scholarly article | Q13442814 |
P356 | DOI | 10.1152/PHYSIOL.00020.2011 |
P698 | PubMed publication ID | 22013190 |
P50 | author | Heide Schatten | Q87470672 |
P2093 | author name string | Qing-Yuan Sun | |
Zhen-Bo Wang | |||
P2860 | cites work | Maternal age-related differential global expression profiles observed in human oocytes | Q48789155 |
Distribution and expression of phosphorylated histone H3 during porcine oocyte maturation | Q48799260 | ||
Regulation of chromatin and chromosome morphology by histone H3 modifications in pig oocytes | Q48801281 | ||
Ageing-associated aberration in meiosis of oocytes from senescence-accelerated mice | Q48849840 | ||
Sorting out chromosome errors | Q48857879 | ||
Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation | Q48861937 | ||
The meiotic competence of in-vitro matured human oocytes is influenced by donor age: evidence that folliculogenesis is compromised in the reproductively aged ovary | Q48944266 | ||
Influence of maternal age on meiotic spindle assembly in oocytes from naturally cycling women | Q48983154 | ||
Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis | Q49034131 | ||
Meiosis I in human oocytes | Q49074034 | ||
Dynamic changes in histone acetylation during sheep oocyte maturation. | Q50639569 | ||
Alterations in epigenetic modifications during oocyte growth in mice. | Q50639929 | ||
Proper chromatin condensation and maintenance of histone H3 phosphorylation during mouse oocyte meiosis requires protein phosphatase activity. | Q50641231 | ||
Bub1 prevents chromosome misalignment and precocious anaphase during mouse oocyte meiosis. | Q50645006 | ||
Histone phosphorylation and pericentromeric histone modifications in oocyte meiosis. | Q50645014 | ||
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21. | Q50646900 | ||
Resolution of chiasmata in oocytes requires separase-mediated proteolysis. | Q50647080 | ||
Histone deacetylation is required for orderly meiosis. | Q50650949 | ||
A molecular model for sporadic human aneuploidy. | Q50652249 | ||
Evidence of a high proportion of premature unbalanced separation of sister chromatids in the first polar bodies of women of advanced age. | Q50653770 | ||
SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. | Q50656030 | ||
Post-ovulatory aging of mouse oocytes leads to decreased MAD2 transcripts and increased frequencies of premature centromere separation and anaphase. | Q50656870 | ||
Restaging the spindle assembly checkpoint in female mammalian meiosis I. | Q50663157 | ||
Nuclear origin of aging-associated meiotic defects in senescence-accelerated mice. | Q50672953 | ||
Maternal age and trisomy--a unifying mechanism of formation. | Q50719907 | ||
Bub3 is a spindle assembly checkpoint protein regulating chromosome segregation during mouse oocyte meiosis | Q21142712 | ||
Unified mode of centromeric protection by shugoshin in mammalian oocytes and somatic cells | Q24303869 | ||
Association between maternal age and meiotic recombination for trisomy 21. | Q24530760 | ||
Gene expression in the fetal mouse ovary is altered by exposure to low doses of bisphenol A | Q24618528 | ||
Structure and function of the PP2A-shugoshin interaction | Q24648497 | ||
Shugoshin-2 is essential for the completion of meiosis but not for mitotic cell division in mice | Q24652898 | ||
The spindle-assembly checkpoint in space and time | Q27860766 | ||
Association between spindle assembly checkpoint expression and maternal age in human oocytes | Q28141354 | ||
Cohesin component dynamics during meiotic prophase I in mammalian oocytes | Q28260099 | ||
The bisphenol A experience: a primer for the analysis of environmental effects on mammalian reproduction | Q28391785 | ||
Bisphenol A exposure in utero disrupts early oogenesis in the mouse | Q28469120 | ||
Mps1 at kinetochores is essential for female mouse meiosis I | Q28504960 | ||
RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females | Q28589265 | ||
Female germ cell aneuploidy and embryo death in mice lacking the meiosis-specific protein SCP3 | Q28590016 | ||
ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes | Q28591500 | ||
Differences in spindle association of the mitotic checkpoint protein Mad2 in mammalian spermatogenesis and oogenesis | Q28592359 | ||
Human exposure to bisphenol A (BPA) | Q29547406 | ||
Bisphenol a exposure causes meiotic aneuploidy in the female mouse | Q29615674 | ||
To err (meiotically) is human: the genesis of human aneuploidy | Q29618613 | ||
Dynamic alterations of specific histone modifications during early murine development | Q30434243 | ||
Changing Mad2 levels affects chromosome segregation and spindle assembly checkpoint control in female mouse meiosis I. | Q33307520 | ||
Epigenetic modification of histone 3 at lysine 9 in sheep zygotes and its relationship with DNA methylation | Q33338295 | ||
Aging predisposes oocytes to meiotic nondisjunction when the cohesin subunit SMC1 is reduced | Q33384436 | ||
TGF-beta Sma/Mab signaling mutations uncouple reproductive aging from somatic aging | Q33521309 | ||
Irregular telomeres impair meiotic synapsis and recombination in mice | Q33695241 | ||
Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects | Q33708697 | ||
Requirement of functional telomeres for metaphase chromosome alignments and integrity of meiotic spindles | Q33757640 | ||
Mad2 prevents aneuploidy and premature proteolysis of cyclin B and securin during meiosis I in mouse oocytes | Q33763645 | ||
Acetaldehyde and microtubules | Q37768692 | ||
Gene expression profiles of single human mature oocytes in relation to age. | Q38346535 | ||
Sister-chromatid cohesion in mitosis and meiosis | Q40613969 | ||
The teratogenic effects of alcohol following exposure during pregnancy, and its influence on the chromosome constitution of the pre-ovulatory egg. | Q41432866 | ||
Histone acetylation and subcellular localization of chromosomal protein BRD4 during mouse oocyte meiosis and mitosis. | Q42831446 | ||
BubR1 is a spindle assembly checkpoint protein regulating meiotic cell cycle progression of mouse oocyte | Q43125814 | ||
Glycogen synthase kinase-3 regulates mouse oocyte homologue segregation | Q44208187 | ||
Metaphase I arrest upon activation of the Mad2-dependent spindle checkpoint in mouse oocytes | Q44587845 | ||
Functionality of the spindle checkpoint during the first meiotic division of mammalian oocytes. | Q44606276 | ||
Regulation of histone acetylation during meiotic maturation in mouse oocytes | Q45006644 | ||
Localization of mitotic arrest deficient 1 (MAD1) in mouse oocytes during the first meiosis and its functions as a spindle checkpoint protein | Q45040800 | ||
Dynamics of cohesin proteins REC8, STAG3, SMC1 beta and SMC3 are consistent with a role in sister chromatid cohesion during meiosis in human oocytes | Q45046784 | ||
Follicle-stimulating hormone affects metaphase I chromosome alignment and increases aneuploidy in mouse oocytes matured in vitro | Q45061653 | ||
Reduced expression of MAD2, BCL2, and MAP kinase activity in pig oocytes after in vitro aging are associated with defects in sister chromatid segregation during meiosis II and embryo fragmentation after activation | Q45094738 | ||
Changes in histone modifications during in vitro maturation of porcine oocytes | Q45286455 | ||
Defective deacetylation of histone 4 K12 in human oocytes is associated with advanced maternal age and chromosome misalignment | Q45354821 | ||
Cohesin SMC1 beta is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination | Q45875368 | ||
Epigenetic modifications and related mRNA expression during bovine oocyte in vitro maturation. | Q45945850 | ||
Differential remodeling of mono- and trimethylated H3K27 during porcine embryo development. | Q45964205 | ||
Changes in histone methylation during human oocyte maturation and IVF- or ICSI-derived embryo development. | Q46036784 | ||
Changes in acetylation on lysine 12 of histone H4 (acH4K12) of murine oocytes during maternal aging may affect fertilization and subsequent embryo development | Q46088660 | ||
Effects of selected endocrine disruptors on meiotic maturation, cumulus expansion, synthesis of hyaluronan and progesterone by porcine oocyte-cumulus complexes | Q46151679 | ||
Age-Related Meiotic Segregation Errors in Mammalian Oocytes Are Preceded by Depletion of Cohesin and Sgo2 | Q46305683 | ||
A model system for increased meiotic nondisjunction in older oocytes | Q46378427 | ||
Differential acetylation of histone H4 lysine during development of in vitro fertilized, cloned and parthenogenetically activated bovine embryos | Q46433280 | ||
Bisphenol-A induces cell cycle delay and alters centrosome and spindle microtubular organization in oocytes during meiosis | Q46477739 | ||
Mad2 is required for inhibiting securin and cyclin B degradation following spindle depolymerisation in meiosis I mouse oocytes. | Q46831372 | ||
Changes in H3K79 methylation during preimplantation development in mice | Q46899764 | ||
BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice | Q47315084 | ||
Increasing age influences uterine integrity, but not ovarian function or oocyte quality, in the cheetah (Acinonyx jubatus). | Q48673434 | ||
Increased zona pellucida thickness and meiotic spindle disruption in oocytes from cigarette smoking mice. | Q48683422 | ||
Regulation of APC/C activity in oocytes by a Bub1-dependent spindle assembly checkpoint. | Q48725350 | ||
Defective cohesin is associated with age-dependent misaligned chromosomes in oocytes | Q48765831 | ||
Continuous exposure to bisphenol A during in vitro follicular development induces meiotic abnormalities | Q48770023 | ||
Insulin signaling in mouse oocytes | Q48787782 | ||
Changes in histone acetylation during postovulatory aging of mouse oocyte | Q48789063 | ||
Frequency of aneuploidy related to age in porcine oocytes | Q33893761 | ||
Smoking and reproduction: gene damage to human gametes and embryos | Q33899642 | ||
Evidence that weakened centromere cohesion is a leading cause of age-related aneuploidy in oocytes. | Q34126610 | ||
Oocyte Cohesin Expression Restricted to Predictyate Stages Provides Full Fertility and Prevents Aneuploidy | Q34153758 | ||
Roles for transforming growth factor beta superfamily proteins in early folliculogenesis | Q34161992 | ||
TGF-β and insulin signaling regulate reproductive aging via oocyte and germline quality maintenance | Q34204996 | ||
Rec8-containing cohesin maintains bivalents without turnover during the growing phase of mouse oocytes | Q34289002 | ||
Germline stem cells and follicular renewal in the postnatal mammalian ovary | Q34304906 | ||
Deterioration without replenishment--the misery of oocyte cohesin | Q34362374 | ||
Chromosomal abnormalities in oocytes | Q34384550 | ||
Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females | Q34450618 | ||
Inadequate histone deacetylation during oocyte meiosis causes aneuploidy and embryo death in mice | Q34624496 | ||
Spindle formation, chromosome segregation and the spindle checkpoint in mammalian oocytes and susceptibility to meiotic error | Q34728135 | ||
Production of offspring from a germline stem cell line derived from neonatal ovaries | Q34975362 | ||
Oocyte-specific differences in cell-cycle control create an innate susceptibility to meiotic errors | Q35576326 | ||
New insights into the genetic regulation of homologue disjunction in mammalian oocytes. | Q35576437 | ||
Involvement of Mitogen-Activated Protein Kinase Cascade During Oocyte Maturation and Fertilization in Mammals1 | Q35582237 | ||
Female and male lifestyle habits and IVF: what is known and unknown | Q36040101 | ||
SYCE2 is required for synaptonemal complex assembly, double strand break repair, and homologous recombination | Q36117975 | ||
A spindle assembly checkpoint protein functions in prophase I arrest and prometaphase progression | Q36193146 | ||
Effect of meiotic recombination on the production of aneuploid gametes in humans | Q36271551 | ||
Changes in histone acetylation during mouse oocyte meiosis | Q36323055 | ||
Keeping sister chromatids together: cohesins in meiosis | Q36328649 | ||
Age-associated increase in aneuploidy and changes in gene expression in mouse eggs | Q36642995 | ||
Shugoshin1 may play important roles in separation of homologous chromosomes and sister chromatids during mouse oocyte meiosis | Q36938393 | ||
The origin of human aneuploidy: where we have been, where we are going | Q36958145 | ||
Meiosis in oocytes: predisposition to aneuploidy and its increased incidence with age. | Q37033768 | ||
Human female meiosis: what makes a good egg go bad? | Q37055902 | ||
Heterochromatin-mediated association of achiasmate homologs declines with age when cohesion is compromised | Q37152661 | ||
Faulty spindle checkpoint and cohesion protein activities predispose oocytes to premature chromosome separation and aneuploidy | Q37216524 | ||
Heterozygosity for a Bub1 mutation causes female-specific germ cell aneuploidy in mice. | Q37293388 | ||
Evidence that a defective spindle assembly checkpoint is not the primary cause of maternal age-associated aneuploidy in mouse eggs | Q37369753 | ||
Cohesin SMC1beta protects telomeres in meiocytes | Q37402354 | ||
Oocyte aging: cellular and molecular changes, developmental potential and reversal possibility | Q37476388 | ||
P433 | issue | 5 | |
P304 | page(s) | 314-325 | |
P577 | publication date | 2011-10-01 | |
P1433 | published in | Physiology | Q1091804 |
P1476 | title | Why is chromosome segregation error in oocytes increased with maternal aging? | |
P478 | volume | 26 |
Q33784903 | Arrested human embryos are more likely to have abnormal chromosomes than developing embryos from women of advanced maternal age. |
Q41605192 | DNA microarray reveals that high proportions of human blastocysts from women of advanced maternal age are aneuploid and mosaic |
Q38038996 | Epigenetic changes associated with oocyte aging |
Q90655817 | Functions and dysfunctions of the mammalian centrosome in health, disorders, disease, and aging |
Q35938140 | Increased DNA damage and repair deficiency in granulosa cells are associated with ovarian aging in rhesus monkey |
Q36235524 | Lack of response to unaligned chromosomes in mammalian female gametes |
Q39612655 | Oocyte-specific deletion of N-WASP does not affect oocyte polarity, but causes failure of meiosis II completion. |
Q38282802 | Polar bodies in assisted reproductive technology: current progress and future perspectives |
Q38915548 | Predictive value of spindle retardance in embryo implantation rate |
Q33953122 | Reduced ability to recover from spindle disruption and loss of kinetochore spindle assembly checkpoint proteins in oocytes from aged mice. |
Q34979054 | The impact of mitochondrial function/dysfunction on IVF and new treatment possibilities for infertility |
Q37445023 | The prevalence of chromosomal deletions relating to developmental delay and/or intellectual disability in human euploid blastocysts |
Q48504865 | Transfer of autologous mitochondria from adipose tissue-derived stem cells rescues oocyte quality and infertility in aged mice |
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