Actin Assembly and Endocytosis: From Yeast to Mammals

Lipid rafts and signal transduction

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Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products.

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The Interaction between N-WASP and the Arp2/3 Complex Links Cdc42-Dependent Signals to Actin Assembly

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Protein regulation by monoubiquitin

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Induction of mutant dynamin specifically blocks endocytic coated vesicle formation.

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Curvature of clathrin-coated pits driven by epsin

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Myosins: a diverse superfamily

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Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae.

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Salmonella interactions with host cells: type III secretion at work.

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Phosphorylated l-caldesmon is involved in disassembly of actin stress fibers and postmitotic spreading

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Ndel1, Nudel ( Noodle): Flexible in the cell?

Chansard, M., Hong, J., Park, Y., Park, S. K., & Nguyen, M. D. (2011) · Cytoskeleton · doi:10.1002/cm.20532 · Cited by 33

Huntingtin-associated protein-1 (HAP1) regulates endocytosis and interacts with multiple trafficking-related proteins

Mackenzie, K. D., Lim, Y. P., Duffield, M. D., Chataway, T., Zhou, X., & Keating, D. J. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.02.023 · Cited by 33

Phosphatidylinositol 4,5-bisphosphate in the Control of Membrane Trafficking

Li, S., Ghosh, C., Xing, Y., & Sun, Y. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.49665 · Cited by 33

Polarization of the endomembrane system is an early event in fucoid zygote development

Hadley, R., Hable, W. E., & Kropf, D. L. (2006) · BMC Plant Biology · doi:10.1186/1471-2229-6-5 · Cited by 33

Lipid requirements for endocytosis in yeast

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Phosphoinositide 3-Kinase C2α Links Clathrin to Microtubule-dependent Movement

Zhao, Y., Gaidarov, I., & Keen, J. H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606998200 · Cited by 33

Endocytosis: Actin in the Driving Seat

Ayscough, K. R. (2004) · Current Biology · doi:10.1016/j.cub.2004.01.021 · Cited by 33

Chapter 1 Macromolecular Trafficking and Immune Evasion in African Trypanosomes

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Trio, a Rho Family GEF, Interacts with the Presynaptic Active Zone Proteins Piccolo and Bassoon

Terry-Lorenzo, R. T., Torres, V. I., Wagh, D. A., Galaz, J., Swanson, S. K., Florens, L. A., Washburn, M. P., Waites, C. L., Gundelfinger, E. D., Reimer, R. J., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0167535 · Cited by 29

Different Contributions of Clathrin- and Caveolae-Mediated Endocytosis of Vascular Endothelial Cadherin to Lipopolysaccharide-Induced Vascular Hyperpermeability

Zhang, Y., Zhang, L.-Y., Li, Y., Sun, S., & Tan, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106328 · Cited by 31

Dual‐colour fluorescence microscopy using yEmCherry‐/GFP‐tagging of eisosome components Pil1 and Lsp1 in Candida albicans

Reijnst, P., Walther, A., & Wendland, J. (2010) · Yeast · doi:10.1002/yea.1841 · Cited by 31

Clathrin-Mediated Endocytosis

McPherson, P. S., Ritter, B., & Wendland, B. (2009) · Springer eBooks · doi:10.1007/978-0-387-93877-6_9 · Cited by 31

The role of F-actin in modulating Clathrin-mediated endocytosis: Lessons from neurons in health and neuropsychiatric disorder

Loebrich, S. (2014) · Communicative & Integrative Biology · doi:10.4161/cib.28740 · Cited by 30

Integrative studies put cell wall synthesis on the yeast functional map

Firon, A., Lesage, G., & Bussey, H. (2004) · Current Opinion in Microbiology · doi:10.1016/j.mib.2004.10.015 · Cited by 30

The Vacuole Import and Degradation Pathway Utilizes Early Steps of Endocytosis and Actin Polymerization to Deliver Cargo Proteins to the Vacuole for Degradation

Brown, C. R., Dunton, D., & Chiang, H.-L. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.028241 · Cited by 29

Internalization of Titanium Dioxide Nanoparticles Is Mediated by Actin-Dependent Reorganization and Clathrin- and Dynamin-Mediated Endocytosis in H9c2 Rat Cardiomyoblasts

Huerta-García, E., Ramos‐Godínez, M. D. P., Saavedra, A. L., Alfaro‐Moreno, E., Gómez-Crisóstomo, N. P., Colín-Val, Z., Sánchez-Barrera, H., & López‐Marure, R. (2019) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.8b00284 · Cited by 29

Lysosomal peptidases—intriguing roles in cancer progression and neurodegeneration

Kos, J., Mitrović, A., Nanut, M. P., & Pišlar, A. H. (2022) · FEBS Open Bio · doi:10.1002/2211-5463.13372 · Cited by 29

Shear Stress-induced Redistribution of Vascular Endothelial-Protein-tyrosine Phosphatase (VE-PTP) in Endothelial Cells and Its Role in Cell Elongation

Mantilidewi, K. I., Murata, Y., Mori, M., Otsubo, C., Kotani, T., Kusakari, S., Ohnishi, H., & Matozaki, T. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529503 · Cited by 29

Characterization of PXK as a Protein Involved in Epidermal Growth Factor Receptor Trafficking

Takeuchi, H., Takeuchi, T., Gao, J., Cantley, L. C., & Hirata, M. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01105-09 · Cited by 29

Environmental Toxicity of Nanomaterials

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Big gulps: specialized membrane domains for rapid receptor-mediated endocytosis

McNiven, M. A. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.08.007 · Cited by 29

Lsb5p interacts with actin regulators Sla1p and Las17p, ubiquitin and Arf3p to couple actin dynamics to membrane trafficking processes

Costa, R., Warren, D. T., & Ayscough, K. R. (2005) · Biochemical Journal · doi:10.1042/bj20041729 · Cited by 29

Peptide Motifs: Building the Clathrin Machinery

McPherson, P. S., & Ritter, B. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:1:073 · Cited by 29

Retromer Dysfunction and Neurodegenerative Disease

Reitz, C. (2017) · Current Genomics · doi:10.2174/1389202919666171024122809 · Cited by 28

Vid30 is required for the association of Vid vesicles and actin patches in the vacuole import and degradation pathway

Alibhoy, A. A., Giardina, B. J., Dunton, D. D., & Chiang, H.-L. (2012) · Autophagy · doi:10.4161/auto.8.1.18104 · Cited by 27

Characterization of large yellow croaker (Pseudosciaena crocea) β-actin promoter supports β-actin gene as an internal control for gene expression modulation and its potential application in transgenic studies in fish

Xiao, X., Li, M., Wang, K., Qin, Q., & Chen, X. (2011) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2011.02.008 · Cited by 27

SILAC-Based Proteome Analysis of Starmerella bombicola Sophorolipid Production

Ciesielska, K., Li, B., Groeneboer, S., Bogaert, I. V., Lin, Y., Soetaert, W., de Peer, Y. V., & Devreese, B. V. (2013) · Journal of Proteome Research · doi:10.1021/pr400392a · Cited by 27

Allele-specific Effects of Thoracic Aortic Aneurysm and Dissection α-Smooth Muscle Actin Mutations on Actin Function

Bergeron, S. E., Wedemeyer, E. W., Lee, R. A., Wen, K., McKane, M., Pierick, A. R., Berger, A. P., Rubenstein, P. A., & Bartlett, H. L. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.203174 · Cited by 27

The Low-Density Lipoprotein Receptor Is Regulated by Estrogen and Forms a Functional Complex with the Estrogen-Regulated Protein Ezrin in Pituitary GH3 Somatolactotropes

Smith, P. M., Cowan, A. E., & White, B. A. (2004) · Endocrinology · doi:10.1210/en.2004-0228 · Cited by 27

The life cycle of human equilibrative nucleoside transporter 1: From ER export to degradation

Nivillac, N. M. I., Bacani, J., & Coe, I. R. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.03.008 · Cited by 27

Single-Molecule Microscopy Reveals Dynamic FLNA Interactions Governing SSTR2 Clustering and Internalization

Treppiedi, D., Jobin, M., Peverelli, E., Giardino, E., Sungkaworn, T., Zabel, U., Arosio, M., Spada, A., Mantovani, G., & Calebiro, D. (2018) · Endocrinology · doi:10.1210/en.2018-00368 · Cited by 27

Lipid determinants of endocytosis and exocytosis in budding yeast

Degreif, D., Cucu, B., Budin, I., Thiel, G., & Bertl, A. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.03.007 · Cited by 27

Structure of Sla1p homology domain 1 and interaction with the NPFxD endocytic internalization motif

Mahadev, R. K., Pietro, S. M. D., Olson, J. M., Piao, H. L., Payne, G. S., & Overduin, M. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601646 · Cited by 27

Immunolocalization of Actin in Paramecium Cells

Kissmehl, R., Sehring, I. M., Wagner, E., & Plattner, H. (2004) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.4a6379.2004 · Cited by 27

Dynamin- and Rab5-dependent endocytosis is required to preventDrosophilaphotoreceptor degeneration

Pinal, N., & Pichaud, F. (2011) · Journal of Cell Science · doi:10.1242/jcs.082115 · Cited by 27

The Roles of the Actin Cytoskeleton in Fear Memory Formation

Lamprecht, R. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00039 · Cited by 26

Actin microfilaments in fungi

Walker, S. K., & Garrill, A. (2006) · Mycologist · doi:10.1016/j.mycol.2005.11.001 · Cited by 26

Disturbance of endomembrane trafficking by brefeldin A and calyculin A reorganizes the actin cytoskeleton of Lilium longiflorum pollen tubes

Hörmannseder, K., Obermeyer, G., & Foissner, I. (2005) · PROTOPLASMA · doi:10.1007/s00709-005-0132-4 · Cited by 26

Thoracic Aortic Aneurysm (TAAD)-causing Mutation in Actin Affects Formin Regulation of Polymerization

Malloy-Walton, L. E., Wen, K., Pierick, A. R., Wedemeyer, E. W., Bergeron, S. E., Vanderpool, N. D., McKane, M., Rubenstein, P. A., & Bartlett, H. L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.371914 · Cited by 26

End3p-Mediated Endocytosis Is Required for Spore Wall Formation in Saccharomyces cerevisiae

Morishita, M., & Engebrecht, J. (2005) · Genetics · doi:10.1534/genetics.105.041459 · Cited by 26

Endocytosis against high turgor pressure is made easier by partial coating and freely rotating base

Ma, R., & Berro, J. (2021) · Biophysical Journal · doi:10.1016/j.bpj.2021.02.033 · Cited by 26

Swf1p, a Member of the DHHC-CRD Family of Palmitoyltransferases, Regulates the Actin Cytoskeleton and Polarized Secretion Independently of Its DHHC Motif

Dighe, S. A., & Kozminski, K. G. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-03-0252 · Cited by 26

Transcript Profiles of Candida albicans Cortical Actin Patch Mutants Reflect Their Cellular Defects: Contribution of the Hog1p and Mkc1p Signaling Pathways

Oberholzer, U., Nantel, A., Berman, J. G., & Whiteway, M. S. (2006) · Eukaryotic Cell · doi:10.1128/ec.00385-05 · Cited by 26

Functional Characterization of Myosin I Tail Regions in Candida albicans

Oberholzer, U., Iouk, T. L., Thomas, D. Y., & Whiteway, M. S. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1272-1286.2004 · Cited by 26

Presynaptic Kv3 channels are required for fast and slow endocytosis of synaptic vesicles

Wu, X., Subramanian, S., Zhang, Y., Shi, B., Xia, J., Li, T., Guo, X., El‐Hassar, L., Szigeti‐Buck, K., Henao‐Mejia, J., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.006 · Cited by 25

Yeast Rsp5 ubiquitin ligase affects the actin cytoskeleton in vivo and in vitro

Kamińska, J., Spiess, M., Stawiecka-Mirota, M., Monkaityte, R., Haguenauer‐Tsapis, R., Urban‐Grimal, D., Winsor, B., & Żołądek, T. (2011) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2011.08.002 · Cited by 25

Initial Polarized Bud Growth by Endocytic Recycling in the Absence of Actin Cable–dependent Vesicle Transport in Yeast

Yamamoto, T. G., Mochida, J., Kadota, J., Takeda, M., Bi, E., & Tanaka, K. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-05-0412 · Cited by 25

Closing the loops: new insights into the role and regulation of actin during cell polarization

Wedlich‐Söldner, R., & Li, R. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.08.011 · Cited by 25

Duffy Antigen Receptor for Chemokines Mediates Chemokine Endocytosis through a Macropinocytosis-Like Process in Endothelial Cells

Zhao, Y., Mangalmurti, N. S., Xiong, Z., Prakash, B. V., Guo, F., Stolz, D. B., & Lee, J. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0029624 · Cited by 25

V-ATPase-dependent luminal acidification is required for endocytic recycling of a yeast cell wall stress sensor, Wsc1p

Ueno, K., Saito, M., Nagashima, M., Kojima, A., Nishinoaki, S., Toshima, J. Y., & Toshima, J. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.12.008 · Cited by 24

Uncommon Endocytic and Trafficking Pathway of the Natural Killer Cell CD94/NKG2A Inhibitory Receptor

Masilamani, M., Narayanan, S., Prieto, M., Borrego, F., & Coligan, J. E. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00738.x · Cited by 24

Endocytosis and Intracellular Trafficking of Human Natural Killer Cell Receptors

Masilamani, M., Peruzzi, G., Borrego, F., & Coligan, J. E. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00973.x · Cited by 24

Yeast as a Model to Understand Actin-Mediated Cellular Functions in Mammals—Illustrated with Four Actin Cytoskeleton Proteins

Akram, Z., Ahmed, I., Mack, H., Kaur, R., da Silva, R. C., Castilho, B. A., Friant, S., Sattlegger, E., & Munn, A. L. (2020) · Cells · doi:10.3390/cells9030672 · Cited by 24

The Structural And Functional Diversity Of The Myosin Family Of Actin-Based Molecular Motors

Mooseker, M. S., & Foth, B. J. (2007) · Springer eBooks · doi:10.1007/978-1-4020-6519-4_1 · Cited by 24

Interaction of the Saccharomyces cerevisiae Cortical Actin Patch Protein Rvs167p With Proteins Involved in ER to Golgi Vesicle Trafficking

Friesen, H., Colwill, K., Robertson, K., Schub, O., & Andrews, B. (2005) · Genetics · doi:10.1534/genetics.104.040063 · Cited by 24

Cyclase‐Associated Protein is Essential for the Functioning of the Endo‐Lysosomal System and Provides a Link to the Actin Cytoskeleton

Sultana, H., Rivero, F., Blau‐Wasser, R., Schwager, S., Balbo, A., Bozzaro, S., Schleicher, M., & Noegel, A. A. (2005) · Traffic · doi:10.1111/j.1600-0854.2005.00330.x · Cited by 23

The endocytosis gene END3 is essential for the glucose‐induced rapid decline of small vesicles in the extracellular fraction in Saccharomyces cerevisiae

Giardina, B. J., Stein, K. R., & Chiang, H. (2014) · Journal of Extracellular Vesicles · doi:10.3402/jev.v3.23497 · Cited by 23

Vps34p Is Required for the Decline of Extracellular Fructose-1,6-bisphosphatase in the Vacuole Import and Degradation Pathway

Alibhoy, A. A., Giardina, B. J., Dunton, D. D., & Chiang, H.-L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.360412 · Cited by 23

Differentiation-dependent rearrangements of actin filaments and microtubules hinder apical endocytosis in urothelial cells

Tratnjek, L., Romih, R., & Kreft, M. E. (2017) · Histochemistry and Cell Biology · doi:10.1007/s00418-017-1566-4 · Cited by 23

Role of Src-family kinases in formation of the cortical actin cap at the dorsal cell surface

Kuga, T., Hoshino, M., Nakayama, Y., Kasahara, K., Ikeda, K., Obata, Y., Takahashi, A., Higashiyama, Y., Fukumoto, Y., & Yamaguchi, N. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.03.018 · Cited by 23

Spatially Defined EGF Receptor Activation Reveals an F-Actin-Dependent Phospho-Erk Signaling Complex

Singhai, A., Wakefield, D. L., Bryant, K. L., Hammes, S. R., Holowka, D., & Baird, B. A. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.09.048 · Cited by 23

Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy

Walsh, M. B., Janzen, E., Wingrove, E., Hosseinibarkooie, S., Muela, N. R., Davidow, L., Dimitriadi, M., Norabuena, E. M., Rubin, L. L., Wirth, B., et al. (2020) · BMC Biology · doi:10.1186/s12915-020-00845-w · Cited by 22

Clathrin Light Chains: Not to Be Taken so Lightly

Das, J., Tiwari, M., & Subramanyam, D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.774587 · Cited by 22

Annexin A2 is SUMOylated on its N‐terminal domain: Regulation by insulin

Caron, D., Boutchueng-Djidjou, M., Tanguay, R. M., & Faure, R. L. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.03.007 · Cited by 22

A selective autophagy pathway that degrades gluconeogenic enzymes during catabolite inactivation

Brown, C. R., & Chiang, H.-L. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.7711 · Cited by 22

Coupled elasticity–diffusion model for the effects of cytoskeleton deformation on cellular uptake of cylindrical nanoparticles

Wang, J., & Li, L. (2014) · Journal of The Royal Society Interface · doi:10.1098/rsif.2014.1023 · Cited by 22

Imaging Clathrin Dynamics in Drosophila melanogaster Hemocytes Reveals a Role for Actin in Vesicle Fission

Kochubey, O., Majumdar, A., & Klingauf, J. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00492.x · Cited by 22

Directed motility of phagosomes inTetrahymena thermophila requires actin and Myo1p, a novel unconventional myosin

Hosein, R. E., Williams, S. A., & Gavin, R. H. (2005) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20065 · Cited by 21

Discovery of a vezatin-like protein for dynein-mediated early endosome transport

Yao, X., Arst, H. N., Wang, X., & Xiang, X. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-08-0602 · Cited by 21

Requirement for the Polarisome and Formin Function in Ssk2p-Mediated Actin Recovery From Osmotic Stress in Saccharomyces cerevisiae

Bettinger, B. T., Clark, M. G., & Amberg, D. C. (2007) · Genetics · doi:10.1534/genetics.106.063370 · Cited by 21

Capacitance-based assay for real-time monitoring of endocytosis and cell viability

Lee, R., Kim, J., Kim, S. Y., Jang, S. M., Lee, S., Choi, I., Park, S. W., Shin, J., & Yoo, K. (2012) · Lab on a Chip · doi:10.1039/c2lc21236f · Cited by 20

Nucleocytoplasmic Trafficking Is Required for Functioning of the Adaptor Protein Sla1p in Endocytosis

Gardiner, F. C., Costa, R., & Ayscough, K. R. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00534.x · Cited by 20

Clathrin: An Amazing Multifunctional Dreamcoat?

Pauly, B. S., & Drubin, D. G. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.10.007 · Cited by 20

Ras-like Small GTPases Form a Large Family of Proteins in the Marine Sponge Suberites domuncula

Ćetković, H., Mikoč, A., Müller, W. E. G., & Gamulin, V. (2007) · Journal of Molecular Evolution · doi:10.1007/s00239-006-0081-3 · Cited by 20

Regulation of clathrin coat assembly by Eps15 homology domain–mediated interactions during endocytosis

Suzuki, R. H., Toshima, J. Y., & Toshima, J. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-04-0380 · Cited by 20

Serum starvation improves transient transfection efficiency in differentiating embryonic stem cells

Wallenstein, E. J., Barminko, J., Schloss, R. S., & Yarmush, M. L. (2010) · Biotechnology Progress · doi:10.1002/btpr.472 · Cited by 20

Membrane trafficking at the ER/Golgi interface: Functional implications of RhoA and Rac1

Matas, O. B., Fritz, S., Luna, A., & Egea, G. (2005) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2005.05.001 · Cited by 19

Production of human β-actin and a mutant using a bacterial expression system with a cold shock vector

TAMURA, M. N., Ito, K., Kunihiro, S., Yamasaki, C., & Haragauchi, M. (2010) · Protein Expression and Purification · doi:10.1016/j.pep.2010.09.007 · Cited by 19

Effect of low pH on organization of the actin cytoskeleton in Saccharomyces cerevisiae

Motizuki, M., Yokota, S., & Tsurugi, K. (2007) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2007.10.003 · Cited by 19

Yeast Eps15-like endocytic protein Pan1p regulates the interaction between endocytic vesicles, endosomes and the actin cytoskeleton

Toshima, J. Y., Furuya, E., Nagano, M., Kanno, C., Sakamoto, Y., Ebihara, M., Siekhaus, D. E., & Toshima, J. (2016) · eLife · doi:10.7554/elife.10276 · Cited by 19

Cytoplasmic cleavage of DPPA3 is required for intracellular trafficking and cleavage-stage development in mice

Shin, S., Vogt, E.-J., Jiménez‐Movilla, M., Baibakov, B. A., & Dean, J. (2017) · Nature Communications · doi:10.1038/s41467-017-01387-6 · Cited by 19

Conserved roles for yeast Rho1 and mammalian RhoA GTPases in clathrin-independent endocytosis

Prosser, D. C., & Wendland, B. (2012) · Small GTPases · doi:10.4161/sgtp.21631 · Cited by 19

Syp1 regulates the clathrin-mediated and clathrin-independent endocytosis of multiple cargo proteins through a novel sorting motif

Apel, A. R., Hoban, K., Chuartzman, S. G., Tonikian, R., Sidhu, S. S., Schuldiner, M., Wendland, B., & Prosser, D. C. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-10-0731 · Cited by 18

Contributions of Wiskott–Aldrich syndrome family cytoskeletal regulatory adapters to immune regulation

Zhang, J., Dong, B., & Siminovitch, K. A. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00846.x · Cited by 19

Electrical Stimulation Promotes Endocytosis of Magnetic Nanoparticles by Cancer Cells

Wang, C., Zhou, G., Guo, X., Zhang, W., & Wu, C. (2024) · Small · doi:10.1002/smll.202403381 · Cited by 17

A Second Las17 Monomeric Actin‐Binding Motif Functions in Arp2/3‐Dependent Actin Polymerization During Endocytosis

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