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The diminution of heterochromatic chromosomal segments in Cyclops (Crustacea, Copepoda)
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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/jez.1401410302openalex-snapshot
Experimental research on chromosome elimination in cecidomyidae (Diptera)
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Bernhard John and Kenneth R. Lewis, The Chromosome Cycle (Protoplasmatologia, Band VI. Kern‐ und Zellteilung B.). 125 S., 45 Abb. Wien‐New York 1969: Springer Verlag 455 s
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F. Dahl, Die Tierwelt Deutschlands. 9. Teil: Krebstiere oder Crustacea. I. (O. Pesta, Ruderfüßer oder Copepoda.) 1928. 136 S., 115 Abb. Preis geh. 8 Mark
inferredcites →https://doi.org/10.1007/bf00281999openalex-snapshot
On the function of the germ line chromosomes in the oogenesis of Wachtliella persicariae (Cecidomyiidae)
inferredcites →https://doi.org/10.1007/bf00283386openalex-snapshot
The development of the macronucleus in the ciliated protozoan Stylonychia mytilus
inferredcites →https://doi.org/10.1007/bf00283827openalex-snapshot
The DNA content of sperm and hemocyte nuclei of the silkworm, Bombyx mori L.
inferredcites →https://doi.org/10.1007/bf00284071openalex-snapshot
Chromosome-sized DNA molecules from Drosophila
inferredcites →https://doi.org/10.1007/bf00284900openalex-snapshot
Giemsa banding: karyotype differences in some species of Anemone and in Hepatica nobilis
inferredcites →https://doi.org/10.1007/bf00285809openalex-snapshot
Heterochromatic chromosomes and satellite DNAs of Drosophila nasutoides
inferredcites →https://doi.org/10.1007/bf00326268openalex-snapshot
The chromosomal distribution of satellite DNA in the germ-line and somatic tissues of the gall midge, Heteropeza pygmaea
inferredcites →https://doi.org/10.1007/bf00326379openalex-snapshot
The DNA content of sperm of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00326871openalex-snapshot
A polymorphism for heterochromatic supernumerary segments in Chorthippus parallelus
inferredcites →https://doi.org/10.1007/bf00326875openalex-snapshot
Karyotyp und DNS-Gehalt von Bufo bufo, B. viridis, B. bufo � B. viridis und B. calamita (Amphibia, Anura)
inferredcites →https://doi.org/10.1007/bf00328664openalex-snapshot
Untersuchungen �ber Geschlechtsbestimmungsmechanismen bei Copepoden
inferredcites →https://doi.org/10.1007/bf00329721openalex-snapshot
Die Struktur der Pachyt�nchromosomen in Euchromatin und Heterochromatin und ihre Auswirkung auf die Chiasmabildung bei Salvia-Arten
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Untersuchungen �ber den einflu� �u�erer saktoren auf die dauer der embryonalentwicklung und den H�utungsrhythmus von Cyclops vicinus
inferredcites →https://doi.org/10.1007/bf00396586openalex-snapshot
Chromatin-Diminution bei Copepoden
inferredcites →https://doi.org/10.1007/bf00396588openalex-snapshot
Cytogenetic analysis of major heterochromatic elements (especially Xh and Y) in Drosophila melanogaster, and the theory of “heterochromatin”
inferredcites →https://doi.org/10.1007/bf00573440openalex-snapshot
Die Blastomerendifferenzierung f�r Soma und Keimbahn beiParascaris equorum
inferredcites →https://doi.org/10.1007/bf00591922openalex-snapshot
Chromosomale Soma-Keimbahn-Differenzierung bei Chironomiden
inferredcites →https://doi.org/10.1007/bf01259940openalex-snapshot
Stoffe und Str�mungen in der Spindel von Cyclops strenuus
inferredcites →https://doi.org/10.1007/bf01259947openalex-snapshot
Weibliche Heterogametie bei Copepoden
inferredcites →https://doi.org/10.1007/bf02906666openalex-snapshot
Ueber die Selbständigkeit der väterlichen und Mütterlichen Kernbestandtheile während der Embryonalentwicklung von Cyclops
inferredcites →https://doi.org/10.1007/bf02933881openalex-snapshot
Ueber generative und embryonale Mitosen, sowie über pathologische Kerntheilungsbilder
inferredcites →https://doi.org/10.1007/bf02975388openalex-snapshot
Die Keimbahn von Cyclops Neue Beiträge zur Kenntniss der Geschlechtszellen-Sonderung
inferredcites →https://doi.org/10.1016/0012-1606(72)90097-8openalex-snapshot
Molecular aspects of chromatin elimination in Ascaris lumbricoides
inferredcites →https://doi.org/10.1016/0012-1606(74)90052-9openalex-snapshot
Histones and histone synthesis in sea urchin development
inferredcites →https://doi.org/10.1016/0014-4827(62)90209-4openalex-snapshot
Variations of the deoxyribonucleic acid (DNA) content in embryonal cells of Cyclops strenuus
inferredcites →https://doi.org/10.1016/0047-2484(80)90077-9openalex-snapshot
Animal cytology and evolution
inferredcites →https://doi.org/10.1016/s0074-7696(08)60944-4openalex-snapshot
The Problem of Germ Cell Determinants
inferredcites →https://doi.org/10.1038/1811479a0openalex-snapshot
Action of Deoxyribonuclease on Lampbrush Chromosomes
inferredcites →https://doi.org/10.1038/198036a0openalex-snapshot
Kinetics of Deoxyribonuclease Action on Chromosomes
inferredcites →https://doi.org/10.1038/231383a0openalex-snapshot
Sea Bottom Velocity Profiles on the Continental Shelf south-west of England
inferredcites →https://doi.org/10.1038/231385a0openalex-snapshot
Biological Sciences: X Chromosome Inactivation studied by Injection of a Single Cell into the Mouse Blastocyst
inferredcites →https://doi.org/10.1038/259055a0openalex-snapshot
Complexity of germline and somatic DNA in Ascaris
inferredcites →https://doi.org/10.1073/pnas.43.1.122openalex-snapshot
THE ORGANIZATION AND DUPLICATION OF CHROMOSOMES AS REVEALED BY AUTORADIOGRAPHIC STUDIES USING TRITIUM-LABELED THYMIDINEE
inferredcites →https://doi.org/10.1093/genetics/54.2.567openalex-snapshot
A QUANTITATIVE STUDY OF CHROMATIN DIMINUTION IN EMBRYONIC MITOSES OF CYCLOPS FURCIFER
inferredcites →https://doi.org/10.1093/genetics/56.3.483openalex-snapshot
PHENOTYPIC AND CHROMOSOMAL ABNORMALITIES ASSOCIATED WITH THE INTRODUCTION OF HETEROCHROMATIN FROM NICOTIANA OTOPHORA INTO N. TABACUM
inferredcites →https://doi.org/10.1111/j.1438-8677.1929.tb01609.xopenalex-snapshot
32. E. Heitz: Heterochromatin, Chromocentren, Chromomeren
inferredcites →https://doi.org/10.1126/science.145.3628.130openalex-snapshot
Heterochromatic Chromosomes in the Coccids
inferredcites →https://doi.org/10.1177/14.8.601openalex-snapshot
FEULGEN HYDROLYSIS: EFFECT OF ACID AND TEMPERATURE
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Chromatin diminution as a tool to study some biological problems
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Cyclops heberti n.sp. and Cyclops singularis n.sp., two new species within the genus Cyclops (‘strenuus-subgroup’) (Crust. Copepoda) from ephemeral ponds in southern Germany
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The effects of chromatin diminution on the pattern of C-banding in the chromosomes of Acanthocyclops vernalis Fischer (Copepoda: Crustacea)
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inferred← citeshttps://doi.org/10.1007/bf00286428openalex-snapshot
Underreplication of a polytene chromosome arm in the chironomid Prodiamesa olivacea
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Restriction enzyme analysis of the germ line limited DNA of Ascaris suum
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inferred← citeshttps://doi.org/10.1007/bf00293130openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00293524openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00293839openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00295135openalex-snapshot
Co-replication of satellite DNA of Chironomus melanotus with mainband DNA during polytenization
inferred← citeshttps://doi.org/10.1007/bf00327390openalex-snapshot
Chromatin elimination and the genetic organisation of the macronucleus in Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1007/bf00328079openalex-snapshot
Heterochromatin variation in Cryptobothrus chrysophorus
inferred← citeshttps://doi.org/10.1007/bf00331248openalex-snapshot
Circular and linear structures in chromatin diminution of Cyclops
inferred← citeshttps://doi.org/10.1007/bf00352285openalex-snapshot
Replication forks are not found in a Drosophila minichromosome demonstrating a gradient of polytenization
inferred← citeshttps://doi.org/10.1007/bf00397988openalex-snapshot
Eliminated sequences with different copy numbers clustered in the micronuclear genome of Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1007/bf01190750openalex-snapshot
Satellite DNA properties of the germ line limited DNA and the organization of the somatic genomes in the nematodesAscaris suum andParascaris equorum
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inferred← citeshttps://doi.org/10.1016/0012-1606(87)90123-0openalex-snapshot
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Sexual Differentiation
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EXTRACHROMOSOMAL DNA IN POLYTENE NUCLEI OF SARCOPHAGA11This work was supported by USPHS grants HD-174 and CA-19265.
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The Special Case of the Hypotrichs
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inferred← citeshttps://doi.org/10.1016/s0074-7696(07)62005-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61435-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61473-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0092-8674(00)81324-0openalex-snapshot
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The DNA content of chromosome division figures and interphase nuclei classifies ulcerative colitis
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Dynamic changes of DNA sequences in Schistosoma mansoni in the course of development
inferred← citeshttps://doi.org/10.1017/s0424820100140993openalex-snapshot
DNA levels in somatic and germ line cells of a freshwater crustacean, Mesocyclops edax
inferred← citeshttps://doi.org/10.1017/s1431927600007844openalex-snapshot
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inferred← citeshttps://doi.org/10.1023/a:1003806912364openalex-snapshot
The contributions of Ulrich K. Einsle to the taxonomy of the copepoda
inferred← citeshttps://doi.org/10.1023/a:1003819809155openalex-snapshot
Interpopulation differentiation within C. kolensis and C. strenuus strenuus (Crustacea: Copepoda): evidence from cytogenetic methods
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inferred← citeshttps://doi.org/10.1023/a:1015294001575openalex-snapshot
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inferred← citeshttps://doi.org/10.1023/a:1015578811571openalex-snapshot
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inferred← citeshttps://doi.org/10.1023/a:1021207310080openalex-snapshot
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inferred← citeshttps://doi.org/10.1023/a:1022419506918openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41576-026-01004-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1042/bst20190951openalex-snapshot
Programmed DNA elimination: silencing genes and repetitive sequences in somatic cells
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Chromatin elimination – an oddity or a common mechanism in differentiation and development?
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Specific DNA rearrangements in synchronously developing nuclei of Tetrahymena.
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Distribution of Chromosomes into Discrete Groups in Colchicine-Induced C-Metaphases of Barley
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Distribution of Chromosomes into Discrete Groups in Colchicine-Induced C-Metaphases of Barley
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Karyology of the northern Baltic peracaridan Crustacea
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Chromosomes and nuclear DNA of Crustacea
inferred← citeshttps://doi.org/10.1083/jcb.92.3.783openalex-snapshot
Elimination of specific DNA sequences from the somatic nucleus of the ciliate Tetrahymena.
inferred← citeshttps://doi.org/10.1089/dna.2008.0806openalex-snapshot
The Unusual Way to Make a Genetically Active Nucleus
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The Genome Architecture of the Copepod Eurytemora carolleeae — the Highly Invasive Atlantic Clade of the Eurytemora affinis Species Complex
inferred← citeshttps://doi.org/10.1093/jcbiol/ruab043openalex-snapshot
Genome size in cyclopoid copepods (Copepoda: Cyclopoida): chromatin diminution as a hypothesized mechanism of evolutionary constraint
inferred← citeshttps://doi.org/10.1093/jcbiol/ruag029openalex-snapshot
Species delineation in Cyclops Müller, 1776 (Copepoda: Cyclopoida: Cyclopidae) based on morphology, DNA sequences, genome size, and chromatin diminution
inferred← citeshttps://doi.org/10.1093/molbev/msn032openalex-snapshot
The Dynamic Nature of Eukaryotic Genomes
inferred← citeshttps://doi.org/10.1093/nar/10.11.3495openalex-snapshot
Chromatin diminution inAscaris suum: nucleotide sequence of the eliminated satellite DNA
inferred← citeshttps://doi.org/10.1093/nar/18.4.845openalex-snapshot
Internal eliminated sequenc are removed prior to chromosome fragmentation during development inEuplotes crassus
inferred← citeshttps://doi.org/10.1093/nar/19.10.2677openalex-snapshot
The highly variable pentameric repeats of the AT-rich germline limited DNA in Parascaris univalens are the telomeric repeats of somatic chromosomes
inferred← citeshttps://doi.org/10.1093/nar/21.10.2409openalex-snapshot
A micronucleus-specific sequence exists in the 5′-upstream region of calmodulin gene inTetrahymena thermophila
inferred← citeshttps://doi.org/10.1093/nar/24.22.4415openalex-snapshot
Sequential Excision of Internal Eliminated DNA Sequences in the Differentiating Macronucleus of the Hypotrichous Ciliate Stylonychia Lemnae
inferred← citeshttps://doi.org/10.1093/nar/gkae579openalex-snapshot
End resection and telomere healing of DNA double-strand breaks during nematode programmed DNA elimination
inferred← citeshttps://doi.org/10.1093/nar/gkf579openalex-snapshot
A PIWI homolog is one of the proteins expressed exclusively during macronuclear development in the ciliate Stylonychia lemnae
inferred← citeshttps://doi.org/10.1093/oso/9780199634057.003.0001openalex-snapshot
| The discovery and significance of mobile genetic elements
inferred← citeshttps://doi.org/10.1101/gad.1.4.323openalex-snapshot
Nucleic acid splicing events occur frequently during macronuclear development in the protozoan Oxytricha nova and involve the elimination of unique DNA.
inferred← citeshttps://doi.org/10.1101/gad.1864609openalex-snapshot
Subtraction by addition: domesticated transposases in programmed DNA elimination: Figure 1.
inferred← citeshttps://doi.org/10.1101/gr.2794604openalex-snapshot
The molecular structure of the DNA fragments eliminated during chromatin diminution in Cyclops kolensis
inferred← citeshttps://doi.org/10.1111/brv.12796openalex-snapshot
Delete and survive: strategies of programmed genetic material elimination in eukaryotes
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2006.tb01103.xopenalex-snapshot
GENETIC ARCHITECTURE OF THE CRYPTIC SPECIES COMPLEX OF ACANTHOCYCLOPS VERNALIS (CRUSTACEA: COPEPODA). II. CROSSBREEDING EXPERIMENTS, CYTOGENETICS, AND A MODEL OF CHROMOSOMAL EVOLOUTION
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2006.00610.xopenalex-snapshot
Genome sizes of cyclopoid copepods (Crustacea): evidence of evolutionary constraint
inferred← citeshttps://doi.org/10.1111/j.1432-0436.1991.tb00236.xopenalex-snapshot
Genomic potential in mammals
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2011.01305.xopenalex-snapshot
Developmentally programmed, RNA‐directed genome rearrangement in Tetrahymena
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1990.tb01424.xopenalex-snapshot
QUANTITATIVE VARIATIONS OF NUCLEAR DNA DURING PLANT DEVELOPMENT: A CRITICAL ANALYSIS
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2000.tb00059.xopenalex-snapshot
Coincidence, coevolution, or causation? DNA content, cellsize, and the C‐value enigma
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1986.tb05551.xopenalex-snapshot
Alternative Processing of Sequences During Macronuclear Development in Tetrahymena thermophila1
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1998.tb04524.xopenalex-snapshot
A Developmentally Eliminated Sequence in the Flanking Region of the Histone H1 Gene in Tetrahymena thermophila Contains Short Repeats
inferred← citeshttps://doi.org/10.1111/j.1601-5223.1980.tb01043.xopenalex-snapshot
Classification of genes, rearrangements and chromosomes according to the chromosome field
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2006.00041.xopenalex-snapshot
Changes in nuclear morphology associated with elevated DNA levels during gametogenesis in cyclopoid copepods with chromatin diminution
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1999.tb08862.xopenalex-snapshot
Genome System Architecture and Natural Genetic Engineering in Evolution
inferred← citeshttps://doi.org/10.1111/j.1768-322x.1989.tb00781.xopenalex-snapshot
Development of the large nucleolus in the oocytes of the copepod Acanthocyclops vernalis: an electron microscope study
inferred← citeshttps://doi.org/10.1126/science.15739260openalex-snapshot
The Significance of Responses of the Genome to Challenge
inferred← citeshttps://doi.org/10.1126/science.3544215openalex-snapshot
Programmed Gene Rearrangements Altering Gene Expression
inferred← citeshttps://doi.org/10.1128/9781555817954.ch30openalex-snapshot
Genome‐Wide Rearrangements of DNA in Ciliates
inferred← citeshttps://doi.org/10.1128/mcb.17.3.1254openalex-snapshot
The Structure of Heterochromatic DNA Is Altered in Polyploid Cells of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1128/mcb.19.8.5631openalex-snapshot
Flanking Regulatory Sequences of the Tetrahymena R Deletion Element Determine the Boundaries of DNA Rearrangement
inferred← citeshttps://doi.org/10.1128/mcb.3.11.1909openalex-snapshot
Germ line-specific DNA sequences are present on all five micronuclear chromosomes in Tetrahymena thermophila.
inferred← citeshttps://doi.org/10.1128/mcb.3.11.1909-1919.1983openalex-snapshot
Germ Line-Specific DNA Sequences Are Present on All Five Micronuclear Chromosomes in Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1128/mcb.5.6.1260openalex-snapshot
Gene Amplification in Tetrahymena thermophila: Formation of Extrachromosomal Palindromic Genes Coding for rRNA
inferred← citeshttps://doi.org/10.1128/mcb.5.8.2039openalex-snapshot
Reproducible and variable genomic rearrangements occur in the developing somatic nucleus of the ciliate Tetrahymena thermophila.
inferred← citeshttps://doi.org/10.1128/mcb.5.8.2039-2050.1985openalex-snapshot
Reproducible and Variable Genomic Rearrangements Occur in the Developing Somatic Nucleus of the Ciliate Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1134/s160767290603015xopenalex-snapshot
The conservatism of the genome structure of Cyclops kolensis (Copepoda, Crustacea) populations inhabiting Moscow Ponds and Lake Baikal
inferred← citeshttps://doi.org/10.1134/s1607672908060057openalex-snapshot
Characterization of Cyclops kolensis inter-simple sequence repeats in germline and postdiminution somatic cells
inferred← citeshttps://doi.org/10.1134/s1990519x13020053openalex-snapshot
Cytophotometric determination of genome size in two species of Cyclops of Lake Baikal (Crustacea: Copepoda, Cyclopoida) in ontogenetic development
inferred← citeshttps://doi.org/10.1139/g04-014openalex-snapshot
DNA–Feulgen cytophotometric determination of genome size for the freshwater-invading copepod Eurytemora affinis
inferred← citeshttps://doi.org/10.1139/g06-022openalex-snapshot
Chromatin diminution in the copepod Mesocyclops edax: diminution of tandemly repeated DNA families from somatic cells
inferred← citeshttps://doi.org/10.1139/g06-155openalex-snapshot
Amphipod genome sizes: first estimates for Arctic species reveal genomic giants
inferred← citeshttps://doi.org/10.1139/g08-053openalex-snapshot
Do phosphorus requirements for RNA limit genome size in crustacean zooplankton?
inferred← citeshttps://doi.org/10.1139/g09-027openalex-snapshot
Survey of genome size in 28 hydrothermal vent species covering 10 families
inferred← citeshttps://doi.org/10.1139/g80-053openalex-snapshot
BIVALENT FORMING RACE OFMESOCYCLOPS EDAX(COPEPODA, CRUSTACEA)
inferred← citeshttps://doi.org/10.1139/g82-056openalex-snapshot
UNUSUAL VARIATIONS IN NUCLEAR DNA CONTENTS IN THE MARINE COPEPODPSEUDOCALANUS
inferred← citeshttps://doi.org/10.1139/g95-012openalex-snapshot
Unusually high numbers of ribosomal RNA genes in copepods (Arthropoda: Crustacea) and their relationship to genome size
inferred← citeshttps://doi.org/10.1139/gen-2012-0097openalex-snapshot
Chromatin diminution in the copepod Mesocyclops edax: elimination of both highly repetitive and nonhighly repetitive DNA
inferred← citeshttps://doi.org/10.1139/z83-095openalex-snapshot
Similar nucleus numbers among copepods
inferred← citeshttps://doi.org/10.1146/annurev.ea.12.050184.001333openalex-snapshot
Rates of Evolution and the Notion of "Living Fossils"
inferred← citeshttps://doi.org/10.1146/annurev.genet.30.1.557openalex-snapshot
GENOME DOWNSIZING DURING CILIATE DEVELOPMENT: Nuclear Division of Labor through Chromosome Restructuring
inferred← citeshttps://doi.org/10.1146/annurev.genet.39.073003.095906openalex-snapshot
RNA-Guided DNA Deletion in Tetrahymena: An RNAi-Based Mechanism for Programmed Genome Rearrangements
inferred← citeshttps://doi.org/10.1159/000064037openalex-snapshot
Adult murine neurons: their chromatin and chromosome changes and failure to support embryonic development as revealed by nuclear transfer
inferred← citeshttps://doi.org/10.1159/000494157openalex-snapshot
Chromatin Diminution in Cyclops kolensis Lill. (Copepoda, Crustacea) as a Radical Way to Inactivate Redundant Genome in Somatic Cells
inferred← citeshttps://doi.org/10.1163/156854083x00235openalex-snapshot
Karyology and Chromosome Evolution in the Genus Tisbe (Copepoda)
inferred← citeshttps://doi.org/10.1163/1937240x-00002473openalex-snapshot
Embryonic development and a quantitative model of programmed DNA elimination in Mesocyclops edax (S. A. Forbes, 1891) (Copepoda: Cyclopoida)
inferred← citeshttps://doi.org/10.1177/002215540104900615openalex-snapshot
Evidence for Endoreduplication: Germ Cell DNA Levels Prior to Chromatin Diminution in Mesocyclops edax
inferred← citeshttps://doi.org/10.1186/1471-2164-15-186openalex-snapshot
Billions of basepairs of recently expanded, repetitive sequences are eliminated from the somatic genome during copepod development
inferred← citeshttps://doi.org/10.1186/gb-2001-2-2-research0005openalex-snapshot
Both subtelomeric regions are required and sufficient for specific DNA fragmentation during macronuclear development in Stylonychia lemnae
inferred← citeshttps://doi.org/10.1242/dev.57.1.61openalex-snapshot
Qualitative changes in DNA indicating differential DNA replication during early embryogenesis of the newt Triturus vulgaris
inferred← citeshttps://doi.org/10.1242/dev.83.supplement.7openalex-snapshot
Chromosomal changes associated with changes in development
inferred← citeshttps://doi.org/10.1353/pbm.1993.0024openalex-snapshot
Nonconventional Genetic Systems
inferred← citeshttps://doi.org/10.1371/journal.pone.0002330openalex-snapshot
The Pathway to Detangle a Scrambled Gene
inferred← citeshttps://doi.org/10.1508/cytologia.71.189openalex-snapshot
An Analysis of Chromosomes in the Uzi Fly, Blepharipa zebina Walker (Diptera: Tachinidae) Using C- and Q-banding
inferred← citeshttps://doi.org/10.1554/05-310.1openalex-snapshot
GENETIC ARCHITECTURE OF THE CRYPTIC SPECIES COMPLEX OF ACANTHOCYCLOPS VERNALIS (CRUSTACEA: COPEPODA). II. CROSSBREEDING EXPERIMENTS, CYTOGENETICS, AND A MODEL OF CHROMOSOMAL EVOLUTION
inferred← citeshttps://doi.org/10.1651/07-2847r.1openalex-snapshot
Gonomery and Chromatin Diminution in Mesocyclops Longisetus (Copepoda)
inferred← citeshttps://doi.org/10.1651/c-2558openalex-snapshot
Variability in Genetic Architecture of the Cryptic Species Complex of Acanthocyclops Vernalis (Copepoda). I. Evidence from Karyotypes, Genome Size, and Ribosomal DNA Sequences
inferred← citeshttps://doi.org/10.20381/ruor-6139openalex-snapshot
Chromatin Diminution in 'Mesocyclops edax' (Crustacea, Copepoda): Similarity of the Pre- and Post-diminution Euchromatic Genomes.
inferred← citeshttps://doi.org/10.21105/joss.07385openalex-snapshot
delfies: a Python package for the detection of DNA breakpoints with neo-telomere addition
inferred← citeshttps://doi.org/10.3390/genes10100832openalex-snapshot
Germline-Specific Repetitive Elements in Programmatically Eliminated Chromosomes of the Sea Lamprey (Petromyzon marinus)
inferred← citeshttps://doi.org/10.3897/compcytogen.v15.i4.64350openalex-snapshot
Study of chromatin diminution in Cyclops kolensis (Copepoda, Crustacea) by radiobiological methods
inferred← citeshttps://doi.org/10.3897/compcytogen.v8i1.5913openalex-snapshot
Chromatin diminution in Copepoda (Crustacea): pattern, biological role and evolutionary aspects
inferred← citeshttps://doi.org/10.47021/0320-3557-2025-70-75openalex-snapshot
APPLICATION OF RADIOBIOLOGICAL METHODS IN STUDYING CHROMATIN DIMINUTION IN CYCLOPS (COPEPODA, CRUSTACEA)
inferred← citeshttps://doi.org/10.53846/goediss-669openalex-snapshot
Molekularbiologische und Röntgenmikroskopische Charakterisierung der Heterochromatinproteine des Nematoden Caenorhabditis elegans
inferred← citeshttps://doi.org/10.5586/asbp.2003.002openalex-snapshot
Nuclear morphology, polyploidy, and chromatin elimination in tissue culture of Allium fistulosum L.
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