Gotowa bibliografia na temat „Testing of teratogens”
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Artykuły w czasopismach na temat "Testing of teratogens"
Amacher, David E., Jeanne Stadler, Shelli J. Schomaker i Christian Verseil. "The Comparative Testing of Eight Coded Chemicals in the Rat Limb Bud Micromass and Rat Embryo Culture Systems". Alternatives to Laboratory Animals 24, nr 6 (grudzień 1996): 945–52. http://dx.doi.org/10.1177/026119299602400609.
Pełny tekst źródłaPiersma, Aldert H., Rudolf Bechter, Nathalie Krafft, Beat P. Schmid, Jeanne Stadler, Aart Verhoef, Christian Verseil i Jacob Zijlstra. "An Interlaboratory Evaluation of Five Pairs of Teratogens and Non-teratogens in Post-implantation Rat Embryo Culture". Alternatives to Laboratory Animals 24, nr 2 (marzec 1996): 201–9. http://dx.doi.org/10.1177/026119299602400211.
Pełny tekst źródłaUretsky, Michael E., i Ralf G. Rahwan. "Problems of Conditioning Xenopus Laevis Tadpoles with Standard Avoidance-Response Learning Paradigms". Psychological Reports 79, nr 3 (grudzień 1996): 763–73. http://dx.doi.org/10.2466/pr0.1996.79.3.763.
Pełny tekst źródłaBell, Susan Givens. "Drug Screening in Neonates". Neonatal Network 35, nr 5 (2016): 321–26. http://dx.doi.org/10.1891/0730-0832.35.5.321.
Pełny tekst źródłaBrent, Robert L. "Utilization of Animal Studies to Determine the Effects and Human Risks of Environmental Toxicants (Drugs, Chemicals, and Physical Agents)". Pediatrics 113, Supplement_3 (1.04.2004): 984–95. http://dx.doi.org/10.1542/peds.113.s3.984.
Pełny tekst źródłaLauschke, Karin, Andreas Frederik Treschow, Mikkel Aabech Rasmussen, Nichlas Davidsen, Bjørn Holst, Jenny Emnéus, Camilla Taxvig i Anne Marie Vinggaard. "Creating a human-induced pluripotent stem cell-based NKX2.5 reporter gene assay for developmental toxicity testing". Archives of Toxicology 95, nr 5 (4.03.2021): 1659–70. http://dx.doi.org/10.1007/s00204-021-03018-y.
Pełny tekst źródłaSennsfelder, Laëtitia, Susie Guilly, Sébastien Leruste, Ludovic Hoareau, Willy Léocadie, Pauline Beuvain, Meïssa Nekaa i in. "Description of Copy Number Variations in a Series of Children and Adolescents with FASD in Reunion Island". Children 10, nr 4 (7.04.2023): 694. http://dx.doi.org/10.3390/children10040694.
Pełny tekst źródłaTing, Keh-Chuh, Modan Gill i Orlando Garbin. "GC/MS Screening Method for Phthalate Esters in Children's Toys". Journal of AOAC INTERNATIONAL 92, nr 3 (1.05.2009): 951–58. http://dx.doi.org/10.1093/jaoac/92.3.951.
Pełny tekst źródłaSethi, Nikunj, Rohit Mahar, Sanjeev K. Shukla, Akhilesh Kumar i Neeraj Sinha. "A novel approach for testing the teratogenic potential of chemicals on the platform of metabolomics: studies employing HR-MAS nuclear magnetic resonance spectroscopy". RSC Advances 5, nr 33 (2015): 26027–39. http://dx.doi.org/10.1039/c5ra00671f.
Pełny tekst źródłaSethi, Nikunj, Rohit Mahar, Sanjeev K. Shukla, Akhilesh Kumar i Neeraj Sinha. "Correction: A novel approach for testing the teratogenic potential of chemicals on the platform of metabolomics: studies employing HR-MAS nuclear magnetic resonance spectroscopy". RSC Advances 5, nr 66 (2015): 53341. http://dx.doi.org/10.1039/c5ra90058a.
Pełny tekst źródłaRozprawy doktorskie na temat "Testing of teratogens"
Carro, Tiffany. "Development and evaluation of a viable chicken egg assay to determine the metabolic fate of xenobiotic and other teratogenic compounds". Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 137 p, 2007. http://proquest.umi.com/pqdweb?did=1372020111&sid=5&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Pełny tekst źródłaPerez, Castiglioni Monica Patricia. "Le statut juridique des cellules souches : de la greffe d’organes à la thérapie cellulaire". Electronic Thesis or Diss., Paris 8, 2021. http://www.theses.fr/2021PA080048.
Pełny tekst źródłaStem cells as cellular products for therapeutic purposes (PCT) or as advanced therapy drugs (ITNs) within the framework of regenerative medicine have revolutionized the medicine of the 21st century. Faced with recent discoveries of new stem cells created by researchers (parthenotes, cloned stem cells, iPS cells), other possibilities for regenerative therapy are emerging over time.The law, which has always accompanied the scientific and technical development of cell therapy since the 17th century, must be more present than ever to protect human beings who lend themselves to new treatments or to experimentation. The historical development of this therapeutic revolution allows us to show the importance of legal and ethical reflection for scientific progress.Old questions, such as the status of the prenatal being and the authorization for cryopreservation of autologous tissues or cells, are re-emerging in the face of the presence of supernumerary human embryonic stem cells and the success of regenerative therapy. Teratogenic treatments and episodes of child abuse during pregnancy have destroyed or damaged thousands of unborn children. Recognition of prenatal life is offered in certain circumstances to protect the embryo and fetus before birth
Pavlíková, Zuzana. "Testování embryotoxicity vybraných lidských teratogenů na zárodcích kuřete". Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-312523.
Pełny tekst źródłaKsiążki na temat "Testing of teratogens"
Southeast, Asian Workshop on Short-term Assays for Detecting Environmental Mutagens Carcinogens and Teratogens (2nd 1989 Bangkok and Chiang Mai Thailand). Environmental mutagens, carcinogens, and teratogens: Principles and short-term assays : proceedings of the Second Southeast Asian Workshop on Short-term Assays for Detecting Environmental Mutagens, Carcinogens, and Teratogens, held in Bangkok and Chiang Mai, Thailand, February 6-17, 1989. Chiang Mai, Thailand: Star Press, 1991.
Znajdź pełny tekst źródłaNational Research Council (U.S.). Subcommittee on Reproductive and Developmental Toxicology. Evaluating chemical and other agent exposures for reproductive and developmental toxicity. Washington, D.C: National Academy Press, 2001.
Znajdź pełny tekst źródłaJoint American-Swiss Seminar on Alternative Embryotoxicity and Teratogenicity Tests (1984 Zurich, Switzerland). In vitro embryotoxicity and teratogenicity tests: Joint American-Swiss Seminar on Alternative Embryotoxicity and Teratogenicity Tests, Zürich, November 12, 1984. Redaktorzy Homburger Freddy i Goldberg Alan M. Basel, Switzerland: New York, 1985.
Znajdź pełny tekst źródłaBrusick, David. Principles of genetic toxicology. Wyd. 2. New York: Plenum Press, 1987.
Znajdź pełny tekst źródłaPersaud, T. V. N. Teratological Testing. Springer, 2012.
Znajdź pełny tekst źródłaTeratogenicity Testing Methods in Molecular Biology Hardcover. Humana Press, 2012.
Znajdź pełny tekst źródłaEnvironmental mutagens, carcinogens, and teratogens: Principles and short-term assays : Proceedings of the Second Southeast Asian Workshop on Short-term ... Chiang Mai, Thailand, February 6-17, 1989. Star Press, 1991.
Znajdź pełny tekst źródłaMohl, Virginia Kathleen. Genetic differences in the murine heat shock response: Implications in testing for teratogen susceptibility. 1988.
Znajdź pełny tekst źródłaMathiesen, Amber, i Kali Roy. Foundations of Perinatal Genetic Counseling. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190681098.001.0001.
Pełny tekst źródła(US), National Research Council, Board on Environmental Studies and Toxicology, Committee on Toxicology i Subcommittee on Reproductive and Developmental Toxicity. Evaluating Chemical and Other Agent Exposures For Reproductive and Developmental Toxicity. National Academies Press, 2001.
Znajdź pełny tekst źródłaCzęści książek na temat "Testing of teratogens"
Abel, Ernest L. "Testing Animal Behavioral Teratogens". W Behavioral Teratogenesis and Behavioral Mutagenesis, 195–226. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0735-8_7.
Pełny tekst źródłaAlves-Pimenta, Sofia, Bruno Colaço, Paula A. Oliveira i Carlos Venâncio. "Biological Concerns on the Selection of Animal Models for Teratogenic Testing". W Methods in Molecular Biology, 61–93. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7883-0_3.
Pełny tekst źródłaAlves-Pimenta, Sofia, Bruno Colaço, Paula A. Oliveira i Carlos Venâncio. "Development Features on the Selection of Animal Models for Teratogenic Testing". W Methods in Molecular Biology, 67–104. New York, NY: Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3625-1_3.
Pełny tekst źródłaSteele, Christopher E., i Graham P. Copping. "Teratogen testing". W Postiplantation Mammalian Embryos, 221–34. Oxford University PressOxford, 1990. http://dx.doi.org/10.1093/oso/9780199630882.003.0012.
Pełny tekst źródłaClark, Robin D., i Cynthia J. Curry. "Intrauterine Growth Restriction". W Genetic Consultations in the Newborn, redaktorzy Robin D. Clark i Cynthia J. Curry, 11–16. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199990993.003.0002.
Pełny tekst źródłaClark, Robin D., i Cynthia J. Curry. "Craniosynostoses". W Genetic Consultations in the Newborn, redaktorzy Robin D. Clark i Cynthia J. Curry, 91–100. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199990993.003.0013.
Pełny tekst źródła"Induction of Low-Molecular-Weight Heat-Shock Proteins in Drosophila and Human Embryonic Lineage Cells After Teratogen Exposure". W Advances In Animal Alternatives For Safety And Efficacy Testing, 131–44. CRC Press, 1997. http://dx.doi.org/10.1201/9781439805817-20.
Pełny tekst źródłaAbbott, Barbara D. "Experimental Models for the Study of Oral Clefts". W Cleft Lip And Palate, 193–202. Oxford University PressNew York, NY, 2002. http://dx.doi.org/10.1093/oso/9780195139068.003.0015.
Pełny tekst źródła"Cancer Institute (NCI), the National Institute for Environmental Health Sciences (NIEHS), the National Center for Toxicological Research (NCTR) and the National Institute for Occupational Safety and Health (NIOSH). Within the NTP Carcinogenesis Testing Program, a cancer bioassay is a two-sex, two-species, lifetime study of experimental animals, usually rats and mice; beginning at weaning, ending 104 weeks after initiation, and using multiple dose levels of the chemical being tested. This bioassay used to determine if a chemical causes cancer, and if it produces damaging effects on certain organ systems: liver, lung, kidney, endocrine systems, etc. The study of a single compound expensive, costing about five hundred thousand dollars, and takes up to five years to complete. The National Toxicology Program publishes a technical report upon completion of a bioassay and review of the results by an indepen-dent Board of Scientific Counselors. Reproductive and Developmental Toxicology Program The National Toxicology Program has a program to assess the effects of chemicals on reproductive function and development. Structural teratology testing (the testing of chemicals to determine if they produce malformations) was begun in FY79. Eight to ten chemicals are tested for teratogenic effects annually. Fetuses are examined at two different levels: gross, readily apparent malformations are noted; and 2) histopathological examinations are conducted to pinpoint less readily apparent, microscopic malformations. Selected priority chemicals are also screened to determine potential reproductive hazard through germ-cell mutations. C. Genetic Toxicology Program The Genetic Toxicology Program tests chemicals for mutagenici-ty, validates existing test systems and develops new short-term test methods. The mutagenicity testing program divided into three phases. Phase I involves Salmonella mutagenicity assays and mammalian cell cultures. Phase II includes Drosophila systems. Phase III utilizes in vivo mammalian assays. All chemicals selected for general toxicology and lifetime bioassays are tested first using the Salmonella mutagenesis". W Dangerous Properties of Industrial and Consumer Chemicals, 16. CRC Press, 1994. http://dx.doi.org/10.1201/9781482293500-9.
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