PLoS One. 2012. PMID: 22393366 Free PMC article.

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