On the public citation graph
Insights into regeneration from the genome, transcriptome and metagenome analysis of Eisenia fetida
0 signed · 104 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/9780470015902.a0022103.pub2openalex-snapshot
Evolutionary Aspects of Annelid Regeneration
inferredcites →https://doi.org/10.1002/cne.901270405openalex-snapshot
The microscopic anatomy and ulrastructure of the nervous system in the earthworm (Lumbricus sp.) with emphasis on the relationship between glial cells and neurons
inferredcites →https://doi.org/10.1002/dvdy.10190openalex-snapshot
Expression of Brachyury during development of the dendrobatid frog Colostethus machalilla
inferredcites →https://doi.org/10.1002/dvdy.20849openalex-snapshot
Molecular approach to annelid regeneration: cDNA subtraction cloning reveals various novel genes that are upregulated during the large‐scale regeneration of the oligochaete, Enchytraeus japonensis
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02409.xopenalex-snapshot
The human mid‐size neurofilament subunit: a repeated protein sequence and the relationship of its gene to the intermediate filament gene family.
inferredcites →https://doi.org/10.1002/jez.1401110307openalex-snapshot
Segment frequencies in anterior regeneration in the earthworm, Eisenia foetida
inferredcites →https://doi.org/10.1006/dbio.1995.1090openalex-snapshot
The Chick Brachyury Gene: Developmental Expression Pattern and Response to Axial Induction by Localized Activin
inferredcites →https://doi.org/10.1006/dbio.1998.9177openalex-snapshot
Expression Pattern of Brachyury and Not in the Sea Urchin: Comparative Implications for the Origins of Mesoderm in the Basal Deuterostomes
inferredcites →https://doi.org/10.1007/978-0-387-74943-3openalex-snapshot
Biology and Ecology of Earthworms
inferredcites →https://doi.org/10.1007/bf00928909openalex-snapshot
Isolation of genomic DNA from the earthworm speciesEisenia fetida
inferredcites →https://doi.org/10.1007/s00441-004-0874-xopenalex-snapshot
Earthworm leukocyte populations specifically harbor lysosomal enzymes that may respond to bacterial challenge
inferredcites →https://doi.org/10.1007/s12013-010-9097-9openalex-snapshot
Identification of a Novel Mouse Brachyury (T) Allele Causing a Short Tail Mutation in Mice
inferredcites →https://doi.org/10.1007/s12031-008-9102-6openalex-snapshot
Changes in the Expression of PACAP-like Compounds During the Embryonic Development of the Earthworm Eisenia fetida
inferredcites →https://doi.org/10.1007/s12031-008-9125-zopenalex-snapshot
Expression of PACAP-Like Compounds During the Caudal Regeneration of the Earthworm Eisenia fetida
inferredcites →https://doi.org/10.1016/0038-0717(92)90124-gopenalex-snapshot
Earthworm communities of tropical rain forests
inferredcites →https://doi.org/10.1016/0145-305x(92)90010-aopenalex-snapshot
Formation of brown bodies in the coelomic cavity of the earthworm Eisenia fetida andrei and attendant changes in shape and adhesive capacity of constitutive cells
inferredcites →https://doi.org/10.1016/j.apsoil.2015.02.010openalex-snapshot
DNA barcoding of earthworms (Eisenia fetida/andrei complex) from 28 ecotoxicological test laboratories
inferredcites →https://doi.org/10.1016/j.ccr.2013.04.020openalex-snapshot
Sox4 Is a Master Regulator of Epithelial-Mesenchymal Transition by Controlling Ezh2 Expression and Epigenetic Reprogramming
inferredcites →https://doi.org/10.1016/j.celrep.2013.03.008openalex-snapshot
A Single Aplysia Neurotrophin Mediates Synaptic Facilitation via Differentially Processed Isoforms
inferredcites →https://doi.org/10.1016/j.celrep.2014.06.031openalex-snapshot
Sox4 Links Tumor Suppression to Accelerated Aging in Mice by Modulating Stem Cell Activation
inferredcites →https://doi.org/10.1016/j.chnaes.2011.04.004openalex-snapshot
The regeneration capacity of an earthworm, Eisenia fetida, in relation to the site of amputation along the body
inferredcites →https://doi.org/10.1016/j.cub.2015.06.068openalex-snapshot
Spiralian Phylogeny Informs the Evolution of Microscopic Lineages
inferredcites →https://doi.org/10.1016/j.jprot.2013.08.004openalex-snapshot
Proteomic and metabolomic analysis of earthworm Eisenia fetida exposed to different concentrations of 2,2′,4,4′-tetrabromodiphenyl ether
inferredcites →https://doi.org/10.1016/j.pedobi.2003.04.001openalex-snapshot
Mitochondrial COII sequences indicate that the parthenogenetic earthworm Octolasion tyrtaeum (Savigny 1826) constitutes of two lineages differing in body size and genotype
inferredcites →https://doi.org/10.1016/j.pedobi.2007.05.003openalex-snapshot
Identifying earthworms through DNA barcodes
inferredcites →https://doi.org/10.1016/j.tcb.2010.05.006openalex-snapshot
The Hydra model: disclosing an apoptosis-driven generator of Wnt-based regeneration
inferredcites →https://doi.org/10.1016/j.ydbio.2009.02.004openalex-snapshot
Multiple Wnts are involved in Hydra organizer formation and regeneration
inferredcites →https://doi.org/10.1016/s0168-9525(99)01693-5openalex-snapshot
T-box genes: what they do and how they do it
inferredcites →https://doi.org/10.1016/s0304-419x(97)00016-4openalex-snapshot
Tales of tails: Brachyury and the T-box genes
inferredcites →https://doi.org/10.1017/cbo9780511754760openalex-snapshot
An Introduction to the Invertebrates
inferredcites →https://doi.org/10.1021/es0716352openalex-snapshot
Toxicogenomic Analysis Provides New Insights into Molecular Mechanisms of the Sublethal Toxicity of 2,4,6-Trinitrotoluene in Eisenia fetida
inferredcites →https://doi.org/10.1029/ce060p0125openalex-snapshot
Macrofaunal burrows and irrigation in marine sediment: Microbiological and biogeochemical interactions
inferredcites →https://doi.org/10.1038/nature09115openalex-snapshot
Functionally defective germline variants of sialic acid acetylesterase in autoimmunity
inferredcites →https://doi.org/10.1038/nature11696openalex-snapshot
Insights into bilaterian evolution from three spiralian genomes
inferredcites →https://doi.org/10.1038/nature12111openalex-snapshot
The zebrafish reference genome sequence and its relationship to the human genome
inferredcites →https://doi.org/10.1038/nbt.1883openalex-snapshot
Full-length transcriptome assembly from RNA-Seq data without a reference genome
inferredcites →https://doi.org/10.1046/j.1440-169x.1999.413435.xopenalex-snapshot
Expression of five novel T‐box genes and brachyury during embryogenesis, and in developing and regenerating limbs and tails of newts
inferredcites →https://doi.org/10.1073/pnas.0907931107openalex-snapshot
Latent regeneration abilities persist following recent evolutionary loss in asexual annelids
inferredcites →https://doi.org/10.1073/pnas.20.5.276openalex-snapshot
Linkage Studies of Brachyury (Short Tail) in the House Mouse
inferredcites →https://doi.org/10.1074/jbc.m111.324186openalex-snapshot
Sialidase NEU4 Hydrolyzes Polysialic Acids of Neural Cell Adhesion Molecules and Negatively Regulates Neurite Formation by Hippocampal Neurons
inferredcites →https://doi.org/10.1084/jem.20081399openalex-snapshot
B cell antigen receptor signal strength and peripheral B cell development are regulated by a 9-O-acetyl sialic acid esterase
inferredcites →https://doi.org/10.1093/bioinformatics/btu555openalex-snapshot
Poretools: a toolkit for analyzing nanopore sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/btu638openalex-snapshot
HTSeq—a Python framework to work with high-throughput sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/btv351openalex-snapshot
BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs
inferredcites →https://doi.org/10.1093/gbe/evv243openalex-snapshot
Timing and Scope of Genomic Expansion within Annelida: Evidence from Homeoboxes in the Genome of the Earthworm Eisenia fetida
inferredcites →https://doi.org/10.1093/genetics/141.1.305openalex-snapshot
Complete sequence of the mitochondrial DNA of the annelid worm Lumbricus terrestris.
inferredcites →https://doi.org/10.1093/glycob/cws057openalex-snapshot
Mammalian sialidases: Physiological and pathological roles in cellular functions
inferredcites →https://doi.org/10.1093/icb/icj051openalex-snapshot
Distribution of segment regeneration ability in the Annelida
inferredcites →https://doi.org/10.1093/molbev/mst133openalex-snapshot
miRNAs: Small Genes with Big Potential in Metazoan Phylogenetics
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003925openalex-snapshot
Complete Mitochondrial Genome Sequence of the Polychaete Annelid Platynereis dumerilii
inferredcites →https://doi.org/10.1098/rsbl.2008.0456openalex-snapshot
Grunting for worms: seismic vibrations cause Diplocardia earthworms to emerge from the soil
inferredcites →https://doi.org/10.1098/rsbl.2015.0763openalex-snapshot
Cambrian stem-group annelids and a metameric origin of the annelid head
inferredcites →https://doi.org/10.1098/rspb.2009.1340openalex-snapshot
MicroRNAs resolve an apparent conflict between annelid systematics and their fossil record
inferredcites →https://doi.org/10.1099/ijs.0.65174-0openalex-snapshot
Verminephrobacter eiseniae gen. nov., sp. nov., a nephridial symbiont of the earthworm Eisenia foetida (Savigny)
inferredcites →https://doi.org/10.1101/gad.14.5.596openalex-snapshot
The Caenorhabditis elegans fate-determining gene mab-9 encodes a T-box protein required to pattern the posterior hindgut
inferredcites →https://doi.org/10.1101/gad.1475106openalex-snapshot
Wnt/β-catenin signaling regulates vertebrate limb regeneration
inferredcites →https://doi.org/10.1101/gad.8.18.2137openalex-snapshot
Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta.
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03931.xopenalex-snapshot
Opening a can of worms: unprecedented sympatric cryptic diversity within British lumbricid earthworms
inferredcites →https://doi.org/10.1111/j.1471-8286.2005.01219.xopenalex-snapshot
Microsatellite markers for the earthworm Lumbricus rubellus
inferredcites →https://doi.org/10.1111/j.1471-8286.2007.01776.xopenalex-snapshot
Development and characterization of novel microsatellite markers for the common earthworm (Lumbricus terrestris L.)
inferredcites →https://doi.org/10.1111/j.1525-142x.2005.05061.xopenalex-snapshot
caudal and even‐skipped in the annelid Platynereis dumerilii and the ancestry of posterior growth
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00302.xopenalex-snapshot
The deep evolution of metazoan microRNAs
inferredcites →https://doi.org/10.1111/j.1749-6632.2012.06517.xopenalex-snapshot
Multifarious roles of sialic acids in immunity
inferredcites →https://doi.org/10.1126/science.282.5396.2012openalex-snapshot
Genome Sequence of the Nematode C. elegans : A Platform for Investigating Biology
inferredcites →https://doi.org/10.1126/science.287.5461.2185openalex-snapshot
The Genome Sequence of Drosophila melanogaster
inferredcites →https://doi.org/10.1146/annurev-genet-120213-092023openalex-snapshot
A Uniform System for the Annotation of Vertebrate microRNA Genes and the Evolution of the Human microRNAome
inferredcites →https://doi.org/10.1146/annurev.micro.61.080706.093139openalex-snapshot
As the Worm Turns: The Earthworm Gut as a Transient Habitat for Soil Microbial Biomes
inferredcites →https://doi.org/10.1186/1471-2105-9-386openalex-snapshot
The metagenomics RAST server – a public resource for the automatic phylogenetic and functional analysis of metagenomes
inferredcites →https://doi.org/10.1186/1471-213x-11-50openalex-snapshot
A novel amniote model of epimorphic regeneration: the leopard gecko, Eublepharis macularius
inferredcites →https://doi.org/10.1186/1471-2164-13-287openalex-snapshot
Transcriptome characterization via 454 pyrosequencing of the annelid Pristina leidyi, an emerging model for studying the evolution of regeneration
inferredcites →https://doi.org/10.1186/1471-2164-9-s1-s15openalex-snapshot
Transcriptomic analysis of RDX and TNT interactive sublethal effects in the earthworm Eisenia fetida
inferredcites →https://doi.org/10.1186/1741-7007-6-25openalex-snapshot
'Systems toxicology' approach identifies coordinated metabolic responses to copper in a terrestrial non-model invertebrate, the earthworm Lumbricus rubellus
inferredcites →https://doi.org/10.1186/2041-9139-3-24openalex-snapshot
Developmental and evolutionary origins of the pharyngeal apparatus
inferredcites →https://doi.org/10.1186/2041-9139-3-8openalex-snapshot
Expression of the pair-rule gene homologs runt, Pax3/7, even-skipped-1 and even-skipped-2 during larval and juvenile development of the polychaete annelid Capitella teleta does not support a role in segmentation
inferredcites →https://doi.org/10.1186/gb-2009-10-3-r25openalex-snapshot
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1242/dev.02812openalex-snapshot
H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration
inferredcites →https://doi.org/10.1242/dev.033985openalex-snapshot
Suppression of the immune response potentiates tadpole tail regeneration during the refractory period
inferredcites →https://doi.org/10.1242/dev.120.1.115openalex-snapshot
Expression of the Brachyury gene during mesoderm development in differentiating embryonal carcinoma cell cultures
inferredcites →https://doi.org/10.1242/dev.120.4.1009openalex-snapshot
no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene
inferredcites →https://doi.org/10.1242/dev.126.5.999openalex-snapshot
HyBra1, a Brachyury homologue, acts during head formation in Hydra
inferredcites →https://doi.org/10.1242/jeb.83.1.231openalex-snapshot
The Rapid Escape Response of the Earthworm Lumbricus Terrestris L.: Overlapping Sensory Fields of the Median and Lateral Giant Fibres
inferredcites →https://doi.org/10.1271/bbb.80391openalex-snapshot
Gene Expression Profile in the Anterior Regeneration of the Earthworm Using Expressed Sequence Tags
inferredcites →https://doi.org/10.1371/journal.pone.0013102openalex-snapshot
Use of ITS2 Region as the Universal DNA Barcode for Plants and Animals
inferredcites →https://doi.org/10.1371/journal.pone.0079257openalex-snapshot
Microbial Environment Affects Innate Immunity in Two Closely Related Earthworm Species Eisenia andrei and Eisenia fetida
inferredcites →https://doi.org/10.1387/ijdb.9879709openalex-snapshot
Expression of two even-skipped genes eve1 and evx2 during zebrafish fin morphogenesis and their regulation by retinoic acid
inferredcites →https://doi.org/10.1523/jneurosci.08-02-00664.1988openalex-snapshot
Expression of nerve growth factor receptors by Schwann cells of axotomized peripheral nerves: ultrastructural location, suppression by axonal contact, and binding properties
inferredcites →https://doi.org/10.2174/138920212800793348openalex-snapshot
Building a Robust A-P Axis
inferredcites →https://doi.org/10.2307/1537668openalex-snapshot
THE LOCATION OF FACTORS OF HEAD REGENERATION IN THE EARTHWORM
inferredcites →https://doi.org/10.2307/1538195openalex-snapshot
REGENERATION IN AN EARTHWORM, EISENIA FOETIDA (SAVIGNY) 1826. I. ANTERIOR REGENERATION
inferredcites →https://doi.org/10.2307/1538597openalex-snapshot
REGENERATION IN AN EARTHWORM, EISENIA FOETIDA (SAVIGNY) 1826. II. POSTERIOR REGENERATION
inferredcites →https://doi.org/10.2307/3279630openalex-snapshot
A New Parasitic Polychaetous Annelid (Arabellidae) from the Bahamas
inferredcites →https://doi.org/10.3389/fmicb.2014.00128openalex-snapshot
The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
inferredcites →https://doi.org/10.3969/j.issn.1673-5374.2012.08.010openalex-snapshot
Neurofilament proteins in axonal regeneration and neurodegenerative diseases.
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
inferredcites →https://doi.org/10.5962/bhl.title.19795openalex-snapshot
Observations on some interesting phenomena in animal physiology, exhibited by several species of Planariae
inferredcites →https://doi.org/10.7717/peerj.250openalex-snapshot
Escape and avoidance learning in the earthworm Eisenia hortensis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148636openalex-snapshot
Profiling microRNAs of earthworm, Perionyx excavatus and deciphering the expression of distinct novel miRNAs regulating epimorphosis regeneration
inferred← citeshttps://doi.org/10.1101/2024.10.27.619232openalex-snapshot
Exploring The Genome of The Oribatid Mite, Oppia Nitens – Environmental Stress Response and Toxicity Adaptation
inferred← citeshttps://doi.org/10.18466/cbayarfbe.390277openalex-snapshot
Genome-wide EST-SSR Marker Identification in Red Wiggler Worm Eisenia fetida (Savigny, 1826)
inferred← citeshttps://doi.org/10.26508/lsa.202201513openalex-snapshot
Molecular insights into high-altitude adaption and acclimatisation ofAporrectodea caliginosa
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.