A Family of IFN-γ–Inducible 65-kD GTPases Protects Against Bacterial Infection

Human IRGM Induces Autophagy to Eliminate Intracellular Mycobacteria

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Immune Control of Tuberculosis by IFN-γ-Inducible LRG-47

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An Atg4B Mutant Hampers the Lipidation of LC3 Paralogues and Causes Defects in Autophagosome Closure

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p62 targeting to the autophagosome formation site requires self-oligomerization but not LC3 binding

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Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis

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Inborn errors of interferon (IFN)‐mediated immunity in humans: insights into the respective roles of IFN‐α/β, IFN‐γ, and IFN‐λ in host defense

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Structure of human guanylate-binding protein 1 representing a unique class of GTP-binding proteins

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Lysosomal killing of Mycobacterium mediated by ubiquitin-derived peptides is enhanced by autophagy

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Delivery of Cytosolic Components by Autophagic Adaptor Protein p62 Endows Autophagosomes with Unique Antimicrobial Properties

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The interferon-inducible p47 (IRG) GTPases in vertebrates: loss of the cell autonomous resistance mechanism in the human lineage

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Tupaia guanylate-binding protein 1 interacts with vesicular stomatitis virus phosphoprotein and represses primary transcription of the viral genome

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Heparan sulfate-dependent RAGE oligomerization is indispensable for pathophysiological functions of RAGE

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Caspase-11 drives macrophage hyperinflammation in models of Polg-related mitochondrial disease

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Context-enriched interactome powered by proteomics helps the identification of novel regulators of macrophage activation

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Type I IFNs facilitate innate immune control of the opportunistic bacteria Burkholderia cenocepacia in the macrophage cytosol

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Antibody-Mediated LILRB2-Receptor Antagonism Induces Human Myeloid-Derived Suppressor Cells to Kill Mycobacterium tuberculosis

Singh, V. K., Khan, A., Xu, Y., Mai, S., Zhang, L., Mishra, A., Restrepo, B. I., Pan, P., Chen, S., & Jagannath, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.865503 · Cited by 14

Transcriptome profiling and differential expression analysis of altered immune-related genes in goldfish (Carassius auratus) infected with Aeromonas hydrophila

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Safe haven under constant attack-TheChlamydia-containing vacuole

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C57BL/6 and 129 inbred mouse strains differ in Gbp2 and Gbp2b expression in response to inflammatory stimuli in vivo

Clough, B., Finethy, R., Khan, R. T., Fisch, D., Jordan, S., Patel, H., Coers, J., & Frickel, E.-M. (2019) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15329.1 · Cited by 14

Mycobacterial Cord Factor Reprograms the Macrophage Response to IFN-γ towards Enhanced Inflammation yet Impaired Antigen Presentation and Expression of GBP1

Huber, A., Killy, B., Grummel, N., Bodendorfer, B., Paul, S., Wiesmann, V., Naschberger, E., Zimmer, J., Wirtz, S. J., Schleicher, U., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000337 · Cited by 14

Porcine reproductive and respiratory syndrome virus non-structural protein 4 cleaves guanylate-binding protein 1 via its cysteine proteinase activity to antagonize GBP1 antiviral effect

Duan, H. Q., Dong, H., Wu, S., Ren, J., Zhang, M., Chen, C., Du, Y., Zhang, G., & Zhang, A. (2022) · Veterinary Research · doi:10.1186/s13567-022-01071-8 · Cited by 13

Guanylate-binding protein-5 is involved in inflammasome activation by bacterial DNA but only the cooperation of multiple GBPs accounts for control of Brucella abortus infection

Marinho, F. V., Brito, C. F., de Araujo, A. C. V. S. C., & Oliveira, S. C. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1341464 · Cited by 13

Utilizing AI for the Identification and Validation of Novel Therapeutic Targets and Repurposed Drugs for Endometriosis

Liu, B. H. M., Lin, Y., Long, X., Hung, S. W., Gaponova, A. V., Ren, F., Zhavoronkov, A. A., Pun, F. W., & Wang, C. C. (2024) · Advanced Science · doi:10.1002/advs.202406565 · Cited by 16

Elimination of intracellularly residingMycobacterium tuberculosisthrough targeting of host and bacterial signaling mechanisms

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Recombinant BCG-LTAK63 Vaccine Candidate for Tuberculosis Induces an Inflammatory Profile in Human Macrophages

dos Santos, C. C., Walburg, K. V., van Veen, S., Wilson, L. G., Trufen, C. E. M., Nascimento, I. P., Ottenhoff, T. H. M., Leite, L. C. C., & Haks, M. C. (2022) · Vaccines · doi:10.3390/vaccines10060831 · Cited by 13

Restricting genomic actions of innate immune mediators on fetal hematopoietic progenitor cells

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Guanylate-Binding Proteins: Niche Recruiters for Antimicrobial Effectors

Dupont, C. D., & Hunter, C. A. (2012) · Immunity · doi:10.1016/j.immuni.2012.08.005 · Cited by 13

Cryo-ET of a human GBP coatomer governing cell-autonomous innate immunity to infectionPreprint

Zhu, S., Bradfield, C. J., Mamińska, A., Park, E., Kim, B.-H., Kumar, P., Huang, S., Zhang, Y., Bewersdorf, J., & MacMicking, J. D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.26.457804 · Cited by 13

Domain motions, dimerization, and membrane interactions of the murine guanylate binding protein 2

Loschwitz, J., Steffens, N., Wang, X., Schäffler, M., Pfeffer, K., Degrandi, D., & Strodel, B. (2023) · Scientific Reports · doi:10.1038/s41598-023-27520-8 · Cited by 12

Type I interferons induce guanylate-binding proteins and lysosomal defense in hepatocytes to control malaria

Marques-da-Silva, C., Schmidt-Silva, C., Bowers, C., Charles-Chess, N. A. E., Samuel, C., Shiau, J. C., Park, E., Yuan, Z., Kim, B.-H., Kyle, D. E., et al. (2025) · Cell Host & Microbe · doi:10.1016/j.chom.2025.03.008 · Cited by 12

IFN-γ-induced macrophage antileishmanial mechanisms in mice: A role for immunity-related GTPases, Irgm1 and Irgm3, in Leishmania donovani infection in the liver

Murray, H. W., Mitchell-Flack, M., Taylor, G. A., & Ma, X. (2015) · Experimental Parasitology · doi:10.1016/j.exppara.2015.07.005 · Cited by 12

Knockdown of GBP1 inhibits BCG-induced apoptosis in macrophage RAW 264.7 cells via p38/JNK pathway

Wang, J., Liu, Z., Wu, L., Yu, J., & Zhang, D. (2021) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2021.105158 · Cited by 12

Guanylate-Binding protein 2b regulates the AMPK/mTOR/ULK1 signalling pathway to induce autophagy during Mycobacterium bovis infection

Yu, Y., Pan, J., Liu, M., Jiang, H., Xiong, J., Tao, L., Xue, F., Tang, F., Wang, H., & Dai, J. (2022) · Virulence · doi:10.1080/21505594.2022.2073024 · Cited by 12

Tumor suppressor p53 protects mice against Listeria monocytogenes infection

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ERAP1 and PDE8A Are Downregulated in Cattle Protected against Bovine Tuberculosis

Blanco, F. C., Soria, M. A., Klepp, L. I., & Bigi, F. (2017) · Microbial Physiology · doi:10.1159/000479183 · Cited by 12

Caspase-4 binds to LPS membranes with positive curvature for non-canonical inflammasome activation

Began, J., Boegli, A., Anton, L., Biriukov, D., Vairamuthu, J., Santos, J. C., & Brož, P. (2026) · Immunity · doi:10.1016/j.immuni.2025.12.017 · Cited by 13

Identification of human guanylate-binding protein 1 gene (hGBP1) as a direct transcriptional target gene of p53

Zhu, Z., Wei, J., Shi, Z., Yang, Y., Shao, D., Li, B., Wang, X., & Ma, Z. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.05.074 · Cited by 11

Effects of Bacillus cereus PAS38 on Immune-Related Differentially Expressed Genes of Spleen in Broilers

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TMT-based quantitative proteomic analysis reveals the spleen regulatory network of dexamethasone-induced immune suppression in chicks

Guo, Y., Su, A., Tian, H., Ding, M., Wang, Y., Tian, Y., Li, K., Sun, G., Jiang, R., Han, R., et al. (2021) · Journal of Proteomics · doi:10.1016/j.jprot.2021.104353 · Cited by 11

Interferon inducible guanylate binding protein 1 restricts the growth of Leishmania donovani by modulating the level of cytokines/chemokines and MAP kinases

Kumar, R., & Kushawaha, P. K. (2022) · Microbial Pathogenesis · doi:10.1016/j.micpath.2022.105568 · Cited by 10

Lactoferrin deficiency during lactation increases the risk of depressive-like behavior in adult mice

Wang, W., Cheng, Z., Wang, X., An, Q., Huang, K., Dai, Y., Meng, Q., & Zhang, Y. (2023) · BMC Biology · doi:10.1186/s12915-023-01748-2 · Cited by 10

An Update on the Study of the Molecular Mechanisms Involved in Autophagy during Bacterial Pathogenesis

Rahman, M. A., Sarker, A., Ayaz, M., Shatabdy, A. R., Haque, N., Jalouli, M., Rahman, M. H., Mou, T. J., Dey, S. K., Apu, E. H., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12081757 · Cited by 11

Immobilization of Biotinylated hGBP1 in a Defined Orientation on Surfaces Is Crucial for Uniform Interaction with Analyte Proteins and Catalytic Activity

Syguda, A., Kerstan, A., Ladnorg, T., Stüben, F., Wöll, C., & Herrmann, C. (2012) · Langmuir · doi:10.1021/la3008359 · Cited by 10

Pathogenic Biohacking: Induction, Modulation and Subversion of Host Transcriptional Responses by Listeria monocytogenes

Eldridge, M. J. G., Cossart, P., & Hamon, M. A. (2020) · Toxins · doi:10.3390/toxins12050294 · Cited by 11

Inflammasomes primarily restrict cytosolic Salmonella replication within human macrophagesPreprint

Egan, M. S., O'Rourke, E. A., Mageswaran, S. K., Zuo, B., Martynyuk, I., Demissie, T., Hunter, E. N., Bass, A. R., Chang, Y., Brodsky, I. E., et al. (2023) · eLife · doi:10.7554/elife.90107 · Cited by 10

Activation and manipulation of inflammasomes and pyroptosis during bacterial infections

Bernard, E. M., & Brož, P. (2022) · Biochemical Journal · doi:10.1042/bcj20220051 · Cited by 10

Syntaxin 11 Contributes to the Interferon-Inducible Restriction of Coxiella burnetii Intracellular Infection

Ganesan, S., Alvarez, N. N., Steiner, S., Fowler, K. M., Corona, A. K., & Roy, C. R. (2023) · mBio · doi:10.1128/mbio.03545-22 · Cited by 9

Biochemical and structural characterization of murine GBP7, a guanylate binding protein with an elongated C-terminal tail

Legewie, L., Loschwitz, J., Steffens, N., Prescher, M., Wang, X., Smits, S. H. J., Schmitt, L., Strodel, B., Degrandi, D., & Pfeffer, K. (2019) · Biochemical Journal · doi:10.1042/bcj20190364 · Cited by 9

IFN-induced cell-autonomous immune mechanisms in the control of intracellular protozoa

Skariah, S., Sultan, A. A., & Mordue, D. G. (2022) · Parasitology Research · doi:10.1007/s00436-022-07514-7 · Cited by 10

A new blood-based RNA signature (R9), for monitoring effectiveness of tuberculosis treatment in a South Indian longitudinal cohort

Thakur, C., Tripathi, A. P., Ravichandran, S., Shivananjaiah, A., Chakraborty, A., Varadappa, S., Chikkavenkatappa, N., Nagarajan, D., Lakshminarasimhaiah, S., Singh, A., et al. (2022) · iScience · doi:10.1016/j.isci.2022.103745 · Cited by 8

Genetic polymorphisms of inflammatory and bone metabolism related proteins in a population with dental implants of the Basque Country. A case-control study

de Mendoza, I. L., Marichalar‐Mendía, X., Setien‐Olarra, A., García-De-La-Fuente, A.-M., Llamosas, R. M.-C., & Aguirre‐Urizar, J. M. (2024) · BMC Oral Health · doi:10.1186/s12903-024-04319-1 · Cited by 9

The ΔfbpAΔsapM candidate vaccine derived from Mycobacterium tuberculosis H37Rv is markedly immunogenic in macrophages and induces robust immunity to tuberculosis in mice

Mishra, A., Khan, A., Singh, V. K., Glyde, E. F., Saikolappan, S., Garnica, O., Das, K., Veerapandian, R., Dhandayuthapani, S., & Jagannath, C. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1321657 · Cited by 8

Restriction and evasion: a review of IFNγ-mediated cell-autonomous defense pathways during genital Chlamydia infection

Reitano, J. R., & Coers, J. (2024) · Pathogens and Disease · doi:10.1093/femspd/ftae019 · Cited by 9

Cellular and molecular determinants of bacterial burden in leprosy granulomas revealed by single-cell multimodal omics

Mi, Z., Wang, Z., Wang, Y., Xue, X., Liao, X., Wang, C., Sun, L., Lin, Y., Wang, J., Guo, D., et al. (2024) · EBioMedicine · doi:10.1016/j.ebiom.2024.105342 · Cited by 8

Antigen-specific CD4+ T cells promote monocyte recruitment and differentiation into glycolytic lung macrophages to control Mycobacterium tuberculosis

Becker, S. H., Ronayne, C. E., Bold, T. D., & Jenkins, M. K. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013208 · Cited by 11

Guanylate‐binding protein 5‐mediated cell‐autonomous immunity suppresses inflammation in dental pulpitis: An in vitro study

Huang, M., Zhan, C., Yang, B., Lu, Y., Yang, X., & Hou, J. L. (2023) · International Endodontic Journal · doi:10.1111/iej.14006 · Cited by 8

Bacteria disarm host-defence proteins

MacMicking, J. D. (2017) · Nature · doi:10.1038/nature24157 · Cited by 8

Immunoprotective Effects of Two Histone H2A Variants in the Grass Carp Against Flavobacterium columnare Infection

Yang, Y. Y., Zheng, S. Y., Fang, H., Wu, X. M., Zhang, J., & Chang, M. X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.939464 · Cited by 8

Select Inflammasome Assembly

Caffrey, D. R., & Fitzgerald, K. A. (2012) · Science · doi:10.1126/science.1222362 · Cited by 8

A hierarchical GBP network promotes cytosolic LPS recognition and sepsisPreprint

Park, E., Kim, B.-H., Kumar, P., Tretina, K., Mamińska, A., Philbrick, W. M., Flavell, R. A., & MacMicking, J. D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.25.457662 · Cited by 7

Single-cell analysis of graft-infiltrating host cells identifies caspase-1 as a potential therapeutic target for heart transplant rejection

Wu, Z., Liang, J., Zhu, S., Liu, N., Zhao, M., Xiao, F., Li, G., Yu, C., Jin, C., Ma, J., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1251028 · Cited by 7

Hycanthone Inhibits Inflammasome Activation and Neuroinflammation-Induced Depression-Like Behaviors in Mice

Boo, K.-J., Gonzales, E. L., Remonde, C. G., Seong, J. Y., Jeon, S. J., Park, Y., Ham, B., & Shin, C. Y. (2022) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2022.073 · Cited by 7

Markers of immune dysregulation in response to the ageing gut: insights from aged murine gut microbiota transplants

Giannos, P., Prokopidis, K., Isanejad, M., & Wright, H. L. (2022) · BMC Gastroenterology · doi:10.1186/s12876-022-02613-2 · Cited by 7

Demarcation of Viral Shelters Results in Destruction by Membranolytic GTPases: Antiviral Function of Autophagy Proteins and Interferon‐Inducible GTPases

Brown, H. M., Biering, S. B., Zhu, A. C., Choi, J., & Hwang, S. (2018) · BioEssays · doi:10.1002/bies.201700231 · Cited by 7

Autophagy and Noroviruses

Furlong, K., & Hwang, S. (2019) · Viruses · doi:10.3390/v11030244 · Cited by 7

Interferon inducible guanylate‐binding protein 1 modulates the lipopolysaccharide‐induced cytokines/chemokines and mitogen‐activated protein kinases in macrophages

Kumar, R., & Kushawaha, P. K. (2024) · Microbiology and Immunology · doi:10.1111/1348-0421.13123 · Cited by 6

Dual mechanism of inflammation sensing by the hematopoietic progenitor genome

Tran, V. L., Liu, P., Katsumura, K. R., Soukup, A. A., Kopp, A., Ahmad, Z. S., Mattina, A. E., Brand, M., Johnson, K. D., & Bresnick, E. H. (2025) · Science Advances · doi:10.1126/sciadv.adv3169 · Cited by 6

Crystal structures reveal nucleotide-induced conformational changes in G motifs and distal regions in human guanylate-binding protein 2

Roy, S., Wang, B., Roy, K., Tian, Y., Bhattacharya, M., Williams, S., & Yin, Q. (2025) · Communications Biology · doi:10.1038/s42003-025-07727-3 · Cited by 6

Observation of autophagosome maturation in the interferon-γ-primed and lipopolysaccharide-activated macrophages using a tandem fluorescent tagged LC3

Fujiwara, E., Washi, Y., & Matsuzawa, T. (2013) · Journal of Immunological Methods · doi:10.1016/j.jim.2013.05.009 · Cited by 6

Guanylate-Binding Protein 1 Regulates Infection-Induced Autophagy through TBK1 Phosphorylation

Hikichi, M., Toh, H., Minowa‐Nozawa, A., Nozawa, T., & Nakagawa, I. (2022) · Cellular Microbiology · doi:10.1155/2022/8612113 · Cited by 6

Class Ⅰ histone deacetylase inhibitor regulate of Mycobacteria–Driven guanylate-binding protein 1 gene expression

Wei, M., Qin, Y., Qian, K., Shang, S., Zhao, Y., Xie, T., Xi, J., & Tang, B. (2022) · Microbial Pathogenesis · doi:10.1016/j.micpath.2022.105655 · Cited by 7

Mouse guanylate‐binding protein 1 does not mediate antiviral activity against influenza virus in vitro or in vivo

Tessema, M. B., Tuipulotu, D. E., Oates, C. V. L., Brööks, A. G., Man, S. M., Londrigan, S. L., & Reading, P. C. (2023) · Immunology and Cell Biology · doi:10.1111/imcb.12627 · Cited by 6

GBPs take AIM at Francisella

Fitzgerald, K. A., & Rathinam, V. A. K. (2015) · Nature Immunology · doi:10.1038/ni.3144 · Cited by 6

Genome-Wide Profiling of In Vivo LPS-Responsive Genes in Splenic Myeloid Cells

Lee, M. S., Kim, B., Lee, S.-M., Cho, W.-C., Lee, W., Kang, J.-S., Choi, U. Y., Lyu, J., & Kim, Y.-J. (2013) · Molecules and Cells · doi:10.1007/s10059-013-2349-y · Cited by 7

Crossing the Rubicon: New Roads Lead to Host Defense

Bradfield, C. J., Kim, B.-H., & MacMicking, J. D. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.02.005 · Cited by 7

Meta-Analysis of Pulmonary Transcriptomes from Differently Primed Mice Identifies Molecular Signatures to Differentiate Immune Responses following Bordetella pertussis Challenge

Raeven, R. H. M., Pennings, J. L. A., van Riet, E., Kersten, G. F. A., & Metz, B. (2017) · Journal of Immunology Research · doi:10.1155/2017/8512847 · Cited by 6

Identification of compounds that decrease numbers of Mycobacteria in human macrophages in the presence of serum amyloid P

Xiang, W., Cox, N., & Gomer, R. H. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.1a0317-118rr · Cited by 6

Identification of key genes and pathways in regulating immune‑induced diseases of dendritic cells by bioinformatic analysis

Zheng, Y., Zheng, X., Li, S., Zhang, H., Liu, M., Yang, Q., Zhang, M., Sun, Y., Wu, J., & Yu, B. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.8834 · Cited by 6

Guanylate-Binding Protein 1 Promotes Migration and Invasion of Human Periodontal Ligament Stem Cells

Bai, S., Chen, T., & Deng, X. (2018) · Stem Cells International · doi:10.1155/2018/6082956 · Cited by 6

A chronic hypoxic response in photoreceptors alters the vitreous proteome in mice

Schori, C., Trachsel, C., Grossmann, J., Barben, M., Klee, K., Storti, F., Samardzija, M., & Grimm, C. (2019) · Experimental Eye Research · doi:10.1016/j.exer.2019.107690 · Cited by 6

Emerging Roles of Autophagy in the Stressed Kidney Allograft

Pallet, N. (2013) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2013.11.006 · Cited by 6

Proteomic analysis of chicken bone marrow-derived dendritic cells in response to an inactivated IBV + NDV poultry vaccine

van den Biggelaar, R. H. G. A., van der Maas, L., Meiring, H. D., Pennings, J. L. A., van Eden, W., Rutten, V. P. M. G., & Jansen, C. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-89810-3 · Cited by 6

Precision tumor immunotherapy via a dual-gated macrophage–bacterial activation platform

Li, L., Wu, L., Qiao, L., Zhang, S., Luan, X., Qiu, J., Qiao, X., Li, C., Sun, Y., Wang, B., et al. (2025) · Trends in biotechnology · doi:10.1016/j.tibtech.2025.09.013 · Cited by 5

Clearance of bacteria from lymph nodes in sheep immunized with Brucella suis S2 vaccine is associated with M1 macrophage activation

Chen, S., Chen, Y., Jiao, Z., Wang, C., Zhao, D., Liu, Y., Zhang, W., Zhao, S., Yang, B., Zhao, Q., et al. (2023) · Veterinary Research · doi:10.1186/s13567-023-01147-z · Cited by 5

Genome-wide association with footrot in hair and wool sheep

Çınar, M. U., Oliveira, R. D., Hadfield, T. S., Lichtenwalner, A. B., Brzozowski, R. J., Settlemire, C. T., Schoenian, S., Parker, C., Neibergs, H. L., Cockett, N. E., et al. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2023.1297444 · Cited by 6

Role of guanylate-binding protein 5 in inflammatory diseases, immune diseases, cancers, and its potential therapeutic implications

Sun, X., Jin, G., Zhou, H., Wang, Y., Dai, F., & Zhou, G. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-01727-9 · Cited by 6

Autophagy: the misty lands of Chlamydia trachomatis infection

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GBP1 recruitment to actin-rich pedestals of extracellular Gram-negative bacteria promotes pyroptosis

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Deciphering the origins of guanylate-binding proteins in mammals (Monotreme, Marsupials and Placentals)

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This Week in Science

(2011) · Science · doi:10.1126/science.2011.332.6030.twis

A Cluster of Interferon-γ-Inducible p65 GTPases Plays a Critical Role in Host Defense against Toxoplasma gondii

Yamamoto, M., Okuyama, M., Su, J., Kimura, T., Kamiyama, N., Saiga, H., Ohshima, J., Sasai, M., Kayama, H., Okamoto, T., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.06.009 · Cited by 334

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

Degrandi, D., Konermann, C., Beuter-Gunia, C., Kresse, A., Wuerthner, J., Kurig, S., Beer, S., & Pfeffer, K. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.11.7729 · Cited by 209

ID: 165

Pfeffer, K., Degrandi, D., & Kravets, E. (2015) · Cytokine · doi:10.1016/j.cyto.2015.08.036

IFN-Inducible GTPases in Host Cell Defense

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