review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Janna Morrison | Q42531528 |
Kimberley Wang | Q82726517 | ||
P2093 | author name string | Song Zhang | |
Kimberley J Botting | |||
I Caroline McMillen | |||
Shervi Lie | |||
Severence M MacLaughlin | |||
Monalisa Padhee | |||
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Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19 | Q24615581 | ||
Methylation analysis of KvDMR1 in human oocytes | Q24647913 | ||
DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific | Q24656230 | ||
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) | Q24678681 | ||
Genomic imprinting and assisted reproduction | Q24793282 | ||
Cardiomyocyte proliferation contributes to heart growth in young humans | Q36567874 | ||
In vitro maturation of human oocytes for assisted reproduction | Q36601570 | ||
A methyl-deficient diet fed to rats during the pre- and peri-conception periods of development modifies the hepatic proteome in the adult offspring | Q36620040 | ||
Embryo culture medium: which is the best? | Q36647382 | ||
Pregnancy recognition and conceptus implantation in domestic ruminants: roles of progesterone, interferons and endogenous retroviruses. | Q36772059 | ||
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An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs | Q36808158 | ||
Suboptimal in vitro culture conditions: an epigenetic origin of long-term health effects. | Q36808803 | ||
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Neuronatin: a new inflammation gene expressed on the aortic endothelium of diabetic mice. | Q36906395 | ||
The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region | Q36927144 | ||
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Peri-implantation undernutrition programs blunted angiotensin II evoked baroreflex responses in young adult sheep | Q37126772 | ||
DNA methylation and gene expression differences in children conceived in vitro or in vivo | Q37357616 | ||
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Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span | Q37383999 | ||
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Eight-fold increased risk for congenital heart defects in children carrying the nicotinamide N-methyltransferase polymorphism and exposed to medicines and low nicotinamide | Q40098410 | ||
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The longer-term health outcomes for children born as a result of IVF treatment. Part II--Mental health and development outcomes | Q27011215 | ||
Primary prevention of coronary heart disease in women through diet and lifestyle | Q28140155 | ||
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Birth after the reimplantation of a human embryo | Q28241508 | ||
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Can assisted reproduction technology compensate for the natural decline in fertility with age? A model assessment | Q28267616 | ||
Reproduction in females: the role of the early life environment | Q28296200 | ||
Persistent epigenetic differences associated with prenatal exposure to famine in humans | Q28298905 | ||
Periconception window: advising the pregnancy-planning couple | Q28385505 | ||
Epigenetics in human disease and prospects for epigenetic therapy | Q29547437 | ||
Genomic imprinting: parental influence on the genome | Q29616227 | ||
Role for DNA methylation in genomic imprinting | Q29618669 | ||
Transient regenerative potential of the neonatal mouse heart | Q29620371 | ||
Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth | Q30408297 | ||
Genomic imprinting: review and relevance to human diseases. | Q30501672 | ||
Pregnancy outcomes after assisted reproductive technology | Q33241644 | ||
Insulin sensitivity is normalized in the third generation (F3) offspring of developmentally programmed insulin resistant (F2) rats fed an energy-restricted diet | Q33377584 | ||
In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model | Q33532631 | ||
Maternal nutrition at conception modulates DNA methylation of human metastable epialleles | Q33587336 | ||
From endothelial dysfunction to atherosclerosis | Q33647535 | ||
Maternal undernutrition significantly impacts ovarian follicle number and increases ovarian oxidative stress in adult rat offspring | Q33778461 | ||
Ovarian stimulation and endometrial receptivity | Q33848140 | ||
Embryonic origins of health: long-term effects of IVF in human and livestock | Q33873791 | ||
Reflections on the golden anniversary of the first embryo transfer to produce a calf | Q33873834 | ||
Economical and ecological importance of indigenous livestock and the application of assisted reroduction to their preservation | Q33873918 | ||
Side of ovulation and cycle characteristics in normally fertile women | Q33896099 | ||
Initial and cyclic recruitment of ovarian follicles | Q33899556 | ||
Epigenetics and assisted reproductive technology: a call for investigation | Q33909693 | ||
Review of media used in ART laboratories | Q34024263 | ||
Systemic and pulmonary vascular dysfunction in children conceived by assisted reproductive technologies | Q34031202 | ||
Investigation of the infertile couple: investigation of the infertile couple in the era of assisted reproductive technology: a time for reappraisal | Q34072693 | ||
Cytokine cross-talk between mother and the embryo/placenta | Q34095118 | ||
Zygote donor nitrogen metabolism and in vitro embryo culture perturbs in utero development and IGF2R expression in ovine fetal tissues. | Q50648009 | ||
The impact of ovarian stimulation on implantation and fetal development in mice. | Q50719700 | ||
Periconception maternal characteristics and embryonic growth trajectories: the Rotterdam Predict study. | Q50765851 | ||
Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line | Q50792932 | ||
Ovine fetal development is more sensitive to perturbation by the presence of serum in embryo culture before rather than after compaction. | Q51112005 | ||
Culture of viable human blastocysts in defined sequential serum-free media. | Q51193428 | ||
Pregnancy in aged rats that were born small: cardiorenal and metabolic adaptations and second-generation fetal growth. | Q51326987 | ||
Imprinted gene expression in the rat embryo-fetal axis is altered in response to periconceptional maternal low protein diet. | Q51792533 | ||
Periconceptional tobacco smoking and isolated congenital heart defects in the neonatal period. | Q51796903 | ||
Adaptive responses by mouse early embryos to maternal diet protect fetal growth but predispose to adult onset disease. | Q51972926 | ||
In vitro fertilization causes epigenetic modifications to the onset of gene expression from the zygotic genome in mice. | Q52141601 | ||
Aberrant fetal growth and development after in vitro culture of sheep zygotes. | Q52143928 | ||
Cleavage anomalies in early human embryos and survival after prolonged culture in-vitro. | Q52144237 | ||
Post-natal growth and development of Simmental calves derived from in vivo or in vitro embryos. | Q52172752 | ||
Changes with age in the level and duration of fertility in the menstrual cycle. | Q53670811 | ||
Impact of elective single embryo transfer on the twin pregnancy rate. | Q53999820 | ||
Fetal growth restriction and the programming of heart growth and cardiac insulin-like growth factor 2 expression in the lamb. | Q54570427 | ||
Fetal, Infant, and Childhood Growth and Adult Blood Pressure | Q57273887 | ||
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies | Q58133996 | ||
Demethylation of the zygotic paternal genome | Q59066150 | ||
Mitochondria and the death of oocytes | Q59075483 | ||
Congenital malformations in infants born after in vitro fertilization in Sweden | Q61851236 | ||
Children born after assisted fertilization have an increased rate of major congenital anomalies | Q61856931 | ||
Altered pregnancy outcomes in mice following treatment with the hyperglycaemia mimetic, glucosamine, during the periconception period | Q48629528 | ||
Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner | Q48712348 | ||
Ontogeny of expression of a receptor for platelet-activating factor in mouse preimplantation embryos and the effects of fertilization and culture in vitro on its expression | Q48923628 | ||
Single embryo transfer and multiple pregnancy rate reduction in IVF/ICSI: a 5-year appraisal | Q49027521 | ||
Cell allocation to the inner cell mass and the trophectoderm in bovine embryos cultured in two different media | Q49174832 | ||
Assessment of human oocyte developmental competence by cumulus cell morphology and circulating hormone profile. | Q50640545 | ||
Maternal periconceptional and gestational low protein diet affects mouse offspring growth, cardiovascular and adipose phenotype at 1 year of age. | Q34110322 | ||
Long-term effects on offspring of exposure of oocytes and embryos to chemical and physical agents | Q34113340 | ||
In-utero overgrowth in ruminants following embryo culture: lessons from mice and a warning to men. | Q34192204 | ||
Reproductive technologies and the risk of birth defects | Q34272832 | ||
Hox genes and the evolution of vertebrate axial morphology. | Q34311983 | ||
Embryo culture media and IVF/ICSI success rates: a systematic review | Q34326455 | ||
The longer-term health outcomes for children born as a result of IVF treatment: Part I--General health outcomes | Q34330313 | ||
Ovarian follicular growth and development in mammals | Q34338272 | ||
Developmental consequences of embryo and cell manipulation in mice and farm animals | Q34380410 | ||
Regulation of ovarian follicular development in primates: facts and hypotheses | Q34389038 | ||
Epigenetic reprogramming in mammals | Q34408807 | ||
Trends in the incidence of births and multiple births and the factors that determine the probability of multiple birth after IVF treatment | Q34451126 | ||
In vitro fertilization is associated with an increase in major birth defects | Q34465920 | ||
Large offspring syndrome and other consequences of ruminant embryo culture in vitro: relevance to blastocyst culture in human ART. | Q34530622 | ||
Incidence of retinoblastoma in children born after in-vitro fertilisation | Q34530916 | ||
Outcome of assisted reproduction. | Q34581482 | ||
A review of known imprinting syndromes and their association with assisted reproduction technologies. | Q34595528 | ||
Clinical practice. In vitro fertilization | Q34605968 | ||
Epigenetics and cardiovascular disease | Q34788746 | ||
The molecular foundations of the maternal to zygotic transition in the preimplantation embryo | Q34806720 | ||
Assisted reproductive technology and major structural birth defects in the United States | Q34880868 | ||
Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritance | Q34915073 | ||
Carotid intima-media thickness, arterial stiffness and risk of cardiovascular disease: current evidence | Q35021450 | ||
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. | Q35058363 | ||
Endothelial dysfunction: a marker of atherosclerotic risk | Q35067247 | ||
Epigenetics and the Environment | Q35118498 | ||
Delaying childbearing: effect of age on fecundity and outcome of pregnancy | Q35179619 | ||
Prevention of congenital abnormalities by periconceptional multivitamin supplementation | Q35188572 | ||
Sizing up the heart: development redux in disease. | Q35189905 | ||
Coronary heart disease after prenatal exposure to the Dutch famine, 1944-45 | Q35377069 | ||
Maternal obesity and the early origins of childhood obesity: weighing up the benefits and costs of maternal weight loss in the periconceptional period for the offspring | Q35607176 | ||
Mouse embryo culture induces changes in postnatal phenotype including raised systolic blood pressure | Q35720294 | ||
Assisted reproduction treatment and epigenetic inheritance. | Q35766037 | ||
Epigenetic reprogramming during early development in mammals. | Q35791053 | ||
The embryo and its future | Q35816174 | ||
Mismatched pre- and postnatal nutrition leads to cardiovascular dysfunction and altered renal function in adulthood. | Q35839676 | ||
The effect of oocyte quality on development | Q35912032 | ||
Imprinted gene expression in fetal growth and development | Q35946496 | ||
Implantation mechanisms: insights from the sheep. | Q35972997 | ||
Epigenetics and the germline | Q36032685 | ||
Developmental origins of the metabolic syndrome: prediction, plasticity, and programming | Q36079011 | ||
Blastocysts don't go it alone. Extrinsic signals fine-tune the intrinsic developmental program of trophoblast cells | Q36121178 | ||
Molecular mechanisms of epigenetics | Q36126545 | ||
Cardiomyocytes structure, function and associated pathologies | Q36160056 | ||
Assisted reproduction: the epigenetic perspective | Q36182585 | ||
IVF/ICSI twin pregnancies: risks and prevention | Q36241038 | ||
DNA methylation, insulin resistance, and blood pressure in offspring determined by maternal periconceptional B vitamin and methionine status | Q36288582 | ||
Errors in development of fetuses and placentas from in vitro-produced bovine embryos | Q36305050 | ||
Periconceptional undernutrition in sheep affects adult phenotype only in males | Q36308220 | ||
The developmental origins of adult disease (Barker) hypothesis | Q36379536 | ||
IVF results: optimize not maximize | Q36386956 | ||
Major advances associated with reproduction in dairy cattle | Q36421492 | ||
Imprinted genes and their role in human fetal growth. | Q36436584 | ||
Selective single blastocyst transfer reduces the multiple pregnancy rate and increases pregnancy rates: a pre- and postintervention study | Q36477504 | ||
Low protein diet fed exclusively during mouse oocyte maturation leads to behavioural and cardiovascular abnormalities in offspring. | Q42646815 | ||
CCAAT/enhancer binding protein alpha (C/EBPalpha) in adipose tissue regulates genes in lipid and glucose metabolism and a genetic variation in C/EBPalpha is associated with serum levels of triglycerides | Q42808906 | ||
Cardiomyocyte cell cycle control and growth estimation in vivo--an analysis based on cardiomyocyte nuclei | Q43195307 | ||
Absence of insulin resistance and low-grade inflammation despite early metabolic syndrome manifestations in children born after in vitro fertilization | Q43203345 | ||
The risk of major birth defects after intracytoplasmic sperm injection and in vitro fertilization | Q43640466 | ||
Assisted reproductive technologies are associated with cardiovascular remodeling in utero that persists postnatally. | Q43735871 | ||
Long-term outcomes in children born after assisted conception | Q43850241 | ||
The impact of ovarian stimulation on the expression of candidate reprogramming genes in mouse preimplantation embryos | Q43866478 | ||
Impact of maternal undernutrition during the periconceptional period, fetal number, and fetal sex on the development of the hypothalamo-pituitary adrenal axis in sheep during late gestation | Q43967689 | ||
Nature, nurture or nutrition? Impact of maternal nutrition on maternal care, offspring development and reproductive function | Q44014777 | ||
Periconceptional nutrition programs development of the cardiovascular system in the fetal sheep | Q44107256 | ||
Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure | Q44141812 | ||
Effects of pre- and periconceptional undernutrition on arterial function in adult female sheep are vascular bed dependent | Q44543815 | ||
Maternal periconceptional alcohol consumption and risk for conotruncal heart defects | Q44744158 | ||
Programming of adult cardiovascular function after early maternal undernutrition in sheep. | Q44771522 | ||
Transfer of bovine embryos produced in vivo or in vitro: survival and fetal development | Q44863236 | ||
Impact of periconceptional nutrition on maternal and fetal leptin and fetal adiposity in singleton and twin pregnancies. | Q44932407 | ||
Periconceptional undernutrition in sheep accelerates maturation of the fetal hypothalamic-pituitary-adrenal axis in late gestation | Q44942767 | ||
Congenital anomalies in infants conceived by assisted reproductive techniques | Q45010655 | ||
Zygote intrafallopian transfer as a successful treatment for unexplained infertility | Q45077794 | ||
Periconceptional undernutrition alters growth trajectory and metabolic and endocrine responses to fasting in late-gestation fetal sheep | Q45253931 | ||
Congenital malformations associated with assisted reproductive technology: a California statewide analysis. | Q46014488 | ||
Neonatal outcome and congenital malformations in children born after in-vitro fertilization | Q46351468 | ||
Plasma pigment epithelium-derived factor is positively associated with obesity in Caucasian subjects, in particular with the visceral fat depot | Q46372820 | ||
The International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) Revised Glossary on ART Terminology, 2009. | Q46377235 | ||
Risk of congenital heart defects associated with assisted reproductive technologies: a population-based evaluation | Q46491122 | ||
Maternal smoking and congenital heart defects | Q46670059 | ||
Transmission of raised blood pressure and endothelial dysfunction to the F2 generation induced by maternal protein restriction in the F0, in the absence of dietary challenge in the F1 generation | Q46730534 | ||
Cardiometabolic differences in children born after in vitro fertilization: follow-up study | Q46745143 | ||
IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch | Q46747937 | ||
Gamete intrafallopian transfer. International cooperative study of the first 800 cases | Q46914686 | ||
Protein restriction during fetal and neonatal development in the rat alters reproductive function and accelerates reproductive ageing in female progeny | Q46960418 | ||
Low and very low birth weight in infants conceived with use of assisted reproductive technology | Q47191285 | ||
Selective loss of imprinting in the placenta following preimplantation development in culture | Q47232748 | ||
Relation of weight and rate of increase in weight during childhood and adolescence to body size, blood pressure, fasting insulin, and lipids in young adults. The Minneapolis Children's Blood Pressure Study | Q47269372 | ||
Gamete intrafallopian transfer (GIFT): historic perspective | Q47323678 | ||
Lamb birth weight is affected by culture system utilized during in vitro pre-elongation development of ovine embryos | Q47343059 | ||
ESHRE guidelines for good practice in IVF laboratories. Committee of the Special Interest Group on Embryology of the European Society of Human Reproduction and Embryology | Q47587060 | ||
Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice | Q47675900 | ||
Effect of periconceptional undernutrition and gender on hypothalamic-pituitary-adrenal axis function in young adult sheep. | Q48450970 | ||
Zygote intrafallopian transfer (ZIFT): evaluation of 42 cases | Q68486665 | ||
Optimization and simplification of culture conditions in human in vitro fertilization (IVF) and preembryo replacement by serum-free media | Q68782062 | ||
Gene expression during oogenesis and oocyte development in mammals | Q69123329 | ||
Zygote intra-fallopian transfer as an alternative treatment for male infertility | Q69652712 | ||
Mitoses and binucleated cells in perinatal human hearts | Q69859960 | ||
Gamete intra-fallopian transfer (GIFT): a new treatment for infertility | Q69866710 | ||
Congenital malformations after in-vitro fertilisation | Q69909561 | ||
Improved pregnancy rate in human in vitro fertilization with the use of a medium based on the composition of human tubal fluid | Q69913154 | ||
Transfer of a human zygote | Q70001048 | ||
Gamete intrafallopian transfer | Q71327658 | ||
Study of non-muscle cells of the adult mammalian heart: a fine structural analysis and distribution | Q71358031 | ||
Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development | Q71699187 | ||
Cardiomyocyte DNA synthesis and binucleation during murine development | Q71839305 | ||
In vitro fertilization/embryo transfer in unexplained infertility and minimal peritoneal endometriosis | Q71905373 | ||
Activation of embryonic genes during preimplantation rat development | Q72102558 | ||
Mammalian embryo culture in the absence of serum or somatic cell support | Q72127118 | ||
Myocardial cell hypertrophy or hyperplasia | Q72834770 | ||
Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture | Q73435273 | ||
Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes | Q73509793 | ||
Effect of male age on fertility: evidence for the decline in male fertility with increasing age | Q73513619 | ||
Effects of different reproduction techniques: AI MOET or IVP, on health and welfare of bovine offspring | Q73588111 | ||
Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo | Q73811130 | ||
Timing of compaction and inner cell allocation in bovine embryos produced in vivo after superovulation | Q73879279 | ||
Growth and maturation of cardiac myocytes in fetal sheep in the second half of gestation | Q73940580 | ||
The developmental origins of adult disease | Q73942742 | ||
Superovulation of female mice delays embryonic and fetal development | Q73959103 | ||
Maternal undernutrition during the preimplantation period of rat development causes blastocyst abnormalities and programming of postnatal hypertension | Q74281065 | ||
Congenital malformations in 4224 children conceived after IVF | Q74549976 | ||
Large offspring syndrome in cattle and sheep | Q77602906 | ||
Common carotid intima-media thickness and arterial stiffness: indicators of cardiovascular risk in high-risk patients. The SMART Study (Second Manifestations of ARTerial disease) | Q78195734 | ||
Myocyte enlargement, differentiation, and proliferation kinetics in the fetal sheep heart | Q79378147 | ||
In vitro fertilization (IVF) in Sweden: risk for congenital malformations after different IVF methods | Q81335319 | ||
A comprehensive assessment of outcomes in pregnancies conceived by in vitro fertilization/intracytoplasmic sperm injection | Q83144756 | ||
A persistent misperception: assisted reproductive technology can reverse the "aged biological clock" | Q83564783 | ||
The double hit of growth restriction: its origins and outcome on this generation and the next | Q83595006 | ||
Manipulating nature: Might there be a cardiovascular price to pay for the miracle of assisted conception? | Q83706059 | ||
Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring | Q84114090 | ||
Growth during infancy and early childhood in relation to blood pressure and body fat measures at age 8-18 years of IVF children and spontaneously conceived controls born to subfertile parents | Q84334836 | ||
Gamete intra-fallopian transfer | Q93636976 | ||
Association between arterial stiffness and atherosclerosis: the Rotterdam Study | Q95751064 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cardiovascular disease | Q389735 |
pregnancy outcome | Q66057507 | ||
physiological phenomenon | Q66615932 | ||
biomedical investigative technique | Q66648976 | ||
P304 | page(s) | 1378-1425 | |
P577 | publication date | 2015-02-18 | |
P1433 | published in | Nutrients | Q7070485 |
P1476 | title | The periconceptional environment and cardiovascular disease: does in vitro embryo culture and transfer influence cardiovascular development and health? | |
P478 | volume | 7 |
Q90237484 | Alteration in the expression of the renin-angiotensin system in the myocardium of mice conceived by in vitro fertilization |
Q53794703 | Changes of Phospholipids in Fetal Liver of Mice Conceived by In Vitro Fertilization. |
Q41696561 | Clinical review of 24-35 year olds conceived with and without in vitro fertilization: study protocol. |
Q47145367 | Embryo cell allocation patterns are not altered by biopsy but can be linked with further development |
Q102055480 | Impact of in vitro embryo culture and transfer on blood pressure regulation in the adolescent lamb |
Q92142500 | In vitro fertilization and embryo transfer alter human placental function through trophoblasts in early pregnancy |
Q42531434 | Nutrition in Pregnancy: Optimising Maternal Diet and Fetal Adaptations to Altered Nutrient Supply |
Q30245567 | Placental Origins of Chronic Disease |
Q98878610 | Self-reported physical health status of donor sperm-conceived adults |
Q38546947 | The programming of cardiovascular disease. |
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