Gotowa bibliografia na temat „Early immune surveillance”
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Artykuły w czasopismach na temat "Early immune surveillance"
Schaller, Julien, i Judith Agudo. "Metastatic Colonization: Escaping Immune Surveillance". Cancers 12, nr 11 (16.11.2020): 3385. http://dx.doi.org/10.3390/cancers12113385.
Pełny tekst źródłaK, Geetha, i Lisa Anna Louis. "A Rare Case of Chorioangioma / Non Immune Fetal Hydrops". Indian Journal of Obstetrics and Gynecology 11, nr 3 (15.09.2023): 31–34. http://dx.doi.org/10.21088/ijog.2321.1636.11323.4.
Pełny tekst źródłaMitra, Roshni, Sarvjeet Singh i Ashok Khar. "Antitumour immune responses". Expert Reviews in Molecular Medicine 5, nr 3 (13.01.2003): 1–22. http://dx.doi.org/10.1017/s1462399403005623.
Pełny tekst źródłaFRIEDMANN, P. S., I. STRICKLAND, A. A. MEMON i P. M. JOHNSON. "Early time course of recruitment of immune surveillance in human skin after chemical provocation". Clinical & Experimental Immunology 91, nr 3 (28.06.2008): 351–56. http://dx.doi.org/10.1111/j.1365-2249.1993.tb05908.x.
Pełny tekst źródłaSopper, Sieghart, Satu Mustjoki, Angelica Loskog, Bjorn T. Gjertsen, Richard Greil, Alois Lang, Werner Linkesch i in. "Immune Monitoring In Patients With Early Chronic Phase Chronic Myelogenous Leukemia (CML-CP) Treated With Frontline Nilotinib". Blood 122, nr 21 (15.11.2013): 2731. http://dx.doi.org/10.1182/blood.v122.21.2731.2731.
Pełny tekst źródłaBrandlmaier, Matthias, Magdalena Hoellwerth, Peter Koelblinger, Roland Lang i Andrea Harrer. "Adjuvant PD-1 Checkpoint Inhibition in Early Cutaneous Melanoma: Immunological Mode of Action and the Role of Ultraviolet Radiation". Cancers 16, nr 8 (11.04.2024): 1461. http://dx.doi.org/10.3390/cancers16081461.
Pełny tekst źródłaUrie, Russell R., Chengchuan Xiao, Elizabeth Hughes, Elizabeth Lombard, Judy Chen, Aaron Morris, Diana Farris, Daniel Goldstein i Lonnie Shea. "Tissue Engineering Scaffolds Remotely Surveil Presymptomatic Allograft Rejection". Journal of Immunology 210, nr 1_Supplement (1.05.2023): 173.40. http://dx.doi.org/10.4049/jimmunol.210.supp.173.40.
Pełny tekst źródłaBayó, Cristina, Gerhard Jung, Marta Español-Rego, Francesc Balaguer i Daniel Benitez-Ribas. "Vaccines for Non-Viral Cancer Prevention". International Journal of Molecular Sciences 22, nr 20 (9.10.2021): 10900. http://dx.doi.org/10.3390/ijms222010900.
Pełny tekst źródłaMorgado, Manuel, Ana Plácido, Sandra Morgado i Fátima Roque. "Management of the Adverse Effects of Immune Checkpoint Inhibitors". Vaccines 8, nr 4 (1.10.2020): 575. http://dx.doi.org/10.3390/vaccines8040575.
Pełny tekst źródłaHamatake, Kiyonori, i Kazuaki Kojima. "Initiatives for immune-related adverse events by the outpatient pharmacist clinic". Trends in Immunotherapy 6, nr 1 (10.01.2022): 3. http://dx.doi.org/10.24294/ti.v6.i1.1385.
Pełny tekst źródłaRozprawy doktorskie na temat "Early immune surveillance"
Pereira, Abrantes Manuela. "Hétérogénéité des neutrophiles et leurs écosystèmes dans l’immunosurveillance au cours de la tumorigenèse". Electronic Thesis or Diss., Lyon 1, 2023. http://www.theses.fr/2023LYO10147.
Pełny tekst źródłaThe neutrophil is the most abundant immune cell in the human blood that migrates rapidly to the inflammatory site. The role of neutrophils has been extensively described in infectious, autoimmune, and allergic contexts, but it remains controversial in cancer, particularly in early immune surveillance mechanisms. Neutrophils are a heterogeneous population, both phenotypically and functionally. The origin and understanding of neutrophil heterogeneity are emerging and increasingly studied, albeit to date, no study has described the evolution of neutrophil heterogeneity at different stages. The aim of my thesis is to characterize this heterogeneity within tissues during tumorigenesis, using two models. My first project focused on colorectal cancer (CRC) in humans, taking advantage of a privileged access to fresh, synchronous, and paired adjacent colorectal tissue samples (AT), preneoplastic tissues (polyps, P), and adenocarcinomas (ADK), from patients undergoing partial or total colectomies. Proteomic quantification demonstrated that neutrophils represent the main increase in the innate immune compartment within ADK. For the first time, transcriptomic profiles of FACS-sorted neutrophils and their cellular partners using RNA-seq and single-cell RNA-seq (scRNA-seq) throughout tumorigenesis were established and integrated to decipher the heterogeneity, evolution, and key cellular interactions of neutrophils in CRC. While the microenvironment of P and ADK were similar and distinct from AT, the transcriptome of P and AT neutrophils were correlated but different from ADK-associated neutrophils. These results suggest a pre-inflammatory niche in P that favors neutrophil modifications, preceding cancer-related inflammation, promoting migration and activation of myeloid cells. P-associated neutrophils exhibited functional properties (e.g. degranulation, activation, cytokine production), while ADK-associated neutrophils showed an "exhausted" state associated with a more pro-tumoral profile (i.e. loss of canonical functions and pro-tumoral profile). scRNA-seq of FACS-sorted neutrophils identified 8 distinct clusters, two of which were specifically enriched in AT and ADK. The AT-enriched cluster was associated with anti-tumoral signatures, while the ADK-enriched cluster demonstrated pro-tumoral characteristics, based on enrichment analyses of publicly available data signatures. Trajectory analyses showed a continuum from AT to P and ADK with three distinct trajectories, where a unique ADK-enriched cluster of neutrophils expressing interferon-stimulated genes stood out from the others. The second project was based on a mouse model of spontaneous mammary carcinogenesis, MMTV-NeuT, for which, unlike the human model, we have access to breast tissues at different stages as well as blood and primary (bone marrow) and secondary (spleen) lymphoid organs. Transcriptomic analysis of FACS-sorted neutrophils revealed distinct phenotypic and functional states depending on the organ and tumor stage. Interestingly, we unveiled the existence of a unique EpCAM+ neutrophil population in tumor tissues, representing 60 to 90% of total neutrophils throughout tumorigenesis. EpCAM expression was not endogenous but seemed to originate from exogenous membrane fragments on the surface of neutrophils, suggesting a mechanism of trogocytosis or even trogoptosis of preneoplastic and tumor cells. Further functional studies will elucidate the mechanism and the role of EpCAM+ neutrophils
Książki na temat "Early immune surveillance"
Stewart, Alex G., Sam Ghebrehewet i Peter MacPherson. New and emerging infectious diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198745471.003.0026.
Pełny tekst źródłaCzęści książek na temat "Early immune surveillance"
Alshammary, Amal F., Mashael Al-Toub, Talat Abdullah Albukhari i Waheed A. Filimban. "Cancer Surveillance". W Molecular Targets and Cancer Therapeutics (Part 2), 271–341. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815124606123010009.
Pełny tekst źródłaRasheed Anjum, Faisal, Sidra Anam, Muhammad Luqman, Ameena A. AL-surhanee, Abdullah F. Shater, Muhammad Wasim Usmani, Sajjad ur Rahman, Muhammad Sohail Sajid, Farzana Rizvi i Muhammad Zulqarnain Shakir. "Fungal Immunology: Mechanisms of Host Innate Immune Recognition and Evasion by Pathogenic Fungi". W Fungal Reproduction and Growth [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101415.
Pełny tekst źródłaCrowcroft, Natasha, i Elizabeth Miller. "Pertussis epidemiology". W Pertussis, 66–86. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198811879.003.0004.
Pełny tekst źródłaMonaco, John J. "Molecular tnechanistns of antigen processing". W Molecular Immunology, 211–47. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780199633791.003.0005.
Pełny tekst źródłaElmaleh, David R., Matthew A. Downey, Ljiljana Kundakovic, Jeremy E. Wilkinson, Ziv Neeman i Eran Segal. "New Approaches to Profile the Microbiome for Treatment of Neurodegenerative Disease". W Advances in Alzheimer’s Disease. IOS Press, 2022. http://dx.doi.org/10.3233/aiad220008.
Pełny tekst źródłaStreszczenia konferencji na temat "Early immune surveillance"
Zhang, Yuan, Jinyang Wang, Yi Xiao, Xiangliang Yuan, Ping Li, Yimin Duan, Victoria L. Seewaldt i Dihua Yu. "Abstract 2592: Boosting immune surveillance by low-dose PI3K inhibitor facilitates early intervention of breast cancer". W Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-2592.
Pełny tekst źródłaWeygant, Nathaniel, Jiannan Yao, Dongfeng Qu, Parthasarathy Chandrakesan, Guangyu An i Courtney W. Houchen. "Abstract 2594: A multigene recurrence signature identifies highly proliferative tumors that escape immune surveillance in early stage lung and pancreas adenocarcinoma". W Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-2594.
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