CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry, 180 Assays - Citations

CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry, 180 Assays - Citations

View additional product information for CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry - Citations (C34573, C34567)

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Citations & References
Abstract
Deriving Quantitative Cell Biological Information from Dye-Dilution Lymphocyte Proliferation Experiments.
AuthorsRoy K, Shokhirev MN, Mitchell S, Hoffmann A,
JournalMethods Mol Biol
PubMed ID29388101
'The dye-dilution assay is a powerful tool to study lymphocyte expansion dynamics. By combining time course dye-dilution experiments with computational analysis, quantitative information about cell biological parameters, such as percentage of cells dividing, time of division, and time of death, can be produced. Here, we describe the method to generate ... More
Triple co-culture of human alveolar epithelium, endothelium and macrophages for studying the interaction of nanocarriers with the air-blood barrier.
AuthorsCosta A, de Souza Carvalho-Wodarz C, Seabra V, Sarmento B, Lehr CM,
JournalActa Biomater
PubMed ID31004840
'Predictive in vitro models are valuable alternatives to animal experiments for evaluating the transport of molecules and (nano)particles across biological barriers. In this work, an improved triple co-culture of air-blood barrier was set-up, being exclusively constituted by human cell lines that allowed to perform experiments at air-liquid interface. Epithelial NCI-H441 ... More
The genomic landscape of pediatric myelodysplastic syndromes.
AuthorsSchwartz JR, Ma J, Lamprecht T, Walsh M, Wang S, Bryant V, Song G, Wu G, Easton J, Kesserwan C, Nichols KE, Mullighan CG, Ribeiro RC, Klco JM,
JournalNat Commun
PubMed ID29146900
Myelodysplastic syndromes (MDS) are uncommon in children and have a poor prognosis. In contrast to adult MDS, little is known about the genomic landscape of pediatric MDS. Here, we describe the somatic and germline changes of pediatric MDS using whole exome sequencing, targeted amplicon sequencing, and/or RNA-sequencing of 46 pediatric ... More
Autoreactive, Low-Affinity T Cells Preferentially Drive Differentiation of Short-Lived Memory B Cells at the Expense of Germinal Center Maintenance.
AuthorsJain RW, Parham KA, Tesfagiorgis Y, Craig HC, Romanchik E, Kerfoot SM,
JournalCell Rep
PubMed ID30566861
B cell fate decisions within a germinal center (GC) are critical to determining the outcome of the immune response to a given antigen. Here, we characterize GC kinetics and B cell fate choices in a response to the autoantigen myelin oligodendrocyte glycoprotein (MOG) and compare the response with a standard ... More
BATF-dependent IL-7RhiGM-CSF+ T cells control intestinal graft-versus-host disease.
AuthorsUllrich E, Abendroth B, Rothamer J, Huber C, Büttner-Herold M, Buchele V, Vogler T, Longerich T, Zundler S, Völkl S, Beilhack A, Rose-John S, Wirtz S, Weber GF, Ghimire S, Kreutz M, Holler E, Mackensen A, Neurath MF, Hildner K,
JournalJ Clin Invest
PubMed ID29376889
Acute graft-versus-host disease (GVHD) represents a severe, T cell-driven inflammatory complication following allogeneic hematopoietic cell transplantation (allo-HCT). GVHD often affects the intestine and is associated with a poor prognosis. Although frequently detectable, proinflammatory mechanisms exerted by intestinal tissue-infiltrating Th cell subsets remain to be fully elucidated. Here, we show that ... More
Colorectal tumor-on-a-chip system: A 3D tool for precision onco-nanomedicine.
AuthorsCarvalho MR, Barata D, Teixeira LM, Giselbrecht S, Reis RL, Oliveira JM, Truckenmüller R, Habibovic P,
JournalSci Adv
PubMed ID31131324
Awareness that traditional two-dimensional (2D) in vitro and nonrepresentative animal models may not completely emulate the 3D hierarchical complexity of tissues and organs is on the rise. Therefore, posterior translation into successful clinical application is compromised. To address this dearth, on-chip biomimetic microenvironments powered by microfluidic technologies are being developed ... More
Subdominance and poor intrinsic immunogenicity limit humoral immunity targeting influenza HA stem.
AuthorsTan HX, Jegaskanda S, Juno JA, Esterbauer R, Wong J, Kelly HG, Liu Y, Tilmanis D, Hurt AC, Yewdell JW, Kent SJ, Wheatley AK,
JournalJ Clin Invest
PubMed ID30521496
Both natural influenza infection and current seasonal influenza vaccines primarily induce neutralizing antibody responses against highly diverse epitopes within the