Interferon‐Induced Mx Proteins: Dynamin‐Like GTPases with Antiviral Activity

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Mx proteins: mediators of innate resistance to RNA viruses

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Mammalian Dynamin-like Protein DLP1 Tubulates Membranes

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Interferon induces a unique protein in mouse cells bearing a gene for resistance to influenza virus.

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Domain structure and intramolecular regulation of dynamin GTPase

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Antivirally active MxA protein sequesters La Crosse virus nucleocapsid protein into perinuclear complexes

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Dynamin family of mechanoenzymes

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Inhibition of Hepatitis B Virus Replication by the Interferon-Inducible MxA Protein

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Transgenic mice with intracellular immunity to influenza virus

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Human MxA Protein Protects Mice Lacking a Functional Alpha/Beta Interferon System against La Crosse Virus and Other Lethal Viral Infections

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Mx proteins: GTPases with antiviral activity

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Interferon-induced human protein MxA is a GTPase which binds transiently to cellular proteins

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Mechanism of human MxA protein action: variants with changed antiviral properties.

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Human MxA Protein Confers Resistance to Semliki Forest Virus and Inhibits the Amplification of a Semliki Forest Virus-Based Replicon in the Absence of Viral Structural Proteins

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The central interactive region of human MxA GTPase is involved in GTPase activation and interaction with viral target structures

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Human MxB Protein, an Interferon-α-inducible GTPase, Contains a Nuclear Targeting Signal and Is Localized in the Heterochromatin Region beneath the Nuclear Envelope

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The Antiviral Dynamin Family Member, MxA, Tubulates Lipids and Localizes to the Smooth Endoplasmic Reticulum

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Signaling mechanistics: Aluminum fluoride for molecule of the year

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Interferon-induced protein Mx accumulates in nuclei of mouse cells expressing resistance to influenza viruses

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Dominant-negative mutants of human MxA protein: domains in the carboxy-terminal moiety are important for oligomerization and antiviral activity

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Crystal structure of a dynamin GTPase domain in both nucleotide‐free and GDP‐bound forms

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Cloning and sequence analyses of cDNAs for interferon- and virus-induced human Mx proteins reveal that they contain putative guanine nucleotide-binding sites: functional study of the corresponding gene promoter

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Interferon-induced Mx proteins form oligomers and contain a putative leucine zipper.

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Dynamin Assembles into Spirals under Physiological Salt Conditions upon the Addition of GDP and γ-Phosphate Analogues

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Self-assembly of Human MxA GTPase into Highly Ordered Dynamin-like Oligomers

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Nuclear localization of mouse Mx1 protein is necessary for inhibition of influenza virus

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A Monomeric GTPase-Negative MxA Mutant with Antiviral Activity

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Interferon-Induced Antiviral Mx1 GTPase Is Associated with Components of the SUMO-1 System and Promyelocytic Leukemia Protein Nuclear Bodies

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Structure of mouse Mx1 protein. Molecular assembly and GTP-dependent conformational change

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Unexpected Structural Requirements for GTPase Activity of the Interferon-induced MxA Protein

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Domains Mediating Intramolecular Folding and Oligomerization of MxA GTPase

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Inhibition of Coxsackievirus B4 Replication in Stably Transfected Cells Expressing Human MxA Protein

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The dynamin A ring complex: molecular organization and nucleotide‐dependent conformational changes

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Intramolecular Backfolding of the Carboxyl-terminal End of MxA Protein Is a Prerequisite for Its Oligomerization

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Nuclear Cotransport Mechanism of Cytoplasmic Human MxB Protein

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MxA GTPase: Oligomerization and GTP-Dependent Interaction with Viral RNP Target Structures

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Antiviral determinants of rat Mx GTPases map to the carboxy-terminal half

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The dynamin superfamily: universal membrane tubulation and fission molecules?

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The interferon response circuit: Induction and suppression by pathogenic viruses

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The airway epithelium: soldier in the fight against respiratory viruses

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Mx GTPases: dynamin-like antiviral machines of innate immunity

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Multiple Anti-Interferon Actions of the Influenza A Virus NS1 Protein

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Human MxA Protein: An Interferon-Induced Dynamin-Like GTPase with Broad Antiviral Activity

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Mx Proteins: Antiviral Gatekeepers That Restrain the Uninvited

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Novel Insights into Hepatitis C Virus Replication and Persistence

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The human model: a genetic dissection of immunity to infection in natural conditions

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An Interferon-α-Induced Tethering Mechanism Inhibits HIV-1 and Ebola Virus Particle Release but Is Counteracted by the HIV-1 Vpu Protein

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An overview of polymyositis and dermatomyositis

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Enhanced type I interferon signalling promotes Th1‐biased inflammation in cutaneous lupus erythematosus

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Evasion of Influenza A Viruses from Innate and Adaptive Immune Responses

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Induction of MxA Gene Expression by Influenza A Virus Requires Type I or Type III Interferon Signaling

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Quantitative expression profiling of immune response genes in rainbow trout following infectious haematopoietic necrosis virus (IHNV) infection or DNA vaccination

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Inhibition of Infectious Pancreatic Necrosis Virus Replication by Atlantic Salmon Mx1 Protein

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Intra- and Intermolecular Domain Interactions of the C-terminal GTPase Effector Domain of the Multimeric Dynamin-like GTPase Drp1

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IFN-inducible GTPases and immunity to intracellular pathogens

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Inverse Interference: How Viruses Fight the Interferon System

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Extensive Characterization of IFN-Induced GTPases mGBP1 to mGBP10 Involved in Host Defense

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African Swine Fever Virus Multigene Family 360 and 530 Genes Affect Host Interferon Response

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IFN-λ: Novel Antiviral Cytokines

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Replication fitness determines high virulence of influenza A virus in mice carrying functional Mx1 resistance gene

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La Crosse Bunyavirus Nonstructural Protein NSs Serves To Suppress the Type I Interferon System of Mammalian Hosts

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The Mx GTPase family of interferon-induced antiviral proteins

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Mucosal Cytokine Response After Short-Term Gluten Challenge in Celiac Disease and Non-Celiac Gluten Sensitivity

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The role of type I interferons in non‐viral infections

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Interferon, Mx, and viral countermeasures

Haller, O., Kochs, G., & Weber, F. (2007) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2007.06.001 · Cited by 179 · see citing works

Nonstructural Proteins NS1 and NS2 of Bovine Respiratory Syncytial Virus Block Activation of Interferon Regulatory Factor 3

Bossert, B., Marozin, S., & Conzelmann, K. (2003) · Journal of Virology · doi:10.1128/jvi.77.16.8661-8668.2003 · Cited by 173 · see citing works

Dynamin‐related proteins and Pex11 proteins in peroxisome division and proliferation

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Tula and Puumala hantavirus NSs ORFs are functional and the products inhibit activation of the interferon‐beta promoter

Jääskeläinen, K. M., Kaukinen, P., Minskaia, E., Plyusnina, A., Vapalahti, O. P., Elliott, R. M., Weber, F., Vaheri, A. I., & Plyusnin, A. (2007) · Journal of Medical Virology · doi:10.1002/jmv.20948 · Cited by 165 · see citing works

Nrf2 expression modifies influenza A entry and replication in nasal epithelial cells

Kesic, M. J., Simmons, S. O., Bauer, R. N., & Jaspers, I. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.04.027 · Cited by 164 · see citing works

Macromolecular Transport and Signaling Through Plasmodesmata

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The Interferon-Inducible GTPases

Martens, S., & Howard, J. C. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104619 · Cited by 162 · see citing works

Antiviral effects of the interferon‐induced protein guanylate binding protein 1 and its interaction with the hepatitis C virus NS5B protein†

Itsui, Y., Sakamoto, N., Kakinuma, S., Nakagawa, M., Sekine‐Osajima, Y., Tasaka‐Fujita, M., Nishimura‐Sakurai, Y., Suda, G., Karakama, Y., Mishima, K., et al. (2009) · Hepatology · doi:10.1002/hep.23195 · Cited by 159 · see citing works

Cytokine imbalance with increased production of interferon-α in psoriasiform eruptions associated with antitumour necrosis factor-α treatments

Sénéschal, J., Milpied, B., Vergier, B., Lepreux, S., Schaeverbeke, T., & Taı̈eb, A. (2009) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2009.09329.x · Cited by 159 · see citing works

Novel functions of proteins encoded by viral stress-inducible genes

Sarkar, S. N., & Sen, G. C. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.07.007 · Cited by 157 · see citing works

The fight between the teleost fish immune response and aquatic viruses

Workenhe, S. T., Rise, M. L., Kibenge, M., & Kibenge, F. S. B. (2010) · Molecular Immunology · doi:10.1016/j.molimm.2010.06.009 · Cited by 157 · see citing works

Interferon and cytokine responses to SARS-coronavirus infection

Thiel, V., & Weber, F. (2008) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2008.01.001 · Cited by 149 · see citing works

Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

Zhu, P.-P., Patterson, A. D., Lavoie, B. A., Stadler, J., Shoeb, M., Patel, R. P., & Blackstone, C. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306702200 · Cited by 153 · see citing works

Trafficking of viral genomic RNA into and out of the nucleus: influenza, Thogoto and Borna disease viruses

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Tumor selective replication of Newcastle disease virus: Association with defects of tumor cells in antiviral defence

Fiola, C., Peeters, B. P. H., Fournier, P., Arnold, A., Bucur, M., & Schirrmacher, V. (2006) · International Journal of Cancer · doi:10.1002/ijc.21821 · Cited by 147 · see citing works

Effects of Low Concentrations of Arsenic on the Innate Immune System of the Zebrafish (Danio Rerio)

Nayak, A. S., Lage, C. R., & Kim, C. H. (2007) · Toxicological Sciences · doi:10.1093/toxsci/kfm072 · Cited by 143 · see citing works

Quantitative Proteomic Analyses of Influenza Virus-Infected Cultured Human Lung Cells

Coombs, K. M., Berard, A. R., Xu, W., Krokhin, O. V., Meng, X., Cortens, J. P., Kobasa, D., Wilkins, J. A., & Brown, E. G. (2010) · Journal of Virology · doi:10.1128/jvi.00431-10 · Cited by 141 · see citing works

Human genetics of infectious diseases: a unified theory

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The expression pattern of interferon-inducible proteins reflects the characteristic histological distribution of infiltrating immune cells in different cutaneous lupus erythematosus subsets

Wenzel, J., Zahn, S., Mikus, S., Wiechert, A., Bieber, T. R. M., & Tüting, T. (2007) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2007.08137.x · Cited by 142 · see citing works

IRG proteins: key mediators of interferon-regulated host resistance to intracellular pathogens

Taylor, G. A. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.00916.x · Cited by 139 · see citing works

Human MxA Protein Inhibits the Replication of Crimean-Congo Hemorrhagic Fever Virus

Andersson, I., Bladh, L., Mousavi‐Jazi, M., Magnusson, K., Lundkvist, Å., Haller, O., & Mirazimi, A. (2004) · Journal of Virology · doi:10.1128/jvi.78.8.4323-4329.2004 · Cited by 139 · see citing works

Expression kinetics of interferon and interferon-induced genes in Atlantic salmon (Salmo salar) following infection with infectious pancreatic necrosis virus and infectious salmon anaemia virus

McBeath, A., SNOW, M., Secombes, C. J., ELLIS, A., & Collet, B. (2006) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2006.05.004 · Cited by 138 · see citing works

Classical Swine Fever Virus Interferes with Cellular Antiviral Defense: Evidence for a Novel Function of Npro

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Nodavirus increases the expression of Mx and inflammatory cytokines in fish brain

Poisa-Beiro, L., Dios, S., Montes, A., Aranguren, R., Figueras, A. J., & Novoa, B. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.04.016 · Cited by 136 · see citing works

Scarring skin lesions of discoid lupus erythematosus are characterized by high numbers of skin-homing cytotoxic lymphocytes associated with strong expression of the type I interferon-induced protein MxA

Wenzel, J., Uerlich, M., Wörenkämper, E., Freutel, S., Bieber, T. R. M., & Tüting, T. (2005) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2005.06784.x · Cited by 136 · see citing works

Countermeasures against viral diseases of farmed fish

Kibenge, F. S. B., Godoy, M., Fast, M. D., Workenhe, S. T., & Kibenge, M. (2012) · Antiviral Research · doi:10.1016/j.antiviral.2012.06.003 · Cited by 131 · see citing works

A comprehensive map of the influenza A virus replication cycle

Matsuoka, Y., Matsumae, H., Katoh, M., Eisfeld, A. J., Neumann, G., Hase, T., Ghosh, S., Shoemaker, J. E., Lopes, T. J. S., Watanabe, T., et al. (2013) · BMC Systems Biology · doi:10.1186/1752-0509-7-97 · Cited by 132 · see citing works

Type I interferon‐associated cytotoxic inflammation in lichen planus

Wenzel, J., Scheler, M., Proelss, J., Bieber, T. R. M., & Tüting, T. (2006) · Journal of Cutaneous Pathology · doi:10.1111/j.1600-0560.2006.00527.x · Cited by 132 · see citing works

Antiviral Activity of Salmonid Gamma Interferon against Infectious Pancreatic Necrosis Virus and Salmonid Alphavirus and Its Dependency on Type I Interferon

Sun, B., Skjæveland, I., Svingerud, T., Zou, J., Jørgensen, J. B., & Robertsen, B. (2011) · Journal of Virology · doi:10.1128/jvi.00319-11 · Cited by 130 · see citing works

Type I interferon-associated skin recruitment of CXCR3+ lymphocytes in dermatomyositis

Wenzel, J., Schmidt, R., Proelss, J., Zahn, S., Bieber, T. R. M., & Tüting, T. (2006) · Clinical and Experimental Dermatology · doi:10.1111/j.1365-2230.2006.02150.x · Cited by 129 · see citing works

Dynamin as a mover and pincher during cell migration and invasion

Kruchten, A. E., & McNiven, M. A. (2006) · Journal of Cell Science · doi:10.1242/jcs.02963 · Cited by 123 · see citing works

Rhinovirus Induces Airway Epithelial Gene Expression through Double-Stranded RNA and IFN-Dependent Pathways

Chen, Y., Hamati, E., Lee, P.-K., Lee, W.-M., Wachi, S., Schnurr, D. P., Yagi, S., Dolganov, G., Boushey, H. A., Avila, P. C., et al. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2004-0417oc · Cited by 123 · see citing works

Flavonoids Activation of the Transcription Factor Nrf2 as a Hypothesis Approach for the Prevention and Modulation of SARS-CoV-2 Infection Severity

Mendonca, P., & Soliman, K. F. A. (2020) · Antioxidants · doi:10.3390/antiox9080659 · Cited by 123 · see citing works

Early antiviral response and virus-induced genes in fish

Verrier, E. R., Langevin, C., Benmansour, A., & Boudinot, P. (2011) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2011.03.012 · Cited by 121 · see citing works

Nuclear body movement is determined by chromatin accessibility and dynamics

Görisch, S. M., Wachsmuth, M., Ittrich, C., Bacher, C. P., Rippe, K., & Lichter, P. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402958101 · Cited by 120 · see citing works

Inhibition of nuclear import and cell-cycle progression by mutated forms of the dynamin-like GTPase MxB

King, M. C., Raposo, G., & Lemmon, M. A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403167101 · Cited by 118 · see citing works

Dynamin-like MxA GTPase: Structural Insights into Oligomerization and Implications for Antiviral Activity

Haller, O., Gao, S., von der Malsburg, A., Daumke, O., & Kochs, G. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.r110.145839 · Cited by 112 · see citing works

Type I Interferon Production of Plasmacytoid Dendritic Cells under Control

Bencze, D., Fekete, T., & Pázmándi, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084190 · Cited by 114 · see citing works

Missorting of LaCrosse Virus Nucleocapsid Protein by the Interferon‐Induced MxA GTPase Involves Smooth ER Membranes

Reichelt, M., Stertz, S., Krijnse‐Locker, J., Haller, O., & Kochs, G. (2004) · Traffic · doi:10.1111/j.1600-0854.2004.00219.x · Cited by 110 · see citing works

Advances in cholangiocyte immunobiology

Syal, G., Fausther, M., & Dranoff, J. A. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00227.2012 · Cited by 105 · see citing works

Differential Antiviral Response of Endothelial Cells after Infection with Pathogenic and Nonpathogenic Hantaviruses

Kraus, A., Raftery, M. J., Giese, T., Ulrich, R. G., Zawatzky, R., Hippenstiel, S., Suttorp, N., Krüger, D. H., & Schönrich, G. (2004) · Journal of Virology · doi:10.1128/jvi.78.12.6143-6150.2004 · Cited by 105 · see citing works

Hantaviral Proteins: Structure, Functions, and Role in Hantavirus Infection

Muyangwa-Semenova, M., Martynova, E. V., Khaiboullina, S. F., Morzunov, S. P., & Rizvanov, A. A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01326 · Cited by 103 · see citing works

Infectious salmon anemia virus is a powerful inducer of key genes of the type I interferon system of Atlantic salmon, but is not inhibited by interferon

Kileng, Ø., Brundtland, M. I., & Robertsen, B. (2006) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2006.11.011 · Cited by 103 · see citing works

IIGP1, an Interferon-γ-inducible 47-kDa GTPase of the Mouse, Showing Cooperative Enzymatic Activity and GTP-dependent Multimerization

Uthaiah, R. C., Praefcke, G. J. K., Howard, J. C., & Herrmann, C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211973200 · Cited by 102 · see citing works

Growth and Division of Peroxisomes

Schrader, M., & Fahimi, H. D. (2006) · International review of cytology · doi:10.1016/s0074-7696(06)55005-3 · Cited by 100 · see citing works

Type I Interferon-Associated Recruitment of Cytotoxic Lymphocytes

Wenzel, J., Bekisch, B., Uerlich, M., Haller, O., Bieber, T. R. M., & Tüting, T. (2005) · American Journal of Clinical Pathology · doi:10.1309/4ej9-kl7c-gden-vvle · Cited by 99 · see citing works

Atlantic salmon ISG15: Expression and conjugation to cellular proteins in response to interferon, double-stranded RNA and virus infections

Røkenes, T. P., LARSEN, R., & Robertsen, B. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.03.016 · Cited by 98 · see citing works

Biological markers of interferon-beta therapy: comparison among interferon-stimulated genes MxA, TRAIL and XAF-1

Gilli, F., Marnetto, F., Caldano, M., Sala, A., Malucchi, S., Capobianco, M. A. N., & Bertolotto, A. (2005) · Multiple Sclerosis Journal · doi:10.1191/135248506ms1245oa · Cited by 96 · see citing works

MxA, a Member of the Dynamin Superfamily, Interacts with the Ankyrin-like Repeat Domain of TRPC

Lussier, M. P., Cayouette, S., Lepage, P. K., Bernier, C., Francoeur, N. J., St‐Hilaire, M., Pinard, M., & Boulay, G. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m500391200 · Cited by 96 · see citing works

Evolutional Conservation of Molecular Structure and Antiviral Function of a Viral RNA Receptor, LGP2, in Japanese Flounder, Paralichthys olivaceus

Ohtani, M., Hikima, J.-I., Kondo, H., Hırono, I., Jung, T. S., & Aoki, T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001850 · Cited by 95 · see citing works

Infectious pancreatic necrosis virus suppresses type I interferon signalling in rainbow trout gonad cell line but not in Atlantic salmon macrophages

Collet, B., Munro, E. S., Gahlawat, S. K., Acosta, F., Cabrera, J. A. G., Roemelt, C., Zou, J., Secombes, C. J., & Ellis, A. E. (2006) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2006.03.011 · Cited by 94 · see citing works

Inhibition of the Type I Interferon Antiviral Response During Arenavirus Infection

Borrow, P., Martínez‐Sobrido, L., & de la Torre, J. C. (2010) · Viruses · doi:10.3390/v2112443 · Cited by 87 · see citing works

Hantavirus nucleocapsid protein: a multifunctional molecule with both housekeeping and ambassadorial duties

Kaukinen, P., Vaheri, A. I., & Plyusnin, A. (2005) · Archives of Virology · doi:10.1007/s00705-005-0555-4 · Cited by 89 · see citing works

Endogenous IFN-α Production by Plasmacytoid Dendritic Cells Exerts an Antiviral Effect on Thymic HIV-1 Infection

Gurney, K. B., Colantonio, A. D., Blom, B., Spits, H., & Uíttenbogaart, C. H. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.12.7269 · Cited by 89 · see citing works

From APOBEC to ZAP: Diverse mechanisms used by cellular restriction factors to inhibit virus infections

Chemudupati, M., Kenney, A. D., Bonifati, S., Zani, A., McMichael, T. M., Wu, L. J., & Yount, J. S. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.09.012 · Cited by 87 · see citing works

Protective role of interferon-induced Mx GTPases against influenza viruses

Haller, O., Staeheli, P., & Kochs, G. (2009) · Scientific and Technical Review (World Organisation for Animal Health) · doi:10.20506/rst.28.1.1867 · Cited by 87 · see citing works

Increased Sensitivity of Sars-Coronavirus to a Combination of Human Type I and Type II Interferons

Scagnolari, C., Vicenzi, E., Bellomi, F., Stillitano, M. G., Pinna, D., Poli, G., Clementi, M., DIANZANI, F., & Antonelli, G. (2004) · Antiviral Therapy · doi:10.1177/135965350400900618 · Cited by 87 · see citing works

Inhibition of nervous necrosis virus propagation by fish Mx proteins

Lin, C., John, J. A. C., Lin, C.-H., & Chang, C. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.063 · Cited by 86 · see citing works

The antiviral effect of interferon-beta against SARS-Coronavirus is not mediated by MxA protein

Spiegel, M., Pichlmair, A., Mühlberger, E., Haller, O., & Weber, F. (2004) · Journal of Clinical Virology · doi:10.1016/j.jcv.2003.11.013 · Cited by 85 · see citing works

Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21

Li, C.-M., Guo, M., Salas, M. C., Schupf, N., Silverman, W. P., Zigman, W. B., Husain, S., Warburton, D., Thaker, H. M., & Tycko, B. (2006) · BMC Medical Genetics · doi:10.1186/1471-2350-7-24 · Cited by 85 · see citing works

Interferon-induced Mx proteins in antiviral host defense

Haller, O., Staeheli, P., & Kochs, G. (2007) · Biochimie · doi:10.1016/j.biochi.2007.04.015 · Cited by 371 · see citing works

Assay and Functional Analysis of Dynamin‐Like Mx Proteins

Kochs, G., Reichelt, M., Danino, D., Hinshaw, J. E., & Haller, O. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)04055-3 · Cited by 44 · see citing works

Mx GTPases: efficient host defense against viral intruders.

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Human MxA Protein: An Interferon-Induced Dynamin-Like GTPase with Broad Antiviral Activity

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The Mx GTPase family of interferon-induced antiviral proteins

Haller, O., Stertz, S., & Kochs, G. (2007) · Microbes and Infection · doi:10.1016/j.micinf.2007.09.010 · Cited by 189 · see citing works