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Artykuły w czasopismach na temat "BCR intraclonal analysis"
Ng, Anita, Andrew Shih, Martina Cardillo, Kristin Lynn Sticco, Houman Khalili, Lita Crichton, William Plunkett, Varsha Gandhi i Nicholas Chiorazzi. "Investigation into Intraclonal Heterogeneity of CXCR4 DimCD5 Bright Chronic Lymphocytic Leukemia Cells Identifies Distinct Activation Signatures". Blood 142, Supplement 1 (28.11.2023): 3259. http://dx.doi.org/10.1182/blood-2023-187957.
Pełny tekst źródłaJulien, Sylvie, Mirjana Radosavljevic, Nathalie Labouret, Sophie Camilleri-Broet, Frederic Davi, Martine Raphael, Thierry Martin i Jean-Louis Pasquali. "AIDS Primary Central Nervous System Lymphoma: Molecular Analysis of the Expressed VH Genes and Possible Implications for Lymphomagenesis". Journal of Immunology 162, nr 3 (1.02.1999): 1551–58. http://dx.doi.org/10.4049/jimmunol.162.3.1551.
Pełny tekst źródłavan Bergen, Cornelis A. M., Marvyn T. Koning, Edwin Quinten, Agnieszka Mykowiecka, Julieta Sepulveda, Ramin Monajemi, Ruben A. L. De Groen i in. "High-Throughput BCR Sequencing and Single-Cell Transcriptomics Reveal Distinct Transcriptional Profiles Associated with Subclonal Evolution of Follicular Lymphoma". Blood 134, Supplement_1 (13.11.2019): 298. http://dx.doi.org/10.1182/blood-2019-130508.
Pełny tekst źródłaZaragoza-Infante, Laura, Andreas Agathangelidis, Valentin Junet, Nikos Pechlivanis, Triantafylia Koletsa, Alessio Bruscaggin, Zadie Davis i in. "Distinct Modes of Ongoing Antigen Interactions Shape Intraclonal Dynamics in Splenic Marginal Zone Lymphoma". Blood 138, Supplement 1 (5.11.2021): 1330. http://dx.doi.org/10.1182/blood-2021-148722.
Pełny tekst źródłaYan, Xiao J., Wentian Li, Sophia Yancopoulos, Igor Dozmorov, Carlo Calissano, Sonia Marsilio, Rajendra N. Damle i in. "Gene Expression Profiles Document That Recently- and Previously-Divided CLL Fractions Represent a Continuum but Suggest Differing Modes of Activation for These Fractions in U-CLL and M-CLL". Blood 120, nr 21 (16.11.2012): 317. http://dx.doi.org/10.1182/blood.v120.21.317.317.
Pełny tekst źródłaSutton, Lesley-Ann, Efterpi Kostareli, Anastasia Hadzidimitriou, Nikos Darzentas, Athanasios Tsaftaris, Achilles Anagnostopoulos, Richard Rosenquist i Kostas Stamatopoulos. "Extensive Intraclonal Diversification in a Subgroup of Chronic Lymphocytic Leukemia Patients with Stereotyped IGHV4-34/IGKV2-30 B cell Receptors: Implications for Ongoing Interactions with Antigen." Blood 114, nr 22 (20.11.2009): 2337. http://dx.doi.org/10.1182/blood.v114.22.2337.2337.
Pełny tekst źródłaPackham, Graham, Serge Krysov, Vania Coelho, Peter Johnson i Freda K. Stevenson. "A “Universal” Lectin-Mediated Interaction Drives B-Cell Receptor Signaling In Primary Follicular Lymphoma Cells". Blood 122, nr 21 (15.11.2013): 4291. http://dx.doi.org/10.1182/blood.v122.21.4291.4291.
Pełny tekst źródłaSutton, Lesley-Ann, Efterpi Kostareli, Evangelia Stalika, Athanasios Tsaftaris, Achilles Anagnostopoulos, Nikos Darzentas, Richard Rosenquist i Kostas Stamatopoulos. "Active Crosstalk with the Microenvironment Leading to Clonal Evolution in Chronic Lymphocytic Leukemia with Stereotyped IGHV4–34/IGKV2–30 Antigen Receptors." Blood 120, nr 21 (16.11.2012): 2878. http://dx.doi.org/10.1182/blood.v120.21.2878.2878.
Pełny tekst źródłaLinley, Adam J., Beatriz Valle-Argos, Andrew J. Steele, Freda K. Stevenson, Francesco Forconi i Graham Packham. "Increased Reactive Oxygen Species and the B-Cell Receptor in Chronic Lymphocytic Leukemia Signaling". Blood 124, nr 21 (6.12.2014): 3291. http://dx.doi.org/10.1182/blood.v124.21.3291.3291.
Pełny tekst źródłaBaaklini, Sabrina, Alexandre Sarrabay, Camille Barthelemy, Laila Dahbi, Laurine Gil, Noushin Mossadegh-Keller, Jean-Marc Navarro i in. "A Single Cell Atlas of Diffuse Large B Cell Lymphomas Reveals Distinct Cellular States Predictive of Outcomes". Blood 142, Supplement 1 (28.11.2023): 848. http://dx.doi.org/10.1182/blood-2023-173929.
Pełny tekst źródłaRozprawy doktorskie na temat "BCR intraclonal analysis"
Abdollahi, Nika. "B cell receptor repertoire analysis in clinical context : new approaches for clonal grouping, intra-clonal diversity studies, and repertoire visualization". Electronic Thesis or Diss., Sorbonne université, 2021. http://www.theses.fr/2021SORUS063.
Pełny tekst źródłaNext-generation sequencing has enabled researchers to conduct in-depth analyses of the immunological repertoire landscape. However, a significant concern in these studies is the computational cost of analyzing millions of sequences with inherent complexity, variability, and mutational capacity, imposing computational challenges and necessitating the development of efficient methods. This challenge is even more evident in the clinical context that does not necessarily have access to professionals with computing skills or robust computational resources. Thus, the main goal of this thesis is to develop a set of dedicated and integrated tools to be used in the clinical environment, for medical diagnostic and patient care, and in the research environment, to perform large-scale and in-depth repertoire analysis. We have designed and implemented multiple algorithms and gathered them in a user-friendly interactive BCR repertoire visualization pipeline to facilitate the process of integrating BCR repertoire analysis into medical practices