| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1028204354 |
| P356 | DOI | 10.1186/1471-2148-13-253 |
| P932 | PMC publication ID | 4225663 |
| P698 | PubMed publication ID | 24238092 |
| P5875 | ResearchGate publication ID | 258633384 |
| P50 | author | Bernhard Hausdorf | Q21390358 |
| Achim Meyer | Q54006623 | ||
| Maximilian P Nesnidal | Q117272023 | ||
| Thomas Hankeln | Q117272024 | ||
| Torsten H. Struck | Q33145773 | ||
| Iris Bruchhaus | Q34580960 | ||
| Bernhard Lieb | Q34581188 | ||
| P2093 | author name string | Ingo Ebersberger | |
| Alexander Witek | |||
| Martin Helmkampf | |||
| P2860 | cites work | Resolving difficult phylogenetic questions: why more sequences are not enough | Q21092718 |
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| Phylogenetic position of Nemertea derived from phylogenomic data | Q31144220 | ||
| Gnathostomulida--an enigmatic metazoan phylum from both morphological and molecular perspectives | Q32110170 | ||
| Bilaterian phylogeny based on analyses of a region of the sodium-potassium ATPase beta-subunit gene | Q33200251 | ||
| The complete mitochondrial genome of Flustrellidra hispida and the phylogenetic position of Bryozoa among the Metazoa | Q33240220 | ||
| Spiralian phylogenomics supports the resurrection of Bryozoa comprising Ectoprocta and Entoprocta | Q33301887 | ||
| HaMStR: profile hidden markov model based search for orthologs in ESTs | Q33479760 | ||
| Phylogenetic relationships within the lophophorate lineages (Ectoprocta, Brachiopoda and Phoronida). | Q33521577 | ||
| Compositional heterogeneity and phylogenomic inference of metazoan relationships | Q33552016 | ||
| A Monte Carlo approach successfully identifies randomness in multiple sequence alignments: a more objective means of data exclusion | Q33595512 | ||
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| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bias | Q742736 |
| phylogenomics | Q3381973 | ||
| P304 | page(s) | 253 | |
| P577 | publication date | 2013-11-17 | |
| P1433 | published in | BMC Evolutionary Biology | Q13418959 |
| P1476 | title | New phylogenomic data support the monophyly of Lophophorata and an Ectoproct-Phoronid clade and indicate that Polyzoa and Kryptrochozoa are caused by systematic bias | |
| P478 | volume | 13 |
| Q46254926 | A Microsporidian Infection in Phoronids (Phylum Phoronida): Microsporidium phoronidi n. sp. from a Phoronis embryolabi |
| Q104455359 | A New Phoronid Species, Phoronis savinkini sp. n., from the South China Sea and an Analysis of the Taxonomic Diversity of Phoronida |
| Q57585277 | A phylogenomic resolution of the sea urchin tree of life |
| Q104457090 | Anatomy of the coelomic system in Novocrania anomala (Brachiopoda, Craniiformea) and relationships within brachiopods |
| Q38367980 | Can quartet analyses combining maximum likelihood estimation and Hennigian logic overcome long branch attraction in phylogenomic sequence data? |
| Q30847199 | Cleavage modification did not alter blastomere fates during bryozoan evolution |
| Q64891321 | Dicyemida and Orthonectida: Two Stories of Body Plan Simplification. |
| Q46436447 | Distribution of serotonin and FMRF-amide in the nervous system of different zooidal types of cheilostome bryozoa: A case study of Arctonula arctica |
| Q28269438 | Ediacaran skeletal metazoan interpreted as a lophophorate |
| Q35791282 | Evolution and development of the adelphophagic, intracapsular Schmidt's larva of the nemertean Lineus ruber. |
| Q55871227 | Genomics and the animal tree of life: conflicts and future prospects |
| Q43205920 | Innervation of the lophophore suggests that the phoronid Phoronis ovalis is a link between phoronids and bryozoans |
| Q89595235 | Key novelties in the evolution of the aquatic colonial phylum Bryozoa: evidence from soft body morphology |
| Q35497778 | Mesodermal gene expression during the embryonic and larval development of the articulate brachiopod Terebratalia transversa |
| Q30670478 | Metamorphic remodeling of morphology and the body cavity in Phoronopsis harmeri (Lophotrochozoa, Phoronida): the evolution of the phoronid body plan and life cycle |
| Q28649316 | Modern Data on the Innervation of the Lophophore in Lingula anatina (Brachiopoda) Support the Monophyly of the Lophophorates |
| Q35681830 | Muscular anatomy of an entoproct creeping-type larva reveals extraordinary high complexity and potential shared characters with mollusks |
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| Q34416122 | Platyzoan paraphyly based on phylogenomic data supports a noncoelomate ancestry of spiralia |
| Q45728964 | Reconstructing the muscular ground pattern of phylactolaemate bryozoans: first data from gelatinous representatives. |
| Q67234679 | Revisiting metazoan phylogeny with genomic sampling of all phyla |
| Q38651284 | The first data on the innervation of the lophophore in the rhynchonelliform brachiopod Hemithiris psittacea: what is the ground pattern of the lophophore in lophophorates? |
| Q28588404 | The life of the freshwater bryozoan Stephanella hina (Bryozoa, Phylactolaemata)-a crucial key to elucidating bryozoan evolution |
| Q35830904 | The lophophore innervation pattern of the inarticulate brachiopod Lingula anatina (Brachiopoda) supports monophyly of Lophophorata |
| Q59795600 | The nervous system in the cyclostome bryozoan as revealed by transmission electron and confocal laser scanning microscopy |
| Q41668135 | The nervous system of Paludicella articulata - first evidence of a neuroepithelium in a ctenostome ectoproct |
| Q36124428 | The nervous system of the lophophore in the ctenostome Amathia gracilis provides insight into the morphology of ancestral ectoprocts and the monophyly of the lophophorates |
| Q64107197 | The neuroanatomy of (Entoprocta, Coloniales) reveals significant differences between bryozoan and entoproct nervous systems |
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| Q35807806 | The serotonin-lir nervous system of the Bryozoa (Lophotrochozoa): a general pattern in the Gymnolaemata and implications for lophophore evolution of the phylum |
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| Q38807570 | Ultrastructure of the coelom in the brachiopod Lingula anatina. |
| Q60916139 | gene expression in postmetamorphic juveniles of the brachiopod |
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