scispace - formally typeset
C

Christina DeCoste

Researcher at Princeton University

Publications -  13
Citations -  1639

Christina DeCoste is an academic researcher from Princeton University. The author has contributed to research in topics: Stem cell & Wnt signaling pathway. The author has an hindex of 9, co-authored 13 publications receiving 1465 citations.

Papers
More filters
Journal ArticleDOI

Dissecting self-renewal in stem cells with RNA interference

TL;DR: This work uses short hairpin RNA (shRNA) loss-of-function techniques to downregulate a set of gene products whose expression patterns suggest self-renewal regulatory functions, and focuses on transcriptional regulators and identifies seven genes for which shRNA-mediated depletion negatively affects self-Renewal.
Journal ArticleDOI

ΔNp63 promotes stem cell activity in mammary gland development and basal-like breast cancer by enhancing Fzd7 expression and Wnt signalling

TL;DR: It is shown that the ΔNp63 isoform of the Trp63 transcription factor promotes normal mammary stem cell activity by increasing the expression of the Wnt receptor Fzd7, thereby enhancing Wnt signalling and governs tumour-initiating activity of the basal subtype of breast cancer.
Journal ArticleDOI

Notch ligand Dll1 mediates cross-talk between mammary stem cells and the macrophageal niche

TL;DR: Dll1cKO mice have a reduced number of MaSCs at different stages of mammary gland development in virgin and pregnant animals, and it is demonstrated that Dll1+ Ma SCs can both basal and luminal cells generate the important cellular components of the Mammary gland stem cell niche through inter-turning.
Journal ArticleDOI

Elf5 regulates mammary gland stem/progenitor cell fate by influencing notch signaling.

TL;DR: It is demonstrated that in addition to regulating terminal differentiation of alveolar cells, Elf5 also plays a critical role in determining cell fate and in regulating the stem/progenitor function of the mammary epithelium.
Journal ArticleDOI

Normal and cancerous mammary stem cells evade interferon-induced constraint through the miR-199a–LCOR axis

TL;DR: It is shown that miR-199a promotes stem cell properties in mammary stem cells and breast CSCs by directly repressing nuclear receptor corepressor LCOR, which primes interferon (IFN) responses.