Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2000-10-5
pubmed:abstractText
The growth of both cancer cells and fetal tissue is rapid; however, cancer cells de-differentiate and proliferate in a disorderly manner, whereas fetal tissues differentiate and proliferate in an orderly manner. Thus, there may be both common and different factors that are involved in the process of the uncontrolled cell growth of pancreatic cancers and the development of the fetal pancreas. The common part of the mechanisms should be in the regulation of the cell cycle, resulting in rapid proliferation via such mechanisms as growth stimulation and avoidance of apoptosis. Therefore, in the current study we investigated the expression of apoptosis-related proteins in fetal pancreatic tissues.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/BAX protein, human, http://linkedlifedata.com/resource/pubmed/chemical/BCL2L1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Glucagon, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proliferating Cell Nuclear Antigen, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/bcl-2-Associated X Protein, http://linkedlifedata.com/resource/pubmed/chemical/bcl-X Protein, http://linkedlifedata.com/resource/pubmed/chemical/myeloid cell leukemia sequence 1...
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0169-4197
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
113-22
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:10862510-Apoptosis, pubmed-meshheading:10862510-Embryonic and Fetal Development, pubmed-meshheading:10862510-Fetus, pubmed-meshheading:10862510-Glucagon, pubmed-meshheading:10862510-Humans, pubmed-meshheading:10862510-Immunohistochemistry, pubmed-meshheading:10862510-In Situ Nick-End Labeling, pubmed-meshheading:10862510-Insulin, pubmed-meshheading:10862510-Neoplasm Proteins, pubmed-meshheading:10862510-Pancreas, pubmed-meshheading:10862510-Proliferating Cell Nuclear Antigen, pubmed-meshheading:10862510-Proteins, pubmed-meshheading:10862510-Proto-Oncogene Proteins, pubmed-meshheading:10862510-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:10862510-Staining and Labeling, pubmed-meshheading:10862510-bcl-2-Associated X Protein, pubmed-meshheading:10862510-bcl-X Protein
pubmed:year
2000
pubmed:articleTitle
Immunohistochemical analysis of apoptosis-related proteins in human embryonic and fetal pancreatic tissues.
pubmed:affiliation
Department of Surgery and Surgical Basic Science, Kyoto University, Sakyo, Japan. khiro@kuhp.kyoto-u.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't