Computer Visualization of Three-Dimensional Image Data Using IMOD

A cryo-ET survey of microtubules and intracellular compartments in mammalian axons

Foster, H. E., Ventura Santos, C., & Carter, A. P. (2022) · Journal of Cell Biology · doi:10.1083/jcb.202103154 · Cited by 69

Implementation and performance evaluation of reconstruction algorithms on graphics processors

Castaño Díez, D., Mueller, H., & Frangakis, A. S. (2007) · Journal of Structural Biology · doi:10.1016/j.jsb.2006.08.010 · Cited by 68

Regulation of melanosome number, shape and movement in the zebrafish retinal pigment epithelium by OA1 and PMEL

Burgoyne, T., O'Connor, M. N., Seabra, M. C., Cutler, D. F., & Futter, C. E. (2015) · Journal of Cell Science · doi:10.1242/jcs.164400 · Cited by 68

Variable microtubule architecture in the malaria parasite

Ferreira, J. L., Pražák, V., Vasishtan, D., Siggel, M., Hentzschel, F., Binder, A. M., Pietsch, E., Kosinski, J., Frischknecht, F., Gilberger, T. W., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36627-5 · Cited by 68

Molecular-scale visualization of sarcomere contraction within native cardiomyocytes

Burbaum, L., Schneider, J., Scholze, S., Böttcher, R. T., Baumeister, W., Schwille, P., Plitzko, J. M., & Jasnin, M. (2021) · Nature Communications · doi:10.1038/s41467-021-24049-0 · Cited by 67

Ultrastructural Imaging of Activity-Dependent Synaptic Membrane-Trafficking Events in Cultured Brain Slices

Imig, C., López-Murcia, F. J., Maus, L., García-Plaza, I. H., Mortensen, L. S., Schwark, M., Schwarze, V., Angibaud, J., Nägerl, U. V., Taschenberger, H., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.004 · Cited by 66

Lipid saturation controls nuclear envelope function

Romanauska, A., & Köhler, A. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01207-8 · Cited by 65

Myelin replacement triggered by single-cell demyelination in mouse cortex

Snaidero, N., Schifferer, M., Mezydlo, A., Zalc, B., Kerschensteiner, M., & Misgeld, T. (2020) · Nature Communications · doi:10.1038/s41467-020-18632-0 · Cited by 63

Identification of a Munc13-sensitive step in chromaffin cell large dense-core vesicle exocytosis

Man, K. N. M., Imig, C., Walter, A. M., Pinheiro, P. S., Stevens, D. R., Rettig, J., Sørensen, J. B., Cooper, B. H., Brose, N., & Wojcik, S. M. (2015) · eLife · doi:10.7554/elife.10635 · Cited by 63

PACRG and FAP20 form the inner junction of axonemal doublet microtubules and regulate ciliary motility

Dymek, E. E., Lin, J., Fu, G., Porter, M. E., Nicastro, D., & Smith, E. F. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-01-0063 · Cited by 61

The Structure of Immature Virus-Like Rous Sarcoma Virus Gag Particles Reveals a Structural Role for the p10 Domain in Assembly

Schur, F. K. M., Dick, R. A., Hagen, W. J. H., Vogt, V. M., & Briggs, J. A. G. (2015) · Journal of Virology · doi:10.1128/jvi.01502-15 · Cited by 61

Scaffold subunits support associated subunit assembly in the Chlamydomonas ciliary nexin–dynein regulatory complex

Gui, L., Song, K., Tritschler, D., Bower, R., Yan, S., Dai, A., Augspurger, K., Sakizadeh, J., Grzemska, M., Ni, T., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910960116 · Cited by 60

Conserved and Variable Features of Gag Structure and Arrangement in Immature Retrovirus Particles

de Marco, A., Davey, N. E., Ulbrich, P., Phillips, J. M., Lux, V., Riches, J. D., Fuzik, T., Ruml, T., Kräusslich, H.-G., Vogt, V. M., et al. (2010) · Journal of Virology · doi:10.1128/jvi.01423-10 · Cited by 59

Structural basis of microRNA biogenesis by Dicer-1 and its partner protein Loqs-PB

Jouravleva, K., Golovenko, D., Demo, G., Dutcher, R. C., Hall, T. M. T., Zamore, P. D., & Korostelev, A. A. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.09.002 · Cited by 57

Tetrahymena RIB72A and RIB72B are microtubule inner proteins in the ciliary doublet microtubules

Stoddard, D., Zhao, Y., Bayless, B. A., Gui, L., Louka, P., Dave, D., Suryawanshi, S., Tomasi, R. F.-X., Dupuis-Williams, P., Baroud, C. N., et al. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-06-0405 · Cited by 53

Structural insight into microtubule stabilization and kinesin inhibition by Tau family MAPs

Shigematsu, H., Imasaki, T., Doki, C., Sumi, T., Aoki, M., Uchikubo-Kamo, T., Sakamoto, A., Tokuraku, K., Shirouzu, M., & Nitta, R. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201711182 · Cited by 54

Clostridioides difficile ferrosome organelles combat nutritional immunity

Pi, H., Sun, R., McBride, J. R., Kruse, A. R. S., Gibson-Corley, K. N., Krystofiak, E. S., Nicholson, M. R., Spraggins, J. M., Zhou, Q., & Skaar, E. P. (2023) · Nature · doi:10.1038/s41586-023-06719-9 · Cited by 54

Coupling of melanocyte signaling and mechanics by caveolae is required for human skin pigmentation

Domingues, L., Hurbain, I., Gilles-Marsens, F., Sirés-Campos, J., André, N., Dewulf, M., Romao, M., Viaris de Lesegno, C., Macé, A.-S., Blouin, C., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16738-z · Cited by 53

Electron cryo-tomography reveals the subcellular architecture of growing axons in human brain organoids

Hoffmann, P. C., Giandomenico, S. L., Ganeva, I., Wozny, M. R., Sutcliffe, M., Lancaster, M. A., & Kukulski, W. (2021) · eLife · doi:10.7554/elife.70269 · Cited by 53

In situ single particle classification reveals distinct 60S maturation intermediates in cells

Lucas, B. A., Zhang, K., Loerch, S., & Grigorieff, N. (2022) · eLife · doi:10.7554/elife.79272 · Cited by 53

Structural mechanism of angiogenin activation by the ribosome

(2024) · doi:10.1038/s41586-024-07508-8 · Cited by 51

Structure of Anabaena flos-aquae gas vesicles revealed by cryo-ET

Dutka, P., Metskas, L. A., Hurt, R. C., Salahshoor, H., Wang, T.-Y., Malounda, D., Lu, G. J., Chou, T.-F., Shapiro, M. G., & Jensen, G. J. (2023) · Structure · doi:10.1016/j.str.2023.03.011 · Cited by 51

Autophagy preferentially degrades non-fibrillar polyQ aggregates

(2024) · doi:10.1016/j.molcel.2024.04.018 · Cited by 51

Different priming states of synaptic vesicles underlie distinct release probabilities at hippocampal excitatory synapses

Aldahabi, M., Balint, F., Holderith, N., Lorincz, A., Reva, M., & Nusser, Z. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.035 · Cited by 50

Cryo-EM structures reveal high-resolution mechanism of a DNA polymerase sliding clamp loader

Gaubitz, C., Liu, X., Pajak, J., Stone, N. P., Hayes, J. A., Demo, G., & Kelch, B. A. (2022) · eLife · doi:10.7554/elife.74175 · Cited by 50

Structural basis for lipid transfer by the ATG2A–ATG9A complex

(2024) · doi:10.1038/s41594-024-01376-6 · Cited by 50

Determinants shaping the nanoscale architecture of the mouse rod outer segment

Pöge, M., Mahamid, J., Imanishi, S. S., Plitzko, J. M., Palczewski, K., & Baumeister, W. (2021) · eLife · doi:10.7554/elife.72817 · Cited by 50

Structural organization of the C1a-e-c supercomplex within the ciliary central apparatus

Fu, G., Zhao, L., Dymek, E., Hou, Y., Song, K., Phan, N., Shang, Z., Smith, E. F., Witman, G. B., & Nicastro, D. (2019) · Journal of Cell Biology · doi:10.1083/jcb.201906006 · Cited by 48

α- and β-Tubulin Lattice of the Axonemal Microtubule Doublet and Binding Proteins Revealed by Single Particle Cryo-Electron Microscopy and Tomography

Maheshwari, A., Obbineni, J. M., Bui, K. H., Shibata, K., Toyoshima, Y. Y., & Ishikawa, T. (2015) · Structure · doi:10.1016/j.str.2015.06.017 · Cited by 47

Ist1 regulates ESCRT-III assembly and function during multivesicular endosome biogenesis in Caenorhabditis elegans embryos

Frankel, E. B., Shankar, R., Moresco, J. J., Yates, J. R., Volkmann, N., & Audhya, A. (2017) · Nature Communications · doi:10.1038/s41467-017-01636-8 · Cited by 46

High-resolution reconstruction of a Jumbo-bacteriophage infecting capsulated bacteria using hyperbranched tail fibers

Ouyang, R., Costa, A. R., Cassidy, C. K., Otwinowska, A., Williams, V. C. J., Latka, A., Stansfeld, P. J., Drulis-Kawa, Z., Briers, Y., Pelt, D. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34972-5 · Cited by 46

The ϕPA3 phage nucleus is enclosed by a self-assembling 2D crystalline lattice

(2023) · doi:10.1038/s41467-023-36526-9 · Cited by 45

Cofilactin filaments regulate filopodial structure and dynamics in neuronal growth cones

Hylton, R. K., Heebner, J. E., Grillo, M. A., & Swulius, M. T. (2022) · Nature Communications · doi:10.1038/s41467-022-30116-x · Cited by 45

In-cell structural insight into the stability of sperm microtubule doublet

(2023) · doi:10.1038/s41421-023-00606-3 · Cited by 45

Nanostructure and pore size control of template-free synthesised mesoporous magnesium carbonate

Cheung, O., Zhang, P., Frykstrand, S., Zheng, H., Yang, T., Sommariva, M., Zou, X., & Strømme, M. (2016) · RSC Advances · doi:10.1039/c6ra14171d · Cited by 43

In situ cryo-electron tomography reveals local cellular machineries for axon branch development

Nedozralova, H., Basnet, N., Ibiricu, I., Bodakuntla, S., Biertümpfel, C., & Mizuno, N. (2022) · Journal of Cell Biology · doi:10.1083/jcb.202106086 · Cited by 43

Induced Maturation of Human Immunodeficiency Virus

Mattei, S., Anders, M., Konvalinka, J., Kräusslich, H.-G., Briggs, J. A. G., & Müller, B. (2014) · Journal of Virology · doi:10.1128/jvi.02271-14 · Cited by 42

CSPP1 stabilizes growing microtubule ends and damaged lattices from the luminal side

(2023) · doi:10.1083/jcb.202208062 · Cited by 42

A tuneable minimal cell membrane reveals that two lipid species suffice for life

Justice, I., Kiesel, P., Safronova, N., von Appen, A., & Saenz, J. P. (2023) · doi:10.1101/2023.10.24.563757 · Cited by 41

A tuneable minimal cell membrane reveals that two lipid species suffice for life

Justice, I., Kiesel, P., Safronova, N., von Appen, A., & Saenz, J. P. (2024) · Nature Communications · doi:10.1038/s41467-024-53975-y · Cited by 41

Integrative modeling reveals the molecular architecture of the intraflagellar transport A (IFT-A) complex

McCafferty, C. L., Papoulas, O., Jordan, M. A., Hoogerbrugge, G., Nichols, C., Pigino, G., Taylor, D. W., Wallingford, J. B., & Marcotte, E. M. (2022) · eLife · doi:10.7554/elife.81977 · Cited by 40

Bile canaliculi remodeling activates YAP via the actin cytoskeleton during liver regeneration

Meyer, K., Morales‐Navarrete, H., Seifert, S., Wilsch‐Braeuninger, M., Dahmen, U., Tanaka, E. M., Brusch, L., Kalaidzidis, Y., & Zerial, M. (2020) · Molecular Systems Biology · doi:10.15252/msb.20198985 · Cited by 39

Dendritic synthesis and release of the neuropeptide galanin: morphological evidence from studies on rat locus coeruleus neurons

Vila‐Porcile, É., Xu, Z. D., Mailly, P., Nagy, F., Calas, A., Hökfelt, T., & Landry, M. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.22105 · Cited by 37

Cryo-electron tomography pipeline for plasma membranes

Sun, W. W., Michalak, D. J., Sochacki, K. A., Kunamaneni, P., Alfonzo-Méndez, M. A., Arnold, A. M., Strub, M.-P., Hinshaw, J. E., & Taraska, J. W. (2025) · Nature Communications · doi:10.1038/s41467-025-56045-z · Cited by 35

Interdigitated immunoglobulin arrays form the hyperstable surface layer of the extremophilic bacterium Deinococcus radiodurans

von Kügelgen, A., van Dorst, S., Yamashita, K., Sexton, D. L., Tocheva, E. I., Murshudov, G., Alva, V., & Bharat, T. A. M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2215808120 · Cited by 35

RNF26 binds perinuclear vimentin filaments to integrate ER and endolysosomal responses to proteotoxic stress

Cremer, T., Voortman, L. M., Bos, E., Jongsma, M. L., ter Haar, L. R., Akkermans, J. J., Talavera Ormeño, C. M., Wijdeven, R. H., de Vries, J., Kim, R. Q., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022111252 · Cited by 35

‘Generating chromosome geometries in a minimal cell from cryo-electron tomograms and chromosome conformation capture maps’

Gilbert, B. R., Thornburg, Z. R., Lam, V., Rashid, F.-Z. M., Glass, J. I., Villa, E., Dame, R. T., & Luthey-Schulten, Z. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.644133 · Cited by 30

SynapsEM: Computer-Assisted Synapse Morphometry

Watanabe, S., Davis, M. W., Kusick, G. F., Iwasa, J., & Jorgensen, E. M. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.584549 · Cited by 34

The giant mimivirus 1.2 Mb genome is elegantly organized into a 30-nm diameter helical protein shield

Villalta, A., Schmitt, A., Estrozi, L. F., Quemin, E. R., Alempic, J.-M., Lartigue, A., Pražák, V., Belmudes, L., Vasishtan, D., Colmant, A. M., et al. (2022) · eLife · doi:10.7554/elife.77607 · Cited by 34

Visualising the cytoskeletal machinery in neuronal growth cones using cryo-electron tomography

Atherton, J., Stouffer, M., Francis, F., & Moores, C. A. (2022) · Journal of Cell Science · doi:10.1242/jcs.259234 · Cited by 34

Molecular architecture of synaptic vesicles

Kravčenko, U., Ruwolt, M., Kroll, J., Yushkevich, A., Zenkner, M., Ruta, J., Lotfy, R., Wanker, E. E., Rosenmund, C., Liu, F., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2407375121 · Cited by 33

Intracellular Ebola virus nucleocapsid assembly revealed by in situ cryo-electron tomography

Watanabe, R., Zyla, D., Parekh, D., Hong, C., Jones, Y., Schendel, S. L., Wan, W., Castillon, G., & Saphire, E. O. (2024) · Cell · doi:10.1016/j.cell.2024.08.044 · Cited by 33

The kidney slit diaphragm resembles a fishnet

Birtasu, A. N., Wieland, K., Ermel, U. H., Arghittu, S. M., Manger, S., Kocylowski, M. K., Fakler, B., Scheffer, M. P., Covino, R., Grahammer, F., et al. (2025) · Kidney International · doi:10.1016/j.kint.2025.08.028 · Cited by 32

CryoEM structure of the outer membrane secretin channel pIV from the f1 filamentous bacteriophage

Conners, R., McLaren, M., Łapińska, U., Sanders, K., Stone, M. R. L., Blaskovich, M. A. T., Pagliara, S., Daum, B., Rakonjac, J., & Gold, V. A. M. (2021) · Nature Communications · doi:10.1038/s41467-021-26610-3 · Cited by 32

The ER ladder is a unique morphological feature of developing mammalian axons

Zamponi, E., Meehl, J. B., & Voeltz, G. K. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.05.002 · Cited by 32

Structure and activation of the RING E3 ubiquitin ligase TRIM72 on the membrane

Park, S. H., Han, J., Jeong, B.-C., Song, J. H., Jang, S. H., Jeong, H., Kim, B. H., Ko, Y.-G., Park, Z.-Y., Lee, K. E., et al. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-01111-7 · Cited by 31

Safe and effective two-in-one replicon-and-VLP minispike vaccine for COVID-19: Protection of mice after a single immunization

Hennrich, A. A., Sawatsky, B., Santos-Mandujano, R., Banda, D. H., Oberhuber, M., Schopf, A., Pfaffinger, V., Wittwer, K., Riedel, C., Pfaller, C. K., et al. (2021) · PLOS Pathogens · doi:10.1371/journal.ppat.1009064 · Cited by 30

Developmental Transitions Coordinate Assembly of the Coxiella burnetii Dot/Icm Type IV Secretion System

Park, D., Steiner, S., Shao, M., Roy, C. R., & Liu, J. (2022) · Infection and Immunity · doi:10.1128/iai.00410-22 · Cited by 30

Nanodiamond integration into niosomes as an emerging and efficient gene therapy nanoplatform for central nervous system diseases

AL Qtaish, N., Gallego, I., Paredes, A. J., Villate-Beitia, I., Soto-Sánchez, C., Martínez-Navarrete, G., Sainz-Ramos, M., Lopez-Mendez, T. B., Fernández, E., Puras, G., et al. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c02182 · Cited by 29

Discovery, structure, and function of filamentous 3-methylcrotonyl-CoA carboxylase

Hu, J. J., Lee, J. K. J., Liu, Y.-T., Yu, C., Huang, L., Aphasizheva, I., Aphasizhev, R., & Zhou, Z. H. (2023) · Structure · doi:10.1016/j.str.2022.11.015 · Cited by 29

In situ structure of a bacterial flagellar motor at subnanometre resolution reveals adaptations for increased torque

(2025) · doi:10.1038/s41564-025-02012-9 · Cited by 28

Directed growth and fusion of membrane-wall microdomains requires CASP-mediated inhibition and displacement of secretory foci

Barbosa, I. C. R., De Bellis, D., Flückiger, I., Bellani, E., Grangé-Guerment, M., Hématy, K., & Geldner, N. (2023) · Nature Communications · doi:10.1038/s41467-023-37265-7 · Cited by 28

Architecture of the biofilm-associated archaic Chaperone-Usher pilus CupE from Pseudomonas aeruginosa

(2023) · doi:10.1371/journal.ppat.1011177 · Cited by 27

Three-dimensional reconstructions of extracellular matrix polymers using automated electron tomography

Baldock, C., Gilpin, C. J., Koster, A. J., Ziese, U., Kadler, K. E., Kielty, C. M., & Holmes, D. F. (2002) · Journal of Structural Biology · doi:10.1016/s1047-8477(02)00028-x · Cited by 27

In Vitro Assembly of Virus-Like Particles of a Gammaretrovirus, the Murine Leukemia Virus XMRV

Hadravová, R., de Marco, A., Ulbrich, P., Štokrová, J., Doležal, M., Pichová, I., Ruml, T., Briggs, J. A. G., & Rumlová, M. (2012) · Journal of Virology · doi:10.1128/jvi.05564-11 · Cited by 26

FilamentID reveals the composition and function of metabolic enzyme polymers during gametogenesis

Hugener, J., Xu, J., Wettstein, R., Ioannidi, L., Velikov, D., Wollweber, F., Henggeler, A., Matos, J., & Pilhofer, M. (2024) · Cell · doi:10.1016/j.cell.2024.04.026 · Cited by 26

StableMARK-decorated microtubules in cells have expanded lattices

de Jager, L., Jansen, K. I., Hoogebeen, R., Akhmanova, A., Kapitein, L. C., Förster, F., & Howes, S. C. (2025) · Journal of Cell Biology · doi:10.1083/jcb.202206143 · Cited by 25

Structure of the ciliary tip central pair reveals the unique role of the microtubule-seam binding protein SPEF1

(2025) · doi:10.1016/j.cub.2025.06.020 · Cited by 25

A role for Vps13-mediated lipid transfer at the ER–endosome contact site in ESCRT-mediated sorting

(2024) · doi:10.1083/jcb.202307094 · Cited by 24

In situ formation of magnetopolymersomes via electroporation for MRI

Bain, J., Ruiz-Pérez, L., Kennerley, A. J., Muench, S. P., Thompson, R., Battaglia, G., & Staniland, S. S. (2015) · Scientific Reports · doi:10.1038/srep14311 · Cited by 24

RNA and Nucleocapsid Are Dispensable for Mature HIV-1 Capsid Assembly

Mattei, S., Flemming, A., Anders-Össwein, M., Kräusslich, H.-G., Briggs, J. A. G., & Müller, B. (2015) · Journal of Virology · doi:10.1128/jvi.00750-15 · Cited by 24

Structure of the mature Rous sarcoma virus lattice reveals a role for IP6 in the formation of the capsid hexamer

Obr, M., Ricana, C. L., Nikulin, N., Feathers, J.-P. R., Klanschnig, M., Thader, A., Johnson, M. C., Vogt, V. M., Schur, F. K. M., & Dick, R. A. (2021) · Nature Communications · doi:10.1038/s41467-021-23506-0 · Cited by 23

Multi-modal cryo-EM reveals trimers of protein A10 to form the palisade layer in poxvirus cores

Datler, J., Hansen, J. M., Thader, A., Schlögl, A., Bauer, L. W., Hodirnau, V.-V., & Schur, F. K. M. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-01201-6 · Cited by 23

Integrated structural biology of the native malarial translation machinery and its inhibition by an antimalarial drug

Anton, L., Cheng, W., Haile, M. T., Dziekan, J. M., Cobb, D. W., Zhu, X., Han, L., Li, E., Nair, A., Lee, C. L., et al. (2025) · Nature Structural & Molecular Biology · doi:10.1038/s41594-025-01632-3 · Cited by 21

The postsynaptic density in excitatory synapses is composed of clustered, heterogeneous nanoblocks

Sun, R., Allen, J. P., Mao, Z., Wilson, L., Haider, M., Alten, B., Zhou, Z., Wang, X., & Zhou, Q. (2025) · Journal of Cell Biology · doi:10.1083/jcb.202406133 · Cited by 20

A second DNA binding site on RFC facilitates clamp loading at gapped or nicked DNA

Liu, X., Gaubitz, C., Pajak, J., & Kelch, B. A. (2022) · eLife · doi:10.7554/elife.77483 · Cited by 19

Endosomal phosphatidylinositol 3-phosphate controls synaptic vesicle cycling and neurotransmission

Liu, G., Kochlamazashvili, G., Puchkov, D., Müller, R., Schultz, C., Mackintosh, A. I., Vollweiter, D., Haucke, V., & Soykan, T. (2022) · The EMBO Journal · doi:10.15252/embj.2021109352 · Cited by 19

The consequence of ATP synthase dimer angle on mitochondrial morphology studied by cryo-electron tomography

(2024) · doi:10.1042/bcj20230450 · Cited by 19

Self-Assembly of Nanofilaments in Cyanobacteria for Protein Co-localization

Zedler, J. A. Z., Schirmacher, A. M., Russo, D. A., Hodgson, L., Gundersen, E., Matthes, A., Frank, S., Verkade, P., & Jensen, P. E. (2023) · ACS Nano · doi:10.1021/acsnano.3c08600 · Cited by 17

MAP9/MAPH-9 supports axonemal microtubule doublets and modulates motor movement

Tran, M. V., Khuntsariya, D., Fetter, R. D., Ferguson, J. W., Wang, J. T., Long, A. F., Cote, L. E., Wellard, S. R., Vázquez-Martínez, N., Sallee, M. D., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2023.12.001 · Cited by 18

The palisade layer of the poxvirus core is composed of flexible A10 trimers

(2024) · doi:10.1038/s41594-024-01218-5 · Cited by 18

FAP106 is an interaction hub for assembling microtubule inner proteins at the cilium inner junction

Shimogawa, M. M., Wijono, A. S., Wang, H., Zhang, J., Sha, J., Szombathy, N., Vadakkan, S., Pelayo, P., Jonnalagadda, K., Wohlschlegel, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40230-z · Cited by 18

Mapping the ultrastructural topology of the corynebacterial cell surface

Isbilir, B., Yeates, A., Alva, V., & Bharat, T. A. M. (2025) · PLOS Biology · doi:10.1371/journal.pbio.3003130 · Cited by 18

Behaviourally modulated hippocampal theta oscillations in the ferret persist during both locomotion and immobility

Dunn, S. L. S., Town, S. M., Bizley, J. K., & Bendor, D. (2022) · Nature Communications · doi:10.1038/s41467-022-33507-2 · Cited by 17

Structure and organization of full-length epidermal growth factor receptor in extracellular vesicles by cryo-electron tomography

Gonzalez-Magaldi, M., Gullapalli, A., Papoulas, O., Liu, C., Leung, A. Y.-H., Guo, L., Brilot, A. F., Marcotte, E. M., Ke, Z., & Leahy, D. J. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2424678122 · Cited by 17

Condensation of the fusion focus by the intrinsically disordered region of the formin Fus1 is essential for cell-cell fusion

Billault-Chaumartin, I., Muriel, O., Michon, L., & Martin, S. G. (2022) · Current Biology · doi:10.1016/j.cub.2022.09.026 · Cited by 17

Mmp14 is required for matrisome homeostasis and circadian rhythm in fibroblasts

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