标题
Genetics of Oocyte Maturation Defects and Early Embryo Development Arrest
作者
关键词
-
出版物
Genes
Volume 13, Issue 11, Pages 1920
出版商
MDPI AG
发表日期
2022-10-24
DOI
10.3390/genes13111920
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Transcriptional control of human gametogenesis
- (2022) Fang Fang et al. HUMAN REPRODUCTION UPDATE
- Novel Homozygous PADI6 Variants in Infertile Females with Early Embryonic Arrest
- (2022) Yao Xu et al. Frontiers in Cell and Developmental Biology
- Mutations in OOEP and NLRP5 identified in infertile patients with early embryonic arrest
- (2022) Xiaomei Tong et al. HUMAN MUTATION
- Identification of Novel Variants of Thyroid Hormone Receptor Interaction Protein 13 That Cause Female Infertility Characterized by Zygotic Cleavage Failure
- (2022) Huiling Hu et al. Frontiers in Physiology
- A novel homozygous mutation in the PADI6 gene causes early embryo arrest
- (2022) Xiaoxia Wang et al. Reproductive Health
- Homozygous variants in PANX1 cause human oocyte death and female infertility
- (2021) Weijie Wang et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Zp4 is completely dispensable for fertility in female rats†
- (2021) Ming-Hua Zeng et al. BIOLOGY OF REPRODUCTION
- Mutant Zp1 impedes incorporation of ZP3 and ZP4 in the zona pellucida, resulting in zona absence and female infertility in rats
- (2021) Chao Lv et al. BIOLOGY OF REPRODUCTION
- A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility
- (2021) Yiming Sun et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome
- (2021) Jing Wang et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- The Recurrent Mutation in PATL2 Inhibits Its Degradation Thus Causing Female Infertility Characterized by Oocyte Maturation Defect Through Regulation of the Mos-MAPK Pathway
- (2021) Qiqi Cao et al. Frontiers in Cell and Developmental Biology
- Essential shared and species-specific features of mammalian oocyte maturation-associated transcriptome changes impacting oocyte physiology
- (2021) Peter Z Schall et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Epigenetic transgenerational inheritance, Gametogenesis and Germline Development
- (2021) Millissia Ben Maamar et al. BIOLOGY OF REPRODUCTION
- The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility
- (2021) Wei Zheng et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility
- (2021) Lin Zhao et al. Frontiers in Cell and Developmental Biology
- Pannexins and Connexins: Their Relevance for Oocyte Developmental Competence
- (2021) Paweł Kordowitzki et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Diagnosis and Management of Infertility
- (2021) Sandra Ann Carson et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development
- (2021) Juan Liu et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- The homozygous p.Tyr228Cys variant in CDC20 causes oocyte maturation arrest: an additional evidence supporting the causality between CDC20 mutation and female infertility
- (2021) Yao Xu et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Novel WEE2 compound heterozygous mutations identified in patients with fertilization failure or poor fertilization
- (2021) Jiamin Jin et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Two mutations in TUBB8 cause developmental arrest in human oocytes and early embryos
- (2021) Tianqi Cao et al. REPRODUCTIVE BIOMEDICINE ONLINE
- TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure
- (2021) Zhenxing Liu et al. Reproductive Sciences
- Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality
- (2021) Manyu Zhang et al. Frontiers in Genetics
- Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest
- (2020) Zhenxing Liu et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations
- (2020) Jing Lin et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- The tubulin code and its role in controlling microtubule properties and functions
- (2020) Carsten Janke et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- FIGLA, LHX8 and SOHLH1 transcription factor networks regulate mouse oocyte growth and differentiation
- (2020) Zhengpin Wang et al. NUCLEIC ACIDS RESEARCH
- Bi-allelic Missense Pathogenic Variants in TRIP13Cause Female Infertility Characterized by Oocyte Maturation Arrest
- (2020) Zhihua Zhang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genetic Interactions of Histone Modification Machinery Set1 and PAF1C with the Recombination Complex Rec114-Mer2-Mei4 in the Formation of Meiotic DNA Double-Strand Breaks
- (2020) Ying Zhang et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility
- (2020) Wei Zheng et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human
- (2020) Qiqi Cao et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development
- (2020) Lin Zhao et al. Protein & Cell
- Novel mutations in TUBB8 expand the mutational and phenotypic spectrum of patients with zygotes containing multiple pronuclei
- (2020) Qianqian Sha et al. GENE
- Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
- (2020) Geng Luo et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Identification and rescue of a novel TUBB8 mutation that causes the first mitotic division defects and infertility
- (2020) Yanping Jia et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
- (2020) Maria Vittoria Cubellis et al. Clinical Epigenetics
- Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same family
- (2020) Thomas Eggermann et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Mitochondrial metabolism and DNA methylation: a review of the interaction between two genomes
- (2020) Amanda F. C. Lopes Clinical Epigenetics
- Meiosis interrupted: the genetics of female infertility via meiotic failure
- (2020) Leelabati Biswas et al. REPRODUCTION
- Novel mutations in WEE2 : expanding the spectrum of mutations responsible for human fertilization failure
- (2019) Zhihua Zhang et al. CLINICAL GENETICS
- Mitochondrial DNA can be inherited from fathers, not just mothers
- (2019) Thomas G. McWilliams et al. NATURE
- A pannexin 1 channelopathy causes human oocyte death
- (2019) Qing Sang et al. Science Translational Medicine
- Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest
- (2019) Jian Mu et al. JOURNAL OF MEDICAL GENETICS
- Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure
- (2019) Xiaoyu Yang et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization
- (2019) Jing Dai et al. FERTILITY AND STERILITY
- Novel WEE2 gene variants identified in patients with fertilization failure and female infertility
- (2019) Shuai Zhao et al. FERTILITY AND STERILITY
- Genetics of human female infertility
- (2019) Svetlana A Yatsenko et al. BIOLOGY OF REPRODUCTION
- REC114 Partner ANKRD31 Controls Number, Timing, and Location of Meiotic DNA Breaks
- (2019) Michiel Boekhout et al. MOLECULAR CELL
- NLRP7 is expressed in ovine ovary and associated with in vitro preimplantation embryo development
- (2019) Guangdong Li et al. REPRODUCTION
- Deleterious mtDNA Mutations are Common in Mature Oocytes
- (2019) Hong Ma et al. BIOLOGY OF REPRODUCTION
- New biallelic mutations in PADI6 cause recurrent preimplantation embryonic arrest characterized by direct cleavage
- (2019) Wei Zheng et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Characterization of zygotic genome activation-dependent maternal mRNA clearance in mouse
- (2019) Qian-Qian Sha et al. NUCLEIC ACIDS RESEARCH
- KHDC3L mutation causes recurrent pregnancy loss by inducing genomic instability of human early embryonic cells
- (2019) Weidao Zhang et al. PLOS BIOLOGY
- ZP4 confers structural properties to the zona pellucida essential for embryo development
- (2019) Ismael Lamas-Toranzo et al. eLife
- A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
- (2019) Hannah Demond et al. Genome Medicine
- The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype
- (2019) Angela Sparago et al. Clinical Epigenetics
- Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility
- (2018) Qing Sang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
- (2018) Marie Christou‐Kent et al. EMBO Molecular Medicine
- The Pannexin1 membrane channel: distinct conformations and functions
- (2018) Gerhard Dahl FEBS LETTERS
- Mutation analysis of the TUBB8 gene in primary infertile women with arrest in oocyte maturation
- (2018) An-Cong Wang et al. GYNECOLOGICAL ENDOCRINOLOGY
- Novel mutations in PATL2 cause female infertility with oocyte germinal vesicle arrest
- (2018) Lingli Huang et al. HUMAN REPRODUCTION
- A novel mutation in the TUBB8 gene is associated with complete cleavage failure in fertilized eggs
- (2018) Ping Yuan et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Maternal variants inNLRPand other maternal effect proteins are associated with multilocus imprinting disturbance in offspring
- (2018) Matthias Begemann et al. JOURNAL OF MEDICAL GENETICS
- Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles
- (2018) Ngoc Minh Phuong Nguyen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
- (2018) Biaobang Chen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genetics and Epigenetics of Infertility and Treatments on Outcomes
- (2018) Margareta D Pisarska et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Biparental Inheritance of Mitochondrial DNA in Humans
- (2018) Shiyu Luo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
- (2017) Shawn Yost et al. NATURE GENETICS
- A Maternal Functional Module in the Mammalian Oocyte-To-Embryo Transition
- (2017) Xukun Lu et al. TRENDS IN MOLECULAR MEDICINE
- R383C mutation of human CDC20 results in idiopathic non-obstructive azoospermia
- (2017) Lingwei Li et al. Oncotarget
- ZP3 is Required for Germinal Vesicle Breakdown in Mouse Oocyte Meiosis
- (2017) Lei-Lei Gao et al. Scientific Reports
- Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming
- (2017) Sangeetha Mahadevan et al. Scientific Reports
- Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest
- (2016) Yao Xu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Novel mutations and structural deletions in TUBB8 : expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development
- (2016) Biaobang Chen et al. HUMAN REPRODUCTION
- BTG4 is a meiotic cell cycle–coupled maternal-zygotic-transition licensing factor in oocytes
- (2016) Chao Yu et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Mutations in TUBB8 and Human Oocyte Meiotic Arrest
- (2016) Ruizhi Feng et al. NEW ENGLAND JOURNAL OF MEDICINE
- BTG4 is a key regulator for maternal mRNA clearance during mouse early embryogenesis
- (2016) Yusheng Liu et al. Journal of Molecular Cell Biology
- BTG4 is a meiotic cell cycle–coupled maternal-zygotic-transition licensing factor in oocytes
- (2016) Chao Yu et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- TRIP13 Regulates Both the Activation and Inactivation of the Spindle-Assembly Checkpoint
- (2016) Hoi Tang Ma et al. Cell Reports
- The BTG4 and CAF1 complex prevents the spontaneous activation of eggs by deadenylating maternal mRNAs
- (2016) Michał Pasternak et al. Open Biology
- Oocyte competency is the key to embryo potential
- (2015) David Keefe et al. FERTILITY AND STERILITY
- Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans
- (2015) Louise E. Docherty et al. Nature Communications
- NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16
- (2015) Heike Singer et al. PLoS One
- A single domain of the ZP2 zona pellucida protein mediates gamete recognition in mice and humans
- (2014) Matteo A. Avella et al. JOURNAL OF CELL BIOLOGY
- Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA
- (2014) B. Rebolledo-Jaramillo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The subcortical maternal complex controls symmetric division of mouse zygotes by regulating F-actin dynamics
- (2014) Xing-Jiang Yu et al. Nature Communications
- T4216C mutation in NADH dehydrogenase I gene is associated with recurrent pregnancy loss
- (2013) Abasalt Hosseinzadeh Colagar et al. Mitochondrial DNA
- The biochemistry and function of pannexin channels
- (2012) Silvia Penuela et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
- Molecular control of oocyte meiotic arrest and resumption
- (2012) Lei Liu et al. REPRODUCTION FERTILITY AND DEVELOPMENT
- National, Regional, and Global Trends in Infertility Prevalence Since 1990: A Systematic Analysis of 277 Health Surveys
- (2012) Maya N. Mascarenhas et al. PLOS MEDICINE
- The Role of Mitochondrial DNA Copy Number in Mammalian Fertility1
- (2010) Timothy Wai et al. BIOLOGY OF REPRODUCTION
- Strong inducible knockdown of APC/CCdc20does not cause mitotic arrest in human somatic cells
- (2010) Axel J. Baumgarten et al. CELL CYCLE
- No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss
- (2010) Seyed Mohammad Seyedhassani et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Cdc20 Is Critical for Meiosis I and Fertility of Female Mice
- (2010) Fang Jin et al. PLoS Genetics
- Human zona pellucida glycoproteins: functional relevance during fertilization
- (2009) Satish K. Gupta et al. JOURNAL OF REPRODUCTIVE IMMUNOLOGY
- The signal pathway of gonadotrophins-induced mammalian oocyte meiotic resumption
- (2009) M. Zhang et al. MOLECULAR HUMAN REPRODUCTION
- Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
- (2009) M. G. Vander Heiden et al. SCIENCE
- Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)
- (2009) Esther Meyer et al. PLoS Genetics
- A Subcortical Maternal Complex Essential for Preimplantation Mouse Embryogenesis
- (2008) Lei Li et al. DEVELOPMENTAL CELL
- A Mouse Model of Mitochondrial Disease Reveals Germline Selection Against Severe mtDNA Mutations
- (2008) Weiwei Fan et al. SCIENCE
- Strong Purifying Selection in Transmission of Mammalian Mitochondrial DNA
- (2008) James Bruce Stewart et al. PLOS BIOLOGY
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search