Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-12-7
pubmed:abstractText
Oral malodorous compounds including hydrogen sulfide (H2S) are causative agents of periodontitis because the toxicities are similar to that of cyanate. Previous studies demonstrated that volatile sulfur compounds (VSCs) were highly toxic to periodontal tissues, causing a large reduction in the amount of collagen in human gingival fibroblasts and extracellular matrix as well as, for example, apoptosis, immunologic responses, and matrix metalloproteinase production. The objective of this study was to determine the effect of H2S on the proliferation of osteoblasts and a signaling transduction pathway through the mitogen-activated protein kinase (MAPK).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
D
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Alkaline Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Butadienes, http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen Sulfide, http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 1, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Nitriles, http://linkedlifedata.com/resource/pubmed/chemical/Pyridines, http://linkedlifedata.com/resource/pubmed/chemical/SB 203580, http://linkedlifedata.com/resource/pubmed/chemical/U 0126, http://linkedlifedata.com/resource/pubmed/chemical/p38 Mitogen-Activated Protein...
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1943-3670
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2028-34
pubmed:meshHeading
pubmed-meshheading:19961386-3T3 Cells, pubmed-meshheading:19961386-Alkaline Phosphatase, pubmed-meshheading:19961386-Animals, pubmed-meshheading:19961386-Butadienes, pubmed-meshheading:19961386-Cell Differentiation, pubmed-meshheading:19961386-Cell Proliferation, pubmed-meshheading:19961386-Cells, Cultured, pubmed-meshheading:19961386-DNA, pubmed-meshheading:19961386-Dose-Response Relationship, Drug, pubmed-meshheading:19961386-Enzyme Inhibitors, pubmed-meshheading:19961386-Halitosis, pubmed-meshheading:19961386-Humans, pubmed-meshheading:19961386-Hydrogen Sulfide, pubmed-meshheading:19961386-Imidazoles, pubmed-meshheading:19961386-MAP Kinase Signaling System, pubmed-meshheading:19961386-Mice, pubmed-meshheading:19961386-Mitogen-Activated Protein Kinase 1, pubmed-meshheading:19961386-Mitogen-Activated Protein Kinase 3, pubmed-meshheading:19961386-Mitogen-Activated Protein Kinases, pubmed-meshheading:19961386-Nitriles, pubmed-meshheading:19961386-Osteoblasts, pubmed-meshheading:19961386-Phosphorylation, pubmed-meshheading:19961386-Pyridines, pubmed-meshheading:19961386-p38 Mitogen-Activated Protein Kinases
pubmed:year
2009
pubmed:articleTitle
Oral malodorous compound inhibits osteoblast proliferation.
pubmed:affiliation
Department of Oral Health, School of Life Dentistry at Tokyo, Nippon Dental University, Tokyo, Japan. imai-109@tky.ndu.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't