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A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
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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/gene.20187openalex-snapshot
Generation ofstella-GFP transgenic mice: A novel tool to study germ cell development
inferredcites →https://doi.org/10.1007/bf00210753openalex-snapshot
Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
inferredcites →https://doi.org/10.1016/0006-291x(90)90490-eopenalex-snapshot
Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy
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
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Mapping of mitochondrial DNA of individual sheep and goats: Rapid evolution in the D loop region
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Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: Implications for genetic imprinting
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The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
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Quantification of mtDNA in single oocytes, polar bodies and subcellular components by real-time rapid cycle fluorescence monitored PCR
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Nucleotide sequence evidence for rapid genotypic shifts in the bovine mitochondrial DNA D-loop
inferredcites →https://doi.org/10.1038/ng0398-231openalex-snapshot
Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice
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Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice
inferredcites →https://doi.org/10.1038/ng1096-146openalex-snapshot
Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA
inferredcites →https://doi.org/10.1038/ng1970openalex-snapshot
The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells
inferredcites →https://doi.org/10.1086/318190openalex-snapshot
Random Genetic Drift Determines the Level of Mutant mtDNA in Human Primary Oocytes
inferredcites →https://doi.org/10.1086/515453openalex-snapshot
Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes
inferredcites →https://doi.org/10.1093/genetics/149.4.2135openalex-snapshot
Germline Bottlenecks and the Evolutionary Maintenance of Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/molehr/8.8.719openalex-snapshot
Can mitochondrial DNA mutations cause sperm dysfunction?
inferredcites →https://doi.org/10.1111/j.1365-2184.1980.tb00456.xopenalex-snapshot
KINETICS OF CELL PROLIFERATION IN THE PRE‐IMPLANTED MOUSE EMBRYO IN VIVO AND IN VITRO
inferredcites →https://doi.org/10.1111/j.1432-0436.2005.00049.xopenalex-snapshot
How is the mouse germ-cell lineage established?
inferredcites →https://doi.org/10.1126/science.6857250openalex-snapshot
Nuclear Transplantation in the Mouse Embryo by Microsurgery and Cell Fusion
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Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
inferredcites →https://doi.org/10.1242/dev.110.2.521openalex-snapshot
Primordial germ cells in the mouse embryo during gastrulation
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Staging of gastrulating mouse embryos by morphological landmarks in the dissecting microscope
inferredcites →https://doi.org/10.1242/dev.64.1.133openalex-snapshot
Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/bs.adgen.2017.06.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2017.10.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.02.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2025.10.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.enz.2023.07.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ajhg.2008.07.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ajhg.2008.10.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ajhg.2010.02.023openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ajhg.2011.03.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ajhg.2016.09.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.arr.2022.101578openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.09.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.03.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbagen.2011.10.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.11.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.02.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.06.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.07.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.08.138openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocel.2009.02.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocel.2009.11.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocel.2012.05.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocel.2015.01.023openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocel.2018.10.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biochi.2013.08.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2012.09.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2012.03.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2015.10.019openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cll.2010.04.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.domaniend.2016.03.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.exger.2009.12.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.forsciint.2010.02.029openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fsigen.2017.09.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gde.2016.03.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gde.2016.04.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2023.147985openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2026.115859openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jgg.2013.10.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jgg.2020.04.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jgg.2026.02.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jmb.2018.10.019openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.livsci.2014.05.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mad.2016.02.013openalex-snapshot
Infertility and recurrent miscarriage with complex II deficiency-dependent mitochondrial oxidative stress in animal models
inferred← citeshttps://doi.org/10.1016/j.mad.2016.10.003openalex-snapshot
Low protein to carbohydrate ratio diet delays onset of Parkinsonism like phenotype in Drosophila melanogaster parkin null mutants
inferred← citeshttps://doi.org/10.1016/j.mce.2008.11.009openalex-snapshot
Ultrastructural characterization of spermatogenesis and its evolutionary conservation in the germline: Germinal granules in mammals☆
inferred← citeshttps://doi.org/10.1016/j.mce.2013.06.004openalex-snapshot
Endocrine disorders in mitochondrial disease
inferred← citeshttps://doi.org/10.1016/j.mehy.2017.01.012openalex-snapshot
Should metformin be included in fertility treatment of PCOS patients?
inferred← citeshttps://doi.org/10.1016/j.mito.2009.04.005openalex-snapshot
CPEO and KSS differ in the percentage and location of the mtDNA deletion
inferred← citeshttps://doi.org/10.1016/j.mito.2010.08.011openalex-snapshot
Age related changes in mitochondrial function and new approaches to study redox regulation in mammalian oocytes in response to age or maturation conditions
inferred← citeshttps://doi.org/10.1016/j.mito.2010.09.012openalex-snapshot
Mitochondrial function in the human oocyte and embryo and their role in developmental competence
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.2011.05.004openalex-snapshot
The implications of mitochondrial DNA copy number regulation during embryogenesis
inferred← citeshttps://doi.org/10.1016/j.mito.2015.12.008openalex-snapshot
Mitochondria and mitochondrial DNA in porcine oocytes and cumulus cells — A search for developmental competence marker
inferred← citeshttps://doi.org/10.1016/j.mito.2019.03.003openalex-snapshot
Mitochondrial genome variations in idiopathic dilated cardiomyopathy
inferred← citeshttps://doi.org/10.1016/j.mito.2019.06.007openalex-snapshot
Dynamic of mitochondrial network, cristae, and mitochondrial nucleoids in pancreatic β-cells
inferred← citeshttps://doi.org/10.1016/j.mito.2022.05.007openalex-snapshot
Triplication of HSA21 on alterations in structure and function of mitochondria
inferred← citeshttps://doi.org/10.1016/j.mito.2026.102175openalex-snapshot
Mitochondrial donation and human reproduction: Clinical, ethical and legal aspects
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2008.11.020openalex-snapshot
Clonal expansion of different mtDNA variants without selective advantage in solid tumors
inferred← citeshttps://doi.org/10.1016/j.neuron.2014.11.022openalex-snapshot
Mitochondrial DNA: Impacting Central and Peripheral Nervous Systems
inferred← citeshttps://doi.org/10.1016/j.nmd.2010.05.008openalex-snapshot
174th ENMC International Workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: Implications of scientific advances 19–21 March 2010, Naarden, The Netherlands
inferred← citeshttps://doi.org/10.1016/j.nmd.2012.03.009openalex-snapshot
Single deletions in mitochondrial DNA – Molecular mechanisms and disease phenotypes in clinical practice
inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106466openalex-snapshot
Modulating mitochondrial DNA mutations: factors shaping heteroplasmy in the germ line and somatic cells
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2024.101264openalex-snapshot
Mitochondrial retinopathies and optic neuropathies: The impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and management
inferred← citeshttps://doi.org/10.1016/j.rbmo.2013.10.016openalex-snapshot
Behaviour of cytoplasmic organelles and cytoskeleton during oocyte maturation
inferred← citeshttps://doi.org/10.1016/j.scr.2017.03.004openalex-snapshot
Mitochondrial matters: Mitochondrial bottlenecks, self-assembling structures, and entrapment in the female germline
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.01.028openalex-snapshot
Mitochondrial DNA copy number and replication in reprogramming and differentiation
inferred← citeshttps://doi.org/10.1016/j.stem.2024.06.015openalex-snapshot
Analyzing embryo dormancy at single-cell resolution reveals dynamic transcriptional responses and activation of integrin-Yap/Taz prosurvival signaling
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2008.10.023openalex-snapshot
Cytoplasmic maturation of bovine oocytes: Structural and biochemical modifications and acquisition of developmental competence
inferred← citeshttps://doi.org/10.1016/j.tig.2008.11.007openalex-snapshot
Mitochondrial DNA mutations and aging: devils in the details?
inferred← citeshttps://doi.org/10.1016/j.tig.2011.10.001openalex-snapshot
Recruitment of healthy mitochondria fuels transmissible cancers
inferred← citeshttps://doi.org/10.1016/j.tig.2013.05.005openalex-snapshot
Mitochondrial disorders: aetiologies, models systems, and candidate therapies
inferred← citeshttps://doi.org/10.1016/j.xfss.2021.12.002openalex-snapshot
Cyclic fertilin-derived peptide stimulates in vitro human embryo development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.11.021openalex-snapshot
Germ-line mitochondria exhibit suppressed respiratory activity to support their accurate transmission to the next generation
inferred← citeshttps://doi.org/10.1016/j.ymgme.2019.09.003openalex-snapshot
Resolving complexity in mitochondrial disease: Towards precision medicine
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/10.1016/s1474-4422(10)70116-2openalex-snapshot
A neurological perspective on mitochondrial disease
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/10.1017/cbo9781139135030.027openalex-snapshot
The legacy of mitochondrial DNA
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr1openalex-snapshot
Author comment: Precision mitochondrial medicine — R0/PR1
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr10openalex-snapshot
Decision: Precision mitochondrial medicine — R1/PR10
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr2openalex-snapshot
Review: Precision mitochondrial medicine — R0/PR2
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr3openalex-snapshot
Review: Precision mitochondrial medicine — R0/PR3
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr4openalex-snapshot
Recommendation: Precision mitochondrial medicine — R0/PR4
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr5openalex-snapshot
Decision: Precision mitochondrial medicine — R0/PR5
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr6openalex-snapshot
Author comment: Precision mitochondrial medicine — R1/PR6
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr7openalex-snapshot
Review: Precision mitochondrial medicine — R1/PR7
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr8openalex-snapshot
Review: Precision mitochondrial medicine — R1/PR8
inferred← citeshttps://doi.org/10.1017/pcm.2022.8.pr9openalex-snapshot
Recommendation: Precision mitochondrial medicine — R1/PR9
inferred← citeshttps://doi.org/10.1017/s0967199422000260openalex-snapshot
Assessment of mitochondrial DNA viability ratio in day-4 biopsied embryos as an add-in to select euploid embryos for single embryo transfer
inferred← citeshttps://doi.org/10.1021/jacs.8b05309openalex-snapshot
Direct Visualization of Single-Nucleotide Variation in mtDNA Using a CRISPR/Cas9-Mediated Proximity Ligation Assay
inferred← citeshttps://doi.org/10.1038/cddiscovery.2017.62openalex-snapshot
Mitochondrial DNA haplotypes induce differential patterns of DNA methylation that result in differential chromosomal gene expression patterns
inferred← citeshttps://doi.org/10.1038/ejhg.2014.35openalex-snapshot
A national perspective on prenatal testing for mitochondrial disease
inferred← citeshttps://doi.org/10.1038/embor.2008.242openalex-snapshot
Mouse models of mitochondrial DNA defects and their relevance for human disease
inferred← citeshttps://doi.org/10.1038/eye.2014.37openalex-snapshot
Treatment strategies for inherited optic neuropathies: past, present and future
inferred← citeshttps://doi.org/10.1038/hdy.2008.52openalex-snapshot
Molecular clock debate: Time dependency of molecular rate estimates for mtDNA: this is not the time for wishful thinking
inferred← citeshttps://doi.org/10.1038/hdy.2008.74openalex-snapshot
Lost in the zygote: the dilution of paternal mtDNA upon fertilization
inferred← citeshttps://doi.org/10.1038/nature08368openalex-snapshot
Mitochondrial gene replacement in primate offspring and embryonic stem cells
inferred← citeshttps://doi.org/10.1038/nature11800openalex-snapshot
Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants
inferred← citeshttps://doi.org/10.1038/nbt.3997openalex-snapshot
Assisted reproductive technologies to prevent human mitochondrial disease transmission
inferred← citeshttps://doi.org/10.1038/ncomms9808openalex-snapshot
Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered flies
inferred← citeshttps://doi.org/10.1038/ng.2427openalex-snapshot
Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission
inferred← citeshttps://doi.org/10.1038/ng.258openalex-snapshot
The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes
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