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Inheritance of Extrachromosomal rDNA in Physarum polycephalum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0005-2787(78)90066-7openalex-snapshot
Ribosomal DNA in spores of Physarum polycephalum
inferredcites →https://doi.org/10.1016/0012-1606(75)90024-xopenalex-snapshot
Mating type and the differentiated state in Physarum polycephalum
inferredcites →https://doi.org/10.1016/0022-2836(76)90252-7openalex-snapshot
Structure of ribosomal DNA in Physarum polycephalum
inferredcites →https://doi.org/10.1016/0022-2836(76)90280-1openalex-snapshot
The macronuclear ribosomal DNA of Tetrahymena pyriformis is a palindrome
inferredcites →https://doi.org/10.1016/0022-2836(77)90052-3openalex-snapshot
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
inferredcites →https://doi.org/10.1016/0022-2836(78)90294-2openalex-snapshot
A tandemly repeated sequence at the termini of the extrachromosomal ribosomal RNA genes in Tetrahymena
inferredcites →https://doi.org/10.1016/0022-2836(81)90472-1openalex-snapshot
Sequence homology near the center of the extrachromosomal rDNA palindrome in Tetrahymena
inferredcites →https://doi.org/10.1016/0022-2836(82)90289-3openalex-snapshot
Structure of the central spacer region of extrachromosomal ribosomal DNA in Physarum polycephalum
inferredcites →https://doi.org/10.1016/0076-6879(79)68012-6openalex-snapshot
[10] Elution of DNA from agarose gels after electrophoresis
inferredcites →https://doi.org/10.1016/0092-8674(77)90190-8openalex-snapshot
A single integrated gene for ribosomal RNA in a eucaryote, tetrahymena pyriformis
inferredcites →https://doi.org/10.1016/0092-8674(80)90564-4openalex-snapshot
A family of inverted repeat sequences and specific single-strand gaps at the termini of the Physarum rDNA palindrome
inferredcites →https://doi.org/10.1016/0092-8674(81)90102-1openalex-snapshot
Ribosomal RNA gene amplification in tetrahymena may be associated with chromosome breakage and DNA elimination
inferredcites →https://doi.org/10.1016/0092-8674(81)90141-0openalex-snapshot
Single extrachromosomal ribosomal rna gene copies are synthesized during amplification of the rDNA in tetrahymena
inferredcites →https://doi.org/10.1016/0092-8674(82)90214-8openalex-snapshot
Allele-specific, selective amplification of a ribosomal RNA gene in tetrahymena thermophila
inferredcites →https://doi.org/10.1016/0147-619x(78)90001-xopenalex-snapshot
On plasmid incompatibility
inferredcites →https://doi.org/10.1073/pnas.76.8.3683openalex-snapshot
Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.
inferredcites →https://doi.org/10.1083/jcb.91.1.309openalex-snapshot
Protein tightly bound near the termini of the Physarum extrachromosomal rDNA palindrome.
inferredcites →https://doi.org/10.1086/282022openalex-snapshot
An Analysis of Nuclear Differentiation in the Selfers of Tetrahymena
inferredcites →https://doi.org/10.1093/genetics/101.1.35openalex-snapshot
A GENE, ALCA, AFFECTING THE LIFE CYCLE FORM EXPRESSED IN PHYSARUM POLYCEPHALUM
inferredcites →https://doi.org/10.1093/genetics/78.4.1051openalex-snapshot
GENETIC ANALYSIS IN THE COLONIA STRAIN OF PHYSARUM POLYCEPHALUM: HETEROTHALLIC STRAINS THAT MATE WITH AND ARE PARTIALLY ISOGENIC TO THE COLONIA STRAIN
inferredcites →https://doi.org/10.1093/genetics/97.3-4.513openalex-snapshot
TWO MULTIALLELIC MATING COMPATIBILITY LOCI SEPARATELY REGULATE ZYGOTE FORMATION AND ZYGOTE DIFFERENTIATION IN THE MYXOMYCETE PHYSARUM POLYCEPHALUM
inferredcites →https://doi.org/10.1111/j.1432-1033.1977.tb11582.xopenalex-snapshot
The Organisation of Genes for Transfer RNA and Ribosomal RNA in Amoebae and Plasmodia of Physarum polycephalum
inferredcites →https://doi.org/10.1111/j.1432-1033.1977.tb11912.xopenalex-snapshot
The Replication of Ribosomal DNA in Physarum polycephalum
inferredcites →https://doi.org/10.1111/j.1550-7408.1966.tb01971.xopenalex-snapshot
Multiple Alleles and Other Factors Affecting Plasmodium Formation in the True Slime Mold Physarum polycephalum Schw*
inferredcites →https://doi.org/10.1128/jb.131.2.473-476.1977openalex-snapshot
Viability of Physarum polycephalum spores and ploidy of plasmodial nuclei
inferredcites →https://doi.org/10.1139/g81-002openalex-snapshot
MULTIPLE ALLELISM AT THEMATB LOCUS INPHYSARUM POLYCEPHALUM
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.399.3.5zenodo-depositor-declared
Towards a phylogenetic classification of the Myxomycetes
inferred← citeshttps://doi.org/10.1002/jez.b.21056openalex-snapshot
Evolution of developmentally regulated genome rearrangements in eukaryotes
inferred← citeshttps://doi.org/10.1007/978-1-4613-2203-0_3openalex-snapshot
Molecular Organization of the Physarum Genome
inferred← citeshttps://doi.org/10.1007/978-1-4615-3872-1_1openalex-snapshot
New mechanisms of gene amplification in drug resistance (the episome model)
inferred← citeshttps://doi.org/10.1007/978-1-4684-5251-8_33openalex-snapshot
Extrachromosomal DNA Elements in the Nucleus of Dictyostelium Discoideum
inferred← citeshttps://doi.org/10.1007/bf00339605openalex-snapshot
Non-mendelian inheritance of mitochondrial DNA and ribosomal DNA in the myxomycete, Didymium iridis
inferred← citeshttps://doi.org/10.1007/bf00425714openalex-snapshot
Ribosomal DNA inheritance and recombination in Neurospora crassa
inferred← citeshttps://doi.org/10.1007/s13127-015-0230-xopenalex-snapshot
Sex or no sex? Group I introns and independent marker genes reveal the existence of three sexual but reproductively isolated biospecies in Trichia varia (Myxomycetes)
inferred← citeshttps://doi.org/10.1016/0092-8674(89)90247-xopenalex-snapshot
A mobile group I intron in the nuclear rDNA of physarum polycephalum
inferred← citeshttps://doi.org/10.1016/0378-1119(85)90314-2openalex-snapshot
Nucleotide sequence of the central non-transcribed spacer region of Physarum polycephalum rDNA
inferred← citeshttps://doi.org/10.1016/b978-0-12-805089-7.00003-2openalex-snapshot
The Phylogeny of Myxomycetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-824281-0.00008-7openalex-snapshot
The phylogeny and phylogenetically based classification of myxomycetes
inferred← citeshttps://doi.org/10.1016/j.protis.2016.03.003openalex-snapshot
What an Intron May Tell: Several Sexual Biospecies Coexist in Meriderma spp. (Myxomycetes)
inferred← citeshttps://doi.org/10.1016/j.protis.2019.125681openalex-snapshot
Evidence of Intra-individual SSU Polymorphisms in Dark-spored Myxomycetes (Amoebozoa)
inferred← citeshttps://doi.org/10.1016/j.tree.2003.10.007openalex-snapshot
Genome diversity in microbial eukaryotes
inferred← citeshttps://doi.org/10.1016/s0021-9258(17)31771-4openalex-snapshot
Tetrahymena ribozyme disrupts rRNA processing in yeast.
inferred← citeshttps://doi.org/10.1016/s0065-2911(08)60096-xopenalex-snapshot
Patterns of Inheritance, Development and the Mitotic Cycle in the Protist Physarum polycephalum
inferred← citeshttps://doi.org/10.1093/nar/11.23.8519openalex-snapshot
Localization and DNA sequence around the initiation site of ribosomal RNA transcription inPhysarum polycephalum
inferred← citeshttps://doi.org/10.1093/nar/12.4.2047openalex-snapshot
Direct repeats surrounding the ribosomal RNA genes ofPhysarum polycephalum
inferred← citeshttps://doi.org/10.1093/nar/gkg348openalex-snapshot
Sequence and structure of the extrachromosomal palindrome encoding the ribosomal RNA genes in Dictyostelium
inferred← citeshttps://doi.org/10.1111/1755-0998.12725openalex-snapshot
Genetic barcoding of dark‐spored myxomycetes (Amoebozoa)—Identification, evaluation and application of a sequence similarity threshold for species differentiation in NGS studies
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1986.tb09696.xopenalex-snapshot
Two‐dimensional gel analysis of repetitive nuclear DNA sequences in the genome of Physarum polycephalum
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2012.00248.xopenalex-snapshot
Comparative genomics in the A moebozoa clade
inferred← citeshttps://doi.org/10.1111/mec.16239openalex-snapshot
Genetic structure of the protist Physarum albescens (Amoebozoa) revealed by multiple markers and genotyping by sequencing
inferred← citeshttps://doi.org/10.1128/mcb.5.2.273openalex-snapshot
Inheritance of extrachromosomal ribosomal DNA during the asexual life cycle of Dictyostelium discoideum: examination by use of DNA polymorphisms.
inferred← citeshttps://doi.org/10.1128/mcb.5.2.273-280.1985openalex-snapshot
Inheritance of Extrachromosomal Ribosomal DNA During the Asexual Life Cycle of Dictyostelium discoideum: Examination by Use of DNA Polymorphisms
inferred← citeshttps://doi.org/10.1186/s12860-026-00587-7openalex-snapshot
Telomere-to-telomere characterization of rDNA chromosome in the myxomycete Didymium iridis
inferred← citeshttps://doi.org/10.1186/s13100-022-00280-4openalex-snapshot
Mobile group I introns at nuclear rDNA position L2066 harbor sense and antisense homing endonuclease genes intervened by spliceosomal introns
inferred← citeshttps://doi.org/10.1242/jcs.99.2.265openalex-snapshot
Genetic analysis of the relationships between the amoebal extranuclear spindle-organizing centre and the plasmodial intranuclear spindleorganizing centre of Physarum during conjugation
inferred← citeshttps://doi.org/10.1371/journal.pone.0174825openalex-snapshot
Speciation in progress? A phylogeographic study among populations of Hemitrichia serpula (Myxomycetes)
inferred← citeshttps://doi.org/10.15407/ukrbotj72.02.147openalex-snapshot
The prospects and perspectives of the phylogenetic system of myxomycetes (Myxogastrea)
inferred← citeshttps://doi.org/10.6084/m9.figshare.21303116openalex-snapshot
Additional file 1 of Mobile group I introns at nuclear rDNA position L2066 harbor sense and antisense homing endonuclease genes intervened by spliceosomal introns
inferred← citeshttps://doi.org/10.6084/m9.figshare.21303119openalex-snapshot
Additional file 2 of Mobile group I introns at nuclear rDNA position L2066 harbor sense and antisense homing endonuclease genes intervened by spliceosomal introns
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