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Chromosome Dynamics Regulating Genomic Dispersion and Alteration of Nucleolus Organizer Regions (NORs)
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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/jmor.1050150204openalex-snapshot
Comparative cytological studies, with especial regard to the morphology of the nucleolus
inferredcites →https://doi.org/10.1006/jtbi.1999.0913openalex-snapshot
Cytological, Genetic and Evolutionary Functions of Chiasmata Based on Chiasma Graph Analysis
inferredcites →https://doi.org/10.1007/bf00164027openalex-snapshot
Analysis of GC-rich repetitive nucleotide sequences in great apes
inferredcites →https://doi.org/10.1007/bf00226528openalex-snapshot
Chromosomal location of rDNA in Allium: in situ hybridization using biotin- and fluorescein-labelled probe
inferredcites →https://doi.org/10.1007/bf00292037openalex-snapshot
Abundance of protein-bound sulfhydryl and bisulfide groups at chromosomal nucleolus organizing regions
inferredcites →https://doi.org/10.1007/bf00292368openalex-snapshot
Silver staining of nucleolus organizer regions during human spermatogenesis
inferredcites →https://doi.org/10.1007/bf00292792openalex-snapshot
Chromosomal polymorphisms involving telomere fusion, centromeric inactivation and centromere shift in the ant Myrmecia (pilosula) n=1
inferredcites →https://doi.org/10.1007/bf00293725openalex-snapshot
Detection of nucleolus organizer regions in chromosomes of human, chimpanzee, gorilla, orangutan and gibbon
inferredcites →https://doi.org/10.1007/bf00295797openalex-snapshot
Non-random association of human acrocentric chromosomes
inferredcites →https://doi.org/10.1007/bf00328466openalex-snapshot
In situ hybridization confirms jumping nucleolus organizing regions in Allium
inferredcites →https://doi.org/10.1007/bf00328483openalex-snapshot
Chromosomal distribution of rDNA in Pan paniscus, Gorilla gorilla beringei, and Symphalangus syndactylus: Comparison to related primates
inferredcites →https://doi.org/10.1007/bf00329388openalex-snapshot
Distribution of 18+28S ribosomal genes in mammalian genomes
inferredcites →https://doi.org/10.1007/bf00329389openalex-snapshot
Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining
inferredcites →https://doi.org/10.1007/bf00368009openalex-snapshot
Multiplication of 28S rDNA and NOR activity in chromosome evolution among ants of the Myrmecia pilosula species complex
inferredcites →https://doi.org/10.1007/bf00710609openalex-snapshot
Inverted and satellited Y chromosome in the orangutan (Pongo pygmaeus)
inferredcites →https://doi.org/10.1007/bf01990741openalex-snapshot
Differential staining of the satellite regions of human acrocentric chromosomes
inferredcites →https://doi.org/10.1007/bf02509500openalex-snapshot
Genomic dispersion of 28S rDNA during karyotypic evolution in the ant genusMyrmecia (Formicidae)
inferredcites →https://doi.org/10.1007/s00018-006-6463-2openalex-snapshot
Telomeres and meiosis in health and disease
inferredcites →https://doi.org/10.1007/s003359900680openalex-snapshot
Concerted evolution of members of the multisequence family chAB4 located on various nonhomologous chromosomes
inferredcites →https://doi.org/10.1007/s10577-006-1092-zopenalex-snapshot
Ribosomal DNA locus evolution in Nemesia: transposition rather than structural rearrangement as the key mechanism?
inferredcites →https://doi.org/10.1007/s10577-007-1149-7openalex-snapshot
Telomere regulation and function during meiosis
inferredcites →https://doi.org/10.1007/s10577-019-09615-zopenalex-snapshot
Structural variations of subterminal satellite blocks and their source mechanisms as inferred from the meiotic configurations of chimpanzee chromosome termini
inferredcites →https://doi.org/10.1016/0168-9525(91)90184-ropenalex-snapshot
Chromosome banding by A.T. Sumner, Unwin & Hyman, 1990. £60.00 (xiv+434 pages) ISBN 0 04 4455279 9
inferredcites →https://doi.org/10.1016/0303-2647(81)90007-1openalex-snapshot
Karyotypic fission theory and the evolution of old world monkeys and apes
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.014openalex-snapshot
The SUN Rises on Meiotic Chromosome Dynamics
inferredcites →https://doi.org/10.1016/j.jsb.2007.06.012openalex-snapshot
Positioning of NORs and NOR-bearing chromosomes in relation to nucleoli
inferredcites →https://doi.org/10.1016/j.tig.2019.07.011openalex-snapshot
Ribosomal DNA and the Nucleolus as Keystones of Nuclear Architecture, Organization, and Function
inferredcites →https://doi.org/10.1016/s0074-7696(08)61645-9openalex-snapshot
The Nucleolar Structure
inferredcites →https://doi.org/10.1016/s0140-6736(61)92647-2openalex-snapshot
NUCLEOLUS-ORGANISERS IN THE CAUSATION OF CHROMOSOMAL ANOMALIES IN MAN
inferredcites →https://doi.org/10.1016/s0960-9822(00)00175-5openalex-snapshot
Chromosomal homogeneity of Drosophila ribosomal DNA arrays suggests intrachromosomal exchanges drive concerted evolution
inferredcites →https://doi.org/10.1016/s1097-2765(01)00317-3openalex-snapshot
Molecular Mechanisms Mediating Methylation-Dependent Silencing of Ribosomal Gene Transcription
inferredcites →https://doi.org/10.1023/a:1009207600920openalex-snapshot
Tandem duplication of nucleolus organizer region (NOR) in the Japanese macaque, Macaca fuscata fuscata
inferredcites →https://doi.org/10.1023/a:1009237412155openalex-snapshot
Genomic Differentiation of 18S Ribosomal DNA and β-Satellite DNA in the Hominoid and its Evolutionary Aspects
inferredcites →https://doi.org/10.1023/a:1016523909096openalex-snapshot
Cytogenetic differentiation of two sympatric tree shrew taxa found in the southern part of the Isthmus of Kra
inferredcites →https://doi.org/10.1023/b:chro.0000013168.61359.43openalex-snapshot
Activity of the En/Spm-like transposons in meiosis as a base for chromosome repatterning in a small, isolated, peripheral population of Aegilops speltoides Tausch.
inferredcites →https://doi.org/10.1023/b:chro.0000021911.43225.ebopenalex-snapshot
Transcriptional repression mechanisms of nucleolus organizer regions (NORs) in humans and chimpanzees
inferredcites →https://doi.org/10.1038/290731a0openalex-snapshot
Springcleaning ribosomal DNA: a model for multigene evolution?
inferredcites →https://doi.org/10.1038/nature10331openalex-snapshot
Protection of repetitive DNA borders from self-induced meiotic instability
inferredcites →https://doi.org/10.1038/ncb2896openalex-snapshot
The TRF1-binding protein TERB1 promotes chromosome movement and telomere rigidity in meiosis
inferredcites →https://doi.org/10.1038/ng0194-52openalex-snapshot
A subterminal satellite located adjacent to telomeres in chimpanzees is absent from the human genome
inferredcites →https://doi.org/10.1073/pnas.69.11.3394openalex-snapshot
Location of Ribosomal DNA in the Human Chromosome Complement
inferredcites →https://doi.org/10.1073/pnas.77.12.7323openalex-snapshot
Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes.
inferredcites →https://doi.org/10.1073/pnas.77.4.2158openalex-snapshot
Rapid duplication and loss of genes coding for the alpha chains of hemoglobin.
inferredcites →https://doi.org/10.1091/mbc.11.12.4189openalex-snapshot
Mammalian Meiotic Telomeres: Protein Composition and Redistribution in Relation to Nuclear Pores
inferredcites →https://doi.org/10.1093/molbev/msz156openalex-snapshot
High Satellite Repeat Turnover in Great Apes Studied with Short- and Long-Read Technologies
inferredcites →https://doi.org/10.1101/gad.260703.115openalex-snapshot
A localized nucleolar DNA damage response facilitates recruitment of the homology-directed repair machinery independent of cell cycle stage
inferredcites →https://doi.org/10.1101/gad.331892.119openalex-snapshot
Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions
inferredcites →https://doi.org/10.1101/gr.157941.113openalex-snapshot
The shared genomic architecture of human nucleolar organizer regions
inferredcites →https://doi.org/10.1111/j.1469-1809.1974.tb01843.xopenalex-snapshot
A cytogenetic survey of 11,680 newborn infants
inferredcites →https://doi.org/10.1126/science.7063861openalex-snapshot
The Origin of Man: A Chromosomal Pictorial Legacy
inferredcites →https://doi.org/10.1146/annurev.ge.20.120186.000501openalex-snapshot
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
inferredcites →https://doi.org/10.1159/000014977openalex-snapshot
Chromosomal localization of rDNA in the gorilla
inferredcites →https://doi.org/10.1159/000056817openalex-snapshot
Dynamic of nucleolus organizer regions and karyotype evolution in Indian pygmy field mice
inferredcites →https://doi.org/10.1159/000080823openalex-snapshot
Chimpanzee chromosomes: retrotransposable compound repeat DNA organization (RCRO) and its influence on meiotic prophase and crossing-over
inferredcites →https://doi.org/10.1159/000121084openalex-snapshot
Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes
inferredcites →https://doi.org/10.1159/000130006openalex-snapshot
Quantitative studies on the arrangement of human metaphase chromosomes
inferredcites →https://doi.org/10.1159/000130821openalex-snapshot
The chromosomal location of rDNA in selected lower primates
inferredcites →https://doi.org/10.1159/000131298openalex-snapshot
Nonhomologous associations of C-heterochromatin at human male meiotic prophase
inferredcites →https://doi.org/10.1159/000131972openalex-snapshot
A direct demonstration of somatically paired heterochromatin of human chromosomes
inferredcites →https://doi.org/10.1159/000132054openalex-snapshot
NOR associations with heterochromatin
inferredcites →https://doi.org/10.1159/000336694openalex-snapshot
Chromosome Analysis of 82 Species of Scarabaeoidea (Coleoptera), with Special Focus on NOR Localization
inferredcites →https://doi.org/10.1159/000448931openalex-snapshot
Interstitial NORs, Fragile Sites, and Chromosome Evolution: A Not So Simple Relationship - The Example of Melolontha melolontha and Genus Protaetia (Coleoptera: Scarabaeidae)
inferredcites →https://doi.org/10.1159/000449145openalex-snapshot
Hypervariability of Nucleolus Organizer Regions in Bengal Slow Lorises, Nycticebus bengalensis (Primates, Lorisidae)
inferredcites →https://doi.org/10.1159/000486441openalex-snapshot
The Relationship between the (In-)Stability of NORs and Their Chromosomal Location: The Example of Cercopithecidae and a Short Review of Other Primates
inferredcites →https://doi.org/10.1186/1471-2148-11-124openalex-snapshot
Are ribosomal DNA clusters rearrangement hotspots? A case study in the genus Mus (Rodentia, Muridae)
inferredcites →https://doi.org/10.1186/1471-2148-12-225openalex-snapshot
Distribution of 45S rDNA sites in chromosomes of plants: Structural and evolutionary implications
inferredcites →https://doi.org/10.1242/jcs.114.23.4207openalex-snapshot
Nucleolus-associated telomere clustering and pairing precede meiotic chromosome synapsis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1266/jjg.63.159openalex-snapshot
Modes of spontaneous chromosomal mutation and karyotype evolution in ants with reference to the minimum interaction hypothesis.
inferredcites →https://doi.org/10.1266/jjg.69.137openalex-snapshot
Experimental bases for the minimum interaction theory. I. Chromosome evolution in ants of the Myrmecia pilosula species complex (Hymenoptera: Formicidae: Myrmeciinae).
inferredcites →https://doi.org/10.1385/1-59259-793-9:379openalex-snapshot
FISH Mapping for Helminth Genome
inferredcites →https://doi.org/10.1534/genetics.106.059733openalex-snapshot
The Meiotic Bouquet Promotes Homolog Interactions and Restricts Ectopic Recombination inSchizosaccharomyces pombe
inferredcites →https://doi.org/10.1534/genetics.107.071399openalex-snapshot
Finely Orchestrated Movements: Evolution of the Ribosomal RNA Genes
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.jcz.2022.11.008zenodo-depositor-declared
Comparative molecular cytogenetics in five species of stingless bees (Hymenoptera, Apidae)
inferred← citeshttps://doi.org/10.3897/compcytogen.18.125235zenodo-depositor-declared
Physical chromosomal mapping of major ribosomal genes in 15 ant species with a review of hypotheses regarding evolution of the number and position of NORs in ants
inferred← citeshttps://doi.org/10.1007/s13592-021-00904-3openalex-snapshot
Inter- and intra-population B chromosome variability in Partamona helleri (Apidae: Meliponini)
inferred← citeshttps://doi.org/10.1007/s13592-021-00906-1openalex-snapshot
Karyotypic variation in the stingless bee Trigona spinipes (Hymenoptera: Apidae: Meliponini) from different geographical regions of Brazil
inferred← citeshttps://doi.org/10.1007/s13592-023-01002-2openalex-snapshot
Comparative cytogenetic analysis reveals chromosomal variability in five stingless bees of the genus Trigona (Apidae, Apinae, Meliponini)
inferred← citeshttps://doi.org/10.1016/j.bios.2022.114058openalex-snapshot
Nucleolar RNA in action: Ultrastructure revealed during protein translation through a terpyridyl manganese(II) complex
inferred← citeshttps://doi.org/10.1016/j.jcz.2021.07.012openalex-snapshot
Cytogenetics of Strumigenys louisianae Roger, 1863 (Formicidae: Myrmicinae) from North-eastern Amazonia shed light on a difficult species complex
inferred← citeshttps://doi.org/10.1080/00218839.2023.2179228openalex-snapshot
Cytotaxonomy and karyotype evolution in Neotropical Meliponini (Hymenoptera: Apidae) inferred by chromosomal mapping of 18S rDNA and five microsatellites
inferred← citeshttps://doi.org/10.1111/cpr.13805openalex-snapshot
HN1 Functions in Protein Synthesis Regulation via mTOR ‐ RPS6 Axis and Maintains Nucleolar Integrity
inferred← citeshttps://doi.org/10.1111/ens.12593openalex-snapshot
Karyotype diversity of Polybia (gr. occidentalis) species complex (Hymenoptera: Vespidae ): Taxonomic and evolutionary implications
inferred← citeshttps://doi.org/10.1111/imb.12699openalex-snapshot
Evolutionary insights into the genomic organization of major ribosomal DNA in ant chromosomes
inferred← citeshttps://doi.org/10.1139/gen-2021-0129openalex-snapshot
Karyotype conservation and genomic organization of repetitive sequences in the leaf-cutting ant Atta cephalotes (Linnaeus, 1758) (Formicidae: Myrmicinae)
inferred← citeshttps://doi.org/10.1139/gen-2023-0132openalex-snapshot
Chromosomal organization of different repetitive sequences in four wasp species of the genus Trypoxylon Latreille (Hymenoptera: Crabronidae) and insights into the composition of wasp telomeres
inferred← citeshttps://doi.org/10.1159/000533431openalex-snapshot
Supernumerary B Chromosomes of Tetragonisca fiebrigi Share Repeat Content with Standard Chromosome Set of both T. fiebrigi and Tetragonisca angustula (Apidae: Meliponini)
inferred← citeshttps://doi.org/10.1159/000542295openalex-snapshot
Karyotypes and Chromosomal Mapping of Some Repetitive DNAs in Two Stingless Bee Species (Apidae: Meliponini), with the Description of a B Chromosome in Plebeia Genus
inferred← citeshttps://doi.org/10.13057/biodiv/d220205openalex-snapshot
Classical and molecular cytogenetics of Belontia hasselti (Perciformes: Osphronemidae): Insights into the ZZ/ZW sex chromosome system
inferred← citeshttps://doi.org/10.15407/agrisp11.01.070openalex-snapshot
Investigation of some nucleoli traits in interphase leukocytes of two rabbit breeds and their hybrid
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2020-0068openalex-snapshot
Reconstruction of the Doradinae (Siluriformes-Doradidae) ancestral diploid number and NOR pattern reveals new insights about the karyotypic diversification of the Neotropical thorny catfishes
inferred← citeshttps://doi.org/10.32634/0869-8155-2022-360-6-20-26openalex-snapshot
Prospects for the use of modern methods of staining nucleolar organizers regions of cells for the diagnosis of diseases in animals
inferred← citeshttps://doi.org/10.3390/biology10090844openalex-snapshot
Repetitive Sequence Distribution on Saguinus, Leontocebus and Leontopithecus Tamarins (Platyrrhine, Primates) by Mapping Telomeric (TTAGGG) Motifs and rDNA Loci
inferred← citeshttps://doi.org/10.3390/biology12040563openalex-snapshot
High Chromosomal Reorganization and Presence of Microchromosomes in Chactidae Scorpions from the Brazilian Amazon
inferred← citeshttps://doi.org/10.3390/genes12070961openalex-snapshot
Antagonising Chromatin Remodelling Activities in the Regulation of Mammalian Ribosomal Transcription
inferred← citeshttps://doi.org/10.3390/insects12050385openalex-snapshot
Cytogenetic Analysis, Heterochromatin Characterization and Location of the rDNA Genes of Hycleus scutellatus (Coleoptera, Meloidae); A Species with an Unexpected High Number of rDNA Clusters
inferred← citeshttps://doi.org/10.3390/insects15080593openalex-snapshot
Structure and Evolution of Ribosomal Genes of Insect Chromosomes
inferred← citeshttps://doi.org/10.36253/caryologia-1106openalex-snapshot
Cytogenetic survey of eight ant species from the Amazon rainforest
inferred← citeshttps://doi.org/10.47328/ufvbbt.2022.295openalex-snapshot
Organização cromossômica e dinâmica evolutiva de sequências repetitivas em formigas cultivadoras de fungos (Myrmicinae: Attini: Attina)
inferred← citeshttps://doi.org/10.47328/ufvbbt.2022.441openalex-snapshot
Citogenética clássica e molecular em formigas do gênero Crematogaster Lund 1831 (Formicidae: Hymenoptera) com sondas específicas e de DNA repetitivo
inferred← citeshttps://doi.org/10.7124/feeo.v30.1458openalex-snapshot
Nucleus-nucleolus features of certain species of the Pinaceae family
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