1 - 2 |
From structural architecture to cellular organization: Celebrating the scientific contributions of Ueli Aebi on the occasion of his retirement Lim RYH, Herrmann H |
3 - 13 |
Looking back at a quarter-century of research at the Maurice E. Muller Institute for Structural Biology Muller SA, Engel A |
14 - 23 |
Inroads into the structure and function of intermediate filament networks Goldman RD, Cleland MM, Murthy SNP, Mahammad S, Kuczmarski ER |
24 - 31 |
Nuclear lamina at the crossroads of the cytoplasm and nucleus Gerace L, Huber MD |
32 - 39 |
Formins filter modified actin subunits during processive elongation Chen Q, Nag S, Pollard TD |
40 - 45 |
Fascin and VASP synergistically increase the Young's modulus of actin comet tails Suei S, Plastino J, Kreplak L |
46 - 53 |
Stabilization of vimentin coil2 fragment via an engineered disulfide Chernyatina AA, Strelkov SV |
54 - 62 |
Complex formation and kinetics of filament assembly exhibited by the simple epithelial keratins K8 and K18 Lichtenstern T, Mucke N, Aebi U, Mauermann M, Herrmann H |
63 - 69 |
From skeletal muscle to cancer: Insights learned elucidating the function of tropomyosin Choi C, Kim D, Kim S, Jeong S, Song E, Helfman DM |
70 - 80 |
An antiparallel actin dimer is associated with the endocytic pathway in mammalian cells Silvan U, Boiteux C, Sutterlin R, Schroeder U, Mannherz HG, Jockusch BM, Berneche S, Aebi U, Schoenenberger CA |
81 - 89 |
Domain topology of nucleoporin Nup98 within the nuclear pore complex Chatel G, Desai SH, Mattheyses AL, Powers MA, Fahrenkrog B |
90 - 98 |
Nuclear transport of baculovirus: Revealing the nuclear pore complex passage Au S, Pante N |
99 - 105 |
Analysis of the yeast nucleoporin Nup188 reveals a conserved S-like structure with similarity to karyopherins Flemming D, Devos DP, Schwarz J, Amlacher S, Lutzmann M, Hurt E |
106 - 112 |
Structural and physiological phenotypes of disease-linked lamin mutations in C. elegans Bank EM, Ben-Harush K, Feinstein N, Medalia O, Gruenbaum Y |
113 - 118 |
Filaments assembly of ectopically expressed Caenorhabditis elegans lamin within Xenopus oocytes Grossman E, Dahan I, Stick R, Goldberg MW, Gruenbaum Y, Medalia O |
119 - 127 |
Metallothionein as a clonable high-density marker for cryo-electron microscopy Bouchet-Marquis C, Pagratis M, Kirmse R, Hoenger A |
128 - 134 |
Connecting mu-fluidics to electron microscopy Kemmerling S, Ziegler J, Schweighauser G, Arnold SA, Giss D, Muller SA, Ringler P, Goldie KN, Goedecke N, Hierlemann A, Stahlberg H, Engel A, Braun T |
135 - 144 |
Automated segmentation of electron tomograms for a quantitative description of actin filament networks Rigort A, Gunther D, Hegerl R, Baum D, Weber B, Prohaska S, Medalia O, Baumeister W, Hege HC |
145 - 151 |
Cryo-EM study of Hepatitis B virus core antigen capsids decorated with antibodies from a human patient Kandiah E, Watts NR, Cheng NG, Cardone G, Stahl SJ, Heller T, Liang TJ, Wingfield PT, Steven AC |
152 - 159 |
Regulation of alternative splicing within the supraspliceosome Sebbag-Sznajder N, Raitskin O, Angenitzki M, Sato TA, Sperling J, Sperling R |
160 - 167 |
Interaction of mammalian end binding proteins with CAP-Gly domains of CLIP-170 and p150(glued) Bjelic S, De Groot CO, Scharer MA, Jaussi R, Bargsten K, Salzmann M, Frey D, Capitani G, Kammerer RA, Steinmetz MO |
168 - 176 |
Optimizing the refolding conditions of self-assembling polypeptide nanoparticles that serve as repetitive antigen display systems Yang YK, Ringler P, Muller SA, Burkhard P |