Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-3-1
pubmed:abstractText
Identification of extracellular matrix proteins (ECM) associated with tumor cell metastasis may generate targets for future therapy against pancreatic cancer metastases. We hypothesized that comparison of ECM-associated gene expression in primary and metastatic pancreatic tumors would identify ECM proteins associated with pancreatic metastasis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1072-7515
pubmed:author
pubmed:issnType
Print
pubmed:volume
200
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
371-7
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15737847-Adenocarcinoma, pubmed-meshheading:15737847-Animals, pubmed-meshheading:15737847-Antibodies, Neoplasm, pubmed-meshheading:15737847-Cluster Analysis, pubmed-meshheading:15737847-Cysteine-Rich Protein 61, pubmed-meshheading:15737847-Extracellular Matrix Proteins, pubmed-meshheading:15737847-Female, pubmed-meshheading:15737847-Gene Expression Regulation, Neoplastic, pubmed-meshheading:15737847-Humans, pubmed-meshheading:15737847-Immediate-Early Proteins, pubmed-meshheading:15737847-Immunohistochemistry, pubmed-meshheading:15737847-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:15737847-Mice, pubmed-meshheading:15737847-Mice, Nude, pubmed-meshheading:15737847-Neoplasm Transplantation, pubmed-meshheading:15737847-Pancreatic Neoplasms, pubmed-meshheading:15737847-Peritoneal Neoplasms, pubmed-meshheading:15737847-RNA, Messenger, pubmed-meshheading:15737847-RNA, Neoplasm, pubmed-meshheading:15737847-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15737847-Tumor Cells, Cultured
pubmed:year
2005
pubmed:articleTitle
Increased expression of Cyr61 (CCN1) identified in peritoneal metastases from human pancreatic cancer.
pubmed:affiliation
Division of Surgical Oncology, Department of Surgery, Hamon Center for Therapeutic Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390-8593, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't