Extracellular matrix in plants and animals: hooks and locks for viruses

Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin

Aziz, J., Shezali, H., Radzi, Z., Yahya, N. A., Abu Kassim, N. H., Czernuszka, J., & Rahman, M. T. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000447017 · Cited by 7,323 · see citing works

Remodelling the extracellular matrix in development and disease

Bonnans, C., Chou, J., & Werb, Z. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3904 · Cited by 4,367 · see citing works

The extracellular matrix at a glance

Frantz, C., Stewart, K. M., & Weaver, V. M. (2010) · Journal of Cell Science · doi:10.1242/jcs.023820 · Cited by 4,334 · see citing works

Extracellular matrix structure

Theocharis, A. D., Skandalis, S. S., Gialeli, C., & Karamanos, N. K. (2016) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2015.11.001 · Cited by 2,598 · see citing works

Mechanotransduction and extracellular matrix homeostasis

Humphrey, J. D., Dufresne, E. R., & Schwartz, M. A. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3896 · Cited by 2,187 · see citing works

The structure, function, and biosynthesis of plant cell wall pectic polysaccharides

Caffall, K. H., & Mohnen, D. (2009) · Carbohydrate Research · doi:10.1016/j.carres.2009.05.021 · Cited by 1,645 · see citing works

Pectin methylesterases: cell wall enzymes with important roles in plant physiology

Micheli, F. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02045-3 · Cited by 974 · see citing works

New insights into pectin methylesterase structure and function

Pelloux, J., Rustérucci, C., & Mellerowicz, E. J. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.04.001 · Cited by 884 · see citing works

Functional structure and composition of the extracellular matrix

Bosman, F. T., & Stamenkovic, I. (2003) · The Journal of Pathology · doi:10.1002/path.1437 · Cited by 823 · see citing works

How Viruses Enter Animal Cells

Smith, A. E., & Helenius, A. (2004) · Science · doi:10.1126/science.1094823 · Cited by 735 · see citing works

Virus entry: molecular mechanisms and biomedical applications

Dimitrov, D. S. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro817 · Cited by 701 · see citing works

Heterogeneity in the chemistry, structure and function of plant cell walls

Burton, R. A., Gidley, M. J., & Fincher, G. B. (2010) · Nature Chemical Biology · doi:10.1038/nchembio.439 · Cited by 663 · see citing works

Pectin-Induced Changes in Cell Wall Mechanics Underlie Organ Initiation in Arabidopsis

Peaucelle, A., Braybrook, S. A., Guillou, L. L., Bron, É., Kuhlemeier, C. J., & Höfte, H. (2011) · Current Biology · doi:10.1016/j.cub.2011.08.057 · Cited by 627 · see citing works

The Cell Biology of Cellulose Synthesis

McFarlane, H. E., Döring, A., & Persson, S. (2014) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050213-040240 · Cited by 623 · see citing works

Oligogalacturonides: Plant damage-associated molecular patterns and regulators of growth and development

Ferrari, S. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00049 · Cited by 573 · see citing works

Plant Cell Walls

Keegstra, K. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.161240 · Cited by 561 · see citing works

The extracellular matrix: Structure, composition, age-related differences, tools for analysis and applications for tissue engineering

Kular, J. K., Basu, S., & Sharma, R. I. (2014) · Journal of Tissue Engineering · doi:10.1177/2041731414557112 · Cited by 557 · see citing works

Callose Biosynthesis Regulates Symplastic Trafficking during Root Development

Vatén, A., Dettmer, J., Wu, S., Stierhof, Y., Miyashima, S., Yadav, S. R., Roberts, C., Campilho, A., Bulone, V., Lichtenberger, R., et al. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.10.006 · Cited by 485 · see citing works

Plant viral movement proteins: Agents for cell-to-cell trafficking of viral genomes

Lucas, W. J. (2005) · Virology · doi:10.1016/j.virol.2005.09.026 · Cited by 459 · see citing works

Plant cell wall dynamics and wall-related susceptibility in plant–pathogen interactions

Bellincampi, D., Cervone, F., & Lionetti, V. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00228 · Cited by 452 · see citing works

Characterization of the Cell-Wall Polysaccharides of Arabidopsis thaliana Leaves

Zablackis, E., Huang, J., Muller, B., Darvill, A. G., & Albersheim, P. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.4.1129 · Cited by 409 · see citing works

Degradation of Fibrillar Collagen in a Human Melanoma Xenograft Improves the Efficacy of an Oncolytic Herpes Simplex Virus Vector

McKee, T. D., Grandi, P., Mok, W., Alexandrakis, G., Insin, N., Zimmer, J. P., Bawendi, M. G., Boucher, Y., Breakefield, X. O., & Jain, R. K. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-2242 · Cited by 397 · see citing works

A Molecular Description of Cellulose Biosynthesis

McNamara, J. T., Morgan, J. L. W., & Zimmer, J. (2015) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060614-033930 · Cited by 388 · see citing works

The sweet spot: defining virus–sialic acid interactions

Stencel-Baerenwald, J., Reiß, K., Reiter, D. M., Stehle, T., & Dermody, T. S. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3346 · Cited by 385 · see citing works

Virus cell-to-cell transmission

Mothes, W., Sherer, N. M., Jin, J., & Zhong, P. (2010) · Journal of Virology · doi:10.1128/jvi.00443-10 · Cited by 353 · see citing works

Interaction between the tobacco mosaic virus movement protein and host cell pectin methylesterases is required for viral cell‐to‐cell movement

Chen, M., Sheng, J., Hínd, G., Handa, A. K., & Citovsky, V. (2000) · The EMBO Journal · doi:10.1093/emboj/19.5.913 · Cited by 323 · see citing works

Clathrin Mediates Endocytosis and Polar Distribution of PIN Auxin Transporters in Arabidopsis

Kitakura, S., Vanneste, S., Robert, S., Löfke, C., Teichmann, T., Tanaka, H., & Friml, J. (2011) · The Plant Cell · doi:10.1105/tpc.111.083030 · Cited by 319 · see citing works

The Collagen Binding α1β1 Integrin VLA-1 Regulates CD8 T Cell-Mediated Immune Protection against Heterologous Influenza Infection

Ray, S. J., Franki, S. N., Pierce, R. H., Dimitrova, S., Koteliansky, V., Sprague, A., Doherty, P. C., de Fougerolles, A. R., & Topham, D. J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00021-4 · Cited by 317 · see citing works

Biology of callose (β-1,3-glucan) turnover at plasmodesmata

Zavaliev, R., Ueki, S., Epel, B. L., & Citovsky, V. (2010) · PROTOPLASMA · doi:10.1007/s00709-010-0247-0 · Cited by 316 · see citing works

Movement of plant viruses is delayed in a β‐1,3‐glucanase‐deficient mutant showing a reduced plasmodesmatal size exclusion limit and enhanced callose deposition

Iglesias, V. A., & Meins, F. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00658.x · Cited by 306 · see citing works

Viral entry mechanisms: cellular and viral mediators of herpes simplex virus entry

Akhtar, J., & Shukla, D. (2009) · The FEBS Journal · doi:10.1111/j.1742-4658.2009.07402.x · Cited by 292 · see citing works

Biology of Plant Rhabdoviruses

Jackson, A. O., Dietzgen, R. G., Goodin, M. M., Bragg, J. N., & Deng, M. (2005) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.43.011205.141136 · Cited by 292 · see citing works

Methyl esterification of pectin plays a role during plant–pathogen interactions and affects plant resistance to diseases

Lionetti, V., Cervone, F., & Bellincampi, D. (2012) · Journal of Plant Physiology · doi:10.1016/j.jplph.2012.05.006 · Cited by 287 · see citing works

Sialic Acid Receptors of Viruses

Matrosovich, M. N., Herrler, G., & Klenk, H. D. (2013) · Topics in current chemistry · doi:10.1007/128_2013_466 · Cited by 286 · see citing works

MMP generated matrikines

Wells, J. M., Gaggar, A., & Blalock, J. E. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.01.016 · Cited by 263 · see citing works

Structural Basis for the Interaction between Pectin Methylesterase and a Specific Inhibitor Protein

Matteo, A. D., Giovane, A., Raiola, A., Camardella, L., Bonivento, D., Lorenzo, G. D., Cervone, F., Bellincampi, D., & Tsernoglou, D. (2005) · The Plant Cell · doi:10.1105/tpc.104.028886 · Cited by 232 · see citing works

Cell-to-cell transmission of viruses

Zhong, P., Agosto, L. M., Munro, J. B., & Mothes, W. (2013) · Current Opinion in Virology · doi:10.1016/j.coviro.2012.11.004 · Cited by 231 · see citing works

Three Pectin Methylesterase Inhibitors Protect Cell Wall Integrity for Arabidopsis Immunity to Botrytis

Lionetti, V., Fabri, E., Caroli, M. D., Hansen, A. R., Willats, W. G. T., Piro, G., & Bellincampi, D. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01185 · Cited by 213 · see citing works

Auxin-Callose-Mediated Plasmodesmal Gating Is Essential for Tropic Auxin Gradient Formation and Signaling

Han, X., Hyun, T. K., Zhang, M., Kumar, R., Koh, E.-J., Kang, B., Lucas, W. J., & Kim, J. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.008 · Cited by 211 · see citing works

Engineering the cell wall by reducing de-methyl-esterified homogalacturonan improves saccharification of plant tissues for bioconversion

Lionetti, V., Francocci, F., Ferrari, S., Volpi, C., Bellincampi, D., Galletti, R., D'Ovidio, R., Lorenzo, G. D., & Cervone, F. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907549107 · Cited by 211 · see citing works

Dysregulation of cell-to-cell connectivity and stomatal patterning by loss-of-function mutation in Arabidopsis CHORUS ( GLUCAN SYNTHASE-LIKE 8 )

Guseman, J. M., Lee, J. S., Bogenschutz, N. L., Peterson, K. M., Virata, R. E., Xie, B., Kanaoka, M. M., Hong, Z., & Torii, K. U. (2010) · Development · doi:10.1242/dev.049197 · Cited by 210 · see citing works

Hyaluronidase Expression by an Oncolytic Adenovirus Enhances Its Intratumoral Spread and Suppresses Tumor Growth

Guedan, S., Rojas, J. J., Gros, A., Mercadé, E., Cascalló, M., & Alemany, R. (2010) · Molecular Therapy · doi:10.1038/mt.2010.79 · Cited by 206 · see citing works

Nanomechanical mapping of first binding steps of a virus to animal cells

Alsteens, D., Newton, R., Schubert, R., Martínez-Martín, D., Delguste, M., Roska, B., & Müller, D. J. (2016) · Nature Nanotechnology · doi:10.1038/nnano.2016.228 · Cited by 202 · see citing works

Matrix metalloproteinases in cardiovascular disease

Liu, P. X., Sun, M., & Sader, S. (2006) · Canadian Journal of Cardiology · doi:10.1016/s0828-282x(06)70983-7 · Cited by 184 · see citing works

Unusual Life Style of Giant Chlorella Viruses

Etten, J. L. V. (2003) · Annual Review of Genetics · doi:10.1146/annurev.genet.37.110801.143915 · Cited by 181 · see citing works

Callose homeostasis at plasmodesmata: molecular regulators and developmental relevance

Storme, N. D., & Geelen, D. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00138 · Cited by 179 · see citing works

Super-Resolution Imaging of Plasmodesmata Using Three-Dimensional Structured Illumination Microscopy

Fitzgibbon, J., Bell, K., King, E. M. J., & OPARKA, K. J. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.157941 · Cited by 167 · see citing works

A glycoprotein inhibitor of pectin methylesterase in kiwi fruit (Actinidia chinensis)

Balestrieri, C., Castaldo, D., Giovane, A., Quagliuolo, L., & Servillo, L. (1990) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1990.tb19321.x · Cited by 158 · see citing works

Cellular growth in plants requires regulation of cell wall biochemistry

Chebli, Y., & Geitmann, A. (2017) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2017.01.002 · Cited by 158 · see citing works

Viral entry mechanisms: human papillomavirus and a long journey from extracellular matrix to the nucleus

Sapp, M. J., & Bienkowska‐Haba, M. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07400.x · Cited by 154 · see citing works

Systemic movement of a tobamovirus requires host cell pectin methylesterase

Chen, M., & Citovsky, V. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01818.x · Cited by 152 · see citing works

Tomato spotted wilt virus—positive steps towards negative success

Adkins, S. T. (2000) · Molecular Plant Pathology · doi:10.1046/j.1364-3703.2000.00022.x · Cited by 148 · see citing works

Surface-exposed Amino Acid Residues of HPV16 L1 Protein Mediating Interaction with Cell Surface Heparan Sulfate

Knappe, M., Bodevin, S., Selinka, H., Spillmann, D., Streeck, R. E., Chen, X. S., Lindahl, U., & Sapp, M. J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705127200 · Cited by 139 · see citing works

Subcellular Dynamics and Role of Arabidopsis β-1,3-Glucanases in Cell-to-Cell Movement of Tobamoviruses

Zavaliev, R., Levy, A., Gera, A., & Epel, B. L. (2013) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-03-13-0062-r · Cited by 139 · see citing works

The Permeability of Plant Cell Walls as Measured by Gel Filtration Chromatography

Tepfer, M. M., & Taylor, I. E. P. (1981) · Science · doi:10.1126/science.213.4509.761 · Cited by 137 · see citing works

Intracellular Transport of Viruses and Their Components: Utilizing the Cytoskeleton and Membrane Highways

Harries, P. A., Schoelz, J. E., & Nelson, R. S. (2010) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-05-10-0121 · Cited by 136 · see citing works

Plasmodesmata enable multicellularity: new insights into their evolution, biogenesis, and functions in development and immunity

Brunkard, J. O., & Zambryski, P. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2016.11.007 · Cited by 135 · see citing works

Molecular Mechanisms of HTLV-1 Cell-to-Cell Transmission

Christine, G., & Thoma‐Kress, A. K. (2016) · Viruses · doi:10.3390/v8030074 · Cited by 132 · see citing works

TIP, A Novel Host Factor Linking Callose Degradation with the Cell-to-Cell Movement of Potato virus X

Fridborg, I., Grainger, J., Page, A. M., Coleman, M. J., Findlay, K., & Angell, S. M. (2003) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2003.16.2.132 · Cited by 129 · see citing works

Spatial Regulation of Pectic Polysaccharides in Relation to Pit Fields in Cell Walls of Tomato Fruit Pericarp

Orfila, C., & Knox, J. P. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.3.775 · Cited by 123 · see citing works

Hepatitis C virus molecular clones and their replication capacity in vivo and in cell culture

Bartenschlager, R. F. W., & Sparacio, S. (2007) · Virus Research · doi:10.1016/j.virusres.2007.02.022 · Cited by 112 · see citing works

Plant viruses spread by diffusion on ER-associated movement-protein-rafts through plasmodesmata gated by viral induced host β-1,3-glucanases

Epel, B. L. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.05.010 · Cited by 111 · see citing works

Herpes simplex virus type 1 glycoprotein H binds to αvβ3 integrins

Parry, C. M., Bell, S., Minson, T., & Browne, H. M. (2004) · Journal of General Virology · doi:10.1099/vir.0.80567-0 · Cited by 103 · see citing works

Dengue virus receptor

Hidari, K. I. P. J., & Suzuki, T. (2011) · Tropical Medicine and Health · doi:10.2149/tmh.2011-s03 · Cited by 99 · see citing works

Cellular factors in plant virus movement: At the leading edge of macromolecular trafficking in plants

Harries, P. A., & Ding, B. (2011) · Virology · doi:10.1016/j.virol.2010.12.021 · Cited by 92 · see citing works

Early Bunyavirus-Host Cell Interactions

Albornoz, A., Hoffmann, A., Lozach, P., & Tischler, N. D. (2016) · Viruses · doi:10.3390/v8050143 · Cited by 89 · see citing works

The plant secretory pathway for the trafficking of cell wall polysaccharides and glycoproteins

Kim, S., & Brandizzí, F. (2016) · Glycobiology · doi:10.1093/glycob/cww044 · Cited by 84 · see citing works

HA metabolism in skin homeostasis and inflammatory disease

Kavasi, R., Berdiaki, A., Spyridaki, I., Corsini, E., Tsatsakis, A. M., Tzanakakis, G. N., & Nikitovic, D. (2017) · Food and Chemical Toxicology · doi:10.1016/j.fct.2017.01.012 · Cited by 83 · see citing works

Transgenic expression of pectin methylesterase inhibitors limits tobamovirus spread in tobacco and A rabidopsis

Lionetti, V., Raiola, A., Cervone, F., & Bellincampi, D. (2013) · Molecular Plant Pathology · doi:10.1111/mpp.12090 · Cited by 82 · see citing works

Cell wall integrity

Pogorelko, G. V., Lionetti, V., Bellincampi, D., & Zabotina, O. A. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.25435 · Cited by 81 · see citing works

ANK, a Host Cytoplasmic Receptor for the Tobacco mosaic virus Cell-to-Cell Movement Protein, Facilitates Intercellular Transport through Plasmodesmata

Ueki, S., Spektor, R., Natale, D. M., & Citovsky, V. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001201 · Cited by 77 · see citing works

Endoplasmic reticulum export and vesicle formation of the movement protein of Chinese wheat mosaic virus are regulated by two transmembrane domains and depend on the secretory pathway

Andika, I. B., Zheng, S., Tan, Z., Sun, L., Kondō, H., Zhou, X., & Chen, J. (2012) · Virology · doi:10.1016/j.virol.2012.10.024 · Cited by 69 · see citing works

Characterization of Cellulose Synthesis in Plant Cells

Maleki, S. S., Mohammadi, K., & Ji, K. (2016) · The Scientific World JOURNAL · doi:10.1155/2016/8641373 · Cited by 69 · see citing works

Cruising the cellular highways: how human papillomavirus travels from the surface to the nucleus

DiGiuseppe, S., Bienkowska-Haba, M., Guion, L. G., & Sapp, M. (2017) · Virus Research · doi:10.1016/j.virusres.2016.10.015 · Cited by 67 · see citing works

Roles and regulation of plant cell walls surrounding plasmodesmata

Knox, J. P., & Benitez‐Alfonso, Y. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.09.009 · Cited by 63 · see citing works

Human Immunodeficiency Virus Type 1 Envelope gp120 Induces a Stop Signal and Virological Synapse Formation in Noninfected CD4+T Cells

Vasiliver-Shamis, G., Tuen, M., Wu, T. W., Starr, T., Cameron, T. O., Thomson, R. P., Kaur, G., Liu, J., Visciano, M. L., Li, H., et al. (2008) · Journal of Virology · doi:10.1128/jvi.00835-08 · Cited by 62 · see citing works

No Stress! Relax! Mechanisms Governing Growth and Shape in Plant Cells

Guerriero, G., Hausman, J.-F., & Cai, G. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15035094 · Cited by 61 · see citing works

Immunogold localization of pectin methylesterases in the cortical tissues of flax hypocotyl

Morvan, O., Quentin, M., Jauneau, A., Mareck, A., & Morvan, C. (1998) · PROTOPLASMA · doi:10.1007/bf01282545 · Cited by 59 · see citing works

Plasma matrix metalloproteinases are associated with incident cardiovascular disease and all-cause mortality in patients with type 1 diabetes: a 12-year follow-up study

Peeters, S. A., Engelen, L., Buijs, J., Jorsal, A., Parving, H. ‐., Tarnow, L., Rossing, P. R., Schalkwijk, C., & Stehouwer, C. D. A. (2017) · Cardiovascular Diabetology · doi:10.1186/s12933-017-0539-1 · Cited by 57 · see citing works

Association of the degree of methylation of intercellular pectin with plant resistance to aphids and with induction of aphid biotypes

Dreyer, D. L., & Campbell, B. C. (1984) · Cellular and Molecular Life Sciences · doi:10.1007/bf01963612 · Cited by 51 · see citing works

The inside and outside: topological issues in plant cell wall biosynthesis and the roles of nucleotide sugar transporters

Temple, H., Saez‐Aguayo, S., Reyes, F. C., & Orellana, A. (2016) · Glycobiology · doi:10.1093/glycob/cww054 · Cited by 45 · see citing works

Plant cell wall in pathogenesis, parasitism and symbiosis

Lionetti, V., & Métraux, J.-P. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00612 · Cited by 44 · see citing works

Histology and cell wall biochemistry of stone cells in the physical defence of conifers against insects

Whitehill, J. G. A., Henderson, H., Schuetz, M., Skyba, O., Yuen, M. M. S., King, J., Samuels, L., Mansfield, S. D., & Bohlmann, J. (2015) · Plant Cell & Environment · doi:10.1111/pce.12654 · Cited by 43 · see citing works

Cell-to-cell movement of viruses via plasmodesmata

Kumar, D., V, Kumar, R., Hyun, T. K., & Kim, J. (2014) · Journal of Plant Research · doi:10.1007/s10265-014-0683-6 · Cited by 42 · see citing works

Oncolysis by paramyxoviruses: preclinical and clinical studies

Matveeva, O. V., Guo, Z. S., Senin, V. M., Senina, A. V., Shabalina, S. A., & Chumakov, P. M. (2015) · Molecular Therapy — Oncolytics · doi:10.1038/mto.2015.17 · Cited by 40 · see citing works

A lower content of de-methylesterified homogalacturonan improves enzymatic cell separation and isolation of mesophyll protoplasts in Arabidopsis

Lionetti, V., Cervone, F., & Lorenzo, G. D. (2014) · Phytochemistry · doi:10.1016/j.phytochem.2014.07.025 · Cited by 37 · see citing works

Roles of membrane trafficking in plant cell wall dynamics

Ebine, K., & Ueda, T. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00878 · Cited by 37 · see citing works

Human Papillomavirus Species-Specific Interaction with the Basement Membrane-Resident Non-Heparan Sulfate Receptor

Richards, K. F., Mukherjee, S., Bienkowska‐Haba, M., Pang, J., & Sapp, M. J. (2014) · Viruses · doi:10.3390/v6124856 · Cited by 34 · see citing works

Polarized Cell Migration during Cell-to-Cell Transmission of Herpes Simplex Virus in Human Skin Keratinocytes

Abaitua, F., Zia, F. R., Hollinshead, M. S., & O’Hare, P. (2013) · Journal of Virology · doi:10.1128/jvi.01172-13 · Cited by 30 · see citing works

Extracellular matrix constituents interfere with Newcastle disease virus spread in solid tissue and diminish its potential oncolytic activity

Yaacov, B., Lazar, I., Tayeb, S., Frank, S., Izhar, U., Lotem, M., Perlman, R., Ben-Yehuda, D., Zakay-Rones, Z., & Panet, A. (2012) · Journal of General Virology · doi:10.1099/vir.0.043281-0 · Cited by 29 · see citing works

Human T-cell leukemia virus type 1 Tax transactivates the matrix metalloproteinase 7 gene via JunD/AP-1 signaling

Nakachi, S., Nakazato, T., Ishikawa, C., Kimura, R., Mann, D. A., Senba, M., Masuzaki, H., & Mori, N. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.02.002 · Cited by 26 · see citing works

Plant virus uncoating as a result of virus-cell wall interactions

Gaard, G., & de Zoeten, G. A. (1979) · Virology · doi:10.1016/0042-6822(79)90168-5 · Cited by 26 · see citing works

Integrin α4β7 Expression Increases HIV Susceptibility in Activated Cervical CD4+ T Cells by an HIV Attachment-Independent Mechanism

Ding, J., Tasker, C., Lespinasse, P. F., Dai, J., Fitzgerald-Bocarsly, P. A., Lu, W., Heller, D. S., & Chang, T. L.-Y. (2015) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000000676 · Cited by 25 · see citing works

How do pectin methylesterases and their inhibitors affect the spreading of tobamovirus?

Lionetti, V., Raiola, A., Cervone, F., & Bellincampi, D. (2014) · Plant Signaling & Behavior · doi:10.4161/15592316.2014.972863 · Cited by 25 · see citing works

[Extracellular matrix--regulation of cancer invasion and metastasis].

Watanabe, H. (2010) · PubMed · Cited by 24 · see citing works

Immune Response to Extracellular Matrix Collagen in Chronic Hepatitis C–Induced Liver Fibrosis

Borg, B. B., Seetharam, A. B., Subramanian, V., Basha, H. I., Lisker‐Melman, M., Korenblat, K., Anderson, C. D., Shenoy, S., Chapman, W. C., Crippin, J. S., et al. (2011) · Liver Transplantation · doi:10.1002/lt.22303 · Cited by 22 · see citing works

Proteins involved in extracellular matrix dynamics are associated with respiratory syncytial virus disease severity

Schuurhof, A., Bont, L., Hodemaekers, H. M., de Klerk, A., de Groot, H., Hofland, R. W., van de Pol, A. C., Kimpen, J. L. L., & Janssen, R. (2012) · European Respiratory Journal · doi:10.1183/09031936.00012311 · Cited by 22 · see citing works

Virus Transmission—Getting Out and In

Blanc, S. (2007) · Springer eBooks · doi:10.1007/7089_2006_099 · Cited by 19 · see citing works

Virus-induced gene silencing of pectin methylesterase protects Nicotiana benthamiana from lethal symptoms caused by Tobacco mosaic virus

Bubici, G., Carluccio, A. V., Cillo, F., & Stavolone, L. (2014) · European Journal of Plant Pathology · doi:10.1007/s10658-014-0546-y · Cited by 11 · see citing works

Early Events In Plant Virus Infections

Shaw, J. G. (2018) · CRC Press eBooks · doi:10.1201/9781351074780-1 · Cited by 8 · see citing works

The Extracellular Matrix in Skin Inflammation and Infection

Pfisterer, K., Shaw, L. E., Symmank, D., & Weninger, W. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.682414 · Cited by 244 · see citing works

Polymers for Agri-Food Applications

Pereira, A. E. S., de Sousa, B. T., Iglesias, M. J., Alvarez, V. A., Casalongué, C. A., Oliveira, H. C., & Fraceto, L. F. (2019) · Springer eBooks · doi:10.1007/978-3-030-19416-1 · Cited by 171 · see citing works

Is Chickpea a Potential Substitute for Soybean? Phenolic Bioactives and Potential Health Benefits

de Camargo, A. C., Favero, B. T., Morzelle, M. C., Franchin, M., ́Álvarez-Parrilla, E., la Rosa, L. A. D., Geraldi, M. V., Maróstica, M. R., Shahidi, F., & Schwember, A. R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112644 · Cited by 147 · see citing works

Scaffolding technologies for the engineering of cultured meat: Towards a safe, sustainable, and scalable production

Levi, S., Yen, F.-C., Baruch, L., & Machluf, M. (2022) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2022.05.011 · Cited by 122 · see citing works

Plant Cell Wall Integrity Perturbations and Priming for Defense

Swaminathan, S., Lionetti, V., & Zabotina, O. A. (2022) · Plants · doi:10.3390/plants11243539 · Cited by 92 · see citing works

Exploring the Role of Cell Wall-Related Genes and Polysaccharides during Plant Development

Tucker, M. R., Lou, H., Aubert, M. K., Wilkinson, L. G., Little, A., Houston, K., Pinto, S. C., & Shirley, N. J. (2018) · Plants · doi:10.3390/plants7020042 · Cited by 82 · see citing works

In-cell NMR: Why and how?

Theillet, F., & Luchinat, E. (2022) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2022.04.002 · Cited by 82 · see citing works

Key checkpoints in the movement of plant viruses through the host

Navarro, J. A., Sánchez-Navarro, J. Á., & Pallás, V. (2019) · Advances in virus research · doi:10.1016/bs.aivir.2019.05.001 · Cited by 73 · see citing works

Plant Cell Wall Dynamics in Compatible and Incompatible Potato Response to Infection Caused by Potato Virus Y (PVYNTN)

Otulak-Kozieł, K., Kozieł, E., & Lockhart, B. E. L. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19030862 · Cited by 69 · see citing works

Foliar Application of Chitosan and Phosphorus Alleviate the Potato virus Y-Induced Resistance by Modulation of the Reactive Oxygen Species, Antioxidant Defense System Activity and Gene Expression in Potato

Al-Mokadem, A. Z., ALNAGGAR, A. E. M., Mancy, A., Sofy, A. R., Sofy, M. R., Mohamed, A. K. S. H., ghazala, M. M. A., El-Zabalawy, K. M., Salem, N. F. G., Elnosary, M. E., et al. (2022) · Agronomy · doi:10.3390/agronomy12123064 · Cited by 50 · see citing works

Modulation of bacterial multicellularity via spatio-specific polysaccharide secretion

Islam, S. T., Alvarez, I. V., Saïdi, F., Guiseppi, A., VINOGRADOV, E. V., Sharma, G., Espinosa, L., Morrone, C., Brasseur, G., Guillemot, J.-F., et al. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000728 · Cited by 47 · see citing works

Thermoplastic polyurethane with controllable degradation and critical anti-fouling properties

Wang, H., Liu, X., Christiansen, D. E., Fattahpour, S., Wang, K., Song, H., Mehraeen, S., & Cheng, G. (2020) · Biomaterials Science · doi:10.1039/d0bm01967d · Cited by 44 · see citing works

Dual Peptide-Based Gene Delivery System for the Efficient Transfection of Plant Callus Cells

Miyamoto, T., Tsuchiya, K., & Numata, K. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c00481 · Cited by 43 · see citing works

CRISPR-Cas assisted diagnostics of plant viruses and challenges

Jaybhaye, S. G., Chavhan, R. L., Hinge, V. R., Deshmukh, A. S., & Kadam, U. S. (2024) · Virology · doi:10.1016/j.virol.2024.110160 · Cited by 36 · see citing works

Viral spillover risk increases with climate change in High Arctic lake sediments

Lemieux, A., Colby, G. A., Poulain, A. J., & Aris‐Brosou, S. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2022.1073 · Cited by 33 · see citing works

A Review on Transcriptional Responses of Interactions between Insect Vectors and Plant Viruses

Catto, M. A., Mugerwa, H., Myers, B. K., Pandey, S., Dutta, B., & Srinivasan, R. (2022) · Cells · doi:10.3390/cells11040693 · Cited by 28 · see citing works

The dispersion of viscoelastic properties of fascicle bundles within the tendon results from the presence of interfascicular matrix and flow of body fluids

Młyniec, A., Dąbrowska, S., Heljak, M. K., Węglarz, W. P., Wójcik, K., Ekiert, M., Obuchowicz, R., & Święszkowski, W. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.112435 · Cited by 25 · see citing works

Modulating Mechanical Properties of Collagen–Lignin Composites

Belgodere, J. A., Zamin, S. A., Kalinoski, R. M., Astete, C. E., Penrod, J. C., Hamel, K. M., Lynn, B. C., Rudra, J. S., Shi, J., & Jung, J. P. (2019) · ACS Applied Bio Materials · doi:10.1021/acsabm.9b00444 · Cited by 21 · see citing works

To-Do and Not-To-Do in Model Studies of the Uptake, Fate and Metabolism of Metal-Containing Nanoparticles in Plants

Wojcieszek, J., Lamana, J. J., Ruzik, L., Szpunar, J., & Jarosz, M. (2020) · Nanomaterials · doi:10.3390/nano10081480 · Cited by 21 · see citing works

Glycine can prevent and fight virus invasiveness by reinforcing the extracellular matrix

Meléndez‐Hevia, E., de Paz-Lugo, P., & Sánchez, G. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104318 · Cited by 20 · see citing works

3D-printed airway model as a platform for SARS-CoV-2 infection and antiviral drug testing

Lee, Y., Lee, M. K., Lee, H., Kim, B., Kim, M., & Jung, S. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122689 · Cited by 20 · see citing works

Allelic RNA Motifs in Regulating Systemic Trafficking of Potato Spindle Tuber Viroid

Takeda, R., Zirbel, C. L., Leontis, N. B., Wang, Y., & Ding, B. (2018) · Viruses · doi:10.3390/v10040160 · Cited by 20 · see citing works

Microbial Biofilms: Human T-cell Leukemia Virus Type 1 First in Line for Viral Biofilm but Far Behind Bacterial Biofilms

Maali, Y., Journo, C., Mahieux, R., & Dutartre, H. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.02041 · Cited by 21 · see citing works

Overexpression of Chicken IRF7 Increased Viral Replication and Programmed Cell Death to the Avian Influenza Virus Infection Through TGF-Beta/FoxO Signaling Axis in DF-1

Kim, T. H., & Zhou, H. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00415 · Cited by 20 · see citing works

Bioinspired microstructures through decellularization of plants for tissue engineering applications

Arslan, Y., Paradiso, A., Celiktas, N., Erdogan, T., Yeşil-Çeliktaş, Ö., & Święszkowski, W. (2023) · European Polymer Journal · doi:10.1016/j.eurpolymj.2023.112415 · Cited by 20 · see citing works

Decellularized plant-derived vasculature-on-a-chip interacting with breast cancer spheroids to evaluate a dual-drug therapy

Filiz, Y., Arslan, Y., Duran, E., Saglam‐Metiner, P., Horozoglu, S., Paradiso, A., Martinez, D. C., Takanlou, M. S., Heljak, M. K., Jaroszewicz, J., et al. (2023) · Applied Materials Today · doi:10.1016/j.apmt.2023.102015 · Cited by 16 · see citing works

Development of pro-angiogenic wound dressings from 2-deoxy-D-ribose (2dDR)-loaded decellularized plant leaves

Dıkıcı, S., & Çavdaroğlu, Ç. (2023) · Journal of Materials Science · doi:10.1007/s10853-023-09064-4 · Cited by 15 · see citing works

Productive biofilms: from prokaryotic to eukaryotic systems

Schmeckebier, A., Zayed, A., & Ulber, R. (2022) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.7208 · Cited by 15 · see citing works

Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda

Pigeyre, L., Schatz, M., Ravallec, M., Gasmi, L., Nègre, N., Clouet, C., Sevéno, M., Koulali, K. E., Decourcelle, M., Guérardel, Y., et al. (2019) · Viruses · doi:10.3390/v11090870 · Cited by 12 · see citing works

Viral tropism in plants, reproductive tissues, and seeds

Núñez-Muñoz, L. A., Calderón-Pérez, B., Ruíz‐Medrano, R., Xoconostle‐Cázares, B., & Torre-Almaráz, R. D. L. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04353-9 · Cited by 12 · see citing works

Mapping Extracellular Space Features of Viral Encephalitis to Evaluate the Proficiency of Anti‐Viral Drugs

Wang, L., Chen, H., Wang, Z., Ning, D., Zhao, W. G., Rat, V., Lamb, D. C., Pang, D., & Liu, S. (2024) · Advanced Materials · doi:10.1002/adma.202311457 · Cited by 9 · see citing works

Potential Use of Polymeric Particles for the Regulation of Plant Growth

Pereira, A. D. E. S., de Sousa, B. T., Iglesias, M. J., Álvarez, V. A., Casalongué, C. A., Oliveira, H. C., & Fraceto, L. F. (2019) · Springer eBooks · doi:10.1007/978-3-030-19416-1_4 · Cited by 8 · see citing works

Equid Herpesvirus-1 Exploits the Extracellular Matrix of Mononuclear Cells to Ensure Transport to Target Cells

Kamel, M., Pavulraj, S., Fauler, B., Mielke, T., & Azab, W. (2020) · iScience · doi:10.1016/j.isci.2020.101615 · Cited by 7 · see citing works

Editorial: Plant cell wall in pathogenesis, parasitism and symbiosis, Volume II

Vicré‐Gibouin, M., & Lionetti, V. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1230438 · Cited by 6 · see citing works

Proteins, Small Peptides and Other Signaling Molecules Identified as Inconspicuous but Possibly Important Players in Microspores Reprogramming Toward Embryogenesis

Dubas, E., Żur, I., Moravčí­ková, J., Fodor, J., Krzewska, M., Surówka, E., Nowicka, A. M., & Gerši, Z. (2021) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2021.745865 · Cited by 5 · see citing works

Starch Plays a Key Role in Sporosorus Formation by the Powdery Scab PathogenSpongospora subterranea

Kamal, H., Lynch-Holm, V., Pappu, H. R., & Tanaka, K. (2023) · Phytopathology · doi:10.1094/phyto-07-23-0224-r · Cited by 5 · see citing works

A perfusable decellularized plant-based air-liquid-interface-on-a-chip for investigating inorganic dust aerosol exposure

Sert, O., Erdogan, T., Arslan, Y., & Yeşil-Çeliktaş, Ö. (2025) · Scientific Reports · doi:10.1038/s41598-025-33930-7 · Cited by 4 · see citing works

Biomatrices that mimic the cancer extracellular environment

Amorim, S., Reis, R. L., & Pires, R. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818128-7.00004-6 · Cited by 4 · see citing works

Spatiotemporal distribution of the glycoprotein pherophorin II reveals stochastic geometry of the growing ECM of Volvox carteri

von der Heyde, B., Srinivasan, A., Birwa, S. K., von der Heyde, E. L., Höhn, S. S. M. H., Goldstein, R. E., & Hallmann, A. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2425759122 · Cited by 2 · see citing works

Effects of Nutrient Elements on Growth and Expression of Insect-Defense Response Genes in Zanthoxylum bungeanum Maxim

Kassen, K., Niyazbekova, Z., Zhang, T., Nasir, M., Li, F., & Meng-lou, L. (2022) · Forests · doi:10.3390/f13091365 · Cited by 3 · see citing works

Moonlight-like proteins are actually cell wall components in Pseudocercospora fijiensis

Canto‐Canché, B., Burgos-Canul, Y. Y., Chi-Chuc, D., Tzec-Simá, M., Ku, A. F., Brito-Argáez, L. G., Carrillo-Pech, M., Santos-Briones, C. D. L., Canseco-Pérez, M. A., Luna-Moreno, D., et al. (2023) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-023-03676-3 · Cited by 3 · see citing works

Heparan sulfate is the attachment factor associated with channel catfish virus infection on host cells

Yu, F., Chen, H., Xu, J., Wang, Y., Nie, C., Song, S., Meng, L., Hao, K., & Zhao, Z. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2023.1260002 · Cited by 3 · see citing works

A change in the cell wall status initiates the elimination of the nucellus in Arabidopsis

Iannaccone, M., Xu, W., Gómez-Páez, D.-M., Choinard, S., Maricchiolo, E., Peaucelle, A., Voxeur, A., Haas, K. T., Lapierre, C., Jiménez‐Gómez, J. M., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2515702123 · Cited by 2 · see citing works

Potential role of ice-binding protein in mitochondria-lipid and ATP mechanisms during freezing of plant callus

Kim, E., Kwon, G.-S., Choi, S., Kim, S., Heo, K. Y., Kim, Y. S., Kim, C. Y., Kim, S. Y., Jeong, J. C., Hwang, J., et al. (2024) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2024.108866 · Cited by 2 · see citing works

Mechanisms of HAHV-1 Interaction with Hemocytes in Haliotis diversicolor supertexta: An In Vitro Study

Wei, M.-L., Li, Y., Wang, J.-L., Ma, C., Kang, H.-G., Li, P.-J., Zhang, X., Huang, B.-W., & Bai, C.-M. C. (2025) · Biology · doi:10.3390/biology14020121 · Cited by 1 · see citing works

Assessment of In Vitro Models of the Human Buccal Mucosa for Vaccine and Adjuvant Development

Davis, M. M., Bajrovic, I., & Croyle, M. A. (2025) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.4c01186 · Cited by 1 · see citing works

Self-generated hydrogel ejects bacterial cells for localized biofilm dispersion

Chou, T. K.-T., Dau-Martinez, A., Vicens-Figueres, J., Gouttumukkala, A., Galera-Laporta, L., García‐Ojalvo, J., & Süel, G. M. (2026) · Nature Microbiology · doi:10.1038/s41564-026-02413-4 · Cited by 1 · see citing works

Incorporation of Lignin in Natural and Synthetic Biomaterials to Alter Mechanical and Biochemical Properties for Enhanced Wound Healing

Belgodere, J. A. (2020) · doi:10.31390/gradschool_dissertations.5412 · Cited by 1 · see citing works

A change in the cell wall status initiates the elimination of the nucellus in ArabidopsisPreprint

Xu, W., Gómez-Páez, D.-M., Choinard, S., Iannaccone, M., Maricchiolo, E., Peaucelle, A., Voxeur, A., Haas, K. T., Pompa, A., & Magnani, E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.23.590775 · Cited by 1 · see citing works

Spatiotemporal distribution of the glycoprotein pherophorin II reveals stochastic geometry of the growing ECM of Volvox carteriPreprint

von der Heyde, B., Srinivasan, A., Birwa, S. K., von der Heyde, E. L., Höhn, S. S. M. H., Goldstein, R. E., & Hallmann, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.06.625376 · Cited by 1 · see citing works

Characterization of the Arabidopsis At5-MMP Matrix Metalloproteinase

Tang, G., Wu, S., Zhao, B., & Flinn, B. S. (2022) · Journal of Plant Biology · doi:10.1007/s12374-022-09369-y

Deficient of glycosylation site in the envelop protein attenuated Zika virus replication in mosquito cells

Wang, W., Wang, Z.-H., Li, J., Ma, S.-Y., He, M., Liu, M.-X., Zhan, Y.-F., Jin, F., Qu, G., Yin, C., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1603083

Proteomic insights into antiviral immunity: Comparative analysis of diploid, triploid, and allotetraploid cells reveals ploidy-specific defense mechanisms against SVCV infection

Zeng, D., Yao, K., Chen, X. L., Sun, G., Tan, T., Li, W., Li, Y., Xiao, J., & Feng, H. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.103230

Cell wall charge gates iron availability in plant rootsPreprint

Liu, C., Dobrogojski, J., Miranda, P. R., Woelki, D., Marconi, M., Ulbrich, N., González-Delgado, A., Kang, H. S., Kubalová, M., Fendrych, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.15.711884

Franchissement de la barrière intestinale du lépidoptère Spodoptera frugiperda par le Densovirus JcDV

Pigeyre, L. (2019) · doi:10.70675/f27cee72ze782z4b7ez8a0fzb520aaa7bbbe

Regulation and synthesis of EPS production in Myxococcus xanthus

Alvarez, I. V. (2020) · doi:10.70675/3da738efz2f8ez468az9af8z5e5a3062baae

Heterodera schachtii enolase does not elicit canonical immune responses in Arabidopsis thaliana

Euler, M. F., Sumaya, N. P. D., Aslam, S., Lerch, J., Mendy, B., & Grundler, F. M. W. (2026) · Scientific Reports · doi:10.1038/s41598-026-56477-7

Comparative Wound Healing Processes in Plants and Animals: Bioinspired Strategies for Advancing Regenerative Medicine

Najafi, F., de Paula, N. A., Lima, F. R., Fronza, M., Vargas-Rechia, C. G., & Frade, M. A. C. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27135899

Neurotropic virus-induced astrocyte remodeling links collagen-rich extracellular matrix to the LINC00460–miR-4443 regulatory axisPreprint

Jean, F., Bautista-Sánchez, D., Schulz, A. L., Hong, C. Y., Gordon, D. G., Chang, V., Wang, H. H., Vogl, A. W., & Flibotte, S. (2026) · Research Square · doi:10.21203/rs.3.rs-10923543/v1

Breaking Through to the Other Side: How Plant Viruses Modify Plasmodesmata and the Plant Cell Wall

Burch‐Smith, T. M. (2026) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-011325-010500

Interfering with Viral Infection: Plants Do It Too

Smith, H. B. (1999) · The Plant Cell · doi:10.1105/tpc.11.7.1191 · Cited by 4 · see citing works

Distinct Effects of the Extracellular Matrix on Tumor Organization and Response to Cancer VirotherapyPreprint

Supino, I., Visscher, F., Boerma, A., Wouters, A. K., Joshi, M., Heemskerk, M. H. M., & Bhatt, D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.20.739578

Virus-Host Interactions during Movement Processes

Boevink, P. C., & OPARKA, K. J. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.066761 · Cited by 152 · see citing works

Key checkpoints in the movement of plant viruses through the host

Navarro, J. A., Sánchez-Navarro, J. Á., & Pallás, V. (2019) · Advances in virus research · doi:10.1016/bs.aivir.2019.05.001 · Cited by 73 · see citing works