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dc.contributor.authorHoward, B
dc.contributor.authorAshworth, A
dc.date.accessioned2018-06-11T11:45:27Z
dc.date.issued2006-08-01
dc.identifier.citationPLoS genetics, 2006, 2 (8), pp. e112 - ?
dc.identifier.issn1553-7390
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1815
dc.identifier.eissn1553-7404
dc.identifier.doi10.1371/journal.pgen.0020112
dc.description.abstractSpecification of mammary epithelial cell fate occurs during embryogenesis as cells aggregate to form the mammary anlage. Within the embryonic mammary bud, a population of epithelial cells exists that will subsequently proliferate to form a ductal tree filling the stromal compartment, and which can produce milk upon terminal differentiation after birth. Subsequently, these structures can be remodelled and returned to a basal state after weaning before regenerating in future pregnancies. The plasticity of the mammary epithelial cell, and its responsiveness to hormone receptors, facilitates this amazing biological feat, but aberrant signalling may also result in unintended consequences in the form of frequent malignancies. Reflecting this intimate connection, a considerable number of signalling pathways have been implicated in both mammary gland morphogenesis and carcinogenesis.
dc.formatPrint
dc.format.extente112 - ?
dc.languageeng
dc.language.isoeng
dc.publisherPUBLIC LIBRARY SCIENCE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectBreast
dc.subjectMammary Glands, Animal
dc.subjectEpithelial Cells
dc.subjectStem Cells
dc.subjectMesoderm
dc.subjectAnimals
dc.subjectHumans
dc.subjectMice
dc.subjectBreast Neoplasms
dc.subjectMammary Neoplasms, Animal
dc.subjectNeuregulins
dc.subjectIntracellular Signaling Peptides and Proteins
dc.subjectT-Box Domain Proteins
dc.subjectSignal Transduction
dc.subjectMorphogenesis
dc.subjectWnt Proteins
dc.subjectFibroblast Growth Factor 10
dc.subjectEctodysplasins
dc.titleSignalling pathways implicated in early mammary gland morphogenesis and breast cancer.
dc.typeJournal Article
rioxxterms.versionofrecord10.1371/journal.pgen.0020112
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2006-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfPLoS genetics
pubs.issue8
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Endocrine control mechanisms
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Gene Function
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Gene Function
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Endocrine control mechanisms
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Gene Function
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Gene Function
pubs.publication-statusPublished
pubs.volume2
pubs.embargo.termsNot known
icr.researchteamEndocrine control mechanisms
icr.researchteamGene Function
dc.contributor.icrauthorHoward, Beatrice


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