Immunological Variation Between Inbred Laboratory Mouse Strains: Points to Consider in Phenotyping Genetically Immunomodified Mice

Pattern Recognition Receptors and Inflammation

Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631

Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells

Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992

Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages

Harrington, L. E., Hatton, R. D., Mangan, P. R., Turner, H., Murphy, T. L., Murphy, K. M., & Weaver, C. T. (2005) · Nature Immunology · doi:10.1038/ni1254 · Cited by 4,742

M-1/M-2 Macrophages and the Th1/Th2 Paradigm

Mills, C. D., Kincaid, K., Alt, J. M., Heilman, M. J., & Hill, A. M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.12.6166 · Cited by 3,287

MicroRNAs Modulate Hematopoietic Lineage Differentiation

Chen, C.-Z., Li, L., Lodish, H. F., & Bartel, D. P. (2004) · Science · doi:10.1126/science.1091903 · Cited by 3,257

Immunol. Cell Biol.

Fitzgerald, M., Hayward, I. P., Thomas, A. C., Campbell, J. H., & CAMPBELL, G. R. (1995) · Cited by 2,552

NALP3 Forms an IL-1β-Processing Inflammasome with Increased Activity in Muckle-Wells Autoinflammatory Disorder

Agostini, L., Martinon, F., Burns, K., McDermott, M. F., Hawkins, P. N., & Tschopp, J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00046-9 · Cited by 1,768

Trained Immunity: A Memory for Innate Host Defense

Netea, M. G., Quintin, J., & van der Meer, J. W. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.04.006 · Cited by 1,760

Signalling through C-type lectin receptors: shaping immune responses

Geijtenbeek, T. B. H., & Gringhuis, S. I. (2009) · Nature reviews. Immunology · doi:10.1038/nri2569 · Cited by 1,449

FELASA recommendations for the health monitoring of mouse, rat, hamster, guinea pig and rabbit colonies in breeding and experimental units

FELASA working group on revision of guidelines for health monitoring of rodents and rabbits, Mähler (Convenor), M., Berard, M., Feinstein, R., Gallagher, A., Illgen-Wilcke, B., Pritchett-Corning, K., & Raspa, M. (2014) · Laboratory Animals · doi:10.1177/0023677213516312 · Cited by 646

Cross-Species Single-Cell Analysis Reveals Divergence of the Primate Microglia Program

Geirsdottir, L., David, E., Keren-Shaul, H., Weiner, A., Bohlen, S. C., Neuber, J., Balic, A., Giladi, A., Sheban, F., Dutertre, C.-A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.11.010 · Cited by 461

Heterogeneity of the gut microbiome in mice: guidelines for optimizing experimental design

Laukens, D., Brinkman, B. M. N., Raes, J., Vos, M. D., & Vandenabeele, P. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv036 · Cited by 402

Development of Immunotherapy Combination Strategies in Cancer

Yap, T. A., Parkes, E. E., Peng, W., Moyers, J. T., Curran, M. A., & Tawbi, H. A. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-1209 · Cited by 352

Meta-analysis of clinical and preclinical studies comparing the anticancer efficacy of liposomal versus conventional non-liposomal doxorubicin

Petersen, G. H., Alzghari, S. K., Chee, W., Sankari, S. S., & La-Beck, N. M. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.04.028 · Cited by 291

The comparative immunology of wild and laboratory mice, Mus musculus domesticus

Abolins, S., King, E. C., Lazarou, L., Weldon, L., Hughes, L., Drescher, P., Raynes, J. G., Hafalla, J. C. R., Viney, M., & Riley, E. M. (2017) · Nature Communications · doi:10.1038/ncomms14811 · Cited by 294

Platelets in Sepsis: An Update on Experimental Models and Clinical Data

Assinger, A., Schrottmaier, W. C., Salzmann, M., & Rayes, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01687 · Cited by 294

Practical murine hematopathology: a comparative review and implications for research.

O'Connell, K. E., Mikkola, A. M., Stepanek, A. M., Vernet, A., Hall, C. D., Sun, C. C., Yildirim, E., Staropoli, J. F., Lee, J. T., & Brown, D. E. (2015) · PubMed Central · Cited by 259

Age-Associated Resident Memory CD8 T Cells in the Central Nervous System Are Primed To Potentiate Inflammation after Ischemic Brain Injury

Ritzel, R. M., Crapser, J. D., Patel, A. R., Verma, R., Grenier, J. M., Chauhan, A., Jellison, E. R., & McCullough, L. D. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502021 · Cited by 187

Heterogeneity in the lymphatic vascular system and its origin

Ulvmar, M. H., & Mäkinen, T. (2016) · Cardiovascular Research · doi:10.1093/cvr/cvw175 · Cited by 168

Leukocyte infiltration in experimental stroke

Sørensen, N. V., Johansen, F. F., Kristiansen, U., & Hasseldam, H. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-115 · Cited by 163

Murine Models of Sepsis and Trauma: Can We Bridge the Gap?

Stortz, J. A., Raymond, S. L., Mira, J. C., Moldawer, L. L., Mohr, A. M., & Efron, P. A. (2017) · ILAR Journal · doi:10.1093/ilar/ilx007 · Cited by 171

Mouse Models of Acute Respiratory Distress Syndrome

Aeffner, F., Bolon, B. N., & Davis, I. C. (2015) · Toxicologic Pathology · doi:10.1177/0192623315598399 · Cited by 157

Dual roles of neutrophils in metastatic colonization are governed by the host NK cell status

Li, P., Lü, M., Shi, J., Hua, L., Gong, Z., Li, Q., Shultz, L. D., & Ren, G. (2020) · Nature Communications · doi:10.1038/s41467-020-18125-0 · Cited by 152

Integrative Physiology: At the Crossroads of Nutrition, Microbiota, Animal Physiology, and Human Health

Leulier, F., MacNeil, L. T., Lee, W., Rawls, J. F., Cani, P. D., Schwarzer, M., Zhao, L., & Simpson, S. J. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.02.001 · Cited by 152

The Antitumor Activity of Combinations of Cytotoxic Chemotherapy and Immune Checkpoint Inhibitors Is Model-Dependent

Grasselly, C., Denis, M., Bourguignon, A., Talhi, N., Mathé, D., Tourette, A., Serre, L., Jordheim, L. P., Matera, E. L., & Dumontet, C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02100 · Cited by 129

Complement-dependent synapse loss and microgliosis in a mouse model of multiple sclerosis

Hammond, J. W., Bellizzi, M. J., Ware, C., Qiu, W. Q., Saminathan, P., Li, H., Luo, S., Ma, S. A., Li, Y., & Gelbard, H. A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.03.004 · Cited by 118

Characterization of immune cell subtypes in three commonly used mouse strains reveals gender and strain-specific variations

Hensel, J. A., Khattar, V., Ashton, R., & Ponnazhagan, S. (2018) · Laboratory Investigation · doi:10.1038/s41374-018-0137-1 · Cited by 114

The CTLA-4 x OX40 bispecific antibody ATOR-1015 induces anti-tumor effects through tumor-directed immune activation

Kvarnhammar, A. M., Veitonmäki, N., Hägerbrand, K., Dahlman, A., Smith, K. E., Fritzell, S., von Schantz, L., Thagesson, M., Werchau, D., Smedenfors, K., et al. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0570-8 · Cited by 116

Safe Recombinant Outer Membrane Vesicles that Display M2e Elicit Heterologous Influenza Protection

Watkins, H. C., Rappazzo, C. G., Higgins, J. S., Sun, X., Brock, N., Chau, A., Misra, A., Cannizzo, J. P. B., King, M. R., Maines, T. R., et al. (2017) · Molecular Therapy · doi:10.1016/j.ymthe.2017.01.010 · Cited by 109

Immunopathology of RSV: An Updated Review

Bergeron, H. C., & Tripp, R. A. (2021) · Viruses · doi:10.3390/v13122478 · Cited by 116

Effects of Influenza on Alveolar Macrophage Viability Are Dependent on Mouse Genetic Strain

Califano, D., Furuya, Y., & Metzger, D. W. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701406 · Cited by 88

Cancer nanomedicine and the complement system activation paradigm: Anaphylaxis and tumour growth

Moghimi, S. M. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.03.051 · Cited by 87

Cell-Based Delivery of Interleukin-13 Directs Alternative Activation of Macrophages Resulting in Improved Functional Outcome after Spinal Cord Injury

Dooley, D., Lemmens, E., Vangansewinkel, T., Blon, D. L., Hoornaert, C., Ponsaerts, P., & Hendrix, S. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.11.005 · Cited by 89

Use of C57BL/6N mice on the variety of immunological researches

Song, H. K., & Hwang, D. Y. (2017) · Laboratory Animal Research · doi:10.5625/lar.2017.33.2.119 · Cited by 87

Translating Mouse Models

Sellers, R. S. (2016) · Toxicologic Pathology · doi:10.1177/0192623316675767 · Cited by 83

Just so stories: The random acts of anti-cancer nanomedicine performance

Moghimi, S. M., & Farhangrazi, Z. S. (2014) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2014.04.011 · Cited by 75

Translational Animal Models of Atopic Dermatitis for Preclinical Studies.

Martel, B. C., Lovato, P., Bäumer, W., & Olivry, T. (2017) · Europe PMC (PubMed Central) · Cited by 74

Microbial Regulation of Enteric Eosinophils and Its Impact on Tissue Remodeling and Th2 Immunity

Jiménez‐Saiz, R., Anipindi, V. C., Galipeau, H. J., Ellenbogen, Y., Chaudhary, R., Koenig, J. F. E., Gordon, M. E., Walker, T. D., Mandur, T. S., Abed, S., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00155 · Cited by 61

Animal models for analysis of immunological responses to nanomaterials: Challenges and considerations

Zamboni, W. C., Szebeni, J., Kozlov, S., Lucas, A. T., Piscitelli, J. A., & Dobrovolskaia, M. A. (2018) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.09.012 · Cited by 63

Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease

McCarthy, G. M., Blasio, A., Donovan, O. G., Schaller, L. B., Bock-Hughes, A., Magraner, J. M., Suh, J. H., Tattersfield, C. F., Stillman, I. E., Shah, S. S., et al. (2021) · Disease Models & Mechanisms · doi:10.1242/dmm.048952 · Cited by 64

Advances in Rodent Experimental Models of Sepsis

Cai, L., Rodgers, E. G., Schoenmann, N., & Raju, R. P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119578 · Cited by 66

Reassessing the Evolutionary Importance of Inflammasomes

Maltez, V. I., & Miao, E. A. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502060 · Cited by 62

Defects in intracellular trafficking of fungal cell wall synthases lead to aberrant host immune recognition

Esher, S. K., Ost, K. S., Kohlbrenner, M. A., Pianalto, K. M., Telzrow, C. L., Campuzano, A., Nichols, C. B., Munro, C. A., Wormley, F. L., & Alspaugh, J. A. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007126 · Cited by 55

Human microbiota-transplanted C57BL/6 mice and offspring display reduced establishment of key bacteria and reduced immune stimulation compared to mouse microbiota-transplantation

Lundberg, R., Toft, M., Metzdorff, S. B., Hansen, C. H. F., Licht, T. R., Bahl, M. I., & Hansen, A. K. (2020) · Scientific Reports · doi:10.1038/s41598-020-64703-z · Cited by 59

Advances in Preclinical Research Models of Radiation-Induced Cardiac Toxicity

Schlaak, R. A., SenthilKumar, G., Boerma, M., & Bergom, C. R. (2020) · Cancers · doi:10.3390/cancers12020415 · Cited by 62

Clinically relevant preclinical animal models for testing novel cranio‐maxillofacial bone 3D‐printed biomaterials

Hatt, L. P., Thompson, K., Helms, J. A., Stoddart, M. J., & Armiento, A. R. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.690 · Cited by 62

The Expression of Toll-like Receptors in Normal Human and Murine Gastrointestinal Organs and the Effect of Microbiome and Cancer

Huhta, H. I., Helminen, O., Kauppila, J. H., Salo, T. A., Porvari, K., Saarnio, J., Lehenkari, P. P., & Karttunen, T. J. (2016) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155416656154 · Cited by 55

Salmonella enterica Causes More Severe Inflammatory Disease in C57/BL6 Nramp1 G169 Mice Than Sv129S6 Mice

Brown, D. E., Libby, S. J., Moreland, S. M., McCoy, M. W., Brabb, T., Stepanek, A., Fang, F. C., & Detweiler, C. S. (2013) · Veterinary Pathology · doi:10.1177/0300985813478213 · Cited by 48

NLRP6 modulates neutrophil homeostasis in bacterial pneumonia-derived sepsis

Cai, S., Paudel, S., Jin, L., Ghimire, L., Taylor, C. M., Wakamatsu, N., Bhattarai, D., & Jeyaseelan, S. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-00357-4 · Cited by 52

Autoimmunity linked protein phosphatase PTPN22 as a target for cancer immunotherapy

Cubas, R. A., Khan, Z., Gong, Q., Москаленко, М., Xiong, H., Ou, Q., Pai, C., Rodriguez, R., Cheung, J., & Chan, A. C. (2020) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2020-001439 · Cited by 49

Genomic copy number variation in Mus musculus

Locke, M. E. O., Milojevic, M., Eitutis, S. T., Patel, N., Wishart, A. E., Daley, M., & Hill, K. A. (2015) · BMC Genomics · doi:10.1186/s12864-015-1713-z · Cited by 51

Faithful preclinical mouse models for better translation to bedside in the field of immuno-oncology

Saito, R., Kobayashi, T., Kashima, S., Matsumoto, K., & Ogawa, O. (2019) · International Journal of Clinical Oncology · doi:10.1007/s10147-019-01520-z · Cited by 53

Immunobiology of Crimean-Congo hemorrhagic fever

Rodriguez, S. E., Hawman, D. W., Sorvillo, T. E., O’Neal, J. T., Bird, B. H., Rodrı́guez, L. L., Bergeron, É., Nichol, S. T., Montgomery, J. M., Spiropoulou, C. F., et al. (2022) · Antiviral Research · doi:10.1016/j.antiviral.2022.105244 · Cited by 48

A Focus on “Bio” in Bio–Nanoscience: The Impact of Biological Factors on Nanomaterial Interactions

Cortez‐Jugo, C., Czuba‐Wojnilowicz, E., Tan, A. E. Q., & Caruso, F. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202100574 · Cited by 46

Gut microbiota and host genetics modulate the effect of diverse diet patterns on metabolic health

Huda, M. N., Salvador, A. C., Barrington, W. T., Gacasan, C. A., D’Souza, E. M., Ramirez, L. D., Threadgill, D. W., & Bennett, B. J. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.896348 · Cited by 51

Intestinal dysbiosis promotes epithelial-mesenchymal transition by activating tumor-associated macrophages in ovarian cancer

Xu, S., Liu, Z., Lv, M., Chen, Y., & Liu, Y. (2019) · Pathogens and Disease · doi:10.1093/femspd/ftz019 · Cited by 46

An obligatory role for club cells in preventing obliterative bronchiolitis in lung transplants

Liu, Z., Liao, F., Scozzi, D., Furuya, Y., Pugh, K. N., Hachem, R. R., Chen, D. L., Cano, M., Green, J. M., Krupnick, A. S., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.124732 · Cited by 44

Hormonal Regulation of Physiology, Innate Immunity and Antibody Response to H1N1 Influenza Virus Infection During Pregnancy

Littauer, E. Q., & Skountzou, I. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02455 · Cited by 43

Gut microbial metabolite targets HDAC3-FOXK1-interferon axis in fibroblast-like synoviocytes to ameliorate rheumatoid arthritis

Chen, H., Fu, X., Wu, X., Zhao, J., Qiu, F., Wang, Z., Wang, Z., Chen, X., Xie, D., Huang, J., et al. (2024) · Bone Research · doi:10.1038/s41413-024-00336-6 · Cited by 47

Regulation of NF-κB by the p105-ABIN2-TPL2 complex and RelAp43 during rabies virus infection

Besson, B., Sonthonnax, F., Duchateau, M., Khalifa, Y. B., Larrous, F., Eun, H., Hourdel, V., Matondo, M., Chamot‐Rooke, J., Grailhe, R., et al. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006697 · Cited by 42

Enhanced protection of C57 BL/6 vs Balb/c mice to melanoma liver metastasis is mediated by NK cells

Foerster, F., Boegel, S., Heck, R., Pickert, G., Rüssel, N., Rosigkeit, S., Bros, M., Strobl, S., Kaps, L., Aslam, M., et al. (2017) · OncoImmunology · doi:10.1080/2162402x.2017.1409929 · Cited by 43

Time Response of Oxidative/Nitrosative Stress and Inflammation in LPS-Induced Endotoxaemia—A Comparative Study of Mice and Rats

Steven, S., Dib, M., Roohani, S., Kashani, F., Münzel, T. F., & Daiber, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102176 · Cited by 41

Urine Cytokine and Chemokine Levels Predict Urinary Tract Infection Severity Independent of Uropathogen, Urine Bacterial Burden, Host Genetics, and Host Age

Armbruster, C. E., Smith, S. N., Mody, L., & Mobley, H. L. T. (2018) · Infection and Immunity · doi:10.1128/iai.00327-18 · Cited by 39

An Immunomodulatory Gallotanin-Rich Fraction From Caesalpinia spinosa Enhances the Therapeutic Effect of Anti-PD-L1 in Melanoma

Lasso, P., Gomez‐Cadena, A., Urueña, C. P., Donda, A., Martínez-Usatorre, A., Romero, P. J., Barreto, A., & Susana Fiorentino, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.584959 · Cited by 41

Burn-Induced Local and Systemic Immune Response: Systematic Review and Meta-Analysis of Animal Studies

Mulder, P. P. G., Koenen, H. J. P. M., Vlig, M., Joosten, I., de Vries, R. B. M., & Boekema, B. K. H. L. (2022) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2022.05.004 · Cited by 42

Probiotics against airway allergy: host factors to consider

Spacova, I., Ceuppens, J. L., Seys, S., Petrova, M., & Lebeer, S. (2018) · Disease Models & Mechanisms · doi:10.1242/dmm.034314 · Cited by 39

Intestinal dysbacteriosis activates tumor-associated macrophages to promote epithelial-mesenchymal transition of colorectal cancer

Wan, G., Xie, M., Yu, H., & Chen, H. (2018) · Innate Immunity · doi:10.1177/1753425918801496 · Cited by 39

The immune response of inbred laboratory mice to Litomosoides sigmodontis: A route to discovery in myeloid cell biology

Finlay, C. M., & Allen, J. E. (2020) · Parasite Immunology · doi:10.1111/pim.12708 · Cited by 36

A poly(beta-amino ester) activates macrophages independent of NF-κB signaling

Dold, N. M., Zeng, Q., Zeng, X., & Jewell, C. M. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.12.040 · Cited by 37

Zika Virus Infection Preferentially Counterbalances Human Peripheral Monocyte and/or NK Cell Activity

Lum, F., Lee, D., Chua, T., Tan, J. J. L., Lee, C. Y., Liu, X., Fang, Y., Lee, B. T. K., Yee, W., Rickett, N. Y., et al. (2018) · mSphere · doi:10.1128/mspheredirect.00120-18 · Cited by 36

Targeted Transcriptomic Analysis of C57BL/6 and BALB/c Mice During Progressive Chronic Toxoplasma gondii Infection Reveals Changes in Host and Parasite Gene Expression Relating to Neuropathology and Resolution

Bergersen, K. V., Barnes, A., Worth, D., David, C. N., & Wilson, E. H. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.645778 · Cited by 38

Characterization of pathogenesis of and immune response to Burkholderia pseudomallei K96243 using both inhalational and intraperitoneal infection models in BALB/c and C57BL/6 mice

Bearss, J. J., Hunter, M., Dankmeyer, J. L., Fritts, K. A., Klimko, C. P., Weaver, C. H., Shoe, J. L., Quirk, A. V., Toothman, R. G., Webster, W. M., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172627 · Cited by 36

Conserved T-cell epitopes of respiratory syncytial virus (RSV) delivered by recombinant live attenuated influenza vaccine viruses efficiently induce RSV-specific lung-localized memory T cells and augment influenza-specific resident memory T-cell responses

Matyushenko, V., Kotomina, T. S., Kudryavtsev, I. V., Mezhenskaya, D. А., Prokopenko, P., Matushkina, A., Сивак, К. В., Muzhikyan, A., Георгиевна, Р. Л., & Isakova–Sivak, I. (2020) · Antiviral Research · doi:10.1016/j.antiviral.2020.104864 · Cited by 35

Characterization of sex-related differences in allergen house dust mite-challenged airway inflammation, in two different strains of mice

Mostafa, D. H. D., Hemshekhar, M., Piyadasa, H., Altieri, A., Halayko, A. J., Pascoe, C. D., & Mookherjee, N. (2022) · Scientific Reports · doi:10.1038/s41598-022-25327-7 · Cited by 35

CCR5 limits cortical viral loads during West Nile virus infection of the central nervous system

Durrant, D. M., Daniels, B. P., Pasieka, T., Dorsey, D. A., & Klein, R. S. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0447-9 · Cited by 34

Microfluidic assay for precise measurements of mouse, rat, and human neutrophil chemotaxis in whole-blood droplets

Jones, C. N., Hoang, A. N., Martel, J. M., Dimisko, L., Mikkola, A. M., Inoue, Y., Kuriyama, N., Yamada, M., Hamza, B. M., Kaneki, M., et al. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.5ta0715-310rr · Cited by 35

Pathology Principles and Practices for Analysis of Animal Models

Knoblaugh, S. E., Hohl, T. M., & Perle, K. M. D. L. (2018) · ILAR Journal · doi:10.1093/ilar/ilz001 · Cited by 34

Phenotypic characteristics of commonly used inbred mouse strains

Tam, W. Y., & Cheung, K. (2020) · Journal of Molecular Medicine · doi:10.1007/s00109-020-01953-4 · Cited by 36

Strain-Dependent Variation in Acute Ischemic Muscle Injury

Schmidt, C. A., Amorese, A. J., RYAN, T. E., Goldberg, E. J., Tarpey, M. D., Green, T. D., Karnekar, R. R., Yamaguchi, D. J., Spangenburg, E. E., & McClung, J. M. (2018) · American Journal Of Pathology · doi:10.1016/j.ajpath.2018.01.008 · Cited by 33

The NADPH Oxidase and Microbial Killing by Neutrophils, With a Particular Emphasis on the Proposed Antimicrobial Role of Myeloperoxidase within the Phagocytic Vacuole

Levine, A. P., & Segal, A. W. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0018-2015 · Cited by 33

Immune System Sex Differences May Bridge the Gap Between Sex and Gender in Fibromyalgia

Meester, I., Rivera‐Silva, G., & González‐Salazar, F. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01414 · Cited by 37

Protection Elicited by Attenuated Live Yersinia pestis Vaccine Strains against Lethal Infection with Virulent Y. pestis

Cote, C. K., Biryukov, S. S., Klimko, C. P., Shoe, J. L., Hunter, M., Rosario-Acevedo, R., Fetterer, D. P., Moody, K. L., Meyer, J. R., Rill, N. O., et al. (2021) · Vaccines · doi:10.3390/vaccines9020161 · Cited by 32

A comprehensive approach to modeling maternal immune activation in rodents

Bucknor, M. C., Gururajan, A., Dale, R. C., & Hofer, M. J. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1071976 · Cited by 37

Tumor immunology CRISPR screening: present, past, and future

Dong, M. B., Tang, K., Zhou, X., Zhou, J. J., & Chen, S. (2021) · Trends in cancer · doi:10.1016/j.trecan.2021.11.009 · Cited by 32

Mycobacterium tuberculosis PPE18 protein inhibits MHC class II antigen presentation and B cell response in mice

Dolasia, K., Nazar, F., & Mukhopadhyay, S. (2020) · European Journal of Immunology · doi:10.1002/eji.201848071 · Cited by 28

The Influence of Genetic and Environmental Factors and Their Interactions on Immune Response to Helminth Infections

Oyesola, O. O., Souza, C. O. S., & Loke, P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.869163 · Cited by 35

A novel approach for emerging and antibiotic resistant infections: Innate defense regulators as an agnostic therapy

North, J. R., Takenaka, S., Rozek, A., Kielczewska, A., Opal, S. M., Morici, L. A., Finlay, B. B., Schaber, C. J., Straube, R., & Donini, O. (2016) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2016.03.032 · Cited by 29

Generation of a C57BL/6 MYC -Driven Mouse Model and Cell Line of Prostate Cancer

Ellis, L., Ku, S., Li, Q., Azabdaftari, G., Seliski, J., Olson, B. M., Netherby, C. S., Tang, D. G., Abrams, S. I., Goodrich, D. W., et al. (2016) · The Prostate · doi:10.1002/pros.23206 · Cited by 30

Necroptosis inhibition as a therapy for Niemann-Pick disease, type C1: inhibition of RIP kinases and combination therapy with 2-hydroxypropyl-β-cyclodextrin

Cougnoux, A., Clifford, S., Salman, A., Ng, S.-L., Bertin, J., & Porter, F. (2018) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2018.10.009 · Cited by 29

Influence of fracture stability on Staphylococcus epidermidis and Staphylococcus aureus infection in a murine femoral fracture model

Bresco, M. S., O’Mahony, L., Zeiter, S., Kluge, K., Ziegler, M., Berset, C., Nehrbass, D., Richards, R. G., & Moriarty, T. F. (2017) · European Cells and Materials · doi:10.22203/ecm.v034a20 · Cited by 28

Preclinical models and evaluation criteria of prostatitis

He, H., Luo, H., Xu, H., Qian, B., Zou, X., Zhang, G., Zeng, F., & Zou, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1183895 · Cited by 27

Defining the optimal animal model for translational research using gene set enrichment analysis

Weidner, C., Steinfath, M., Opitz, E., Oelgeschläger, M., & Schönfelder, G. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201506025 · Cited by 27

Autophagy diminishes the early interferon-β response to influenza A virus resulting in differential expression of interferon-stimulated genes

Pérot, B. P., Boussier, J., Yatim, N., Rossman, J. S., Ingersoll, M. A., & Albert, M. L. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0546-5 · Cited by 27

Mouse Strain and Sex-Dependent Differences in Long-term Behavioral Abnormalities and Neuropathologies after Developmental Zika Infection

Snyder‐Keller, A., Kramer, L. D., Zink, S. D., & Bolivar, V. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2666-18.2019 · Cited by 25

Cecal Slurry Injection in Neonatal and Adult Mice

Rincon, J. C., Efron, P. A., Moldawer, L. L., & Larson, S. D. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1488-4_4 · Cited by 25

New Insights and Implications of Natural Killer Cells in Parkinson’s Disease

Menees, K. B., & Lee, J. (2022) · Journal of Parkinson s Disease · doi:10.3233/jpd-223212 · Cited by 26

Trade-off between tolerance and resistance to infections: an experimental approach with malaria parasites in a passerine bird

Arriero, E., Pérez‐Tris, J., Ramírez, Á., & Remacha, C. (2018) · Oecologia · doi:10.1007/s00442-018-4290-4 · Cited by 25

Immune Relevant and Immune Deficient Mice: Options and Opportunities in Translational Research

Radaelli, E., Santagostino, S. F., Sellers, R. S., & Brayton, C. F. (2018) · ILAR Journal · doi:10.1093/ilar/ily026 · Cited by 27

Interstrain Differences in CO2-Induced Pulmonary Hemorrhage in Mice.

Fisher, S., Burgess, W., Hines, K. D., Mason, G. L., & Owiny, J. R. (2016) · PubMed Central · Cited by 24

Kinetics and Phenotype of the CD4 T Cell Response to Influenza Virus Infections

Hornick, E. E., Zacharias, Z. R., & Legge, K. L. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02351 · Cited by 24

MicroRNA-155 deletion promotes tumorigenesis in the azoxymethane-dextran sulfate sodium model of colon cancer

Velázquez, K. T., Enos, R. T., McClellan, J. L., Cranford, T. L., Chatzistamou, I., Singh, U. P., Nagarkatti, M., Nagarkatti, P. S., Fan, D., & Murphy, E. A. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00326.2015 · Cited by 24

Restriction of chronic Escherichia coli urinary tract infection depends upon T cell‐derived interleukin‐17, a deficiency of which predisposes to flagella‐driven bacterial persistence

Chamoun, M. N., Sullivan, M. J., Goh, K. G. K., Acharya, D., Ipe, D. S., Katupitiya, L., Gosling, D., Peters, K. M., Sweet, M. J., Sester, D. P., et al. (2020) · The FASEB Journal · doi:10.1096/fj.202000760r · Cited by 23

Macrophage cytokine responses to commensal Gram-positive Lactobacillus salivarius strains are TLR2-independent and Myd88-dependent

Udayan, S., Buttó, L. F., Rossini, V., Velmurugan, J., Martínez‐López, M., Sancho, D., Melgar, S., O’Toole, P. W., & Nally, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-85347-7 · Cited by 23

Immunogenicity differences of a 15-valent pneumococcal polysaccharide conjugate vaccine (PCV15) based on vaccine dose, route of immunization and mouse strain

Caro-Aguilar, I., Indrawati, L., Kaufhold, R. M., Gaunt, C., Zhang, Y., Nawrocki, D. K., Giovarelli, C., Winters, M. A., Smith, W. J., Heinrichs, J. H., et al. (2017) · Vaccine · doi:10.1016/j.vaccine.2016.12.055 · Cited by 23

Comparison of response to LPS-induced sepsis in three DBA/2 stocks derived from different sources

Park, J. W., Lee, S. J., Kim, J. E., Kang, M. J., Bae, S. J., Choi, Y. J., Gong, J. E., Kim, K., Jung, Y., Cho, J., et al. (2021) · Laboratory Animal Research · doi:10.1186/s42826-020-00079-5 · Cited by 22

Murine cancer cachexia models replicate elevated catabolic pembrolizumab clearance in humans

Castillo, A. M. M., Vu, T. T., Liva, S. G., Chen, M., Xie, Z., Thomas, J. W., Remaily, B., Guo, Y., Subrayan, U. L., Costa, T., et al. (2021) · JCSM Rapid Communications · doi:10.1002/rco2.32 · Cited by 21

The bias of experimental design, including strain background, in the determination of critical Streptococcus suis serotype 2 virulence factors

Auger, J.-P., Chuzeville, S., Roy, D., Mathieu‐Denoncourt, A., Xu, J., Grenier, D., & Gottschalk, M. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181920 · Cited by 22

Parasites in brains of wild rodents (Arvicolinae and Murinae) in the city of Leipzig, Germany

Waindok, P., ÖZBAKIŞ-BECERİKLİSOY, G., Janecek, E., Springer, A., Pfeffer, M., Leschnik, M. W., & Strübe, C. (2019) · International Journal for Parasitology Parasites and Wildlife · doi:10.1016/j.ijppaw.2019.09.004 · Cited by 21

Distinct iron homeostasis in C57BL/6 and Balb/c mouse strains

Saha, P., Xiao, X., Li, Y., Golonka, R. M., Abokor, A. A., Yeoh, B. S., & Vijay–Kumar, M. (2020) · Physiological Reports · doi:10.14814/phy2.14441 · Cited by 21

Immunological Variation Between Inbred Laboratory Mouse Strains: Points to Consider in Phenotyping Genetically Immunomodified

Sellers, R. S., Clifford, C. B., Treuting, P. M., & Brayton, C. (2016)

Wild-derived mice: from genetic diversity to variation in immune responses

Poltorak, A. N., Апалько, С. В., & Sherbak, S. (2018) · Mammalian Genome · doi:10.1007/s00335-018-9766-3 · Cited by 20

New tools for defining the 'genetic background' of inbred mouse strains

Ridgway, W. M., Healy, B. C., Smink, L. J., Rainbow, D., & Wicker, L. S. (2007) · Nature Immunology · doi:10.1038/ni0707-669 · Cited by 26

Genetic variants and strains of the laboratory mouse

Lyon, M. F. (1989)

Inbred and Genetically Defined Strains of Laboratory Animals: Part 1. Mouse and Rat

Glynn, L. E. (1980) · Immunology · Cited by 67