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Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer

Detalles Bibliográficos
Autores principales: Gee, Julia MW, Giles, Martin G, Nicholson, Robert I
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468673/
https://www.ncbi.nlm.nih.gov/pubmed/15217488
http://dx.doi.org/10.1186/bcr904
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author Gee, Julia MW
Giles, Martin G
Nicholson, Robert I
author_facet Gee, Julia MW
Giles, Martin G
Nicholson, Robert I
author_sort Gee, Julia MW
collection PubMed
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language English
publishDate 2004
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spelling pubmed-4686732004-07-16 Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer Gee, Julia MW Giles, Martin G Nicholson, Robert I Breast Cancer Res Viewpoint BioMed Central 2004 2004-06-09 /pmc/articles/PMC468673/ /pubmed/15217488 http://dx.doi.org/10.1186/bcr904 Text en Copyright © 2004 BioMed Central Ltd
spellingShingle Viewpoint
Gee, Julia MW
Giles, Martin G
Nicholson, Robert I
Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title_full Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title_fullStr Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title_full_unstemmed Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title_short Extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
title_sort extreme growth factor signalling can promote oestrogen receptor-α loss: therapeutic implications in breast cancer
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468673/
https://www.ncbi.nlm.nih.gov/pubmed/15217488
http://dx.doi.org/10.1186/bcr904
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