| P50 | author | Thomas Cavalier-Smith | Q454117 |
| P2860 | cites work | The nuclear matrix of Euglena gracilis (euglenophyta): a stage of nuclear matrix evolution? | Q73952436 |
| | Eukaryotic non-coding DNA is functional: evidence from the differential scaling of cryptomonad genomes | Q74023124 |
| | Reproducible but dynamic positioning of DNA in chromosomes during mitosis | Q74307648 |
| | Feast and famine in plant genomes | Q74630698 |
| | [Desoxyribonucleic acid volume & content per nucleus] | Q74739777 |
| | Prokaryotic structural maintenance of chromosomes (SMC) proteins: distribution, phylogeny, and comparison with MukBs and additional prokaryotic and eukaryotic coiled-coil proteins | Q77166393 |
| | Classification of common conserved sequences in mammalian intergenic regions | Q77816264 |
| | Chromatin of Trypanosoma cruzi: in situ analysis revealed its unusual structure and nuclear organization | Q77986163 |
| | Live imaging of telomeres: yKu and Sir proteins define redundant telomere-anchoring pathways in yeast | Q78708973 |
| | The high genomic mutation rate | Q80506082 |
| | Evolution of DNA amounts across land plants (embryophyta) | Q22066091 |
| | The highly reduced genome of an enslaved algal nucleus | Q22122376 |
| | Selfish DNA: the ultimate parasite | Q22122417 |
| | Selfish genes, the phenotype paradigm and genome evolution | Q22122418 |
| | The genome sequence of the filamentous fungus Neurospora crassa | Q22122516 |
| | Genome sequence of the human malaria parasite Plasmodium falciparum | Q22122524 |
| | Histone sumoylation is associated with transcriptional repression | Q24656259 |
| | HA95 and LAP2 beta mediate a novel chromatin-nuclear envelope interaction implicated in initiation of DNA replication | Q24675954 |
| | Four signature motifs define the first class of structurally related large coiled-coil proteins in plants | Q24806409 |
| | Polo-like kinase Cdc5 promotes chiasmata formation and cosegregation of sister centromeres at meiosis I. | Q27933588 |
| | Functional genomics identifies monopolin: a kinetochore protein required for segregation of homologs during meiosis i. | Q27934438 |
| | Kinetochore recruitment of two nucleolar proteins is required for homolog segregation in meiosis I. | Q27939356 |
| | Arabidopsis TERMINAL FLOWER 2 gene encodes a heterochromatin protein 1 homolog and represses both FLOWERING LOCUS T to regulate flowering time and several floral homeotic genes | Q28182172 |
| | Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma | Q28185889 |
| | Chromosomal cohesin forms a ring | Q28185991 |
| | Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin | Q28187783 |
| | The root of the eukaryote tree pinpointed | Q28205101 |
| | The phagotrophic origin of eukaryotes and phylogenetic classification of Protozoa | Q28212529 |
| | The neomuran origin of archaebacteria, the negibacterial root of the universal tree and bacterial megaclassification | Q28218259 |
| | A mitochondrial remnant in the microsporidian Trachipleistophora hominis | Q28218819 |
| | Principles of protein and lipid targeting in secondary symbiogenesis: euglenoid, dinoflagellate, and sporozoan plastid origins and the eukaryote family tree | Q28261633 |
| | The origin of eukaryotic and archaebacterial cells | Q28290673 |
| | A general model for the origin of allometric scaling laws in biology | Q28306671 |
| | The desoxyribonucleic acid content of animal cells and its evolutionary significance | Q28756221 |
| | Chloroplast protein and centrosomal genes, a tRNA intron, and odd telomeres in an unusually compact eukaryotic genome, the cryptomonad nucleomorph | Q28776379 |
| | Microsporidia: Biology and Evolution of Highly Reduced Intracellular Parasites | Q29307168 |
| | Heterochromatin and epigenetic control of gene expression | Q29618486 |
| | Nuclear DNA C-values in 30 species double the familial representation in pteridophytes | Q30845029 |
| | Remarkable compartmentalization of transposable elements and pseudogenes in the heterochromatin of the Tetraodon nigroviridis genome | Q30860364 |
| | Is small indel bias a determinant of genome size? | Q30980345 |
| | Coding properties of macronuclear DNA molecules in Sterkiella nova (Oxytricha nova). | Q31059864 |
| | The fractal nature of nature: power laws, ecological complexity and biodiversity | Q31085782 |
| | Dependence of heterochromatic histone H3 methylation patterns on the Arabidopsis gene DDM1. | Q44037194 |
| | Interplay between two epigenetic marks. DNA methylation and histone H3 lysine 9 methylation | Q44113626 |
| | Critical nuclear DNA size and distribution associated with S phase initiation. Peripheral location of initiation and termination sites | Q44239508 |
| | Methylation of histone H3 in euchromatin of plant chromosomes depends on basic nuclear DNA content | Q44358708 |
| | Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassa | Q44393142 |
| | The carboxyl-terminal region common to lamins A and C contains a DNA binding domain. | Q44419994 |
| | Evolution of genome size: new approaches to an old problem | Q47220744 |
| | Evolutionary implications of the relationship between genome size and body size in flatworms and copepods | Q47241976 |
| | Intron-genome size relationship on a large evolutionary scale | Q47258179 |
| | r- and K-tactics in the evolution of protist developmental systems: Cell and genome size, phenotype diversifying selection, and cell cycle patterns | Q47301605 |
| | The paleontology of intergene retrotransposons of maize | Q47750190 |
| | The large-scale genomic organization of repetitive DNA families at the telomeres of rye chromosomes | Q48069559 |
| | Congruent evidence from alpha-tubulin and beta-tubulin gene phylogenies for a zygomycete origin of microsporidia | Q48251993 |
| | Origin of an apparent B chromosome by mutation, chromosome fragmentation and specific DNA sequence amplification | Q48270072 |
| | Mutations in LIKE HETEROCHROMATIN PROTEIN 1 affect flowering time and plant architecture in Arabidopsis. | Q48330316 |
| | Nuclear lamina and the structural organization of the nuclear envelope | Q49487452 |
| | Mathematical model of the cell division cycle of fission yeast. | Q52015697 |
| | Variation across species in the size of the nuclear genome supports the junk-DNA explanation for the C-value paradox | Q52230315 |
| | The changing sizes of genes. | Q52551550 |
| | Multiple regimes of constrained chromosome motion are regulated in the interphase Drosophila nucleus. | Q52590760 |
| | Characterisation and high-resolution distribution of a matrix attachment region-binding protein (MFP1) in proliferating cells of onion | Q58285053 |
| | Selfish DNA | Q59071461 |
| | Changes in the Amount of DNA in Cell Nuclei during Vertebrate Evolution | Q59085694 |
| | Electron Microscopic Evidence for Chloroplast Fusion in Zygotes of Chlamydomonos reinhardii | Q59092224 |
| | Towards a blueprint of the cell cycle | Q61071722 |
| | Identification of proteins immunologically related to vertebrate lamins in the nuclear matrix of the myxomycete Physarum polycephalum | Q72564216 |
| | Immunological characterization of lamins in the nuclear matrix of onion cells | Q72680750 |
| | Phase transitions in nuclei and chromatin. Is nuclear volume controlled by the chromatin or by the nuclear matrix? | Q72752807 |
| | Spontaneous formation of nucleus-like structures around bacteriophage DNA microinjected into Xenopus eggs | Q72791838 |
| | One gene determines maize B chromosome accumulation by preferential fertilisation; another gene(s) determines their meiotic loss | Q73121019 |
| | Bacterial catalase in the microsporidian Nosema locustae: implications for microsporidian metabolism and genome evolution. | Q33193875 |
| | Arabidopsis MSI1 is required for epigenetic maintenance of reproductive development | Q33338362 |
| | Nucleus-encoded, plastid-targeted glyceraldehyde-3-phosphate dehydrogenase (GAPDH) indicates a single origin for chromalveolate plastids | Q33338581 |
| | Model scenarios for evolution of the eukaryotic cell cycle | Q33546752 |
| | Large-scale chromatin structure and function. | Q33680832 |
| | The skeletal function of non-genic nuclear DNA: new evidence from ancient cell chimaeras | Q33858685 |
| | The fourth dimension of life: fractal geometry and allometric scaling of organisms. | Q33863970 |
| | Membrane heredity and early chloroplast evolution | Q33877286 |
| | Rooting the eukaryote tree by using a derived gene fusion | Q33960025 |
| | The Closest Unicellular Relatives of Animals | Q33962095 |
| | Phylogeny of Choanozoa, Apusozoa, and Other Protozoa and Early Eukaryote Megaevolution | Q33965494 |
| | Interphase nuclear envelope lamins form a discontinuous network that interacts with only a fraction of the chromatin in the nuclear periphery | Q34030313 |
| | Allometric scaling of metabolic rate from molecules and mitochondria to cells and mammals | Q34116835 |
| | Chromatin proteins are determinants of centromere function | Q34131328 |
| | Origin of the cell nucleus | Q34164886 |
| | Kleisins: a superfamily of bacterial and eukaryotic SMC protein partners | Q34187210 |
| | Centrosome number is controlled by a centrosome-intrinsic block to reduplication | Q34199885 |
| | How selfish is DNA? | Q34286255 |
| | DNA methylation controls histone H3 lysine 9 methylation and heterochromatin assembly in Arabidopsis. | Q34361252 |
| | Evolution of the cell cycle | Q34373045 |
| | A relationship between DNA content, nuclear volume, and minimum mitotic cycle time | Q34397261 |
| | Genome evolution in the genus Sorghum (Poaceae) | Q34582856 |
| | Kinetic analysis of a molecular model of the budding yeast cell cycle | Q34675369 |
| | Mutational equilibrium model of genome size evolution | Q34776798 |
| | Functional and evolutionary analysis of a eukaryotic parasitic genome | Q34921839 |
| | Chromosome cohesion: ring around the sisters? | Q34942956 |
| | Nucleomorphs: enslaved algal nuclei | Q35012166 |
| | Involvement of p34cdc2 in establishing the dependency of S phase on mitosis | Q35013567 |
| | Chromatin silencing: RNA in the driving seat | Q35044493 |
| | Controlling S-phase onset in fission yeast | Q35132566 |
| | The laminopathies: nuclear structure meets disease | Q35145852 |
| | Modeling the fission yeast cell cycle: quantized cycle times in wee1- cdc25Delta mutant cells | Q35170247 |
| | Erasure of CpG methylation in Arabidopsis alters patterns of histone H3 methylation in heterochromatin | Q35170859 |
| | The nuclear lamina and its functions in the nucleus | Q35200844 |
| | Genomic reduction and evolution of novel genetic membranes and protein-targeting machinery in eukaryote-eukaryote chimaeras (meta-algae). | Q35213429 |
| | ROLES OF DEOXYRIBONUCLEIC ACID IN INHERITANCE. | Q35458397 |
| | Structure, Function, and Regulation of Budding Yeast Kinetochores | Q35564845 |
| | ACE2 is required for daughter cell-specific G1 delay in Saccharomyces cerevisiae | Q35917950 |
| | The relationship of DNA content to nuclear and chromosome volumes and to radiosensitivity (LD50) | Q35974320 |
| | Nuclear actin and protein 4.1: essential interactions during nuclear assembly in vitro. | Q35977914 |
| | MFP1 is a thylakoid-associated, nucleoid-binding protein with a coiled-coil structure | Q36247510 |
| | Lamin-binding fragment of LAP2 inhibits increase in nuclear volume during the cell cycle and progression into S phase | Q36275039 |
| | The budding yeast silencing protein Sir1 is a functional component of centromeric chromatin. | Q36335566 |
| | A complex history of rearrangement in an orthologous region of the maize, sorghum, and rice genomes | Q36349471 |
| | Intron phylogeny: a new hypothesis | Q37778081 |
| | A prokaryotic condensin/cohesin-like complex can actively compact chromosomes from a single position on the nucleoid and binds to DNA as a ring-like structure | Q38351923 |
| | Target sites for SINE integration in Brassica genomes display nuclear matrix binding activity | Q38498177 |
| | Conservation of matrix attachment region-binding filament-like protein 1 among higher plants | Q38500218 |
| | Matrix attachment region binding protein MFP1 is localized in discrete domains at the nuclear envelope | Q38501083 |
| | The maintenance of transposable elements in natural populations | Q39274824 |
| | Testing a mathematical model of the yeast cell cycle | Q39354553 |
| | Cell size and the concept of wasteful and frugal evolutionary strategies | Q39502814 |
| | Buffering: a possible passive-homeostasis role for redundant DNA. | Q39562229 |
| | A polymer model for large-scale chromatin organization in lower eukaryotes | Q39617256 |
| | Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the DNA C-value paradox | Q39791026 |
| | Nuclear DNA content and minimum generation time in herbaceous plants | Q39907465 |
| | The cytoplasmic control of nuclear activity in animal development | Q39970305 |
| | Skeletal DNA and the evolution of genome size | Q40335452 |
| | Cell size and nuclear DNA content in vertebrates | Q40498694 |
| | From morphogenes to morphogenesis | Q40931274 |
| | A quantitative model for the cdc2 control of S phase and mitosis in fission yeast | Q41150534 |
| | At the heart of the budding yeast cell cycle | Q41203319 |
| | Bacterial DNA segregation: its motors and positional control | Q41316772 |
| | Cell cycle-dependent expression of an essential SMC-like protein and dynamic chromosome localization in the archaeon Halobacterium salinarum | Q42527387 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 147-75 | |
| P577 | publication date | 2005-01-01 | |
| P1433 | published in | Annals of Botany | Q1821243 |
| P1476 | title | Economy, speed and size matter: evolutionary forces driving nuclear genome miniaturization and expansion | |
| P478 | volume | 95 | |