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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2009-11-26
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pubmed:abstractText |
Despite many published studies on ERbeta, progress towards understanding its role in breast cancer remains slow. This is largely due to discordant data between mRNA and protein studies as well as failure to take into account the biologically distinct ERbeta isoforms and their heterogeneous expression profile.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1875-8606
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
467-73
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pubmed:meshHeading |
pubmed-meshheading:19940362-Breast Neoplasms,
pubmed-meshheading:19940362-Epithelial Cells,
pubmed-meshheading:19940362-Estrogen Receptor beta,
pubmed-meshheading:19940362-Female,
pubmed-meshheading:19940362-Fibroblasts,
pubmed-meshheading:19940362-Gene Expression Profiling,
pubmed-meshheading:19940362-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:19940362-Humans,
pubmed-meshheading:19940362-Lasers,
pubmed-meshheading:19940362-Microdissection,
pubmed-meshheading:19940362-Protein Isoforms,
pubmed-meshheading:19940362-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:19940362-Stromal Cells
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pubmed:year |
2009
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pubmed:articleTitle |
Gene expression of ERbeta isoforms in laser microdissected human breast cancers: implications for gene expression analyses.
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pubmed:affiliation |
Leeds Institute of Molecular Medicine, St. James's University Hospital, Leeds, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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