Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy

[1]  D. Medina,et al.  Re-evaluation of mammary stem cell biology based on in vivo transplantation , 2008, Breast Cancer Research.

[2]  C. Boulanger,et al.  Stem cells and the mammary microenvironment. , 2008, Breast disease.

[3]  M. Smalley,et al.  Mammary stem cells and breast cancer. , 2007, Cellular and molecular life sciences : CMLS.

[4]  Carlos Caldas,et al.  Molecular heterogeneity of breast carcinomas and the cancer stem cell hypothesis , 2007, Nature Reviews Cancer.

[5]  T. Rando,et al.  High Incidence of Non-Random Template Strand Segregation and Asymmetric Fate Determination In Dividing Stem Cells and their Progeny , 2007, PLoS biology.

[6]  M. Smalley,et al.  Common Molecular Mechanisms of Mammary Gland Development and Breast Cancer , 2007, Cellular and Molecular Life Sciences.

[7]  B. W. Booth,et al.  Estrogen receptor-α and progesterone receptor are expressed in label-retaining mammary epithelial cells that divide asymmetrically and retain their template DNA strands , 2006, Breast Cancer Research.

[8]  François Vaillant,et al.  Steroid hormone receptor status of mouse mammary stem cells. , 2006, Journal of the National Cancer Institute.

[9]  Barbara Gayraud-Morel,et al.  Asymmetric division and cosegregation of template DNA strands in adult muscle satellite cells , 2006, Nature Cell Biology.

[10]  P. Chambon,et al.  Paracrine signaling through the epithelial estrogen receptor α is required for proliferation and morphogenesis in the mammary gland , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Lothar Hennighausen,et al.  Information networks in the mammary gland , 2005, Nature Reviews Molecular Cell Biology.

[12]  Gilbert H. Smith,et al.  Label-retaining epithelial cells in mouse mammary gland divide asymmetrically and retain their template DNA strands , 2005, Development.

[13]  R. Clarke,et al.  Stem Cells and Tissue Homeostasis in Mammary Glands , 2005, Journal of Mammary Gland Biology and Neoplasia.

[14]  Gilbert H. Smith,et al.  Experimental mammary epithelial morphogenesis in anin vivo model: Evidence for distinct cellular progenitors of the ductal and lobular phenotype , 2005, Breast Cancer Research and Treatment.

[15]  E. Nisoli,et al.  Reversible transdifferentiation of secretory epithelial cells into adipocytes in the mammary gland. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[16]  R. Clarke,et al.  Steroid Receptors and Cell Cycle in Normal Mammary Epithelium , 2004, Journal of Mammary Gland Biology and Neoplasia.

[17]  A. Neville,et al.  Basal clear cells of the normal human breast , 2004, Virchows Archiv A.

[18]  J. Sherley,et al.  Cosegregation of chromosomes containing immortal DNA strands in cells that cycle with asymmetric stem cell kinetics. , 2002, Cancer research.

[19]  C. Boulanger,et al.  Mammary stem cell repertoire: new insights in aging epithelial populations , 2002, Mechanisms of Ageing and Development.

[20]  J. Cairns.  Somatic stem cells and the kinetics of mutagenesis and carcinogenesis , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Christopher S Potten,et al.  Intestinal stem cells protect their genome by selective segregation of template DNA strands. , 2002, Journal of cell science.

[22]  A. Andres,et al.  Vascular remodelling during the normal and malignant life cycle of the mammary gland , 2001, Microscopy research and technique.

[23]  N. Zeps,et al.  Murine Progesterone Receptor Expression in Proliferating Mammary Epithelial Cells During Normal Pubertal Development and Adult Estrous Cycle: Association with ERα and ERβ Status , 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[24]  M. Bissell,et al.  Human mammary luminal epithelial cells contain progenitors to myoepithelial cells. , 1999, Developmental biology.

[25]  G. Smith,et al.  An entire functional mammary gland may comprise the progeny from a single cell. , 1998, Development.

[26]  N. Zeps,et al.  Estrogen receptor-negative epithelial cells in mouse mammary gland development and growth. , 1998, Differentiation; research in biological diversity.

[27]  G H Smith,et al.  Three division-competent, structurally-distinct cell populations contribute to murine mammary epithelial renewal. , 1997, Tissue & cell.

[28]  N. Zeps,et al.  Detection of a population of long-lived cells in mammary epithelium of the mouse , 1996, Cell and Tissue Research.

[29]  W. Muller,et al.  Roles of platelet/endothelial cell adhesion molecule-1 (PECAM-1, CD31) in natural killer cell transendothelial migration and beta 2 integrin activation. , 1996, Journal of immunology.

[30]  D. Medina,et al.  A morphologically distinct candidate for an epithelial stem cell in mouse mammary gland. , 1988, Journal of cell science.

[31]  J. Cairns,et al.  The segregation of DNA in epithelial stem cells , 1978, Cell.

[32]  John Cairns,et al.  Mutation selection and the natural history of cancer , 1975, Nature.

[33]  Jing Hao.  Figure , 1972, Analysing Scientific Discourse From a Systemic Functional Linguistic Perspective.

[34]  H. Traurig,et al.  A radioautographic study of cell proliferation in the mammary gland of the pregnant mouse , 1967, The Anatomical record.

[35]  F. Bresciani.  EFFECT OF OVARIAN HORMONES ON DURATION OF DNA SYNTHESIS IN CELLS OF THE C3H MOUSE MAMMARY GLAND. , 1965, Experimental cell research.

[36]  F. Bresciani.  DNA Synthesis in Alveolar Cells of the Mammary Gland: Acceleration by Ovarian Hormones , 1964, Science.

[37]  C. F. Morgan,et al.  Autoradiographic Studies of the Epithelium of Mammary Gland as Influenced by Ovarian Hormones.∗ , 1964, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.