Meng Q - Search Results

1

NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.

Han J, Zhang N, Cao Q, Shi X, Wang C, Rui X, Ding J, Zhao C, Zhang J, Ling X, Li H, Guan Y, Meng Q, Huo R. Han J, et al. Among authors: meng q. J Mol Med (Berl). 2023 Jun;101(6):717-729. doi: 10.1007/s00109-023-02322-7. Epub 2023 May 6. J Mol Med (Berl). 2023. PMID: 37148315

2

[Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].

Chen Y, Kan HJ, Mao J, Ding J, Meng QX, Li HB, Cheng HB, Liu MJ, Sun Y, Yan WH, Li H. Chen Y, et al. Zhonghua Er Ke Za Zhi. 2011 Apr;49(4):316-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21624212 Chinese.

3

[Relationship of sperm morphology with the outcomes of in vitro fertilization and embryo transfer].

Shi YC, Shen LY, Cheng HB, Wang JX, Song D, Wang GG, Yang SM, Zheng AY, Ding J, Gu B, Xu YL, Meng QX, Zou QY, Wang W, Li H. Shi YC, et al. Zhonghua Nan Ke Xue. 2014 Aug;20(8):690-6. Zhonghua Nan Ke Xue. 2014. PMID: 25195363 Chinese.

4

Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection.

Ou J, Wang W, Feng T, Liao L, Meng Q, Zou Q, Ding J, Zheng A, Duan C, Li P, Liu Q, Lin C, Li H. Ou J, et al. Among authors: meng q. Mol Cytogenet. 2015 Dec 30;8:105. doi: 10.1186/s13039-015-0207-7. eCollection 2015. Mol Cytogenet. 2015. PMID: 26719770 Free PMC article.

5

Efficiency of mild ovarian stimulation with clomiphene on poor ovarian responders during IVF\ICSI procedures: a meta-analysis.

Song D, Shi Y, Zhong Y, Meng Q, Hou S, Li H. Song D, et al. Among authors: meng q. Eur J Obstet Gynecol Reprod Biol. 2016 Sep;204:36-43. doi: 10.1016/j.ejogrb.2016.07.498. Epub 2016 Aug 3. Eur J Obstet Gynecol Reprod Biol. 2016. PMID: 27521596 Review.

6

Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling.

Cheng H, Zhang Q, Wang W, Meng Q, Wang F, Liu M, Mao J, Shi Y, Wang W, Li H. Cheng H, et al. Among authors: meng q. Int J Pediatr Otorhinolaryngol. 2018 Mar;106:113-119. doi: 10.1016/j.ijporl.2018.01.005. Epub 2018 Jan 31. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29447883

7

Fetal liver mesenchymal stem cells restore ovarian function in premature ovarian insufficiency by targeting MT1.

Huang B, Qian C, Ding C, Meng Q, Zou Q, Li H. Huang B, et al. Among authors: meng q. Stem Cell Res Ther. 2019 Nov 29;10(1):362. doi: 10.1186/s13287-019-1490-8. Stem Cell Res Ther. 2019. PMID: 31783916 Free PMC article.

8

Human amnion mesenchymal stem cells restore spermatogenesis in mice with busulfan-induced testis toxicity by inhibiting apoptosis and oxidative stress.

Qian C, Meng Q, Lu J, Zhang L, Li H, Huang B. Qian C, et al. Among authors: meng q. Stem Cell Res Ther. 2020 Jul 16;11(1):290. doi: 10.1186/s13287-020-01803-7. Stem Cell Res Ther. 2020. PMID: 32678012 Free PMC article.

9

Importance of a semen analysis report for determining the relationship between SCSA sperm DNA fragmentation index and assisted reproductive technology pregnancy rate.

Cheng H, Han M, Ding J, Wang F, Wang G, Shen L, Wang J, Zheng B, Meng Q, Wang W, Yang S, Li H. Cheng H, et al. Among authors: meng q. Reprod Biol. 2020 Dec;20(4):460-464. doi: 10.1016/j.repbio.2019.09.002. Epub 2020 Aug 12. Reprod Biol. 2020. PMID: 32798137

10

Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility.

Zhao L, Guan Y, Meng Q, Wang W, Wu L, Chen B, Hu J, Zhu J, Zhang Z, Mu J, Chen Y, Sun Y, Wu T, Wang W, Zhou Z, Dong J, Zeng Y, Liu R, Li Q, Du J, Kuang Y, Sang Q, Wang L. Zhao L, et al. Among authors: meng q. Front Cell Dev Biol. 2021 Apr 9;9:647130. doi: 10.3389/fcell.2021.647130. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33898437 Free PMC article.

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