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1

Lenchenko, Ekaterina M., Dmitry A. Blumenkrants, Vladislav V. Ponomarev, Inna B. Pavlova, and Galina S. Tolmacheva. "METHODOLOGICAL ASPECTS OF RESEARCH OF COMPOSITION OF BIOFILMS in vitro, ex vivo, in vivo." Problems of veterinary sanitation, hygiene and ecology 1, no. 41 (2022): 73–82. http://dx.doi.org/10.36871/vet.san.hyg.ecol.202201009.

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The article presents the general patterns of formation of a three-dimensional multilayer heterogeneous structure biofilms in vitro, ex vivo, in vivo. It was found, that the mass fraction of cells of biofilms was 86,8-91,4%, of the matrix – 8,9-13,2%, which is due to the structure of the cell wall of microorganisms synthesizing the extracellular matrix. The advantages of transmission and scanning electron microscopy are the visualization of L-shapes and the quantitative assessment of the diameter, perimeter, height, area, volume and chemical composition of cells and the extracellular matrix of microorganisms. Laser modulation interference microscopy made it possible to study biofilms in real time without fixing and staining microorganisms; phase-contrast microscopy – intrapopulation and interpopulation interactions depending on changes in the pH of the environment, oxygen content and other chemical and physical factors. Fluorescent microscopy is a promising method for detection of non-culturable viable cells of microorganisms. The use a modified Gram stain, the use of solution of «Crocus sativus» made it possible to differentiate gram-negative and gram-positive microorganisms and to assess the degree of repair of tissue. The developed new methodological approach made it possible to scientifically substantiate and experimentally confirm the effectiveness of the use of nutrient media containing components for the repair of the cell wall of microorganisms.
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Shishatskaya, Ekaterina I. "Biodegradation of PHA in vivo." Journal of Siberian Federal University. Biology 9, no. 1 (March 2016): 21–32. http://dx.doi.org/10.17516/1997-1389-2016-9-1-21-32.

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3

van Luijk, S. J., F. Scheele, and C. P. M. van der Vleuten. "Toetsing in vivo bij ‘In VIVO’." Tijdschrift voor Medisch Onderwijs 27, no. 6 (December 2008): 279–87. http://dx.doi.org/10.1007/bf03078290.

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4

Mitterhauser, Markus, Stefan Toegel, Wolfgang Wadsak, Rupert R. Lanzenberger, Leonhard-Key Mien, Claudia Kuntner, Thomas Wanek, et al. "Pre vivo, ex vivo and in vivo evaluations of [68Ga]-EDTMP." Nuclear Medicine and Biology 34, no. 4 (May 2007): 391–97. http://dx.doi.org/10.1016/j.nucmedbio.2007.03.002.

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5

Huven, Paula. "Reativar o vivo, atravessar a floresta." MODOS: Revista de História da Arte 7, no. 1 (February 13, 2023): 344–68. http://dx.doi.org/10.20396/modos.v7i1.8670588.

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A partir de variadas expressões poéticas – fotográfica, cinematográfica, pictórica e literária – proponho contornar a ideia de vivo. Minha série fotográfica Água viva desenha a aproximação de uma menina com as águas correntes da cachoeira. A criança entra em contato com a matéria do mundo e com o invisível da natureza, sem margens que os distingam. Naomi Kawase, em seu filme Floresta dos Lamentos, mostra-nos que atravessar a floresta é, necessariamente, ser atravessada por ela. A artista Wilma Martins constrói pictoricamente irrupções da floresta no cenário domiciliar e, assim, ela dá forma ao vínculo entre o real e o imaginário; entre o selvagem e o domesticado. A personagem G.H., de Clarice Lispector, vive uma epifania a partir do encontro com uma barata – ser arcaico, remoto, imemorial, travessia íntima e subjetiva que faz emergir o mais primitivo de si. Entre o mundo que olhamos e o que vemos, o visível e o invisível, a matéria e o espírito, humano e não humano, somos atravessados pela energia do vivo. Reativar, palavra-chave no vocabulário da filósofa belga Isabelle Stengers, leva-nos de volta em direção ao vínculo com os deuses, os espíritos, a terra e, com estas alianças, reativar o vivo se compõe.
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6

Ilinskaya, O. N., and H. Fret. "Genotoxical effects of ribonuclease in vivo." Biopolymers and Cell 16, no. 4 (July 20, 2000): 270–74. http://dx.doi.org/10.7124/bc.000570.

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7

Gurova, S. V., T. M. Kecheryukova, A. S. Goncharova, E. N. Kolesnikov, M. A. Kozhushko, and M. Z. Tatimov. "MODELS OF LIVER CANCER IN VIVO." Современные проблемы науки и образования (Modern Problems of Science and Education), no. 4 2023 (2023): 14. http://dx.doi.org/10.17513/spno.32707.

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8

Chen, Gong. "In vivo confusion over in vivo conversion." Molecular Therapy 29, no. 11 (November 2021): 3097–98. http://dx.doi.org/10.1016/j.ymthe.2021.10.017.

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9

Borgström, L. "In vitro, ex vivo, in vivo veritas." Allergy 54, s49 (March 1999): 88–92. http://dx.doi.org/10.1111/j.1398-9995.1999.tb04394.x.

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10

Tümmler, Burkhard. "In-vivo and ex-vivo functional assessment." Journal of Cystic Fibrosis 3 (August 2004): 149–50. http://dx.doi.org/10.1016/j.jcf.2004.05.031.

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11

Ivanović, Zoran. "Ex vivo expansion of hematopoietic cells today." Scripta Medica 42, no. 2 (2011): 92–96. http://dx.doi.org/10.5937/scrimed1102092i.

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12

Montiel, Luis. "Historia y filosofía del ser vivo." Asclepio 53, no. 1 (June 30, 2001): 313–18. http://dx.doi.org/10.3989/asclepio.2001.v53.i1.182.

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13

Rigue, Fernanda Monteiro, and Alice Copetti Dalmaso. "ESTAR VIVO: APRENDER." Criar Educação 9, no. 3 (December 3, 2020): 130. http://dx.doi.org/10.18616/ce.v9i3.6354.

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Nestes escritos, empreendemos um convite em atentar às exigências das forças que nos tomam e pedem passagem nos dias atuais. Com novos ou velhos gestos, atos, palavras, formas e conteúdos, vamos dando conta, temporariamente, de nossos anseios, sobretudo às dimensões desagregadoras a que estamos expostos, mas que, invariavelmente, permite que se crie algo novo: aprender, ao estar vivo. Estar vivo implica um processo ininterrupto de aprender, resingularizações de sentir o que se passa entre nós e os acontecimentos, convidando-nos a procurar novas formas e trejeitos de viver, experimentar a vida que se tem. Pensamos que aí - como uma onda que chega, interpela e permanece em nossas células - residirá alguma coisa fluida, atualizando processos de aprendizagens que estejam em curso: passagem rica e viva de algo novo que nasce e (se) experimenta em nós.Palavras-chave: aprender; atenção; estar vivo; experimentação.
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14

Sansi Roca, Roger. "`Dinheiro Vivo'." Critique of Anthropology 27, no. 3 (September 2007): 319–39. http://dx.doi.org/10.1177/0308275x07080360.

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15

Demming, Anna. "Nanotechnologyin vivo." Nanotechnology 21, no. 14 (March 16, 2010): 140201. http://dx.doi.org/10.1088/0957-4484/21/14/140201.

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16

Pínnola, Fabián Marcelo. "En Vivo." Revista del ISM, no. 5 (November 29, 2005): 50–74. http://dx.doi.org/10.14409/ism.v1i5.513.

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Vivo, Teatro. "Teatro Vivo." Index on Censorship 14, no. 1 (February 1985): 2–3. http://dx.doi.org/10.1080/03064228508533822.

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18

Jakubowski, Hieronim. "Proofreadingin Vivo." Journal of Biological Chemistry 270, no. 30 (July 28, 1995): 17672–73. http://dx.doi.org/10.1074/jbc.270.30.17672.

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19

Kim, Tae Woo, Hesson Chung, Ick Chan Kwon, Ha Chin Sung, and Seo Young Jeong. "In Vivo." Molecules and Cells 10, no. 2 (2000): 135. http://dx.doi.org/10.1007/s100590050004.

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20

Dayanne, Rose. "“VIVO SONHANDO”." Cadernos Miroslav Milovic 1, no. 1 (February 11, 2023): 165–72. http://dx.doi.org/10.46550/cadernosmilovic.v1i1.26.

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O texto tem o objetivo de indicar as ressonâncias políticas no pensamento de Miroslav Milovic e Jacques Derrida. Em tempos de terror, esses dois filósofos destacaram a importância da democracia radical compreendida como possibilidade do impossível. Para entender as implicações desta questão, o artigo se divide em duas seções. O ponto de partida é o luto infinito, singular e coletivo, consequência das catástrofes políticas. A segunda seção investiga as relações de amizade imbricadas nas questões políticas. Nesse artigo, a fonte que a pesquisa utiliza é a correspondência de Mario Castellani a Miroslav Milovic acerca do tema “A democracia não tem fim”, alusão a obra Voyous de Derrida. A correspondência foi encontrada nos Manuscritos direito como potência, acervo que se mostra exitoso para novas pesquisas acerca do pensamento de Milovic. No final, ganha relevância a responsabilidade do sobrevivente em semear a espectralidade do outro, pois o mais importante do amor incondicional não é a semente, é o semear.
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21

Havlicek, V., M. Lopatarova, S. Cech, R. Dolezel, T. Huber, A. Pavlok, G. Brem, and U. Besenfelder. "In vivo culture of bovine embryos and quality assessment of in vivo vs. in vitro produced embryos." Veterinární Medicína 50, No. 4 (March 28, 2012): 149–58. http://dx.doi.org/10.17221/5608-vetmed.

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Routine access to the bovine oviduct for in vivo culture accomplishes various demands on embryo production for scientific as well as commercial purposes. The experiments conducted in the present study focused on the efficiency of recovery methods after temporary in vivo culture of bovine embryos in oviducts of the homologous species using transvaginal endoscopy (Experiment I) and on the quality assessment of recovered blastocysts (Experiment II). In Experiment I in vitro matured oocytes were fertilized, cultured for 1 to 3 days and transferred unilaterally into the ipsilateral oviducts of 54 heifers by the means of transvaginal endoscopy. After 4 to 6 days of in vivo culture embryos were re-collected either by non-surgical flushing of uterine horns (U-group) or by combined flushing of the oviducts and uterine horns (OU-group). In total the recovery rate was 38.4% (780/2029). After flushing at day seven, 106 blastocysts (blastocyst rate: 13.6% ) were found. The additional 24 h of in vitro culture (day eight) resulted in 153 blastocysts (blastocyst rate: 19.6% ). The recovery rate in the OU-group was twice as efficient as in the U-group (390/1358 vs. 390/671, P < 0.01). The recovery rates among the different stages of transferred embryos did not differ significantly; likewise cross-effects among the stages and the recovery methods were non-significant. The recovery methods (P < 0.001) and the interaction between the recovery methods and the stages of transferred embryos (P < 0.01) had an influence on blastocyst yields on day seven (U-group 37/1358 vs. OU-group 69/671) and day eight (U-group 48/1358 vs. OU-group 105/671). In Experiment II embryo quality was assessed by the survival rate of blastocysts after freezing in ethylene glycol. Day seven embryos were produced in vitro (in vitro group D7) or by IVM/IVF followed by a combined culture procedure (2 to 3 days in vitro prior to 4 to 5 days in vivo) (in vivo group D7) or after superovulation and collection at day seven (superovulation group). Embryos from in vitro group D7 re-expanded only for 6 h after thawing, embryos from in vivo group D7 and superovulation group were alive for 24 h and 72 h of culture, respectively. Only embryos derived by superovulation showed hatching activity. Blastocysts from the in vitro group D7 and the in vivo group D7 that were held in culture medium for additional 24 h (day eight) showed an analogous post-thawing culture behaviour. In conclusion, the results of the present study demonstrated that some embryos transferred for in vivo culture remain in the oviduct even at day seven. Hence, combined flushing of oviducts and uterine horns after in vivo culture in the bovine oviduct is necessary for effective embryo re-collection. The quality of recovered embryos after temporary in vivo culture assessed by cryotolerance was in-between those produced in vitro or recovered after superovulation.
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22

Kobirumaki-Shimozawa, Fuyu, Kotaro Oyama, Seine A. Shintani, Erisa Hirokawa, Togo Shimozawa, Takako Terui, Shin'ich Ishiwata, and Norio Fukuda. "3SDA-04 Real-time high-resolution cardiac imaging in vivo(3SDA Biophysics toward In Vivo work,Symposium)." Seibutsu Butsuri 53, supplement1-2 (2013): S104. http://dx.doi.org/10.2142/biophys.53.s104_4.

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23

Zhelavskyi, M. A. "APROBATION OF PLATELET AGGREGATION INHIBITOR FROM ECHIS MULTISQUAMATIS SNAKE VENOM IN VITRO, IN VIVO AND EX VIVO." Biotechnologia Acta 16, no. 5 (October 31, 2023): 55–60. http://dx.doi.org/10.15407/biotech16.05.055.

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Snake venom-derived platelet aggregation inhibitors can be promising antiplatelet medications that can allow to avoid the risk of bleeding and treatment resistance, particularly in aspirin-resistant patients. Our study aimed to assess the effectiveness of a platelet aggregation inhibitor derived from Echis multisquamatis snake venom in various settings, including in vitro, in vivo, and ex vivo. Methods. We examined a polypeptide from Echis multisquamatis venom, purified using a recently developed chromatography protocol, across multiple models. This polypeptide was introduced into platelet-rich blood plasma and administered intravenously to rats. The effects on platelet aggregation were assessed using aggregometry, focusing on ADP-induced aggregation. Results & Discussion. Our findings revealed that a concentration of 0.040 mg/ml significantly reduced platelet aggregation in vitro. Remarkably, this dosage also proved effective when administered intravenously in laboratory animals, reaffirming its potential as a robust antiplatelet agent. In the final phase of our study, the polypeptide demonstrated its ability to inhibit platelet aggregation in blood plasma of pregnant woman with aspirin resistance, presenting a promising avenue for innovative treatment approaches in such cases. Conclusion. This study underscores the potential of the Echis multisquamatis venom-derived polypeptide as a promising antiplatelet agent, effective in diverse scenarios, including aspirin resistance. Further research and clinical trials are imperative to fully harness its therapeutic potential.
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Kerr, Andrew S., Julio Osende, John T. Fallon, and Juan Badimon. "Aortic Slimgraft: Ex vivo and in vivo study." Journal of Vascular Surgery 34, no. 2 (August 2001): 350–52. http://dx.doi.org/10.1067/mva.2001.115814.

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25

Esteban-Martínez, Lorena, and Patricia Boya. "Autophagic flux determination in vivo and ex vivo." Methods 75 (March 2015): 79–86. http://dx.doi.org/10.1016/j.ymeth.2015.01.008.

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HASHIMOTO, Hitoshi, and Norihito SHINTANI. "In vivo functional analysis of the neuropeptide PACAP using gene-targeted mice." Folia Pharmacologica Japonica 122, no. 5 (2003): 427–35. http://dx.doi.org/10.1254/fpj.122.427.

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Bochkarev, A. A., A. A. Stekolnikov, M. A. Nausbaeva, E. A. Lakovnikov, and A. O. Blusma. "Cytochemical verification of induced osteoblasts in vivo." "Veterinary Medicine" Journal 22, no. 09 (September 2019): 42–46. http://dx.doi.org/10.30896/0042-4846.2019.22.9.42-46.

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Bagryantseva, O. V., I. V. Gmoshinskii, A. D. Evstratova, E. N. Trushina, O. K. Mustafina, Kh S. Soto, V. A. Shipelin, A. A. Shumakova, A. D. Panova, and S. A. Khotimchenko. "TOXICITY OF YESSOTOXIN IN EXPERIMENT IN VIVO." Health Risk Analysis, no. 3 (September 2018): 112–19. http://dx.doi.org/10.21668/health.risk/2018.3.12.

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29

Berdichevsky, Berdichevsky V. B., Berdichevsky B. A. Berdichevsky, Sapozhenkova E. V. Sapozhenkova, Pavlova I. V. Pavlova, Gonyaev A. A. Gonyaev, Boldyrev A. L. Boldyrev, Korabelnikov M. A. Korabelnikov, Petrov D. I. Petrov, and Spirina D. S. Spirina. "Clinical evaluation of uropathogen selection in vivo." Nephrology 1_2023 (March 3, 2023): 65–69. http://dx.doi.org/10.18565/nephrology.2023.1.65-69.

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Rorbach-Dolata, Anna, Ewa Żurawska-Płaksej, Zofia Marchewka, and Agnieszka Piwowar. "In vivo and ex vivo impact of nutritional xenobiotics – acrylamide and sodium nitrates – on plasma antioxidant properties." Annales Academiae Medicae Silesiensis 73 (August 13, 2019): 154–62. http://dx.doi.org/10.18794/aams/108959.

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YOSHIMURA, Megumu, Hidemasa FURUE, Go KATO, Atsushi DOI, Masaharu MIZUNO, and Toshihiko KATAFUCHI. "Application of in vivo patch-clamp technique to pharmacological analysis of synaptic transmission in the CNS." Folia Pharmacologica Japonica 124, no. 2 (2004): 111–18. http://dx.doi.org/10.1254/fpj.124.111.

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32

Wang, Lei-Lei, and Chun-Li Zhang. "Reply to In vivo confusion over in vivo conversion." Molecular Therapy 30, no. 3 (March 2022): 986–87. http://dx.doi.org/10.1016/j.ymthe.2022.01.027.

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Yamamoto, Ryo, Adam C. Wilkinson, and Hiromitsu Nakauchi. "In vivo and ex vivo haematopoietic stem cell expansion." Current Opinion in Hematology 27, no. 4 (May 20, 2020): 273–78. http://dx.doi.org/10.1097/moh.0000000000000593.

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34

Opitz, Alexander, Arnaud Falchier, Gary S. Linn, Michael P. Milham, and Charles E. Schroeder. "Limitations of ex vivo measurements for in vivo neuroscience." Proceedings of the National Academy of Sciences 114, no. 20 (May 1, 2017): 5243–46. http://dx.doi.org/10.1073/pnas.1617024114.

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A long history of postmortem studies has provided significant insight into human brain structure and organization. Cadavers have also proven instrumental for the measurement of artifacts and nonneural effects in functional imaging, and more recently, the study of biophysical properties critical to brain stimulation. However, death produces significant changes in the biophysical properties of brain tissues, making an ex vivo to in vivo comparison complex, and even questionable. This study directly compares biophysical properties of electric fields arising from transcranial electric stimulation (TES) in a nonhuman primate brain pre- and postmortem. We show that pre- vs. postmortem, TES-induced intracranial electric fields differ significantly in both strength and frequency response dynamics, even while controlling for confounding factors such as body temperature. Our results clearly indicate that ex vivo cadaver and in vivo measurements are not easily equitable. In vivo examinations remain essential to establishing an adequate understanding of even basic biophysical phenomena in vivo.
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35

Gorog, D. A., S. Saraf, and V. Markides. "Coronary thrombosis: In vivo, ex vivo and in vitro." Case Reports 2009, apr07 2 (April 14, 2009): bcr0920080983. http://dx.doi.org/10.1136/bcr.09.2008.0983.

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36

Stockinger, Pia, Andreas Berlin, Daniel Kampik, Christine Schmitt, Jost Hillenkamp, Jeffrey D. Messinger, Martina C. Herwig-Carl, and Thomas Ach. "Vergleichende In-vivo‑/Ex-vivo-Bildgebung des hinteren Augenabschnitts." Der Ophthalmologe 117, no. 12 (September 23, 2020): 1188–95. http://dx.doi.org/10.1007/s00347-020-01228-w.

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37

Moore, Malcolm A. S. "Stem cell proliferation: Ex vivo and in vivo observations." Stem Cells 15, S2 (April 1997): 239–51. http://dx.doi.org/10.1002/stem.5530150832.

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Fésűs, Luca. "Innovative in vivo imaging techniques in dermatology." Bőrgyógyászati és Venerológiai Szemle 98, no. 3 (July 12, 2022): 133–41. http://dx.doi.org/10.7188/bvsz.2022.98.3.5.

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As a result of advances in the development of medical imaging, the toolbox of dermatological imaging in the XXI. century expanded considerably. In addition to the histological examination that is currently the gold standard in diagnostics, a number of noninvasive imaging methods have emerged in recent decades that have become part of the clinical and preclinical practice. The characteristics of many dermatological diseases have been described in vivo studies with commercially available devices. The authors summarize the principles of terahertz imaging, photoacoustic imaging, reflectance and autofluorescence imaging, near-infrared spectroscopy, and nonlinear microscopy, as well as the in vivo dermatological results and clinical applications of these modalities.
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Kang, Dae-Gyu, and Kwang-Man Lee. "In-vivo Dose verification using MOSFET dosimeter." Journal of Sensor Science and Technology 15, no. 2 (March 31, 2006): 102–5. http://dx.doi.org/10.5369/jsst.2006.15.2.102.

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Monastyrska, Ewelina, and Oliwia Beck. "Psychological and legal aspects of ex vivo transplantation." Medycyna Ogólna i Nauki o Zdrowiu 20, no. 2 (July 8, 2014): 145–48. http://dx.doi.org/10.5604/20834543.1112228.

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ŞAHAN, M. Heval, Engin ARAS, Mine DÜNDAR ÇÖMLEKOĞLU, and Celal ARTUNÇ. "In Vivo Evaluation of Motility on Ocular Prosthesis." Turkiye Klinikleri Journal of Dental Sciences 21, no. 3 (2015): 196–206. http://dx.doi.org/10.5336/dentalsci.2015-43726.

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Saakyan, S. V., А. Yu Tsygankov, N. I. Moiseeva, and А. F. Karamysheva. "Assessment of uveal melanoma cells chemosensitivity ex vivo." Cell Technologies in Biology and Medicine, no. 3 (2020): 185–90. http://dx.doi.org/10.47056/1814-3490-2020-3-185-190.

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TÜTÜNCÜ, Sena, Hülya TEZEL, Aylin BALCI ÖZYURT, Anıl YİRÜN, Terken BAYDAR, and Pınar ERKEKOĞLU. "Alzheimer's Disease In Vivo Models: A Traditional Review." Journal of Literature Pharmacy Sciences 12, no. 1 (2023): 8–19. http://dx.doi.org/10.5336/pharmsci.2022-90431.

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44

Legonkova, O. A., A. V. Chupin, A. S. Ogannisian, A. V. Nikitina, V. V. Stafford, I. P. Savchenkova, A. B. Varava, S. V. Sapelkin, and S. V. Pozyabin. "In Vivo research of liquid embolic compound." Bulletin of Experimental Biology and Medicine 170, no. 9 (2020): 357–60. http://dx.doi.org/10.47056/0365-9615-2020-170-9-357-360.

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45

KIKUCHI, Jun, and Kenji AKAMINE. "In vivo NMR." Journal of the Spectroscopical Society of Japan 55, no. 5 (2006): 320–30. http://dx.doi.org/10.5111/bunkou.55.320.

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46

Aldabó Pallás, T. "Donante vivo: legislación." Cuadernos de Medicina Forense 21, no. 1-2 (June 2015): 24–33. http://dx.doi.org/10.4321/s1135-76062015000100004.

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47

Oliveira, Fabrício Marques de. "O enterrado vivo." Revista Literária do Corpo Discente da Universidade Federal de Minas Gerais 30, no. 26 (January 31, 1996): 71. http://dx.doi.org/10.17851/0103-5878.30.26.71-74.

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48

Schavelev, Sergei P. "Science in vivo." Epistemology & Philosophy of Science 55, no. 1 (2018): 236–41. http://dx.doi.org/10.5840/eps201855119.

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49

Pereira, Cláudia Sousa. "Literatura Ao Vivo." Cultura, no. 38 (December 31, 2019): 39–57. http://dx.doi.org/10.4000/cultura.5471.

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50

Magloire, Nadine, and Beth Lellis. "Autopsy in Vivo." Callaloo 15, no. 2 (1992): 481. http://dx.doi.org/10.2307/2931261.

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