On the public citation graph
Retroposons—Seeds of Evolution
0 signed · 385 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known work and none has been retracted — and get a dated CiteStamped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/j.1460-2075.1986.tb04323.xopenalex-snapshot
The use of incomplete genes for the construction of a Trypanosoma equiperdum variant surface glycoprotein gene.
inferredcites →https://doi.org/10.1002/j.1460-2075.1990.tb08271.xopenalex-snapshot
Zfa is an expressed retroposon derived from an alternative transcript of the Zfx gene.
inferredcites →https://doi.org/10.1007/978-3-642-86659-3openalex-snapshot
Evolution by Gene Duplication
inferredcites →https://doi.org/10.1016/0092-8674(87)90189-9openalex-snapshot
A hyperconversion mechanism generates the chicken light chain preimmune repertoire
inferredcites →https://doi.org/10.1016/0888-7543(90)90275-yopenalex-snapshot
A testis-specific form of the human pyruvate dehydrogenase E1α subunit is coded for by an intronless gene on chromosome 4
inferredcites →https://doi.org/10.1016/s0074-7696(08)61375-3openalex-snapshot
The Origin and Evolution of Retroposons
inferredcites →https://doi.org/10.1017/s0094837300004310openalex-snapshot
Exaptation—a Missing Term in the Science of Form
inferredcites →https://doi.org/10.1038/284601a0openalex-snapshot
Selfish genes, the phenotype paradigm and genome evolution
inferredcites →https://doi.org/10.1038/326501a0openalex-snapshot
Human testis-specific PGK gene lacks introns and possesses characteristics of a processed gene
inferredcites →https://doi.org/10.1038/347294a0openalex-snapshot
Frequent activation of N-myc genes by hepadnavirus insertion in woodchuck liver tumours
inferredcites →https://doi.org/10.1073/pnas.86.17.6686openalex-snapshot
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources.
inferredcites →https://doi.org/10.1128/mcb.10.6.2513openalex-snapshot
Retroviral and Pseudogene Insertion Sites Reveal the Lineage of Human Salivary and Pancreatic Amylase Genes from a Single Gene during Primate Evolution
inferredcites →https://doi.org/10.1128/mcb.7.9.3107openalex-snapshot
The testis-specific phosphoglycerate kinase gene pgk-2 is a recruited retroposon.
inferredcites →https://doi.org/10.1128/mcb.7.9.3324openalex-snapshot
Primate Brain-Specific Cytoplasmic Transcript of the Alu Repeat Family
inferredcites →https://doi.org/10.1146/annurev.bi.55.070186.003215openalex-snapshot
NONVIRAL RETROPOSONS: GENES, PSEUDOGENES, AND TRANSPOSABLE ELEMENTS GENERATED BY THE REVERSE FLOW OF GENETIC INFORMATION
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4663101openalex-extracted
Genome-Wide Identification of Nac Family Genes in Common Oat (Avena Sativa L.) and Functional Characterization of Asnac109 in Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1002/(sici)1097-0169(1997)38:2<120::aid-cm2>3.0.co;2-bopenalex-snapshot
Vertebrates have conserved capping protein α isoforms with specific expression patterns
inferred← citeshttps://doi.org/10.1002/(sici)1521-1878(200002)22:2<148::aid-bies6>3.0.co;2-zopenalex-snapshot
SINE insertions: powerful tools for molecular systematics
inferred← citeshttps://doi.org/10.1002/9781119079453.ch10openalex-snapshot
Using evolutionary algorithms to study the evolution of gene regulatory networks controlling biological development
inferred← citeshttps://doi.org/10.1002/ajpa.21439openalex-snapshot
Nonadaptive processes in primate and human evolution
inferred← citeshttps://doi.org/10.1002/bies.201100177openalex-snapshot
Newly evolved genes: Moving from comparative genomics to functional studies in model systems
inferred← citeshttps://doi.org/10.1002/bies.20544openalex-snapshot
The relationship between non‐protein‐coding DNA and eukaryotic complexity
inferred← citeshttps://doi.org/10.1002/biuz.19910210510openalex-snapshot
Die Rolle virus‐ähnlicher Partikel bei parasitoiden Insekten
inferred← citeshttps://doi.org/10.1002/ece3.400openalex-snapshot
Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE ‐Thrust hypothesis
inferred← citeshttps://doi.org/10.1002/ece3.7507openalex-snapshot
Genome‐wide analysis of European sea bass provides insights into the evolution and functions of single‐exon genes
inferred← citeshttps://doi.org/10.1002/humu.20420openalex-snapshot
Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons
inferred← citeshttps://doi.org/10.1002/humu.22519openalex-snapshot
Primary Immunodeficiency Caused by an Exonized Retroposed Gene Copy Inserted in theCYBBGene
inferred← citeshttps://doi.org/10.1002/j.1460-2075.1994.tb06854.xopenalex-snapshot
The roles of starvation and selective substrates in the emergence of araB‐lacZ fusion clones.
inferred← citeshttps://doi.org/10.1006/jmbi.2001.4725openalex-snapshot
Birth of a gene: locus of neuronal BC200 snmRNA in three prosimians and human BC200 pseudogenes as archives of change in the Anthropoidea lineage
inferred← citeshttps://doi.org/10.1007/978-1-4612-0411-4_26openalex-snapshot
An in vitro Human Mammary Epithelial Model System for Studies of Differentiation and Carcinogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4613-1407-3_8openalex-snapshot
Reverse Transcriptase: Mediator of Genomic Plasticity
inferred← citeshttps://doi.org/10.1007/978-1-4615-2592-9_2openalex-snapshot
Growth, differentiation, and transformation of human mammary epithelial cells in culture
inferred← citeshttps://doi.org/10.1007/978-1-4615-3372-6_1openalex-snapshot
Origin and General Nature of Retroviruses
inferred← citeshttps://doi.org/10.1007/978-1-4615-3372-6_4openalex-snapshot
Retroelements in Microorganisms
inferred← citeshttps://doi.org/10.1007/978-1-4939-9074-0_6openalex-snapshot
Transposable Elements: Classification, Identification, and Their Use As a Tool For Comparative Genomics
inferred← citeshttps://doi.org/10.1007/978-1-61779-582-4_12openalex-snapshot
Transposable Elements and Their Identification
inferred← citeshttps://doi.org/10.1007/978-3-032-04125-8_1openalex-snapshot
Transposable Elements and Genome Evolution in Vertebrates
inferred← citeshttps://doi.org/10.1007/978-3-642-30425-5_16openalex-snapshot
Functional Retrogenes in Animal Genomes
inferred← citeshttps://doi.org/10.1007/978-3-642-55606-7_1openalex-snapshot
Genome System Architecture and Natural Genetic Engineering
inferred← citeshttps://doi.org/10.1007/978-3-662-21930-0_1openalex-snapshot
Cell Surface Receptors and the G Protein-Coupled Receptor Superfamily
inferred← citeshttps://doi.org/10.1007/978-3-7091-1130-7openalex-snapshot
Plant Genome Diversity Volume 1
inferred← citeshttps://doi.org/10.1007/978-3-7091-1130-7_3openalex-snapshot
The Impact of Transposable Elements on Gene and Genome Evolution
inferred← citeshttps://doi.org/10.1007/978-94-010-0229-5_1openalex-snapshot
The contribution of RNAs and retroposition to evolutionary novelties
inferred← citeshttps://doi.org/10.1007/978-94-010-0229-5_8openalex-snapshot
Transposable elements and vertebrate protein diversity
inferred← citeshttps://doi.org/10.1007/978-94-010-0263-9_1openalex-snapshot
Gene duplication and other evolutionary strategies: from the RNA world to the future
inferred← citeshttps://doi.org/10.1007/978-94-011-2028-9_16openalex-snapshot
Transposable DNA elements and life history traits
inferred← citeshttps://doi.org/10.1007/978-94-011-2028-9_24openalex-snapshot
Natural genetic engineering in evolution
inferred← citeshttps://doi.org/10.1007/978-94-011-2028-9_9openalex-snapshot
Genome canalization: the coevolution of Transposable and Interspersed Repetitive Elements with single copy DNA
inferred← citeshttps://doi.org/10.1007/978-94-011-4156-7_23openalex-snapshot
Genomes were forged by massive bombardments with retroelements and retrosequences
inferred← citeshttps://doi.org/10.1007/978-94-011-4898-6_15openalex-snapshot
Plant S1 SINEs as a model to study retroposition
inferred← citeshttps://doi.org/10.1007/978-981-16-3997-5_11openalex-snapshot
De Novo Evolution of Genes in Rice
inferred← citeshttps://doi.org/10.1007/bf00021787openalex-snapshot
A major cysteine proteinase, EPB, in germinating barley seeds: structure of two intronless genes and regulation of expression
inferred← citeshttps://doi.org/10.1007/bf00132576openalex-snapshot
Increased concentration of some transcription factor binding sites in human retroposons of theAlu family
inferred← citeshttps://doi.org/10.1007/bf00133714openalex-snapshot
Natural genetic engineering in evolution
inferred← citeshttps://doi.org/10.1007/bf00133716openalex-snapshot
Modular transposition and the dynamical structure of eukaryote regulatory evolution
inferred← citeshttps://doi.org/10.1007/bf00133717openalex-snapshot
Transposable DNA elements and life history traits
inferred← citeshttps://doi.org/10.1007/bf00133722openalex-snapshot
Genome canalization: the coevolution of transposable and interspersed repetitive elements with single copy DNA
inferred← citeshttps://doi.org/10.1007/bf00160270openalex-snapshot
An analysis of retroposition in plants based on a family of SINEs from Brassica napus
inferred← citeshttps://doi.org/10.1007/bf00163206openalex-snapshot
The role and amplification of the HS Alu subfamily founder gene
inferred← citeshttps://doi.org/10.1007/bf00163211openalex-snapshot
Computer simulation of transposable element evolution: Random template and strict master models
inferred← citeshttps://doi.org/10.1007/bf00173420openalex-snapshot
Evolution of secondary structure in the family of 7SL-like RNAs
inferred← citeshttps://doi.org/10.1007/bf01435251openalex-snapshot
The mammalian genome shaping activity of reverse transcriptase
inferred← citeshttps://doi.org/10.1007/bf01728656openalex-snapshot
Reverse transcriptase: Mediator of genomic plasticity
inferred← citeshttps://doi.org/10.1007/bf02069557openalex-snapshot
Functional domains of the gonadotropin-releasing hormone receptor
inferred← citeshttps://doi.org/10.1007/bf02259494openalex-snapshot
Evolution of B2 repeats: the muroid explosion
inferred← citeshttps://doi.org/10.1007/pl00006264openalex-snapshot
The Evolution of MHC Diversity by Segmental Duplication and Transposition of Retroelements
inferred← citeshttps://doi.org/10.1007/pl00006426openalex-snapshot
The BC200 RNA Gene and Its Neural Expression Are Conserved in Anthropoidea (Primates)
inferred← citeshttps://doi.org/10.1007/s00018-007-7369-3openalex-snapshot
Conserved eukaryotic transposable elements and the evolution of gene regulation
inferred← citeshttps://doi.org/10.1007/s00239-013-9609-5openalex-snapshot
On the Origin and Evolution of Plant Brassinosteroid Receptor Kinases
inferred← citeshttps://doi.org/10.1007/s00239-018-9838-8openalex-snapshot
Evolution of Melanoma Antigen-A11 (MAGEA11) During Primate Phylogeny
inferred← citeshttps://doi.org/10.1007/s002390010087openalex-snapshot
Evolutionary History of B1 Retroposons in the Genus Mus
inferred← citeshttps://doi.org/10.1007/s00299-008-0520-2openalex-snapshot
AtCopeg1, the unique gene originated from AtCopia95 retrotransposon family, is sensitive to external hormones and abiotic stresses
inferred← citeshttps://doi.org/10.1007/s003359901092openalex-snapshot
The functional intronless S-adenosylmethionine decarboxylase gene of the mouse ( Amd-2 ) is linked to the ornithine decarboxylase gene ( Odc ) on Chromosome 12 and is present in distantly related species of the genus Mus
inferred← citeshttps://doi.org/10.1007/s00438-021-01797-8openalex-snapshot
A prescient evolutionary model for genesis, duplication and differentiation of MIR160 homologs in Brassicaceae
inferred← citeshttps://doi.org/10.1007/s10709-005-3086-8openalex-snapshot
ALU-ring elements in the primate genomes
inferred← citeshttps://doi.org/10.1007/s10709-010-9474-8openalex-snapshot
Drcd-1 related: a positively selected spermatogenesis retrogene in Drosophila
inferred← citeshttps://doi.org/10.1007/s11427-018-9447-8openalex-snapshot
Exaptation at the molecular genetic level
inferred← citeshttps://doi.org/10.1007/s11427-018-9449-0openalex-snapshot
Transposable elements significantly contributed to the core promoters in the human genome
inferred← citeshttps://doi.org/10.1007/s11515-013-1268-9openalex-snapshot
Development and utilization of new sequenced characterized amplified region markers specific for E genome of Thinopyrum
inferred← citeshttps://doi.org/10.1007/s12041-013-0212-8openalex-snapshot
Gene duplication as a major force in evolution
inferred← citeshttps://doi.org/10.1016/0014-5793(91)81370-nopenalex-snapshot
The evolution of placental mammals
inferred← citeshttps://doi.org/10.1016/0022-2836(92)90626-uopenalex-snapshot
Alu RNA transcripts in human embryonal carcinoma cells
inferred← citeshttps://doi.org/10.1016/0076-6879(93)24023-nopenalex-snapshot
[22] Molecular approaches to mammalian retrotransposon isolation
inferred← citeshttps://doi.org/10.1016/0092-8674(93)90318-kopenalex-snapshot
Transposons in place of telomeric repeats at a Drosophila telomere
inferred← citeshttps://doi.org/10.1016/0168-9525(94)90254-2openalex-snapshot
Alu sequences in the coding regions of mRNA: a source of protein variability
inferred← citeshttps://doi.org/10.1016/0378-1119(92)90654-8openalex-snapshot
A highly repetitive DNA sequence possibly unique to canids
inferred← citeshttps://doi.org/10.1016/0734-9750(95)02011-xopenalex-snapshot
Multifactional glucanases
inferred← citeshttps://doi.org/10.1016/b978-0-12-357490-9.50008-0openalex-snapshot
Genes, Genome Organization, and Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-415874-0.00004-4openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-815230-0.00004-2openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-012357031-4/50023-6openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-012444562-8/50018-5openalex-snapshot
Gn-RH as an Autocrine Regulator in the Human Ovary
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2016.08.005openalex-snapshot
Diversity, expansion, and evolutionary novelty of plant DNA-binding transcription factor families
inferred← citeshttps://doi.org/10.1016/j.ceb.2017.11.008openalex-snapshot
Novel gene function and regulation in neocortex expansion
inferred← citeshttps://doi.org/10.1016/j.cj.2018.12.008openalex-snapshot
Retrotransposon-mediated DELLA transcriptional reprograming underlies semi-dominant dwarfism in foxtail millet
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.12.046openalex-snapshot
Interpopulation differences of retroduplication variations (RDVs) in rice retrogenes and their phenotypic correlations
inferred← citeshttps://doi.org/10.1016/j.envres.2021.110913openalex-snapshot
Phenotype profiles and adaptive preference of Acinetobacter johnsonii isolated from Ba River with different environmental backgrounds
inferred← citeshttps://doi.org/10.1016/j.exphem.2016.06.251openalex-snapshot
Transposable elements: The enemies within
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.01.070openalex-snapshot
Functional and evolutionary analyses on expressed intronless genes in the mouse genome
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.08.042openalex-snapshot
The role of mRNA‐based duplication in the evolution of the primate genome
inferred← citeshttps://doi.org/10.1016/j.gde.2009.10.013openalex-snapshot
Transposable elements in gene regulation and in the evolution of vertebrate genomes
inferred← citeshttps://doi.org/10.1016/j.gene.2005.09.036openalex-snapshot
Transposable elements as a significant source of transcription regulating signals
inferred← citeshttps://doi.org/10.1016/j.gene.2007.07.012openalex-snapshot
Transposable element fragments in protein-coding regions and their contributions to human functional proteins
inferred← citeshttps://doi.org/10.1016/j.gene.2007.10.008openalex-snapshot
Newly discovered young CORE-SINEs in marsupial genomes
inferred← citeshttps://doi.org/10.1016/j.gene.2008.04.022openalex-snapshot
Retroposons of salmonoid fishes (Actinopterygii: Salmonoidei) and their evolution
inferred← citeshttps://doi.org/10.1016/j.gene.2009.06.008openalex-snapshot
The adaptive role of transposable elements in the Drosophila genome
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e14466openalex-snapshot
The origin of genetic and metabolic systems: Evolutionary structuralinsights
inferred← citeshttps://doi.org/10.1016/j.ins.2015.02.012openalex-snapshot
Forced evolution in silico by artificial transposons and their genetic operators: The ant navigation problem
inferred← citeshttps://doi.org/10.1016/j.jia.2024.12.002openalex-snapshot
SiDWARF4 encodes an ent-copalyl diphosphate synthase (CPS) required for gibberellin biosynthesis and morphogenesis in foxtail millet
inferred← citeshttps://doi.org/10.1016/j.jmb.2004.06.045openalex-snapshot
Neuronal MAP2 mRNA: Species-dependent Differential Dendritic Targeting Competence
inferred← citeshttps://doi.org/10.1016/j.jmb.2005.03.058openalex-snapshot
An Unusual Primate Locus that Attracted Two Independent Alu Insertions and Facilitates their Transcription
inferred← citeshttps://doi.org/10.1016/j.margen.2011.03.004openalex-snapshot
Comparative analysis of intronless genes in teleost fish genomes: Insights into their evolution and molecular function
inferred← citeshttps://doi.org/10.1016/j.mcn.2006.10.009openalex-snapshot
Loss of neurturin in frog—Comparative genomics study of GDNF family ligand-receptor pairs
inferred← citeshttps://doi.org/10.1016/j.tibs.2012.11.001openalex-snapshot
Translational control at the synapse: role of RNA regulators
inferred← citeshttps://doi.org/10.1016/j.tig.2006.03.006openalex-snapshot
Do transposable elements really contribute to proteomes?
inferred← citeshttps://doi.org/10.1016/j.tig.2007.03.003openalex-snapshot
The ambiguous boundary between genes and pseudogenes: the dead rise up, or do they?
inferred← citeshttps://doi.org/10.1016/j.tree.2004.08.002openalex-snapshot
SINEs of speciation: tracking lineages with retroposons
inferred← citeshttps://doi.org/10.1016/j.ygeno.2008.01.004openalex-snapshot
Organization and evolution of mitochondrial gene clusters in human
inferred← citeshttps://doi.org/10.1016/j.ygeno.2008.09.006openalex-snapshot
Quality of regulatory elements in Drosophila retrogenes
inferred← citeshttps://doi.org/10.1016/s0021-9258(19)49826-8openalex-snapshot
Gene and pseudogene of the mouse cation-dependent mannose 6-phosphate receptor. Genomic organization, expression, and chromosomal localization.
inferred← citeshttps://doi.org/10.1016/s0021-9258(19)89484-xopenalex-snapshot
Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene
inferred← citeshttps://doi.org/10.1016/s0065-230x(08)60824-6openalex-snapshot
Genomic Instability and Tumor Progression: Mechanistic Considerations
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61050-5openalex-snapshot
Control of Genes by Mammalian Retroposons
inferred← citeshttps://doi.org/10.1016/s0079-6603(08)60148-8openalex-snapshot
Alu: Structure, Origin, Evolution, Significance, and Function of One-Tenth of Human DNA
inferred← citeshttps://doi.org/10.1016/s0079-6603(08)60964-2openalex-snapshot
Evolution, Expression, and Possible Function of a Master Gene for Amplification of an Interspersed Repeated DNA Family in Rodents
inferred← citeshttps://doi.org/10.1016/s0168-9525(99)01783-7openalex-snapshot
Many G-protein-coupled receptors are encoded by retrogenes
inferred← citeshttps://doi.org/10.1016/s0378-1119(00)00436-4openalex-snapshot
Genomic scrap yard: how genomes utilize all that junk
inferred← citeshttps://doi.org/10.1016/s0378-1119(97)00289-8openalex-snapshot
A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7A)
inferred← citeshttps://doi.org/10.1016/s0378-1119(99)00227-9openalex-snapshot
RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements
inferred← citeshttps://doi.org/10.1016/s0378-1119(99)00229-2openalex-snapshot
Origin of new genes and source for N-terminal domain of the chimerical gene, jingwei, in Drosophila
inferred← citeshttps://doi.org/10.1016/s0925-4773(00)00307-5openalex-snapshot
Tissue-specific developmental expression of OAX, a Xenopus repetitive element
inferred← citeshttps://doi.org/10.1016/s0955-0674(02)00338-1openalex-snapshot
SINEs and LINEs: the art of biting the hand that feeds you
inferred← citeshttps://doi.org/10.1016/s0959-437x(00)00252-5openalex-snapshot
Evolution of novel genes
inferred← citeshttps://doi.org/10.1016/s1673-8527(08)60085-5openalex-snapshot
On the origin and evolution of new genes—a genomic and experimental perspective
inferred← citeshttps://doi.org/10.1023/a:1004018519722openalex-snapshot
Genomes were forged by massive bombardments with retroelements and retrosequences
inferred← citeshttps://doi.org/10.1023/a:1016024131097openalex-snapshot
Expansion of genome coding regions by acquisition of new genes
inferred← citeshttps://doi.org/10.1023/a:1018377411475openalex-snapshot
Plant S1 SINEs as a model to study retroposition
inferred← citeshttps://doi.org/10.1023/a:1022627311114openalex-snapshot
Gene duplication and other evolutionary strategies: from the RNA world to the future
inferred← citeshttps://doi.org/10.1023/a:1024105726123openalex-snapshot
Transposable Elements and Vertebrate Protein Diversity
inferred← citeshttps://doi.org/10.1023/a:1024141306559openalex-snapshot
The Contribution of RNAs and Retroposition to Evolutionary Novelties
inferred← citeshttps://doi.org/10.1038/74184openalex-snapshot
Human LINE retrotransposons generate processed pseudogenes
inferred← citeshttps://doi.org/10.1038/ng.2649openalex-snapshot
DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape
inferred← citeshttps://doi.org/10.1038/ng.600openalex-snapshot
Transposable elements have rewired the core regulatory network of human embryonic stem cells
inferred← citeshttps://doi.org/10.1038/ng1338openalex-snapshot
Duplication-degeneration as a mechanism of gene fission and the origin of new genes in Drosophila species
inferred← citeshttps://doi.org/10.1038/nrg1204openalex-snapshot
The origin of new genes: glimpses from the young and old
inferred← citeshttps://doi.org/10.1038/nrg2337openalex-snapshot
Transposable elements and the evolution of regulatory networks
inferred← citeshttps://doi.org/10.1038/s41438-018-0104-4openalex-snapshot
Expansion of PmBEAT genes in the Prunus mume genome induces characteristic floral scent production
inferred← citeshttps://doi.org/10.1038/s41438-019-0211-xopenalex-snapshot
Evolution and roles of cytokinin genes in angiosperms 1: Do ancient IPTs play housekeeping while non-ancient IPTs play regulatory roles?
inferred← citeshttps://doi.org/10.1038/s41438-020-0246-zopenalex-snapshot
Evolution and roles of cytokinin genes in angiosperms 2: Do ancient CKXs play housekeeping roles while non-ancient CKXs play regulatory roles?
inferred← citeshttps://doi.org/10.1038/s41559-017-0283-7openalex-snapshot
Adaptive evolution by spontaneous domain fusion and protein relocalization
inferred← citeshttps://doi.org/10.1038/s41588-024-02059-0openalex-snapshot
Functional innovation through new genes as a general evolutionary process
inferred← citeshttps://doi.org/10.1038/s41598-020-77381-8openalex-snapshot
MicroRNA retrocopies generated via L1-mediated retrotransposition in placental mammals help to reveal how their parental genes were transcribed
inferred← citeshttps://doi.org/10.1038/s41598-021-82735-xopenalex-snapshot
The enhancer activity of long interspersed nuclear element derived microRNA 625 induced by NF-κB
inferred← citeshttps://doi.org/10.1038/s43587-025-00852-yopenalex-snapshot
The retrotransposon-derived capsid genes PNMA1 and PNMA4 maintain reproductive capacity
inferred← citeshttps://doi.org/10.1038/sj.leu.2403340openalex-snapshot
Split-signal FISH for detection of chromosome aberrations in acute lymphoblastic leukemia
inferred← citeshttps://doi.org/10.1046/j.1365-2583.1999.00144.xopenalex-snapshot
DEC: a new miniature inverted‐repeat transposable element from the genome of the beetle Tenebrio molitor
inferred← citeshttps://doi.org/10.1046/j.1365-2583.1999.810141.xopenalex-snapshot
Is the insect glutathione S‐transferase I gene family intronless?
inferred← citeshttps://doi.org/10.1073/pnas.0511307103openalex-snapshot
Evolutionary fate of retroposed gene copies in the human genome
inferred← citeshttps://doi.org/10.1073/pnas.072066399openalex-snapshot
Origin of sphinx , a young chimeric RNA gene in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1073/pnas.2206025119openalex-snapshot
Silencing RNAs expressed from W-linked PxyMasc “retrocopies” target that gene during female sex determination in Plutella xylostella
inferred← citeshttps://doi.org/10.1073/pnas.88.20.9175openalex-snapshot
Multiple human D5 dopamine receptor genes: a functional receptor and two pseudogenes.
inferred← citeshttps://doi.org/10.1073/pnas.89.22.10706openalex-snapshot
On "genomenclature": a comprehensive (and respectful) taxonomy for pseudogenes and other "junk DNA".
inferred← citeshttps://doi.org/10.1073/pnas.90.24.11563openalex-snapshot
BC200 RNA: a neural RNA polymerase III product encoded by a monomeric Alu element.
inferred← citeshttps://doi.org/10.1073/pnas.91.13.5992openalex-snapshot
Evolutionary selection against change in many Alu repeat sequences interspersed through primate genomes.
inferred← citeshttps://doi.org/10.1073/pnas.91.21.10153openalex-snapshot
Species-specific amplification of tRNA-derived short interspersed repetitive elements (SINEs) by retroposition: a process of parasitization of entire genomes during the evolution of salmonids.
inferred← citeshttps://doi.org/10.1073/pnas.91.9.3607openalex-snapshot
Rodent BC1 RNA gene as a master gene for ID element amplification.
inferred← citeshttps://doi.org/10.1073/pnas.93.3.1077openalex-snapshot
DANA elements: a family of composite, tRNA-derived short interspersed DNA elements associated with mutational activities in zebrafish (Danio rerio).
inferred← citeshttps://doi.org/10.1074/jbc.270.10.5642openalex-snapshot
Cloning and Sequencing of an Intronless Mouse S-Adenosylmethionine Decarboxylase Gene Coding for a Functional Enzyme Strongly Expressed in the Liver
inferred← citeshttps://doi.org/10.1074/jbc.274.35.24849openalex-snapshot
A Set of Highly Conserved RNA-binding Proteins, αCP-1 and αCP-2, Implicated in mRNA Stabilization, Are Coexpressed from an Intronless Gene and Its Intron-containing Paralog
inferred← citeshttps://doi.org/10.1074/jbc.m101760200openalex-snapshot
Characterization of Sptrx, a Novel Member of the Thioredoxin Family Specifically Expressed in Human Spermatozoa
inferred← citeshttps://doi.org/10.1074/jbc.m205358200openalex-snapshot
Biological Potential of a Functional Human SNAILRetrogene
inferred← citeshttps://doi.org/10.1074/jbc.m412450200openalex-snapshot
Cloning, Sequencing, and Characterization of Alternatively Spliced Glutaredoxin 1 cDNA and Its Genomic Gene
inferred← citeshttps://doi.org/10.1080/07352689.2019.1682791openalex-snapshot
The Hot and the Colorful: Understanding the Metabolism, Genetics and Evolution of Consumer Preferred Metabolic Traits in Pepper and Related Species
inferred← citeshttps://doi.org/10.1080/10245330512331389980openalex-snapshot
Split-signal FISH for detection of chromosome aberrations
inferred← citeshttps://doi.org/10.1080/106351500750049851openalex-snapshot
SINE Evolution, Missing Data, and the Origin of Whales
inferred← citeshttps://doi.org/10.1080/10635150601077634openalex-snapshot
Exploring Frontiers in the DNA Landscape: An Introduction to the Symposium “Genome Analysis and the Molecular Systematics of Retroelements”
inferred← citeshttps://doi.org/10.1083/jcb.201310045openalex-snapshot
Interactions of noncanonical motifs with hnRNP A2 promote activity-dependent RNA transport in neurons
inferred← citeshttps://doi.org/10.1089/dna.1992.11.1openalex-snapshot
Sequence Alignment of the G-Protein Coupled Receptor Superfamily
inferred← citeshttps://doi.org/10.1089/dna.1994.13.605openalex-snapshot
Structure of the Mouse Gonadotropin-Releasing Hormone Receptor Gene: Variant Transcripts Generated by Alternative Processing
inferred← citeshttps://doi.org/10.1089/dna.1995.14.485openalex-snapshot
Molecular Cloning and Characterization of the Mouse Dopamine D 3 Receptor Gene: An Additional Intron and an mRNA Variant
inferred← citeshttps://doi.org/10.1089/dna.1998.17.1009openalex-snapshot
Identification of CXorfl , a Novel Intronless Gene in Xq27.3, Expressed in Human Hippocampus
inferred← citeshttps://doi.org/10.1089/jir.1995.15.815openalex-snapshot
An Alu Cassette in the Cytoplasmic Domain of an Interferon Receptor Subunit
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199642274.003.0011openalex-snapshot
Evolutionary interactions between sex chromosomes and autosomes
inferred← citeshttps://doi.org/10.1093/bioinformatics/btg1056openalex-snapshot
How significant is 98.5% ‘junk’ in mammalian genomes?
inferred← citeshttps://doi.org/10.1093/database/bax038openalex-snapshot
RetrogeneDB–a database of plant and animal retrocopies
inferred← citeshttps://doi.org/10.1093/g3journal/jkad233openalex-snapshot
Comparative transcriptomics reveals divergence in pathogen response gene families amongst 20 forest tree species
inferred← citeshttps://doi.org/10.1093/gbe/evac141openalex-snapshot
Multiple Horizontal Acquisitions of Plant Genes in the Whitefly Bemisia tabaci
inferred← citeshttps://doi.org/10.1093/gbe/evad178openalex-snapshot
Insights into the Evolution of Ohnologous Sequences and Their Epigenetic Marks Post-WGD in Malus Domestica
inferred← citeshttps://doi.org/10.1093/gbe/evq021openalex-snapshot
PiggyBac-ing on a Primate Genome: Novel Elements, Recent Activity and Horizontal Transfer
inferred← citeshttps://doi.org/10.1093/gbe/evt155openalex-snapshot
Alternative Processing as Evolutionary Mechanism for the Origin of Novel Nonprotein Coding RNAs
inferred← citeshttps://doi.org/10.1093/gbe/evy098openalex-snapshot
Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
inferred← citeshttps://doi.org/10.1093/gbe/evy193openalex-snapshot
Factors Influencing Gene Family Size Variation Among Related Species in a Plant Family, Solanaceae
inferred← citeshttps://doi.org/10.1093/gbe/evz185openalex-snapshot
The Genomic Substrate for Adaptive Radiation: Copy Number Variation across 12 Tribes of African Cichlid Species
inferred← citeshttps://doi.org/10.1093/jhered/esp047openalex-snapshot
Distinguishing Among Evolutionary Models for the Maintenance of Gene Duplicates
inferred← citeshttps://doi.org/10.1093/molbev/msl090openalex-snapshot
Fast Protein Evolution and Germ Line Expression of a Drosophila Parental Gene and Its Young Retroposed Paralog
inferred← citeshttps://doi.org/10.1093/molbev/msl201openalex-snapshot
Drosophila mojoless, a Retroposed GSK-3, Has Functionally Diverged to Acquire an Essential Role in Male Fertility
inferred← citeshttps://doi.org/10.1093/molbev/msm083openalex-snapshot
Novel SINE Families from Salmons Validate Parahucho (Salmonidae) as a Distinct Genus and Give Evidence that SINEs Can Incorporate LINE-related 3′-Tails of Other SINEs
inferred← citeshttps://doi.org/10.1093/molbev/msn105openalex-snapshot
Duplication and Functional Diversification of HAP3 Genes Leading to the Origin of the Seed-Developmental Regulatory Gene, LEAFY COTYLEDON1 (LEC1), in Nonseed Plant Genomes
inferred← citeshttps://doi.org/10.1093/molbev/msq260openalex-snapshot
Primate and Rodent Specific Intron Gains and the Origin of Retrogenes with Splice Variants
inferred← citeshttps://doi.org/10.1093/molbev/mss147openalex-snapshot
Parallel Relaxation of Stringent RNA Recognition in Plant and Mammalian L1 Retrotransposons
inferred← citeshttps://doi.org/10.1093/molbev/mss235openalex-snapshot
"Orphan" Retrogenes in the Human Genome
inferred← citeshttps://doi.org/10.1093/molbev/msu139openalex-snapshot
RetrogeneDB—A Database of Animal Retrogenes
inferred← citeshttps://doi.org/10.1093/nar/19.23.6533openalex-snapshot
The structure of the gene coding for the mouse cell adhesion molecule uvomorulin
showing the first 200 of 367 · page through all 367
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.