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A clinical study of preimplantation DNA methylation screening in assisted reproductive technology.辅助生殖技术中植入前DNA甲基化筛查的临床研究。
Cell Res. 2023 Jun;33(6):483-485. doi: 10.1038/s41422-023-00809-z. Epub 2023 May 8.
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Technology requirements for preimplantation genetic diagnosis to improve assisted reproduction outcomes.胚胎植入前遗传学诊断技术对提高辅助生殖结局的要求。
Fertil Steril. 2010 Jul;94(2):408-30. doi: 10.1016/j.fertnstert.2009.02.091. Epub 2009 May 5.
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Micromanipulation in assisted reproductive technology: intracytoplasmic sperm injection, assisted hatching, and preimplantation genetic diagnosis.
Clin Obstet Gynecol. 2006 Mar;49(1):73-84. doi: 10.1097/01.grf.0000197500.99334.20.
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Use of preimplantation genetic diagnosis and preimplantation genetic screening in the United States: a Society for Assisted Reproductive Technology Writing Group paper.在美国使用植入前遗传学诊断和植入前遗传学筛查:辅助生殖技术学会工作组论文。
Fertil Steril. 2011 Oct;96(4):865-8. doi: 10.1016/j.fertnstert.2011.07.1139. Epub 2011 Aug 26.
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Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology.胚胎植入前遗传学诊断作为辅助生殖技术中的一种治疗和诊断工具。
Fertil Steril. 2003 Aug;80(2):467-8. doi: 10.1016/s0015-0282(03)00605-8.
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Current controversies in prenatal diagnosis 4: preimplantation genetic screening should be routinely offered to all preimplantation genetic diagnosis cases.产前诊断的当前争议4:对于所有植入前基因诊断病例,都应常规提供植入前基因筛查。
Prenat Diagn. 2016 Jan;36(1):25-8. doi: 10.1002/pd.4757. Epub 2016 Jan 4.
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[Preimplantation genetic testing].植入前基因检测
Ugeskr Laeger. 2021 Nov 29;183(48).
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Prediction of a rare chromosomal aberration simultaneously with next generation sequencing-based comprehensive chromosome screening in human preimplantation embryos for recurrent pregnancy loss.在反复妊娠丢失的人类植入前胚胎中,与基于下一代测序的全面染色体筛查同时进行罕见染色体畸变的预测。
J Assist Reprod Genet. 2018 Jan;35(1):171-176. doi: 10.1007/s10815-017-1044-x. Epub 2017 Sep 30.

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The clinical application and challenges of preimplantation genetic testing.胚胎植入前基因检测的临床应用与挑战
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Advances and applications in single-cell and spatial genomics.单细胞和空间基因组学的进展与应用
Sci China Life Sci. 2024 Dec 20. doi: 10.1007/s11427-024-2770-x.
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Multi-omics PGT: re-evaluation of euploid blastocysts for implantation potential based on RNA sequencing.多组学植入前基因检测:基于RNA测序对整倍体囊胚的着床潜力进行重新评估。
Hum Reprod. 2024 Dec 1;39(12):2861-2872. doi: 10.1093/humrep/deae237.
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Obstetrical and neonatal outcomes after vitrified-warmed blastocyst transfer in day 1 rescue intracytoplasmic sperm injection cycles: a retrospective cohort study.玻璃化冷冻-解冻囊胚移植在第 1 天补救胞浆内单精子注射周期中的产科和新生儿结局:一项回顾性队列研究。
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An artificial intelligence model for embryo selection in preimplantation DNA methylation screening in assisted reproductive technology.一种用于辅助生殖技术中植入前DNA甲基化筛查胚胎选择的人工智能模型。
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Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure.新型 MEI1 突变导致染色体和 DNA 甲基化异常,从而导致胚胎停滞和着床失败。
Mol Genet Genomics. 2024 Feb 28;299(1):18. doi: 10.1007/s00438-024-02113-w.

本文引用的文献

1
Live Birth with or without Preimplantation Genetic Testing for Aneuploidy.有无胚胎植入前遗传学检测非整倍体的活产。
N Engl J Med. 2021 Nov 25;385(22):2047-2058. doi: 10.1056/NEJMoa2103613.
2
Management of Pregnancy in Women of Advanced Maternal Age: Improving Outcomes for Mother and Baby.高龄孕产妇的孕期管理:改善母婴结局
Int J Womens Health. 2021 Aug 10;13:751-759. doi: 10.2147/IJWH.S283216. eCollection 2021.
3
Reproductive technologies, female infertility, and the risk of imprinting-related disorders.生殖技术、女性不孕与印记相关疾病的风险
Clin Epigenetics. 2020 Dec 11;12(1):191. doi: 10.1186/s13148-020-00986-3.
4
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial.胚胎植入前遗传学检测非整倍体与形态学作为选择标准用于预后良好患者的单个冻融胚胎移植:一项多中心随机临床试验。
Fertil Steril. 2019 Dec;112(6):1071-1079.e7. doi: 10.1016/j.fertnstert.2019.07.1346. Epub 2019 Sep 21.
5
Promoter methylation of SEPT9 as a potential biomarker for early detection of cervical cancer and its overexpression predicts radioresistance.SEPT9 启动子甲基化作为宫颈癌早期检测的潜在生物标志物,其过表达预测放射抵抗。
Clin Epigenetics. 2019 Aug 19;11(1):120. doi: 10.1186/s13148-019-0719-9.
6
Insights into imprinting from parent-of-origin phased methylomes and transcriptomes.从亲本来源的相定甲基化组和转录组中洞察印迹。
Nat Genet. 2018 Nov;50(11):1542-1552. doi: 10.1038/s41588-018-0232-7. Epub 2018 Oct 22.
7
Comprehensive meta-analysis reveals association between multiple imprinting disorders and conception by assisted reproductive technology.综合荟萃分析揭示了多种印迹疾病与辅助生殖技术受孕之间的关联。
J Assist Reprod Genet. 2018 Jun;35(6):943-952. doi: 10.1007/s10815-018-1173-x. Epub 2018 Apr 25.
8
Genome wide abnormal DNA methylome of human blastocyst in assisted reproductive technology.人类辅助生殖技术中胚胎的全基因组异常 DNA 甲基组。
J Genet Genomics. 2017 Oct 20;44(10):475-481. doi: 10.1016/j.jgg.2017.09.001. Epub 2017 Sep 6.
9
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.单亲二倍体个体的DNA甲基化谱绘制出人类基因组中亲本表观遗传偏向图谱。
Am J Hum Genet. 2016 Sep 1;99(3):555-566. doi: 10.1016/j.ajhg.2016.06.032. Epub 2016 Aug 25.
10
Programming and inheritance of parental DNA methylomes in mammals.哺乳动物中亲本 DNA 甲基组的编程和遗传。
Cell. 2014 May 8;157(4):979-991. doi: 10.1016/j.cell.2014.04.017.

A clinical study of preimplantation DNA methylation screening in assisted reproductive technology.

作者信息

Gao Yuan, Yi Lizhi, Zhan Jianhong, Wang Lijuan, Yao Xuelong, Yan Junhao, Jian Sijing, Gao Lei, Farangez Mamadboqirova, Gao Ming, Zou Yang, Gao Xuan, Wu Keliang, Liu Jiang, Chen Zi-Jiang

机构信息

Center for Reproductive Medicine, Shandong University, Jinan, Shandong, China.

Shandong Key Laboratory of Reproductive Medicine, Shandong Provincial Clinical Research Center for Reproductive Health, Shandong Technology Innovation Center for Reproductive Health, Jinan, Shandong, China.

出版信息

Cell Res. 2023 Jun;33(6):483-485. doi: 10.1038/s41422-023-00809-z. Epub 2023 May 8.

DOI:10.1038/s41422-023-00809-z
PMID:37150776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10235035/
Abstract
摘要