In the in-house database 178 test chemicals had oral [LD.sub.50] values (10) that were collected from publicly available databases (e.g., ChemIDplus, IUCLID, RTECS, and HSDB
), Merck index, EU Risk Assessment Reports, Sax's Dangerous Properties of Industrial Materials, and the published literature.
For quality control, each sample was run as a standard curve for TTC3, RPL17, and HSDB
(endogenous control) with 3.75, 7.5, and 15 ng of purified WGA.
(Horse single nucleotide polymorphism and expression database (HSDB
) provides the unexplored genomic variants which still remain to be identified in the horse genome including rare variants by using horse population genome sequencing.
(10) See CATASTROPHE STUDY, supra note 1, at 58-59; HSDB
, supra note 6; see also COLEMAN, supra note 7, at 17-18 (noting the concentration that the German used against the Allies at Ypres was near 1000 ppm.).
Toxnet platform [the Chemical Carcinogenesis Research Information System (CCRIS) (NIH and TOXNETa), DART, Toxicology Literature Online (TOXLINE) (NIH and TOXNETd), and Hazardous Substances Data Bank (HSDB
) (NIH and TOXNETc) databases, which are collections of publicly available information] and the Registry of Toxic Effects of Chemical Substances (RTECS) database (Biovia).
(5.9) TOXNET/HSDB, MEDLINE, NIH sponsors and maintains several PubMed, other databases databases for toxicology and (NIH); via http://www.nih.gov; environmental health applications, for example, TOXNET/HSDB; including TOXNET and the Hazardous http://toxnet.nlm.nih.gov/ Substances Data Bank (HSDB
.htm Haz-Map (occupational health database), PubMed, and MEDLINE, with links to biomedical journals.
A cluster of databases on toxicology, chemicals and related substances produced or made available by the National Library of Medicine: HSDB[R] (Hazardous Substances Databank), IRIS (Integrated Risk Information System), CCRIS (Chemical Carcinogenesis Research Information System), GENE-TOX, TOXLINE[R], DART/ETIC (Developmental and Reproductive Toxicology/Environmental Teratology Information Center), TRI (Toxic Release Inventory), ChemIDplus (Chemical IDentification file), HSDB
Structures, and NCI-3D.
2012; NLM 2016); 2,4-dichlorophenol is used in the production of certain pesticides; and 2,5-dichlorophenol is a major metabolite of 1,4-dichlorobenzene, which is used in moth balls and room deodorizers (Crinnion 2010; HSDB
databases: IRIS (Integrated Risk Information System), RTECS (Registry of Toxic Effects of Chemical Substances) and the HSDB
(Hazardous Substances Data Bank).
EPA 2005a, 2005b), and toxicological databases [CCRIS (Household Products Database; http://hpd.nlm.nih.gov/), HSDB
(Hazardous Substances Data Bank; http://toxnet.nlm.nih.
2,5-Dichlorophenol (2,5-DCP) is a major metabolite of 1,4-dichlorobenzene (1,4-D), which has been used as a chemical intermediate for the manufacture of dyes and pharmaceutical and agricultural products, as a moth repellent, and as a space deodorant for industrial and indoor home applications [Hazardous Substances Data Bank (HSDB
) 2014; International Programme on Chemical Safety (IPCS) 1989].