A B-cell subset uniquely responsive to innate stimuli accumulates in aged mice

PD-1 expression on HIV-specific T cells is associated with T-cell exhaustion and disease progression

Day, C. L., Kaufmann, D. E., Kiepiela, P., Brown, J. A., Moodley, E. S., Reddy, S., Mackey, E. W., Miller, J. D., Leslie, A. J., DePierres, C., et al. (2006) · Nature · doi:10.1038/nature05115 · Cited by 2,680

Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection

Blackburn, S. D., Shin, H., Haining, W. N., Zou, T., Workman, C. J., Polley, A., Betts, M. R., Freeman, G. J., Vignali, D. A. A., & Wherry, E. J. (2009) · Nature Immunology · doi:10.1038/ni.1679 · Cited by 2,062

Chromatin–IgG complexes activate B cells by dual engagement of IgM and Toll-like receptors

Leadbetter, E. A., Rifkin, I. R., Hohlbaum, A. M., Beaudette-Zlatanova, B. C., Shlomchik, M. J., & Marshak‐Rothstein, A. (2002) · Nature · doi:10.1038/416603a · Cited by 1,929

Viral Persistence Alters CD8 T-Cell Immunodominance and Tissue Distribution and Results in Distinct Stages of Functional Impairment

Wherry, E. J., Blattman, J. N., Murali‐Krishna, K., der Most, R. G. V., & Ahmed, R. (2003) · Journal of Virology · doi:10.1128/jvi.77.8.4911-4927.2003 · Cited by 1,645

Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals

Moir, S. L., Ho, J., Malaspina, A., Wang, W., DiPoto, A. C., O’Shea, M. A., Roby, G. A., Kottilil, S., Arthos, J. A., Proschan, M. A., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072683 · Cited by 894

T Helper 17 Cells Promote Cytotoxic T Cell Activation in Tumor Immunity

Martín‐Orozco, N., Muranski, P. J., Chung, Y., Yang, X. O., Yamazaki, T., Lu, S., Hwu, P., Restifo, N. P., Overwijk, W. W., & Dong, C. (2009) · Immunity · doi:10.1016/j.immuni.2009.09.014 · Cited by 829

T‐cell exhaustion: characteristics, causes and conversion

Yi, J. S., Cox, M. A., & Zajac, A. J. (2010) · Immunology · doi:10.1111/j.1365-2567.2010.03255.x · Cited by 675

Effector and regulatory B cells: modulators of CD4+ T cell immunity

Lund, F. E., & Randall, T. D. (2010) · Nature reviews. Immunology · doi:10.1038/nri2729 · Cited by 636

Regulation of B Lymphocyte Responses to Foreign and Self-Antigens by the CD19/CD21 Complex

Fearon, D. T., Carroll, M. C., & Carroll, M. C. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.393 · Cited by 529

Complement receptor 2/CD21− human naive B cells contain mostly autoreactive unresponsive clones

Isnardi, I., Ng, Y.-S., Menard, L. C., Meyers, G., Saadoun, D., Srdanovic, I., Samuels, J., Berman, J., Buckner, J. H., Cunningham‐Rundles, C., et al. (2010) · Blood · doi:10.1182/blood-2009-09-243071 · Cited by 483

Increased Fascin1 and Pak1 Expressions Enhance Age‐Associated B‐Cell Actin Cytoskeleton Remodeling and Motility

Fujiwara, M., Kondo, R., Sugiyama, Y., Maruyama, M., & Nishikimi, A. (2025) · Cell Biochemistry and Function · doi:10.1002/cbf.70090 · Cited by 1

Glutaredoxin2 reduces age-associated B cell differentiation through maintaining redox homeostasis

Jiang, Y. Y., Sun, C., He, Q., Liu, S., Tian, S., Zhang, Y., Du, Y., Li, F., & Zhang, H. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1593816 · Cited by 2

Analysis of immune cell remodeling and functional alterations induced by aging and obesity in mice

Sim, H. B., Choi, Y.-J., Mun, S., Ramos, S., Park, D.-H., Lee, J.-B., Jeong, S., & Kim, J.-J. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115735 · Cited by 1

Follicle-like niches outside the cortex? 3D phase-contrast µCT revealed medullary B cell nodules in mucosa-draining lymph nodes

Schütz, P., Schwarzenberg, F. L., Weber, L. J., Hammel, J. U., Siebels, B., Nissen, P., Leising, N., Jarick, K. J., Walkenfort, B., Irvine, S. C., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1674997 · Cited by 1

From discovery to complexity: the evolving role of age-associated B cells in immunity, aging, and disease

Carsetti, R. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf232 · Cited by 1

The impact of growth hormone (GH) on immunosenescence: exploring the role of B and T cells

Bashir, B., van Hoolwerff, M., Benencia, F., Duran‐Ortiz, S., List, E. O., Kopchick, J. J., & Berryman, D. E. (2026) · Pituitary · doi:10.1007/s11102-025-01632-y · Cited by 2

Predictive value of interferon regulatory factor 5 nuclear translocation in B cells for disease activity and flare in systemic lupus erythematosus: A prospective observational cohort study

Kanayama, Y., Ban, T., Sato, G. R., Arinuma, Y., Matsueda, Y., Yamaoka, K., & Tamura, T. (2026) · Modern Rheumatology · doi:10.1093/mr/roag024 · Cited by 1

Age-related B cell dysfunction at the aging-cancer nexus: from shared manifestations to therapeutic potential

Liu, L.-T., Wang, H., Zhang, S.-W., Shao, Z., & Jiang, Y. (2026) · Cancer Letters · doi:10.1016/j.canlet.2026.218436 · Cited by 1

Immunosenescence in elderly patients with advanced non-small cell lung cancer: Mechanisms and therapeutic implications

Wang, N., Wang, C., Wang, X., Meng, Y., Cui, S., Zhao, K., Jia, Y., & Kong, F. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189587 · Cited by 1

Bridging aging and colorectal cancer: synergistic roles of inflammaging and immunosenescence

Zaongo, S. D., Yang, Q., Han, M., Xi, T., Luo, Z., Wang, X., Yang, J., & Ouyang, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1792954 · Cited by 2

Type I interferons enhance B cell activation and promote differentiation of double negative 2 cells in SLE

Faheem, Z., Boukhaled, G. M., Nassar, C., Manion, K., Kim, M., Bonilla, D., Gladman, D. D., Garcia, L. P. W., Touma, Z., Brooks, D. G., et al. (2026) · Lupus Science & Medicine · doi:10.1136/lupus-2026-002042 · Cited by 1

Loss of ST8Sia6 mediated α-2,8-linked di-sialylation enhances T cell-dependent antibody responses and promotes autoimmunity in aged mice

Brüchert, R., Hinzpeter-Schmidt, M., Röder, B., Krause, M., Brey, S., Winkler, T., Buettner, F. F. R., Mühlenhoff, M., & Nitschke, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1874115 · Cited by 1

Age-associated B cells (ABCs) develop from a CNS-localized progenitor pool into a pro-inflammatory phenotype after stroke

McAtee, A. M., Kenwood, M. R., Ujas, T. A., Colson, M. K., Watkins, J., Winford, E. D., Cotter, K. M., Britsch, D. R. S., Betz, D., Turchan-Cholewo, J. T., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-04044-2 · Cited by 1

Pattern of Tumor-Infiltrating Lymphocytes in Mixed Epithelial and Stromal Tumor of the Kidney: A Review of Five Cases

Lee, H. W., Lee, H., Park, C., Oh, W. J., Kim, T. J., Kwon, G. Y., & Seo, S. I. (2021) · Cells · doi:10.3390/cells10040917 · Cited by 1

Characteristics of senescent cells

Schmitt, R., & Melk, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823318-4.00035-4 · Cited by 1

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Barnas, J. L., Meffre, E., & Anolik, J. H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820583-9.00036-1 · Cited by 1

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Cancro, M. P. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.07.008 · Cited by 1

Rho-kinase inhibitors to deplete age-associated B cells in systemic autoimmunity

Sachinidis, A., & Garyfallos, A. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.09.004 · Cited by 1

Weaker SARS-CoV-2 vaccine responses in nonalcoholic fatty liver disease with advanced liver fibrosis

Hakimian, D., Amer, J., Jammal, A., Shafrir, A., Milgrom, Y., Masarowah, M., Hazou, W., Ishay, Y., Imam, A., Francis, A., et al. (2023) · Vaccine X · doi:10.1016/j.jvacx.2023.100359 · Cited by 1

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Zvarych, L., Panchenko, V. V., Golyarnik, N., Belayev, O. A., & Bаzyка, D. (2023) · Проблеми радіаційної медицини та радіобіології = Problems of Radiation Medicine and Radiobiology · doi:10.33145/2304-8336-2023-28-286-315 · Cited by 2

ZEB2 drives the differentiation of age-associated B cell in autoimmune diseases

Li, C., Li, C., Wang, Y., Zhang, S., & Liu, W. (2024) · 中国科学通报：英文版 · doi:10.1016/j.scib.2024.03.041 · Cited by 1

T cell Dissimilarities in B Cell Activating Factor–Deficient Versus B Cell Activating Factor Receptor 3–Deficient Systemic Lupus Erythematosus‐Prone NZM 2328 Mice as Contributors to Their Divergent Clinical Outcomes

Stohl, W., Wu, Y., & Stohl, M. (2024) · ACR Open Rheumatology · doi:10.1002/acr2.11712 · Cited by 1

What's atypical about human B cells after allogeneic stem cell transplantation?

Bracken, S. J., Poe, J. C., & Sarantopoulos, S. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf048 · Cited by 1

Pattern Recognition Receptors and Aging

Shalaby, K. H. (2013) · Springer eBooks · doi:10.1007/978-3-642-39495-9_8 · Cited by 1

Antibodies control metabolism by regulating insulin homeostasisPreprint

Amendt, T., Allies, G., Nicolò, A., Ayoubi, O. E., Young, M., Rőszer, T., Setz, C. S., Warnatz, K., & Jumaa, H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.10.455644 · Cited by 1

Age-associated B cells are long-lasting effectors that restrain reactivation of latent γHV68Preprint

Mouat, I. C., Shanina, I., & Horwitz, M. S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.29.474434 · Cited by 1

Chronic BCR signaling generates and maintains age-associated B cells from anergic B cellsPreprint

Imabayashi, K., Yada, Y., Ushijima, M., Yoshimura, M., Iwasaki, T., Akashi, K., Niiro, H., & Baba, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.26.550463 · Cited by 1

Activation of Autoreactive Lymphocytes in the Lung by STING Gain-of-function Mutation Radioresistant CellsPreprint

Gao, K. M., Nündel, K., Chiang, K., Yin, X., Utz, P. J., Fitzgerald, K. A., & Marshak‐Rothstein, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.28.551002 · Cited by 1

The Immune Landscape of Murine Skeletal Muscle Regeneration and AgingPreprint

Sousa, N. S., Bica, M., Brás, M. F., Antunes, I. B., Encarnação, I. A., Costa, T., Martins, I. B., Barbosa‐Morais, N. L., Sousa‐Victor, P., & Neves, J. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4663954 · Cited by 1

Age-associated B-cells are expanded in early arthritis linked to atherosclerosis and immune circuits - a potential role as a biomarker for risk stratificationPreprint

Miranda-Prieto, D., Alpéri, M., Pérez-Álvarez, Á. I., Alonso-Castro, S., Suárez, A., & Rodríguez‐Carrio, J. (2025) · medRxiv · doi:10.1101/2025.01.14.25320531 · Cited by 1

Effect of Age on Xenobiotic-Induced AutoimmunityPreprint

de Ocampo, C., Peiss, A. K., Leung, H. Y., Janssen, L., Kono, D. H., Mayeux, J., & Pollard, K. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.22.655368 · Cited by 2

Is there a role for B cells in Alzheimer's disease?

Charavner, E.-L., Fillatreau, S., & El Behi, M. (2026) · Cellular Immunology · doi:10.1016/j.cellimm.2026.105154

Fas Pathway of Cell Death and B Cell Dysregulation in SLE

Paganelli, R., Paganelli, A., & Maria, C. (2012) · InTech eBooks · doi:10.5772/26509

New Cells in Old Mice: The ABCs of Humoral Immunosenescence

Hao, Y. (2012) · Open Longevity Science · doi:10.2174/1876326x01206010112

Pivotal Functions of Plasmacytoid Dendritic Cells in Systemic Autoimmune

Cao, W. (2014)

Hematopoietic Stem Cell Aging and Leukemogenesis

Henry, C. J., Rozhok, A. I., & DeGregori, J. V. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1232-8_13

The Aging Immune System, Vaccine Efficacy, and the Lung

Bartley, J. M., & Haynes, L. (2015) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814635011_0009

Regulation of B cell metabolic activation, germinal center responses and autoimmunity by Tandem PH domain-containing proteins

Jayachandran, N. (2016) · Mspace (University of Manitoba)

Ageing and vaccination in transplant patients

Wang, L. (2021) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.33612/diss.160954435

Uncontrolled CD21 low age-associated and B1 B cell accumulation caused by failure of an EGR2/3 tolerance checkpointPreprint

Masle‐Farquhar, E., Peters, T. J., Miosge, L. A., Parish, I. A., Weigel, C., Oakes, C. C., Reed, J. H., & Goodnow, C. C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.01.450650

MULTI-FUNCTIONAL EFFECTOR RESPONSES ELICITED FROM IgM MEMORY STEM CELLS

Kenderes, K. J. (2017) · SUNY Digital Repository Support (State University of New York System)

CD11C+ T-BET+ B CELLS IN INFECTION AND AUTOIMMUNITY

Levack, R. C. (2020) · SUNY Digital Repository Support (State University of New York System)

Permutational immune analysis reveals architectural similarities between inflammaging, Down syndrome and autoimmunityPreprint

Lambert, K., Moo, K. G., Arnett, A., Goel, G., Flynn, K. J., Speake, C., WIEDEMAN, A. E., Greenbaum, C. J., Long, S. A., Partridge, R., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.13.460115

Longitudinal dynamics of human B-cell response at single-cell level in response to Tdap vaccinationPreprint

Khatri, I., Diks, A. M., van den Akker, E. B., Oosten, L. E. M., Zwaginga, J. J., Reinders, M. J. T., van Dongen, J. J. M., & Berkowska, M. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.08.463649

Overactive STAT3 Drives Accumulation of Disease-Associated CD21 low B CellsPreprint

Masle‐Farquhar, E., Peters, T. J., Jackson, K., Singh, M., Ma, C. S., Suan, D., Uzel, G., Chua, I. C., Leiding, J. W., Heiskanen, K., et al. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3996405

Faculty Opinions recommendation of Role of nucleic acid-sensing TLRs in diverse autoantibody specificities and anti-nuclear antibody-producing B cells.

Manser, T. L. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718010590.793476777

Aging blood factors promote CD8+ T cell infiltration in the adult mouse brainPreprint

van Olst, L., Kamermans, A., van der Pol, S. M. A., Hulshof, L. A., van Dijk, R. E., Vonk, D., Schouten, M., Witte, M. E., de Vries, H. E., & Middeldorp, J. (2022) · Research Square · doi:10.21203/rs.3.rs-1266205/v1

B Cell Repertoire Changes in Mouse Models of Aging

Scholz, J. L., Hao, Y., Quinn, W. J., & Cancro, M. P. (2017) · Springer eBooks · doi:10.1007/978-3-319-64597-1_20-1

B Cell Repertoire Changes in Mouse Models of Aging

Scholz, J. L., Hao, Y., Quinn, W. J., & Cancro, M. P. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_20

Anti-DNA antibodies

Malkiel, S., Atisha‐Fregoso, Y., & Diamond, B. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814551-7.00027-1

Faculty Opinions recommendation of Commensal bacteria contribute to insulin resistance in aging by activating innate B1a cells.

Berzofsky, J. A. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734431272.793569295

Single-Cell Analysis of the Peripheral Immune Landscape in Alzheimer's Disease Reveals a Distinct Adaptive Immune SignaturePreprint

van Olst, L., van der Pol, S. M. A., Kamermans, A., Verberk, I. M. W., Wessels, D. W. R., Verberk, S. G. S., Rodriguez, E., Rodriguez-Mogeda, C., Verhoeff, J., Wouters, D., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4112546

Age-associated B cells are long-lasting effectors that impede latent gHV68 reactivationPreprint

Mouat, I. C., Shanina, I., & Horwitz, M. S. (2022) · Research Square · doi:10.21203/rs.3.rs-1832698/v1

Fate and plasticity of SARS-CoV-2-specific B cells during memory and recall response in humansPreprint

Zurbuchen, Y., Michler, J., Taeschler, P., Adamo, S., Cervia, C., Raeber, M. E., Acar, İ. E., Nilsson, J., Warnatz, K., Soyka, M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.07.511336 · Cited by 1

Increased of Fascin1 and Pak1 expression enhances age-associated B cell actin cytoskeleton remodelingPreprint

Fujiwara, M., Kondo, R., Sugiyama, Y., Maruyama, M., & Nishikimi, A. (2023) · Research Square · doi:10.21203/rs.3.rs-2659669/v1

Upregulated Fcrl5 disrupts B cell anergy and causes autoimmunityPreprint

Ono, C., Tanaka, S., Myouzen, K., Iwasaki, T., Ueda, M. T., Oda, Y., Yamamoto, K., Kochi, Y., & Baba, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.20.549843

The Effects of Aging on Solid Organ Transplantation—Characteristics and Consequences of Immunosenescence

Rollenhagen, C., & Maltzman, J. S. (2023) · Current Transplantation Reports · doi:10.1007/s40472-023-00405-5

Memory B Cells and Plasma Cells

McGrath, M., Weisel, F. J., Radbruch, A., & Shlomchik, M. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95895-0.00011-8

Bye-bye My-HSC: Antibody Depletion of Myeloid-biased Stem Cells Revitalizes Aged Blood and Boosts Immunity

Shen, Y., & Psaila, B. (2024) · The Hematologist · doi:10.1182/hem.v21.4.2024412

Contributions of each of the BAFF receptors to the lymphocyte profiles in C57BL /6 mice

Stohl, W., Wu, Y. T., & Stohl, M. (2024) · Immunology · doi:10.1111/imm.13856

Research progress of immune cell therapy for spinal cord injury

Zhu, S.-Y. (2024) · New discovery. · doi:10.61958/ndwm5390

Personalized Immune Profiling in Pediatric Transplant Recipients: Linking Atypical B Cells to Vaccine ResponsePreprint

Wedel, J., Tang, Y., Alsairafi, B., Do, V., Maslyar, M., Fleming, R., Schwartz, M. A., Gerdemann, U., Albanese, A., Mitsialis, V., et al. (2025) · medRxiv · doi:10.1101/2025.03.25.25324615

Evolving Approach to Clinical Cytometry for Immunodeficiencies and Other Immune Disorders

Akha, A. A. S., Csomós, K., Ujházi, B., Walter, J. E., & Kumánovics, A. (2025) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2025.01.009

Inmunosenescencia y autoinmunidad: mecanismos e implicaciones patológicas

Ibarra, A. S. P., Criado-Villamizar, J., Niebles-Navas, M., Rojas-Castro, G., Monsalve, D. M., Acosta‐Ampudia, Y., & Ramı́rez-Santana, C. (2024) · Medicina · doi:10.56050/01205498.2336 · Cited by 1

Tribute to Mike Cancro – Former editor-in-chief at Cellular Immunology

Fillatreau, S., & Hao, Y. (2025) · Cellular Immunology · doi:10.1016/j.cellimm.2025.104973

P75NTR activation limits CD21lo B cell subsets expansion in response to autoimmune-inducing challenges

Luo, C., Zha, A., Luo, R., Hu, Z., Shen, W., & Dai, R. (2025) · iScience · doi:10.1016/j.isci.2025.113055

Remembering Michael P. Cancro: modern Renaissance Man

Tomayko, M. M., & Scholz, J. L. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf079

CD11c+ Tbet+ B cells constrain obesity- and vaccination-induced germinal center B cells and T helper cellsPreprint

Vanz, C., Enslow, B. T., Collins, E., Dominguez-Lowry, M., Liendo, N. S., Dudley, E. A., & Leadbetter, E. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.01.673552

Epigenomic and Transcriptomic Germ-Free Ageing Atlas Reveals Sterile Inflammation as an Intrinsic Ageing FeaturePreprint

Twilhaar, W. N., Chang, J.-C., Terooatea, T. W., Yabukami, H., Kato, S., Hetherington, N. A., Satoh‐Takayama, N., Ahmadi, A., Hsieh, T.-H., Jeyamohan, P., et al. (2025) · SSRN Electronic Journal · doi:10.1101/2025.11.19.689100 · Cited by 1

Additional file 14 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711651

Additional file 3 of Altered transcriptional responses in the lungs of aged mice after influenza infection

Hernandez, A. M., Mossman, J. A., Toapanta, F. R., Previte, D. M., Ross, T. M., & Nau, G. J. (2022) · Figshare · doi:10.6084/m9.figshare.19959739

Additional file 4 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711621

Additional file 2 of Altered transcriptional responses in the lungs of aged mice after influenza infection

Hernandez, A. M., Mossman, J. A., Toapanta, F. R., Previte, D. M., Ross, T. M., & Nau, G. J. (2022) · Figshare · doi:10.6084/m9.figshare.19959736

Additional file 10 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711639

Additional file 15 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711654

Additional file 1 of Changes in T and B cell subsets in end stage renal disease patients before and after kidney transplantation

Wang, L., Rondaan, C., de Joode, A. A. E., Raveling‐Eelsing, E., Bos, N. A., & Westra, J. (2021) · Figshare · doi:10.6084/m9.figshare.16960328

Additional file 5 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711624

Additional file 21 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711672

Additional file 1 of Altered transcriptional responses in the lungs of aged mice after influenza infection

Hernandez, A. M., Mossman, J. A., Toapanta, F. R., Previte, D. M., Ross, T. M., & Nau, G. J. (2022) · Figshare · doi:10.6084/m9.figshare.19959733

Additional file 9 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711636

Additional file 11 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711642

Additional file 16 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711657

Additional file 18 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711663

Additional file 7 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711630

Additional file 13 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711648

Additional file 2 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25687615

Additional file 8 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711633

Additional file 12 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711645

Additional file 1 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25687445

Additional file 3 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711618

Additional file 20 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711669

Additional file 6 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711627

Additional file 19 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711666

Additional file 17 of Adaptive immune changes associate with clinical progression of Alzheimer’s disease

van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26711660

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