Academic literature on the topic 'Tweed (Tissus)'

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Journal articles on the topic "Tweed (Tissus)"

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Roux, Huguette, C. Paass, Konan Djaha, G. Agneroh-Eboi, and A. Aka. "Triangle de TWEED. Équilibre de la denture et des tissus mous. Étude sur une population de jeunes Ivoiriens." Revue d'Orthopédie Dento-Faciale 27, no. 3 (1993): 297–304. http://dx.doi.org/10.1051/odf/1993030.

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Meehan, J. T., R. C. Cutlip, and H. D. Lehmkuhl. "Evaluation of Ethylenediaminetetraacetic Acid, Tetrasodium Salt Dihydrate (EDTA)-Tween 20 Treatment versus Protease Digestion of Formalin-fixed Tissue Sections for Detection of Bovine Respiratory Syncytial Virus Antigen in Infected Ovine Lung." Veterinary Pathology 26, no. 4 (1989): 322–25. http://dx.doi.org/10.1177/030098588902600406.

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The efficacy of protease and ethylenediaminetetraacetic acid, tetrasodium salt dihydrate (EDTA)-Tween 20 in unmasking bovine respiratory syncytial virus (BRSV) antigens in formalin-fixed lung tissue was compared using avidin-biotin immunoperoxidase procedure. Tissues were taken from experimentally infected lambs. BRSV antigen stained in both techniques. Treatment with EDTA-Tween 20 resulted in more intense staining of BRSV infected cells, more uniform cytoplasmic staining, less non-specific background, and superior cellular detail in comparison to protease digestion.
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Karimifar, Haddis, Mina Allameh, Arsalan Soleimanian, Asghar Zeyni-Esfahani, and Abdolamir Allameh. "Augmentation of lipid peroxidation and tissue injuries in rats exposed by sub-acute inhalation to nano-silver particles containing tween-20." Interdisciplinary Toxicology 13, no. 4 (2020): 121–27. https://doi.org/10.2478/intox-2020-0017.

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Abstract Nanosilver particles (NSPs) used by customers may contain detergents/solvents. However, in most of the toxicological studies, nanosilvers are prepared in water and very little is known about the interaction of these agents with NSPs in causing adverse effects. The aim of this study was to investigate the interaction of NSPs and tween-20 in causing tissue injuries after inhalation. In this experiment, 16 rats were divided into four groups (n=4/group) as follows. Controls, exposed to water vapors; Tween-treated exposed to tween-20 alone (0.01% V/V); NSP-tween group exposed to 1000 ppm c
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Lust, Cody A. C., Xinjie Lin, Erin M. Rock, Cheryl L. Limebeer, Linda A. Parker, and David W. L. Ma. "Short communication: Tissue distribution of major cannabinoids following intraperitoneal injection in male rats." PLOS ONE 17, no. 1 (2022): e0262633. http://dx.doi.org/10.1371/journal.pone.0262633.

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Currently, peripheral tissue distribution of cannabinoids after treatment is poorly understood. This pilot study sought to examine the early tissue distribution of major cannabinoids 30 minutes following an intraperitoneal injection of vehicle (1:9 Tween 80/SAL), and doses of THC (1 mg/kg) and CBD (5 mg/kg) that are feasible for human consumption in serum, adipose, brain, lung, liver, jejunum, and muscle of male Sprague-Dawley rats. The jejunum and adipose were most enriched in THC. Similarly, CBD was enriched in the jejunum and adipose but also the liver. In contrast, the brain had the lowest
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Lownds, N. K., and M. J. Bukovac. "Surfactant-induced Ethylene Production by Leaf Tissue." Journal of the American Society for Horticultural Science 114, no. 3 (1989): 449–54. http://dx.doi.org/10.21273/jashs.114.3.449.

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Abstract Ethylene evolution induced by nonionic (Triton X-100, Triton X-405, Tween 20, Ortho X-77 and Regulaid), anionic (Aerosol OT and Dupanol ME), and cationic (Arquad C-50 and Arquad 2C-75) surfactants was characterized using cowpea [Vigna unguiculata (L.) Walp. supsb. unguiculata ‘Dixielee’] seedlings. Representative surfactants of each ionogenic class induced ethylene evolution. Time course studies revealed an increased rate of ethylene evolution during the first 6 to 12 hr after treatment, followed by a slow decrease for the next 12 to 36 hr, and a return to control levels within 48 hr.
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Lu, Huihui, Francesco Floris, Marc Rensing, and Stefan Andersson-Engels. "Fluorescence Spectroscopy Study of Protoporphyrin IX in Optical Tissue Simulating Liquid Phantoms." Materials 13, no. 9 (2020): 2105. http://dx.doi.org/10.3390/ma13092105.

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Fluorescence spectroscopy has been extensively investigated for disease diagnosis. In this framework, optical tissue phantoms are widely used for validating the biomedical device system in a laboratory environment outside of clinical procedures. Moreover, it is fundamental to consider that there are several scattering components and chromophores inside biological tissues and the interplay between scattering and absorption may result in a distortion of the emitted fluorescent signal. In this work, the photophysical behaviour of a set of liquid, tissue-like phantoms containing different composit
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Morita, Tetsuo, and Tatsuo Shimada. "Surface morphology of Purkinje cells and myocardial cells following chemical digestion." Proceedings, annual meeting, Electron Microscopy Society of America 48, no. 3 (1990): 420–21. http://dx.doi.org/10.1017/s0424820100159643.

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From light and transmission electron microscopic studies, it has been long known that Purkinje cells of mammalian hearts have morphological characteristics different from ordinary myocardial cells. In the present study, not only Purkinje cells and myocardial cells but also connective tissue sheaths surrounding these cells were investigated by combined scanning electron microscopy(SEM) and chemical digestion.The moderator band of adult sheep heart was used because it possessed both Purkinje cells and myocardial cells (Fig.1). Tissue blocks were immersed in Karnovsky’s fixative for 3hr or longer
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Gagné, François. "Isolation and Quantification of Polystyrene Nanoplastics in Tissues by Low Pressure Size Exclusion Chromatography." Journal of Xenobiotics 12, no. 2 (2022): 109–21. http://dx.doi.org/10.3390/jox12020010.

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Ecotoxicity investigations of plastic nanoparticles (NPs) should pay more attention to their ability to pass barriers, accumulate, and initiate toxicity in cells. The purpose of this study was to develop a simple size exclusion chromatography (SEC) methodology to measure plastic NPs in biological tissues. A SEC column was prepared using a high-resolution gel for large macromolecules to separate plastic NPs from the protein/lipid pools in tissues. It was necessary to prepare the samples in high salt and non-ionic detergent (0.5 M NaCl and 0.2% Tween-20) and apply 0.2% Tween-20 containing 14 mM
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Kshitiza, Pathak, and Pathak Akshay. "CROSS-SECTIONAL ASSESSMENT OF ASSOCIATION BETWEEN GRADE OF AS-THI SARATA AND INCIDENCE OF DENTAL CARIES." International Ayurvedic Medical Journal 8, no. 8 (2020): 4032–35. http://dx.doi.org/10.46607/iamj0108082020.

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Dashavidha Karanadi Pariksha (Ten-fold examination) elaborated in Charaka Samhita imparts complete knowledge of patient’s condition by means of specific investigations. It is done for knowledge of lifespan, degree of strength of body and disease and exact treatment perspective. Accordingly, a patient should be examined in respect of Dhatu Sarata (excellence of body tissues) i.e. as per the best qualities of Dhatu (body tissues). Drudh Danta (strongness of teeth) has been described as a characteristic of Asthi Sarata. Thus, an observational cross-sectional study was planned to assess the probab
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Bytov, Maksim V., Irina M. Petrova, Sergey L. Khatsko, Olga V. Sokolova, and Irina A. Shkuratova. "Protocol refinement for quenching autofluorescence of red blood cells in FFPE sections of organ samples from cattle, pigs and chickens." BIO Web of Conferences 108 (2024): 01034. http://dx.doi.org/10.1051/bioconf/202410801034.

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One of the most common problem that researchers encounter when using fluorescence to visualize immunohistochemistry is the autofluorescence of the studied organ tissue sections and cell cultures. Autofluorescence quenching is necessary for a wide variety of organs and tissues, as well as for different methods of fixation and histochemical processing of sections. In addition to autofluorescence quenching, it is necessary to take into account the need for histological readability of tissue sections when using counterstains afterwards. Such protocol refinement for fluorescent immunohistochemistry
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Books on the topic "Tweed (Tissus)"

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Tweed. Bloomsbury Academic, an imprint of Bloomsbury Publishing Plc, 2017.

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Tweed. Bloomsbury Publishing Plc, 2016.

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Tweed. Bloomsbury Publishing Plc, 2016.

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Book chapters on the topic "Tweed (Tissus)"

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Cumming, Riciiard, and Rachel Fallon. "Subcellular Localization of Biological Molecules." In Radioisotopes in Biology. Oxford University PressOxford, 1990. http://dx.doi.org/10.1093/oso/9780199630806.003.0007.

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Abstract The complexity of higher organisms is due in part to the wide variety of tissues and cells which have become specialized for different functions. Cells can often be differentiated from each other on the basis of size, shape, fine structural differences and on the basis of phenotypic molecular markers. Techniques such as tissue culture can help to elucidate the function of individual cell types by growing them and manipulating them under controlled conditions. A further degree of complexity comes from the organization of structures within the cell; at the simplest level we can divide t
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Conference papers on the topic "Tweed (Tissus)"

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"Hepatoprotective Effect of Typhonium flagelliforme against Thioacetamide Induced Liver Cirrhosis in Rats." In 4th International Conference on Biological & Health Sciences (CIC-BIOHS’2022). Cihan University, 2022. http://dx.doi.org/10.24086/biohs2022/paper.643.

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Typhonium flagelliforme (T. flagelliforme) was utilized in outdated medication for handling numerous syndromes. This study aimed to investigate hepatoprotection effects of T. flagelliforme against thioacetamide (TAA) hepatotoxicity in rodents.Thirty rodents arbitrarily separated five clusters. Collection 1 was intraperitoneally injected distilled water thrice /week and fed (p.o) daily with 10% Tween 20 to eight weeks. Collection 2-5 i.p. injected with 200 mg/kg TAA three times thrice per week for 8 weeks and fed 10% Tween 20, 50 mg/kg silymarin, 250 and 500 mg/kg of T. flagelliforme extract da
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Harris, R., L. Garcia Frade, S. Poole, M. Mahmoud, A. D. Curtis, and P. J. Gaffney. "CATABOLIC BEHAVIOUR OF RECOMBINANT TISSUE PLASMINOGEN ACTIVATOR (R-t-PA) IN THE RAT." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643175.

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To compliment ongoing experimentation on the use of tissue plasminogen activator (t-PA) as a thrombolytic agent in a rat thrombosis model, clearance data for labelled R-t-PA in the rat were investigated. Both Iodogen and Chloramine T labelling procedures for incorporation yielded similar biological activity in the resultant labelled t-PA, while the half-lives in the rat circulation for Iodogen- and Chloramine T-label led materials were 5 1/2 and 7 1/2 minutes respectively. Clearance data using promoter based and ELISA assays support that obtained with 125j_ labelled t-PA. Following fractionati
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