Relevant bibliographies by topics / Non-lymphoid cells

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Non-lymphoid cells'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Non-lymphoid cells"

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Crouse, David A., James B. Turpen, and J. Graham Sharp. "Thymic non-lymphoid cells." Survey of Immunologic Research 4, no. 2 (1985): 120–34. http://dx.doi.org/10.1007/bf02918808.

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Deyev, Sergey M., Andre Lieber, Boris V. Radko, and Oleg L. Polanovsky. "Production of recombinant antibodies in lymphoid and non-lymphoid cells." FEBS Letters 330, no. 2 (1993): 111–13. http://dx.doi.org/10.1016/0014-5793(93)80253-q.

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Kuper, C. F., D. M. H. Hameleers, J. P. Bruijntjes, I. van der Ven, J. Biewenga, and T. Sminia. "Lymphoid and non-lymphoid cells in nasal-associated lymphoid tissue (NALT) in the rat." Cell and Tissue Research 259, no. 2 (1990): 371–77. http://dx.doi.org/10.1007/bf00318460.

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Abdulla, Zainalabideen, Helen Turley, Kevin Gatter, and Francesco Pezzella. "Immunohistological recognition of cyclin D1 expression by non-lymphoid cells among lymphoid neoplastic cells." APMIS 122, no. 3 (2013): 183–91. http://dx.doi.org/10.1111/apm.12123.

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PALMEN, M. J. H. J., L. A. DIELEMAN, M. B. ENDE, et al. "Non-lymphoid and lymphoid cells in acute, chronic and relapsing experimental colitis." Clinical & Experimental Immunology 99, no. 2 (2008): 226–32. http://dx.doi.org/10.1111/j.1365-2249.1995.tb05537.x.

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Vezzoni, Paolo, Sonia Levi, Elena Gabri, Maria Rosa Pozzi, Silvia Spinazze, and Paolo Arosio. "Ferritins in malignant and non-malignant lymphoid cells." British Journal of Haematology 62, no. 1 (1986): 105–10. http://dx.doi.org/10.1111/j.1365-2141.1986.tb02905.x.

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Dugast, A. S., and B. Vanhove. "Immune regulation by non-lymphoid cells in transplantation." Clinical & Experimental Immunology 156, no. 1 (2009): 25–34. http://dx.doi.org/10.1111/j.1365-2249.2009.03877.x.

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SMINIA, T., A. VANASSELT, M. VDENDE, D. OFHISTOLOGYMEDICAL, and F. FREEUNIVERSITYAMSTERDAMTHEN. "Ontogeny of non-lymphoid cells in rat thymus." Developmental & Comparative Immunology 10, no. 1 (1986): 119. http://dx.doi.org/10.1016/0145-305x(86)90094-7.

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Dijkstra, C. D., and G. Kraal. "Non-lymphoid cells in the splenic white pulp." Research in Immunology 142, no. 4 (1991): 325–28. http://dx.doi.org/10.1016/0923-2494(91)90083-u.

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Huggins, Matthew A., Changwei Peng, Kelsey M. Wanhainen, Abigail R. Gress, Stephen C. Jameson, and Sara E. Hamilton. "Circulating KLRG1+ memory CD8 T cells support immune responses in non-lymphoid tissues." Journal of Immunology 206, no. 1_Supplement (2021): 98.25. http://dx.doi.org/10.4049/jimmunol.206.supp.98.25.

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Abstract The memory T cell population must be durable and capable of responding with rapid effector functions during re-encounter with pathogens. This is accomplished by forming a memory CD8 T cell pool containing multiple distinct subsets of cells that combine varying functional and homing characteristics. At steady-state, memory T cells expressing KLRG1 are restricted to circulation and patrol the host from within the vasculature. These cells convey robust protection during acute rechallenge with pathogens delivered intravenously. Given their localization pattern, we questioned whether KLRG1
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Dissertations / Theses on the topic "Non-lymphoid cells"

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Roake, Justin Alan. "Studies on the properties and migration of non-lymphoid dendritic cells." Thesis, University of Oxford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317810.

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Roubanis, Aristeidis. "Investigating the metabolism of regulatory T cells in non-lymphoid tissues using a genetic approach and an in vivo adaptation of SCENITH." Electronic Thesis or Diss., Sorbonne université, 2024. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2024SORUS321.pdf.

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La régulation du métabolisme cellulaire est un élément central gouvernant le destin et la fonction des cellules T. Parmi les cellules T, les cellules T régulatrices CD4+ Foxp3+ (Tregs) sont essentielles pour le maintien de la tolérance au soi et de l'homéostasie immunitaire. Les Tregs sont présentes dans les tissus lymphoïdes où elles contrôlent les réponses immunitaires et dans divers tissus non-lymphoïdes où elles maintiennent l'homéostasie tissulaire. Les précurseurs des Tregs colonisant les tissus non-lymphoïdes sont présents dans la rate et les ganglions lymphatiques et subissent des étap
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Vieira, Élodie. "Contribution des cellules innées lymphoïdes de groupe 1 dans le développement de la stéatohépathie non alcoolique du foie." Electronic Thesis or Diss., Université Côte d'Azur, 2020. http://www.theses.fr/2020COAZ6009.

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Les maladies chroniques du foie associées à l’obésité représentent un problème de santé publique avec une incidence croissante dans les pays occidentaux. Ces complications se développent à partir d’un foie gras (accumulation de lipides dans les hépatocytes) qui peut évoluer vers la stéatohépatite (NASH) caractérisée par une inflammation et une mort hépatocytaire importante. Ce stade peut alors progresser vers des complications plus sévères comme la fibrose, la cirrhose et le carcinome hépatocellulaire. L’accumulation de lipides toxiques provenant du tissu adipeux et les produits bactériens att
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Nikitin, Artemii. "Role of nuclear receptor RORα in regulatory T cells". Thesis, Université de Lille (2018-2021), 2019. http://www.theses.fr/2019LILUS073.

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Les facteurs de transcription de la superfamille des récepteurs nucléaires jouent de multiples rôles dans le développement et la fonction des lymphocytes T régulateurs (TREG). Les TREG sont des cellules régulatrices/suppressives qui contrôlent les réponses d’autres types cellulaires et l’homéostasie locale des tissus.Comme les TREG sont actives au sein de divers organes, tant à l’homéostasie qu’en conditions inflammatoires,ils doivent répondre à la fois aux contexte local au sein du tissus et à un environnement immunologiquement agressif tout en préservant leurs propriétés tolérogéniques au co
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Bourinet, Manon. "Contribution des cellules innées lymphoïdes NKp46+ et régulation de leurs fonctions par CD44 au cours de la stéatohépatite métabolique." Electronic Thesis or Diss., Université Côte d'Azur, 2024. http://www.theses.fr/2024COAZ6008.

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La maladie hépatique stéatotique associée à un dysfonctionnement métabolique (MASLD) est l'une des principales causes de maladies chroniques du foie avec une prévalence mondiale de 33% en 2022. La MASLD regroupe un spectre de lésions hépatiques allant de la stéatose, (accumulation de lipides dans les hépatocytes) vers la stéatohépatite associée au métabolisme (MASH), caractérisée par une inflammation et une mort hépatocytaire. La MASH est la forme évolutive de la maladie qui peut progresser vers des stades plus sévères comme la fibrose/ cirrhose et le carcinome hépatocellulaire. Des acteurs in
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Olurinde, Mobolaji O. "Antigen-specific memory T cell distribution in non-lymphoid tissue." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/40951.

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Thesis (S.M.)--Massachusetts Institute of Technology, Biological Engineering Division, 2007.<br>Includes bibliographical references (leaves 28-34).<br>CD8+ T cells are the main adaptive immune system cell type responding to intracellular pathogens, particularly viruses, and tumor antigens. In the case of influenza, activated T cells migrate from the mediastinal (draining) lymph nodes to the lung where they perform their cytolytic function. After pathogen clearance, memory CD8+ T cells are generated, giving rise to long-term protection from reinfection. However, these cells are no longer detect
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Barbier, Nicolas. "Étude du rôle des mécanismes épigénétiques dans la transition des cellules stromales mésenchymateuses en fibroblastes associés au cancer et dans l’acquisition de leurs propriétés pro-tumorales dans le lymphome folliculaire." Electronic Thesis or Diss., Université de Rennes (2023-....), 2024. http://www.theses.fr/2024URENB011.

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Le lymphome folliculaire (FL) est le lymphome non-hodgkinien indolent le plus fréquent qui représente 20 à 25% des cas. Le FL est dans 90% des cas caractérisé par la translocation chromosomique t(14;18) des lymphocytes B, qui entraine la surexpression de BCL-2. Pour se développer, le FL est dépendant de son microenvironnement qui fournit notamment des signaux de survie et de prolifération aux lymphocytes B. Ce microenvironnement est composé en partie de cellules stromales lymphoïdes (LSC), qui, dans un contexte physiologique, structurent l’organe et soutiennent la mise en place de réactions im
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Petitprez, Florent. "Integrated analysis and clinical impact of immune and stromal microenvironments in solid tumors Quantitative analyses of the tumor microenvironment composition and orientation in the era of precision medicine Transcriptomic analysis of the tumor microenvironment to guide prognosis and immunotherapies Tumor microenvironment quantification tool draws a comprehensive map of the tumor microenvironment of non-hematologic human cancers The mMCP-counter method to estimate abundance of tissue-infiltrating immune and stromal cell populations using gene expression in murine samples Immune sub-classes in sarcoma predict survival and immunotherapy response Intra-tumoral tertiary lymphoid structures are associated with a low risk of hepatocellular carcinoma early recurrence Association of IL-36γ with tertiary lymphoid structures and inflammatory immune infiltrates in human colorectal cancer Immune-based identification of cancer patients at high risk of progression Tumor-infiltrating and peripheral blood T-cell immunophenotypes predict early relapse in localized clear cell renal cell carcinoma PD-L1 expression and CD8+ T-cell infiltrate are associated with clinical progression in patients with node-positive prostate cancer Intratumoral classical complement pathway activation promotes cancer progression". Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCB104.

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Les tumeurs sont composées de cellules malignes et d'une grande variété de cellules non-tumorales, en particulier des cellules immunitaires qui forment le micro-environnement tumoral (MET). Il a été démontré que la composition du MET était associée au devenir clinique des patients, en termes de survie et de réponses thérapeutiques. Avec le développement récent des immunothérapies qui ciblent des éléments spécifiques du MET, l'immunité anti-tumorale a soulevé un intérêt majeur. Plusieurs méthodologies ont été mises au point afin d'étudier la composition du MET, avec une précision toujours plus
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Bai, Li-Yuan, and 白禮源. "Treating B-cell lymphoid malignancies with non-conventional chemotherapeutic agents: study of compounds targeting p38 MAPK, Akt pathways or histone deacetylase." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/00407222502301962749.

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博士<br>中國醫藥大學<br>臨床醫學研究所博士班<br>99<br>Hematological malignancies can be grouped as either myeloid or lymphoid disorders. The standard treatment strategy for lymphoid malignancies is chemotherapeutic agents, usually in combination with monoclonal antibodies which have introduced great impact on the clinical situation. Although certain subtypes of lymphoid malignancies, e.g. diffuse large B cell lymphoma, have good response to initial treatment, some of patients will succumb to the disease because of development of drug resistance. Still others are primarily refractory to initial therapy. The prog
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Books on the topic "Non-lymphoid cells"

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Cerhan, James R., Claire M. Vajdic, and John J. Spinelli. The Non-Hodgkin Lymphomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0040.

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The non-Hodgkin lymphomas (NHL) are a heterogeneous group of over forty lymphoid neoplasms that have undergone a major redefinition over the last twenty-five years, in part due to advances in immunology and genetics as well as implementation of the WHO classification system. NHLs are considered clonal tumors of B-cells, T-cells, or natural killer (NK) cells arrested at various stages of differentiation, regardless of whether they present in the blood (lymphoid leukemia) or lymphoid tissues (lymphoma). In the United States, the age-standardized NHL incidence rate (per 100,000) doubled from 1973
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Cytological basis of immune functions of the spleen: Immunocytochemical characterization of lymphoid and non-lymphoid cells involved in the "in situ" immune response. Fischer, 1989.

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Cytological Basis of Immune Functions of the Spleen: Immunocytochemical Characterization of Lymphoid and Non-Lymphoid Cells Involved in the in Situ I (Progress in Histochemistry and Cytochemistry). Gustav Fischer, 1989.

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Albert, Tyler J., and Erik R. Swenson. The blood cells and blood count. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0265.

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Blood is a dynamic fluid consisting of cellular and plasma components undergoing constant regeneration and recycling. Like most physiological systems, the concentrations of these components are tightly regulated within narrow limits under normal conditions. In the critically-ill population, however, haematological abnormalities frequently occur and are largely due to non-haematological single- or multiple-organ pathology. Haematopoiesis originates from the pluripotent stem cell, which undergoes replication, proliferation, and differentiation, giving rise to cells of the erythroid, myeloid, and
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Batchelor, Tracy, Joshua P. Klein, Andrés José María Ferreri, and Lisa M. DeAngelis, eds. Oxford Textbook of Neurohaematology. Oxford University PressOxford, 2024. http://dx.doi.org/10.1093/med/9780198884903.001.0001.

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Abstract The Oxford Textbook of Neurohaematology is the first dedicated source of knowledge on the diverse neurological conditions associated with malignant and classical haematological diseases. The book is divided into three sections. In the first section, neurological conditions associated with malignant haematological diseases are covered. This section begins with chapters on primary haematological malignancies of the nervous system, including primary central nervous system lymphomas, vitreoretinal lymphoma, and other rare primary malignancies such as Hodgkin disease and lymphoproliferativ
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Carton, James. Haematopathology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198759584.003.0015.

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This chapter discusses haematopathology, including iron deficiency anaemia, anaemia of chronic disease, megaloblastic anaemias, hereditary spherocytosis, glucose-6-phosphate dehydrogenase deficiency, thalassaemias, sickle-cell disorders, idiopathic thrombocytopenic purpura (ITP), thrombotic thrombocytopenic purpura (TTP), von Willebrand disease, haemophilia, thrombophilia, acute B-lymphoblastic leukaemia, acute myeloid leukaemias, chronic lymphocytic leukaemia (CLL), chronic myelogenous leukaemia, polycythaemia vera (PV), essential thrombocythaemia (ET), primary myelofibrosis (PMF), myelodyspl
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Batchelor, Tracy T., Oussama Abla, Zhong-ping Chen, Dennis C. Shrieve, and Samar Issa. Tumours of the haematopoietic system. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0013.

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‘Tumours of the haematopoietic system’ examines the epidemiology, the pathogenesis, and the clinical features of adult and childhood primary central nervous system lymphomas (PCNSLs), extranodal forms of non-Hodgkin lymphoma, as well as the histiocytoses included in the World Health Organization (WHO) classification of central nervous system (CNS) tumours. It reviews these features in the most common PCNSL, primary central nervous system diffuse large B-cell lymphoma, as well as the other rare histopathological PCNSL variants including lymphomatoid granulomatosis, T-cell lymphoma, anaplastic l
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Cassidy, Jim, Donald Bissett, Roy A. J. Spence OBE, Miranda Payne, and Gareth Morris-Stiff. Bone and soft tissue malignancies. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199689842.003.0025.

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Haematological malignancies examines the epidemiology, genetics, clinical presentation and classification of these diseases, and presents current treatment approaches for each. First are the acute leukaemias, and the management of acute lymphoblastic leukaemia (ALL) and acute myeloid leukaemia (AML). Chronic myeloid leukaemia, its genetics and sensitivity to tyrosine kinase inhibitors, is described. Myelodysplastic syndromes and their management, are followed by chronic lymphoid leukaemias, a large heterogeneous group of diseases, and their treatment. Hodgkin lymphoma, its pathology and presen
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Book chapters on the topic "Non-lymphoid cells"

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Pelchen-Matthews, Annegret, Jane E. Armes, and Mark Marsh. "Endocytosis of CD4 in Lymphoid and Non-Lymphoid Cells." In Endocytosis. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84295-5_44.

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Roake, J. A., A. S. Rao, C. P. Larsen, and J. M. Austyn. "Migration and maturation of non-lymphoid dendritic cells." In Mononuclear Phagocytes. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-015-8070-0_10.

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Breel, M., M. B. van der Ende, T. Sminia, and G. Kraal. "Subpopulations of Non-Lymphoid Cells in Bronchus Associated Lymphoid Tissue and Lung of the Mouse." In Advances in Experimental Medicine and Biology. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5535-9_92.

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Cattoretti, Giorgio, Domenico Delia, Luciana Parola, et al. "Heterogeneous Expression of Myelo-Monocytic Markers on Selected Non-Lymphoid Cells." In Leukocyte Typing II. Springer New York, 1986. http://dx.doi.org/10.1007/978-1-4612-4850-7_18.

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Palmen, Mary J. H. J., Marja B. van der Ende, A. Salvador Peña, and Emmelien P. van Rees. "Non-Lymphoid Cells in Acute and Chronic Experimental Inflammatory Bowel Disease." In In Vivo Immunology. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2492-2_48.

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Beelen, Robert H. J., Ellen van Vugt, Joke J. E. Steenbergen, Michiel G. H. Betjes, Carin E. G. Havenith, and Eduard W. A. Kamperdijk. "Dendritic Cells Isolated From Rat and Human Non-Lymphoid Tissue are Very Potent Accessory Cells." In Advances in Experimental Medicine and Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2930-9_21.

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Ward, Eleanor Jayne, Hongmei Fu, and Federica Marelli-Berg. "Monitoring Migration of Activated T Cells to Antigen-Rich Non-lymphoid Tissue." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6931-9_15.

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Plaisance, S., A. Alileche, D. Han, et al. "Expression and Role of Surface Markers of Immunocompetent Cells in Non Lymphoid Systems." In Flow Cytometry. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_6.

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W. Hoskin, D., R. A. Murgita, S. Hamel, and K.-O. Gronvik. "PREGNANCY INTERRUPTION BY A MONOCLONAL ANTIBODY THAT RECOGNIZES NON-T SUPPRESSOR CELLS IN MATERNAL LYMPHOID TISSUE." In Pregnancy Proteins in Animals, edited by Jann Hau. De Gruyter, 1986. http://dx.doi.org/10.1515/9783110858167-035.

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Sripada, Anand, Kapil Sirohi, and Rafeul Alam. "Isolation and Characterization of Conventional and Non-conventional Type 2 Innate Lymphoid Cells (ILC2s) from Human Peripheral Blood Mononuclear Cells (PBMCs)." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2364-0_13.

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Conference papers on the topic "Non-lymphoid cells"

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Rosenbluth, Michael J., Wilbur A. Lam, and Daniel A. Fletcher. "Contribution of Cell Mechanics to Acute Leukemia." In ASME 2004 International Mechanical Engineering Congress and Exposition. ASMEDC, 2004. http://dx.doi.org/10.1115/imece2004-59881.

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Leukostasis is a life-threatening condition that occurs when leukemia cells accumulate in the vasculature of organs such as the brain and lungs. Recent evidence has shown that leukostasis is not simply due to the physical overcrowding of leukemia cells, as previously thought, but may result from specific mechanical properties of the cells and interactions between cells. Using atomic force microscopy (AFM), we obtained direct measurements of two mechanical properties that are likely involved in this condition: (1) stiffness of individual leukemia cells and (2) non-specific adhesion forces betwe
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Jonckheere, A., B. Steelant, S. Seys, et al. "The potential role of innate lymphoid cells in non-allergic neutrophilic asthma model." In ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.lsc-0010.

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Jonckheere, Anne-Charlotte, Brecht Steelant, Sven Seys, et al. "The potential role of innate lymphoid cells in non-allergic neutrophilic asthma model." In ERS Lung Science Conference 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/23120541.lsc-2022.10.

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Meunier, I., I. Marois, M. Richter, and G. Boire. "SAT0002 Innate lymphoid cells (ILCS) are differentially distributed in inflammatory and non-inflammatory joint diseases." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.4095.

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Matsuyama, Takahiro, Yoshihisa Tokunaga, Xiaotian Ju, et al. "A comparative analyses of group 2 innate lymphoid cells in sputum from patients with non-asthmatic eosinophilic bronchitis and allergic asthma." In ERS Congress 2024 abstracts. European Respiratory Society, 2024. http://dx.doi.org/10.1183/13993003.congress-2024.oa1073.

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Falang, A., G. M. Alessio, M. Donati, and T. A. Barbui. "DISSEMINATED INTRAVASCULAR COAGULATION (DIC) AND ACUTE LEUKEMIA:IDENTIFICATION OF A NEW CELLULAR PROCOAGULANT." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643661.

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There is an enhanced incidence (&gt;50%) of severe coagulopathy in association with several types of acute leukemias. Cell associated procoagulants are considered important in this context. So far only a Tissue Factor (TF)-type procoagulant has been described in leukemic cells. We have set up here the experimentalconditions to identify other possible cellular procoagulants in leukemia. We have tested blast cell extracts from 21 patients with 5 different cytological subtypes (from Ml to M5 of acute non lymphoid leukemia (ANLL), according to theFAB classification, in order to assay whether they
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Engelhard, Victor H., David Peske, Amber Woods, Nithya Srinivasan, Colin Brinkman, and Andrew Ferguson. "Abstract IA23: T cell trafficking in lymphoid and non-lymphoid tissues." In Abstracts: AACR Special Conference: Tumor Immunology and Immunotherapy: A New Chapter; December 1-4, 2014; Orlando, FL. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/2326-6074.tumimm14-ia23.

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Goi, Mariana Copetti, Ana Paula Santana de z. Abreu, Sheila Cristina Lordelo Wludarski, Joaquim Teodoro de Araújo Neto, and Edison Mantovani Barbosa. "Primary breast lymphoma associated with invasive breast carcinoma: a case report." In XXVI Brazilian Mastology Congress. Mastology, 2024. https://doi.org/10.29289/259453942024v34s2039.

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Introduction: This case report describes a 54-year-old patient who developed invasive breast carcinoma in her left breast without further specifications, of the luminal B molecular subtype, concurrently with a primary breast lymphoma (diffuse large B-cell lymphoma with the germinal center B-cell subtype), which was definitively diagnosed only after surgical intervention. Synchronous occurrence of breast cancer and non-Hodgkin lymphoma (NHL) is an uncommon situation, with only 38 cases reported in the literature. It is extremely rare for both tumors to present as a collision tumor within the sa
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Segura, Rossana Natalia Lazcano, Andre Catao, Luisa M. Solis, et al. "Abstract 399: Tertiary lymphoid structures features associate with outcome in non-small cell lung carcinoma." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-399.

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van Zelst, C., J. In'T Veen, G. De Boer, et al. "Differences in Innate Lymphoid Cell profiles between COPD, asthma, smoking controls and non-smoking healthy controls." In ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.3635.

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