Xu Y - Search Results

1

Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.

Chen B, Li B, Li D, Yan Z, Mao X, Xu Y, Mu J, Li Q, Jin L, He L, Kuang Y, Sang Q, Wang L. Chen B, et al. Among authors: xu y. Hum Reprod. 2017 Feb;32(2):457-464. doi: 10.1093/humrep/dew322. Epub 2016 Dec 17. Hum Reprod. 2017. PMID: 27989988

2

Deep mRNA sequencing analysis to capture the transcriptome landscape of zebrafish embryos and larvae.

Yang H, Zhou Y, Gu J, Xie S, Xu Y, Zhu G, Wang L, Huang J, Ma H, Yao J. Yang H, et al. Among authors: xu y. PLoS One. 2013 May 20;8(5):e64058. doi: 10.1371/journal.pone.0064058. Print 2013. PLoS One. 2013. PMID: 23700457 Free PMC article.

3

A possible new mechanism in the pathophysiology of polycystic ovary syndrome (PCOS): the discovery that leukocyte telomere length is strongly associated with PCOS.

Li Q, Du J, Feng R, Xu Y, Wang H, Sang Q, Xing Q, Zhao X, Jin L, He L, Wang L. Li Q, et al. Among authors: xu y. J Clin Endocrinol Metab. 2014 Feb;99(2):E234-40. doi: 10.1210/jc.2013-3685. Epub 2013 Dec 3. J Clin Endocrinol Metab. 2014. PMID: 24302747

4

Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome.

Sang Q, Li X, Wang H, Wang H, Zhang S, Feng R, Xu Y, Li Q, Zhao X, Xing Q, Jin L, He L, Wang L. Sang Q, et al. Among authors: xu y. PLoS One. 2014 Feb 5;9(2):e88013. doi: 10.1371/journal.pone.0088013. eCollection 2014. PLoS One. 2014. PMID: 24505354 Free PMC article. Clinical Trial.

5

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: xu y. 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

6

MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro.

Feng R, Sang Q, Zhu Y, Fu W, Liu M, Xu Y, Shi H, Xu Y, Qu R, Chai R, Shao R, Jin L, He L, Sun X, Wang L. Feng R, et al. Among authors: xu y. Sci Rep. 2015 Mar 3;5:8689. doi: 10.1038/srep08689. Sci Rep. 2015. PMID: 25732513 Free PMC article.

7

ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42.

Sang Q, Li W, Xu Y, Qu R, Xu Z, Feng R, Jin L, He L, Li H, Wang L. Sang Q, et al. Among authors: xu y, xu z. Biol Open. 2015 Mar 27;4(4):411-8. doi: 10.1242/bio.201410876. Biol Open. 2015. PMID: 25819842 Free PMC article.

8

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: xu y. 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.

9

Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.

Qu R, Sang Q, Xu Y, Feng R, Jin L, He L, Wang L. Qu R, et al. Among authors: xu y. Int J Pediatr Otorhinolaryngol. 2016 May;84:43-7. doi: 10.1016/j.ijporl.2016.02.036. Epub 2016 Mar 5. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27063751

10

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos.

Feng R, Yan Z, Li B, Yu M, Sang Q, Tian G, Xu Y, Chen B, Qu R, Sun Z, Sun X, Jin L, He L, Kuang Y, Cowan NJ, Wang L. Feng R, et al. Among authors: xu y. J Med Genet. 2016 Oct;53(10):662-71. doi: 10.1136/jmedgenet-2016-103891. Epub 2016 Jun 6. J Med Genet. 2016. PMID: 27273344 Free PMC article.

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