Guo T - Search Results

1

NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic arrest by impairing cytoplasmic UHRF1 abundance.

Zhang W, Zhang R, Wu L, Zhu C, Zhang C, Xu C, Zhao S, Liu X, Guo T, Lu Y, Gao Z, Yu X, Li L, Chen ZJ, Qin Y, Jiao X. Zhang W, et al. Among authors: guo t. Cell Rep. 2023 Dec 26;42(12):113531. doi: 10.1016/j.celrep.2023.113531. Epub 2023 Dec 6. Cell Rep. 2023. PMID: 38060382 Free article.

2

Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).

Qin Y, Zhao H, Xu J, Shi Y, Li Z, Qiao J, Liu J, Qin C, Ren C, Li J, Chen S, Cao Y; China POF Study Group; Simpson JL, Chen ZJ. Qin Y, et al. Hum Mol Genet. 2012 Jan 15;21(2):430-6. doi: 10.1093/hmg/ddr462. Epub 2011 Oct 11. Hum Mol Genet. 2012. PMID: 21989058

3

FMR1 premutation is an uncommon explanation for premature ovarian failure in Han Chinese.

Guo T, Qin Y, Jiao X, Li G, Simpson JL, Chen ZJ. Guo T, et al. PLoS One. 2014 Jul 22;9(7):e103316. doi: 10.1371/journal.pone.0103316. eCollection 2014. PLoS One. 2014. PMID: 25050920 Free PMC article.

4

CSB-PGBD3 Mutations Cause Premature Ovarian Failure.

Qin Y, Guo T, Li G, Tang TS, Zhao S, Jiao X, Gong J, Gao F, Guo C, Simpson JL, Chen ZJ. Qin Y, et al. Among authors: guo c, guo t. PLoS Genet. 2015 Jul 28;11(7):e1005419. doi: 10.1371/journal.pgen.1005419. eCollection 2015 Jul. PLoS Genet. 2015. PMID: 26218421 Free PMC article.

5

Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficiency.

Dou X, Guo T, Li G, Zhou L, Qin Y, Chen ZJ. Dou X, et al. Among authors: guo t. Fertil Steril. 2016 Nov;106(6):1485-1489.e2. doi: 10.1016/j.fertnstert.2016.08.018. Epub 2016 Sep 9. Fertil Steril. 2016. PMID: 27573988 Free article.

6

Mutations in MSH5 in primary ovarian insufficiency.

Guo T, Zhao S, Zhao S, Chen M, Li G, Jiao X, Wang Z, Zhao Y, Qin Y, Gao F, Chen ZJ. Guo T, et al. Hum Mol Genet. 2017 Apr 15;26(8):1452-1457. doi: 10.1093/hmg/ddx044. Hum Mol Genet. 2017. PMID: 28175301 Free PMC article.

7

Wdr62 is involved in female meiotic initiation via activating JNK signaling and associated with POI in humans.

Zhou Y, Qin Y, Qin Y, Xu B, Guo T, Ke H, Chen M, Zhang L, Han F, Li Y, Chen M, Behrens A, Wang Y, Xu Z, Chen ZJ, Gao F. Zhou Y, et al. Among authors: guo t. PLoS Genet. 2018 Aug 13;14(8):e1007463. doi: 10.1371/journal.pgen.1007463. eCollection 2018 Aug. PLoS Genet. 2018. PMID: 30102701 Free PMC article.

8

Novel FSHR mutations in Han Chinese women with sporadic premature ovarian insufficiency.

Liu H, Guo T, Gong Z, Yu Y, Zhang Y, Zhao S, Qin Y. Liu H, et al. Among authors: guo t. Mol Cell Endocrinol. 2019 Jul 15;492:110446. doi: 10.1016/j.mce.2019.05.005. Epub 2019 May 9. Mol Cell Endocrinol. 2019. PMID: 31077743

9

FANCL gene mutations in premature ovarian insufficiency.

Yang Y, Guo T, Liu R, Ke H, Xu W, Zhao S, Qin Y. Yang Y, et al. Among authors: guo t. Hum Mutat. 2020 May;41(5):1033-1041. doi: 10.1002/humu.23997. Epub 2020 Feb 24. Hum Mutat. 2020. PMID: 32048394

10

Novel pathogenic mutations in minichromosome maintenance complex component 9 (MCM9) responsible for premature ovarian insufficiency.

Guo T, Zheng Y, Li G, Zhao S, Ma J, Qin Y. Guo T, et al. Fertil Steril. 2020 Apr;113(4):845-852. doi: 10.1016/j.fertnstert.2019.11.015. Epub 2020 Mar 4. Fertil Steril. 2020. PMID: 32145932 Free article.

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