scholarly article | Q13442814 |
P356 | DOI | 10.1002/MRD.22461 |
P698 | PubMed publication ID | 25728573 |
P50 | author | Mohammad-Hossein Nasr-Esfahani | Q64900574 |
P2093 | author name string | S M Hosseini | |
M Hajian | |||
V Asgari | |||
H R Rahmani | |||
F Jafarpour | |||
M A Edriss | |||
A Bakhtari | |||
E Bonakdar | |||
N Sadeghi Boroujeni | |||
P2860 | cites work | Coactivator as a target gene specificity determinant for histone H3 lysine 4 methyltransferases | Q24305587 |
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints | Q24322379 | ||
In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene | Q24532045 | ||
Beckwith-Wiedemann syndrome and IVF: a case-control study | Q24533595 | ||
The product of the imprinted H19 gene is an oncofetal RNA | Q24609254 | ||
A decade of exploring the cancer epigenome - biological and translational implications | Q24614467 | ||
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19 | Q24615581 | ||
Mammalian ASH1L is a histone methyltransferase that occupies the transcribed region of active genes | Q24680558 | ||
Conceptual links between DNA methylation reprogramming in the early embryo and primordial germ cells | Q26864904 | ||
Eaf1 is the platform for NuA4 molecular assembly that evolutionarily links chromatin acetylation to ATP-dependent exchange of histone H2A variants | Q27931128 | ||
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality | Q28131773 | ||
Epigenetic reprogramming in mammalian development | Q28212171 | ||
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method | Q28237886 | ||
Developmental-specific activity of the FGF-4 enhancer requires the synergistic action of Sox2 and Oct-3 | Q28291574 | ||
The impact of supraphysiologic serum estradiol levels on peri-implantation embryo development and early pregnancy outcome following in vitro fertilization cycles | Q28395271 | ||
PGC7/Stella protects against DNA demethylation in early embryogenesis | Q28506319 | ||
A novel octamer binding transcription factor is differentially expressed in mouse embryonic cells | Q28506765 | ||
Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine | Q28585429 | ||
5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming | Q28588147 | ||
Chromatin modification and epigenetic reprogramming in mammalian development | Q29617802 | ||
Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth | Q30408297 | ||
Dynamic reprogramming of DNA methylation in the early mouse embryo. | Q34108785 | ||
Placental-specific IGF-II is a major modulator of placental and fetal growth. | Q34135795 | ||
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology | Q34183041 | ||
Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency. | Q34249450 | ||
Embryo culture media and IVF/ICSI success rates: a systematic review | Q34326455 | ||
Epigenetic reprogramming in mammals | Q34408807 | ||
Trithorax-group protein ASH1 methylates histone H3 lysine 36. | Q34633633 | ||
Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development | Q34786920 | ||
On the nature of human housekeeping genes | Q34825854 | ||
Nuclear reprogramming in cells | Q34907992 | ||
Dynamic CpG island methylation landscape in oocytes and preimplantation embryos | Q35135165 | ||
Chromosome methylation patterns during mammalian preimplantation development | Q35205639 | ||
Ovarian stimulation and low birth weight in newborns conceived through in vitro fertilization | Q35228727 | ||
Loss of genomic imprinting in mouse embryos with fast rates of preimplantation development in culture. | Q35779087 | ||
Jumonji domain-containing protein 3 regulates histone 3 lysine 27 methylation during bovine preimplantation development | Q35787162 | ||
Epigenetic reprogramming during early development in mammals. | Q35791053 | ||
Generation and replication-dependent dilution of 5fC and 5caC during mouse preimplantation development. | Q35979229 | ||
Stage-specific roles for tet1 and tet2 in DNA demethylation in primordial germ cells | Q36934066 | ||
Genomic imprinting mechanisms in mammals. | Q37105077 | ||
The clinical significance of the retrieval of a low number of oocytes following mild ovarian stimulation for IVF: a meta-analysis | Q37353447 | ||
DNA methylation and gene expression differences in children conceived in vitro or in vivo | Q37357616 | ||
Intracytoplasmic sperm injection may increase the risk of imprinting defects | Q37361933 | ||
Histone modifications during mammalian oocyte maturation: dynamics, regulation and functions | Q37740910 | ||
Epigenetic reprogramming in mouse pre-implantation development and primordial germ cells | Q37965513 | ||
Parallel mechanisms of epigenetic reprogramming in the germline | Q37990242 | ||
Genomic imprints as a model for the analysis of epigenetic stability during assisted reproductive technologies | Q38041530 | ||
Epigenetic programming and reprogramming during development | Q38086774 | ||
Gadd45a promotes epigenetic gene activation by repair-mediated DNA demethylation. | Q40176354 | ||
Pw1, a novel zinc finger gene implicated in the myogenic and neuronal lineages | Q41179526 | ||
Vitrification at the germinal vesicle stage does not affect the methylation profile of H19 and KCNQ1OT1 imprinting centers in human oocytes subsequently matured in vitro | Q41608013 | ||
DNA integrity, growth pattern, spindle formation, chromosomal constitution and imprinting patterns of mouse oocytes from vitrified pre-antral follicles | Q41608683 | ||
Higher survival rate of vitrified and thawed in vitro produced bovine blastocysts following culture in defined medium supplemented with beta-mercaptoethanol | Q41614244 | ||
Gadd45 in stress signaling | Q42130318 | ||
Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection | Q43202295 | ||
Microarray assessment of methylation in individual mouse blastocyst stage embryos shows that in vitro culture may have widespread genomic effects | Q43407643 | ||
Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure | Q44141812 | ||
Peak serum estradiol level during controlled ovarian hyperstimulation is associated with increased risk of small for gestational age and preeclampsia in singleton pregnancies after in vitro fertilization | Q45135212 | ||
Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoa | Q46329417 | ||
Maintenance of genomic methylation patterns during preimplantation development requires the somatic form of DNA methyltransferase 1. | Q46874788 | ||
Changes in H3K79 methylation during preimplantation development in mice | Q46899764 | ||
Low and very low birth weight in infants conceived with use of assisted reproductive technology | Q47191285 | ||
Assisted reproductive technology in Europe, 2008: results generated from European registers by ESHRE. | Q47394116 | ||
Active and passive demethylation of male and female pronuclear DNA in the mammalian zygote | Q47981749 | ||
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. | Q48125063 | ||
Trim28 is required for epigenetic stability during mouse oocyte to embryo transition. | Q48652732 | ||
Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner | Q48712348 | ||
Peg3/Pw1 is involved in p53-mediated cell death pathway in brain ischemia/hypoxia | Q48731045 | ||
Superovulation alters the expression of imprinted genes in the midgestation mouse placenta | Q48764255 | ||
Transmission of modified nucleosomes from the mouse male germline to the zygote and subsequent remodeling of paternal chromatin. | Q50745250 | ||
Extending the maternal-zygotic effect with genomic imprinting. | Q51910884 | ||
Nanog promotes transfer of pluripotency after cell fusion. | Q52014295 | ||
Genomic imprinting: mother maintains methylation marks. | Q52132092 | ||
Epigenetic reprogramming in mouse primordial germ cells | Q57086629 | ||
P433 | issue | 3 | |
P304 | page(s) | 191-206 | |
P577 | publication date | 2015-03-01 | |
P1433 | published in | Molecular Reproduction and Development | Q6895976 |
P1476 | title | A physiological, rather than a superovulated, post-implantation environment can attenuate the compromising effect of assisted reproductive techniques on gene expression in developing mice embryos | |
P478 | volume | 82 |
Q37628615 | Global DNA methylation levels are altered by modifiable clinical manipulations in assisted reproductive technologies |
Q37479026 | Methylation Status of H19/IGF2 Differentially Methylated Region in in vitro Human Blastocysts Donated by Healthy Couples. |
Q47573145 | Overweight negatively affects outcome of superovulation treatment in female mice |
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