| scholarly article | Q13442814 |
| P50 | author | Filippo M Rijli | Q89836921 |
| Shigeru Kuratani | Q30518801 | ||
| P2093 | author name string | Rie Kusakabe | |
| Yasunori Murakami | |||
| Shigehiro Kuraku | |||
| Massimo Pasqualetti | |||
| Yuichi Narita | |||
| Yoko Takio | |||
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| Peripheral development of cranial nerves in a cyclostome, Lampetra japonica: morphological distribution of nerve branches and the vertebrate body plan | Q73592371 | ||
| A new evolutionary scenario for the vertebrate jaw | Q81407737 | ||
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| Organizing axes in time and space; 25 years of colinear tinkering | Q34215299 | ||
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| Archetypal organization of the amphioxus Hox gene cluster. | Q34322671 | ||
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| Organization of Hox genes in ascidians: present, past, and future | Q36103648 | ||
| Evolution of the brain developmental plan: Insights from agnathans | Q36121152 | ||
| Evolutionary patterns of cranial nerve efferent nuclei in vertebrates | Q36299296 | ||
| Cephalic neural crest cells and the evolution of craniofacial structures in vertebrates: morphological and embryological significance of the premandibular-mandibular boundary | Q36340780 | ||
| Ciona intestinalis Hox gene cluster: Its dispersed structure and residual colinear expression in development | Q37589522 | ||
| Time scale for cyclostome evolution inferred with a phylogenetic diagnosis of hagfish and lamprey cDNA sequences | Q40247553 | ||
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| Targeted misexpression of Hox-4.6 in the avian limb bud causes apparent homeotic transformations | Q41089950 | ||
| Light- and electron-microscopic observations of the tail bud of the larval lamprey (Lampetra japonica), with special reference to neural tube formation | Q42462285 | ||
| Spatially restricted expression of Dlx-1, Dlx-2 (Tes-1), Gbx-2, and Wnt- 3 in the embryonic day 12.5 mouse forebrain defines potential transverse and longitudinal segmental boundaries | Q42483474 | ||
| Evidence that Hensen's node is a site of retinoic acid synthesis | Q43668261 | ||
| Importance of SoxE in neural crest development and the evolution of the pharynx | Q44186629 | ||
| Additional hox clusters in the zebrafish: divergent expression patterns belie equivalent activities of duplicate hoxB5 genes | Q47073084 | ||
| Evidence that mechanisms of fin development evolved in the midline of early vertebrates. | Q47193446 | ||
| Amphioxus and ascidian Dmbx homeobox genes give clues to the vertebrate origins of midbrain development | Q47333141 | ||
| Evolutionary biology: lamprey Hox genes and the evolution of jaws. | Q47576549 | ||
| Programming neural Hoxd10: in vivo evidence that early node-associated signals predominate over paraxial mesoderm signals at posterior spinal levels | Q47663302 | ||
| Colinear and segmental expression of amphioxus Hox genes | Q47936870 | ||
| Molecular evolution ofHox gene regulation: Cloning and transgenic analysis of the lampreyHoxQ8 gene | Q48040987 | ||
| Teleost HoxD and HoxA genes: comparison with tetrapods and functional evolution of the HOXD complex | Q48067479 | ||
| Hox cluster disintegration with persistent anteroposterior order of expression in Oikopleura dioica | Q48175053 | ||
| Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling | Q48203653 | ||
| Isolation and expression of the homeobox gene Gbx1 during mouse development | Q48208107 | ||
| The expression of gbx-2 during zebrafish embryogenesis | Q48313260 | ||
| Expression of Gbx-2 during early development of the chick embryo | Q48378620 | ||
| Molecular Dissection of Hox Gene Induction and Maintenance in the Hindbrain | Q48416031 | ||
| Stereotyped axonal bundle formation and neuromeric patterns in embryos of a cyclostome, Lampetra japonica | Q48495630 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Lethenteron japonicum | Q106373086 |
| P304 | page(s) | 606-620 | |
| P577 | publication date | 2007-05-17 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Hox gene expression patterns in Lethenteron japonicum embryos--insights into the evolution of the vertebrate Hox code | |
| P478 | volume | 308 |
| Q42961210 | A Hox regulatory network of hindbrain segmentation is conserved to the base of vertebrates |
| Q64099213 | A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates |
| Q28742260 | A new mechanistic scenario for the origin and evolution of vertebrate cartilage |
| Q46474639 | Amphioxus and the evolution of head segmentation |
| Q91884924 | An atlas of anterior hox gene expression in the embryonic sea lamprey head: Hox-code evolution in vertebrates |
| Q36310996 | Ancestral mesodermal reorganization and evolution of the vertebrate head |
| Q42057926 | Broken colinearity of the amphioxus Hox cluster. |
| Q33890433 | CTCF binding landscape in jawless fish with reference to Hox cluster evolution. |
| Q46753584 | Characterization of two neurogenin genes from the brook lamprey lampetra planeri and their expression in the lamprey nervous system |
| Q42681646 | Craniofacial development of hagfishes and the evolution of vertebrates. |
| Q54352428 | Development and evolution of the lateral plate mesoderm: comparative analysis of amphioxus and lamprey with implications for the acquisition of paired fins |
| Q50449375 | Development of the viscerocranial skeleton during embryogenesis of the sea lamprey, Petromyzon Marinus |
| Q50736562 | Developmental expression and evolution of muscle-specific microRNAs conserved in vertebrates. |
| Q37218531 | Evidence for at least six Hox clusters in the Japanese lamprey (Lethenteron japonicum). |
| Q28748945 | Evidence for the prepattern/cooption model of vertebrate jaw evolution |
| Q26992068 | Evolution of Hoxgene clusters in deuterostomes |
| Q28661238 | Evolution of bilaterian central nervous systems: a single origin? |
| Q37871675 | Evolution of motor innervation to vertebrate fins and limbs |
| Q51914503 | Evolution of oropharyngeal patterning mechanisms involving Dlx and endothelins in vertebrates. |
| Q26861644 | Evolution of patterning systems and circuit elements for locomotion |
| Q51868845 | Evolution of repeated structures along the body axis of jawed vertebrates, insights from the Scyliorhinus canicula Hox code. |
| Q35610087 | Evolution of retinoic acid receptors in chordates: insights from three lamprey species, Lampetra fluviatilis, Petromyzon marinus, and Lethenteron japonicum |
| Q38047031 | Evolution of the vertebrate jaw from developmental perspectives |
| Q47678956 | Evolvability of the vertebrate craniofacial skeleton |
| Q51896859 | Expression and interaction of muscle-related genes in the lamprey imply the evolutionary scenario for vertebrate skeletal muscle, in association with the acquisition of the neck and fins. |
| Q48363371 | Expression patterns of Sema3A in developing amniote limbs: With reference to the diversification of peripheral nerve innervation. |
| Q64990497 | FGF- and SHH-based molecular signals regulate barbel and craniofacial development in catfish. |
| Q33360531 | Fishing for jaws in early vertebrate evolution: a new hypothesis of mandibular confinement |
| Q46791394 | Genoarchitecture of the rostral hindbrain of a shark: basis for understanding the emergence of the cerebellum at the agnathan-gnathostome transition |
| Q58483255 | Hagfish and lamprey Hox genes reveal conservation of temporal colinearity in vertebrates |
| Q37908390 | Hox Gene Clusters of Early Vertebrates: Do They Serve as Reliable Markers for Genome Evolution? |
| Q27014950 | Hox genes: choreographers in neural development, architects of circuit organization |
| Q37570826 | Hox networks and the origins of motor neuron diversity |
| Q51956803 | Identification of four Engrailed genes in the Japanese lamprey, Lethenteron japonicum |
| Q42631620 | Involvement of Slit-Robo signaling in the development of the posterior commissure and concomitant swimming behavior in Xenopus laevis |
| Q36648629 | Lampreys as Diverse Model Organisms in the Genomics Era. |
| Q28602223 | Mode of reduction in the number of pharyngeal segments within the sarcopterygians |
| Q37494809 | Modularity, comparative embryology and evo-devo: developmental dissection of evolving body plans |
| Q27348054 | Mosaic hoxb4a neuronal pleiotropism in zebrafish caudal hindbrain |
| Q28709583 | Non-parsimonious evolution of hagfish Dlx genes |
| Q36638668 | Noncanonical role of Hox14 revealed by its expression patterns in lamprey and shark. |
| Q38644036 | Segmental arithmetic: summing up the Hox gene regulatory network for hindbrain development in chordates. |
| Q37084577 | The lamprey in evolutionary studies. |
| Q50166588 | The neural crest and evolution of the head/trunk interface in vertebrates |
| Q36203683 | The origin and diversification of the developmental mechanisms that pattern the vertebrate head skeleton. |
| Q47395804 | The proepicardium keeps a potential for glomerular marker expression which supports its evolutionary origin from the pronephros |
| Q38793552 | The vertebrate Hox gene regulatory network for hindbrain segmentation: Evolution and diversification: Coupling of a Hox gene regulatory network to hindbrain segmentation is an ancient trait originating at the base of vertebrates. |
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