Coronavirus Spike Proteins in Viral Entry and Pathogenesis

Coiled Coils in Both Intracellular Vesicle and Viral Membrane Fusion

Skehel, J. J., & Wiley, D. C. (1998) · Cell · doi:10.1016/s0092-8674(00)81710-9 · Cited by 411 · see citing works

Retargeting of Coronavirus by Substitution of the Spike Glycoprotein Ectodomain: Crossing the Host Cell Species Barrier

Kuo, L., Godeke, G.-J., Raamsman, M. J. B., Masters, P. S., & Rottier, P. J. M. (2000) · Journal of Virology · doi:10.1128/jvi.74.3.1393-1406.2000 · Cited by 366 · see citing works

Localization of neutralizing epitopes and the receptor-binding site within the amino-terminal 330 amino acids of the murine coronavirus spike protein

Kubo, H., Yamada, Y. K., & Taguchi, F. (1994) · Journal of Virology · doi:10.1128/jvi.68.9.5403-5410.1994 · Cited by 286 · see citing works

Targeted Recombination Demonstrates that the Spike Gene of Transmissible Gastroenteritis Coronavirus Is a Determinant of Its Enteric Tropism and Virulence

Sánchez, C. M., Izeta, A., Sánchez-Morgado, J. M., Alonso, S., Sola, I., Balasch, M., Plana-Durán, J., & Enjuanes, L. (1999) · Journal of Virology · doi:10.1128/jvi.73.9.7607-7618.1999 · Cited by 220 · see citing works

Alteration of the pH dependence of coronavirus-induced cell fusion: effect of mutations in the spike glycoprotein

Gallagher, T., Escarmı́s, C., & Buchmeier, M. J. (1991) · Journal of Virology · doi:10.1128/jvi.65.4.1916-1928.1991 · Cited by 164 · see citing works

Conformational change of the coronavirus peplomer glycoprotein at pH 8.0 and 37 degrees C correlates with virus aggregation and virus-induced cell fusion

Sturman, L. S., Ricard, C. S., & Holmes, K. V. (1990) · Journal of Virology · doi:10.1128/jvi.64.6.3042-3050.1990 · Cited by 161 · see citing works

Pathogenesis of Chimeric MHV4/MHV-A59 Recombinant Viruses: the Murine Coronavirus Spike Protein Is a Major Determinant of Neurovirulence

Phillips, J. J., Chua, M. M., Lavi, E., & Weiss, S. R. (1999) · Journal of Virology · doi:10.1128/jvi.73.9.7752-7760.1999 · Cited by 157 · see citing works

Cytokine induction during T-cell-mediated clearance of mouse hepatitis virus from neurons in vivo

Pearce, B. D., Hobbs, M. V., McGraw, T., & Buchmeier, M. J. (1994) · Journal of Virology · doi:10.1128/jvi.68.9.5483-5495.1994 · Cited by 149 · see citing works

LearnCoil-VMF: computational evidence for coiled-coil-like motifs in many viral membrane-fusion proteins

Singh, M., Berger, B., & Kim, P. S. (1999) · Journal of Molecular Biology · doi:10.1006/jmbi.1999.2796 · Cited by 145 · see citing works

Mouse hepatitis virus strain A59 and blocking antireceptor monoclonal antibody bind to the N-terminal domain of cellular receptor.

Dveksler, G. S., Pensiero, M. N., Dieffenbach, C. W., et al. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.1716 · Cited by 114 · see citing works

Episodic evolution mediates interspecies transfer of a murine coronavirus

Baric, R. S., Yount, B. L., Hensley, L. E., et al. (1997) · Journal of Virology · doi:10.1128/jvi.71.3.1946-1955.1997 · Cited by 108 · see citing works

The V5A13.1 envelope glycoprotein deletion mutant of mouse hepatitis virus type-4 is neuroattenuated by its reduced rate of spread in the central nervous system

Fazakerley, J. K., Parker, S. E., Bloom, F. E., et al. (1992) · Virology · doi:10.1016/0042-6822(92)90306-a · Cited by 104 · see citing works

Roles in Cell-to-Cell Fusion of Two Conserved Hydrophobic Regions in the Murine Coronavirus Spike Protein

Luo, Z., & Weiss, S. R. (1998) · Virology · doi:10.1006/viro.1998.9121 · Cited by 97 · see citing works

Variations in Disparate Regions of the Murine Coronavirus Spike Protein Impact the Initiation of Membrane Fusion

Krueger, D. K., Kelly, S. M., Lewicki, D. N., Ruffolo, R., & Gallagher, T. M. (2001) · Journal of Virology · doi:10.1128/jvi.75.6.2792-2802.2001 · Cited by 94 · see citing works

Sequence analysis of the spike protein gene of murine coronavirus variants: Study of genetic sites affecting neuropathogenicity

Wang, F.-I., Fleming, J. O., & Lai, M. M. C. (1992) · Virology · doi:10.1016/0042-6822(92)90041-m · Cited by 82 · see citing works

Identification of spike protein residues of murine coronavirus responsible for receptor-binding activity by use of soluble receptor-resistant mutants

Saeki, K., Ohtsuka, N., & Taguchi, F. (1997) · Journal of Virology · doi:10.1128/jvi.71.12.9024-9031.1997 · Cited by 75 · see citing works

A role for naturally occurring variation of the murine coronavirus spike protein in stabilizing association with the cellular receptor

Gallagher, T. (1997) · Journal of Virology · doi:10.1128/jvi.71.4.3129-3137.1997 · Cited by 69 · see citing works

Identification of a Contiguous 6-Residue Determinant in the MHV Receptor That Controls the Level of Virion Binding to Cells

Rao, P. V., Kumari, S., & Gallagher, T. M. (1997) · Virology · doi:10.1006/viro.1997.8446 · Cited by 46 · see citing works

Role of virus receptor-bearing endothelial cells of the blood-brain barrier in preventing the spread of mouse hepatitis virus-A59 into the central nervous system

Godfraind, C., Havaux, N., Holmes, K. V., et al. (1997) · Journal of NeuroVirology · doi:10.3109/13550289709031188 · Cited by 29 · see citing works

21 Specificity of Coronavirus/Receptor InteractionsPreprint

Holmes, K. V., & Dveksler, G. S. (1994) · Cold Spring Harbor Monograph Archive · doi:10.1101/087969429.28.403 · Cited by 19 · see citing works

Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus

Li, W., Moore, M. J., Vasilieva, N., Sui, J., Wong, S. K., Berne, M. A., Somasundaran, M., Sullivan, J. L., Luzuriaga, K., Greenough, T. C., et al. (2003) · Nature · doi:10.1038/nature02145 · Cited by 5,923 · see citing works

A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2

Chi, X., Yan, R., Zhang, J., Zhang, G., Zhang, Y., Hao, M., Zhang, Z., Fan, P., Dong, Y., Yang, Y., et al. (2020) · Science · doi:10.1126/science.abc6952 · Cited by 1,385 · see citing works

Coronavirus Pathogenesis and the Emerging Pathogen Severe Acute Respiratory Syndrome Coronavirus

Weiss, S. R., & Navas-Martin, S. (2005) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.69.4.635-664.2005 · Cited by 1,256 · see citing works

Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry

Hofmann, H., Pyrc, K., van der Hoek, L., Geier, M., Berkhout, B., & Pöhlmann, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409465102 · Cited by 824 · see citing works

Computational analysis of microRNA-mediated interactions in SARS-CoV-2 infection

Saçar Demirci, M. D., & Adan, A. (2020) · PeerJ · doi:10.7717/peerj.9369 · Cited by 190 · see citing works

Antigenic and Immunogenic Characterization of Recombinant Baculovirus-Expressed Severe Acute Respiratory Syndrome Coronavirus Spike Protein: Implication for Vaccine Design

He, Y., Li, J., Heck, S., Lustigman, S., & Jiang, S. (2006) · Journal of Virology · doi:10.1128/jvi.00083-06 · Cited by 135 · see citing works

Proteomic approaches to uncovering virus–host protein interactions during the progression of viral infection

Lum, K. K., & Cristea, I. M. (2016) · Expert Review of Proteomics · doi:10.1586/14789450.2016.1147353 · Cited by 113 · see citing works

Central nervous system stromal cells control local CD8 + T cell responses during virus-induced neuroinflammation.

Cupovic, J., Onder, L., Gil-Cruz, C., Weiler, E., Caviezel-Firner, S., Perez-Shibayama, C., Rülicke, T., Bechmann, I., & Ludewig, B. (2016) · Immunity · doi:10.1016/j.immuni.2015.12.022 · Cited by 98 · see citing works

Artificial Intelligence Technologies for COVID-19 De Novo Drug Design

Floresta, G., Zagni, C., Gentile, D., Patamia, V., & Rescifina, A. (2022) · doi:10.20944/preprints202203.0032.v1 · Cited by 67 · see citing works

Renin-angiotensin system in human coronavirus pathogenesis

Wevers, B. A., & Hoek, L. V. D. (2010) · Future Virology · doi:10.2217/fvl.10.4 · Cited by 51 · see citing works

Predicting Potential SARS-COV-2 Drugs—In Depth Drug Database Screening Using Deep Neural Network Framework SSnet, Classical Virtual Screening and Docking

Karki, N., Verma, N., Trozzi, F., Tao, P., Kraka, E., & Zoltowski, B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041573 · Cited by 43 · see citing works

COVID-19 as a Risk Factor for Alzheimer’s Disease

Golzari-Sorkheh, M., Weaver, D. F., & Reed, M. A. (2023) · Journal of Alzheimer's Disease · doi:10.3233/jad-220800 · Cited by 39 · see citing works

A novel system to study adenovirus tropism to normal and malignant colon tissues

Kolodkin‐Gal, D., Zamir, G. A., Pikarski, E., et al. (2006) · Virology · doi:10.1016/j.virol.2006.07.048 · Cited by 19 · see citing works

Short Communication: Causal Relationships between HIV-1 Coreceptor Utilization, Tropism, and Pathogenesis in Human Thymus

Berkowitz, R. D., Alexander, S. A., & McCune, J. M. (2000) · AIDS Research and Human Retroviruses · doi:10.1089/08892220050075291 · Cited by 21 · see citing works

Demyelinating and Nondemyelinating Strains of Mouse Hepatitis Virus Differ in Their Neural Cell Tropism

Sarma, J. D., Iacono, K. T., Gard, L., Marek, R. A., Kenyon, L. C., Koval, M. H., & Weiss, S. R. (2008) · Journal of Virology · doi:10.1128/jvi.01488-07 · Cited by 49 · see citing works

Characterization of Attenuated Mutants of MHV3 : Importance of the E2 Protein in Organ Tropism and Infection of Isolated Liver Cells

Martin, J. P., Chen, W., Obert, G., et al. (1990) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-5823-7_55 · Cited by 7 · see citing works

Low-virulent mouse hepatitis viruses exhibiting various tropisms in macrophages, T and B cell subpopulations, and thymic stromal cells.

Lamontagne, L., & Jolicoeur, P. (1994) · PubMed · Cited by 11 · see citing works