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Molecular control of mitochondrial function in preimplantation mouse embryos
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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/(sici)1098-2795(199904)52:4<427::aid-mrd12>3.0.co;2-gopenalex-snapshot
Changes in poly(A) tail length of maternal transcripts during in vitro maturation of bovine oocytes and their relation with developmental competence
inferredcites →https://doi.org/10.1002/(sici)1098-2795(199905)53:1<8::aid-mrd2>3.0.co;2-kopenalex-snapshot
Alterations in the relative abundance of gene transcripts in preimplantation bovine embryos cultured in medium supplemented with either serum or PVA
inferredcites →https://doi.org/10.1002/dvg.1020130502openalex-snapshot
The genetic program for preimplantation development
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb04770.xopenalex-snapshot
A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication.
inferredcites →https://doi.org/10.1002/mrd.1080400105openalex-snapshot
Mitochondrial biogenesis in early mouse embryos: Expression of the mRNAs for subunits IV, Vb, and VIIc of cytochrome c oxidase and subunit 9 (P1) of H+‐ATP synthase
inferredcites →https://doi.org/10.1016/0012-1606(76)90253-0openalex-snapshot
Number of mitochondria and some properties of mitochondrial DNA in the mouse egg
inferredcites →https://doi.org/10.1016/0012-1606(87)90395-2openalex-snapshot
Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos
inferredcites →https://doi.org/10.1016/0092-8674(77)90286-0openalex-snapshot
Mouse L cell mitochondrial DNA molecules are selected randomly for replication throughout the cell cycle
inferredcites →https://doi.org/10.1016/0092-8674(84)90343-xopenalex-snapshot
Precise identification of individual promoters for transcription of each strand of human mitochondrial DNA
inferredcites →https://doi.org/10.1016/s0093-691x(01)00481-2openalex-snapshot
The maternal legacy to the embryo: cytoplasmic components and their effects on early development
inferredcites →https://doi.org/10.1016/s0168-9525(01)02238-7openalex-snapshot
What regulates mitochondrial DNA copy number in animal cells?
inferredcites →https://doi.org/10.1016/s1472-6483(10)61277-1openalex-snapshot
Mitochondrial DNA turnover occurs during preimplantation development and can be modulated by environmental factors
inferredcites →https://doi.org/10.1038/ng0398-231openalex-snapshot
Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice
inferredcites →https://doi.org/10.1038/ng909openalex-snapshot
Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA
inferredcites →https://doi.org/10.1071/rd04084openalex-snapshot
Role of the mitochondrial genome in preimplantation development and assisted reproductive technologies
inferredcites →https://doi.org/10.1073/pnas.91.4.1309openalex-snapshot
Activation of the human mitochondrial transcriptionfactor A gene by nuclear respiratory factors: a potential regulatory linkbetween nuclear and mitochondrial gene expression in organellebiogenesis.
inferredcites →https://doi.org/10.1074/jbc.274.21.14779openalex-snapshot
Functional Interactions of Mitochondrial DNA Polymerase and Single-stranded DNA-binding Protein
inferredcites →https://doi.org/10.1074/jbc.m103399200openalex-snapshot
hPop5, a Protein Subunit of the Human RNase MRP and RNase P Endoribonucleases
inferredcites →https://doi.org/10.1083/jcb.135.4.883openalex-snapshot
In situ localization of mitochondrial DNA replication in intact mammalian cells.
inferredcites →https://doi.org/10.1093/humrep/13.10.2857openalex-snapshot
Mitochondrial transfer between oocytes: potential applications of mitochondrial donation and the issue of heteroplasmy
inferredcites →https://doi.org/10.1093/humrep/15.suppl_2.11openalex-snapshot
Transcription and replication of mitochondrial DNA
inferredcites →https://doi.org/10.1093/humrep/16.5.909openalex-snapshot
Mitochondrial aggregation patterns and activity in human oocytes and preimplantation embryos
inferredcites →https://doi.org/10.1093/humupd/1.2.91openalex-snapshot
Culture of preimplantation embryos: facts and artifacts
inferredcites →https://doi.org/10.1093/molehr/gah004openalex-snapshot
Alterations in mitochondrial membrane potential during preimplantation stages of mouse and human embryo development
inferredcites →https://doi.org/10.1093/toxsci/49.2.290openalex-snapshot
Quantitative polymerase chain reaction using an external control mRNA for determination of gene expression in a heterogeneous cell population
inferredcites →https://doi.org/10.1095/biolreprod.102.006320openalex-snapshot
Quantification of Housekeeping Transcript Levels During the Development of Bovine Preimplantation Embryos1
inferredcites →https://doi.org/10.1095/biolreprod62.4.847openalex-snapshot
Energy Metabolism in Preimplantation Bovine Embryos Derived In Vitro or In Vivo1
inferredcites →https://doi.org/10.1095/biolreprod62.6.1866openalex-snapshot
Oxidative Phosphorylation-Dependent and -Independent Oxygen Consumption by Individual Preimplantation Mouse Embryos1
inferredcites →https://doi.org/10.1101/gad.4.6.1023openalex-snapshot
NRF-1: a trans-activator of nuclear-encoded respiratory genes in animal cells.
inferredcites →https://doi.org/10.1128/mcb.22.4.1116-1125.2002openalex-snapshot
A Human Mitochondrial Transcription Factor Is Related to RNA Adenine Methyltransferases and Binds S-Adenosylmethionine
inferredcites →https://doi.org/10.1146/annurev.biochem.66.1.409openalex-snapshot
MITOCHONDRIAL DNA MAINTENANCE IN VERTEBRATES
inferredcites →https://doi.org/10.1242/jcs.110.10.1147openalex-snapshot
Changes in histone synthesis and modification at the beginning of mouse development correlate with the establishment of chromatin mediated repression of transcription
inferredcites →https://doi.org/10.1530/biosciprocs.14.003openalex-snapshot
Cytoplasmic inheritance and its effects on development and performance
inferredcites →https://doi.org/10.1530/jrf.0.0720009openalex-snapshot
Pyruvate and glucose uptake by mouse ova and preimplantation embryos
inferredcites →https://doi.org/10.1530/rep.0.1260197openalex-snapshot
Energy metabolism in pig oocytes and early embryos
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mitochondrial DNA Quantification Correlates with the Developmental Potential of Human Euploid Blastocysts but not with that of Mosaic Blastocysts
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Correlation of the Mitochondrial Activity of Two‐Cell Embryos Produced In Vitro and the Two‐Cell Block In Kunming and B6C3F1 Mice
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Intracellular evolution of mitochondrial DNA (mtDNA) and the tragedy of the cytoplasmic commons
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Expression of mitochondrial transcription factor A (TFAM) during porcine gametogenesis and preimplantation embryo development
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Characterization of a donor mitochondrial DNA transmission bottleneck in nuclear transfer derived cow lineages
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BH4 peptide derived from Bcl‐xL and Bax‐inhibitor peptide suppresses apoptotic mitochondrial changes in heat stressed bovine oocytes
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Modulation of autophagy influences development and apoptosis in mouse embryos developing in vitro
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Stress‐induced alterations in oocyte transcripts are further expressed in the developing blastocyst
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Theory about the Embryo Cryo‐Treatment
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Transmission of Dysfunctional Mitochondrial DNA and Its Implications for Mammalian Reproduction
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Assisted Reproductive Technologies: The Potential to Prevent the Transmission of Mutant mtDNA from One Generation to the Next
inferred← citeshttps://doi.org/10.1007/s00441-012-1444-2openalex-snapshot
Transmission, inheritance and replication of mitochondrial DNA in mammals: implications for reproductive processes and infertility
inferred← citeshttps://doi.org/10.1007/s10815-011-9588-7openalex-snapshot
The contribution of mitochondrial function to reproductive aging
inferred← citeshttps://doi.org/10.1007/s10815-017-1070-8openalex-snapshot
Mitochondrial DNA content is associated with ploidy status, maternal age, and oocyte maturation methods in mouse blastocysts
inferred← citeshttps://doi.org/10.1007/s10815-018-1113-9openalex-snapshot
Blastulation timing is associated with differential mitochondrial content in euploid embryos
inferred← citeshttps://doi.org/10.1007/s10815-019-01520-yopenalex-snapshot
Cleavage stage mitochondrial DNA is correlated with preimplantation human embryo development and ploidy status
inferred← citeshttps://doi.org/10.1007/s10815-020-02045-5openalex-snapshot
Suboptimal trophectoderm mitochondrial DNA level is associated with delayed blastocyst development
inferred← citeshttps://doi.org/10.1007/s10815-023-02952-3openalex-snapshot
The effect of vitrification on blastocyst mitochondrial DNA dynamics and gene expression profiles
inferred← citeshttps://doi.org/10.1007/s11427-022-2349-9openalex-snapshot
KLF4 facilitates chromatin accessibility remodeling in porcine early embryos
inferred← citeshttps://doi.org/10.1007/s12015-009-9058-0openalex-snapshot
The Relationship Between Pluripotency and Mitochondrial DNA Proliferation During Early Embryo Development and Embryonic Stem Cell Differentiation
inferred← citeshttps://doi.org/10.1007/s12015-011-9318-7openalex-snapshot
The Effects of Nuclear Reprogramming on Mitochondrial DNA Replication
inferred← citeshttps://doi.org/10.1007/s12522-011-0101-xopenalex-snapshot
Mitochondrial biology in reproduction
inferred← citeshttps://doi.org/10.1007/s43032-025-01816-8openalex-snapshot
Green Synthesis of Copper Nanoparticles using Rosmarinus officinalis L. Extract Improves the Developmental Competence of Mouse Oocytes during in Vitro Maturation
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64862-6openalex-snapshot
Mitochondria and Embryo Viability
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00005-5openalex-snapshot
Mitochondrial DNA: Structure, Genetics, Replication and Defects
inferred← citeshttps://doi.org/10.1016/b978-0-12-813209-8.00020-0openalex-snapshot
Mitochondria Research in Human Reproduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-816561-4.00009-0openalex-snapshot
Mitochondrial genetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-819621-2.00001-2openalex-snapshot
Tissue specificity of energy metabolism in mitochondria
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00296-0openalex-snapshot
Mitochondria and Embryo Viability
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2017.10.012openalex-snapshot
The Mitochondria and the Regulation of Cell Fitness During Early Mammalian Development
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Effect of peroxiredoxin II on the quality and mitochondrial activity of pre-implantation bovine embryos
inferred← citeshttps://doi.org/10.1016/j.bbabio.2012.03.019openalex-snapshot
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.03.002openalex-snapshot
The inheritance of pathogenic mitochondrial DNA mutations
inferred← citeshttps://doi.org/10.1016/j.bbagen.2011.10.014openalex-snapshot
Prevention of mitochondrial disease inheritance by assisted reproductive technologies: Prospects and challenges
inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.10.036openalex-snapshot
The control of mtDNA replication during differentiation and development
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.08.143openalex-snapshot
Over-expression of Tfam improves the mitochondrial disease phenotypes in a mouse model system
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.07.013openalex-snapshot
Sanguinarine cytotoxicity on mouse melanoma K1735-M2 cells—Nuclear vs. mitochondrial effects
inferred← citeshttps://doi.org/10.1016/j.cdev.2023.203859openalex-snapshot
Cell starvation regulates ceramide-induced autophagy in mouse preimplantation embryo development
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117615openalex-snapshot
ER-mitochondria contacts and mitochondrial fusion correlate with increased mitochondrial activity during vertebrate embryogenesis
inferred← citeshttps://doi.org/10.1016/j.cyto.2018.07.025openalex-snapshot
Interleukin-7 improves in vitro maturation of ovine cumulus-oocyte complexes in a dose dependent manner
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2012.11.031openalex-snapshot
The aging oocyte—can mitochondrial function be improved?
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2018.11.048openalex-snapshot
Mitochondrial unfolded protein response: a stress response with implications for fertility and reproductive aging
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112337openalex-snapshot
Origin and development of uniparental and polyploid blastomeres
inferred← citeshttps://doi.org/10.1016/j.jare.2023.11.033openalex-snapshot
New insights on mitochondrial heteroplasmy observed in ovarian diseases
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.10.019openalex-snapshot
Mitochondrial DNA Purifying Selection in Mammals and Invertebrates
inferred← citeshttps://doi.org/10.1016/j.livsci.2014.05.024openalex-snapshot
Cytoplasmatic inheritance, epigenetics and reprogramming DNA as tools in animal breeding
inferred← citeshttps://doi.org/10.1016/j.mito.2007.05.002openalex-snapshot
Mitochondria in stem cells
inferred← citeshttps://doi.org/10.1016/j.mito.2008.09.001openalex-snapshot
Rat visceral yolk sac (VYS) and placenta mitochondrial features during the placentation period
inferred← citeshttps://doi.org/10.1016/j.mito.2009.12.144openalex-snapshot
Microinjection of serum-starved mitochondria derived from somatic cells affects parthenogenetic development of bovine and murine oocytes
inferred← citeshttps://doi.org/10.1016/j.mito.2010.11.004openalex-snapshot
Therapeutic treatments of mtDNA diseases at the earliest stages of human development
inferred← citeshttps://doi.org/10.1016/j.mito.2010.12.013openalex-snapshot
Dynamic regulation of mitochondrial function in preimplantation embryos and embryonic stem cells
inferred← citeshttps://doi.org/10.1016/j.mito.2016.09.001openalex-snapshot
Alterations of mitochondrial biogenesis in chronic lymphocytic leukemia cells with loss of p53
inferred← citeshttps://doi.org/10.1016/j.mito.2017.10.011openalex-snapshot
The mitochondrial uncoupling protein 2 gene is causal for the spontaneous polycystic liver diseases in mice
inferred← citeshttps://doi.org/10.1016/j.omtn.2021.11.016openalex-snapshot
DdCBE mediates efficient and inheritable modifications in mouse mitochondrial genome
inferred← citeshttps://doi.org/10.1016/j.omtn.2024.102170openalex-snapshot
Secondary follicles enable efficient germline mtDNA base editing at hard-to-edit site
inferred← citeshttps://doi.org/10.1016/j.reprotox.2015.04.007openalex-snapshot
Effects of mono(2-ethylhexyl)phthalate on cytoplasmic maturation of oocytes – The bovine model
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The role of mitochondrial dynamics in oocyte and early embryo development
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Advancing maternal age predisposes to mitochondrial damage and loss during maturation of equine oocytes in vitro
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.06.009openalex-snapshot
Improving the cytoplasmic maturation of bovine oocytes matured in vitro with intracellular and/or extracellular antioxidants is not associated with increased rates of embryo development
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.07.017openalex-snapshot
Mitochondrial DNA content and developmental competence of blastocysts derived from pre-pubertal heifer oocytes
inferred← citeshttps://doi.org/10.1016/j.tice.2025.102819openalex-snapshot
Developmental competence of ovum pick up derived Sahiwal cow oocytes in maturation media supplemented with cysteamine and melatonin
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Mono(2-ethylhexyl) phthalate (MEHP) induces transcriptomic alterations in oocytes and their derived blastocysts
inferred← citeshttps://doi.org/10.1016/j.xfss.2020.05.001openalex-snapshot
Mitochondrial DNA content decreases during in vitro human embryo development: insights into mitochondrial DNA variation in preimplantation embryos donated for research
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Mitochondrial DNA in the Oocyte and the Developing Embryo
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77004-1openalex-snapshot
Mitochondrial DNA and the Mammalian Oocyte
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77009-0openalex-snapshot
Impact of Assisted Reproductive Technologies: A Mitochondrial Perspective of Cytoplasmic Transplantation
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77010-7openalex-snapshot
Nuclear Transfer: Preservation of a Nuclear Genome at the Expense of Its Associated mtDNA Genome(s)
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60409-9openalex-snapshot
Variations in mouse mitochondrial DNA copy number from fertilization to birth are associated with oxidative stress
inferred← citeshttps://doi.org/10.1017/cbo9780511674747.014openalex-snapshot
Description of muscle disease – specific diseases
inferred← citeshttps://doi.org/10.1017/cbo9780511674747.023openalex-snapshot
Mitochondrial myopathies
inferred← citeshttps://doi.org/10.1038/cdd.2014.66openalex-snapshot
Mitochondrial metabolism directs stemness and differentiation in P19 embryonal carcinoma stem cells
inferred← citeshttps://doi.org/10.1038/cddis.2015.34openalex-snapshot
Mitochondrial DNA copy number is regulated by DNA methylation and demethylation of POLGA in stem and cancer cells and their differentiated progeny
inferred← citeshttps://doi.org/10.1038/emboj.2012.71openalex-snapshot
HIF1α induced switch from bivalent to exclusively glycolytic metabolism during ESC‐to‐EpiSC/hESC transition
inferred← citeshttps://doi.org/10.1038/nrg2396openalex-snapshot
Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease
inferred← citeshttps://doi.org/10.1038/s41598-019-41801-1openalex-snapshot
Mitochondrial DNA and genomic DNA ratio in embryo culture medium is not a reliable predictor for in vitro fertilization outcome
inferred← citeshttps://doi.org/10.1038/srep03844openalex-snapshot
Therapeutic potential of somatic cell nuclear transfer for degenerative disease caused by mitochondrial DNA mutations
inferred← citeshttps://doi.org/10.1038/srep23229openalex-snapshot
Restoration of normal embryogenesis by mitochondrial supplementation in pig oocytes exhibiting mitochondrial DNA deficiency
inferred← citeshttps://doi.org/10.1071/rd04084openalex-snapshot
Role of the mitochondrial genome in preimplantation development and assisted reproductive technologies
inferred← citeshttps://doi.org/10.1071/rd08078openalex-snapshot
Molecular control of mitochondrial function in developing rhesus monkey oocytes and preimplantation-stage embryos
inferred← citeshttps://doi.org/10.1071/rd10076openalex-snapshot
Asymmetrical allocation of mitochondrial DNA to blastomeres during the first two cleavages in mouse embryos
inferred← citeshttps://doi.org/10.1071/rd13359openalex-snapshot
Mitochondria and vesicles differ between adult and prepubertal sheep oocytes during IVM
inferred← citeshttps://doi.org/10.1071/rd14300openalex-snapshot
Effects of ovarian hyperstimulation on mitochondria in oocytes and early embryos
inferred← citeshttps://doi.org/10.1071/rd14450openalex-snapshot
Maternal age and in vitro culture affect mitochondrial number and function in equine oocytes and embryos
inferred← citeshttps://doi.org/10.1071/rd14472openalex-snapshot
Effects of aging on gene expression and mitochondrial DNA in the equine oocyte and follicle cells
inferred← citeshttps://doi.org/10.1071/rd17387openalex-snapshot
Mitochondrial DNA replication is initiated at blastocyst formation in equine embryos
inferred← citeshttps://doi.org/10.1071/rd17408openalex-snapshot
The mitochondrial genome: how it drives fertility
inferred← citeshttps://doi.org/10.1080/15569543.2020.1803358openalex-snapshot
Mephedrone as a new synthetic amphetamine induces abortion, morphological alterations and mitochondrial dysfunction in mouse embryos
inferred← citeshttps://doi.org/10.1080/19396368.2022.2145248openalex-snapshot
Mitochondrial DNA copy number in cumulus granulosa cells as a predictor for embryo morphokinetics and chromosome status
inferred← citeshttps://doi.org/10.1089/clo.2006.0081openalex-snapshot
Developmental Arrest and Cytoskeletal Anomalies of Rat Embryos Reconstructed by Somatic Cell Nuclear Transfer
inferred← citeshttps://doi.org/10.1089/rej.2007.0617openalex-snapshot
Mitochondrial DNA Mutations May Contribute to Aging Via Cell Death Caused by Peptides that Induce Cytochrome c Release
inferred← citeshttps://doi.org/10.1093/hmg/ddt040openalex-snapshot
Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis
inferred← citeshttps://doi.org/10.1093/humrep/dev114openalex-snapshot
Relationship between diminished ovarian reserve and mitochondrial biogenesis in cumulus cells
inferred← citeshttps://doi.org/10.1093/humrep/dew203openalex-snapshot
Poor embryo development in post-ovulatory in vivo -aged mouse oocytes is associated with mitochondrial dysfunction, but mitochondrial transfer from somatic cells is not sufficient for rejuvenation
inferred← citeshttps://doi.org/10.1093/humrep/dex292openalex-snapshot
Clinical implications of mitochondrial DNA quantification on pregnancy outcomes: a blinded prospective non-selection study
inferred← citeshttps://doi.org/10.1093/humrep/dez054openalex-snapshot
Maternal ageing impairs mitochondrial DNA kinetics during early embryogenesis in mice
inferred← citeshttps://doi.org/10.1093/humupd/dmi042openalex-snapshot
The transmission of OXPHOS disease and methods to prevent this
inferred← citeshttps://doi.org/10.1093/humupd/dmq002openalex-snapshot
Mitochondrial DNA transmission, replication and inheritance: a journey from the gamete through the embryo and into offspring and embryonic stem cells
inferred← citeshttps://doi.org/10.1093/humupd/dmv024openalex-snapshot
Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing
inferred← citeshttps://doi.org/10.1093/humupd/dmw028openalex-snapshot
Ovarian ageing: the role of mitochondria in oocytes and follicles
inferred← citeshttps://doi.org/10.1093/jhered/esae004openalex-snapshot
Germline ecology: Managed herds, tolerated flocks, and pest control
inferred← citeshttps://doi.org/10.1093/molehr/gah227openalex-snapshot
Mitochondrial DNA deletions in rhesus macaque oocytes and embryos
inferred← citeshttps://doi.org/10.1093/molehr/gau086openalex-snapshot
Mitochondrial DNA in Day 3 embryo culture medium is a novel, non-invasive biomarker of blastocyst potential and implantation outcome
inferred← citeshttps://doi.org/10.1093/nar/gks770openalex-snapshot
Mitochondrial DNA copy number is regulated in a tissue specific manner by DNA methylation of the nuclear-encoded DNA polymerase gamma A
inferred← citeshttps://doi.org/10.1093/nar/gkz542openalex-snapshot
Quantitative proteomics revealed C6orf203/MTRES1 as a factor preventing stress-induced transcription deficiency in human mitochondria
inferred← citeshttps://doi.org/10.1093/narmme/ugaf042openalex-snapshot
The nuclear and mitochondrial genomes need to tango. How is their dance synchronized during development?
inferred← citeshttps://doi.org/10.1093/procel/pwac009openalex-snapshot
Oxidative phosphorylation safeguards pluripotency via UDP-N-acetylglucosamine
inferred← citeshttps://doi.org/10.1093/toxsci/kfv246openalex-snapshot
Ah Receptor Activation by Dioxin Disrupts Activin, BMP, and WNT Signals During the Early Differentiation of Mouse Embryonic Stem Cells and Inhibits Cardiomyocyte Functions
inferred← citeshttps://doi.org/10.1093/toxsci/kfx246openalex-snapshot
Paternal Exposure to Environmental Chemical Stress Affects Male Offspring’s Hepatic Mitochondria
inferred← citeshttps://doi.org/10.1095/biolreprod.106.054536openalex-snapshot
Regulated Mitochondrial DNA Replication During Oocyte Maturation Is Essential for Successful Porcine Embryonic Development
inferred← citeshttps://doi.org/10.1095/biolreprod.106.058040openalex-snapshot
The Influence of Nuclear Content on Developmental Competence of Gaur × Cattle Hybrid In Vitro Fertilized and Somatic Cell Nuclear Transfer Embryos1
inferred← citeshttps://doi.org/10.1095/biolreprod.109.077776openalex-snapshot
Embryo Mitochondrial DNA Depletion Is Reversed During Early Embryogenesis in Cattle1
inferred← citeshttps://doi.org/10.1095/biolreprod.110.087262openalex-snapshot
Impaired Mitochondrial Function in the Preimplantation Embryo Perturbs Fetal and Placental Development in the Mouse1
inferred← citeshttps://doi.org/10.1095/biolreprod.112.101881openalex-snapshot
Incorporation of Coenzyme Q10 into Bovine Oocytes Improves Mitochondrial Features and Alleviates the Effects of Summer Thermal Stress on Developmental Competence1
inferred← citeshttps://doi.org/10.1095/biolreprod.113.115337openalex-snapshot
Integral Proteomic Analysis of Blastocysts Reveals Key Molecular Machinery Governing Embryonic Diapause and Reactivation for Implantation in Mice1
inferred← citeshttps://doi.org/10.1095/biolreprod.115.133017openalex-snapshot
The Infertility of Repeat-Breeder Cows During Summer Is Associated with Decreased Mitochondrial DNA and Increased Expression of Mitochondrial and Apoptotic Genes in Oocytes1
inferred← citeshttps://doi.org/10.1097/gco.0000000000000164openalex-snapshot
Oocyte mitochondrial function and reproduction
inferred← citeshttps://doi.org/10.1097/gco.0000000000000265openalex-snapshot
Mitochondrial DNA supplementation as an enhancer of female reproductive capacity
inferred← citeshttps://doi.org/10.1097/gco.0000000000000274openalex-snapshot
Mitochondrial DNA as a biomarker for in-vitro fertilization outcome
inferred← citeshttps://doi.org/10.1101/2024.06.11.598492openalex-snapshot
Increase in ER-mitochondria contacts and mitochondrial fusion are hallmarks of mitochondrial activation during embryogenesis
inferred← citeshttps://doi.org/10.1111/cge.12557openalex-snapshot
mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development
inferred← citeshttps://doi.org/10.1111/j.1439-0531.2010.01691.xopenalex-snapshot
Mitochondrial Activity and Morphology in Developing Porcine Oocytes and Pre‐implantation Non‐Cultured and Cultured Embryos
inferred← citeshttps://doi.org/10.1111/nyas.12873openalex-snapshot
The control of mitochondrial DNA replication during development and tumorigenesis
inferred← citeshttps://doi.org/10.1111/rda.12929openalex-snapshot
Supplement of autologous ooplasm into porcine somatic cell nuclear transfer embryos does not alter embryo development
inferred← citeshttps://doi.org/10.1124/jpet.107.128017openalex-snapshot
Mitochondrially Targeted Effects of Berberine [Natural Yellow 18, 5,6-dihydro-9,10-dimethoxybenzo(g)-1,3-benzodioxolo(5,6-a) quinolizinium] on K1735-M2 Mouse Melanoma Cells: Comparison with Direct Effects on Isolated Mitochondrial Fractions
inferred← citeshttps://doi.org/10.1126/science.aaa0986openalex-snapshot
Replication-transcription switch in human mitochondria
inferred← citeshttps://doi.org/10.1128/mcb.05629-11openalex-snapshot
A Critical Role of Mitochondrial Phosphatase Ptpmt1 in Embryogenesis Reveals a Mitochondrial Metabolic Stress-Induced Differentiation Checkpoint in Embryonic Stem Cells
inferred← citeshttps://doi.org/10.1134/s1990519x08060072openalex-snapshot
Distribution of foreign mitochondrial DNA during the first splitting of transmitochondrial mouse embryos
inferred← citeshttps://doi.org/10.1146/annurev-genet-021920-105545openalex-snapshot
Mitochondria Are Fundamental for the Emergence of Metazoans: On Metabolism, Genomic Regulation, and the Birth of Complex Organisms
inferred← citeshttps://doi.org/10.1152/ajpendo.00120.2007openalex-snapshot
Responses of mitochondrial biogenesis and function to maternal diabetes in rat embryo during the placentation period
inferred← citeshttps://doi.org/10.11606/d.10.2014.tde-12012015-085943openalex-snapshot
Transferência de citoplasma submetido ao estresse oxidativo como modelo para o estudo da herança de doenças mitocondriais
inferred← citeshttps://doi.org/10.11606/d.41.2018.tde-02042018-150706openalex-snapshot
Heteroplasmia em Bombus morio (Hymenoptera, Apidae) e impactos em estudos evolutivos
inferred← citeshttps://doi.org/10.1186/1477-7827-3-65openalex-snapshot
Increase of mitochondrial DNA content and transcripts in early bovine embryogenesis associated with upregulation of mtTFA and NRF1 transcription factors
inferred← citeshttps://doi.org/10.1186/s12863-016-0375-4openalex-snapshot
The relationship between mitochondrial DNA haplotype and the reproductive capacity of domestic pigs (Sus scrofa domesticus)
inferred← citeshttps://doi.org/10.1186/s12863-017-0523-5openalex-snapshot
Cattle phenotypes can disguise their maternal ancestry
inferred← citeshttps://doi.org/10.1186/s12884-023-05760-wopenalex-snapshot
Mitochondrial DNA quantification correlates with the developmental potential of human euploid blastocysts but not with that of mosaic blastocysts
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/10.1186/s13048-025-01915-9openalex-snapshot
Mechanisms and treatment modalities related to premature ovarian insufficiency in mitochondria: literature review
inferred← citeshttps://doi.org/10.1186/s13578-019-0360-5openalex-snapshot
Autologous mitochondrial microinjection; a strategy to improve the oocyte quality and subsequent reproductive outcome during aging
inferred← citeshttps://doi.org/10.1201/9781315119793-14openalex-snapshot
Mitochondria and Embryo Viability
inferred← citeshttps://doi.org/10.1210/me.2009-0033openalex-snapshot
Maternal Diabetes Causes Mitochondrial Dysfunction and Meiotic Defects in Murine Oocytes
inferred← citeshttps://doi.org/10.1242/dev.114850openalex-snapshot
Mitochondrial dysfunction in oocytes of obese mothers: transmission to offspring and reversal by pharmacological endoplasmic reticulum stress inhibitors
inferred← citeshttps://doi.org/10.1242/dev.162644openalex-snapshot
Regulation of energy metabolism during early mammalian development: TEAD4 controls mitochondrial transcription
inferred← citeshttps://doi.org/10.1242/jcs.016972openalex-snapshot
Mitochondrial DNA replication during differentiation of murine embryonic stem cells
inferred← citeshttps://doi.org/10.1262/jrd.19010openalex-snapshot
Mitochondrial Dysfunction of In Vitro Grown Rabbit Oocytes Results in Preimplantation Embryo Arrest After Activation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1001066openalex-snapshot
Transmission of Mitochondrial DNA Diseases and Ways to Prevent Them
inferred← citeshttps://doi.org/10.1371/journal.pone.0014805openalex-snapshot
Interspecies Somatic Cell Nuclear Transfer Is Dependent on Compatible Mitochondrial DNA and Reprogramming Factors
inferred← citeshttps://doi.org/10.1371/journal.pone.0093287openalex-snapshot
Reference Gene Selection for Gene Expression Analysis of Oocytes Collected from Dairy Cattle and Buffaloes during Winter and Summer
inferred← citeshttps://doi.org/10.1371/journal.pone.0125680openalex-snapshot
Mfn2 Affects Embryo Development via Mitochondrial Dysfunction and Apoptosis
inferred← citeshttps://doi.org/10.1387/ijdb.103202rkopenalex-snapshot
Role of mitochondrial DNA replication during differentiation of reprogrammed stem cells
inferred← citeshttps://doi.org/10.14348/molcells.2015.2285openalex-snapshot
The Mitochondrial Fusion-Related Proteins Mfn2 and OPA1 are Transcriptionally Induced during Differentiation of Bone Marrow Progenitors to Immature Dendritic Cells
inferred← citeshttps://doi.org/10.1530/rep-06-0263openalex-snapshot
Characterization of mitochondrial replication and transcription control during rat early development in vivo and in vitro
inferred← citeshttps://doi.org/10.1530/rep-07-0012openalex-snapshot
Mitochondrial differentiation and oxidative phosphorylation system capacity in rat embryo during placentation period
inferred← citeshttps://doi.org/10.1530/rep-11-0044openalex-snapshot
Nuclear–cytoplasmic incompatibility and inefficient development of pig–mouse cytoplasmic hybrid embryos
inferred← citeshttps://doi.org/10.1530/rep-12-0113openalex-snapshot
Regulation of mitochondrial DNA accumulation during oocyte growth and meiotic maturation in the mouse
inferred← citeshttps://doi.org/10.1530/rep-18-0431openalex-snapshot
Mitochondria in early development: linking the microenvironment, metabolism and the epigenome
inferred← citeshttps://doi.org/10.1530/rep-18-0529openalex-snapshot
Evidence that growth hormone can improve mitochondrial function in oocytes from aged mice
inferred← citeshttps://doi.org/10.1534/genetics.106.070177openalex-snapshot
Contrasting Effects of in Vitro Fertilization and Nuclear Transfer on the Expression of mtDNA Replication Factors
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2019-0095openalex-snapshot
Maternal transmission of mitochondrial diseases
inferred← citeshttps://doi.org/10.17179/excli2017-819openalex-snapshot
Mitochondrial DNA copy number instability in ERBB2-amplified breast cancer tumors
inferred← citeshttps://doi.org/10.17760/d20005089openalex-snapshot
The influence of aging on oocyte quality and the importance of mitochondria
inferred← citeshttps://doi.org/10.17816/maj34657openalex-snapshot
Distribution of introduced human mitochondrial DNA in early stage mouse embryos
inferred← citeshttps://doi.org/10.21203/rs.3.rs-129121/v1openalex-snapshot
Knock out of Specific Maternal Vitellogenins in Zebrafish (Danio Rerio) Evokes Vital Changes in Egg Proteomic Profiles that resemble the Phenotype of Poor Quality Eggs
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2571158/v1openalex-snapshot
Mitochondrial DNA Quantification Correlates with the Developmental Potential of Human Euploid Blastocysts but not with that of Mosaic Blastocysts
inferred← citeshttps://doi.org/10.21926/obm.genet.1901070openalex-snapshot
The Role of Mitochondria in Oocyte and Early Embryo Health
inferred← citeshttps://doi.org/10.23736/s0031-0808.18.03510-3openalex-snapshot
Mitochondria and reproduction: possibilities for testing and treatment
inferred← citeshttps://doi.org/10.23880/oajg-16000187openalex-snapshot
Role of Mitochondrial Unfolding Protein Response in Reproduction and Aging with Utilization of Autologous Mitochondrial Injections in Mitochondrial Diseases along with in Aging Oocytes
inferred← citeshttps://doi.org/10.2527/jas.2014-8625openalex-snapshot
PHYSIOLOGY AND ENDOCRINOLOGY SYMPOSIUM: Cellular and molecular mechanisms of heat stress related to bovine ovarian function1
inferred← citeshttps://doi.org/10.26481/dis.20161115aoopenalex-snapshot
The impact of the mitochondrial bottleneck on mtDNA disease risk and embryogenesis
inferred← citeshttps://doi.org/10.30574/wjarr.2020.7.2.0278openalex-snapshot
Reproductive toxicity of iron oxide nanoparticles, silver nanoparticles and their mixture in male rats: Effects on testicular gene expression
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.4672openalex-snapshot
Characterizing Cytoplasmic Maturation and Improving Competence of Bovine In Vitro Matured Oocytes
inferred← citeshttps://doi.org/10.3168/jds.2017-13389openalex-snapshot
Symposium review: Reduction in oocyte developmental competence by stress is associated with alterations in mitochondrial function
inferred← citeshttps://doi.org/10.33549/physiolres.934982openalex-snapshot
Mitochondria in human reproduction: novel paradigm in the onset of neurodegenerative disorders
inferred← citeshttps://doi.org/10.3389/fcell.2020.590106openalex-snapshot
Reporting on the Role of miRNAs and Affected Pathways on the Molecular Backbone of Ovarian Insufficiency: A Systematic Review and Critical Analysis Mapping of Future Research
inferred← citeshttps://doi.org/10.3389/fcell.2021.664099openalex-snapshot
Mitochondrial DNA Depletion in Granulosa Cell Derived Nuclear Transfer Tissues
inferred← citeshttps://doi.org/10.3389/fcell.2021.791784openalex-snapshot
Differential Expression Profiles and Potential Intergenerational Functions of tRNA-Derived Small RNAs in Mice After Cadmium Exposure
inferred← citeshttps://doi.org/10.3389/fragi.2023.1158510openalex-snapshot
Oocyte aging in comparison to stem cells in mice
inferred← citeshttps://doi.org/10.3390/ani11030741openalex-snapshot
Effect of Interleukin-7 on In Vitro Maturation of Porcine Cumulus-Oocyte Complexes and Subsequent Developmental Potential after Parthenogenetic Activation
inferred← citeshttps://doi.org/10.3390/biology6030035openalex-snapshot
The Role of Oocyte Organelles in Determining Developmental Competence
inferred← citeshttps://doi.org/10.3390/genes15030367openalex-snapshot
Dynamics of Mitochondrial DNA Copy Number and Membrane Potential in Mouse Pre-Implantation Embryos: Responses to Diverse Types of Oxidative Stress
inferred← citeshttps://doi.org/10.3390/genes9050265openalex-snapshot
Influence of Maternal Aging on Mitochondrial Heterogeneity, Inheritance, and Function in Oocytes and Preimplantation Embryos
inferred← citeshttps://doi.org/10.3390/ijms15058893openalex-snapshot
Cancer Stem Cell Theory and the Warburg Effect, Two Sides of the Same Coin?
inferred← citeshttps://doi.org/10.3390/ijms242317047openalex-snapshot
PDGFRβ Activation Induced the Bovine Embryonic Genome Activation via Enhanced NFYA Nuclear Localization
inferred← citeshttps://doi.org/10.4103/wkmp-0152.210693openalex-snapshot
Mitochondrial Dysfunction and Age - related Oocyte Quality
inferred← citeshttps://doi.org/10.4172/2155-6156.1000181openalex-snapshot
Prenatal Effects of Different Intra-Uterine Milieus on Fetal Glucose Sensing Mechanisms during Gestation in Rats
inferred← citeshttps://doi.org/10.4238/2015.october.29.29openalex-snapshot
Mitochondrial DNA dynamics during in vitro culture and pluripotency induction of a bovine Rho0 cell line
inferred← citeshttps://doi.org/10.47749/t/unicamp.2010.773702openalex-snapshot
Estudo do efeito da quantidade de cópias de DNA mitocondrial sobre o desenvolvimento embrionário
inferred← citeshttps://doi.org/10.6084/m9.figshare.26597516openalex-snapshot
Additional file 1 of Mitochondrial DNA quantification correlates with the developmental potential of human euploid blastocysts but not with that of mosaic blastocysts
inferred← citeshttps://doi.org/10.6091/ibj.1400.2015openalex-snapshot
Comparison of Mitochondrial-Related Transcriptional Levels of TFAM, NRF1 and MT-CO1 Genes in Single Human Oocytes at Various Stages of the Oocyte Maturation
inferred← citeshttps://doi.org/10.70675/c0f1a3a3z992az4717zb426z210e51dadf82openalex-snapshot
Rôle du transporteur mitochondrial UCP2 dans la leucémie
inferred← citeshttps://doi.org/10.82308/11866openalex-snapshot
Regulation of mitochondrial DNA accumulation during oogenesis
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