Paper · 15535842
Role of Notch signaling in cell-fate determination of human mammary stem/progenitor cells.
Dontu G and 5 others. Breast Cancer Res, 2004. Cited by 581 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Role of Notch signaling in cell-fate determination of human mammary stem/progenitor cells. Papers, record 15535842. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/15535842
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Role of Notch signaling in cell-fate determination of human mammary stem/progenitor cells.
- PubMed
Topics15
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Mammary Glands, Human | Major topic |
| Proto-Oncogene Proteins | Major topic |
| Receptors, Cell Surface | Major topic |
| Stem Cells | Major topic |
| Transcription Factors | Major topic |
| Cell Differentiation | |
| Cells, Cultured | |
| Epithelial Cells | |
| Female | |
| Humans | |
| Proto-Oncogene Mas | |
| Receptor, Notch1 | |
| Receptor, Notch4 | |
| Receptors, Notch | |
| Signal Transduction |
Source PubMed
Grants4
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
| Grant, as the record writes it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| R01 CA101860 | NCI NIH HHS | United States | R01CA101860 | PubMed and NIH | NIH RePORTER |
| 5 P 30 CA46592 | NCI NIH HHS | United States | P30CA046592 | PubMed and NIH | NIH RePORTER |
| CA101860 | NCI NIH HHS | United States | R01CA101860 | PubMed and NIH | NIH RePORTER |
| CA66233 | NCI NIH HHS | United States | PubMed | PubMed |
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References38
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 10,557,086 | Involvement of Notch1 in the development of mouse mammary tumors. | Oncogene | 1999 | https://conductscience.org/library/papers/10557086 | PubMed |
| 2 | 10,528,225 | Arbiter of differentiation and death: Notch signaling meets apoptosis. | J Cell Physiol | 1999 | https://conductscience.org/library/papers/10528225 | PubMed |
| 3 | 10,645,000 | Identification of a novel NOTCH-4/INT-3 RNA species encoding an activated gene product in certain human tumor cell lines. | Oncogene | 2000 | https://conductscience.org/library/papers/10645000 | PubMed |
| 4 | 10,797,286 | Expression of an activated Notch4(int-3) oncoprotein disrupts morphogenesis and induces an invasive phenotype in mammary epithelial cells in vitro. | Int J Cancer | 2000 | https://conductscience.org/library/papers/10797286 | PubMed |
| 5 | 10,837,027 | Notch signaling is essential for vascular morphogenesis in mice. | Genes Dev | 2000 | https://conductscience.org/library/papers/10837027 | PubMed |
| 6 | 10,850,492 | Transient Notch activation initiates an irreversible switch from neurogenesis to gliogenesis by neural crest stem cells. | Cell | 2000 | https://conductscience.org/library/papers/10850492 | PubMed |
| 7 | 10,882,062 | A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1. | Mol Cell | 2000 | https://conductscience.org/library/papers/10882062 | PubMed |
| 8 | 10,980,592 | Ras pathway signals are required for notch-mediated oncogenesis. | Oncogene | 2000 | https://conductscience.org/library/papers/10980592 | PubMed |
| 9 | 11,010,805 | Notch signaling: a dance of proteins changing partners. | Exp Cell Res | 2000 | https://conductscience.org/library/papers/11010805 | PubMed |
| 10 | 11,182,080 | Notch1 and Notch3 instructively restrict bFGF-responsive multipotent neural progenitor cells to an astroglial fate. | Neuron | 2001 | https://conductscience.org/library/papers/11182080 | PubMed |
1 to 10 of 38
See all 38 referencesCited by379
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 581 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,974,381 | Astrocyte plasticity shapes brain metastasis progression through tumor-astrocyte crosstalk. | Cancer Heterog Plast | 2025 | https://conductscience.org/library/papers/42974381 | PubMed |
| 42,426,902 | Cancer stem cell plasticity: mechanisms, immune microenvironment crosstalk, and therapeutic implications. | J Hematol Oncol | 2026 | https://conductscience.org/library/papers/42426902 | PubMed |
| 41,206,509 | The Glyco-Switch of life: O-GlcNAcylation in cell fate decision. | Glycobiology | 2025 | https://conductscience.org/library/papers/41206509 | PubMed |
| 41,027,955 | Role of Notch gene receptors as prognostic biomarkers in colorectal cancer. | Sci Rep | 2025 | https://conductscience.org/library/papers/41027955 | PubMed |
| 40,733,561 | The Gene Expression Profile of Milk Somatic Cells of Small Ruminant Lentivirus-Seropositive and -Seronegative Dairy Goats (Capra hircus) During Their First Lactation. | Viruses | 2025 | https://conductscience.org/library/papers/40733561 | PubMed |
| 40,080,721 | Signaling pathway dysregulation in breast cancer. | Oncotarget | 2025 | https://conductscience.org/library/papers/40080721 | PubMed |
| 40,006,075 | Drug Treatment Direction Based on the Molecular Mechanism of Breast Cancer Brain Metastasis. | Pharmaceuticals (Basel) | 2025 | https://conductscience.org/library/papers/40006075 | PubMed |
| 40,003,637 | Notch and Hedgehog Signaling Unveiled: Crosstalk, Roles, and Breakthroughs in Cancer Stem Cell Research. | Life (Basel) | 2025 | https://conductscience.org/library/papers/40003637 | PubMed |
| 39,940,912 | Mutanobactin-D, a Streptococcus mutans Non-Ribosomal Cyclic Lipopeptide, Induces Osteogenic/Odontogenic Differentiation of Human Dental Pulp Stem Cells and Human Bone Marrow Stem Cells. | Int J Mol Sci | 2025 | https://conductscience.org/library/papers/39940912 | PubMed |
| 39,853,518 | Targeting breast cancer stem cells in ER-positive breast cancer by repurposing the benzoporphyrin derivative verteporfin as a YAP/TAZ small molecule inhibitor. | Mol Biol Rep | 2025 | https://conductscience.org/library/papers/39853518 | PubMed |
1 to 10 of 379
See all 379 cited byGenes9
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| DLK1 | 8,788 | PubTator's text mining | https://conductscience.org/library/genes/8788 | NCBI Gene |
| EPCAM | 4,072 | PubTator's text mining | https://conductscience.org/library/genes/4072 | NCBI Gene |
| HES1 | 3,280 | PubTator's text mining | https://conductscience.org/library/genes/3280 | NCBI Gene |
| KRT14 | 3,861 | PubTator's text mining | https://conductscience.org/library/genes/3861 | NCBI Gene |
| KRT18 | 3,875 | PubTator's text mining | https://conductscience.org/library/genes/3875 | NCBI Gene |
| MME | 4,311 | PubTator's text mining | https://conductscience.org/library/genes/4311 | NCBI Gene |
| MUC1 | 4,582 | PubTator's text mining | https://conductscience.org/library/genes/4582 | NCBI Gene |
| NOTCH1 | 4,851 | PubTator's text mining | https://conductscience.org/library/genes/4851 | NCBI Gene |
| NOTCH4 | 4,855 | PubTator's text mining | https://conductscience.org/library/genes/4855 | NCBI Gene |
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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