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Effect of oxygen concentration on human embryo development evaluated by time-lapse monitoring
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.1402060108openalex-snapshot
The effect of oxygen on the development of preimplantation mouse embryos in vitro
inferredcites →https://doi.org/10.1002/mrd.1006openalex-snapshot
Protection against reactive oxygen species during mouse preimplantation embryo development: Role of EDTA, oxygen tension, catalase, superoxide dismutase and pyruvate
inferredcites →https://doi.org/10.1002/mrd.20183openalex-snapshot
Oxygen‐regulated expression of GLUT‐1, GLUT‐3, and VEGF in the mouse blastocyst
inferredcites →https://doi.org/10.1002/mrd.20502openalex-snapshot
Influence of in vitro oxygen concentrations on preimplantation embryo development, gene expression and production of hanwoo calves following embryo transfer
inferredcites →https://doi.org/10.1007/s10815-011-9549-1openalex-snapshot
Embryo quality, blastocyst and ongoing pregnancy rates in oocyte donation patients whose embryos were monitored by time-lapse imaging
inferredcites →https://doi.org/10.1007/s10815-012-9750-xopenalex-snapshot
A randomized clinical trial comparing embryo culture in a conventional incubator with a time-lapse incubator
inferredcites →https://doi.org/10.1016/0093-691x(94)90504-copenalex-snapshot
Effect of oxygen concentration in the incubator's gas phase on the development of cultured preimplantation rabbit embryos
inferredcites →https://doi.org/10.1016/j.fertnstert.2003.07.023openalex-snapshot
Single blastocyst transfer: a prospective randomized trial
inferredcites →https://doi.org/10.1016/j.fertnstert.2005.07.038openalex-snapshot
The Comparison of Embryo Developments and Pregnancy Rates in Human in Vitro Culture Conditions at Different Oxygen Gas Phase
inferredcites →https://doi.org/10.1016/j.fertnstert.2006.05.017openalex-snapshot
Effects of oxygen tension on gene expression in preimplantation mouse embryos
inferredcites →https://doi.org/10.1016/j.fertnstert.2006.05.066openalex-snapshot
Effect of reduced oxygen concentrations on the outcome of in vitro fertilization
inferredcites →https://doi.org/10.1016/j.fertnstert.2008.03.051openalex-snapshot
Low-oxygen compared with high-oxygen atmosphere in blastocyst culture, a prospective randomized study
inferredcites →https://doi.org/10.1016/j.fertnstert.2008.07.1707openalex-snapshot
In vitro culture under physiologic oxygen concentration improves blastocyst yield and quality: a prospective randomized survey on sibling oocytes
inferredcites →https://doi.org/10.1016/j.fertnstert.2009.02.048openalex-snapshot
Comparison of 5% and ambient oxygen during days 3–5 of in vitro culture of human embryos
inferredcites →https://doi.org/10.1016/j.fertnstert.2009.03.077openalex-snapshot
A prospective, randomized trial on the effect of atmospheric versus reduced oxygen concentration on the outcome of intracytoplasmic sperm injection cycles
inferredcites →https://doi.org/10.1016/j.fertnstert.2009.07.1561openalex-snapshot
The effect of oxygen concentration on human embryo culture: a prospective randomized controlled trial
inferredcites →https://doi.org/10.1016/j.rbmo.2010.04.028openalex-snapshot
Time-lapse analysis of mouse embryo development in oxygen gradients
inferredcites →https://doi.org/10.1016/j.theriogenology.2004.01.011openalex-snapshot
Effects of oxygen concentration and antioxidants on the in vitro developmental ability, production of reactive oxygen species (ROS), and DNA fragmentation in porcine embryos
inferredcites →https://doi.org/10.1016/j.theriogenology.2004.03.012openalex-snapshot
Effects of oxygen tension on the development and quality of porcine in vitro fertilized embryos
inferredcites →https://doi.org/10.1016/j.theriogenology.2004.10.001openalex-snapshot
The effect of oxygen tension on porcine embryonic development is dependent on embryo type
inferredcites →https://doi.org/10.1016/s0015-0282(16)57305-1openalex-snapshot
Effect of oxygen concentration on in vitro fertilization and embryo culture in the human and the mouse
inferredcites →https://doi.org/10.1016/s0093-691x(98)00227-1openalex-snapshot
Developmental kinetics of the first cell cycles of bovine in vitro produced embryos in relation to their in vitro viability and sex
inferredcites →https://doi.org/10.1016/s1472-6483(10)60199-xopenalex-snapshot
Influence of atmospheric versus reduced oxygen concentration on development of human blastocysts in vitro: a prospective study on sibling oocytes
inferredcites →https://doi.org/10.1016/s1472-6483(10)60222-2openalex-snapshot
Kinetic markers of human embryo quality using time-lapse recordings of IVF/ICSI-fertilized oocytes
inferredcites →https://doi.org/10.1016/s1472-6483(10)60768-7openalex-snapshot
Early cleavage: an additional predictor of high implantation rate following elective single embryo transfer
inferredcites →https://doi.org/10.1016/s1472-6483(10)61136-4openalex-snapshot
Effect of oxygen concentration during the incubation of embryos of women undergoing ICSI and embryo transfer: a prospective randomized study
inferredcites →https://doi.org/10.1016/s1472-6483(10)61276-xopenalex-snapshot
Impact of oxygen concentration on embryonic development of mouse zygotes
inferredcites →https://doi.org/10.1016/s1472-6483(10)61443-5openalex-snapshot
Observations on intrauterine oxygen tension measured by fibre-optic microsensors
inferredcites →https://doi.org/10.1016/s1534-5807(03)00373-3openalex-snapshot
Dynamics of Global Gene Expression Changes during Mouse Preimplantation Development
inferredcites →https://doi.org/10.1016/s1534-5807(03)00404-0openalex-snapshot
A Genome-Wide Study of Gene Activity Reveals Developmental Signaling Pathways in the Preimplantation Mouse Embryo
inferredcites →https://doi.org/10.1017/s0967199411000426openalex-snapshot
Developmental competence of porcine oocytes after in vitro maturation and in vitro culture under different oxygen concentrations
inferredcites →https://doi.org/10.1038/332459a0openalex-snapshot
Human gene expression first occurs between the four- and eight-cell stages of preimplantation development
inferredcites →https://doi.org/10.1038/nbt.1686openalex-snapshot
Non-invasive imaging of human embryos before embryonic genome activation predicts development to the blastocyst stage
inferredcites →https://doi.org/10.1071/bi9790363openalex-snapshot
Foetal and Placental Growth in the Mouse After Pre-implantation Development in Vitro Under Oxygen Concentrations' of 5 and 20%
inferredcites →https://doi.org/10.1071/rd9910601openalex-snapshot
Oxygen concentration and protein source affect the development of preimplantation goat embryos in vitro
inferredcites →https://doi.org/10.1093/biolreprod/87.s1.1openalex-snapshot
Trainee Forum—Writing Winning Grants.
inferredcites →https://doi.org/10.1093/hmg/ddh157openalex-snapshot
The unique transcriptome through day 3 of human preimplantation development
inferredcites →https://doi.org/10.1093/humrep/14.2.465openalex-snapshot
Effect of oxygen concentration on human in-vitro fertilization and embryo culture
inferredcites →https://doi.org/10.1093/humrep/16.12.2652openalex-snapshot
Early embryo cleavage is a strong indicator of embryo quality in human IVF
inferredcites →https://doi.org/10.1095/biolreprod.112.100552openalex-snapshot
Oxygen Regulates Amino Acid Turnover and Carbohydrate Uptake During the Preimplantation Period of Mouse Embryo Development1
inferredcites →https://doi.org/10.1111/j.1447-0756.1999.tb01177.xopenalex-snapshot
Effects of Low Oxygen Condition on the Generation of Reactive Oxygen Species and the Development in Mouse Embryos Cultured in vitro*
inferredcites →https://doi.org/10.1111/j.1749-0774.2006.00018.xopenalex-snapshot
Global gene expression profiling of preimplantation embryos
inferredcites →https://doi.org/10.1113/jphysiol.2005.102681openalex-snapshot
Effect of culturing mouse embryos under different oxygen concentrations on subsequent fetal and placental development
inferredcites →https://doi.org/10.1186/1477-7827-4-54openalex-snapshot
Development to the blastocyst stage, the oxidative state, and the quality of early developmental stage of porcine embryos cultured in alteration of glucose concentrations in vitro under different oxygen tensions
inferredcites →https://doi.org/10.1242/dev.060426openalex-snapshot
Human pre-implantation embryo development
inferredcites →https://doi.org/10.1242/dev.064741openalex-snapshot
Waves of early transcriptional activation and pluripotency program initiation during human preimplantation development
inferredcites →https://doi.org/10.1371/journal.pone.0007844openalex-snapshot
Transcriptome Profiling of Human Pre-Implantation Development
inferredcites →https://doi.org/10.1371/journal.pone.0013615openalex-snapshot
Functional Genomics of 5- to 8-Cell Stage Human Embryos by Blastomere Single-Cell cDNA Analysis
inferredcites →https://doi.org/10.1530/jrf.0.0890573openalex-snapshot
Effect of oxygen concentration on in-vitro development of preimplantation sheep and cattle embryos
inferredcites →https://doi.org/10.1530/jrf.0.0990673openalex-snapshot
Oxygen tension in the oviduct and uterus of rhesus monkeys, hamsters and rabbits
inferredcites →https://doi.org/10.2527/1997.752483xopenalex-snapshot
Effect of oxygen concentration and free radicals on in vitro development of in vitro-produced bovine embryos.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118849613.ch7openalex-snapshot
Clinical Application of Methods to SelectIn VitroFertilized Embryos
inferred← citeshttps://doi.org/10.1002/9781118849613.ch8openalex-snapshot
New Horizons/Developments in Time‐Lapse Morphokinetic Analysis of Mammalian Embryos
inferred← citeshttps://doi.org/10.1002/mrd.23119openalex-snapshot
Embryo responses to stress induced by assisted reproductive technologies
inferred← citeshttps://doi.org/10.1002/stem.3029openalex-snapshot
Metabolomic and Transcriptional Analyses Reveal Atmospheric Oxygen During Human Induced Pluripotent Stem Cell Generation Impairs Metabolic Reprogramming
inferred← citeshttps://doi.org/10.1007/978-1-4614-6651-2_20openalex-snapshot
Metabolism of the Viable Human Embryo
inferred← citeshttps://doi.org/10.1007/978-1-4614-8376-2_22openalex-snapshot
Predicting Embryo Developmental Potential and Viability Using Automated Time-Lapse Analysis (Eeva Test)
inferred← citeshttps://doi.org/10.1007/978-3-319-16892-0_10openalex-snapshot
Prediction of Embryo Viability by Morphokinetic Evaluation to Facilitate Single Transfer
inferred← citeshttps://doi.org/10.1007/978-3-319-17849-3_8openalex-snapshot
Current Status of Time-Lapse Microscopy for Embryo Selection
inferred← citeshttps://doi.org/10.1007/978-3-319-43011-9_42openalex-snapshot
Predicting Embryo Developmental Potential and Viability Using Automated Time-Lapse Analysis (Eeva™ Test)
inferred← citeshttps://doi.org/10.1007/978-3-319-43011-9_74openalex-snapshot
Embryo Culture and Phenotype of the Offspring
inferred← citeshttps://doi.org/10.1007/s00404-023-07235-xopenalex-snapshot
Developmental competence and neonatal outcomes of nonpronuclear zygotes following single vitrified-warmed blastocyst transfers using propensity score matching analysis
inferred← citeshttps://doi.org/10.1007/s10815-014-0178-3openalex-snapshot
Altered cleavage patterns in human tripronuclear embryos and their association to fertilization method: A time-lapse study
inferred← citeshttps://doi.org/10.1007/s10815-014-0250-zopenalex-snapshot
Embryo catheter loading and embryo culture techniques: results of a worldwide web-based survey
inferred← citeshttps://doi.org/10.1007/s10815-014-0341-xopenalex-snapshot
Relative kinetic expressions defining cleavage synchronicity are better predictors of blastocyst formation and quality than absolute time points
inferred← citeshttps://doi.org/10.1007/s10815-015-0488-0openalex-snapshot
Unaltered timing of embryo development in women with polycystic ovarian syndrome (PCOS): a time-lapse study
inferred← citeshttps://doi.org/10.1007/s10815-015-0510-6openalex-snapshot
A critical appraisal of time-lapse imaging for embryo selection: where are we and where do we need to go?
inferred← citeshttps://doi.org/10.1007/s10815-016-0678-4openalex-snapshot
Time-lapse variables and embryo gender: a retrospective analysis of 81 live births obtained following minimal stimulation and single embryo transfer
inferred← citeshttps://doi.org/10.1007/s10815-016-0693-5openalex-snapshot
Comparison of 2, 5, and 20 % O2 on the development of post-thaw human embryos
inferred← citeshttps://doi.org/10.1007/s10815-017-0935-1openalex-snapshot
The effect of follicle size and homogeneity of follicular development on the morphokinetics of human embryos
inferred← citeshttps://doi.org/10.1007/s10815-017-0955-xopenalex-snapshot
Selecting embryos with the highest implantation potential using data mining and decision tree based on classical embryo morphology and morphokinetics
inferred← citeshttps://doi.org/10.1007/s10815-018-1265-7openalex-snapshot
Euploid embryos selected by an automated time-lapse system have superior SET outcomes than selected solely by conventional morphology assessment
inferred← citeshttps://doi.org/10.1007/s10815-018-1396-xopenalex-snapshot
A comparison of morphokinetic markers predicting blastocyst formation and implantation potential from two large clinical data sets
inferred← citeshttps://doi.org/10.1007/s10815-019-01567-xopenalex-snapshot
Performance of Day 5 KIDScore™ morphokinetic prediction models of implantation and live birth after single blastocyst transfer
inferred← citeshttps://doi.org/10.1007/s10815-019-01574-yopenalex-snapshot
Deconstructing the myth of poor prognosis for fast-cleaving embryos on day 3. Is it time to change the consensus?
inferred← citeshttps://doi.org/10.1007/s10815-020-01789-4openalex-snapshot
Between-laboratory reproducibility of time-lapse embryo selection using qualitative and quantitative parameters: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1007/s10815-021-02368-xopenalex-snapshot
GDF9 concentration in embryo culture medium is linked to human embryo quality and viability
inferred← citeshttps://doi.org/10.1007/s10815-023-02943-4openalex-snapshot
Oxygen concentration from days 1 to 3 after insemination affects the embryo culture quality, cumulative live birth rate, and perinatal outcomes
inferred← citeshttps://doi.org/10.1007/s10815-024-03385-2openalex-snapshot
Could cleaved embryo morphology and morphokinetics be associated with prenatal and neonatal outcomes?
inferred← citeshttps://doi.org/10.1007/s13577-021-00516-0openalex-snapshot
The optimal number of embryo cells for effective pregnancy and decrease of multiple pregnancy rate in frozen-thawed embryo transfer
inferred← citeshttps://doi.org/10.1007/s43032-020-00333-0openalex-snapshot
The Anti-oxidative Effects of Encapsulated Cysteamine During Mice In Vitro Matured Oocyte/Morula-Compact Stage Embryo Culture Model: a Comparison of High-Efficiency Nanocarriers for Hydrophilic Drug Delivery—a Pilot Study
inferred← citeshttps://doi.org/10.1007/s43032-021-00670-8openalex-snapshot
Enhanced Synergistic-Antioxidant Activity of Melatonin and Tretinoin by Co-encapsulation into Amphiphilic Chitosan Nanocarriers: During Mice In Vitro Matured Oocyte/Morula-Compact Stage Embryo Culture Model
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64857-2openalex-snapshot
Human Embryo Development and Assessment of Viability
inferred← citeshttps://doi.org/10.1016/b978-0-323-47912-7.00032-9openalex-snapshot
Gamete and Embryo Manipulation
inferred← citeshttps://doi.org/10.1016/j.bpc.2024.107199openalex-snapshot
Dependence of cell's membrane potential on extracellular voltage observed in Chara globularis
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2013.04.021openalex-snapshot
Improving embryo selection using a computer-automated time-lapse image analysis test plus day 3 morphology: results from a prospective multicenter trial
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2013.08.033openalex-snapshot
A time to look back: analysis of morphokinetic characteristics of human embryo development
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.05.043openalex-snapshot
Composition of commercial media used for human embryo culture
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.07.738openalex-snapshot
Clinical validation of embryo culture and selection by morphokinetic analysis: a randomized, controlled trial of the EmbryoScope
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.10.050openalex-snapshot
Is there a relationship between time-lapse parameters and embryo sex?
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.11.003openalex-snapshot
Choosing the best embryo by time lapse versus standard morphology
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.12.111openalex-snapshot
External validation of a time-lapse prediction model
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2015.03.017openalex-snapshot
Clinical significance of intercellular contact at the four-cell stage of human embryos, and the use of abnormal cleavage patterns to identify embryos with low implantation potential: a time-lapse study
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2015.07.1164openalex-snapshot
Influence of different oocyte insemination techniques on early and late morphokinetic parameters: retrospective analysis of 500 time-lapse monitored blastocysts
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2015.10.030openalex-snapshot
Improved implantation rates of day 3 embryo transfers with the use of an automated time-lapse–enabled test to aid in embryo selection
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2015.11.003openalex-snapshot
Time-lapse deselection model for human day 3 in vitro fertilization embryos: the combination of qualitative and quantitative measures of embryo growth
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2016.08.014openalex-snapshot
Structural and morphologic differences in human oocytes after in vitro maturation compared with standard in vitro fertilization
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2016.11.014openalex-snapshot
Examining the efficacy of six published time-lapse imaging embryo selection algorithms to predict implantation to demonstrate the need for the development of specific, in-house morphokinetic selection algorithms
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2017.07.013openalex-snapshot
Impact of 3.5% O2 culture on embryo development and clinical outcomes: a comparative study
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2017.10.036openalex-snapshot
Time-lapse algorithms and morphological selection of day-5 embryos for transfer: a preclinical validation study
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2021.02.002openalex-snapshot
Design and validation of a model for quality control monitoring of dichotomous in vitro fertilization outcomes
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2023.06.006openalex-snapshot
Association between a morphokinetic ploidy prediction model risk score and miscarriage and live birth: a multicentre cohort study
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2023.12.014openalex-snapshot
Impact of oxygen tension during in vitro maturation: a sibling-oocyte prospective double-blinded study
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.142858openalex-snapshot
Histone lactylation regulates early embryonic development through m6A methyltransferase METTL3 in goats
inferred← citeshttps://doi.org/10.1016/j.medre.2022.100118openalex-snapshot
Extended embryo culture up to 14 days
inferred← citeshttps://doi.org/10.1016/j.rbmo.2013.04.013openalex-snapshot
Retrospective analysis of outcomes after IVF using an aneuploidy risk model derived from time-lapse imaging without PGS
inferred← citeshttps://doi.org/10.1016/j.rbmo.2014.03.026openalex-snapshot
Comparison of gender-specific human embryo development characteristics by time-lapse technology
inferred← citeshttps://doi.org/10.1016/j.rbmo.2014.09.005openalex-snapshot
Computer-automated time-lapse analysis results correlate with embryo implantation and clinical pregnancy: A blinded, multi-centre study
inferred← citeshttps://doi.org/10.1016/j.rbmo.2015.02.008openalex-snapshot
Cleavage pattern predicts developmental potential of day 3 human embryos produced by IVF
inferred← citeshttps://doi.org/10.1016/j.rbmo.2016.08.003openalex-snapshot
Combined effects of individual culture and atmospheric oxygen on preimplantation mouse embryos in vitro
inferred← citeshttps://doi.org/10.1016/j.rbmo.2018.12.014openalex-snapshot
Prolonged blastomere movement induced by the delay of pronuclear fading and first cell division adversely affects pregnancy outcomes after fresh embryo transfer on Day 2: a time-lapse study
inferred← citeshttps://doi.org/10.1016/j.rbmo.2019.03.102openalex-snapshot
Individual culture and atmospheric oxygen during culture affect mouse preimplantation embryo metabolism and post-implantation development
inferred← citeshttps://doi.org/10.1016/j.rbmo.2019.10.003openalex-snapshot
‘There is only one thing that is truly important in an IVF laboratory: everything’ Cairo Consensus Guidelines on IVF Culture Conditions
inferred← citeshttps://doi.org/10.1016/j.rbmo.2020.01.026openalex-snapshot
Prospective randomized multicentre comparison on sibling oocytes comparing G-Series media system with antioxidants versus standard G-Series media system
inferred← citeshttps://doi.org/10.1016/j.rbmo.2020.09.030openalex-snapshot
Are morphokinetic parameters of embryo development associated with adverse perinatal outcomes following fresh blastocyst transfer?
inferred← citeshttps://doi.org/10.1016/j.rbmo.2025.104955openalex-snapshot
The Istanbul Consensus update: a revised ESHRE/ALPHA consensus on oocyte and embryo static and dynamic morphological assessment† ‡
inferred← citeshttps://doi.org/10.1016/j.repbio.2015.09.001openalex-snapshot
Assessment of human embryos by time-lapse videography: A comparison of quantitative and qualitative measures between two independent laboratories
inferred← citeshttps://doi.org/10.1016/j.repbio.2020.03.011openalex-snapshot
Mouse embryos exposed to oxygen concentrations that mimic changes in the oviduct and uterus show improvement in blastocyst rate, blastocyst size, and accelerated cell division
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.01.065openalex-snapshot
Label-free microscopy: A non-invasive new tool to assess gametes and embryo quality
inferred← citeshttps://doi.org/10.1016/j.tibtech.2021.01.007openalex-snapshot
Oxygen-Releasing Biomaterials: Current Challenges and Future Applications
inferred← citeshttps://doi.org/10.1016/j.tjog.2017.12.013openalex-snapshot
Effect of morphokinetics and morphological dynamics of cleavage stage on embryo developmental potential: A time-lapse study
inferred← citeshttps://doi.org/10.1017/9781108611633.009openalex-snapshot
The Clinical In-Vitro Fertilization Laboratory
inferred← citeshttps://doi.org/10.1017/9781108611633.012openalex-snapshot
Oocyte Retrieval and Embryo Culture
inferred← citeshttps://doi.org/10.1017/9781108874014.006openalex-snapshot
Culture Media and Embryo Culture
inferred← citeshttps://doi.org/10.1017/9781316569238.035openalex-snapshot
Embryo Culture and Assessment via Time-Lapse Microscopy in the IVF laboratory
inferred← citeshttps://doi.org/10.1017/9781316756744.020openalex-snapshot
Physiology and Culture of the Early Human Embryo
inferred← citeshttps://doi.org/10.1017/cbo9781139059053.018openalex-snapshot
Time-lapse imaging of embryo development: using morphokinetic analysis to select viable embryos
inferred← citeshttps://doi.org/10.1017/s0967199420000179openalex-snapshot
Reactive oxygen species in reproduction: harmful, essential or both?
inferred← citeshttps://doi.org/10.1017/s0967199420000337openalex-snapshot
Effects of oxygen concentrations on developmental competence and transcriptomic profile of yak oocytes
inferred← citeshttps://doi.org/10.1017/s2040174417000368openalex-snapshot
Impact of the IVF laboratory environment on human preimplantation embryo phenotype
inferred← citeshttps://doi.org/10.1038/s41598-021-01488-9openalex-snapshot
Impact of oxygen tension according to embryo stage of development: a prospective randomized study
inferred← citeshttps://doi.org/10.1038/s41598-022-06158-yopenalex-snapshot
The effects of temperature variation treatments on embryonic development: a mouse study
inferred← citeshttps://doi.org/10.1055/s-0040-1718443openalex-snapshot
Follicular Fluid from Infertile Women with Mild Endometriosis Impairs In Vitro Bovine Embryo Development: Potential Role of Oxidative Stress
inferred← citeshttps://doi.org/10.1071/rd19225openalex-snapshot
Morphokinetics of early equine embryo development in vitro using time-lapse imaging, and use in selecting blastocysts for transfer
inferred← citeshttps://doi.org/10.1080/09513590.2018.1462315openalex-snapshot
Low oxygen environment facilitates embryo availability for older ovarian responders (PORs)
inferred← citeshttps://doi.org/10.1080/14647273.2016.1255357openalex-snapshot
How do laboratory embryo transfer techniques affect IVF outcomes? A review of current literature
inferred← citeshttps://doi.org/10.1080/14647273.2018.1425919openalex-snapshot
Assessing efficacy of day 3 embryo time-lapse algorithms retrospectively: impacts of dataset type and confounding factors
inferred← citeshttps://doi.org/10.1080/19396368.2020.1754961openalex-snapshot
The effect of low and ultra-low oxygen tensions on mammalian embryo culture and development in experimental and clinical IVF
inferred← citeshttps://doi.org/10.1080/19396368.2020.1834008openalex-snapshot
Modification of late human embryo development after blastomere removal on day 3 for preimplantation genetic testing
inferred← citeshttps://doi.org/10.1080/19396368.2024.2439838openalex-snapshot
In vitro fertilization, intracytoplasmic sperm injection, in vitro maturation, and embryo culture
inferred← citeshttps://doi.org/10.1093/biolre/ioab031openalex-snapshot
Time-lapse imaging of human embryos fertilized with testicular sperm reveals an impact on the first embryonic cell cycle
inferred← citeshttps://doi.org/10.1093/biolre/ioy229openalex-snapshot
Is differences in embryo morphokinetic development significantly associated with human embryo sex?†
inferred← citeshttps://doi.org/10.1093/hropen/hoaa008openalex-snapshot
Good practice recommendations for the use of time-lapse technology†
inferred← citeshttps://doi.org/10.1093/hropen/hoz036openalex-snapshot
Reduced oxygen concentration during human IVF culture improves embryo utilization and cumulative pregnancy rates per cycle
inferred← citeshttps://doi.org/10.1093/humrep/deac020openalex-snapshot
A double-blind randomized controlled trial investigating a time-lapse algorithm for selecting Day 5 blastocysts for transfer
inferred← citeshttps://doi.org/10.1093/humrep/deaf021openalex-snapshot
The Istanbul consensus update: a revised ESHRE/ALPHA consensus on oocyte and embryo static and dynamic morphological assessment,
inferred← citeshttps://doi.org/10.1093/humrep/det300openalex-snapshot
Time-lapse parameters as predictors of blastocyst development and pregnancy outcome in embryos from good prognosis patients: a prospective cohort study
inferred← citeshttps://doi.org/10.1093/humrep/deu316openalex-snapshot
No benefit of culturing embryos in a closed system compared with a conventional incubator in terms of number of good quality embryos: results from an RCT
inferred← citeshttps://doi.org/10.1093/humrep/deu334openalex-snapshot
Developmental kinetics of cleavage stage mouse embryos are related to their subsequent carbohydrate and amino acid utilization at the blastocyst stage
inferred← citeshttps://doi.org/10.1093/humrep/dev125openalex-snapshot
In vitromaturation is associated with increased early embryo arrest without impairing morphokinetic development of useable embryos progressing to blastocysts
inferred← citeshttps://doi.org/10.1093/humrep/dev296openalex-snapshot
Timing of human preimplantation embryonic development is confounded by embryo origin
inferred← citeshttps://doi.org/10.1093/humrep/dew183openalex-snapshot
Correlation between aneuploidy, standard morphology evaluation and morphokinetic development in 1730 biopsied blastocysts: a consecutive case series study
inferred← citeshttps://doi.org/10.1093/humrep/dew188openalex-snapshot
Development of a generally applicable morphokinetic algorithm capable of predicting the implantation potential of embryos transferred on Day 3
inferred← citeshttps://doi.org/10.1093/humrep/dey091openalex-snapshot
Should extended blastocyst culture include Day 7?
inferred← citeshttps://doi.org/10.1093/humrep/dey386openalex-snapshot
Association between outdoor air pollution during in vitro culture and the outcomes of frozen–thawed embryo transfer
inferred← citeshttps://doi.org/10.1093/humrep/dez085openalex-snapshot
Can novel early non-invasive biomarkers of embryo quality be identified with time-lapse imaging to predict live birth?
inferred← citeshttps://doi.org/10.1093/humupd/dmac022openalex-snapshot
Morphological and morphokinetic associations with aneuploidy: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1093/humupd/dmu064openalex-snapshot
Diagnosis of human preimplantation embryo viability
inferred← citeshttps://doi.org/10.1093/humupd/dmv034openalex-snapshot
The effects of chemical and physical factors on mammalian embryo culture and their importance for the practice of assisted human reproduction
inferred← citeshttps://doi.org/10.1093/molehr/gaw057openalex-snapshot
Assessment of human embryo development using morphological criteria in an era of time-lapse, algorithms and ‘OMICS’: is looking good still important?
inferred← citeshttps://doi.org/10.1097/gco.0000000000000072openalex-snapshot
Time-lapse embryo imaging technology
inferred← citeshttps://doi.org/10.1111/and.13061openalex-snapshot
Influence of human sperm origin, testicular or ejaculated, on embryo morphokinetic development
inferred← citeshttps://doi.org/10.1111/jog.15797openalex-snapshot
The effect of embryo selection using time‐lapse monitoring on IVF / ICSI outcomes: A systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1134/s1062360416020077openalex-snapshot
Hypoxia during mammalian preimplantation development: Extreme circumstance vs. typical environment
inferred← citeshttps://doi.org/10.1155/2017/2874283openalex-snapshot
Pluripotent Stem Cell Metabolism and Mitochondria: Beyond ATP
inferred← citeshttps://doi.org/10.1177/1933719115602761openalex-snapshot
Better Quality and More Usable Embryos Obtained on Day 3 Cultured in 5% Than 20% Oxygen: A Controlled and Randomized Study Using the Sibling Oocytes
inferred← citeshttps://doi.org/10.1177/2058915816663858openalex-snapshot
Morphokinetics of embryos—where are we now?
inferred← citeshttps://doi.org/10.1177/2633494120976921openalex-snapshot
The clinical use of time-lapse in human-assisted reproduction
inferred← citeshttps://doi.org/10.1186/1477-7827-12-54openalex-snapshot
Analysis of embryo morphokinetics, multinucleation and cleavage anomalies using continuous time-lapse monitoring in blastocyst transfer cycles
inferred← citeshttps://doi.org/10.1186/s13048-017-0344-1openalex-snapshot
Low oxygen tension increases mitochondrial membrane potential and enhances expression of antioxidant genes and implantation protein of mouse blastocyst cultured in vitro
inferred← citeshttps://doi.org/10.1201/9781315157269-14openalex-snapshot
Human Embryo Development and Assessment of Viability
inferred← citeshttps://doi.org/10.1371/journal.pone.0178720openalex-snapshot
Does time-lapse imaging have favorable results for embryo incubation and selection compared with conventional methods in clinical in vitro fertilization? A meta-analysis and systematic review of randomized controlled trials
inferred← citeshttps://doi.org/10.1371/journal.pone.0183328openalex-snapshot
Inter-laboratory agreement on embryo classification and clinical decision: Conventional morphological assessment vs. time lapse
inferred← citeshttps://doi.org/10.1371/journal.pone.0274502openalex-snapshot
Nucleation status of Day 2 pre-implantation embryos, acquired by time-lapse imaging during IVF, is associated with live birth
inferred← citeshttps://doi.org/10.1371/journal.pone.0318480openalex-snapshot
Predicting IVF live -birth probability using time-lapse data: Implications of including or excluding age in a day 2 embryo transfer model
inferred← citeshttps://doi.org/10.14715/cmb/2017.63.8.18openalex-snapshot
Morphokinetic analysis of human embryo development and its relationship to the female age: a retrospective time-lapse imaging study
inferred← citeshttps://doi.org/10.1515/almed-2020-0095openalex-snapshot
Transferencia embrionaria única: estrategia clave para reducir el riesgo de embarazo múltiple en reproducción humana asistida
inferred← citeshttps://doi.org/10.1515/almed-2021-0013openalex-snapshot
Single-embryo transfer: a key strategy to reduce the risk for multiple pregnancy in assisted human reproduction
inferred← citeshttps://doi.org/10.1530/rep-20-0322openalex-snapshot
HYPOXIA AND REPRODUCTIVE HEALTH: Hypoxic regulation of preimplantation embryos: lessons from human embryonic stem cells
inferred← citeshttps://doi.org/10.17816/jowd609504openalex-snapshot
TIME-LAPSE technology in modern embryological practice
inferred← citeshttps://doi.org/10.21608/jsrs.2023.331811openalex-snapshot
Efficacy of Laser-Assisted Hatching on Pregnancy and Live-Birth Rates of Human Frozen-Thawed Embryos
inferred← citeshttps://doi.org/10.24425/124296openalex-snapshot
CO2 concentration affects in vitro pig embryo developmental capacity
inferred← citeshttps://doi.org/10.26686/wgtn.22082537openalex-snapshot
Developing In Vitro Models of Human Embryonic Aneuploidy
inferred← citeshttps://doi.org/10.3109/14647273.2014.944417openalex-snapshot
ACE consensus meeting report: Culture systems
inferred← citeshttps://doi.org/10.3389/fcell.2022.881550openalex-snapshot
Update on the Epigenomic Implication of Embryo Cryopreservation Methods Applied in Assisted Reproductive Technologies With Potential Long-Term Health Effects
inferred← citeshttps://doi.org/10.3389/fendo.2020.00246openalex-snapshot
Intraindividual Embryo Morphokinetics Are Not Affected by a Switch of the Ovarian Stimulation Protocol Between GnRH Agonist vs. Antagonist Regimens in Consecutive Cycles
inferred← citeshttps://doi.org/10.3390/biom16030341openalex-snapshot
Impacts of Oxygen Tension on Developmental Competence of Preimplantation Embryos
inferred← citeshttps://doi.org/10.3390/cells12030390openalex-snapshot
Genes Involved in DNA Repair and Mitophagy Protect Embryoid Bodies from the Toxic Effect of Methylmercury Chloride under Physioxia Conditions
inferred← citeshttps://doi.org/10.3390/ijms24010393openalex-snapshot
Sperm Chromatin Condensation Defect Accelerates the Kinetics of Early Embryonic Development but Does Not Modify ICSI Outcome
inferred← citeshttps://doi.org/10.3390/jcm10215173openalex-snapshot
Differences in Morphokinetic Parameters and Incidence of Multinucleations in Human Embryos of Genetically Normal, Abnormal and Euploid Embryos Leading to Clinical Pregnancy
inferred← citeshttps://doi.org/10.3390/jcm11195722openalex-snapshot
Opportunities and Limits of Conventional IVF versus ICSI: It Is Time to Come off the Fence
inferred← citeshttps://doi.org/10.3390/jcm14134596openalex-snapshot
Day 4 Versus Day 5 Fresh Embryo Transfer in In Vitro Fertilization: Is It All About Timing?
inferred← citeshttps://doi.org/10.3390/jcm9082609openalex-snapshot
Metabolic Activity of Human Embryos after Thawing Differs in Atmosphere with Different Oxygen Concentrations
inferred← citeshttps://doi.org/10.3390/jox14040087openalex-snapshot
Environmental Stress-Induced Alterations in Embryo Developmental Morphokinetics
inferred← citeshttps://doi.org/10.3390/pr7070450openalex-snapshot
Do Bioreactor Designs with More Efficient Oxygen Supply to Ovarian Cortical Tissue Fragments Enhance Follicle Viability and Growth In Vitro?
inferred← citeshttps://doi.org/10.4103/2305-0500.298773openalex-snapshot
Time-lapse videography reveals different morphokinetic profiles of human embryos displaying direct or reverse cleavage at different stages of development: A retrospective sibling embryo study
inferred← citeshttps://doi.org/10.5152/jtgga.2014.13068openalex-snapshot
Reproducibility of a time-lapse embryo selection model based on morphokinetic data in a sequential culture media setting
inferred← citeshttps://doi.org/10.5507/bp.2022.052openalex-snapshot
Prediction of live birth - selection of embryos using morphokinetic parameters
inferred← citeshttps://doi.org/10.56093/ijans.v92i10.104284openalex-snapshot
Effect of hypoxia on production of caprine chimeric blastocyst
inferred← citeshttps://doi.org/10.5935/1518-0557.20180041openalex-snapshot
External validation of a time-lapse model; a retrospective study comparing embryo evaluation using a morphokinetic model to standard morphology with live birth as endpoint
inferred← citeshttps://doi.org/10.5935/1518-0557.20180042openalex-snapshot
Morphology vs morphokinetics: a retrospective comparison of interobserver and intra-observer agreement between embryologists on blastocysts with known implantation outcome
inferred← citeshttps://doi.org/10.5935/1518-0557.20200035openalex-snapshot
Morphokinetic parameters as auxiliary criteria for selection of blastocysts cultivated in a time-lapse monitoring system
inferred← citeshttps://doi.org/10.5935/1518-0557.20210051openalex-snapshot
Rate of Post-Fertilization Mitotic Activity Predicts Embryonic Competence via Next Generation Sequencing: An Analysis of 39,301 Cleavage Stage Embryos
inferred← citeshttps://doi.org/10.5935/1518-0557.20210107openalex-snapshot
Time-Lapse Embryo culture: A better understanding of embryo development and clinical application
inferred← citeshttps://doi.org/10.7287/peerj.9738v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Comparing transcriptome profiles of human embryo cultured in closed and standard incubators (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.9738v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Comparing transcriptome profiles of human embryo cultured in closed and standard incubators (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.9738v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Comparing transcriptome profiles of human embryo cultured in closed and standard incubators (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.9738v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Comparing transcriptome profiles of human embryo cultured in closed and standard incubators (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.9738openalex-snapshot
Comparing transcriptome profiles of human embryo cultured in closed and standard incubators
inferred← citeshttps://doi.org/10.7759/cureus.63075openalex-snapshot
Diameter of Human Day Five Blastocysts and Birth Sex
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