Qu R - Search Results

1

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: qu r. 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.

2

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: qu r. 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

3

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: qu r. Sci Rep. 2015 Mar 3;5:8689. doi: 10.1038/srep08689. Sci Rep. 2015. PMID: 25732513 Free PMC article.

4

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: qu r. Biol Open. 2015 Mar 27;4(4):411-8. doi: 10.1242/bio.201410876. Biol Open. 2015. PMID: 25819842 Free PMC article.

5

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. 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

6

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: qu r. 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.

7

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.

Xu Y, Shi Y, Fu J, Yu M, Feng R, Sang Q, Liang B, Chen B, Qu R, Li B, Yan Z, Mao X, Kuang Y, Jin L, He L, Sun X, Wang L. Xu Y, et al. Among authors: qu r. Am J Hum Genet. 2016 Sep 1;99(3):744-752. doi: 10.1016/j.ajhg.2016.06.024. Epub 2016 Aug 18. Am J Hum Genet. 2016. PMID: 27545678 Free PMC article.

8

Expression of ENPP3 in human cyclic endometrium: a novel molecule involved in embryo implantation.

Chen Q, Xin A, Qu R, Zhang W, Li L, Chen J, Lu X, Gu Y, Li J, Sun X. Chen Q, et al. Among authors: qu r. Reprod Fertil Dev. 2018 Oct;30(10):1277-1285. doi: 10.1071/RD17257. Reprod Fertil Dev. 2018. PMID: 29614240

9

Screening of miRNAs in human follicular fluid reveals an inverse relationship between microRNA-663b expression and blastocyst formation.

Fu J, Qu RG, Zhang YJ, Gu RH, Li X, Sun YJ, Wang L, Sang Q, Sun XX. Fu J, et al. Reprod Biomed Online. 2018 Jul;37(1):25-32. doi: 10.1016/j.rbmo.2018.03.021. Epub 2018 Apr 13. Reprod Biomed Online. 2018. PMID: 29703434

10

A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family.

Qu R, Sang Q, Wang X, Xu Y, Chen B, Mu J, Zhang Z, Jin L, He L, Wang L. Qu R, et al. Ann Hum Genet. 2020 Jan;84(1):46-53. doi: 10.1111/ahg.12349. Epub 2019 Sep 8. Ann Hum Genet. 2020. PMID: 31495922

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