Human CD8+ T-cell differentiation in response to viruses

Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

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Phenotypic Analysis of Antigen-Specific T Lymphocytes

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Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products.

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CCR7 Coordinates the Primary Immune Response by Establishing Functional Microenvironments in Secondary Lymphoid Organs

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Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

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Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection

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Effector and memory T-cell differentiation: implications for vaccine development

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Lineage relationship and protective immunity of memory CD8 T cell subsets

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The lineage decisions of helper T cells

MURPHY, K. M. M., & Reiner, S. L. (2002) · Nature reviews. Immunology · doi:10.1038/nri954 · Cited by 1,690

CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes

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Molecular changes associated with increased TNF-α-induced apoptotis in naïve (TN) and central memory (TCM) CD8+ T cells in aged humans

Gupta, S., Su, H., Agrawal, S., & Gollapudi, S. V. S. (2018) · Immunity & Ageing · doi:10.1186/s12979-017-0109-0 · Cited by 16

Jakmip1 Is Expressed upon T Cell Differentiation and Has an Inhibitory Function in Cytotoxic T Lymphocytes

Libri, V., Schulte, D., van Stijn, A., Ragimbeau, J., Rogge, L., & Pellegrini, S. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.9.5847 · Cited by 16

Functional profile of human influenza virus-specific cytotoxic T lymphocyte activity is influenced by interleukin-2 concentration and epitope specificity

Boon, A. C. M., de Mutsert, G., Fouchier, R. A. M., Osterhaus, A. D. M. E., & Rimmelzwaan, G. F. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02880.x · Cited by 16

Induction and Maintenance of Cd8+ T Cells Specific for Persistent Viruses

van Leeuwen, E. M. M., ten Berge, I. J. M., & van Lier, R. A. W. (2007) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-34814-8_9 · Cited by 15

Evaluating antigen-specific cytotoxic T lymphocyte responses by a novel mouse granzyme B ELISPOT assay

Ewen, C., Rong, J., Kokaji, A. I., Bleackley, R. C., & Kane, K. P. (2005) · Journal of Immunological Methods · doi:10.1016/j.jim.2005.10.009 · Cited by 15

A subset of functional effector‐memory CD8+ T lymphocytes in human immunodeficiency virus‐infected patients

Decrion-Barthod, A.-Z., Varin, A., Drobacheff, C., Estavoyer, J., & Herbein, G. (2007) · Immunology · doi:10.1111/j.1365-2567.2007.02589.x · Cited by 15

Flow Cytometry Applications of MHC Tetramers

Altman, J. D. (2004) · Methods in cell biology · doi:10.1016/s0091-679x(04)75017-7 · Cited by 15

The effects of exercise training for eight weeks on immune cell characteristics among breast cancer survivors

Echarri, A. A., Struszczak, L., Beresford, M. J., Campbell, J. P., Thompson, D., & Turner, J. E. (2023) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2023.1163182 · Cited by 14

Phenotypic and functional characteristics of HIV-specific CD8 T cells and gag sequence variability after autologous dendritic cells based therapeutic vaccine

López, A., van der Lubbe, N., Sánchez‐Palomino, S., Arnedo, M., Nomdedéu, M., Castro, P., Guilà, M., Maleno, M. J., García, F., Gallart, T., et al. (2009) · Vaccine · doi:10.1016/j.vaccine.2009.08.021 · Cited by 14

NKp44/HLA-DP-dependent regulation of CD8 effector T cells by NK cells

Padoan, B., Casar, C., Krause, J., Schultheiß, C., Baumdick, M. E., Niehrs, A., Zecher, B. F., Pujantell, M., Yuki, Y., Martin, M. P., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114089 · Cited by 13

Aging, nutrition and immunity – their relationship and interaction

Alam, I., & Pawelec, G. (2012) · Nutrition and Aging · doi:10.3233/nua-130013 · Cited by 13

CD8+ T-cell maturation following lung transplantation: The differential impact of CMV and acute rejection

Westall, G. P., Brööks, A. G., & Kotsimbos, T. C. (2007) · Transplant Immunology · doi:10.1016/j.trim.2007.07.002 · Cited by 13

Autologous cytomegalovirus‐specific T cells as effector cells in immunotherapy of B cell chronic lymphocytic leukaemia

Kater, A. P., Remmerswaal, E. B. M., Nolte, M. A., Eldering, E., van Oers, M. H. J., & van Lier, R. A. W. (2004) · British Journal of Haematology · doi:10.1111/j.1365-2141.2004.05070.x · Cited by 13

Autophagy-enhancing ATG16L1 polymorphism is associated with improved clinical outcome and T-cell immunity in chronic HIV-1 infection

Schreurs, R., Koulis, A., Booiman, T., Boeser‐Nunnink, B., Cloherty, A. P. M., Rader, A. G., Patel, K. S., Kootstra, N. A., & Ribeiro, C. M. S. (2024) · Nature Communications · doi:10.1038/s41467-024-46606-z · Cited by 12

HIV‐1‐Specific Immune Response

Harari, A., & Pantaleo, G. (2008) · Advances in pharmacology · doi:10.1016/s1054-3589(07)56003-5 · Cited by 12

Low Concentrations of Flavonoid - Rich Fraction of Shallot Extract Induce Delayed - Type Hypersensitivity and TH1 Cytokine IFNγ Expression in BALB/c Mice.

Farhadi, L., Mohammadi‐Motlagh, H., Seyfi, P., & Mostafaie, A. (2014) · Europe PMC (PubMed Central) · Cited by 12

Development of monoclonal antibodies (MAbs) to feline interferon (fIFN)- γ as tools to evaluate cellular immune responses to feline infectious peritonitis virus (FIPV)

Satoh, R., Kaku, A., Satomura, M., Kohori, M., Noura, K., Furukawa, T., Kotake, M., Takano, T., & Hohdatsu, T. (2011) · Journal of Feline Medicine and Surgery · doi:10.1016/j.jfms.2011.01.008 · Cited by 12

Immunophenotyping of T Cell Subpopulations in HIV Disease

Chattopadhyay, P. K., & Roederer, M. (2005) · Current Protocols in Immunology · doi:10.1002/0471142735.im1212s65 · Cited by 12

CD45RA expression on HCMV-specific effector memory CD8+ T cells is associated with the duration and intensity of HCMV replication after transplantation

Cantisán, S., Solana, R., Lara, R., Rodríguez‐Benot, A., Vaquero, J. M., Gutiérrez-Aroca, J. B., Gayoso, I., Montejo, M., Rivero, A., & Torre‐Cisneros, J. (2010) · Clinical Immunology · doi:10.1016/j.clim.2010.06.016 · Cited by 11

Persistent Detection of Varicella-Zoster Virus DNA in a Previously Healthy Child after Severe Chickenpox

Vossen, M. T. M., Gent, M.-R., Peters, K. M. C., Dillen, P. M. E. W., Dolman, K. M., van Breda, A., van Lier, R. A. W., & Kuijpers, T. W. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.11.5614-5621.2005 · Cited by 11

IMMUNITY TO MICROBES

Abbas, A. K., Lichtman, A. H., Pillai, S. S., & Baker, D. L. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-3123-9.50024-3 · Cited by 11

Decrease of cytotoxic T cells in allergic asthma correlates with total serum immunglobulin E

Bratke, K., Haupt, F., Kuepper, M., Bade, B., Fähndrich, S., Luttmann, W., & Virchow, J. C., Jr. (2006) · Allergy · doi:10.1111/j.1398-9995.2006.01192.x · Cited by 11

Simultaneous monitoring assay for T-cell receptor stimulation-dependent activation of CD4 and CD8 T cells using inducible markers on the cell surface

Takahama, S., Nogimori, T., Higashiguchi, M., Murakami, H., Akita, H., & Yamamoto, T. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.07.037 · Cited by 10

Monitoring of CMV-specific T-cell levels after organ transplantation / Monitoring CMV-spezifischer T-Zellen nach Organtransplantation

Sester, M., Gärtner, B. C., & Sester, U. (2008) · Journal of Laboratory Medicine · doi:10.1515/jlm.2008.027 · Cited by 10

Normal Numbers of Stem Cell Memory T Cells Despite Strongly Reduced Naive T Cells Support Intact Memory T Cell Compartment in Ataxia Telangiectasia

Weitering, T. J., Melsen, J. E., Dam, M. M. V. O.-T., Weemaes, C. M. R., Schilham, M. W., & van der Burg, M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.686333 · Cited by 10

Integration of Immune Models Using Petri Nets

Na, D., Park, I. H., Lee, K. H., & Lee, D. (2004) · Lecture notes in computer science · doi:10.1007/978-3-540-30220-9_17 · Cited by 10

Monitoring of CD38high expression in peripheral blood CD8+ lymphocytes in patients after kidney transplantation as a marker of cytomegalovirus infection

Tichá, O., Stouracova, M., Kuman, M., Studenı́k, P., Freiberger, T., & Litzman, J. (2010) · Transplant Immunology · doi:10.1016/j.trim.2010.10.002 · Cited by 10

T cell function in the aged: Lessons learned from animal models

Linton, P., Lustgarten, J., & Thoman, M. L. (2006) · Clinical and Applied Immunology Reviews · doi:10.1016/j.cair.2006.06.001 · Cited by 10

CRM197-conjugated peptides vaccine of HCMV pp65 and gH induce maturation of DC and effective viral-specific T cell responses

Zhang, S., Nan, F., Jiang, S., Zhou, X., Niu, D., Li, J., Wang, H., Zhang, X., Zhang, X., & Wang, B. (2023) · Virulence · doi:10.1080/21505594.2023.2169488 · Cited by 9

T cell immune responses to HIV-1

Vasan, S. (2006) · Frontiers in bioscience · doi:10.2741/2235 · Cited by 9

Psychoneuromicrobiology: Cytomegalovirus Infection as a Putative Link Between Stress, Aging, and Immunity

Bosch, J. A., Rector, J. L., Turner, J. E., Riddell, N. E., O’Hartaigh, B. W. J., & Burns, V. E. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4776-4_6 · Cited by 9

T Lymphocytes in Patients With Nijmegen Breakage Syndrome Demonstrate Features of Exhaustion and Senescence in Flow Cytometric Evaluation of Maturation Pathway

Piątosa, B., Wolska‐Kuśnierz, B., Tkaczyk, K., Heropolitańska–Pliszka, E., Grycuk, U., Wakulińska, A., & Gregorek, H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01319 · Cited by 9

Poor Lymphoproliferative Responses with Low Proportion of Gag-Specific CD8 T EMRA Cells in HIV-1-Infected Patients Showing Immunological and Virological Discordance Despite Prolonged Suppression of Plasma Viremia

Sachdeva, N. K., Weinstein, J. E., Ashman, M. R., Sachdeva, M., Brewer, T. H., Gracia, D., & Asthana, D. (2010) · Viral Immunology · doi:10.1089/vim.2009.0069 · Cited by 9

TGF-β superfamily enhances the antigen-induced IFN-γ production by effector/memory CD8+ T cells

Kozawa (2009) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000319 · Cited by 9

HIV-1 and immune control: can we change the course of HIV-1?

Kovács, A., & Connors, M. (2004) · The Lancet · doi:10.1016/s0140-6736(04)15770-x · Cited by 9

Targeted clearance of senescent cells alleviates alcohol-associated liver disease by restoring cellular function and immune balance

Tian, T., Xue, Y., Song, Z., Jin-Smith, B., Barkin, J., Ottallah, M., Mannan, M., Zhirkova, A. M., Zhou, D., & Pi, L. (2025) · GeroScience · doi:10.1007/s11357-025-01952-8 · Cited by 7

Vaccination with a bacterial peptide conjugated to SARS-CoV-2 receptor-binding domain accelerates immunity and protects against COVID-19

Blanas, A., Karsjens, H., de Ligt, A., Huijbers, E. J. M., van Loon, K., Denisov, S. S., Durukan, C., Engbersen, D. J. M., Groen, J., Hennig, S., et al. (2022) · iScience · doi:10.1016/j.isci.2022.104719 · Cited by 7

Immunology of viral co-infections with HIV.

Northfield, J. W., Harcourt, G., Lucas, M., & Klenerman, P. (2005) · UWA Profiles and Research Repository (University of Western Australia) · Cited by 7

Qualitative host factors associated with immunological control of HIV infection by CD8 T cells

Migueles, S. A., Tilton, J. C., & Connors, M. (2006) · Current Opinion in HIV and AIDS · doi:10.1097/01.coh.0000194108.14601.69 · Cited by 7

CD8 T cell dynamics and immune cell trafficking in ZIKV infection: implications for neuroinflammation and therapy

Park, S. J. (2025) · Virology Journal · doi:10.1186/s12985-025-02866-9 · Cited by 7

Transcriptional signature of durable effector T cells elicited by a replication defective HCMV vaccine

Ye, X., Shih, D. J. H., Ku, Z., Hong, J., Barrett, D. F., Rupp, R. E., Zhang, N., Fu, T., Zheng, W. J., & An, Z. (2024) · npj Vaccines · doi:10.1038/s41541-024-00860-w · Cited by 6

Morfometri Limpa Berkaitan dengan Produksi Radikal Bebas dan Antioksidan pada Kelelawar Pemakan Buah Codot Krawar (Cynopterus brachyotis)

Hanadhita, D., Prawira, A. Y., Rahma, A., Satyaningtijas, A. S., & Agungpriyono, S. (2018) · jurnal veteriner · doi:10.19087/jveteriner.2018.19.1.62 · Cited by 6

CD8α+βlow Effector T Cells in Systemic Lupus Erythematosus

Werwitzke, S., Tiede, A., Jacobs, R., Zielinska‐Skowronek, M., Buyny, S., Schmidt, R. E., & Witte, T. (2008) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2008.02093.x · Cited by 6

Immune Response to SARS-CoV-2 Vaccine in 2 Men

Gupta, S., Su, H., & Agrawal, S. (2021) · International Archives of Allergy and Immunology · doi:10.1159/000520046 · Cited by 6

Reciprocal Changes of Naïve and Effector/Memory CD8 + T Lymphocytes in Chronic Hepatitis B Virus Infection

Carotenuto, P., Artsen, A., Osterhaus, A. D. M. E., & Pontesilli, O. (2011) · Viral Immunology · doi:10.1089/vim.2010.0067 · Cited by 5

The interaction between cytomegalovirus and the human immune system

ten Berge, I. J. M., & van Lier, R. A. W. (2014) · Immunology Letters · doi:10.1016/j.imlet.2014.10.009 · Cited by 5

Marked skewing of entire T-cell memory compartment occurs only in a minority of CMV-infected individuals and is unrelated to the degree of memory subset skewing among CMV-specific T-cells

Fuhrmann, S., Reus, B., Frey, O., Pera, A., Picker, L. J., & Kern, F. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1258339 · Cited by 5

Human Purified CD8+T Cells: Ex vivo Expansion Model to Generate a Maximum Yield of Functional Cytotoxic Cells

Al‐Shanti, N., & Aldahoudi, Z. (2006) · Immunological Investigations · doi:10.1080/08820130600991950 · Cited by 5

Dominant Epstein–Barr virus-specific T-cell responses are maintained during moderate and intense immunosuppressive treatment

Daikeler, T. D., Höenger, G., Oehri, I., Tyndall, A., Gratwohl, A. A., Brander, C., Klimkait, T., Gasser, O., & Hess, C. (2010) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2010.129734 · Cited by 3

A review of HLA and COVID-19 association studies

Žunec, R. (2020) · Molecular and experimental biology in medicine · doi:10.33602/mebm.3.2.3 · Cited by 3

Adaptive Cellular Responses following SARS-CoV-2 Vaccination in Primary Antibody Deficiency Patients

Gupta, S., Su, H., Agrawal, S., Demirdağ, Y. Y., Tran, M., & Gollapudi, S. V. S. (2024) · Pathogens · doi:10.3390/pathogens13060514 · Cited by 3

Modulation of T-Cell Mediated Immunity by Cytomegalovirus

Benedict, C. A., Arens, R., Loewendorf, A. I., & Janssen, E. M. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0484-2_7 · Cited by 3

The cellular immune system comes of age

van Lier, R. A. W., & Kuijpers, T. W. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.02.023 · Cited by 3

Persistence of spike-specific immune responses in BNT162b2-vaccinated donors and generation of rapid ex-vivo T cells expansion protocol for adoptive immunotherapy: A pilot study

Mestiri, S., Merhi, M., Inchakalody, V. P., Taib, N., Smatti, M. K., Ahmad, F., Raza, A., Ali, F. H., Hydrose, S., Fernandes, Q., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1061255 · Cited by 2

Screening of Phyllanthus niruri Leaves Phytoconstituents for Antiviral and Antibacterial Activity by Molecular Docking Studies

Manisha, P., Alekhya, K. P., Tejaswini, A., Swathi, K., & Sai, K. V. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-31978-5_9 · Cited by 2

Cytokine responses to major human Cytomegalovirus antigens in mouse model

Essa, S. S., Safar, H. A., & Raghupathy, R. (2024) · Cytokine · doi:10.1016/j.cyto.2024.156546 · Cited by 1

Regulation of T Cell Senescence in Health and Diseases

Mun, S., Choi, S., Kim, J., Kim, J., & Chung, Y. (2026) · Immune Network · doi:10.4110/in.2026.26.e27 · Cited by 1

The Association of EBV and HHV-6 Viral Load with Different NK and CD8+ T Cell Subsets in The Acute Phase of Relapsing-Remitting Multiple Sclerosis.

Salehi, Z., Beheshti, M., Nomanpour, B., Khosravani, P., Naseri, M., Sahraian, M. A., & Izad, M. H. (2021) · PubMed Central · doi:10.22074/cellj.2021.7308 · Cited by 1

Deletion of MIF gene from live attenuated LdCen−/− parasites enhances protective CD4+ T cell immunity

Fiuza, J. A., Gannavaram, S., Gaze, S. T., de Ornellas, L. G., Alves, É. A. R., Ismail, N., Nakhasi, H. L., & Corrêa‐Oliveira, R. (2023) · Scientific Reports · doi:10.1038/s41598-023-34333-2 · Cited by 1

A Systems Biologist's View of Dendritic Cell–Cytotoxic T Lymphocyte Interaction

Ludewig, B., & Bocharov, G. A. (2006) · Wiley eBooks · doi:10.1002/9783527619696.ch23 · Cited by 1

ATUALIZAÇÃO DE CONHECIMENTOS SOBRE A PATOGÊNESE DA SÍNDROME PULMONAR E CARDIOVASCULAR

Borges, A. A., & Figueiredo, L. T. M. (2008) · Revista de Patologia Tropical / Journal of Tropical Pathology · doi:10.5216/rpt.v36i3.3171 · Cited by 1

Immunosenescence

Turner, J. E. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6439-6_101906-1 · Cited by 1

CD8+ lymphocyte and progenitor cell mobilization during acute psychological stress and betaadrenergic stimulation

Riddell, N. E. (2010) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1

Samples isolated by flow cytometry

Appay, V., & Larsen, M. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8334-3_6

Psychosocial and behavioral determinants of immune aging

Rector, J. L. (2015) · University of Birmingham Institutional Research Archive (University of Birmingham)

Specific T-Cell Response to HCMV Infection

Lucchini, G., Pioltelli, P. E., & Lanzetta, M. (2007) · Springer eBooks · doi:10.1007/978-88-470-0374-3_30

Functional competence of CD8+ T cell responses specific to human cytomegalovirus in common variable immunodeficiency

Marashi, S. M. (2011) · UCL Discovery (University College London)

Multimeric Major Histocompatibility Complex Reagents for the Detection and Quantitation of Specific T-Cell Populations

Altman, J. D. (2006) · Wiley eBooks · doi:10.1128/9781555815905.ch23

Immunogenicity Versus Immunomodulation of Perinatal Stem Cells

Lutton, B. V., & Duran‐Struuck, R. (2013) · Wiley eBooks · doi:10.1002/9781118497883.ch7

Characterization of the Mucosal and Systemic Immune Responses Following Virus Vector-Based Gene Delivery into the Colonic Mucosa

Safroneeva, E. (2009) · MacSphere (McMaster University) · doi:10.71548/10686

Immunobiology of Emerging Human DNA Viruses

Kumar, A. (2014) · Työväentutkimus Vuosikirja

The role of immune inhibitory receptors in age-associatedimmune decline

Macaulay, R. (2011) · UCL Discovery (University College London)

The effect of B2 agonists on the immune function

Zalli, A. A. (2013) · University of Birmingham Institutional Research Archive (University of Birmingham)

Homeostasis and function of T cells in healthy individuals and renal transplant recipients

Havenith, S. H. C. (2012) · UvA-DARE (University of Amsterdam)

Comparison of Antiretroviral Therapy (ART) Efficiency and Different HLA Class II Haplotypes

Jasinskis, V. (2014) · Journal of Advances in Medicine and Medical Research · doi:10.9734/bjmmr/2014/5664

Basic and clinical research in the AMC Renal Transplant Unit

ten Berge, I. J. M., & Bemelman, F. J. (2014) · Transplant Immunology · doi:10.1016/j.trim.2014.09.003

The Immune System in the Oldest-Old Clinical and Immunological Studies in the NONA Immune Cohort

Nilsson, B. (2010)

Chronic cytomegalovirus infection drives the accumulation of memory T cells with low functional avidity during ageing

Griffiths, S. (2011) · UCL Discovery (University College London)

Profiles of Cytotoxic Granules in Memory Cd8 t Cells Correlate with Function, Differentiation Stage and Antigen Exposure

Ibarrondo, J., & Brander, C. (2009) · Future Virology · doi:10.2217/fvl.09.16

Efecto del tratamiento con benznidazol sobre la respuesta celular T específica para Trypanosoma cruzi en pacientes en la etapa indeterminada de la enfermedad de Chagas crónica

Mazliah, P., & Eduardo, D. (2011)

Circulation but Not in the Tumor Site T Cells in the + Melanoma-Specific CD8 New Generation Vaccine Induces Effective

Speiser, D. E., Romero, P. J., Leyvraz, S., Rufer, N., Guillaume, P., Krieg, A. Μ., Coupland, S. E., Rimoldi, D., Jandus, C., & Voelter, V. (2015)

Effects of Ageing on Adaptive Immune Responses

Henson, S. M. (2016) · Springer eBooks · doi:10.1007/978-3-319-43365-3_2

HLA-B27-specific Immune Response to Influenza is Critically Dependent on ERAP-1 and on MHC-I Allelic Co-dominant Expression

Akram, A. (2014) · TSpace (University of Toronto)

Global and CMV-specific Immune Assays to Predict Clinical Outcomes and Inform Clinical Practice in Solid Organ Transplant Recipients

Mian, M. F. (2016) · TSpace (University of Toronto)

Immunosenescence

Turner, J. E. (2020) · Springer eBooks · doi:10.1007/978-3-030-39903-0_101906

Immune Activation

Pahwa, S. G., & Phenix, B. N. (2005) · CRC Press eBooks · doi:10.1201/9781420038156.ch11

B4 Microarrays

Wild, S., Bissels, U., Schaffrath, B., & Bosio, A. (2011) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0346-0136-8_15

Screening of Phyllanthus niruri Root Phytoconstituents for Antibacterial, Antifungal, Anticancer, and Antiviral Activities by Molecular Docking Studies

Alekhya, K. P., Manisha, P., Tejaswini, A., Nageswari, P., & Swathi, K. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-31978-5_11

Phenotyping of virus-specific CD8+ effector T-cells over the course of primary EBV infection and the development of PTLD in renal transplant recipientsPreprint

Amirkhan, K. G., van der Putten, C., Frölke, S. C., Kersten, M. J., Remmerswaal, E. B. M., van Aalderen, M. C., & Bemelman, F. J. (2025) · medRxiv · doi:10.1101/2025.05.01.25326787

Markers of immunosenescence and oxidative stress in healthy adults

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