On the public citation graph
Selection for mitochondrial quality drives evolution of the germline
0 signed · 50 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.b.16openalex-snapshot
Phylogenetic considerations of clonality, coloniality, and mode of germline development in animals
inferredcites →https://doi.org/10.1006/abbi.1994.1342openalex-snapshot
Human Skin Mitochondrial DNA Deletions Associated with Light Exposure
inferredcites →https://doi.org/10.1006/jtbi.1996.0089openalex-snapshot
Separate Sexes and the Mitochondrial Theory of Ageing
inferredcites →https://doi.org/10.1007/bf01273895openalex-snapshot
Studies on the development and three-dimensional reconstruction of giant mitochondria and their nuclei in egg cells ofPelargonium zonale Ait.
inferredcites →https://doi.org/10.1007/s00239-008-9069-5openalex-snapshot
Slow Mitochondrial COI Sequence Evolution at the Base of the Metazoan Tree and Its Implications for DNA Barcoding
inferredcites →https://doi.org/10.1007/s00294-004-0522-8openalex-snapshot
The mitochondrial DNA of land plants: peculiarities in phylogenetic perspective
inferredcites →https://doi.org/10.1007/s00294-009-0277-3openalex-snapshot
Studies of mitochondrial morphology and DNA amount in the rice egg cell
inferredcites →https://doi.org/10.1007/s10750-004-2671-7openalex-snapshot
On the taxonomy and presumable evolutionary pathways of planktonic larvae of Ceriantharia (Anthozoa, Cnidaria)
inferredcites →https://doi.org/10.1016/0022-5193(78)90189-3openalex-snapshot
The evolution of anisogamy
inferredcites →https://doi.org/10.1016/j.bbamcr.2013.03.010openalex-snapshot
Maternal inheritance of mitochondrial DNA by diverse mechanisms to eliminate paternal mitochondrial DNA
inferredcites →https://doi.org/10.1016/j.mrrev.2003.11.001openalex-snapshot
Oxidative DNA damage and disease: induction, repair and significance
inferredcites →https://doi.org/10.1016/s0070-2153(06)77004-1openalex-snapshot
Mitochondrial DNA and the Mammalian Oocyte
inferredcites →https://doi.org/10.1016/s0074-7696(08)60169-2openalex-snapshot
Follicular Atresia in the Ovaries of Nonmammalian Vertebrates
inferredcites →https://doi.org/10.1016/s1472-6483(10)61946-3openalex-snapshot
Mitochondrial DNA point mutation in human oocytes is associated with maternal age
inferredcites →https://doi.org/10.1038/35049558openalex-snapshot
The origins, patterns and implications of human spontaneous mutation
inferredcites →https://doi.org/10.1038/462272aopenalex-snapshot
Biodiversity: On the origin of bar codes
inferredcites →https://doi.org/10.1038/nature13400openalex-snapshot
The ctenophore genome and the evolutionary origins of neural systems
inferredcites →https://doi.org/10.1038/ncomms8142openalex-snapshot
Rise to modern levels of ocean oxygenation coincided with the Cambrian radiation of animals
inferredcites →https://doi.org/10.1038/ng.f.94openalex-snapshot
What causes mitochondrial DNA deletions in human cells?
inferredcites →https://doi.org/10.1046/j.1365-2540.2001.00808.xopenalex-snapshot
Cooperation and conflict in the evolution of multicellularity
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01652.xopenalex-snapshot
Slow mitochondrial DNA sequence evolution in the Anthozoa (Cnidaria)
inferredcites →https://doi.org/10.1073/pnas.1312778110openalex-snapshot
Oxygen, ecology, and the Cambrian radiation of animals
inferredcites →https://doi.org/10.1073/pnas.92.25.11331openalex-snapshot
Uniparental inheritance of mitochondrial and chloroplast genes: mechanisms and evolution.
inferredcites →https://doi.org/10.1093/icb/icm027openalex-snapshot
Evolution of the bilaterian germ line: lineage origin and modulation of specification mechanisms
inferredcites →https://doi.org/10.1093/icb/icm045openalex-snapshot
Key transitions in animal evolution: a mitochondrial DNA perspective
inferredcites →https://doi.org/10.1093/oso/9780198548386.001.0001openalex-snapshot
Ecology and Evolution in Anoxic Worlds
inferredcites →https://doi.org/10.1098/rspb.1996.0121openalex-snapshot
Cooperation and conflict in the evolution of individuality. II. Conflict mediation
inferredcites →https://doi.org/10.1098/rspb.2002.2161openalex-snapshot
The evolution of anisogamy: a game-theoretic approach
inferredcites →https://doi.org/10.1098/rspb.2011.1871openalex-snapshot
Selection for mitonuclear co-adaptation could favour the evolution of two sexes
inferredcites →https://doi.org/10.1098/rspb.2013.1920openalex-snapshot
Dynamics of mitochondrial inheritance in the evolution of binary mating types and two sexes
inferredcites →https://doi.org/10.1098/rstb.2000.0727openalex-snapshot
Relatedness and the fraternal major transitions
inferredcites →https://doi.org/10.1098/rstb.2012.0263openalex-snapshot
Energy, ageing, fidelity and sex: oocyte mitochondrial DNA as a protected genetic template
inferredcites →https://doi.org/10.1105/tpc.109.071902openalex-snapshot
The Levels of Male Gametic Mitochondrial DNA Are Highly Regulated in Angiosperms with Regard to Mitochondrial Inheritance
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03982.xopenalex-snapshot
Revealing the hidden complexities of mtDNA inheritance
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102403.114735openalex-snapshot
The Evolution of Multicellularity: A Minor Major Transition?
inferredcites →https://doi.org/10.1186/1471-2148-6-24openalex-snapshot
No variation and low synonymous substitution rates in coral mtDNA despite high nuclear variation
inferredcites →https://doi.org/10.1186/1741-7007-9-61openalex-snapshot
The intriguing evolutionary dynamics of plant mitochondrial DNA
inferredcites →https://doi.org/10.1186/1745-6150-5-42openalex-snapshot
Mitochondrial DNA, chloroplast DNA and the origins of development in eukaryotic organisms
inferredcites →https://doi.org/10.1371/journal.pbio.1001858openalex-snapshot
The Evolutionary Origin of Somatic Cells under the Dirty Work Hypothesis
inferredcites →https://doi.org/10.1371/journal.pgen.1002028openalex-snapshot
Ultra-Deep Sequencing of Mouse Mitochondrial DNA: Mutational Patterns and Their Origins
inferredcites →https://doi.org/10.1371/journal.pone.0086612openalex-snapshot
Fast-Evolving Mitochondrial DNA in Ceriantharia: A Reflection of Hexacorallia Paraphyly?
inferredcites →https://doi.org/10.1387/ijdb.15005568openalex-snapshot
The germ line and somatic stem cell gene Cniwi in the jellyfish Podocoryne carnea.
inferredcites →https://doi.org/10.3109/19401736.2011.624611openalex-snapshot
Extreme mitochondrial evolution in the ctenophoreMnemiopsis leidyi: Insight from mtDNA and the nuclear genome
inferredcites →https://doi.org/10.5962/bhl.title.168967openalex-snapshot
The germ-plasm : a theory of heredity /
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.