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Use of retrotransposon-derived genetic markers to analyse genomic variability in plants

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02728.xopenalex-snapshot
Studies on the introduction and mobility of the maize Activator element in Arabidopsis thaliana and Daucus carota.
inferredcites →https://doi.org/10.1007/978-1-62703-767-9_12openalex-snapshot
Transposon-Based Tagging: IRAP, REMAP, and iPBS
inferredcites →https://doi.org/10.1007/bf00027369openalex-snapshot
BARE-1, a copia-like retroelement in barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1007/bf02174388openalex-snapshot
TheTy1-copia group retrotransposons inVicia species: copy number, sequence heterogeneity and chromosomal localisation
inferredcites →https://doi.org/10.1007/pl00008630openalex-snapshot
Polymorphism of insertion sites of Ty1-copia class retrotransposons and its use for linkage and diversity analysis in pea
inferredcites →https://doi.org/10.1007/s00122-005-0203-0openalex-snapshot
TRIM retrotransposons occur in apple and are polymorphic between varieties but not sports
inferredcites →https://doi.org/10.1007/s00122-010-1311-zopenalex-snapshot
Polymorphism of a new Ty1-copia retrotransposon in durum wheat under salt and light stresses
inferredcites →https://doi.org/10.1007/s00122-010-1398-2openalex-snapshot
iPBS: a universal method for DNA fingerprinting and retrotransposon isolation
inferredcites →https://doi.org/10.1007/s00122-011-1539-2openalex-snapshot
Genetic diversity of cultivated flax (Linum usitatissimum L.) germplasm assessed by retrotransposon-based markers
inferredcites →https://doi.org/10.1007/s00122-012-1925-4openalex-snapshot
A transgenic system for generation of transposon Ac/Ds-induced chromosome rearrangements in rice
inferredcites →https://doi.org/10.1007/s00122-014-2293-zopenalex-snapshot
The Tvv1 retrotransposon family is conserved between plant genomes separated by over 100 million years
inferredcites →https://doi.org/10.1007/s00122-014-2422-8openalex-snapshot
Development of IRAP- and REMAP-derived SCAR markers for marker-assisted selection of the stripe rust resistance gene Yr15 derived from wild emmer wheat
inferredcites →https://doi.org/10.1007/s00438-003-0850-2openalex-snapshot
Comparison of the utility of barley retrotransposon families for genetic analysis by molecular marker techniques
inferredcites →https://doi.org/10.1007/s00438-014-0914-5openalex-snapshot
Prediction of retrotransposons and assessment of genetic variability based on developed retrotransposon-based insertion polymorphism (RBIP) markers in Pyrus L
inferredcites →https://doi.org/10.1007/s004380000326openalex-snapshot
Application of BARE-1 retrotransposon markers to the mapping of a major resistance gene for net blotch in barley
inferredcites →https://doi.org/10.1007/s004380050372openalex-snapshot
Genetic distribution of Bare–1-like retrotransposable elements in the barley genome revealed by sequence-specific amplification polymorphisms (S-SAP)
inferredcites →https://doi.org/10.1007/s00439-012-1165-3openalex-snapshot
Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats
inferredcites →https://doi.org/10.1007/s10265-017-0983-8openalex-snapshot
A transposition-active Phyllostachys edulis long terminal repeat (LTR) retrotransposon
inferredcites →https://doi.org/10.1007/s10577-017-9569-5openalex-snapshot
Transposable elements: genome innovation, chromosome diversity, and centromere conflict
inferredcites →https://doi.org/10.1007/s10681-015-1537-6openalex-snapshot
Retrotransposon molecular markers resolve cocoyam (Xanthosoma sagittifolium) and taro (Colocasia esculenta) by type and variety
inferredcites →https://doi.org/10.1007/s10709-017-9977-7openalex-snapshot
Diversity, distribution and dynamics of full-length Copia and Gypsy LTR retroelements in Solanum lycopersicum
inferredcites →https://doi.org/10.1007/s11033-011-1112-8openalex-snapshot
Isolation of Ty1-copia retrotransposon in myrtle genome and development of S-SAP molecular marker
inferredcites →https://doi.org/10.1007/s11033-018-4146-3openalex-snapshot
Molecular characterization of Fagaceae species using inter-primer binding site (iPBS) markers
inferredcites →https://doi.org/10.1007/s11295-009-0263-4openalex-snapshot
Retrotransposon-based molecular markers for grapevine species and cultivars identification
inferredcites →https://doi.org/10.1007/s12298-017-0446-7openalex-snapshot
Assessment of genetic diversity and population structure of an endemic Moroccan tree (Argania spinosa L.) based in IRAP and ISSR markers and implications for conservation
inferredcites →https://doi.org/10.1007/s13258-017-0619-3openalex-snapshot
Ty3/Gypsy retrotransposons in the Pacific abalone Haliotis discus hannai: characterization and use for species identification in the genus Haliotis
inferredcites →https://doi.org/10.1007/s13258-018-0655-7openalex-snapshot
Retrotransposons in Betula nana, and interspecific relationships in the Betuloideae, based on inter-retrotransposon amplified polymorphism (IRAP) markers
inferredcites →https://doi.org/10.1016/0888-7543(90)90166-ropenalex-snapshot
Alumorphs—Human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers
inferredcites →https://doi.org/10.1016/0955-0674(90)90130-7openalex-snapshot
Transposable elements and DNA transposition in eukaryotes
inferredcites →https://doi.org/10.1016/j.cell.2017.06.013openalex-snapshot
LTR-Retrotransposon Control by tRNA-Derived Small RNAs
inferredcites →https://doi.org/10.1016/j.copbio.2015.01.003openalex-snapshot
Controlled activation of retrotransposition for plant breeding
inferredcites →https://doi.org/10.1016/j.coviro.2013.08.009openalex-snapshot
Retrotransposon replication in plants
inferredcites →https://doi.org/10.1016/j.funbio.2011.08.007openalex-snapshot
Silencing of the PiAvr3a effector-encoding gene from Phytophthora infestans by transcriptional fusion to a short interspersed element
inferredcites →https://doi.org/10.1016/j.pbi.2012.09.001openalex-snapshot
Developmental relaxation of transposable element silencing in plants: functional or byproduct?
inferredcites →https://doi.org/10.1016/j.pbi.2017.03.002openalex-snapshot
Genetic and epigenetic variation of transposable elements in Arabidopsis
inferredcites →https://doi.org/10.1016/j.ygeno.2017.05.005openalex-snapshot
FastPCR: An in silico tool for fast primer and probe design and advanced sequence analysis
inferredcites →https://doi.org/10.1016/j.ympev.2015.03.009openalex-snapshot
A survey of transposable element classification systems – A call for a fundamental update to meet the challenge of their diversity and complexity
inferredcites →https://doi.org/10.1023/a:1014831511810openalex-snapshot
A high-density cytogenetic map of the Aegilops tauschii genome incorporating retrotransposons and defense-related genes: insights into cereal chromosome structure and function
inferredcites →https://doi.org/10.1038/hdy.2009.45openalex-snapshot
Evolutionary conserved lineage of Angela-family retrotransposons as a genome-wide microsatellite repeat dispersal agent
inferredcites →https://doi.org/10.1038/ncomms15407openalex-snapshot
A TRIM insertion in the promoter of Ms2 causes male sterility in wheat
inferredcites →https://doi.org/10.1038/nprot.2006.377openalex-snapshot
IRAP and REMAP for retrotransposon-based genotyping and fingerprinting
inferredcites →https://doi.org/10.1038/s41467-017-01374-xopenalex-snapshot
High-frequency recombination between members of an LTR retrotransposon family during transposition bursts
inferredcites →https://doi.org/10.1038/s41598-017-06084-4openalex-snapshot
RETRACTED ARTICLE: Comparison of traditional and new generation DNA markers declares high genetic diversity and differentiated population structure of wild almond species
inferredcites →https://doi.org/10.1038/srep43766openalex-snapshot
Gene Deletion in Barley Mediated by LTR-retrotransposon BARE
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00004.xopenalex-snapshot
Transposon Display identifies individual transposable elements in high copy number lines
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00556.xopenalex-snapshot
Rapid isolation of plant Ty1‐copia group retrotransposon LTR sequences for molecular marker studies
inferredcites →https://doi.org/10.1073/pnas.0709698105openalex-snapshot
Cassandra retrotransposons carry independently transcribed 5S RNA
inferredcites →https://doi.org/10.1073/pnas.110587497openalex-snapshot
Genome evolution of wild barley ( Hordeum spontaneum ) by BARE -1 retrotransposon dynamics in response to sharp microclimatic divergence
inferredcites →https://doi.org/10.1073/pnas.241341898openalex-snapshot
Terminal-repeat retrotransposons in miniature (TRIM) are involved in restructuring plant genomes
inferredcites →https://doi.org/10.1073/pnas.75.11.5631openalex-snapshot
Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.
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/10.1073/pnas.89.15.7124openalex-snapshot
copia-like retrotransposons are ubiquitous among plants.
inferredcites →https://doi.org/10.1073/pnas.95.21.12432openalex-snapshot
Knock-out mutants from an En-1 mutagenized Arabidopsis thaliana population generate phenylpropanoid biosynthesis phenotypes
inferredcites →https://doi.org/10.1093/aob/mcx078openalex-snapshot
Impact of transposable elements on polyploid plant genomes
inferredcites →https://doi.org/10.1093/bioinformatics/btv281openalex-snapshot
HTT-DB: Horizontally transferred transposable elements database
inferredcites →https://doi.org/10.1093/dnares/dsu015openalex-snapshot
Efficient DNA Fingerprinting Based on the Targeted Sequencing of Active Retrotransposon Insertion Sites Using a Bench-Top High-Throughput Sequencing Platform
inferredcites →https://doi.org/10.1093/gbe/evw243openalex-snapshot
LINEs between Species: Evolutionary Dynamics of LINE-1 Retrotransposons across the Eukaryotic Tree of Life
inferredcites →https://doi.org/10.1093/genetics/54.2.595openalex-snapshot
A MOLECULAR APPROACH TO THE STUDY OF GENIC HETEROZYGOSITY IN NATURAL POPULATIONS. II. AMOUNT OF VARIATION AND DEGREE OF HETEROZYGOSITY IN NATURAL POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/molbev/msx275openalex-snapshot
Horizontal Transfer of Non-LTR Retrotransposons from Arthropods to Flowering Plants
inferredcites →https://doi.org/10.1093/nar/20.14.3639openalex-snapshot
Ty1–copiagroup retrotransposons are ubiquitous and heterogeneous in higher plants
inferredcites →https://doi.org/10.1093/nar/23.21.4407openalex-snapshot
AFLP: a new technique for DNA fingerprinting
inferredcites →https://doi.org/10.1093/nar/gkx1150openalex-snapshot
Diversity-generating retroelements: natural variation, classification and evolution inferred from a large-scale genomic survey
inferredcites →https://doi.org/10.1093/pcp/pcw202openalex-snapshot
Inducible Transposition of a Heat-Activated Retrotransposon in Tissue Culture
inferredcites →https://doi.org/10.1101/gr.10.7.908openalex-snapshot
A Contiguous 66-kb Barley DNA Sequence Provides Evidence for Reversible Genome Expansion
inferredcites →https://doi.org/10.1101/gr.193301openalex-snapshot
Envelope -Class Retrovirus-Like Elements Are Widespread, Transcribed and Spliced, and Insertionally Polymorphic in Plants
inferredcites →https://doi.org/10.1101/gr.6214107openalex-snapshot
Genome-wide comparative analysis of copia retrotransposons in Triticeae, rice, and Arabidopsis reveals conserved ancient evolutionary lineages and distinct dynamics of individual copia families
inferredcites →https://doi.org/10.1104/pp.113.216481openalex-snapshot
The Initiation of Epigenetic Silencing of Active Transposable Elements Is Triggered by RDR6 and 21-22 Nucleotide Small Interfering RNAs
inferredcites →https://doi.org/10.1105/tpc.16.00718openalex-snapshot
Exogenous Transposable Elements Circumvent Identity-Based Silencing, Permitting the Dissection of Expression-Dependent Silencing
inferredcites →https://doi.org/10.1105/tpc.4.10.1283openalex-snapshot
Tourist: A Large Family of Small Inverted Repeat Elements Frequently Associated with Maize Genes
inferredcites →https://doi.org/10.1111/tpj.12285openalex-snapshot
Genome‐wide analysis of short interspersed nuclear elements SINES revealed high sequence conservation, gene association and retrotranspositional activity in wheat
inferredcites →https://doi.org/10.1111/tpj.13481openalex-snapshot
Transposable elements ( TE s) contribute to stress‐related long intergenic noncoding RNA s in plants
inferredcites →https://doi.org/10.1111/tpj.13526openalex-snapshot
DNA methylation of retrotransposons, DNA transposons and genes in sugar beet (Beta vulgaris L.)
inferredcites →https://doi.org/10.1128/mcb.15.6.3310openalex-snapshot
A Novel Mechanism of Self-Primed Reverse Transcription Defines a New Family of Retroelements
inferredcites →https://doi.org/10.1134/s1022795410010060openalex-snapshot
Using IRAP markers for analysis of genetic variability in populations of resource and rare species of plants
inferredcites →https://doi.org/10.1139/g06-074openalex-snapshot
Retrotransposon-based S-SAP as a platform for the analysis of genetic variation and linkage in globe artichoke
inferredcites →https://doi.org/10.1139/g06-119openalex-snapshot
Mapping of major spot-type and net-type net-blotch resistance genes in the Ethiopian barley line CI 9819
inferredcites →https://doi.org/10.1139/g07-036openalex-snapshot
A major gene for grain cadmium accumulation in oat (Avena sativa L.)
inferredcites →https://doi.org/10.1139/g08-040openalex-snapshot
The first doubled haploid linkage map for cultivated oat
inferredcites →https://doi.org/10.1139/gen-2014-0031openalex-snapshot
Efficient screening of long terminal repeat retrotransposons that show high insertion polymorphism via high-throughput sequencing of the primer binding site
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.1openalex-snapshot
HIV-1: Fifteen Proteins and an RNA
inferredcites →https://doi.org/10.1159/000121084openalex-snapshot
Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes
inferredcites →https://doi.org/10.1186/1471-2148-10-44openalex-snapshot
The genetic diversity and evolution of field pea (Pisum) studied by high throughput retrotransposon based insertion polymorphism (RBIP) marker analysis
inferredcites →https://doi.org/10.1186/1471-2156-6-15openalex-snapshot
Rim 2/Hipa CACTA transposon display ; A new genetic marker technique in Oryza species
inferredcites →https://doi.org/10.1186/1471-2164-16-s12-s1openalex-snapshot
ARG-walker: inference of individual specific strengths of meiotic recombination hotspots by population genomics analysis
inferredcites →https://doi.org/10.1186/1759-8753-1-6openalex-snapshot
Transposable elements in a marginal plant population: temporal fluctuations provide new insights into genome evolution of wild diploid wheat
inferredcites →https://doi.org/10.1186/1759-8753-2-4openalex-snapshot
Plant centromeric retrotransposons: a structural and cytogenetic perspective
inferredcites →https://doi.org/10.1186/s12864-016-3337-3openalex-snapshot
Ty1-copia elements reveal diverse insertion sites linked to polymorphisms among flax (Linum usitatissimum L.) accessions
inferredcites →https://doi.org/10.1186/s12864-017-3753-zopenalex-snapshot
Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
inferredcites →https://doi.org/10.1186/s12864-017-4050-6openalex-snapshot
Genome-wide analysis of LTR-retrotransposon diversity and its impact on the evolution of the genus Helianthus (L.)
inferredcites →https://doi.org/10.1186/s12870-017-1108-1openalex-snapshot
Maize RNA PolIV affects the expression of genes with nearby TE insertions and has a genome-wide repressive impact on transcription
inferredcites →https://doi.org/10.1186/s12870-017-1223-zopenalex-snapshot
Genomic abundance and transcriptional activity of diverse gypsy and copia long terminal repeat retrotransposons in three wild sunflower species
inferredcites →https://doi.org/10.1186/s13059-017-1341-9openalex-snapshot
New reference genome sequences of hot pepper reveal the massive evolution of plant disease-resistance genes by retroduplication
inferredcites →https://doi.org/10.1186/s41065-016-0009-xopenalex-snapshot
Assessment of genetic diversity in Nordic timothy (Phleum pratense L.)
inferredcites →https://doi.org/10.1266/jjg.68.35openalex-snapshot
Ty1-copia group retrotransposons as ubiquitous components of plant genomes.
inferredcites →https://doi.org/10.1270/jsbbs.17085openalex-snapshot
Characterization of a heat-activated retrotransposon in Vigna angularis
inferredcites →https://doi.org/10.1371/annotation/4ccaacb2-92d7-445a-87da-313cedf18febopenalex-snapshot
Correction: Next Generation Sequencing-Based Analysis of Repetitive DNA in the Model Dioceous Plant Silene latifolia
inferredcites →https://doi.org/10.1371/journal.pone.0027335openalex-snapshot
Next Generation Sequencing-Based Analysis of Repetitive DNA in the Model Dioceous Plant Silene latifolia
inferredcites →https://doi.org/10.15252/embr.201642743openalex-snapshot
CTRL+INSERT: retrotransposons and their contribution to regulation and innovation of the transcriptome
inferredcites →https://doi.org/10.1534/genetics.111.134643openalex-snapshot
Diversity of Long Terminal Repeat Retrotransposon Genome Distribution in Natural Populations of the Wild Diploid WheatAegilops speltoides
inferredcites →https://doi.org/10.1534/genetics.117.300103openalex-snapshot
Developmental Restriction of Retrotransposition Activated in Arabidopsis by Environmental Stress
inferredcites →https://doi.org/10.1534/genetics.166.3.1437openalex-snapshot
Large Retrotransposon Derivatives: Abundant, Conserved but Nonautonomous Retroelements of Barley and Related Genomes
inferredcites →https://doi.org/10.2144/000113655openalex-snapshot
Adaptation of the AFLP technique as a new tool to detect genetic instability and transposition in interspecific hybrids
inferredcites →https://doi.org/10.3389/fpls.2018.00600openalex-snapshot
Transposon-Derived Non-coding RNAs and Their Function in Plants
inferredcites →https://doi.org/10.3390/agronomy8070107openalex-snapshot
Retrotransposon-Based Genetic Diversity Assessment in Wild Emmer Wheat (Triticum turgidum ssp. dicoccoides)
inferredcites →https://doi.org/10.3390/genes9010023openalex-snapshot
Identification of Transposable Elements Contributing to Tissue-Specific Expression of Long Non-Coding RNAs
inferredcites →https://doi.org/10.4161/mge.34394openalex-snapshot
Interspecific hybridization as a genomic stressor inducing mobilization of transposable elements inDrosophila
inferredcites →https://doi.org/10.5937/ratpov1102261kopenalex-snapshot
The use of retrotransposon-based molecular markers to analyze genetic diversity

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.phytochem.2020.112330zenodo-depositor-declared
Efficiency of RAPD, ISSR, iPBS, SCoT and phytochemical markers in the genetic relationship study of five native and economical important bamboos of North-East India
inferred← citeshttps://doi.org/10.1002/ece3.7095openalex-snapshot
Retrotransposon‐based genetic diversity of Deschampsia antarctica Desv. from King George Island (Maritime Antarctic)
inferred← citeshttps://doi.org/10.1007/978-1-0716-0997-2_15openalex-snapshot
Retrotransposable Elements: DNA Fingerprinting and the Assessment of Genetic Diversity
inferred← citeshttps://doi.org/10.1007/978-1-0716-0997-2_3openalex-snapshot
Isolation and Purification of DNA from Complicated Biological Samples
inferred← citeshttps://doi.org/10.1007/978-1-0716-1799-1_16openalex-snapshot
A Guide to Using FASTPCR Software for PCR, In Silico PCR, and Oligonucleotide Analysis
inferred← citeshttps://doi.org/10.1007/978-3-030-93390-6_3openalex-snapshot
Transposable Elements in Pines
inferred← citeshttps://doi.org/10.1007/978-3-031-10721-4_1openalex-snapshot
Cisgenic Crops: Biodiversity, Ecosystems, and Environment
inferred← citeshttps://doi.org/10.1007/978-981-96-9859-2_6openalex-snapshot
Mobile Genetic Elements and Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-99-1612-2_9openalex-snapshot
Applicability of Molecular Markers in Ascertaining Genetic Diversity and Relationship Between Five Edible Bamboos of North-East India
inferred← citeshttps://doi.org/10.1007/978-981-99-5245-8_11openalex-snapshot
Genetic Diversity Assessment in Cereal Crops
inferred← citeshttps://doi.org/10.1007/s10709-019-00055-5openalex-snapshot
Genetic analysis of the grapevine genotypes of the Russian Vitis ampelographic collection using iPBS markers
inferred← citeshttps://doi.org/10.1007/s11033-020-05246-4openalex-snapshot
High-throughput retrotransposon-based genetic diversity of maize germplasm assessment and analysis
inferred← citeshttps://doi.org/10.1007/s13353-021-00617-4openalex-snapshot
Clustered and dispersed chromosomal distribution of the two classes of Revolver transposon family in rye (Secale cereale)
inferred← citeshttps://doi.org/10.1007/s13353-023-00748-wopenalex-snapshot
The comparison of polymorphism among Avena species revealed by retrotransposon-based DNA markers and soluble carbohydrates in seeds
inferred← citeshttps://doi.org/10.1016/b978-0-12-819715-8.00005-7openalex-snapshot
Genome mapping tools: current research and future prospects
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2019.10.001openalex-snapshot
Retrotransposons shuttling genetic and epigenetic information from the nuclear to the mitochondrial compartment: Do they play a pathogenetic role in scleroderma?
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e08093openalex-snapshot
Basic concepts and methodologies of DNA marker systems in plant molecular breeding
inferred← citeshttps://doi.org/10.1016/j.jarmap.2021.100349openalex-snapshot
Genetic diversity and population structure of Clerodendrum serratum (L.) Moon using CBDP, iPBS and SCoT markers
inferred← citeshttps://doi.org/10.1016/j.lwt.2021.112823openalex-snapshot
Identification and technological characterization of endogenous yeast isolated from fermented black carrot juice, shalgam
inferred← citeshttps://doi.org/10.1016/j.pmpp.2024.102277openalex-snapshot
Genetic and pathogenic characterization of Rhizoctonia solani AG-4 isolates obtained from common bean
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109753openalex-snapshot
Retrotransposon-based genetic variation and population structure of Impatiens macrovexilla Y. L. Chen in natural habitats and the implications for breeding
inferred← citeshttps://doi.org/10.1080/07391102.2019.1654409openalex-snapshot
In silico determination of transposon-derived miRNAs and targets in Aegilops species
inferred← citeshttps://doi.org/10.1080/11263504.2019.1651782openalex-snapshot
Utility of iPBS retrotransposons markers for molecular characterization of African Gnetum species
inferred← citeshttps://doi.org/10.1080/14772000.2020.1827076openalex-snapshot
Retrotransposon-based molecular markers as a tool in delimiting species in section Ryncholotus, a recent radiation group of Macaronesian Lotus
inferred← citeshttps://doi.org/10.1080/15427528.2021.1973171openalex-snapshot
Genetic relationship of the winter barley varieties assessed by the inter-Primer Binding Site (iPBS) DNA profiling method
inferred← citeshttps://doi.org/10.1111/pbr.12960openalex-snapshot
Comparative assessment of microsatellite and retrotransposon‐based markers for genetic characterization of commercial banana cultivars (Musa spp.)
inferred← citeshttps://doi.org/10.1134/s1062359023602008openalex-snapshot
Effect of Mammalian Sex Hormones on Somaclonal Variation of Lotus corniculatus In Vitro Culture
inferred← citeshttps://doi.org/10.1186/s13100-021-00248-wopenalex-snapshot
A 192 bp ERV fragment insertion in the first intron of porcine TLR6 may act as an enhancer associated with the increased expressions of TLR6 and TLR1
inferred← citeshttps://doi.org/10.17557/tjfc.834403openalex-snapshot
POPULATION STRUCTURE AND LINKAGE DISEQUILIBRIUM ANALYSES OF MODEL PLANT Brachypodium distachion THROUGH iPBS MARKERS
inferred← citeshttps://doi.org/10.21203/rs.3.rs-101173/v1openalex-snapshot
An 192 bp ERV insertion in the first intron of TLR6 acts as an enhancer to increase TLR6 and TLR1 expression
inferred← citeshttps://doi.org/10.21203/rs.3.rs-693177/v1openalex-snapshot
SINE Insertion in 5’ Flanking of IGFBP3 May Associated With Gene Expression and Phenotypic Variations
inferred← citeshttps://doi.org/10.21203/rs.3.rs-871689/v1openalex-snapshot
SINE Insertion in 5’ Flanking of Porcine IGFBP3 May Associated with Gene Expression and Phenotypic Variations
inferred← citeshttps://doi.org/10.2174/9789815165555123010011openalex-snapshot
Genetic Stability in Micropropagated Orchids: Assessment by Molecular Markers and Flow Cytometry
inferred← citeshttps://doi.org/10.3103/s0095452721010047openalex-snapshot
Assessing the Levels of Polymorphism and Differentiation in Iris pumila L. Populations Using Three Types of PCR Markers
inferred← citeshttps://doi.org/10.31367/2079-8725-2026-102-1-50-57openalex-snapshot
Using retrotransposons to assess the genetic diversity of a tomato collection
inferred← citeshttps://doi.org/10.3389/fpls.2022.1064847openalex-snapshot
Retrotransposons: How the continuous evolutionary front shapes plant genomes for response to heat stress
inferred← citeshttps://doi.org/10.3390/agronomy12071510openalex-snapshot
Development of Retrotransposon-Based Molecular Markers for Characterization of Persea americana (Avocado) Cultivars and Horticultural Races
inferred← citeshttps://doi.org/10.3390/ani13142355openalex-snapshot
Insertion of 643bp Retrotransposon Upstream of PPARγ CDS Is Associated with Backfat of Large White Pigs
inferred← citeshttps://doi.org/10.3390/biotech10040023openalex-snapshot
Primer Binding Site (PBS) Profiling of Genetic Diversity of Natural Populations of Endemic Species Allium ledebourianum Schult.
inferred← citeshttps://doi.org/10.3390/d15111127openalex-snapshot
Current State of Natural Populations of Paeonia anomala (Paeoniaceae) in East Kazakhstan
inferred← citeshttps://doi.org/10.3390/f11010031openalex-snapshot
Development and Deployment of High-Throughput Retrotransposon-Based Markers Reveal Genetic Diversity and Population Structure of Asian Bamboo
inferred← citeshttps://doi.org/10.3390/genes11101216openalex-snapshot
Comparative Study of Pine Reference Genomes Reveals Transposable Element Interconnected Gene Networks
inferred← citeshttps://doi.org/10.3390/genes14040794openalex-snapshot
Genetic Diversity in Natural Populations of Rhodiola Species of Different Adaptation Strategies
inferred← citeshttps://doi.org/10.3390/genes16121449openalex-snapshot
Genetic Diversity of Rhodiola quadrifida (Crassulaceae) in Altai High-Mountain Populations of Kazakhstan
inferred← citeshttps://doi.org/10.3390/ijms21082931openalex-snapshot
Long Tandem Arrays of Cassandra Retroelements and Their Role in Genome Dynamics in Plants
inferred← citeshttps://doi.org/10.3390/ijms222111387openalex-snapshot
The Dynamism of Transposon Methylation for Plant Development and Stress Adaptation
inferred← citeshttps://doi.org/10.3390/jof7030234openalex-snapshot
Genetic Diversity and Pathogenicity of Rhizoctonia spp. Isolates Associated with Red Cabbage in Samsun (Turkey)
inferred← citeshttps://doi.org/10.3390/plants15152388openalex-snapshot
Evolution of Tat Retrotransposons Reveals Mosaic Phylogenetic Patterns Among Land Plants
inferred← citeshttps://doi.org/10.3390/plants9010015openalex-snapshot
Copy Number Variation of Transposable Elements in Thinopyrum intermedium and Its Diploid Relative Species
inferred← citeshttps://doi.org/10.34101/actaagrar/1/10392openalex-snapshot
Use of molecular marker methods in the classification of bamboo taxa: A review
inferred← citeshttps://doi.org/10.36718/1819-4036-2025-5-47-61openalex-snapshot
USING iPBS MARKERS TO ANALYSE WINTER BARLEY GENOTYPE POLYMORPHISM
inferred← citeshttps://doi.org/10.38058/ijsl.592537openalex-snapshot
Retrotransposon Analyses in Cucurbitaceae family
inferred← citeshttps://doi.org/10.5219/1353openalex-snapshot
Differences between microbiota, phytochemical, antioxidant profile and dna fingerprinting of cabernet sauvignon grape from Slovakia and Macedonia
inferred← citeshttps://doi.org/10.6084/m9.figshare.15253485openalex-snapshot
Additional file 1 of A 192 bp ERV fragment insertion in the first intron of porcine TLR6 may act as an enhancer associated with the increased expressions of TLR6 and TLR1
inferred← citeshttps://doi.org/10.7287/peerj.11702v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genetic analysis and population structure of wild and cultivated wishbone flower (Torenia fournieri Lind.) lines related to specific floral color (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11702v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genetic analysis and population structure of wild and cultivated wishbone flower (Torenia fournieri Lind.) lines related to specific floral color (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11702v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Genetic analysis and population structure of wild and cultivated wishbone flower (Torenia fournieri Lind.) lines related to specific floral color (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.10674openalex-snapshot
DNA profiling and assessment of genetic diversity of relict speciesAllium altaicumPall. on the territory of Altai
inferred← citeshttps://doi.org/10.7717/peerj.11702openalex-snapshot
Genetic analysis and population structure of wild and cultivated wishbone flower ( Torenia fournieri Lind.) lines related to specific floral color
inferred← citeshttps://doi.org/10.7717/peerj.9097openalex-snapshot
Genetic diversity of Alternaria species associated with black point in wheat grains
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.