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Relevant bibliographies by topics / Naine T

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Academic literature on the topic 'Naine T'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Naine T"

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Rodrigues Filho, Vagner A., Júlio C. L. Neves, Sérgio L. R. Donato, and Bruno V. C. Guimarães. "Model for determining nutritional and non-nutritional limitations of Grande Naine banana in the Brazilian semiarid region." Revista Brasileira de Engenharia Agrícola e Ambiental 25, no. 8 (August 2021): 538–46. http://dx.doi.org/10.1590/1807-1929/agriambi.v25n8p538-546.

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ABSTRACT Plant nutrition is essential in attaining higher yields; however, non-nutritional factors play a major role in limiting crop yield. This study aimed to model and determined nutritional and non-nutritional limitations of Grande Naine banana grown in Ceará and Bahia states, Brazil, based on nutritional balance and equilibrium. The data used in this study were collected between 2010 and 2017 from two farms, located in Missão Velha, Ceará (7° 35’ 90” S and 39° 21’ 17” W, and 442 m of altitude), and Ponto Novo, Bahia (10º 51’ 46” S and 40º 08’ 01” W, and 342 m of altitude). Plots with yields greater than the average plus 0.5 standard deviations were defined as high-yielding populations (HYP) and used as a reference population to establish the norms. Plots with yields below this limit, low-yielding populations (LYP), were used for nutritional diagnosis. The database was divided into four. The first and second databases, from the area located in Missão Velha, contained 46 samples from a reference population with a yield greater than 58.84 t ha-1 per year, and 104 samples from an LYP, respectively. The third and four databases, from the area located in Ponto Novo, contained 19 samples from a reference population with a yield greater than 76.12 t ha-1 per year, and 46 samples from an LYP, respectively. Nutritional factors limited Grande Naine banana yield in Ceará and Bahia by 11.17 and 14.79%, while non-nutritional factors limited by 30.11 and 29.41%, respectively. In Grande Naine banana, non-nutritional factors are more yield-limiting than nutritional factors.

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Sousa, Valdemício Ferreira de, Marcos Emanuel da Costa Veloso, Lúcio Flavo Lopes Vasconcelos, Valdenir Queiroz Ribeiro, Valdomiro Aurélio Barbosa de Souza, and Boanerges Siqueira d'Albuquerque Junior. "Nitrogênio e potássio via água de irrigação nas características de produção da bananeira 'Grand Naine'." Pesquisa Agropecuária Brasileira 39, no. 9 (September 2004): 865–69. http://dx.doi.org/10.1590/s0100-204x2004000900005.

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O objetivo deste trabalho foi avaliar o efeito do nitrogênio e do potássio, aplicados via água de irrigação por microaspersão, sobre as características de produção da bananeira, cv. Grand Naine. O delineamento utilizado foi o de blocos casualizados, com quatro repetições. Os tratamentos consistiram de 30, 180, 300, 420 e 570 kg ha-1 ano-1 de N e de 55, 330, 550, 770 e 1.045 kg ha-1 ano-1 de K2O, e testemunha, sem adubação, totalizando onze tratamentos, de acordo com o modelo da matriz experimental de Plan Puebla III. Foram avaliadas as características: massa média de fruto, massa média de cacho e produtividade, referentes ao primeiro e segundo ciclos de produção. No primeiro e segundo ciclos, a massa média de fruto, a massa média de cacho e a produtividade foram influenciadas apenas pelas doses de potássio. Os maiores valores de massa média de fruto (253,47 g), massa média de cacho (28 kg) e produtividade (55,42 t ha-1), no primeiro ciclo, foram obtidos com a aplicação de 938,31, 665,38 e 665,27 kg ha-1 de K2O, respectivamente. No segundo ciclo, os maiores valores em relação à massa média de fruto (174, 22 g), massa média de cacho (32,04 kg) e produtividade (60,08 t ha-1) foram alcançados com a aplicação de 725,50, 907,50 e 933,33 kg ha-1 de K2O, respectivamente. Não houve resposta das características avaliadas ao nitrogênio.

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Bengaly, Zakaria, Peter-Henning Clausen, Hamidou Boly, Augustin Kanwé, and Gérard Duvallet. "Comparaison de la trypanosomose expérimentale chez certaines races de petits ruminants au Burkina Faso." Revue d’élevage et de médecine vétérinaire des pays tropicaux 46, no. 4 (April 1, 1993): 563–70. http://dx.doi.org/10.19182/remvt.9410.

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Pour comparer leurs degrés respectifs de sensibilité à l'égard de la trypanosomose, 24 moutons et chèvres de race naine Djallonké, et 16 moutons et chèvres Peul du Sahel, ont été inoculés avec des souches de Trypanosoma vivax et de Trypanosoma congolense. Un animal de chaque race a servi de témoin. Une anémie est observée chez tous les animaux inoculés. Pour l'infection à T. vivax, 1 chèvre Djallonké sur 6, 3 chèvres sur 4 et 2 moutons sur 4 de race Peul du Sahel sont morts en 16 semaines d'expérimentation. Une seule mortalité sur 4 est enregistrée dans le lot des moutons Peul du Sahel, pour l'infection à T. congolense. Les chutes de poids et de concentration leucocytaire observées ne diffèrent pas significativement entre Djallonké et Peul du Sahel durant 8 semaines. Cette étude montre une bonne résistance des moutons et chèvres Djallonké à l'infection à T. vivax. Par contre, il n'y a pas de différence significative entre les deux races de moutons et de chèvres infectés à T.congolense.

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GOENAGA, R., and H. IRIZARRY. "YIELD OF BANANA GROWN WITH SUPPLEMENTAL DRIP-IRRIGATION ON AN ULTISOL." Experimental Agriculture 34, no. 4 (October 1998): 439–48. http://dx.doi.org/10.1017/s0014479798004062.

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A three-year study was conducted on an Ultisol to determine the water requirement, yield and fruit-quality traits of three ratoon crops (R1, R2, R3) of ‘Grande Naine’ banana (Musa acuminata Colla, AAA group) subjected to four levels of irrigation. The irrigation treatments were based on Class A pan factors ranging from 0.0 (rainfed) to 1.0 in increments of 0.25. When needed, drip irrigation was supplied three times a week on alternate days. Results showed significant (p < 0.01) irrigation treatment and crop effects on bunch weight, yield, bunch mean hand weight, weight and fruit diameter of the third and last hands, and length of fruits of the third hand. Highest marketable yield (47.9 t ha−1) was obtained from the R2 crop with water application according to a pan factor of 1.0. It was concluded that irrigating the crop according to a pan factor of 1.0 was sufficient to justify the investment of a drip-irrigation system for a farm in the mountain region.

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Teixeira, Luiz Antonio Junqueira, Bernardo Van Raij, and José Emílio Bettiol Neto. "Estimativa das necessidades nutricionais de bananeiras do subgrupo Cavendish cultivadas no Estado de São Paulo." Revista Brasileira de Fruticultura 30, no. 2 (June 2008): 540–45. http://dx.doi.org/10.1590/s0100-29452008000200047.

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A acumulação na planta e a exportação de nutrientes pela colheita dos cachos são alguns dos fatores que determinam a necessidade de adubação para a cultura da bananeira. Visando a estimar as quantidades de nutrientes acumulados e exportados por bananeiras do subgrupo Cavendish, nas condições de cultivo do Estado de São Paulo, foram considerados 293 registros de um banco de dados contendo teores de N, P, K, Ca, Mg, S, B, Cu, Fe, Mn e Zn em frutos e em engaços e massa dos cachos das cultivares Grande Naine e Nanicão. Esses registros provieram de experimentos de adubação realizados no Planalto Paulista e no Vale do Ribeira, em áreas irrigadas e de sequeiro, durante sete ciclos de cultivo, variando fontes, doses e formas de aplicação de fertilizantes. Para produzir 40 t ha-1, em média, o nutriente exportado pelos cachos em maior quantidade foi o K (182 kg ha-¹ ) seguido pelo N (68 kg ha-¹), Mg (10 kg ha-¹), P (8 kg ha-¹), Ca (6 kg ha-¹), S (3 kg ha-¹), Mn (191 g ha-¹), Fe (147 g ha-¹), B (89 g ha-¹), Zn (68 g ha-¹) e Cu (25 g ha-¹). A recomendação de adubação para bananeira para o Estado de São Paulo, aparentemente, subestima a necessidade de K na implantação da cultura e preconiza doses de N muito superiores à exportação de N pelos cachos. Para P, a recomendação está coerente com as necessidades estimadas para a cultura.

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Ko, Dong-Woo, and Jung-Jin Yang. "New Exploration to Identify the Naive T Cell-Specific Gene Using Gene Similarity." Journal of Korean Institute of Information Technology 18, no. 2 (February 28, 2020): 33–43. http://dx.doi.org/10.14801/jkiit.2020.18.2.33.

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Pereira, Lair Victor, Sebastião de Oliveira e. Silva, Elio José Alves, and Carlos Ramirez de Rezende e. Silva. "Avaliação de cultivares e hibridos de bananeira em lavras, MG." Ciência e Agrotecnologia 27, no. 1 (February 2003): 17–25. http://dx.doi.org/10.1590/s1413-70542003000100002.

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Avaliaram-se os genótipos de bananeira Nam, Pioneira, Caipira, Prata Anã, Grande Naine, SH36-40, FHIA 18, FHIA 01 e PV 03-44, em condições de sequeiro na região sul de Minas Gerais, com o objetivo de identificar os mais produtivos e com melhor adaptação edafoclimática, em comparação com as cultivares Prata e Prata Anã, tradicionalmente cultivadas nessa região. O ensaio foi conduzido na Fazenda Experimental da EPAMIG, em Lavras, no período de 1997 a 1999. Cada genótipo foi plantado em blocos de 50 plantas, no espaçamento 3,0 x 3,0 m, sendo a parcela útil as 24 plantas centrais e uma por repetição. O híbrido SH36-40 foi superior aos demais em peso médio dos cachos (16,56 kg), frutos (171,00 g), diâmetro (4,21 cm) e comprimento dos frutos (17,64 cm) nos três primeiros ciclos. Isso corresponde a um rendimento de 18,5 t/ha, cerca de duas vezes maior que a produção das cultivares Prata Anã, Pioneira, Nam, Caipira e três vezes maior que a do híbrido PV 03-44. O híbrido SH 36-40 apresentou, ainda, porte médio de 2,75 m, ciclo em torno de 17,5 meses e o menor período da emissão à colheita do cacho, inferior a 4,83 meses para as plantas-mãe, filha e neta. Esse híbrido apresentou também um menor e mais tardio perfilhamento. Os híbridos SH 36-40 e FHIA 01 apresentaram os maiores incrementos nos pesos dos cachos e dos frutos do primeiro para o terceiro ciclo. As cultivares Caipira, Prata Anã, Pioneira e Nam produziram cachos com peso médio inferior a 9,0 kg e o híbrido PV0344, inferior a 6,0 kg. A cv. Caipira foi a mais tardia, com um ciclo em torno de 22 meses e a Prata Anã e Pioneira, as mais precoces, com cerca de 16,6 meses no primeiro ciclo e 15,5 no segundo e terceiro ciclos.

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Helft, Julie, Alexandra Jacquet, Nathalie T. Joncker, Isabelle Grandjean, Guillaume Dorothée, Adrien Kissenpfennig, Bernard Malissen, Polly Matzinger, and Olivier Lantz. "Antigen-specific T-T interactions regulate CD4 T-cell expansion." Blood 112, no. 4 (August 15, 2008): 1249–58. http://dx.doi.org/10.1182/blood-2007-09-114389.

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Abstract The regulation of CD4 T-cell numbers during an immune response should take account of the amount of antigen (Ag), the initial frequency of Ag-specific T cells, the mix of naive versus experienced cells, and (ideally) the diversity of the repertoire. Here we describe a novel mechanism of T-cell regulation that potentially deals with all of these parameters. We found that CD4 T cells establish a negative feedback loop by capturing their cognate major histocompatibility class (MHC)/peptide complexes from Ag-presenting cells and presenting them to Ag-experienced CD4 T cells, thereby inhibiting their recruitment into the response while allowing recruitment of naive T cells. The inhibition is Ag specific, begins at day 2 (long before Ag disappearance), and cannot be overcome by providing new Ag-loaded dendritic cells. In this way, CD4 T-cell proliferation is regulated in a functional relationship to the amount of Ag, while allowing naive T cells to generate repertoire variety.

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Gerlach, Carmen, Jeroen W. J. van Heijst, Erwin Swart, Daoud Sie, Nicola Armstrong, Ron M. Kerkhoven, Dietmar Zehn, Michael J. Bevan, Koen Schepers, and Ton N. M. Schumacher. "One naive T cell, multiple fates in CD8+ T cell differentiation." Journal of Experimental Medicine 207, no. 6 (May 17, 2010): 1235–46. http://dx.doi.org/10.1084/jem.20091175.

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The mechanism by which the immune system produces effector and memory T cells is largely unclear. To allow a large-scale assessment of the development of single naive T cells into different subsets, we have developed a technology that introduces unique genetic tags (barcodes) into naive T cells. By comparing the barcodes present in antigen-specific effector and memory T cell populations in systemic and local infection models, at different anatomical sites, and for TCR–pMHC interactions of different avidities, we demonstrate that under all conditions tested, individual naive T cells yield both effector and memory CD8+ T cell progeny. This indicates that effector and memory fate decisions are not determined by the nature of the priming antigen-presenting cell or the time of T cell priming. Instead, for both low and high avidity T cells, individual naive T cells have multiple fates and can differentiate into effector and memory T cell subsets.

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Klein, Dieter. "HIV latency in naive T cells." Trends in Molecular Medicine 7, no. 7 (July 2001): 285. http://dx.doi.org/10.1016/s1471-4914(01)02071-8.

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Dissertations / Theses on the topic "Naine T"

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Ferreira, Cristina da ConceicÌ§aÌƒo Varandas. "Naive T cell survival : analysis of transgenic monoclonal T cell populations." Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250701.

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Yang, Liang Peng. "The maturation of naive human CD4 T lymphocytes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1996. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/nq21528.pdf.

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Gaß, Nadine [Verfasser], and H. A. [Akademischer Betreuer] Wagenknecht. "PhotoDNAzyme - Asymmetrische Katalyse und Distanzabhängigkeit der T-T-Dimerbildung / Nadine Gaß ; Betreuer: H.-A. Wagenknecht." Karlsruhe : KIT-Bibliothek, 2016. http://d-nb.info/1122461518/34.

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Grebe, Nadine [Verfasser]. "Analyse humaner regulatorischer T-Zellen im humanisierten Mausmodell / Nadine Grebe." Mainz : Universitätsbibliothek Mainz, 2013. http://d-nb.info/103701264X/34.

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Cowan, Teresa. "The TCRBJ and TCRBV repertoire in naive and memory human T-cells." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ34173.pdf.

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Martin, Matthew David. "Naive and memory CD8 T cell responses after antigen stimulation in vivo." Thesis, University of Iowa, 2011. https://ir.uiowa.edu/etd/1246.

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The extent to which the progeny of one primary memory CD8 T cell differs from the progeny of one naïve CD8 T cell of the same specificity remains an important question. In order to explore cell autonomous functional differences between naïve and memory CD8 T cells that are not influenced by differences in the priming environment, an experimental model has been developed in which physiological numbers of both populations of cells were co-transferred into naïve host before antigen-stimulation. Interestingly, naïve CD8 T cells expand in numbers more than primary memory CD8 T cells after various infections or immunizations. The intrinsic ability of one naïve CD8 T cell to give rise to more effector CD8 T cells than one memory CD8 T cell is independent of the number of primary memory CD8 T cells present in vivo. The sustained proliferation of primary, but not the increased death of secondary effectors was shown to contribute to the differences in the observed magnitudes of expansion. In addition, longitudinal analysis of primary and secondary CD8 T cell responses revealed that the ability of naïve CD8 T cells to generate long-lived progeny (`memory generation potential') is better than for primary memory CD8 T cells despite the differences in overall kinetics of both responses after infection. Taken together, the data presented here revealed previously unappreciated differences between naïve and memory CD8 T cells and will help further define the functional potential for both cell types. The goal of immunization is to generate memory CD8 T cells of sufficient quality and quantity, and it has been shown that the naïve to primary memory CD8 T cell differentiation in vivo is controlled, at least in part, by the amount and duration of inflammation present early after the initiation of the response. In experiments where naïve CD8 T cells were co-transferred with increasing numbers of primary memory CD8 T cells, we observed a negative correlation between the number of primary memory present and the magnitude of primary CD8 T cell responses. Interestingly, the conversion of newly recruited (either TCR-Tg or endogenous) primary CD8 T cells into CD8 T cells with the phenotype (CD62Lhi, CD27hi) and function (tissue distribution, Ag-driven proliferation, cytokine production) of long-term memory was facilitated when they were primed in the presence of memory CD8 T cells of the same or unrelated specificity. Therefore, these data suggest that the presence of anti-vectorial immunity will not necessarily decrease the efficacy of CD8 T cell vaccination since newly recruited CD8 T cells, despite their decreased magnitude of expansion, might differentiate into functional memory cells faster.

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Yang, Edward. "The localization of naive and memory CD8⁺ T cells following infection." Diss., [La Jolla] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p1465089.

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Thesis (M.S.)--University of California, San Diego, 2009.
Title from first page of PDF file (viewed June 22, 2009). Available via ProQuest Digital Dissertations. Includes bibliographical references (p. 43-45).

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Correia, Rodolfo Patussi. "Estudo da distribuição de células T naive e subtipos de células T de memória em neoplasias hematológicas." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-19042013-092628/.

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Células T de memória são a marca registrada da imunidade adaptativa, e podem ser caracterizadas em central memory (TCM) e effector memory (TEM) T cells. A participação destas células no curso de doenças hematológicas é descrita como mecanismo relacionado à evolução das mesmas. Neste trabalho, analisamos o sangue periférico de doadores de sangue e pacientes com Mielodisplasia (SMD), Mieloma Múltiplo (MM) e Leucemia linfocítica crônica B (LLC), e avaliamos a distribuição das células T CD4+ e CD8+ naive e de memória. SMD e MM não apresentaram resultados significativos, mas na LLC, as células T CD4+ estavam alteradas e dependentes do prognóstico, com aumento das células TCM somente nos pacientes com prognóstico ruim. Essas evidências sugerem que interações imunológicas entre células B da LLC e células T CD4+ possa ser um mecanismo próprio da doença que venha interferir na fisiopatologia e favorecer a geração de células TCM, que podem fornecer sinais de sobrevivência, como citocinas e CD40L, contribuindo assim para o estabelecimento e agressividade da LLC.
Memory T cells are the hallmark of adaptive immunity and are characterized as central (TCM) and effector memory (TEM) T cells. The influence of T cells in the course of hematological malignancies has been described as a mechanism related to the evolution. In this study, we analyzed the peripheral blood of healthy donors and patients with myelodysplastic syndrome (MDS), multiple myeloma (MM) and chronic lymphocytic leukemia B (CLL), and analyzed the distribution of CD4+ and CD8+ naive and memory T cells. MDS and MM revealed no significant difference, but CLL patients showed changes in CD4+ T cell and it were dependent on the prognosis. Patients with poor prognosis presented increased in frequency and absolute number of TCM cells. These evidences show that immunological interactions between CLL and CD4+ T cells could be a disease mechanism that could interfere in pathophysiology and result in the generation of TCM cells, that provide survival signals to the tumor clone, such as cytokines and CD40L, thus contributing to establishment and more aggressive CLL progression.

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Hoellman, John Richard. "Contact-Dependent Activation of Macrophages by Naive CD4⁺ T cells." [Johnson City, Tenn. : East Tennessee State University], 2000. http://etd-submit.etsu.edu/etd/theses/available/etd-0602100-130806/restricted/electhesisJU21c.pdf.

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Stirk, Emily Ruth. "Stochastic modelling of diversity and ageing in the naive T cell repertoire." Thesis, University of Leeds, 2010. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531516.

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Books on the topic "Naine T"

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s, Louis de (pseud coll ). Boanerge. Actualite de la fin des temps: Biento t le re gne mille naire : historique apologe tique du mille narisme. [S.l.]: L. de Boanerge s, 1993.

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Book chapters on the topic "Naine T"

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Seddon, Benedict, Sanket Rane, and Andrew J. Yates. "Modelling Naive T Cell Homeostasis." In Mathematical, Computational and Experimental T Cell Immunology, 45–64. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-57204-4_3.

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Beverley, P. C. L., M. Merkenschlager, and D. L. Wallace. "Identification of Human Naive and Memory T Cells." In Progress in Immunology, 432–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83755-5_57.

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Gupta, Sudhir, and Ankmalika Gupta. "Molecular Mechanisms of Apoptosis in Naive and Memory Human T-Cell Subsets." In Handbook of Immunosenescence, 1–21. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-64597-1_36-1.

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Gupta, Sudhir, and Ankmalika Gupta. "Molecular Mechanisms of Apoptosis in Naive and Memory Human T Cell Subsets." In Handbook of Immunosenescence, 1139–59. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-99375-1_36.

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Horgan, Kevin J., Yoshiya Tanaka, and Stephen Shaw. "Postthymic Differentiation of CD4 T Lymphocytes: Naive Versus Memory Subsets and Further Specialization among Memory Cells (Part 1 of 2)." In Regulation and Functional Significance of T-Cell Subsets, 72–87. Basel: KARGER, 1992. http://dx.doi.org/10.1159/000319115.

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Horgan, Kevin J., Yoshiya Tanaka, and Stephen Shaw. "Postthymic Differentiation of CD4 T Lymphocytes: Naive Versus Memory Subsets and Further Specialization among Memory Cells (Part 2 of 2)." In Regulation and Functional Significance of T-Cell Subsets, 88–102. Basel: KARGER, 1992. http://dx.doi.org/10.1159/000319116.

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Meng, Xiangzhi, Nicole Riley, Ryan Thompson, and Siddhartha Sharma. "Investigate Global Chromosomal Interaction by Hi-C in Human Naive CD4 T Cells." In Methods in Molecular Biology, 239–52. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7514-3_15.

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Mielke, M. E. A., C. Peters, S. Brocke, and H. Hahn. "Cytokines produced by T cell subset-depleted naive and listeria-immune spleen cells." In Mononuclear Phagocytes, 585–92. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-015-8070-0_78.

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Hinz, S., L. Pagerols-Raluy, H. H. Oberg, D. Wesch, D. Kabelitz, R. Grützmann, F. Fändrich, and H. Kalthoff. "Bedeutung der Expresssion des T-reg Markers FOXP3 in Pankreasadenocarzinomzelllinien in Hinblick auf eine immunmodulatorische Wirkung auf naive T-Zellen." In Chirurgisches Forum 2006, 109–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/3-540-34668-6_36.

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Textor, Johannes, and Jürgen Westermann. "Modeling Migration, Compartmentalization and Exit of Naive T Cells in Lymph Nodes Without Chemotaxis." In Lecture Notes in Computer Science, 228–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-73922-7_20.

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Conference papers on the topic "Naine T"

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Schultz, Liora M., Debra Czerwinski, Chiung-Chi Kuo, Shoshana Levy, and Ronald Levy. "Abstract 2209: Costimulation of T cells by CD81 enhances CAR transduction of naive T cells." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2209.

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Wang, Yuchen. "The difference between Treg cells and naive T cells analyzed by cluster analysis." In 2017 2nd International Conference on Machinery, Electronics and Control Simulation (MECS 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/mecs-17.2017.46.

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Balyan, Renu, Rupali Gund, Chitra Ebenezer, Thyagarajan Krishnamurthy, Amanpreet Singh Chawla, Jeannine Durdik, Anna George, Vineeta Bal, and Satyajit Rath. "Abstract A80: Functionally significant heterogeneity in apparently homogenous naive CD8 T cell populations." In Abstracts: AACR Special Conference on Tumor Immunology and Immunotherapy; October 20-23, 2016; Boston, MA. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/2326-6074.tumimm16-a80.

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Skapenko, A., J. Wendler, PE Lipsky, JR Kalden, and H. Schulze-Koops. "THU0117 The bias for th1 differentiation of rheumatoid arthritis t cells is characteristic of memory but not of naive t cells." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.994.

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Hosgood, H. Dean, Luoping Zhang, Xiaojiang Tang, Roel Vermeulen, Min Shen, Martyn Smith, Chuangyi Qiu, et al. "Abstract 4645: Decreased CD4+ naive and effector memory T cell counts, and CD8+ naïve T cell counts, are associated with trichloroethylene exposure." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4645.

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Baricza, E., N. Marton, P. Királyhidi, OT Kovács, IK Székely, E. Lajkó, L. Kohidai, et al. "P031 In both rheumatoid and psoriatic arthritis naive CD4+ T lymphocytes are predisposed to differentiate towards TH17 cells and have characteristic cytokine profiles." In 38th European Workshop for Rheumatology Research, 22–24 February 2018, Geneva, Switzerland. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-ewrr2018.54.

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Ghafouri, Sanaz Noelle, Christopher Walthers, Mobina Roshandell, Brenda Ji, Jacqueline Trent, Jia Ming Chen, Jacob Naparstek, et al. "Abstract CT007: CD19/CD20 bispecific chimeric antigen receptor (CAR) in naive/memory T-cells for the treatment of relapsed or refractory B-cell lymphomas." In 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-ct007.

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Thatcher, TH, MA Williams, RP Phipps, and PJ Sime. "The Aryl Hydrocarbon Receptor (AhR) Is a Novel Regulator of Dendritic Cell Function: AhR-Deficient DCs Promote a Th2 Phenotype in Naive Wild-Type T Cells." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a6081.

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Johnson, Taylor A., Madison K. Ritter, Mary-Peyton A. Knapp, Robert O. Rainer, Nathalie D. King-Lyons, Terry D. Connell, and Sergio Arce. "Abstract A25: Differentiation of human naive T cells to various effector memory cell subtypes correlates with increased binding of the B subunit of Type-IIb heat-labile enterotoxin (LT-IIb-B5) to its cognate ganglioside receptors." In Abstracts: AACR Special Conference on Tumor Immunology and Immunotherapy; November 17-20, 2019; Boston, MA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/2326-6074.tumimm19-a25.

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Miller, K., J. Cortes, SA Hurvitz, IE Krop, D. Tripathy, S. Verma, K. Riahi, et al. "Abstract OT3-01-01: HERMIONE: A phase 2, randomized, open label trial comparing MM-302 plus trastuzumab with chemotherapy of physician's choice plus trastuzumab, in anthracycline naive HER2-positive, locally advanced/metastatic breast cancer patients previously treated with pertuzumab and ado-trastuzumab emtansine (T-DM1)." In Abstracts: Thirty-Eighth Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 8-12, 2015; San Antonio, TX. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.sabcs15-ot3-01-01.

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Reports on the topic "Naine T"

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Chen, Mao-bing, Hua Wang, Qi-han Zheng, Wei-yan Cui, Hua-lan Xu, and Xu-wen Zheng. Comparative efficacy of the front-line anti-HBV drugs in nucleos(t)ide analogue-naive chronic hepatitis B, A protocol for systematic review and network meta-analysis. INPLASY - International Platform of Registered Systematic Review Protocols, March 2020. http://dx.doi.org/10.37766/inplasy2020.3.0016.

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