| scholarly article | Q13442814 |
| P2093 | author name string | Didier Casane | |
| Patrick Laurenti | |||
| P2860 | cites work | The distribution of fitness effects of new mutations | Q22122013 |
| Evolution of the mutation rate | Q24602069 | ||
| Heterotachy, an important process of protein evolution | Q28212928 | ||
| Genetic drift | Q28251605 | ||
| An endogenous foamy-like viral element in the coelacanth genome | Q28727830 | ||
| A living fossil in the genome of a living fossil: Harbinger transposons in the coelacanth genome | Q28732115 | ||
| Genome biology of the cyclostomes and insights into the evolutionary biology of vertebrate genomes | Q28742395 | ||
| Genetically distinct coelacanth population off the northern Tanzanian coast | Q28743173 | ||
| Complete HOX cluster characterization of the coelacanth provides further evidence for slow evolution of its genome | Q28748470 | ||
| Coelacanth genome sequence reveals the evolutionary history of vertebrate genes | Q28770070 | ||
| Nuclear protein-coding genes support lungfish and not the coelacanth as the closest living relatives of land vertebrates | Q28776039 | ||
| Which side of the tree is more basal? | Q30053816 | ||
| The Darwinian revolution as viewed by a philosophical biologist. | Q30366729 | ||
| The mitochondrial genome of Indonesian coelacanth Latimeria menadoensis (Sarcopterygii: Coelacanthiformes) and divergence time estimation between the two coelacanths | Q31154649 | ||
| Two lamprey Hedgehog genes share non-coding regulatory sequences and expression patterns with gnathostome Hedgehogs | Q33725443 | ||
| A pervasive denigration of natural history misconstrues how biodiversity inventories and taxonomy underpin scientific knowledge. | Q33864616 | ||
| Identifying heterogeneity in rates of morphological evolution: discrete character change in the evolution of lungfish (Sarcopterygii; Dipnoi). | Q34140748 | ||
| Earliest known coelacanth skull extends the range of anatomically modern coelacanths to the Early Devonian | Q34227430 | ||
| Extremely slow rate of evolution in the HOX cluster revealed by comparison between Tanzanian and Indonesian coelacanths | Q34304422 | ||
| Composition and phylogenetic analysis of vitellogenin coding sequences in the Indonesian coelacanth Latimeria menadoensis | Q34308512 | ||
| Evolution of the Australian lungfish (Neoceratodus forsteri) genome: a major role for CR1 and L2 LINE elements. | Q34317231 | ||
| Hox gene clusters in the Indonesian coelacanth, Latimeria menadoensis | Q34328982 | ||
| Conservation of shh cis-regulatory architecture of the coelacanth is consistent with its ancestral phylogenetic position | Q34350972 | ||
| Molecular phylogeny and divergence times of deuterostome animals | Q34437645 | ||
| First discovery of a primitive coelacanth fin fills a major gap in the evolution of lobed fins and limbs | Q34655656 | ||
| Drift-barrier hypothesis and mutation-rate evolution. | Q36389558 | ||
| Unburdening evo-devo: ancestral attractions, model organisms, and basal baloney | Q36492186 | ||
| Adaptation or biased gene conversion? Extending the null hypothesis of molecular evolution | Q36785408 | ||
| Developmental biology of hagfishes, with a report on newly obtained embryos of the Japanese inshore hagfish, Eptatretus burgeri | Q37408280 | ||
| Evolutionary dynamics of rhodopsin type 2 opsins in vertebrates | Q37478050 | ||
| Replication-associated mutational asymmetry in the human genome | Q39582800 | ||
| Evolution of Hox gene clusters in gnathostomes: insights from a survey of a shark (Scyliorhinus canicula) transcriptome. | Q42667284 | ||
| Population divergence in East African coelacanths | Q43938814 | ||
| Epistasis as the primary factor in molecular evolution | Q43975683 | ||
| The "fish-specific" Hox cluster duplication is coincident with the origin of teleosts. | Q44591674 | ||
| Revisiting the origin of the vertebrate Hox14 by including its relict sarcopterygian members | Q46254688 | ||
| Tooth and cranial disparity in the fossil relatives of Sphenodon (Rhynchocephalia) dispute the persistent 'living fossil' label. | Q47182409 | ||
| The phylogenetic relationship of tetrapod, coelacanth, and lungfish revealed by the sequences of forty-four nuclear genes | Q47643476 | ||
| Evolution of repeated structures along the body axis of jawed vertebrates, insights from the Scyliorhinus canicula Hox code. | Q51868845 | ||
| A fork-tailed coelacanth,Rebellatrix divaricerca, gen. et sp. nov. (Actinistia, Rebellatricidae, fam. nov.), from the Lower Triassic of Western Canada | Q54666360 | ||
| The Nearly Neutral Theory of Molecular Evolution | Q55968685 | ||
| Indonesian ‘king of the sea’ discovered | Q56081865 | ||
| Tree thinking for all biology: the problem with reading phylogenies as ladders of progress | Q56967556 | ||
| Hox clusters of the bichir (Actinopterygii, Polypterus senegalus) highlight unique patterns of sequence evolution in gnathostome phylogeny | Q56990653 | ||
| A Living Fish of Mesozoic Type | Q59099141 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 332-338 | |
| P577 | publication date | 2013-02-04 | |
| P1433 | published in | BioEssays | Q4914614 |
| P1476 | title | Why coelacanths are not 'living fossils': a review of molecular and morphological data | |
| P478 | volume | 35 |
| Q92610118 | A thirteen-million-year divergence between two lineages of Indonesian coelacanths |
| Q28650301 | Ancestor-descendant relationships in evolution: origin of the extant pygmy right whale, Caperea marginata |
| Q38406090 | Boom and bust: ancient and recent diversification in bichirs (Polypteridae: Actinopterygii), a relictual lineage of ray-finned fishes |
| Q57898413 | Coelacanths as “almost living fossils” |
| Q54537521 | Current status of the systematics and evolutionary biology of Grylloblattidae (Grylloblattodea) |
| Q45371583 | Evolutionary active transposable elements in the genome of the coelacanth. |
| Q38714433 | Incorporating tree-thinking and evolutionary time scale into developmental biology |
| Q28650419 | Interspecies insertion polymorphism analysis reveals recent activity of transposable elements in extant coelacanths |
| Q38219353 | Is evolutionary biology becoming too politically correct? A reflection on the scala naturae, phylogenetically basal clades, anatomically plesiomorphic taxa, and 'lower' animals. |
| Q55881123 | Macroevolutionary patterns in Rhynchocephalia: is the tuatara (Sphenodon punctatus ) a living fossil? |
| Q41682413 | Model organisms in evo-devo: promises and pitfalls of the comparative approach |
| Q28708974 | Multiple global radiations in tadpole shrimps challenge the concept of 'living fossils' |
| Q35457840 | Permian-Triassic Osteichthyes (bony fishes): diversity dynamics and body size evolution |
| Q28596089 | Phylogeography of Arenaria balearica L. (Caryophyllaceae): evolutionary history of a disjunct endemic from the Western Mediterranean continental islands |
| Q34451105 | Relict species: a relict concept? |
| Q58589081 | Rethinking Living Fossils |
| Q28681093 | Revealing less derived nature of cartilaginous fish genomes with their evolutionary time scale inferred with nuclear genes |
| Q28652544 | The coelacanth rostral organ is a unique low-resolution electro-detector that facilitates the feeding strike |
| Q28607083 | The coelacanth: Can a "living fossil" have active transposable elements in its genome? |
| Q21198717 | The great chain of being is still here |
| Q45077856 | Transcriptional activity of transposable elements in coelacanth |
| Q60232109 | What Is the Meaning of Extreme Phylogenetic Diversity? The Case of Phylogenetic Relict Species |
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