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Journal articles on the topic 'Cellular tests'

Author: Grafiati

Published: 10 May 2022

Last updated: 30 July 2025

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1

Vaganov, A. A., A. S. Timonin, and I. I. Sidelnikov. "Hydraulic tests of cellular packing." Chemical and Petroleum Engineering 46, no. 11-12 (2011): 699–702. http://dx.doi.org/10.1007/s10556-011-9405-2.

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2

Chirumbolo, Salvatore. "Immunotherapy in allergy and cellular tests." Human Vaccines & Immunotherapeutics 10, no. 6 (2014): 1595–610. http://dx.doi.org/10.4161/hv.28592.

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3

Stamenović, Dimitrije, Srboljub M. Mijailovich, Iva Marija Tolić‐Nørrelykke, and Ning Wang. "Experimental tests of the cellular tensegrity hypothesis." Biorheology: The Official Journal of the International Society of Biorheology 40, no. 1-3 (2003): 221–25. http://dx.doi.org/10.1177/0006355x2003040001003024.

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The tensegrity model depicts the cytoskeleton (CSK) as a prestressed network of interconnected filaments. The prestress is generated by the CSK contractile apparatus and is partly balanced by traction at the cell–substrate interface and partly by CSK internal compression elements such as microtubules (MTs). A key feature of tensegrity is that the shear modulus (G) must increase in proportion with the prestress. Here we have tested that prediction as well as the idea that compression of MTs balance a portion of the cell prestress. Airway smooth muscle cells were studied. Traction microscopy was

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4

Ariza, Adriana, Maria Montanez, Tahia Fernandez, James Perkins, and Cristobalina Mayorga. "Cellular Tests for the Evaluation of Drug Hypersensitivity." Current Pharmaceutical Design 22, no. 45 (2017): 6773–83. http://dx.doi.org/10.2174/1381612822666161107165917.

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5

Dowling, V. P., and K. G. Martin. "Radiant Panel Fire Tests on Cellular Plastics Insulation." Journal of Thermal Insulation 8, no. 4 (1985): 314–38. http://dx.doi.org/10.1177/109719638500800407.

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6

Vaganov, A. A., and A. S. Timonin. "Heat- and mass-transfer tests of cellular packing." Chemical and Petroleum Engineering 46, no. 11-12 (2011): 686–91. http://dx.doi.org/10.1007/s10556-011-9402-5.

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7

Sanz, Maria, Pedro Gamboa, and A. De Weck. "Cellular Tests in the Diagnosis of Drug Hypersensitivity." Current Pharmaceutical Design 14, no. 27 (2008): 2803–8. http://dx.doi.org/10.2174/138161208786369722.

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8

Chapman, J. F. "Fire Tests on Plasterboard/Cellular Plastics Insulating Panels." Cellular Polymers 7, no. 1 (1988): 33–55. http://dx.doi.org/10.1177/026248938800700103.

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Small-scale fire and smoke test results are sometimes used — and the results interpreted – beyond their significance to choose materials for use in constructions and to reject others. When this happens, data from other small-scale tests are rarely adequate to correct the erroneous position. Instead, a quantum jump to more realistic tests is needed. A U.K. specifying authority was influenced by test performance claims made for Phenolic Foam to impose a ban on any other rigid foam in plasterboard laminate lining boards for refurbishing its housing property. This paper describes a real fire simul

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9

Bathgate, AJ, JN Plevris, MM Dollinger, and PC Hayes. "Skin tests predict acute cellular rejection in liver transplantation." Gastroenterology 114 (April 1998): A1209. http://dx.doi.org/10.1016/s0016-5085(98)84907-x.

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10

Bathgate, A. J., J. N. Plevris, M. M. Dollinger, and P. C. Hayes. "SKIN TESTS PREDICT ACUTE CELLULAR REJECTION IN LIVER TRANSPLANTATION." Transplantation 67, no. 7 (1999): S260. http://dx.doi.org/10.1097/00007890-199904150-01038.

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11

Fry, Jeffrey R., and Alison H. Hammond. "Assessment of the Functional Integrity of Hepatocytes: A Brief Review." Alternatives to Laboratory Animals 21, no. 3 (1993): 324–29. http://dx.doi.org/10.1177/026119299302100303.

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A variety of approaches to assessment of cellular integrity exist, based on tests of integrity of the plasma membrane, tests of metabolic competence, and asessment of morphology. By definition, such approaches address different aspects of cellular integrity and hence are not interchangeable indices of cellular integrity. Accordingly, it would be most appropriate to characterise hepatocyte preparations on the basis of more than just trypan blue dye exclusion (a test of plasma membrane integrity) as is customary. A scheme for the choice of the most appropriate mix of tests of cellular integrity

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12

Buyuktiryaki, Betul, and Alexandra F. Santos. "Food allergy severity predictions based on cellular in vitro tests." Expert Review of Molecular Diagnostics 20, no. 7 (2020): 679–91. http://dx.doi.org/10.1080/14737159.2020.1782192.

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13

Petrides, Michael. "Use of cellular telephones and performance on tests of attention." Neuroreport 12, no. 4 (2001): A21. http://dx.doi.org/10.1097/00001756-200103260-00001.

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14

Sabovljev, S. A., W. A. Cramp, P. D. Lewis, G. Harris, KeithE Halnan, and J. Lambert. "USE OF RAPID TESTS OF CELLULAR RADIOSENSITIVITY IN RADIOTHERAPEUTIC PRACTICE." Lancet 326, no. 8458 (1985): 787. http://dx.doi.org/10.1016/s0140-6736(85)90674-9.

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15

Avalle, Massimiliano, Giovanni Belingardi, and Andrea Ibba. "Mechanical models of cellular solids: Parameters identification from experimental tests." International Journal of Impact Engineering 34, no. 1 (2007): 3–27. http://dx.doi.org/10.1016/j.ijimpeng.2006.06.012.

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16

Haag, F. C., A. F. Galio, and L. Schaeffer. "Uniaxial compression tests of aluminium foams." Proceedings of the Institution of Mechanical Engineers, Part B: Journal of Engineering Manufacture 216, no. 4 (2002): 633–36. http://dx.doi.org/10.1243/0954405021520148.

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Some cellular aluminium materials have been extensively developed and investigated in recent years. The potential for applying aluminium foams in lightweight construction is mainly based on the stiffness and impact absorption. Because of these characteristics, this work is based mainly on the uniaxial compression resistance of aluminium foam. The aluminium foam was formed with three different compaction presses to verify the influence on density and, subsequently, crushing resistance.

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17

Scherer, Kathrin, Andreas J. Bircher, and Ingmar AFM Heijnen. "Diagnosis of stinging insect allergy: utility of cellular in-vitro tests." Current Opinion in Allergy and Clinical Immunology 9, no. 4 (2009): 343–50. http://dx.doi.org/10.1097/aci.0b013e32832dd1f5.

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18

Röhmel, J., C. Schwarz, D. Staab, and P. Stock. "119 Cellular allergy tests for antibiotic drug hypersensitivity in cystic fibrosis." Journal of Cystic Fibrosis 14 (June 2015): S87. http://dx.doi.org/10.1016/s1569-1993(15)30296-4.

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19

Durif, S., A. Bouchaïr, and O. Vassart. "Experimental tests and numerical modeling of cellular beams with sinusoidal openings." Journal of Constructional Steel Research 82 (March 2013): 72–87. http://dx.doi.org/10.1016/j.jcsr.2012.12.010.

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20

Polienova, E. V., K. P. Makeeva, and A. Yu Valdberg. "Aerodynamic tests of new regular cellular packings for mass-transfer towers." Chemical and Petroleum Engineering 46, no. 11-12 (2011): 692–95. http://dx.doi.org/10.1007/s10556-011-9403-4.

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21

Wang, Ning, Hetao Hou, Youcheng Wang, et al. "Flexural behavior of partially encased cellular beams: Tests and design implications." Engineering Structures 293 (October 2023): 116631. http://dx.doi.org/10.1016/j.engstruct.2023.116631.

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22

Kondo, Andrea Tiemi, and Andreza Alice Feitosa Ribeiro. "Regulatory considerations for Cellular Therapy." JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY 3, no. 1 (2022): 166. http://dx.doi.org/10.46765/2675-374x.2022v3n1p166.

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Advanced therapy products can be an alternative treatment for several disease. Manufacturing steps and product release are critical points to avoid unsafe use of products. Quality controls tests, manufacturing practice, safety testing and efficacy trials need to be properly accessed before releasing to patients. Regulatory system for cell therapy products determines guidelines for production, clinical trials and registration, considering risk-benefit ratios. This article aims to discuss main aspects of National Regulatory for advanced therapy products.

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23

TAN, SYN KIAT, and SHENG-UEI GUAN. "A TRANSFORMATION SEQUENCING APPROACH TO PSEUDORANDOM NUMBER GENERATION." International Journal of Modern Physics C 18, no. 08 (2007): 1293–302. http://dx.doi.org/10.1142/s0129183107011327.

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This paper presents a new approach to designing pseudorandom number generators based on cellular automata. Current cellular automata designs either focus on (i) ensuring desirable sequence properties such as maximum length period, balanced distribution of bits and uniform distribution of n-bit tuples, etc. or (ii) ensuring the generated sequences pass stringent randomness tests. In this work, important design patterns are first identified from the latter approach and then incorporated into cellular automata such that the desirable sequence properties are preserved like in the former approach.

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24

SCOTT, A. "Ophthalmology (Picture Tests)." British Journal of Ophthalmology 82, no. 10 (1998): 1220f. http://dx.doi.org/10.1136/bjo.82.10.1220f.

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25

Doig, W. M. "Clinical Tests: Ophthalmology." British Journal of Ophthalmology 75, no. 3 (1991): 192. http://dx.doi.org/10.1136/bjo.75.3.192-a.

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26

Stronge, W. J., and V. P. W. Shim. "Microdynamics of Crushing in Cellular Solids." Journal of Engineering Materials and Technology 110, no. 2 (1988): 185–90. http://dx.doi.org/10.1115/1.3226029.

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Lightweight, open-celled foams and honeycombs can exhibit deformation localization during static crushing as a result of buckling and plastic collapse of cell walls. Localization of deformation is a manifestation of strain-softening behavior that limits transmitted forces through these shock mitigating materials. Collision tests on two-dimensional cellular solids with strain-softening behavior reveal that with some microstructures, strain-rate effects can stabilize less compliant modes of deformation. When stabilization occurs, it amplifies the intensity of transmitted shocks.

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27

Wood, P. R., L. A. Corner, J. S. Rothel, et al. "A field evaluation of serological and cellular diagnostic tests for bovine tuberculosis." Veterinary Microbiology 31, no. 1 (1992): 71–79. http://dx.doi.org/10.1016/0378-1135(92)90142-g.

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28

Lowe, J. G., J. S. Beck, R. Madhok, et al. "Histometric studies on cellular infiltrates of tuberculin tests in patients with haemophilia." Journal of Clinical Pathology 42, no. 2 (1989): 184–87. http://dx.doi.org/10.1136/jcp.42.2.184.

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29

Lowe, J. G., J. H. Gibbs, R. C. Potts, J. L. Stanford, and J. Swanson Beck. "Histometric studies on cellular infiltrates of tuberculin tests in patients with sarcoidosis." Journal of Clinical Pathology 44, no. 3 (1991): 219–23. http://dx.doi.org/10.1136/jcp.44.3.219.

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30

Penha-Junior, Tarciso, Monica Abreu Pessoa Rodrigues, Vanessa Pecorari, and Maristela Dutra-Correa. "Can cellular cementum in bovine teeth alter the results of microleakage tests?" International Journal of Health Science 4, no. 39 (2024): 2–8. http://dx.doi.org/10.22533/at.ed.1594392418049.

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31

Kurcheva, S. A., D. A. Kovalev, D. G. Ponomarenko, et al. "Qualitative Indicators of Experimental Brucellosis Antigen Preparations Designed for Cellular Tests in vitro." Problems of Particularly Dangerous Infections, no. 3 (October 22, 2020): 83–88. http://dx.doi.org/10.21055/0370-1069-2020-3-83-88.

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In order to develop the most diagnostically informative methods for carrying out antigen-stimulated cellular tests in vitro a careful selection of stimulating agent (antigen) is required, possessing an adequate activating potential and providing specificity of the reaction.Objective of the study was to identify the qualitative indicators of experimental batches of brucellosis antigen preparations designed for cellular tests in vitro.Materials and methods. Initially we produced antigen complexes of brucellosis microbe on the basis of the vaccine strains of three epidemically significant Brucell

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32

Son, Chang-Nam, and Sang-Hyon Kim. "Interpretation of Anti-Nuclear Antibody Tests." Korean Journal of Medicine 96, no. 4 (2021): 337–40. http://dx.doi.org/10.3904/kjm.2021.96.4.337.

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Anti-nuclear antibodies (ANAs) are autoantibodies against nuclear substances or other cellular components. ANA tests are used in the diagnostic process to screen patients with suspected rheumatic or autoimmune diseases. ANA-associated diseases are characterized by a high titer of antinuclear antibodies and include systemic lupus erythematosus, systemic sclerosis, and mixed connective tissue diseases. ANA test results must be cautiously interpreted as they can be positive not only in infections and oncological diseases but also for the healthy general population. The ANA test mainly uses the in

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33

Del Rosso, Stefano, and Lorenzo Iannucci. "On the Compressive Response of Polymeric Cellular Materials." Materials 13, no. 2 (2020): 457. http://dx.doi.org/10.3390/ma13020457.

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This paper presents a series of compression tests performed on a variety of high performance lightweight cellular materials conventionally used in energy absorption applications. Compressive tests were performed over a range of strain rates with a universal testing machine and a single stage gas gun. Experimental results revealed a dependency of the mechanical properties on the polymeric precursor, density, infill topology and strain rates. The dynamic strength of the investigated materials was determined through a material parameter identification study via the finite element (FE) method. Num

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34

Fava-Netto, Celeste, Walderez Gambale, Júlio Croce, Claudete R. Paula, and Sérgio de C. Fava. "Candidin: comparison of two antigens for cutaneous delayed hypersensitivity testing." Revista do Instituto de Medicina Tropical de São Paulo 38, no. 6 (1996): 397–99. http://dx.doi.org/10.1590/s0036-46651996000600002.

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A candidin, which is a suspension of killed yeast cells, is commonly used for intradermal tests of delayed hypersensitivity, to evaluate the immunological cellular competence of the patient, when the test is applied along with other similar tests. When working with a cellular antigen, the histopathology of positive skin tests reveals a cellular infiltrate which not only presents a characteristic hypersensitivity reaction but also a neutrophilic abscess in the central part. This research presents the results of a comparison between the yeast cell suspension and the polysaccharide antigens, both

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35

Chicos, Lucia-Antoneta, Ian Campbell, Sebastian Marian Zaharia, et al. "Experimental and Finite Element Analysis of the Open-Cells Porous Materials Subjected to Compression Mechanical Loading." Materiale Plastice 56, no. 2 (2019): 421–25. http://dx.doi.org/10.37358/mp.19.2.5199.

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Progress in Additive Manufacturing (AM) technology enables the fabrication of complex structures that could not be obtained with traditional manufacturing methods. One AM research area is the development and use of lightweight products with cellular structures, containing complex lattices and pores, which give improved performance and functionality. It is well known that there is a strong link between mechanical properties and architecture of samples with cellular structures. This paper presents a comparison and validation of Finite Element Analysis (FEA) simulations of cellular structures wit

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36

Mïller, Mathias. "Cellular diagnostics: A challenge for laboratory medicine." Jugoslovenska medicinska biohemija 23, no. 3 (2004): 195–200. http://dx.doi.org/10.2298/jmh0403195m.

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Investigating cells for genetic features, malignant transformation, surface characteristics, metabolic functions and signaling will be future key elements for diagnosis of diseases. Integrating this new area into Laboratory Medicine will add new competence and responsibility to Clinical Biochemistry and Laboratory Medicine. Cellular genetics will be a main area for the diagnostic laboratory to investigate risk and prognosis for diseases having also impact on a more individualized medication. With the introduction of flow cytometry a more objective way of cell identification by immunophenotypin

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37

Rogowski, B. F. W. "Fire Performance of Building Elements Incorporating Cellular Polymers." Cellular Polymers 4, no. 5 (1985): 325–38. http://dx.doi.org/10.1177/026248938500400501.

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This paper discusses the use of cellular plastics in buildings, reviews their fire performance and suggests how test procedures can be developed to assist design. Reference is made to a particular series of tests involving the assessment of a range of non-loadbearing partitions or infill panels, based on an extruded polystyrene core.

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38

Lilius, Henrik, and Boris Isomaa. "Fluorescent Probes as Tools in In Vitro Toxicology." Alternatives to Laboratory Animals 24, no. 3 (1996): 423–28. http://dx.doi.org/10.1177/026119299602400318.

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A number of different endpoints reflecting cell viability are commonly used to assess cytotoxicity. These endpoints are then taken to reflect cell death. It is not possible to elucidate the basis of the toxic mechanisms involved in these tests. However, by using a number of different endpoints to monitor different cellular events, the information that can be obtained from in vitro toxicity tests could be increased. Fluorescent probes appear to be promising alternatives for assessing cytotoxicity, and such probes are available for a number of different cellular events. In addition to viability,

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39

Engelken, Jared A., Tobias Butelmann, Fabian Tribukait-Riemenschneider, and V. Prasad Shastri. "Towards a 3D-Printed Millifluidic Device for Investigating Cellular Processes." Micromachines 15, no. 11 (2024): 1348. http://dx.doi.org/10.3390/mi15111348.

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Microfluidic devices (µFDs) have been explored extensively in drug screening and studying cellular processes such as migration and metastasis. However, the fabrication and implementation of microfluidic devices pose cost and logistical challenges that limit wider-spread adoption. Despite these challenges, light-based 3D printing offers a potential alternative to device fabrication. This study reports on the development of millifluidic devices (MiFDs) for disease modeling and elucidates the methods and implications of the design, production, and testing of 3D-printed MiFDs. It further details h

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40

Israeli, Moshe, Tuvia Ben-Gal, Vicktoria Yaari, et al. "Individualized Immune Monitoring of Cardiac Transplant Recipients by Noninvasive Longitudinal Cellular Immunity Tests." Transplantation 89, no. 8 (2010): 968–76. http://dx.doi.org/10.1097/tp.0b013e3181cbabe6.

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41

Demko, J. A., J. E. Fesmire, J. Dookie, J. Bickley, and S. Kraft. "Comparison tests of cellular glass insulation for the development of cryogenic insulation standards." IOP Conference Series: Materials Science and Engineering 101 (December 18, 2015): 012016. http://dx.doi.org/10.1088/1757-899x/101/1/012016.

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42

Ergenc, Ali Fuat, та Nejat Olgac. "New technology for cellular piercing: rotationally oscillating μ-injector, description and validation tests". Biomedical Microdevices 9, № 6 (2007): 885–91. http://dx.doi.org/10.1007/s10544-007-9102-2.

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43

Debray, Julien, Lei Chang, Stéphanie Marquès, et al. "Inhibitors of tissue-nonspecific alkaline phosphatase: Design, synthesis, kinetics, biomineralization and cellular tests." Bioorganic & Medicinal Chemistry 21, no. 24 (2013): 7981–87. http://dx.doi.org/10.1016/j.bmc.2013.09.053.

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44

Tong, Charles C., Charlene A. McQueen, Sharma Ved Brats, and Gary M. Williams. "The lack of genotoxicity of sodium fluoride in a battery of cellular tests." Cell Biology and Toxicology 4, no. 2 (1988): 173–86. http://dx.doi.org/10.1007/bf00119244.

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45

Moreno-Garrido, I., L. M. Lubián, and A. M. V. M. Soares. "Influence of Cellular Density on Determination of EC50 in Microalgal Growth Inhibition Tests." Ecotoxicology and Environmental Safety 47, no. 2 (2000): 112–16. http://dx.doi.org/10.1006/eesa.2000.1953.

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46

Kurihara, Ooki, and Hidenori Takahashi. "Centrifuge Model Tests on Configuration of Cement-Treated Soil Behind Cellular Quay Wall." Japanese Geotechnical Society Special Publication 10, no. 15 (2024): 473–78. http://dx.doi.org/10.3208/jgssp.v10.os-4-05.

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47

Mingomataj, Ervin Ç., and Alketa H. Bakiri. "Approaches to the Management of Presumed Immediate Hymenoptera Venom Allergy and Non-Detectable IgE." Open Allergy Journal 3, no. 1 (2010): 16–23. http://dx.doi.org/10.2174/1874838401003010016.

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Objective: To provide a comprehensive evaluation in patients with a convincing history of immediate insect allergy but negative skin test and/or specific IgE results, adequately addressing the question of how best to manage them. Data sources: Observational peer-reviewed studies and case reports were searched on Pub-Med database from 1998 up to March 2009 using the following keywords: Hymenoptera Allergy & Negative IgE (Negative Skin Tests). Study selection: Studies on supplemental diagnostic tests that provided data from patients with immediate hymenoptera allergy but negative conventiona

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48

Pedersen, Morten Gram, Gianna M. Toffolo, and Claudio Cobelli. "Cellular modeling: insight into oral minimal models of insulin secretion." American Journal of Physiology-Endocrinology and Metabolism 298, no. 3 (2010): E597—E601. http://dx.doi.org/10.1152/ajpendo.00670.2009.

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The oral glucose tolerance test and meal tolerance test are common clinical tests of the glucose-insulin system. Several mathematical models have been suggested as means to extract information about β-cell function from data from oral tolerance tests. Any such model needs to be fairly simple but should at the same time be linked to the underlying biology of the insulin-secreting β-cells. The scope of the present work is to present a way to make such a connection using a recent model describing intracellular mechanisms. We show how the three main components of oral minimal secretion models, der

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49

Sonia, G. B., Mahalakshmi Sundarapandian, G. Ramu, and Priya Raman. "Cellular Dynamics in Passiflora tarminiana: Insights from Histological Investigations." Research Journal of Biotechnology 20, no. 1 (2024): 21–28. https://doi.org/10.25303/201rjbt021028.

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The objective of the study was to investigate the visible and microscopic features of Passiflora tarminiana fruit. The plant specimen was collected in May 2023 from Ooty, The Nilgiris District, Tamil Nadu. The evaluation was carried out using macroscopy, microscopy and histochemical tests. The fruit's characteristic components were identified by dissecting it and their structures were visually documented through photographs. Macroscopy revealed the fruit's sensory properties while microscopy showed the presence of oil globules, stone cells, simple pitted, reticulated and spiral vessels and clu

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50

Kumagai‐Braesch, Makiko, Masahiro Satake, Olle Korsgren, Arne Andersson, and Erna Möller. "Characterization of cellular human anti‐porcine xenoreactivity." Clinical Transplantation 7, no. 3 (1993): 273–80. http://dx.doi.org/10.1111/j.1399-0012.1993.tb00917.x.

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The cellular xenoimmune reactivity of human responder cells reactive against porcine stimulator cells has been characterized. The xenogeneic mixed lymphocyte bulk culture reactivity is slightly lower than the allogeneic response but peak reactivity occurs with similar kinetics and secondary responses of primed lymphocytes are comparable. The xeno‐MLR was directed against pig MHC class II molecules as indicated by blocking using specific monoclonal antibodies. Production of IL‐2 was delayed and significantly lower in the xeno‐MLR. The low proliferative xenoresponse could not be restored by the

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