Guo T - Search Results

1

Deciphering the DNA methylome in women with PCOS diagnosed using the new international evidence-based guidelines.

Wang Y, Gao X, Yang Z, Yan X, He X, Guo T, Zhao S, Zhao H, Chen ZJ. Wang Y, et al. Among authors: guo t. Hum Reprod. 2023 Nov 20;38(Suppl 2):ii69-ii79. doi: 10.1093/humrep/dead191. Hum Reprod. 2023. PMID: 37982419

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

Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency.

Luo W, Guo T, Li G, Liu R, Zhao S, Song M, Zhang L, Wang S, Chen ZJ, Qin Y. Luo W, et al. Among authors: guo t. J Clin Endocrinol Metab. 2020 Oct 1;105(10):dgaa505. doi: 10.1210/clinem/dgaa505. J Clin Endocrinol Metab. 2020. PMID: 32772095

9

DNA repair protein FANCD2 has both ubiquitination-dependent and ubiquitination-independent functions during germ cell development.

Zhao S, Huang C, Yang Y, Xu W, Yu Y, Wen C, Cao L, Gao F, Qin Y, Chen ZJ, Guo T, Zhao S. Zhao S, et al. Among authors: guo t. J Biol Chem. 2023 Mar;299(3):102905. doi: 10.1016/j.jbc.2023.102905. Epub 2023 Jan 13. J Biol Chem. 2023. PMID: 36642183 Free PMC article.

10

Landscape of pathogenic mutations in premature ovarian insufficiency.

Ke H, Tang S, Guo T, Hou D, Jiao X, Li S, Luo W, Xu B, Zhao S, Li G, Zhang X, Xu S, Wang L, Wu Y, Wang J, Zhang F, Qin Y, Jin L, Chen ZJ. Ke H, et al. Among authors: guo t. Nat Med. 2023 Feb;29(2):483-492. doi: 10.1038/s41591-022-02194-3. Epub 2023 Feb 2. Nat Med. 2023. PMID: 36732629 Free PMC article.

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