 |
|
 | Journal of Experimental Zoology 2002, Vol 294 |
| A Force, A Amores, JH Postlethwait | Hox cluster organization in the jawless vertebrate Petromyzon marinus | 30-46 |
| A Ressayre, B Godelle, C Raquin, PH Gouyon | Aperture pattern ontogeny in angiosperms | 122-135 |
| AC Horton, JJ GibsonBrown | Evolution of developmental functions by the Eomesodermin, T-brain-1, Tbx21 subfamily of T-box genes: Insights from amphioxus | 112-121 |
| C Ledje, CB Kim, FH Ruddle | Characterization of Hox genes in the bichir, Polypterus palmas | 107-111 |
| CO Wilke, PRA Campos, JF Fontanari | Genealogical process on a correlated fitness landscape | 274-284 |
| E Meir, EM Munro, GM Odell, G VonDassow | Ingeneue: A versatile tool for reconstituting genetic networks, with examples from the segment polarity network | 216-251 |
| G Satoh, JK Takeuchi, K Yasui, K Tagawa, H Saiga, PJ Zhang, N Satoh | Amphi-Eomes/Tbr1: An amphioxus cognate of vertebrate Eomesodermin and T-Brain1 genes whose expression reveals evolutionarily distinct domain in amphioxus development | 136-145 |
| G VonDassow, GM Odell | Design and constraints of the Drosophila segment polarity module: Robust spatial patterning emerges from intertwined cell state switches | 179-215 |
| GF Stopper, L Hecker, RA Franssen, SK Sessions | How trematodes cause limb deformities in amphibians | 252-263 |
| GP Wagner | What is the scientific impact of MDE? | 177-178 |
| HCE Larsson, GP Wagner | Pentadactyl ground state of the avian wing | 146-151 |
| JL Scemama, M Hunter, J McCallum, V Prince, E Stellwag | Evolutionary divergence of vertebrate Hoxb2 expression patterns and transcriptional regulatory loci | 285-299 |
| K Kitamura, T Shimizu | Segment-specific expression of alkaline phosphatase in the Tubifex embryo requires DNA replication and mRNA synthesis | 68-76 |
| M Harris | Shh-Bmp2 signaling module and the evolutionary origin and diversification of feathers (Vol 294, pg 160, 2002) | 300 |
| M Kundrat, V Seichert, AP Russell, K Smetana | Pentadactyl pattern of the avian wing autopodium and pyramid reduction hypothesis | 152-159 |
| MP Harris, JF Fallon, RO Prum | Shh-Bmp2 signaling module and the evolutionary origin and diversification of feathers | 160-176 |
| MR SanchezVillagra | Comparative patterns of postcranial ontogeny in therian mammals: An analysis of relative timing of ossification events | 264-273 |
| PG Satchell, X Anderton, OH Ryu, XH Luan, AJ Ortega, R Opamen, BJ Berman, DE Witherspoon, JL Gutmann, A Yamane, M ZeichnerDavid, JP Simmer, CF Shuler, TGH Diekwisch | Conservation and variation in enamel protein distribution during vertebrate tooth development | 91-106 |
| PM Mabee, PL Crotwell, NC Bird, AC Burke | Evolution of median fin modules in the axial skeleton of fishes | 77-90 |
| SQ Irvine, JL Carr, WJ Bailey, K Kawasaki, N Shimizu, CT Amemiya, FH Ruddle | Genomic analysis of hox clusters in the sea lamprey Petromyzon marinus | 47-62 |
| TR Jackman, DJ Irschick, K DeQueiroz, JB Losos, A Larson | Molecular phylogenetic perspective on evolution of lizards of the Anolis grahami series | 1-16 |
| WH Powell, ME Hahn | Identification and functional characterization of hypoxia-inducible factor 2 alpha from the estuarine teleost, Fundulus heteroclitus: Interaction of HIF-2 alpha with two ARNT2 splice variants | 17-29 |
| X Huang, HH Cheng, YQ Guo, L Liu, JF Gui, RJ Zhou | A conserved family of doublesex-related genes from fishes | 63-67 |