| 1 - 10 |
Structural origin of the drastic modification of second harmonic generation intensity pattern occurring in tail muscles of climax stages xenopus tadpoles
Recher G, Coumailleau P, Rouede D, Tiaho F |
| 11 - 20 |
NMR structure and dynamics of Q4D059, a kinetoplastid-specific and conserved protein from Trypanosoma cruzi
Lopez-Castilla A, Pons T, Pires JR |
| 21 - 30 |
Crystal structure and substrate-binding mode of GH63 mannosylglycerate hydrolase from Thermus thermophilus HB8
Miyazaki T, Ichikawa M, Iino H, Nishikawa A, Tonozuka T |
| 31 - 37 |
Presence of plicidentine in the oral teeth of the coelacanth Latimeria chalumnae Smith 1939 (Sarcopterygii; Actinistia)
Meunier FJ, Mondejar-Fernandez J, Goussard F, Clement G, Herbin M |
| 38 - 46 |
The insertion domain 1 of class IIA dimeric glycyl-tRNA synthetase is a rubredoxin-like zinc ribbon
Kaur G, Subramanian S |
| 47 - 55 |
CapsidMaps: Protein-protein interaction pattern discovery platform for the structural analysis of virus capsids using Google Maps
Carrillo-Tripp M, Montiel-Garcia DJ, Brooks CL, Reddy VS |
| 56 - 72 |
CNS myelin sheath is stochastically built by homotypic fusion of myelin membranes within the bounds of an oligodendrocyte process
Szuchet S, Nielsen LL, Domowicz MS, Austin JR, Arvanitis DL |
| 73 - 80 |
Changes in the micro- and nanostructure of siliceous valves in the diatom Synedra acus under the effect of colchicine treatment at different stages of the cell cycle
Kharitonenko KV, Bedoshvili YD, Likhoshway YV |
| 81 - 91 |
The leucine-rich amelogenin protein (LRAP) is primarily monomeric and unstructured in physiological solution
Tarasevich BJ, Philo JS, Maluf NK, Krueger S, Buchko GW, Lin GY, Shaw WJ |
