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Genes and Phenes in Tetrahymena
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00267361openalex-snapshot
Galactokinase-deficient mutants of Tetrahymena thermophila: Selection and characterization
inferredcites →https://doi.org/10.1007/bf00282018openalex-snapshot
Distances �lectrophor�tiques entre l'Homme, le Chimpanz� (Pan troglodytes) et le Gorille (Gorilla gorilla) bas�es sur la mobilit� des enzymes �rythrocytaires
inferredcites →https://doi.org/10.1007/bf00485640openalex-snapshot
Intersyngenic variations in the esterases and acid phosphatases of Tetrahymena pyriformis
inferredcites →https://doi.org/10.1007/bf00486091openalex-snapshot
Nucleotide sequence divergence among DNA fractions of different syngens of Tetrahymena pyriformis
inferredcites →https://doi.org/10.1007/bf00504282openalex-snapshot
Molecular polymorphism of ciliary proteins from different species of the ciliate Tetrahymena
inferredcites →https://doi.org/10.1007/bf01975768openalex-snapshot
Elemente der exakten Erblichkeitslehre
inferredcites →https://doi.org/10.1007/bf02602905openalex-snapshot
The sequence ofTetrahymena thermophila 5S ribosomal ribonucleic acid
inferredcites →https://doi.org/10.1016/0005-2787(77)90159-9openalex-snapshot
The structure of Tetrahymena pyriformis mitochondrial DNA
inferredcites →https://doi.org/10.1016/0014-5793(79)81299-5openalex-snapshot
Strain‐dependent variation of the protein composition of Tetrahymena ribosomes
inferredcites →https://doi.org/10.1016/0022-2836(79)90367-xopenalex-snapshot
Extrachromosomal ribosomal RNA genes in Tetrahymena structure and evolution
inferredcites →https://doi.org/10.1016/b978-0-12-575550-4.50016-0openalex-snapshot
A Biochemical Phylogeny
inferredcites →https://doi.org/10.1016/b978-0-12-612983-0.50017-1openalex-snapshot
An Analysis of Cell-Surface Patterning in Tetrahymena
inferredcites →https://doi.org/10.1016/b978-1-4832-3139-6.50011-2openalex-snapshot
The Biochemistry of Ciliates in Pure Culture
inferredcites →https://doi.org/10.1017/cbo9781316145401openalex-snapshot
Elemente der exakten Erblichkeitslehre
inferredcites →https://doi.org/10.1038/276264a0openalex-snapshot
Humans and apes are genetically very similar
inferredcites →https://doi.org/10.1038/290457a0openalex-snapshot
Sequence and organization of the human mitochondrial genome
inferredcites →https://doi.org/10.1038/295430a0openalex-snapshot
Nucleotide sequence of a macronuclear gene for actin in Oxytricha fallax
inferredcites →https://doi.org/10.1042/bj1590193openalex-snapshot
Amino acid sequence of cytochrome c from Tetrahymena pyriformis Phenoset A
inferredcites →https://doi.org/10.1073/pnas.76.2.585openalex-snapshot
Amino-acid sequence of Tetrahymena histone H4 differs from that of higher eukaryotes.
inferredcites →https://doi.org/10.1073/pnas.78.4.2432openalex-snapshot
Evolutionary tree for apes and humans based on cleavage maps of mitochondrial DNA.
inferredcites →https://doi.org/10.1083/jcb.79.3.727openalex-snapshot
Scalar constraints in Tetrahymena evolution. Quantitative basal body variations within and between species.
inferredcites →https://doi.org/10.1086/283593openalex-snapshot
Cytogeometric Constraints in Tetrahymena Evolution: Contractile Vacuole Pore Positions in Nineteen Species of the Tetrahymena pyriformis Complex
inferredcites →https://doi.org/10.1093/genetics/72.2.227openalex-snapshot
TRANSITORY HETEROSIS IN NUMBERS OF BASAL BODIES IN TETRAHYMENA PYRIFORMIS
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a109456openalex-snapshot
Epigenesis and the evolution of social systems
inferredcites →https://doi.org/10.1101/sqb.1961.026.01.009openalex-snapshot
Compositional Correlation between Deoxyribonucleic Acid and Protein
inferredcites →https://doi.org/10.1111/j.1550-7408.1955.tb02419.xopenalex-snapshot
The Breeding System and Distribution of Tetrahymena pyriformis.*
inferredcites →https://doi.org/10.1111/j.1550-7408.1956.tb02440.xopenalex-snapshot
Meiosis and Nuclear Behavior in Tetrahymena pyriformis*
inferredcites →https://doi.org/10.1111/j.1550-7408.1975.tb05848.xopenalex-snapshot
Further Electrophoretic Characterization of Strains of Tetrahymena pyriformis*
inferredcites →https://doi.org/10.1111/j.1550-7408.1977.tb04775.xopenalex-snapshot
Inter‐strain Variability of Structural Proteins in Tetrahymena*
inferredcites →https://doi.org/10.1111/j.1550-7408.1980.tb04274.xopenalex-snapshot
Production of Melanin Precursors By A Mutant of Tetrahymena Thermophila*
inferredcites →https://doi.org/10.1111/j.1550-7408.1980.tb05397.xopenalex-snapshot
Isozymic Characterization of Three Mating Groups of the Tetrahymena pyriformis complex*
inferredcites →https://doi.org/10.1111/j.1550-7408.1981.tb02806.xopenalex-snapshot
Three New “Biological” Species of Tetrahymena (T. hegewischi n. sp., T. sonneborni n. sp., T. nipissingi n. sp.) and Temperature Tolerance of Members of the “pyriformis” Complex1
inferredcites →https://doi.org/10.1111/j.1550-7408.1982.tb05417.xopenalex-snapshot
Scanning Electron Microscopy of Cytoskeletal Elements in the Oral Apparatus of Tetrahymena1
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb00986.xopenalex-snapshot
ELECTROPHORETIC ANALYSIS OF EVOLUTIONARY RELATIONSHIPS INTETRAHYMENA
inferredcites →https://doi.org/10.1126/science.1090005openalex-snapshot
Evolution at Two Levels in Humans and Chimpanzees
inferredcites →https://doi.org/10.1126/science.213.4507.549openalex-snapshot
Nullisomic Tetrahymena: Eliminating Germinal Chromosomes
inferredcites →https://doi.org/10.1126/science.7280679openalex-snapshot
Seeds of Change in Embryonic Development
inferredcites →https://doi.org/10.1242/jcs.49.1.177openalex-snapshot
Evolutionary constraints on quantitative variation and regulation of macronuclear dna content in the genus Tetrahymena
inferredcites →https://doi.org/10.2307/3225391openalex-snapshot
Characterization of the Species of the Tetrahymena pyriformis Complex
inferredcites →https://doi.org/10.2307/3225629openalex-snapshot
The Origin and Early Evolution of Animals
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4375.3.4zenodo-depositor-declared
Molecular delineation of the Agave Red Worm Comadia redtenbacheri (Lepidoptera: Cossidae)
inferred← citeshttps://doi.org/10.4467/16890027ap.12.008.0512openalex-extracted
Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1002/dvg.1020130102openalex-snapshot
Introduction: A tribute to David L. Nanney, an experimental ciliatologist
inferred← citeshttps://doi.org/10.1002/ecm.1517openalex-snapshot
Evaluating thermal performance of closely related taxa: Support for hotter is not better, but for unexpected reasons
inferred← citeshttps://doi.org/10.1006/jtbi.2002.3128openalex-snapshot
The Protein Folds as Platonic Forms: New Support for the Pre-Darwinian Conception of Evolution by Natural Law
inferred← citeshttps://doi.org/10.1007/978-1-4615-6974-9_4openalex-snapshot
Neontological Inferences of Evolutionary Pattern and Process in the Salamander Family Plethodontidae
inferred← citeshttps://doi.org/10.1007/978-1-4684-7612-5_1openalex-snapshot
Physiological Ecology of Free-Living Protozoa
inferred← citeshttps://doi.org/10.1007/978-3-030-64682-0_7openalex-snapshot
The Intersection of Forensic Techniques with Ecological Issues
inferred← citeshttps://doi.org/10.1007/978-3-642-80106-8_4openalex-snapshot
Signal Peptide-Induced Sensory Behavior in Free Ciliates: Bioassays and Cellular Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-662-06278-4_11openalex-snapshot
Super-Species in the calcareous plankton
inferred← citeshttps://doi.org/10.1007/978-90-481-2801-3_10openalex-snapshot
The “Tetrahymena pyriformis” complex of cryptic species
inferred← citeshttps://doi.org/10.1007/978-94-010-0585-2_4openalex-snapshot
Toward a new synthesis: Population genetics and evolutionary developmental biology
inferred← citeshttps://doi.org/10.1007/978-981-97-9859-9_85openalex-snapshot
Environmental Sustainability Using eDNA Metabarcoding
inferred← citeshttps://doi.org/10.1007/bf02099752openalex-snapshot
5S and 5.8S ribosomal RNA evolution in the suborder tetrahymenina (Ciliophora: Hymenostomatida)
inferred← citeshttps://doi.org/10.1007/bf02691601openalex-snapshot
Linear genetics, non-linear epigenetics: Complementary approaches to understanding complex diseases
inferred← citeshttps://doi.org/10.1007/s10531-007-9255-6openalex-snapshot
The “Tetrahymena pyriformis” complex of cryptic species
inferred← citeshttps://doi.org/10.1007/s10709-006-0033-2openalex-snapshot
Evolution of branched regulatory genetic pathways: directional selection on pleiotropic loci accelerates developmental system drift
inferred← citeshttps://doi.org/10.1007/s12526-010-0056-xopenalex-snapshot
Biodiversity and phylogeography of Arctic marine fauna: insights from molecular tools
inferred← citeshttps://doi.org/10.1007/s13225-021-00485-7openalex-snapshot
Species concepts of Dothideomycetes: classification, phylogenetic inconsistencies and taxonomic standardization
inferred← citeshttps://doi.org/10.1016/0022-5193(83)90335-1openalex-snapshot
On the problem of stasis in organismal evolution
inferred← citeshttps://doi.org/10.1016/b978-0-12-656520-1.50012-2openalex-snapshot
Dinoflagellate Genetics
inferred← citeshttps://doi.org/10.1016/j.protis.2016.08.003openalex-snapshot
Cohesion of Clonal Life History, Senescence and Rejuvenation Induced by Autogamy of the Histophagous Ciliate Tetrahymena rostrata
inferred← citeshttps://doi.org/10.1016/j.tree.2014.08.001openalex-snapshot
From barcoding single individuals to metabarcoding biological communities: towards an integrative approach to the study of global biodiversity
inferred← citeshttps://doi.org/10.1016/s0020-7519(97)00167-7openalex-snapshot
The global diversity of protozoa and other small species
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61704-0openalex-snapshot
Protozoological Approaches to the Cellular Basis of Mammalian Stress Repair
inferred← citeshttps://doi.org/10.1016/s0091-679x(08)61527-7openalex-snapshot
Chapter 1 Laboratory and Evolutionary History of Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1016/s0091-679x(08)61528-9openalex-snapshot
Chapter 2 Cell Biology of Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1021/jf403545mopenalex-snapshot
Pyrosequencing as a Tool for Rapid Fish Species Identification and Commercial Fraud Detection
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Freshwater protozoa: biodiversity and ecological function
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Toward a new synthesis: population genetics and evolutionary developmental biology
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Molecular biology running into a cul-de-sac?
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Epigenesis: The Missing Beat in Biotechnology?
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CLOSTERIUM MONILIFERUM‐EHRENBERGII(CHAROPHYCEAE, CHLOROPHYTA) SPECIES COMPLEX VIEWED FROM THE 1506 GROUP I INTRON AND ITS2 OF NUCLEAR rDNA
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What can molecules tell us about evolution∗
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Biodiversity at the Microbial Level: The Number of Free-Living Ciliates in the Biosphere
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Biological identifications through DNA barcodes
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The diversity of microbes: resurgence of the phenotype
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Beach environmental DNA fills gaps in photographic biomonitoring to track spatiotemporal community turnover across 82 phyla
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Evaluation of 11 single‐locus and seven multilocus DNA barcodes in L amium L . ( L amiaceae)
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An update on DNA barcoding: low species coverage and numerous unidentified sequences
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DNA barcoding as a heuristic tool for classifying undescribed Nearctic Myrmica ants (Hymenoptera: Formicidae)
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DEVELOPMENTAL HETEROCHRONY IN CILIATED PROTOZOA: OVERLAP OF ASEXUAL AND SEXUAL CYCLES DURING CONJUGATION
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New Wild Tetrahymena from Southeast Asia, China, and North America, Including T. malaccensis, T. asiatica, T. nanneyi, T. caudata, and T. silvana n. spp.
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The 5S and 5.8S Ribosomal RNA Sequences of Tetrahymena thermophila and T. pyriformis1
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Electrophoretic Characterization of Members of the Crypthecodinium cohnii (Dinophyceae) Species Complex1
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Comparison of Sequence Differences in a Variable 23S rRNA Domain among Sets of Cryptic Species of Ciliated Protozoa
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An emergent science on the brink of irrelevance: a review of the past 8 years of DNA barcoding
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In Memoriam: David L. Nanney (1925–2016)
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Estimates of Genetic Introgression, Gene Tree Reticulation, Taxon Divergence, and Sustainability of DNA Barcoding Based on Genetic Molecular Markers
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