A novel TLE6 mutation, c.541+1G>A, identified using whole‐exome sequencing in a Chinese family with female infertility
Author:
Affiliation:
1. The Reproductive Medicine Hospital of the First Hospital of Lanzhou University Lanzhou Gansu China
Publisher
Wiley
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1743
Reference13 articles.
1. TLE6 mutation causes the earliest known human embryonic lethality
2. Expression of maternally derived KHDC3, NLRP5, OOEP and TLE6is associated with oocyte developmental competence in the ovine species
3. Novel Roles for MLH3 Deficiency and TLE6-Like Amplification in DNA Mismatch Repair-Deficient Gastrointestinal Tumorigenesis and Progression
4. The E2A-HLF Oncoprotein Activates Groucho -Related Genes and Suppresses Runx1
5. Transducin-Like Enhancer of Split-6 (TLE6) Is a Substrate of Protein Kinase A Activity During Mouse Oocyte Maturation1
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1. Total fertilization failure after ICSI: insights into pathophysiology, diagnosis, and management through artificial oocyte activation;Human Reproduction Update;2023-03-28
2. Gene mutations associated with fertilization failure after in vitro fertilization/intracytoplasmic sperm injection;Frontiers in Endocrinology;2022-12-16
3. Roles of transducin-like enhancer of split (TLE) family proteins in tumorigenesis and immune regulation;Frontiers in Cell and Developmental Biology;2022-11-11
4. A novel variant in TLE6 is associated with embryonic developmental arrest (EDA) in familial female infertility;Scientific Reports;2022-10-21
5. Molecular tools for the genomic assessment of oocyte’s reproductive competence;Journal of Assisted Reproduction and Genetics;2022-02-05
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