Chen T - Search Results

1

Limitations of gene editing assessments in human preimplantation embryos.

Liang D, Mikhalchenko A, Ma H, Marti Gutierrez N, Chen T, Lee Y, Park SW, Tippner-Hedges R, Koski A, Darby H, Li Y, Van Dyken C, Zhao H, Wu K, Zhang J, Hou Z, So S, Han J, Park J, Kim CJ, Zong K, Gong J, Yuan Y, Gu Y, Shen Y, Olson SB, Yang H, Battaglia D, O'Leary T, Krieg SA, Lee DM, Wu DH, Duell PB, Kaul S, Kim JS, Heitner SB, Kang E, Chen ZJ, Amato P, Mitalipov S. Liang D, et al. Among authors: chen zj, chen t. Nat Commun. 2023 Mar 7;14(1):1219. doi: 10.1038/s41467-023-36820-6. Nat Commun. 2023. PMID: 36882397 Free PMC article.

2

FADS1-FADS2 gene cluster confers risk to polycystic ovary syndrome.

Tian Y, Zhang W, Zhao S, Sun Y, Bian Y, Chen T, Du Y, Zhang J, Wang Z, Huang T, Peng Y, Yang P, Zhao H, Chen ZJ. Tian Y, et al. Among authors: chen zj, chen t. Sci Rep. 2016 Feb 16;6:21195. doi: 10.1038/srep21195. Sci Rep. 2016. PMID: 26879377 Free PMC article.

3

Mitochondrial replacement by pre-pronuclear transfer in human embryos.

Wu K, Chen T, Huang S, Zhong C, Yan J, Zhang X, Li J, Gao Y, Zhao H, Chen ZJ. Wu K, et al. Among authors: chen zj, chen t. Cell Res. 2017 Jun;27(6):834-837. doi: 10.1038/cr.2017.48. Epub 2017 Apr 4. Cell Res. 2017. PMID: 28374747 Free PMC article. No abstract available.

4

Polar bodies are efficient donors for reconstruction of human embryos for potential mitochondrial replacement therapy.

Wu K, Zhong C, Chen T, Zhang X, Tao W, Zhang J, Li H, Zhao H, Li J, Chen ZJ. Wu K, et al. Among authors: chen zj, chen t. Cell Res. 2017 Aug;27(8):1069-1072. doi: 10.1038/cr.2017.67. Epub 2017 May 12. Cell Res. 2017. PMID: 28497811 Free PMC article. No abstract available.

5

Novel zona pellucida gene variants identified in patients with oocyte anomalies.

Yang P, Luan X, Peng Y, Chen T, Su S, Zhang C, Wang Z, Cheng L, Zhang X, Wang Y, Chen ZJ, Zhao H. Yang P, et al. Among authors: chen zj, chen t. Fertil Steril. 2017 Jun;107(6):1364-1369. doi: 10.1016/j.fertnstert.2017.03.029. Fertil Steril. 2017. PMID: 28577617 Free article.

6

A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.

Chen T, Bian Y, Liu X, Zhao S, Wu K, Yan L, Li M, Yang Z, Liu H, Zhao H, Chen ZJ. Chen T, et al. Among authors: chen zj. Am J Hum Genet. 2017 Sep 7;101(3):459-465. doi: 10.1016/j.ajhg.2017.08.001. Am J Hum Genet. 2017. PMID: 28886344 Free PMC article.

7

Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization.

Yu M, Zhao H, Chen T, Tian Y, Li M, Wu K, Bian Y, Su S, Cao Y, Ning Y, Liu H, Chen ZJ. Yu M, et al. Among authors: chen zj, chen t. J Assist Reprod Genet. 2018 Mar;35(3):539-544. doi: 10.1007/s10815-017-1101-5. Epub 2017 Dec 15. J Assist Reprod Genet. 2018. PMID: 29243140 Free PMC article.

8

Variation Screening of Zygote Arrest 1(ZAR1) in Women with Recurrent Zygote Arrest During IVF/ICSI Programs.

Tian Y, Yang J, Peng Y, Chen T, Huang T, Zhang C, Zhao H. Tian Y, et al. Among authors: chen t. Reprod Sci. 2020 Dec;27(12):2265-2270. doi: 10.1007/s43032-020-00246-y. Epub 2020 Jul 22. Reprod Sci. 2020. PMID: 32700283

9

Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defects.

Yang P, Yin C, Li M, Ma S, Cao Y, Zhang C, Chen T, Zhao H. Yang P, et al. Among authors: chen t. Clin Genet. 2021 Jan;99(1):208-214. doi: 10.1111/cge.13855. Epub 2020 Oct 19. Clin Genet. 2021. PMID: 33009822

10

The critical role of ZP genes in female infertility characterized by empty follicle syndrome and oocyte degeneration.

Yang P, Chen T, Liu Y, Hou Z, Wu K, Cao Y, Zhang J, Wang Z, Zhao H. Yang P, et al. Among authors: chen t. Fertil Steril. 2021 May;115(5):1259-1269. doi: 10.1016/j.fertnstert.2020.11.003. Epub 2020 Dec 4. Fertil Steril. 2021. PMID: 33272616 Free article.

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