1 - 19 |
A model-based parallel origin and for cryoTEM and its application orientation refinement algorithm to the study of virus structures Ji YC, Marinescu DC, Zhang W, Zhang X, Yan XD, Baker TS |
20 - 26 |
Role of each residue in catalysis in the active site of pyrimidine nucleoside phosphorylase from Bacillus subtilis: A hybrid QM/MM study Gao XF, Huang XR, Sun CC |
27 - 41 |
Domains of importin-alpha 2 required for ring canal assembly during Drosophila oogenesis Gorjanacz M, Torok I, Pomozi I, Garab G, Szlanka T, Kiss I, Mechler BM |
42 - 58 |
Mechanisms of antimicrobial peptide action: Studies of indolicidin assembly at model membrane interfaces by in situ atomic force microscopy Shaw JE, Alattia JR, Verity JE, Prive GG, Yip CM |
59 - 67 |
The role of subunit hinges and molecular "switches" in the control of viral capsid polymorphism Tang JH, Johnson JM, Dryden KA, Young MJ, Zlotnick A, Johnson JE |
68 - 78 |
Checking the conformational stability of cystatin C and its L68Q variant by molecular dynamics studies: Why is the L68Q variant amyloidogenic? Rodziewicz-Motowidlo S, Wahlbom M, Wang X, Lagiewka J, Janowski R, Jaskolski M, Grubb A, Grzonka Z |
79 - 88 |
In vivo formation steps of the hard alpha-keratin intermediate filament along a hair follicle: Evidence for structural polymorphism Rafik ME, Briki F, Burghammer M, Doucet J |
89 - 99 |
The flagellar attachment zone of Trypanosoma cruzi epimastigote forms Rocha GM, Brandao BA, Mortara RA, Attias M, de Souza W, Carvalho TMU |
100 - 110 |
Morphological and structural aspects of the giant starch granules from Phajus grandifolius Chanzy H, Putaux JL, Dupeyre D, Davies R, Burghammer M, Montanari S, Riekel C |