We are analyzing https://link.springer.com/article/10.1186/bcr563.

Title:
Erratum to: Functional and molecular characterisation of mammary side population cells | Breast Cancer Research
Description:
It has been brought to our attention that there was an inaccuracy in the above article [1]. In the discussion section the authors state that "One of the assumptions underlying mammary transplant studies is that mammary outgrowths at limiting dilution are clonal (14,000–20,000 cells per cleared fat pad)" and they attribute this to reference 21 "Smith GH: Experimental mammary epithelial morphogenesis in an in vivo model: evidence for distinct cellular progenitors of the ductal and lobular phenotype. Breast Cancer Res Treat 1996, 39:21–31" [2]. In the paper by Smith no claim of clonality is made, rather it is stated that it is not known whether the simultaneous development of both lobular and ductal phenotypes indicates cooperative interaction between the two epithelial progenitors or signals the presence of a third progenitor type capable of producing both ductular and lobular committed daughters. It is, therefore, incorrect that the assumption of clonality based on limiting dilution has been attributed to Gilbert Smith.
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Keywords {🔍}

cancer, article, research, breast, mammary, privacy, cookies, molecular, cells, information, publish, search, download, alvi, clayton, joshi, smalley, smith, lobular, res, cell, institute, content, data, journal, erratum, functional, characterisation, side, population, published, december, enver, ashworth, vivanco, dale, matthew, section, epithelial, progenitors, ductal, discover, london, function, optional, personal, parties, policy, find, track,

Topics {✒️}

progenitor type capable breast cancer res cell privacy choices/manage cookies cancer research authors state article number e1 article alvi netherlands cancer institute european economic area cleared fat pad related subjects conditions privacy policy distinct cellular progenitors clonal accepting optional cookies lobular committed daughters mammary outgrowths journal finder publish tariq enver chirag joshi alan ashworth & maria uk azra original article 000 cells smith gh epithelial progenitors 1186/bcr547 rights article cite privacy policy personal data books a discussion section erratum smalley mj optional cookies manage preferences alvi vivanco section uk trevor data protection essential cookies cookies skip alan ashworth gilbert smith netherlands matthew journal publish article [1] usage analysis social media

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Erratum to: Functional and molecular characterisation of mammary side population cells
         description:It has been brought to our attention that there was an inaccuracy in the above article [1]. In the discussion section the authors state that "One of the assumptions underlying mammary transplant studies is that mammary outgrowths at limiting dilution are clonal (14,000–20,000 cells per cleared fat pad)" and they attribute this to reference 21 "Smith GH: Experimental mammary epithelial morphogenesis in an in vivo model: evidence for distinct cellular progenitors of the ductal and lobular phenotype. Breast Cancer Res Treat 1996, 39:21–31" [2]. In the paper by Smith no claim of clonality is made, rather it is stated that it is not known whether the simultaneous development of both lobular and ductal phenotypes indicates cooperative interaction between the two epithelial progenitors or signals the presence of a third progenitor type capable of producing both ductular and lobular committed daughters. It is, therefore, incorrect that the assumption of clonality based on limiting dilution has been attributed to Gilbert Smith.
         datePublished:2002-12-04T00:00:00Z
         dateModified:2002-12-04T00:00:00Z
         pageStart:1
         pageEnd:1
         sameAs:https://doi.org/10.1186/bcr563
         keywords:
            Cancer Research
            Oncology
            Surgical Oncology
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            name:BioMed Central
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                     name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
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                        name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Helen Clayton
               affiliation:
                     name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
                     address:
                        name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
                        type:PostalAddress
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                        type:PostalAddress
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                     address:
                        name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
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               affiliation:
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                        type:PostalAddress
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                     address:
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                        type:PostalAddress
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               affiliation:
                     name:Section of Cell and Molecular Biology, Institute of Cancer Research
                     address:
                        name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
                        type:PostalAddress
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                        name:Current address: Division of Molecular Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands
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ScholarlyArticle:
      headline:Erratum to: Functional and molecular characterisation of mammary side population cells
      description:It has been brought to our attention that there was an inaccuracy in the above article [1]. In the discussion section the authors state that "One of the assumptions underlying mammary transplant studies is that mammary outgrowths at limiting dilution are clonal (14,000–20,000 cells per cleared fat pad)" and they attribute this to reference 21 "Smith GH: Experimental mammary epithelial morphogenesis in an in vivo model: evidence for distinct cellular progenitors of the ductal and lobular phenotype. Breast Cancer Res Treat 1996, 39:21–31" [2]. In the paper by Smith no claim of clonality is made, rather it is stated that it is not known whether the simultaneous development of both lobular and ductal phenotypes indicates cooperative interaction between the two epithelial progenitors or signals the presence of a third progenitor type capable of producing both ductular and lobular committed daughters. It is, therefore, incorrect that the assumption of clonality based on limiting dilution has been attributed to Gilbert Smith.
      datePublished:2002-12-04T00:00:00Z
      dateModified:2002-12-04T00:00:00Z
      pageStart:1
      pageEnd:1
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         Cancer Research
         Oncology
         Surgical Oncology
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         issn:
            1465-542X
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         type:
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                     type:PostalAddress
                  type:Organization
            type:Person
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            affiliation:
                  name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
                  address:
                     name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
                     type:PostalAddress
                  type:Organization
            type:Person
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            affiliation:
                  name:Section of Gene Function and Regulation, Institute of Cancer Research
                  address:
                     name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
                     type:PostalAddress
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                     name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
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                  address:
                     name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
                     type:PostalAddress
                  type:Organization
            type:Person
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            affiliation:
                  name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
                  address:
                     name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
                     type:PostalAddress
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         name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
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      address:
         name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
         type:PostalAddress
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      address:
         name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
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            address:
               name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
               type:PostalAddress
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      name:Helen Clayton
      affiliation:
            name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
            address:
               name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Chirag Joshi
      affiliation:
            name:Section of Gene Function and Regulation, Institute of Cancer Research
            address:
               name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Tariq Enver
      affiliation:
            name:Section of Gene Function and Regulation, Institute of Cancer Research
            address:
               name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Alan Ashworth
      affiliation:
            name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
            address:
               name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Maria d M Vivanco
      affiliation:
            name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research
            address:
               name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Trevor C Dale
      affiliation:
            name:Section of Cell and Molecular Biology, Institute of Cancer Research
            address:
               name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
      name:Matthew J Smalley
      affiliation:
            name:Section of Cell and Molecular Biology, Institute of Cancer Research
            address:
               name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
               type:PostalAddress
            type:Organization
            name:Netherlands Cancer Institute
            address:
               name:Current address: Division of Molecular Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands
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PostalAddress:
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      name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
      name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
      name:Section of Gene Function and Regulation, Institute of Cancer Research, London, UK
      name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
      name:Breakthrough Toby Robins Breast Cancer Centre, Institute of Cancer Research, London, UK
      name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
      name:Section of Cell and Molecular Biology, Institute of Cancer Research, London, UK
      name:Current address: Division of Molecular Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands

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