Relevant bibliographies by topics / M-cels

Contents

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

Academic literature on the topic 'M-cels'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "M-cels"

1

Mesquita, Hilda de Souza Lima, and Ana Júlia Fernandes. "Variação de curta escala temporal de bactérias, plcofltoplâncton e nanoheterótrofos na região de Ubatuba - SP, Brasil." Revista Brasileira de Oceanografia 44, no. 1 (1996): 47–56. http://dx.doi.org/10.1590/s1413-77391996000100005.

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A variação temporal da comunidade microbiana (bactérias, picofitoplâncton total e nanoheterótrofos) nas águas de Ubatuba (23°S 45°W) foi estudada durante um período de 7 dias (de 27/02 a 04/03/1988). As amostras foram obtidas na termoclina, duas vezes ao dia (na estôfa da maré baixa e da maré alta durante o período diurno. A densidade de nanoheterótrofos variou de 0,9 a 3,5 x 10³ cels m-1 apresentando valor médio de 2,3 x 10³ cels m-1. Picofitoplâncton total foi representado principalmente por cianobactérias cocóides e sua denside de variocões de 1,0 a 7,6 x 10(6) cels m-1. O número de bactéri
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2

Samper Prunera, Emili. "(Algunes) variacions sobre el diable: una proposta de catalogació de dues llegendes satàniques." Estudis de Literatura Oral Popular / Studies in Oral Folk Literature, no. 4 (December 17, 2015): 107. http://dx.doi.org/10.17345/elop2015107-120.

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En el marc del projecte «RondCat: rondalles catalanes», dirigit per Carme Oriol i Josep M. Pujol, i la catalogació de rondalles que no tenen correspondència a l’índex internacional d’Aarne-Thompson-Uther [ATU], es proposa la creació de dos tipus nous: C-103 («Dimoni, on vas?») i C-113 (La fondària del gorg). El punt de partida és l’estudi de la llegenda satànica fet per Josep M. Pujol l’any 1994 («Variacions sobre el diable»), així com el corpus recollit pel folklorista Cels Gomis i Mestre (1841-1915). La proposta de creació dels dos tipus inclou la relació de les versions catalanes localitzad
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3

Magalhaes, Roberto J. Pessoa, María-Belén Vidriales, Bruno Paiva, et al. "Multidimensional Flow Cytometric (MFC) Analysis of the Immune System of Multiple Myeloma (MM) Patients Achieving Long Term Disease Control." Blood 118, no. 21 (2011): 810. http://dx.doi.org/10.1182/blood.v118.21.810.810.

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Abstract Abstract 810FN2 Increasing evidence shows that a small fraction of MM patients (pts) treated with high-dose therapy followed by autologous stem cell transplantation achieve long-term remission. Interestingly, this is not restricted to pts in complete response (CR), since those that revert to a monoclonal gammopathy of undetermined significance (MGUS) profile may also achieve long-term remission, despite the persistence of residual myeloma plasma cells (PCs). These results suggest that in addition to the anti-myeloma therapy, other factors may play a role in the control of the disease.
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Setlow, Jane K. "Genetics in Chinese Hamster Cells Molecular Cell Genetics M. M. Gottesman." BioScience 36, no. 10 (1986): 680–82. http://dx.doi.org/10.2307/1310394.

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Kanaya, Takashi, Kohtaro Miyazawa, Ikuro Takakura, et al. "Differentiation of a murine intestinal epithelial cell line (MIE) toward the M cell lineage." American Journal of Physiology-Gastrointestinal and Liver Physiology 295, no. 2 (2008): G273—G284. http://dx.doi.org/10.1152/ajpgi.00378.2007.

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M cells are a kind of intestinal epithelial cell in the follicle-associated epithelium of Peyer's patches. These cells can transport antigens and microorganisms into underlying lymphoid tissues. Despite the important role of M cells in mucosal immune responses, the origin and mechanisms of differentiation as well as cell death of M cells remain unclear. To clarify the mechanism of M cell differentiation, we established a novel murine intestinal epithelial cell line (MIE) from the C57BL/6 mouse. MIE cells grow rapidly and have a cobblestone morphology, which is a typical feature of intestinal e
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Uemura, N., K. Ozawa, K. Takahashi, et al. "Binding of membrane-anchored macrophage colony-stimulating factor (M- CSF) to its receptor mediates specific adhesion between stromal cells and M-CSF receptor-bearing hematopoietic cells." Blood 82, no. 9 (1993): 2634–40. http://dx.doi.org/10.1182/blood.v82.9.2634.2634.

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Abstract To explore the biologic significance of the membrane-anchored form of macrophage colony-stimulating factor (M-CSF), we examined whether interaction between membrane-bound M-CSF and its receptor mediates intercellular adhesion as well as cell proliferation and differentiation. Human M-CSF receptors were expressed on a murine interleukin-2 (IL-3)-dependent cell line, FDC-P2, by DNA transfection with the c-fms gene (FDC-P2-MCSFR). A human bone marrow-derived stromal cell line, KM102, was used in the cell adhesion assay. The expression of membrane-bound M-CSF on KM102 cells was demonstrat
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Uemura, N., K. Ozawa, K. Takahashi, et al. "Binding of membrane-anchored macrophage colony-stimulating factor (M- CSF) to its receptor mediates specific adhesion between stromal cells and M-CSF receptor-bearing hematopoietic cells." Blood 82, no. 9 (1993): 2634–40. http://dx.doi.org/10.1182/blood.v82.9.2634.bloodjournal8292634.

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To explore the biologic significance of the membrane-anchored form of macrophage colony-stimulating factor (M-CSF), we examined whether interaction between membrane-bound M-CSF and its receptor mediates intercellular adhesion as well as cell proliferation and differentiation. Human M-CSF receptors were expressed on a murine interleukin-2 (IL-3)-dependent cell line, FDC-P2, by DNA transfection with the c-fms gene (FDC-P2-MCSFR). A human bone marrow-derived stromal cell line, KM102, was used in the cell adhesion assay. The expression of membrane-bound M-CSF on KM102 cells was demonstrated by flo
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8

Ebisawa, Masashi, Koji Hase, Daisuke Takahashi, et al. "CCR6hiCD11cint B cells promote M-cell differentiation in Peyer's patch." International Immunology 23, no. 4 (2011): 261–69. http://dx.doi.org/10.1093/intimm/dxq478.

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Lelouard, Hugues, Alain Sahuquet, Hubert Reggio, and Philippe Montcourrier. "Rabbit M cells and dome enterocytes are distinct cell lineages." Journal of Cell Science 114, no. 11 (2001): 2077–83. http://dx.doi.org/10.1242/jcs.114.11.2077.

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We have studied the M cell origin and differentiation pathway in rabbit gut-associated lymphoid tissues. Micro-dissected domes and epithelium isolated by ethylene diamine tetra acetic acid detachment allowed us to view the whole epithelial surface from the bottom of crypts to the top of domes. We used monoclonal antibodies specific to the apex of either M cells or dome enterocytes, lectins, and antibodies to vimentin in appendix, distal Peyer’s patches and caecal patches. The earliest vimentin-labeled M cells were observed in the BrdU-positive proliferative zone of dome-associated crypts. Grad
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Klisuric, Ana, Benjamin Thierry, Ludivine Delon, Clive A. Prestidge, and Rachel J. Gibson. "Identifying human and murine M cells in vitro." Experimental Biology and Medicine 244, no. 7 (2019): 554–64. http://dx.doi.org/10.1177/1535370219838674.

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M cells are an epithelial cell population found in the follicle-associated epithelium overlying gut-associated lymphoid tissues. They are specialized in the transcytosis of luminal antigens. Their transcytotic capacity and location in an immunocompetent environment has prompted the study of these cells as possible targets for oral drug delivery systems. Currently, the models most commonly used to study M cells are restricted to in vivo experiments conducted in mice, and in vitro studies conducted in models comprised either of primary epithelial cells or established cell lines of murine or huma
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Dissertations / Theses on the topic "M-cels"

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Tyrer, Peter Charles, and n/a. "Targeting M-cells for oral vaccine delivery." University of Canberra. Health Sciences, 2004. http://erl.canberra.edu.au./public/adt-AUC20060427.122012.

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An in vitro model of the follicle-associated epithelia that overlie the Peyer's patches of the small intestine was developed and validated to examine the mechanisms of mucosal antigen sampling. This model displays many phenotypic and physiological characteristics of M cells including apical expression of [alpha]5[beta]l integrin and enhanced energy dependent participate transport. CD4+ T-cells were shown to be an important influence on the development of Mlike cells. The model was used to examine the M cell mediated uptake of several putative whole-cell killed bacterial vaccines. Greater numbe
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Blakemore, Louise Margaret. "Curcumin-induced G2/M cell cycle arrest in colorectal cancer cells." Thesis, University of Leicester, 2011. http://hdl.handle.net/2381/9809.

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Curcumin, a diet-derived chemopreventive and chemotherapeutic agent has been shown to induce G2/M cell cycle arrest, and previous studies suggested that microtubule depolymerisation may be linked to M-phase arrest. However, mechanisms involved have not been elucidated and often non-physiological concentrations of curcumin were used. The goal of this study was to characterise in more detail curcumin-induced cell cycle arrest using a panel of human colorectal cancer cell (CRC) lines, HT-29, SW480, HCT116 p53+/+, HCT116 p53-/- and HCT116 p21-/-. Using physiologically relevant concentrations of cu
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Mairopoulos, Dimitrios. "M-Cell assembly." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/99294.

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Thesis: S.M., Massachusetts Institute of Technology, Department of Architecture, June 2015.<br>Cataloged from PDF version of thesis. "June 2015."<br>Includes bibliographical references (page 47).<br>In this thesis I propose a self- assembly procedure called the Morphocell(M-Cell) assembly. This procedure is based on an assembly unit called the M-Cell. The M-Cell is comprised out of two components, the M-Block and the M-Clay (in which the M-Block is embedded). During the assembly procedure the M-Clay acts as the environment of the assembly for the M-Blocks. This allows a global, parallel assemb
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Mason, Caroline Margaret. "Characterisation of intestinal M cells using monoclonal antibodies." Thesis, University of Newcastle Upon Tyne, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260952.

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Sehgal, Anuj. "Investigating the development and function of M cells." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/28738.

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Gut-associated lymphoid tissues such as Peyer’s patches (PP) are inductive sites for immune response in the intestine. Unlike other peripheral lymphoid tissues, gut-associated lymphoid tissues lack afferent lymphatics and can directly sample mucosal antigens by specialized epithelial cells in the follicular associated epithelia (FAE), known as M cells. M cells derive from Lgr5+ intestinal stem cells in intestinal crypts, where the daughter cells of Lgr5+ cells differentiate into M cells after stimulation from the cytokine receptor activator of nuclear factor-κB ligand (RANKL). RANKL is produce
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Schäkel, Knut, Claudia Poppe, Elfriede Mayer, Christine Federle, Gert Riethmüller, and Ernst Peter Rieber. "M-DC8+ Leukocytes – A Novel Human Dendritic Cell Population." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-135252.

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Dendritic cells (DC) constitute a heterogeneous leukocyte population having in common a unique capacity to induce primary T cell responses and are therefore most attractive candidates for immunomodulatory strategies. Two populations of blood DC (CD11c+ CD123dim and CD11c– CD123high) have been defined so far. However, their direct isolation for experimental purposes is hampered by their low frequency and by the lack of selective markers allowing large scale purification from blood. Here we describe the monoclonal antibody (mAb) M-DC8, which was generated by immunizing mice with highly enriched
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Baker, Peter Kenneth. "The role of M-CSF in hairy-cell leukaemia." Thesis, University of Liverpool, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367653.

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Sansom, Nigel P. "Antigen sampling by porcine intestinal Peyer's patch M-cells." Thesis, University of Aberdeen, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322637.

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Schäkel, Knut, Claudia Poppe, Elfriede Mayer, Christine Federle, Gert Riethmüller, and Ernst Peter Rieber. "M-DC8+ Leukocytes – A Novel Human Dendritic Cell Population." Karger, 1999. https://tud.qucosa.de/id/qucosa%3A27632.

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Dendritic cells (DC) constitute a heterogeneous leukocyte population having in common a unique capacity to induce primary T cell responses and are therefore most attractive candidates for immunomodulatory strategies. Two populations of blood DC (CD11c+ CD123dim and CD11c– CD123high) have been defined so far. However, their direct isolation for experimental purposes is hampered by their low frequency and by the lack of selective markers allowing large scale purification from blood. Here we describe the monoclonal antibody (mAb) M-DC8, which was generated by immunizing mice with highly enriched
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Messerly, Erin. "M-CSF Stress-Induced Priming of the Macrophage Cell." Ohio Dominican University Honors Theses / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=oduhonors1449484244.

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Books on the topic "M-cels"

1

Instruments, Texas. 2-[mu]m CMOS standard cell data book. Texas Instruments, 1987.

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International Malpighi Symposium (5th 2003 Rome, Italy). Morphodynamics of cells and tissues: A book in memory of Pietro M. Motta. Editrice Il Sedicesimo, 2005.

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Toci, F. Determination of oxygen potentials and O/M ratios of oxide nuclear reactor fuels by means of an automated solid state galvanic cell. Commission of the European Communities, 1987.

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Resources, United States Congress Senate Committee on Labor and Human. Sickle disease research: An update : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred Third Congress, second session, on to award a grant to the Louisiana Department of Health and Hospitals to establish and construct the National Center for Sickle Cell Disease Research at Southern University in Baton Rouge, LA, and for related facilities and equipment at such center, July 28, 1994. U.S. G.P.O., 1994.

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Branting, Christina. Studies on S øt ør øe øp øt øo øc øo øc øc øu øs ø m øu øt øa øn øs ø glucans with special reference to cell adhesion. Kongl. Carolinska Medico Chirurgiska Institutet, 1988.

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Wolfgang, Holzgreve, and Lessl M. 1966-, eds. Stem cells from cord blood, in utero stem cell development, and transportation-inclusive gene therapy /cW. Holzgreve, M. Lessl, editors. Springer, 2001.

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Federal Energy Technology Center (U.S.) and United States. Dept. of Energy., eds. Developing the second-generation fuel cell: The M-C Power Project. Dept. of Energy, Office of Fossil Energy, Federal Energy Technology Center, 1998.

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Federal Energy Technology Center (U.S.) and United States. Dept. of Energy, eds. Developing the second-generation fuel cell: The M-C Power Project. Dept. of Energy, Office of Fossil Energy, Federal Energy Technology Center, 1998.

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Federal Energy Technology Center (U.S.) and United States. Dept. of Energy., eds. Developing the second-generation fuel cell: The M-C Power Project. Dept. of Energy, Office of Fossil Energy, Federal Energy Technology Center, 1998.

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Federal Energy Technology Center (U.S.) and United States. Dept. of Energy, eds. Developing the second-generation fuel cell: The M-C Power Project. Dept. of Energy, Office of Fossil Energy, Federal Energy Technology Center, 1998.

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Book chapters on the topic "M-cels"

1

Rischin, Danny. "Biomarkers for Immune Modulatory Treatment in Head and Neck Squamous Cell Carcinoma (HNSCC)." In Critical Issues in Head and Neck Oncology. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63234-2_6.

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AbstractImmune checkpoint inhibitors have changed the standard of care for recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC). However, only a minority of patients respond, hence the search for predictive biomarkers. Potential predictive biomarkers for immune checkpoint inhibitors discussed in this chapter include (1) Immune checkpoint ligand expression e.g., PD-L1, (2) biomarkers of a T-cell inflamed tumour microenvironment (TME) such as gene expression profiles of activated T cells, (3) biomarkers of tumour neoepitope burden such as tumour mutation burden (TMB) and (4) multidimensional quantitative techniques. At present only PD-L1 expression has been shown to have clinical utility in head and neck cancer. It enriches for populations more likely to respond, but the false positive predictive value remains high. In the pivotal Keynote−048 trial that established a role for pembrolizumab (anti-PD1) monotherapy and pembrolizumab + chemotherapy as treatment options in first-line R/M HNSCC, primary endpoints included overall survival in defined subgroups based on PD-L1 expression. In this trial the combined positive score (CPS) was used which takes into account PD-L1 expression in tumour and immune cells. Based on this trial regulatory approvals for first-line pembrolizumab in R/M HNSCC require assessment of PD-L1 expression using the CPS. Finally we discuss emerging evidence that locoregionally advanced HPV-associated oropharyngeal cancers that have high expression of CD103 positive CD8 T cells have an excellent prognosis and features that suggest increased probability of responding to anti-PD1/PD-L1, raising the possibility of incorporating these immune therapies as part of a de-escalation trial strategy.
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Jæger, Karoline Horgmo, and Aslak Tveito. "Derivation of a Cell-Based Mathematical Model of Excitable Cells." In Modeling Excitable Tissue. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-61157-6_1.

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Abstract Excitable cells are of vital importance in biology, and mathematical models have contributed significantly to understand their basic mechanisms. However, classical models of excitable cells are based on severe assumptions that may limit the accuracy of the simulation results. Here, we derive a more detailed approach to modeling that has recently been applied to study the electrical properties of both neurons and cardiomyocytes. The model is derived from first principles and opens up possibilities for studying detailed properties of excitable cells.We refer to the model as the EMI model because both the extracellular space (E), the cell membrane (M) and the intracellular space (I) are explicitly represented in the model, in contrast to classical spatial models of excitable cells. Later chapters of the present text will focus on numerical methods and software for solving the model. Also, in the next chapter, the model will be extended to account for ionic concentrations in the intracellular and extracellular spaces.
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Tromba, Anthony J. "T(M) is a Cell." In Teichmüller Theory in Riemannian Geometry. Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-8613-0_4.

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Zámborszky, Judit. "Cell Cycle Transitions, G2/M." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_38.

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Antzelevitch, Charles, Vladislav V. Nesterenko, Wataru Shimizu, and Jose M. Di Diego. "Electrophysiological Characteristics of the M Cell." In Monophasic Action Potentials. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60851-3_13.

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Yamamoto, M., D. W. Pascual, and H. Kiyono. "M Cell-Targeted Mucosal Vaccine Strategies." In Current Topics in Microbiology and Immunology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/82_2011_134.

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Kaufmann, Stefan H. E., and Gennaro De Libero. "Cytolytic Cells in M. tuberculosis Infections." In Infectious Agents and Pathogenesis. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5418-5_7.

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Rischin, Danny. "Update of Immune Therapies in Recurrent/Metastatic Head and Neck Cancer." In Critical Issues in Head and Neck Oncology. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63234-2_19.

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AbstractSince the initial reports of activity of pembrolizumab in recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC), investigation of the role of immune therapies has been the major focus of clinical trials in R/M HNSCC. Randomised trials initially with nivolumab and later with pembrolizumab established overall survival benefit in patients with R/M HNSCC previously treated with platinum compared to physicians choice of 2nd line therapy, and have led to regulatory approval around the world. More recently the Keynote-048 trial has compared both pembrolizumab monotherapy and pembrolizumab + platinum/5FU to the Extreme regimen of platinum/5FU/cetuximab in the first-line R/M setting. The key findings from this trial are that pembrolizumab monotherapy compared to Extreme improved overall survival in patients with PD-L1 combined positive score (CPS) ≥ 20 and ≥ 1, and that pembro/chemotherapy improved OS in CPS ≥ 20, CPS ≥ 1 and the total population. Relative to Extreme there was less toxicity in the monotherapy arm and comparable toxicity in the pembro/chemo arm. Based on this trial use of pembrolizumab as part of first-line treatment for R/M HNSCC is appropriate for the majority of patients, and represents a new standard of care. The focus has now moved to identifying combinations that may be superior to pembrolizumab monotherapy or to chemotherapy + pembrolizumab. Some of the more promising approaches under investigation in HNSCC are discussed in this chapter. In summary, immune therapies are now the cornerstone of management of R/M HNSCC with the approval of pembrolizumab in the first-line R/M setting.
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Gupta, Prem N. "Mucosal Vaccine Delivery and M Cell Targeting." In Advances in Delivery Science and Technology. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-11355-5_9.

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Neutra, Marian R., Philippe Sansonetti, and Jean-Pierre Kraehenbuhl. "Role of Intestinal M Cells in Microbial Pathogenesis." In Microbial Pathogenesis and the Intestinal Epithelial Cell. ASM Press, 2014. http://dx.doi.org/10.1128/9781555817848.ch2.

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Conference papers on the topic "M-cels"

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Lindsay, Alexandra R., Usamah Chaudhary, Taylor N. Terry, Mahdi Haghshenas-Jaryani, and Muthu B. J. Wijesundara. "Interconnected Fluid-Filled Cells Design for Reduction of Linear Acceleration and Force Transfer to Prevent Concussion." In ASME 2019 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/imece2019-10675.

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Abstract Regardless of efforts in improving helmet technologies, sport related concussions continue to be a problem. In an effort for advancing helmet liners, this research investigated a design comprised of interconnected fluid-filled cell structures that consist of a primary cell connecting to one or more secondary cells through a channel. When the primary cell undergoes impact, it deforms and pushes the fluid from the primary to secondary cells, which expand accordingly. This fluid motion absorbs the impact and dissipates energy, thereby reducing the force and acceleration transfer to a con
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Markant, Shirley L., Kelly Barton, Jesse Sun, and Robert Wechsler-Reya. "Abstract 3443: Targeting G2/M cell cycle regulators in medulloblastoma tumor-propagating cells." 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.am2011-3443.

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Sonnet, J., and E. K. Gini. "IMPROVEMENT OF SICKLE CELL DEFORMABILITY BY PIRACETAM IN VITRO AND IN VIVO." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644214.

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Piracetam (P) (2-oxo-pyrrolidine acetamide) has Theological properties and has been used at various dosages over the past decade for the management of psychosenescent syndromes. On maintenance therapy, at the oral dosage of 160 mg/kg/day, in four divided doses, P reduces the number of vaso-occlusive crises in sickle cell homozygous patients, to about a fifth of what could be expected without drug. After oral intake at the latter dosage P's bioavailability in the blood ranges from 0.5to 1 m mol/1. Microsieving on polycarbonate filters, 5 μ m por size, of diluted suspensions (haematocrit 1%) of
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Zhang, Wujie, Geer Yang, Aili Zhang, Lisa X. Xu, and Xiaoming He. "Preferential Vitrification of Water in Small Alginate Microcapsules Significantly Augments Cell Cryopreservation by Vitrification." In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19231.

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A major challenge to the eventual success of the emerging cell-based medical technologies such as tissue engineering, regenerative medicine and cell transplantation is the limited availability of the desired cell sources [1]. This challenge can be alleviated by cell microencapsulation to avoid undesired immune response (i.e., immunoisolation) so that non-autologous cells can be used to treat human diseases, and by cell cryopreservation to establish banks of important living cells for wide distribution to end users so that they are readily available when needed in the future [2,3]. Although cel
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Hoffman, R., B. J. Roth, G. W. Sledge, J. Straneva, and J. Brandt. "ANALYSIS OF PHORBOL ESTER STIMULATED HUMAN MEGAKARYOCYTE DEVELOPMENT." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642951.

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The events that occur during the terminal maturation of human megakaryocytes are poorly characterized. To examine these events, a recently characterized human megakaryocytic cell line (EST-IU, Cancer Res. 46: 2155-2159, 1986) was exposed to 12-0-tetradecanoyl-phorbol-13-acetate (TPA), as well as 2 non-transforming phorbol esters (4 alpha phorbol and 4 beta phorbol 12 alpha, 13 alpha diacetate) at the identical concentrations. Morphologic changes, including cellular attachment to untreated plastic or glass, occurred within 4 hrs of treatment with TPA. Treatment of EST-IU cells with either of th
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Dupuy, E., P. S. Rohrlich, and G. Tobelem. "HEPARIN STIMULATES FIBROBLAST GROWTH INDUCED BY PDGF." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643750.

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Heparin binds to smooth muscle cells and endothelial cells. It inhibits the proliferation of the smooth muscle cells and modulates the growth of endothelial cells. Fibroblasts which represent an other cell type belonging to the vascular wall could also have their growth modified by heparin. We have at first, demonstrated that 125I unfractionated heparin bigds to cultured human skin fibroblasts with a Kd of 1.16 10 M.A low molecular weight heparin fraction (PK 10169) competed (50 %)with I unfractionated heparin, but at aless extent than cold unfractionated heparin(90%).As it has been reported w
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Bubis, Eugenia, Lea Mor, Nissim Sabag, et al. "Electrical Characterization of a Glucose-Fueled Alkaline Fuel Cell." In ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97031.

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This paper is part of an effort to establish design parameters for glucose-fueled room temperature membraneless alkaline fuel cells as possible electricity suppliers for portable devices. We report experimental results for three characteristics of glucose-fueled room temperature membraneless alkaline fuel cells: 1) polarization curve, 2) power density as a function of current density, and 3) internal resistance. The internal resistance of the cell was measured by two independent experimental methods: “Voltage Divider” and “Current Interrupt”. The three characteristics were measured as a functi
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Hsiao, Min-Chien, Shu-Hang Liao, Ming-Yu Yen, et al. "Electrical and Thermal Conductivities of Novel Metal Mesh Hybrid Polymer Composite Bipolar Plates for Proton Exchange Membrane Fuel Cells." In ASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2009. http://dx.doi.org/10.1115/fuelcell2009-85134.

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Novel metal mesh hybrid polymer composite bipolar plates for proton exchange membrane fuel cells (PEMFCs) have been prepared via inserting a copper or alumina mesh in polymer composites. The composition of polymer composites consisted of 70 wt% graphite powder and 0–2 wt% modified multi-walled carbon nanotubes (m-MWCNTs). Results indicated that the inplane electrical conductivity of m-MWCNTs/polymer composite bipolar plates increased from 156 S cm−1 (0 wt% MWCNT) to 643 Scm−1 (with 1 wt% MWCNT) (D.O.E target &gt; 100 S cm−1). The bulk thermal conductivities of the copper and aluminum mesh hybr
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Xiu-juan, Zhang, Huang Qing-ling, and Ji Yu-bin. "Induction of apoptosis and G2/M cell cycle arrest by myricetin in human hepatoma HepG2 cells." In Education (ITIME). IEEE, 2009. http://dx.doi.org/10.1109/itime.2009.5236242.

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Wasi, S., P. Alles, D. Gauthier, et al. "STUDIES ON SMALL MOLECULAR WEIGHT ADHESION PROTEINS (SAPs) FROM CONNECTIVE TISSUES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643556.

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We have identified a family of low molecular weight proteins with cell attachment properties in a variety of soft and mineralised connective tissues (Wong et al., Biochem. J. 232, 119, 1985). For further characterisation of these proteins we extracted porcine bones with 4 M guanidine hydrochloride and purified the proteins on a series of gel filtration columns The purifed SAPs comprise three bands with Mr -14 000 -17 000. All three proteins bound to heparin-sepahrose in both the presence and absence of 4M urea, and when eluted with 2 M NaCl they retained their cell binding capacity. These prot
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Reports on the topic "M-cels"

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Davis, Shelly M., and Shigeki Miyamoto. Exploring a Link Between NF-KB and G2/M Cell Cycle Arrest in Breast Cancer Cells. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada436875.

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Davis, Shelly M. Exploring a Link Between NF-kappaB and G2/M Cell Cycle Arrest in Breast Cancer Cells. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425730.

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Cheever, C. L., and R. W. Rose. Decontamination of hot cells K-1, K-3, M-1, M-3, and A-1, M-Wing, Building 200: Project final report Argonne National Laboratory-East. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/414345.

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Liu, Jingwen. Role of High-Affinity Oncostatin M Receptor in Prevention of Breast Cancer Cell Growth. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada295676.

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Ku, L. P., S. L. Liew, and J. G. Kolibal. Parametric analysis of neutron streaming through major penetrations in the 0. 914 m TFTR test cell floor. Office of Scientific and Technical Information (OSTI), 1985. http://dx.doi.org/10.2172/5200120.

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Arnett, Clint, Justin Lange, Ashley Boyd, Martin Page, and Donald Cropek. Expression and secretion of active Moringa oleifera coagulant protein in Bacillus subtilis. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41546.

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Cationic polypeptide proteins found in the seeds of the tropical plant Moringa oleifera have coagulation efficiencies similar to aluminum and ferric sulfates without their recalcitrant nature. Although these proteins possess great potential to augment or replace traditional coagulants in water treatment, harvesting active protein from seeds is laborious and not cost-effective. Here, we describe an alternative method to express and secrete active M. oleifera coagulant protein (MO) in Bacillus subtilis. A plasmid library containing the MO gene and 173 different types of secretory signal peptides
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McAlpin, Jennifer, and Cassandra Ross. Houston Ship Channel Expansion Channel Improvement Project (ECIP) numerical modeling report : BABUS cell and Bird Island analysis. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41581.

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The Houston Ship Channel (HSC) is one of the busiest deep-draft navigation channels in the United States and must be able to accommodate increasing vessel sizes. The US Army Engineer District, Galveston (SWG), requested the Engineer Research and Development Center, Coastal and Hydraulics Laboratory, perform hydrodynamic and sediment modeling of proposed modifications in Galveston and Trinity Bays and along the HSC. The modeling results are necessary to provide data for hydrodynamic, salinity, and sediment transport analysis. SWG provided three project alternatives that include closing Rollover
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