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Cancer Stem Cells and Side Population Cells in Breast Cancer and Metastasis
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inferredcites →https://doi.org/10.1002/(sici)1097-0215(19990812)82:4<609::aid-ijc23>3.0.co;2-aopenalex-snapshot
Increased resistance to apoptosis by bone marrow CD34+ progenitor cells from tumor-bearing mice
inferredcites →https://doi.org/10.1002/ijc.24349openalex-snapshot
Side population of pancreatic cancer cells predominates in TGF‐β‐mediated epithelial to mesenchymal transition and invasion
inferredcites →https://doi.org/10.1002/path.2457openalex-snapshot
Detection and analysis of mammary gland stem cells
inferredcites →https://doi.org/10.1002/path.2772openalex-snapshot
Finding cancer stem cells: are aldehyde dehydrogenases fit for purpose?
inferredcites →https://doi.org/10.1002/path.2793openalex-snapshot
Cancer stem cells: problems for therapy?
inferredcites →https://doi.org/10.1002/stem.563openalex-snapshot
Aldehyde Dehydrogenase Activity of Breast Cancer Stem Cells Is Primarily Due To Isoform ALDH1A3 and Its Expression Is Predictive of Metastasis
inferredcites →https://doi.org/10.1002/stem.582openalex-snapshot
Side Population is Not Necessary or Sufficient for a Cancer Stem Cell Phenotype in Glioblastoma Multiforme
inferredcites →https://doi.org/10.1006/dbio.2002.0625openalex-snapshot
Sca-1pos Cells in the Mouse Mammary Gland Represent an Enriched Progenitor Cell Population
inferredcites →https://doi.org/10.1007/s00432-008-0407-1openalex-snapshot
Identification of side population cells in human hepatocellular carcinoma cell lines with stepwise metastatic potentials
inferredcites →https://doi.org/10.1007/s10549-008-0072-8openalex-snapshot
Cancer stem/progenitor cell active compound 8-quinolinol in combination with paclitaxel achieves an improved cure of breast cancer in the mouse model
inferredcites →https://doi.org/10.1007/s10911-005-2537-2openalex-snapshot
Stem/Progenitor Cells in Mouse Mammary Gland Development and Breast Cancer
inferredcites →https://doi.org/10.1007/s10911-009-9109-9openalex-snapshot
ABC Transporters, Drug Resistance, and Cancer Stem Cells
inferredcites →https://doi.org/10.1007/s10911-009-9110-3openalex-snapshot
The Epithelial-to-Mesenchymal Transition and Cancer Stem Cells: A Coalition Against Cancer Therapies
inferredcites →https://doi.org/10.1007/s11010-007-9570-yopenalex-snapshot
Identification of a distinct side population of cancer cells in the Cal-51 human breast carcinoma cell line
inferredcites →https://doi.org/10.1007/s12253-010-9271-9openalex-snapshot
The Probable Role of Tumor Stem Cells for Lymph Node Metastasis in Supraglottic Carcinoma
inferredcites →https://doi.org/10.1016/0092-8674(91)90403-lopenalex-snapshot
A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells
inferredcites →https://doi.org/10.1016/j.bbrc.2007.09.007openalex-snapshot
RETRACTED: Blockade of invasion and metastasis of breast cancer cells via targeting CXCR4 with an artificial microRNA
inferredcites →https://doi.org/10.1016/j.bbrc.2007.10.016openalex-snapshot
Most MCF7 and SK-OV3 cells were deprived of their stem nature by Hoechst 33342
inferredcites →https://doi.org/10.1016/j.bbrc.2009.10.042openalex-snapshot
Salinomycin induces apoptosis and overcomes apoptosis resistance in human cancer cells
inferredcites →https://doi.org/10.1016/j.bbrc.2009.12.020openalex-snapshot
Detection and characterization of side population in Ewing’s sarcoma SK-ES-1 cells in vitro
inferredcites →https://doi.org/10.1016/j.biocel.2011.12.020openalex-snapshot
Breast cancer stem cells
inferredcites →https://doi.org/10.1016/j.ccr.2007.01.013openalex-snapshot
Molecular Definition of Breast Tumor Heterogeneity
inferredcites →https://doi.org/10.1016/j.cell.2008.03.027openalex-snapshot
The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells
inferredcites →https://doi.org/10.1016/j.cell.2009.06.034openalex-snapshot
Identification of Selective Inhibitors of Cancer Stem Cells by High-Throughput Screening
inferredcites →https://doi.org/10.1016/j.cell.2009.08.007openalex-snapshot
Breast Cancer Stem Cells: Eradication by Differentiation Therapy?
inferredcites →https://doi.org/10.1016/j.cell.2009.12.007openalex-snapshot
Biological and Molecular Heterogeneity of Breast Cancers Correlates with Their Cancer Stem Cell Content
inferredcites →https://doi.org/10.1016/j.critrevonc.2004.04.007openalex-snapshot
Stem cell origin of cancer and differentiation therapy
inferredcites →https://doi.org/10.1016/j.ctrv.2008.01.007openalex-snapshot
Mechanisms and strategies to overcome chemotherapy resistance in metastatic breast cancer
inferredcites →https://doi.org/10.1016/j.ejca.2010.02.024openalex-snapshot
CD44, a therapeutic target for metastasising tumours
inferredcites →https://doi.org/10.1016/j.febslet.2007.02.071openalex-snapshot
Fluctuation of the SP/non‐SP phenotype in the C6 glioma cell line
inferredcites →https://doi.org/10.1016/j.febslet.2007.05.073openalex-snapshot
Effects of Hoechst 33342 on C2C12 and PC12 cell differentiation
inferredcites →https://doi.org/10.1016/j.ijcard.2008.08.032openalex-snapshot
Differentiation and migration of Sca1+/CD31− cardiac side population cells in a murine myocardial ischemic model
inferredcites →https://doi.org/10.1016/j.ijcard.2010.05.021openalex-snapshot
Stem cell therapy: A role for CXCR4 in homing bone marrow side population cells to areas of myocardial damage
inferredcites →https://doi.org/10.1016/j.jconrel.2007.05.005openalex-snapshot
Tumorigenic stem and progenitor cells: Implications for the therapeutic index of anti-cancer agents
inferredcites →https://doi.org/10.1016/j.jhep.2004.07.029openalex-snapshot
Mature hepatocytes are the source of small hepatocyte-like progenitor cells in the retrorsine model of liver injury
inferredcites →https://doi.org/10.1016/j.semcancer.2008.03.016openalex-snapshot
Can cancer be reversed by engineering the tumor microenvironment?
inferredcites →https://doi.org/10.1016/j.stem.2007.06.002openalex-snapshot
Distinct Populations of Cancer Stem Cells Determine Tumor Growth and Metastatic Activity in Human Pancreatic Cancer
inferredcites →https://doi.org/10.1016/j.stem.2007.08.014openalex-snapshot
ALDH1 Is a Marker of Normal and Malignant Human Mammary Stem Cells and a Predictor of Poor Clinical Outcome
inferredcites →https://doi.org/10.1016/j.stem.2011.01.007openalex-snapshot
Critical Appraisal of the Side Population Assay in Stem Cell and Cancer Stem Cell Research
inferredcites →https://doi.org/10.1016/j.ydbio.2003.09.028openalex-snapshot
Persistent expression of the ATP-binding cassette transporter, Abcg2, identifies cardiac SP cells in the developing and adult heart
inferredcites →https://doi.org/10.1016/j.ydbio.2004.07.044openalex-snapshot
A putative human breast stem cell population is enriched for steroid receptor-positive cells
inferredcites →https://doi.org/10.1016/j.yexcr.2003.11.005openalex-snapshot
Evidence for a resident subset of cells with SP phenotype in the C2C12 myogenic line: a tool to explore muscle stem cell biology
inferredcites →https://doi.org/10.1016/j.yexcr.2004.03.029openalex-snapshot
Growth and differentiation of progenitor/stem cells derived from the human mammary gland
inferredcites →https://doi.org/10.1016/j.yexcr.2004.04.010openalex-snapshot
Demystifying SP cell purification: viability, yield, and phenotype are defined by isolation parameters
inferredcites →https://doi.org/10.1016/j.yexcr.2007.02.025openalex-snapshot
Kinetic analyses as a critical parameter in defining the side population (SP) phenotype
inferredcites →https://doi.org/10.1016/j.yexcr.2010.01.009openalex-snapshot
Mechanisms of resistance to HER family targeting antibodies
inferredcites →https://doi.org/10.1016/j.yexmp.2009.05.001openalex-snapshot
The role of HER2 in early breast cancer metastasis and the origins of resistance to HER2-targeted therapies
inferredcites →https://doi.org/10.1016/s0040-8166(97)80024-9openalex-snapshot
Three division-competent, structurally-distinct cell populations contribute to murine mammary epithelial renewal
inferredcites →https://doi.org/10.1016/s0070-2153(08)60289-6openalex-snapshot
Chapter 8: Teratocarcinoma: Model for A Developmental Concept of Cancer
inferredcites →https://doi.org/10.1016/s0092-8674(00)00179-3openalex-snapshot
The Leukotriene C4 Transporter MRP1 Regulates CCL19 (MIP-3β, ELC)–Dependent Mobilization of Dendritic Cells to Lymph Nodes
inferredcites →https://doi.org/10.1016/s0140-6736(00)49915-0openalex-snapshot
THE DISTRIBUTION OF SECONDARY GROWTHS IN CANCER OF THE BREAST.
inferredcites →https://doi.org/10.1023/b:clin.0000037697.76011.1dopenalex-snapshot
Tamoxifen resistance in breast cancer cells is accompanied by an enhanced motile and invasive phenotype: Inhibition by gefitinib (`Iressa', ZD1839)
inferredcites →https://doi.org/10.1038/35021093openalex-snapshot
Molecular portraits of human breast tumours
inferredcites →https://doi.org/10.1038/35065016openalex-snapshot
Involvement of chemokine receptors in breast cancer metastasis
inferredcites →https://doi.org/10.1038/35102167openalex-snapshot
Stem cells, cancer, and cancer stem cells
inferredcites →https://doi.org/10.1038/nature04372openalex-snapshot
Generation of a functional mammary gland from a single stem cell
inferredcites →https://doi.org/10.1038/nature04496openalex-snapshot
Purification and unique properties of mammary epithelial stem cells
inferredcites →https://doi.org/10.1038/nature05944openalex-snapshot
In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state
inferredcites →https://doi.org/10.1038/nature09091openalex-snapshot
Progesterone induces adult mammary stem cell expansion
inferredcites →https://doi.org/10.1038/ncb0510-419openalex-snapshot
Cancer stem cells: nature versus nurture
inferredcites →https://doi.org/10.1038/nm0901-1028openalex-snapshot
The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype
inferredcites →https://doi.org/10.1038/nrc1098openalex-snapshot
The pathogenesis of cancer metastasis: the 'seed and soil' hypothesis revisited
inferredcites →https://doi.org/10.1038/nrc1212openalex-snapshot
Stem cells and breast cancer: A field in transit
inferredcites →https://doi.org/10.1038/nrc1590openalex-snapshot
Tumour stem cells and drug resistance
inferredcites →https://doi.org/10.1038/nrc1694openalex-snapshot
Migrating cancer stem cells — an integrated concept of malignant tumour progression
inferredcites →https://doi.org/10.1038/nrc2499openalex-snapshot
Cancer stem cells in solid tumours: accumulating evidence and unresolved questions
inferredcites →https://doi.org/10.1038/nrc2627openalex-snapshot
Parallel progression of primary tumours and metastases
inferredcites →https://doi.org/10.1038/nrc2789openalex-snapshot
ABC transporters in cancer: more than just drug efflux pumps
inferredcites →https://doi.org/10.1038/onc.2008.207openalex-snapshot
HER2 regulates the mammary stem/progenitor cell population driving tumorigenesis and invasion
inferredcites →https://doi.org/10.1038/sj.bjc.6605553openalex-snapshot
Side-population cells in luminal-type breast cancer have tumour-initiating cell properties, and are regulated by HER2 expression and signalling
inferredcites →https://doi.org/10.1038/sj.leu.2404859openalex-snapshot
ATP-binding-cassette transporters in hematopoietic stem cells and their utility as therapeutical targets in acute and chronic myeloid leukemia
inferredcites →https://doi.org/10.1038/sj.onc.1207947openalex-snapshot
Self-renewal and solid tumor stem cells
inferredcites →https://doi.org/10.1042/bst0330241openalex-snapshot
ABC transporters in the balance: is there a role in multidrug resistance?
inferredcites →https://doi.org/10.1046/j.1365-2184.36.s.1.6.xopenalex-snapshot
Stem cells in normal breast development and breast cancer
inferredcites →https://doi.org/10.1073/pnas.0400067101openalex-snapshot
A distinct “side population” of cells with high drug efflux capacity in human tumor cells
inferredcites →https://doi.org/10.1073/pnas.0400699101openalex-snapshot
The transforming activity of Wnt effectors correlates with their ability to induce the accumulation of mammary progenitor cells
inferredcites →https://doi.org/10.1073/pnas.0530291100openalex-snapshot
Prospective identification of tumorigenic breast cancer cells
inferredcites →https://doi.org/10.1073/pnas.0603672103openalex-snapshot
Ovarian cancer side population defines cells with stem cell-like characteristics and Mullerian Inhibiting Substance responsiveness
inferredcites →https://doi.org/10.1073/pnas.0606599104openalex-snapshot
WNT/β-catenin mediates radiation resistance of mouse mammary progenitor cells
inferredcites →https://doi.org/10.1073/pnas.0702596104openalex-snapshot
Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance
inferredcites →https://doi.org/10.1073/pnas.0830967100openalex-snapshot
Breast cancer stem cells revealed
inferredcites →https://doi.org/10.1073/pnas.1006732107openalex-snapshot
Cancer stem cells from human breast tumors are involved in spontaneous metastases in orthotopic mouse models
inferredcites →https://doi.org/10.1073/pnas.191367098openalex-snapshot
Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications
inferredcites →https://doi.org/10.1073/pnas.192276999openalex-snapshot
Bcrp1 gene expression is required for normal numbers of side population stem cells in mice, and confers relative protection to mitoxantrone in hematopoietic cells in vivo
inferredcites →https://doi.org/10.1073/pnas.90.23.10914openalex-snapshot
Antioncogenes and human cancer.
inferredcites →https://doi.org/10.1073/pnas.95.12.7024openalex-snapshot
The drug efflux protein, P-glycoprotein, additionally protects drug-resistant tumor cells from multiple forms of caspase-dependent apoptosis
inferredcites →https://doi.org/10.1084/jem.183.4.1797openalex-snapshot
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo.
inferredcites →https://doi.org/10.1093/annonc/mdp427openalex-snapshot
Quantitative analysis of changes in ER, PR and HER2 expression in primary breast cancer and paired nodal metastases
inferredcites →https://doi.org/10.1093/carcin/bgh293openalex-snapshot
Will cancer stem cells provide new therapeutic targets?
inferredcites →https://doi.org/10.1093/carcin/bgr028openalex-snapshot
Breast cancer stem cells: treatment resistance and therapeutic opportunities
inferredcites →https://doi.org/10.1093/humrep/del514openalex-snapshot
Characterization of side-population cells in human normal endometrium
inferredcites →https://doi.org/10.1093/jnci/58.5.1329openalex-snapshot
Ultrastructural Comparison of Differentiation of Stem Cells of Murine Adenocarcinomas of Colon and Breast With Their Normal Counterparts2
inferredcites →https://doi.org/10.1093/jnci/djn123openalex-snapshot
Intrinsic Resistance of Tumorigenic Breast Cancer Cells to Chemotherapy
inferredcites →https://doi.org/10.1093/jnci/djq008openalex-snapshot
Breast Cancer Prognosis and Occult Lymph Node Metastases, Isolated Tumor Cells, and Micrometastases
inferredcites →https://doi.org/10.1111/j.1349-7006.2009.01211.xopenalex-snapshot
Cancer stem cell‐like SP cells have a high adhesion ability to the peritoneum in gastric carcinoma
inferredcites →https://doi.org/10.1111/j.1365-2184.2005.00357.xopenalex-snapshot
Isolation and characterization of human mammary stem cells
inferredcites →https://doi.org/10.1111/j.1600-0463.2005.apm_371.xopenalex-snapshot
Stem cell biology and the cellular pathways of carcinogenesis
inferredcites →https://doi.org/10.1126/science.1171837openalex-snapshot
The Increasing Complexity of the Cancer Stem Cell Paradigm
inferredcites →https://doi.org/10.1126/science.299.5609.1002openalex-snapshot
Tracing the Steps of Metastasis, Cancer's Menacing Ballet
inferredcites →https://doi.org/10.1158/0008-5472.967.65.3openalex-snapshot
Silencing of CXCR4 Blocks Breast Cancer Metastasis
inferredcites →https://doi.org/10.1158/0008-5472.can-04-1844openalex-snapshot
CXCR4 Regulates Growth of Both Primary and Metastatic Breast Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0592openalex-snapshot
Side Population Is Enriched in Tumorigenic, Stem-Like Cancer Cells, whereas ABCG2+ and ABCG2− Cancer Cells Are Similarly Tumorigenic
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0619openalex-snapshot
CD24 Expression Causes the Acquisition of Multiple Cellular Properties Associated with Tumor Growth and Metastasis
inferredcites →https://doi.org/10.1158/0008-5472.can-06-0054openalex-snapshot
Hedgehog Signaling and Bmi-1 Regulate Self-renewal of Normal and Malignant Human Mammary Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-06-3126openalex-snapshot
Cancer Stem Cells—Perspectives on Current Status and Future Directions: AACR Workshop on Cancer Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-06-3557openalex-snapshot
Side Population in Human Lung Cancer Cell Lines and Tumors Is Enriched with Stem-like Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-06-4343openalex-snapshot
Identification of Cancer Stem Cell–Like Side Population Cells in Human Nasopharyngeal Carcinoma Cell Line
inferredcites →https://doi.org/10.1158/0008-5472.can-06-4493openalex-snapshot
Enrichment of a Population of Mammary Gland Cells that Form Mammospheres and Have In vivo Repopulating Activity
inferredcites →https://doi.org/10.1158/0008-5472.can-07-0999openalex-snapshot
Side Population Cells Isolated from Mesenchymal Neoplasms Have Tumor Initiating Potential
inferredcites →https://doi.org/10.1158/0008-5472.can-07-2249openalex-snapshot
MCF7 Side Population Cells with Characteristics of Cancer Stem/Progenitor Cells Express the Tumor Antigen MUC1
inferredcites →https://doi.org/10.1158/0008-5472.can-07-2545openalex-snapshot
ABCG2 Expression and Side Population Abundance Regulated by a Transforming Growth Factor β–Directed Epithelial-Mesenchymal Transition
inferredcites →https://doi.org/10.1158/0008-5472.can-07-6341openalex-snapshot
The Side Population of Ovarian Cancer Cells Is a Primary Target of IFN-α Antitumor Effects
inferredcites →https://doi.org/10.1158/0008-5472.can-08-3343openalex-snapshot
Immune-Induced Epithelial to Mesenchymal Transition In vivo Generates Breast Cancer Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-08-3441openalex-snapshot
Characterization of a Naturally Occurring Breast Cancer Subset Enriched in Epithelial-to-Mesenchymal Transition and Stem Cell Characteristics
inferredcites →https://doi.org/10.1158/0008-5472.can-09-3619openalex-snapshot
CD44posCD49fhiCD133/2hi Defines Xenograft-Initiating Cells in Estrogen Receptor–Negative Breast Cancer
inferredcites →https://doi.org/10.1158/1078-0432.1154.11.3openalex-snapshot
Prevalence of CD44+/CD24−/low Cells in Breast Cancer May Not Be Associated with Clinical Outcome but May Favor Distant Metastasis
inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-1327openalex-snapshot
Tumor-Initiating Cells of HER2-Positive Carcinoma Cell Lines Express the Highest Oncoprotein Levels and Are Sensitive to Trastuzumab
inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-1479openalex-snapshot
Association of Breast Cancer Stem Cells Identified by Aldehyde Dehydrogenase 1 Expression with Resistance to Sequential Paclitaxel and Epirubicin-Based Chemotherapy for Breast Cancers
inferredcites →https://doi.org/10.1158/1078-0432.ccr-09-1630openalex-snapshot
Aldehyde Dehydrogenase 1–Positive Cancer Stem Cells Mediate Metastasis and Poor Clinical Outcome in Inflammatory Breast Cancer
inferredcites →https://doi.org/10.1158/1078-0432.ccr-09-1764openalex-snapshot
Lapatinib Restores Hormone Sensitivity with Differential Effects on Estrogen Receptor Signaling in Cell Models of Human Epidermal Growth Factor Receptor 2–Negative Breast Cancer with Acquired Endocrine Resistance
inferredcites →https://doi.org/10.1158/1541-7786.327.2.6openalex-snapshot
Involvement of the Chemokine Receptor CXCR4 and Its Ligand Stromal Cell-Derived Factor 1α in Breast Cancer Cell Migration Through Human Brain Microvascular Endothelial Cells
inferredcites →https://doi.org/10.1172/jci44540openalex-snapshot
CD44 splice isoform switching in human and mouse epithelium is essential for epithelial-mesenchymal transition and breast cancer progression
inferredcites →https://doi.org/10.1177/0091270005276905openalex-snapshot
Multiple Drug Resistance in Cancer Revisited: The Cancer Stem Cell Hypothesis
inferredcites →https://doi.org/10.1182/blood-2003-09-3064openalex-snapshot
Characterization of clonogenic multiple myeloma cells
inferredcites →https://doi.org/10.1182/blood-2004-02-0448openalex-snapshot
Functional characterization of highly purified human hematopoietic repopulating cells isolated according to aldehyde dehydrogenase activity
inferredcites →https://doi.org/10.1182/blood-2005-02-0655openalex-snapshot
Hematopoietic stem cells do not engraft with absolute efficiencies
inferredcites →https://doi.org/10.1182/blood.v100.4.1224.h81602001224_1224_1232openalex-snapshot
Phase 3 study of the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age and older with acute myeloid leukemia: Cancer and Leukemia Group B Study 9720
inferredcites →https://doi.org/10.1182/blood.v92.6.2041openalex-snapshot
Apoptotic Regulation in Primitive Hematopoietic Precursors
inferredcites →https://doi.org/10.1186/1423-0127-16-100openalex-snapshot
Distinct population of highly malignant cells in a head and neck squamous cell carcinoma cell line established by xenograft model
inferredcites →https://doi.org/10.1186/bcr1610openalex-snapshot
CD44+/CD24-breast cancer cells exhibit enhanced invasive properties: an early step necessary for metastasis
inferredcites →https://doi.org/10.1186/bcr1855openalex-snapshot
Brca1 breast tumors contain distinct CD44+/CD24- and CD133+cells with cancer stem cell characteristics
inferredcites →https://doi.org/10.1186/bcr1982openalex-snapshot
Human breast cancer cell lines contain stem-like cells that self-renew, give rise to phenotypically diverse progeny and survive chemotherapy
inferredcites →https://doi.org/10.1186/bcr547openalex-snapshot
Functional and molecular characterisation of mammary side population cells
inferredcites →https://doi.org/10.1186/bcr627openalex-snapshot
Expression pattern of CXC chemokine receptor-4 is correlated with lymph node metastasis in human invasive ductal carcinoma
inferredcites →https://doi.org/10.1186/bcr709openalex-snapshot
Stem cells in normal breast development and breast cancer
inferredcites →https://doi.org/10.1186/bcr749openalex-snapshot
Introducing the concept of breast cancer stem cells
inferredcites →https://doi.org/10.1196/annals.1349.001openalex-snapshot
Acute Myeloid Leukemia Stem Cells
inferredcites →https://doi.org/10.1200/jco.1999.17.8.2334openalex-snapshot
Significance of Axillary Lymph Node Metastasis in Primary Breast Cancer
inferredcites →https://doi.org/10.1200/jco.2001.19.6.1589openalex-snapshot
Phase I/II Study of the P-Glycoprotein Modulator PSC 833 in Patients With Acute Myeloid Leukemia
inferredcites →https://doi.org/10.1200/jco.2004.07.048openalex-snapshot
Mitoxantrone, Etoposide, and Cytarabine With or Without Valspodar in Patients With Relapsed or Refractory Acute Myeloid Leukemia and High-Risk Myelodysplastic Syndrome: A Phase III Trial (E2995)
inferredcites →https://doi.org/10.1200/jco.2008.17.7436openalex-snapshot
Cancer Stem Cells: A Step Toward the Cure
inferredcites →https://doi.org/10.1200/jco.2009.23.3734openalex-snapshot
Lapatinib Combined With Letrozole Versus Letrozole and Placebo As First-Line Therapy for Postmenopausal Hormone Receptor–Positive Metastatic Breast Cancer
inferredcites →https://doi.org/10.1208/aapsj070112openalex-snapshot
Role of the breast cancer resistance protein (ABCG2) in drug transport
inferredcites →https://doi.org/10.1210/en.2006-1553openalex-snapshot
Characterization of Side Population in Thyroid Cancer Cell Lines: Cancer Stem-Like Cells Are Enriched Partly But Not Exclusively
inferredcites →https://doi.org/10.1210/en.2007-1001openalex-snapshot
Side Population Does Not Define Stem Cell-Like Cancer Cells in the Adrenocortical Carcinoma Cell Line NCI h295R
inferredcites →https://doi.org/10.1242/dev.01609openalex-snapshot
Label-retaining epithelial cells in mouse mammary gland divide asymmetrically and retain their template DNA strands
inferredcites →https://doi.org/10.1245/s10434-009-0730-zopenalex-snapshot
Characterizing the HER2/neu Status and Metastatic Potential of Breast Cancer Stem/Progenitor Cells
inferredcites →https://doi.org/10.1289/ehp.93101s515openalex-snapshot
Cellular origin of cancer: dedifferentiation or stem cell maturation arrest?
inferredcites →https://doi.org/10.1371/journal.pone.0010365openalex-snapshot
Doxorubicin in Combination with a Small TGFβ Inhibitor: A Potential Novel Therapy for Metastatic Breast Cancer in Mouse Models
inferredcites →https://doi.org/10.1371/journal.pone.0011456openalex-snapshot
Characterization of Side Populations in HNSCC: Highly Invasive, Chemoresistant and Abnormal Wnt Signaling
inferredcites →https://doi.org/10.1517/17425255.4.1.1openalex-snapshot
ABCG2: structure, function and role in drug response
inferredcites →https://doi.org/10.1634/stemcells.2004-0170openalex-snapshot
Phenotypic Characterization of Murine Primitive Hematopoietic Progenitor Cells Isolated on Basis of Aldehyde Dehydrogenase Activity
inferredcites →https://doi.org/10.1634/stemcells.2004-0292openalex-snapshot
Characterization of Cells with a High Aldehyde Dehydrogenase Activity from Cord Blood and Acute Myeloid Leukemia Samples
inferredcites →https://doi.org/10.1634/stemcells.2005-0150openalex-snapshot
Contribution of the ABC Transporters Bcrp1 and Mdr1a/1b to the Side Population Phenotype in Mammary Gland and Bone Marrow of Mice
inferredcites →https://doi.org/10.1634/stemcells.2005-0562openalex-snapshot
Prospective Isolation of Murine Hematopoietic Stem Cells by Expression of an Abcg2/GFP Allele
inferredcites →https://doi.org/10.1634/stemcells.2008-0171openalex-snapshot
Characterization of Side Population Cells from Human Airway Epithelium
inferredcites →https://doi.org/10.1634/stemcells.2008-0397openalex-snapshot
Quantitative Mass Spectrometry Identifies Drug Targets in Cancer Stem Cell-Containing Side Population
inferredcites →https://doi.org/10.2174/157488809787169110openalex-snapshot
Breast Cancer Stem Cells and Intrinsic Subtypes: Controversies Rage On
inferredcites →https://doi.org/10.3390/cancers30100716openalex-snapshot
Cancer Stem Cells and Epithelial-to-Mesenchymal Transition (EMT)-Phenotypic Cells: Are They Cousins or Twins?
inferredcites →https://doi.org/10.4049/jimmunol.167.8.4747openalex-snapshot
A Possible Role for CXCR4 and Its Ligand, the CXC Chemokine Stromal Cell-Derived Factor-1, in the Development of Bone Marrow Metastases in Neuroblastoma
inferredcites →https://doi.org/10.4161/cc.4.2.1406openalex-snapshot
A Distinct “Side Population” of Cells in Human Tumor Cells: Implications for Tumor Biology and Therapy
inferredcites →https://doi.org/10.4161/cc.6.20.4911openalex-snapshot
Effects of Low Confluency, Serum Starvation and Hypoxia on the Side Population of Cancer Cell Lines
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.prp.2022.154043openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsami.7b06393openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d6ma00569aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1177/1010428317695915openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12951-022-01607-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s40360-017-0118-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/scrt433openalex-snapshot
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High Percentage of Cancer Stem Cells in Metastatic Locations: Upregulation of circBIRC6 in Highly Metastatic Breast Cancer Subline
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1688863/v2openalex-snapshot
High Percentage of Cancer Stem Cells in Metastatic Locations: Upregulation of circBIRC6 in Highly Metastatic Breast Cancer Subline
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inferred← citeshttps://doi.org/10.32604/biocell.2023.028863openalex-snapshot
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inferred← citeshttps://doi.org/10.34133/bmr.0168openalex-snapshot
Label-Free Enrichment of Highly Metastatic Tumor-Initiating Cells up to a Monoclonal State
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Cancer stem cells in esophageal squamous cell cancer (Review)
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Breast cancer stem cell RNA‑pulsed dendritic cells enhance tumor cell killing by effector T�cells�
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Single-cell RNA-sequencing reveals distinct patterns of cell state heterogeneity in mouse models of breast cancer
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