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秦莹莹 ( 主任医师 ) 赞
个人主页 http://faculty.sdu.edu.cn/qinyingying/zh_CN/index.htm
主任医师

论文成果当前位置：中文主页 >> 科学研究 >> 论文成果

[1] . Live Birth with or without Preimplantation Genetic Testing for Aneuploidy. NEW ENGLAND JOURNAL OF MEDICINE, 385, 2047, 2021.
[2] 朱瑞敏. 新时代医学类研究生招生工作路径探索. 教育教学论坛, 25-28, 2024.
[3] . Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency-2. HUMAN REPRODUCTION, 47, 2023.
[4] 于永泽. UBE2T resolves transcription-replication conflicts and protects common fragile sites in primordia.... CELLULAR AND MOLECULAR LIFE SCIENCES, 92, 2023.
[5] . TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosi.... Journal of Clinical Investigation, 133, 2023.
[6] . FAAP100 is required for the resolution of transcription-replication conflicts in primordial germ .... BMC BIOLOGY, 21, 2023.
[7] . DNA repair protein FANCD2 has both ubiquitination- dependent and ubiquitination-independent funct.... JOURNAL OF BIOLOGICAL CHEMISTRY, 299, 2023.
[8] . NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic ar.... Cell Reports, 42, 2023.
[9] . The TH 22-mediated IL-22 deficiency associated with premature ovarian insufficiency. Am J Reprod Immunol, 89, 2023.
[10] . Autophagy Regulates Differentiation of Ovarian Granulosa Cells through Degradation of WT1. Autophagy, 18, 1864, 2022.
[11] 赵世斗. Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. fertil steril, 548, 2015.
[12] 焦雪. Novel NR5A1 missense mutation in premature ovarian failure: detection in han chinese indicates ca.... Plos one, 2013.
[13] . CSB-PGBD3 Mutations Cause Premature Ovarian Failure. Plos Genetics, 2015.
[14] 秦莹莹. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. fertil steril, 1104, 2014.
[15] 秦莹莹. Genetics of primary ovarian insufficiency: new developments and opportunities. Hum Reprod Update, 787, 2015.

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