Distinct stem cells contribute to mammary gland development and maintenance

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907

Identification of stem cells in small intestine and colon by marker gene Lgr5

Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687

Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121

In vitro propagation and transcriptional profiling of human mammary stem/progenitor cellsPreprint

Dontu, G., Abdallah, W. M., Foley, J. M., Jackson, K. W., Clarke, M. F., Kawamura, M., & Wicha, M. S. (2003) · Genes & Development · doi:10.1101/gad.1061803 · Cited by 2,413

Generation of a functional mammary gland from a single stem cell

Shackleton, M., Vaillant, F., Simpson, K. J., Stingl, J., Smyth, G. K., Asselin-Labat, M.-L., Wu, L., Lindeman, G. J., & Visvader, J. E. (2006) · Nature · doi:10.1038/nature04372 · Cited by 2,005

Purification and unique properties of mammary epithelial stem cells

Stingl, J., Eirew, P. D., Ricketson, I., Shackleton, M. J., Vaillant, F., Choi, D., Li, H. I., & Eaves, C. J. (2006) · Nature · doi:10.1038/nature04496 · Cited by 1,581

Epidermal homeostasis: a balancing act of stem cells in the skin

Blanpain, C., & Fuchs, E. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2636 · Cited by 1,270

Keeping abreast of the mammary epithelial hierarchy and breast tumorigenesisPreprint

Visvader, J. E. (2009) · Genes & Development · doi:10.1101/gad.1849509 · Cited by 603

An entire functional mammary gland may comprise the progeny from a single cell

Kordon, E. C., & Smith, G. H. (1998) · Development · doi:10.1242/dev.125.10.1921 · Cited by 553

Early restriction of peripheral and proximal cell lineages during formation of the lung

Perl, A. T., Wert, S. E., Nagy, A., Lobe, C. G., & Whitsett, J. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152238499 · Cited by 525

CD24 and CD49f expressions of E14.5 mouse mammary anlagen cells define putative distribution of earlier embryonic mammary stem cell activities

Song, J., Ding, F., Li, S., Li, W., Li, N., & Xue, K. (2018) · Biochemistry and Cell Biology · doi:10.1139/bcb-2017-0177 · Cited by 2

Single-Cell Transcriptomic and Epigenetic Analyses of Mouse Mammary Development Starting with the Embryo

Ma, Z., Lytle, N. K., Ramos, C., Naeem, R. F., & Wahl, G. M. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2193-6_3 · Cited by 3

Heterogeneity of Mammary Stem Cells

French, R., & Tornillo, G. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-24108-7_7 · Cited by 2

Laminin alpha 5 is Necessary for Mammary Epithelial Growth and Function by Maintaining Luminal Epithelial Cell IdentityPreprint

Englund, J. I., Cojoc, H., Blaas, L., Ritchie, A., Pentinmikko, N., Döhla, J., Munne, P., Patarroyo, M. E., Klefström, J. T., Ivaska, J., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.27.889451 · Cited by 2

Fine-tuning of Epithelial EGFR signals Supports Coordinated Mammary Gland DevelopmentPreprint

Samocha, A. J., Doh, H. M., Sitarama, V., Nguyen, Q., Gbenedio, O. M., Rudolph, J. D., Eckalbar, W. L., Barczak, A. J., Miao, Y., García, K. C., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.10.291872 · Cited by 2

A Self-Limiting Circuit Regulates Mammary Cap Cell Plasticity Through TGF-beta SignalingPreprint

Guelte, A. L., & Macara, I. G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.04.455067 · Cited by 2

Discovery and evaluation of novel biomarkers reveal dasatinib as a potential treatment for a specific subtype of Triple-Negative Breast CancerPreprint

Ortega-Álvarez, D., Tébar-García, D., Casado-Peláez, M., Castillo-Agea, E., Balibrea-Rull, J., Olivares-Osuna, D., Pérez-Parra, D., Guardia, C., Musulén, E., Vinuesa-Pitarch, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.24.603752 · Cited by 2

Pregnancy Reduces Il33+ Hybrid Progenitor Accumulation in the Aged Mammary GlandPreprint

Olander, A., Ramirez, C. M., Acosta, V. H., Medina, P., Kaushik, S., Jönsson, V. D., & Sikandar, S. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.01.606240 · Cited by 2

Loss of tumor suppressor p53 upregulates stem cell factor SOX9 via Notch signalingPreprint

Sanawar, R., & Guo, W. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.27.656408 · Cited by 2

Intramammary rapamycin administration to calves induces epithelial stem cell self-renewal and latent cell proliferation and milk protein expression

Kosenko, A., Jacoby, S., Salame, T., Ross, M., & Barash, I. (2022) · PLoS ONE · doi:10.1371/journal.pone.0269505 · Cited by 1

A Newly Identified Spliceosomal Protein AHED Is Essential for Homeostasis of the Epidermis

Takaishi, M., Ishimoto, T., Kataoka, S., Yagyu, K.-I., Morisawa, K., Kinjo, S., Ikeo, K., Noma, S., Takahashi, C., Okazaki, Y., et al. (2025) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2025.01.025 · Cited by 1

Intraductal Injection of Adenoviruses to Perform Lineage Tracing in the Mammary Gland

Chen, X., Han, S., Zhao, D., & Li, Z. (2025) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-025-09584-6 · Cited by 2

2D and 3D Differentiation of Human Mammary Basal Cells Long-Term Expanded in YDAC-Supplemented F Medium

Inoko, A. (2025) · Methods in molecular biology · doi:10.1007/7651_2025_665 · Cited by 1

Little women: the relevance and reliance on mouse models for mammary gland research and next steps for translation

Bjerre, L. B., Chalmers, S. B., & Davis, F. M. (2025) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-025-09590-8 · Cited by 1

Shared molecular and cellular programs during regeneration of glandular epithelia

Journot, R. P., Merle, C., & Fré, S. (2026) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2026.102508 · Cited by 1

A reporter mouse line with doxycyclin-inducible expression of β-glucosidase

Jay, F. F., & Schneider, M. R. (2014) · Histochemistry and Cell Biology · doi:10.1007/s00418-014-1255-5 · Cited by 1

‘The charmingest place’: non-coding RNA, lineage tracing, tumor heterogeneity, metastasis and metabolism - new methods in mammary gland development and cancer: the fifth ENBDC Workshop

Clarke, R. B., Stingl, J., Vivanco, M. D., & Bentires‐Alj, M. (2013) · Breast Cancer Research · doi:10.1186/bcr3497 · Cited by 1

Does a Lung Stem Cell Exist?

Ray, S., & Stripp, B. R. (2015) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-16232-4_1 · Cited by 1

Using Mouse Models and Making Sense of Them

Nguyen, D. H. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-25601-6_3 · Cited by 1

Unipotent or Multipotent Mammary Stem/Progenitor Cells in Mouse Mammary Gland Development

Smith, G. H. (2018) · Journal of Tumor Medicine & Prevention · doi:10.19080/jtmp.2018.03.555609 · Cited by 1

Hormonal effects on breast stem/progenitor cells and influence on breast cancer risk

Lambouras, M., & Britt, K. L. (2020) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2020.11.004 · Cited by 1

TRPV Family Ion Channels in the Mammary Epithelium: Role in Normal Tissue Homeostasis and along Breast Cancer Progression

Tojkander, S. (2022) · Biochemistry · doi:10.5772/intechopen.103665 · Cited by 1

Mammary Epithelial Stem Cells

Booth, B. W., Medina, D., & Smith, G. H. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7696-2_18 · Cited by 1

Mechanisms of Regulation of Cell Fate in Breast Development and Cancer

Keymeulen, A. V. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-70875-6_10 · Cited by 1

Recording Lineage History with Cellular Barcodes in the Mammary Epithelium and in Breast Cancer

Merle, C., & Fré, S. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-70875-6_5 · Cited by 2

Long-term expansion of basal cells and the novel differentiation methods identify mechanisms for switching Claudin expression in normal epithelia

Inoko, A., Soga, N., Suzuki, M., Kiyono, T., Ikenouchi, J., Kojima, T., Sato, Y., Saito, D., Miyamoto, T., Goshima, N., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-95463-3 · Cited by 1

Mammary stem cells: from molecular cues to orchestrated regulatory mechanisms and its implications in breast cancer

Zhang, M., Zhang, L., Liu, J., Zhao, J., Mei, J., Zou, J., Luo, Y., & Cai, C. (2025) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2025.04.007 · Cited by 1

Reactivation of Multipotency in the Mammary Gland – a Ripple in the Pond and a Turn of the Tide

Hager, C., Jehanno, C., & Bentires‐Alj, M. (2025) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-025-09586-4 · Cited by 1

RANK and RANKL of Bones, T Cells, and the Mammary Glands

Sigl, V., & Penninger, J. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800571-2.00008-6 · Cited by 1

Mouse Models of Breast Cancer: Deceptions that Reveal the Truth

Couto, J. P., & Bentires‐Alj, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-48848-6_6 · Cited by 1

Plasticity of Epidermal Stem Cells: The Future of Stem Cell-Based Therapeutics to Improve Cutaneous Wound Healing

Sun, X., Qin, H., Yang, S., & Fu, X. (2019) · Springer eBooks · doi:10.1007/978-981-13-3353-8_20 · Cited by 1

Quantification of Self-renewal in Murine Mammosphere Cultures

Vlachou, T., Xieraili, A., D’Elia, E., Santoro, A., Moroni, M. C., & Pelicci, P. G. (2019) · Journal of Visualized Experiments · doi:10.3791/60256 · Cited by 1

The mesenchymal property of mouse mammary anlagen repopulating cell population is associated with its stemness

Song, J., Ding, W., Liu, Y., Lin, L., Jia, M., Liu, S., & Xue, K. (2020) · Gene Expression Patterns · doi:10.1016/j.gep.2020.119151 · Cited by 1

Proteomics of Mammary Gland and Mammary Stem Cells

Kumar, S., Tyagi, N., Mohanty, A. K., & Kaushik, J. K. (2021) · Springer eBooks · doi:10.1007/978-981-16-3464-2_11 · Cited by 1

THE NRF-1/GABP/BRCA1 Transcriptional Network in Mammary Epithelial Differentiation

Thompson, C. (2012) · QSpace (Queen's University Library) · Cited by 1

The Role of ALDH1A3 in Normal and Transformed Mammary Gland Development

Cull, A. (2012) · QSpace (Queen's University Library) · Cited by 1

A miRNA screen identifies a transcriptional program controlling the fate of adult stem cellPreprint

Robert, J., Vlachavas, E., Lemaı̂tre, G., Chatziioannou, A. A., Pucéat, M., Delom, F., & Fessart, D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/314658 · Cited by 1

Buried myoepithelial stem cells as a reservoir for repairing the exposed airway epithelium

Duval, C., Watanabe, M., & Donati, G. (2018) · Stem Cell Investigation · doi:10.21037/sci.2018.11.07 · Cited by 1

Reconstitution of Alveolar Regeneration via novel DATPs by Inflammatory NichesPreprint

Choi, J., Park, J.-E., Tsagkogeorga, G., Yanagita, M., Koo, B., Han, N., & Lee, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.14.151324 · Cited by 1

Single-cell analysis identifies TCF4 and ID3 as a molecular switch of mammary epithelial stem cell differentiationPreprint

Yan, K., Nekritz, E. A., Ju, B., Dong, X., Werner, R. L., Alsina‐Beauchamp, D., Rosencrance, C. D., Mukhopadhyay, P., Pan, Q., Gorbatenko, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.16.249854 · Cited by 1

LMO2 is critical for early metastatic events in breast cancerPreprint

Sikandar, S. S., Antony, J., Gulati, G. S., Kuo, A. H., Ho, W. H. D., Das, S., Steen, C. B., Pereira, T. A., Qian, D., Beachy, P. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.26.443198 · Cited by 1

Breast tumor Insulin-like growth factor receptor regulates cell adhesion and metastasis: Alignment of mouse single cell and human breast cancer transcriptomicsPreprint

Obr, A. E., Chang, Y.-J., Ciliento, V., Lemenze, A., Maingrette, K., Bulatowicz, J. J., Shang, Q., Gallagher, E., LeRoith, D., & Wood, T. L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.31.458283 · Cited by 1

Commentary: DNA Damage Promotes Epithelial Hyperplasia and Fate Mis-specification via Fibroblast Inflammasome Activation

Solano, D., Patel, K. R., Perez, A. B., & Seldin, L. (2022) · Journal of Dermatology and Skin Science · doi:10.29245/2767-5092/2022/2.1154 · Cited by 2

Spatially coordinated cell cycle activity and motility govern mammary ductal growth and tip bifurcationPreprint

Myllymäki, S.-M., Kaczyńska, B., Lan, Q., & Mikkola, M. L. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.29.505725 · Cited by 1

Tumour-derived LAMA5 is critical for tumour initiation and controls progression and phenotype in luminal breast cancerPreprint

Ritchie, A., Dhawan, P., Kailari, E., Lindén, J., Blaas, L., Izzi, V., Katajisto, P., & Englund, J. I. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.26.630367 · Cited by 1

Next-Generation Breast Organoids Capture Human Organogenesis With High-Resolution Live ImagingPreprint

Rauner, G., Traugh, N. C., Trepicchio, C. J., Parrish, M. E., & Kuperwasser, C. (2025) · Qeios · doi:10.32388/mv8sr3 · Cited by 1

Noncanonical Wnt/Ror2 Signaling Regulates Basal Cell Fidelity and Branching Morphogenesis in the Mammary GlandPreprint

Si, H., Mendoza, E. M., Esquivel, M., Creighton, C. J., Xu, J., & Roarty, K. P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.25.640099 · Cited by 1

Single-cell transcriptomics uncover conserved molecular mechanisms and functional diversification in multilayered epitheliaPreprint

Merle, C., Huyghe, M., Kimber, E., Faraldo, M. M., Pantalacci, S., Sémon, M., Fré, S., & Journot, R. P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.14.688286 · Cited by 1

Dysplastic Epithelial Repair Propagates Chronic Pathology Through the Paracrine Transformation of Pulmonary FibroblastsPreprint

Holcomb, N. P., Samuel, R. Z., Klochkova, A., Wong, J., Kass-Gergi, S., Mendoza, M., Maideen, M. M., Martinez, E. A., Abraham, D. M., Singh, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.02.716135 · Cited by 1

Isolation and Characterization of Prostate Stem Cells

Goldstein, A. S., & Witte, O. N. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6498-3_2

Cellular and molecular effects of early pregnancy on mammary epithelial cell subpopulations in mice and their potential relevance for breast cancer protection

Meier‐Abt, F. (2013) · edoc (University of Basel) · doi:10.5451/unibas-006163851

Human Mammary Epithelial Stem/Progenitor Cells

Keller, P. J., Arendt, L. M., & Kuperwasser, C. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7696-2_17

The role of cFLIP in breast cancer stem cells

French, R. (2014) · ORCA Online Research @Cardiff (Cardiff University)

Adult Mammary Stem Cells: Identity, Location, and Functional Assays

Tharmapalan, P., & Khokha, R. (2013) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4614-9569-7_9

Genetic and Environmental Effects on Stem Cells and Breast Cancer

Popkie, A. P., Kakarala, M., & Graveel, C. R. (2014) · Current Pathobiology Reports · doi:10.1007/s40139-013-0037-4

Who do they think they are? Wnt-responsive cells reveal their family trees

Ordonez, L., & Smalley, M. J. (2012) · Breast Cancer Research · doi:10.1186/bcr3351

Effects of porcine jelly matrix (JMX) on gene expression of porcine umbilical cord (PUC) stem cells

Morton, J. M. (2014) · K-State Research Exchange (Kansas State University)

Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells

Gayraud-Morel, B., Chrétien, F. C., Jory, A., Sambasivan, R., Négroni, E., Flamant, P., Soubigou, G., Coppée, J., Santo, J. P. D., Cumano, A., et al. (2012) · Development · doi:10.1242/dev.084186

Cédric Blanpain: The stories stem cells tell

Sedwick, C. E. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.1991pi

potentials for adult skeletal muscle stem cells.

Gayraud-Morel, B., Sambasivan, R., Négroni, E., Flamant, P., & Soubigou, G. (2013)

The Role of BRCA1 in Suppressing Epithelial-Mesenchymal Transition in Mammary Gland and Tumor Development

Pei, X. (2014) · doi:10.21236/ada612714

aaaaaaaaa. Progesterone and Overlooked Endocrine Pathways in Breast Cancer Pathogenesis

Brisken, C., Hess, K. P., & Jeitziner, R. (2015)

Identification of Novel HIF1A Target Genes That Regulate Tumor Progression and Metastasis

Peacock, D. L. (2013) · doi:10.21007/etd.cghs.2013.0241

Investigation of the role of bovine mammary stem cells in the lactation cycle

Bowman, S. R. A. (2017) · The Sydney eScholarship Repository (The University of Sydney)

The mammary stem cell field wakes up to hibernating cells

Michalak, E. M. (2017) · Stem Cell Investigation · doi:10.21037/sci.2017.04.08

Adult Prostate Stem Cells

Lawrence, M. G., Toivanen, R., Takizawa, I., Gargett, C. E., & Risbridger, G. P. (2013) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4614-9569-7_11

The ninth ENBDC Weggis meeting: growth and in-depth characterisation of normal and neoplastic breast cells

Wiese, K. E., Amante, R. J., Vivanco, M. D., Bentires‐Alj, M., & Iggo, R. D. (2017) · Breast Cancer Research · doi:10.1186/s13058-017-0891-9

Fundamental Pathways in Breast Cancer 4: Signaling to Chromatin in Breast Development

Mazzarella, L., & Pelicci, P. G. (2017) · Springer eBooks · doi:10.1007/978-3-319-48848-6_4

Genetic Analysis of Gata3 and Runx1 in Mammary Tumor Formation

Kusdaya, N. A. (2015) · TSpace (University of Toronto)

Efecto de la frecuencia diaria de ordeño sobre la producción y composición de la leche y el estado sanitario de la ubre en ovejas de la raza Assaf: interacción con el nivel de producción y el aporte de vitamina E y selenio = Effect of milking frecuency on milk yield, milk composition and udder health in assaf ewes: interaction with the level of production and vitamin E and selenium supplementation

Chávez, E. E. P. (2017) · doi:10.18002/10612/6913

All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration

Botchkarev, V. A., Sharov, A. A., & Fessing, M. Y. (2018) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-16769-5_1

The Role of Notch in Breast Cancer

Bloodworth, J. C., & Osipo, C. (2018) · Springer eBooks · doi:10.1007/978-1-4939-8859-4_9

Molecular Dissection of Breast Luminal Transcription Networks

Bargiacchi, F. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/yxsj-a431

The effect of alcohol consumption on mammary epithelial cell composition and mammary tumorigenesis

Datar, K. R. (2019) · doi:10.7282/t3-f46z-6662

Inhibitor of Differentiation 4 (ID4) represses myoepithelial differentiation of mammary stem cells through its interaction with HEBPreprint

Holliday, H., Roden, D., Junankar, S., Wu, S. Z., Baker, L. A., Krisp, C., Chan, C.-L., McFarland, A., Skhinas, J. N., Cox, T. R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.06.026963

Mammary stem cells and their niche during aging

Broome, L. E., Bouamar, H., & Sun, L. (2020) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2020.05.003

In vivo Mouse Mammary Gland Formation

Sun, H., Zhang, X., Chan, U., Su, S., Guo, S., Xu, X., & Deng, C. (2020) · BIO-PROTOCOL · doi:10.21769/bioprotoc.3667

Identifying Molecular Mechanisms of Progesterone-responsive Mammary Stem Cell Expansion

Shiah, Y.-J. (2014) · TSpace (University of Toronto)

Early Dietary Exposures Epigenetically Program Mammary Cancer Susceptibility through IGF1-mediated Expansion of Mammary Stem CellsPreprint

Zheng, Y., Luo, L., Lambertz, I. U., & Fuchs‐Young, R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.15.383570

Commercial Artificial Sweeteners Might Affect Pregnant and Nursing Mice Mammary Gland. A Histological Study

Al-Hasan, M. M., & Al-Qudsi, F. (2020) · Journal of Biosciences and Medicines · doi:10.4236/jbm.2020.812010

Lineage-restricted Metabolic Identities of Mammary Epithelial Cells

Mahendralingam, M. J. (2019) · TSpace (University of Toronto)

Single-Cell Transcriptomic Analysis of Mammary Tumors Reveals Distinct Patterns of Hierarchical and Subtype HeterogeneityPreprint

Yeo, S. K., Zhu, X., Okamoto, T., Hao, M., Lu, L. J., & Guan, J. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3316799

Application of Genomic and Epigenomic Methods to Understand Environmental and Dietary Factors in Carcinogenesis.

Colacino, J. A. (2014) · Deep Blue (University of Michigan)

Transcription Factor RFX3 Stabilizes Mammary Basal Cell IdentityPreprint

Tross, E. M., de Caestecker, C. R., Lau, K. S., & Macara, I. G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.13.472491

Potential of Stem Cell Therapy to Combat Mastitis in Dairy Animals

Sharma, N., Devi, S., & Bačić, G. (2021) · Springer eBooks · doi:10.1007/978-981-16-3464-2_5

Orthotopic Transplantation of Mouse Mammary Epithelial Cells

Faraldo, M. M., Glukhova, M. A., & Deugnier, M. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2193-6_6

Lineage Tracing Methods to Study Mammary Epithelial Hierarchies In Vivo

Rodilla, V., & Fré, S. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2193-6_7 · Cited by 2

Faculty Opinions recommendation of Adipocyte hypertrophy and lipid dynamics underlie mammary gland remodeling after lactation.

Macotela, Y. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733951455.793558172

Faculty Opinions recommendation of Myoepithelial cells are a dynamic barrier to epithelial dissemination.

Akhtar, N. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733711378.793576912

Quantification of Self-renewal in Murine Mammosphere Cultures

Vlachou, T., Xieraili, A., D’Elia, E., Santoro, A., Moroni, M. C., & Pelicci, P. G. (2019) · Journal of Visualized Experiments · doi:10.3791/60256-v

Data from Basal but not Luminal Mammary Epithelial Cells Require PI3K/mTOR Signaling for Ras-Driven Overgrowth

Plichta, K. A., Mathers, J. L., Gestl, S. A., Glick, A. B., & Gunther, E. J. (2023) · doi:10.1158/0008-5472.c.6504017.v1

Data from Novel Mouse Models of Bladder Cancer Identify a Prognostic Signature Associated with Risk of Disease Progression

Park, S., Rong, L., Owczarek, T. B., Bernardo, M. D., Shoulson, R. L., Chua, C. W., Kim, J. Y., Lankarani, A., Chakrapani, P., Syed, T., et al. (2023) · doi:10.1158/0008-5472.c.6513832.v1

Avaliação de quimiocinas circulantes em pacientes com câncer de mama, o ardiloso luminal b e as misteriosas quimiocinas

Araújo, R. (2023) · doi:10.14393/ufu.te.2022.586

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