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Andrea V. Cantú

Researcher at University of California, San Francisco

Publications -  12
Citations -  733

Andrea V. Cantú is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Wnt signaling pathway & Embryonic stem cell. The author has an hindex of 9, co-authored 12 publications receiving 664 citations. Previous affiliations of Andrea V. Cantú include Stanford University & University of Texas Medical Branch.

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Influence of Acellular Natural Lung Matrix on Murine Embryonic Stem Cell Differentiation and Tissue Formation

TL;DR: It is found that AC lung allowed for better retention of cells with more differentiation of mESCs into epithelial and endothelial lineages and highlights the critical role played by matrix or scaffold-associated cues in guiding ESC differentiation toward lung-specific lineages.
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In vitro analog of human bone marrow from 3D scaffolds with biomimetic inverted colloidal crystal geometry.

TL;DR: The development of an in vitro artificial bone marrow based on a 3D scaffold with inverted colloidal crystal (ICC) geometry mimicking the structural topology of actual bone marrow matrix being shown to be critical for production of B cells and antigen-specific antibodies is reported.
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Neurogenic and neuro-protective potential of a novel subpopulation of peripheral blood-derived CD133+ ABCG2+CXCR4+ mesenchymal stem cells: development of autologous cell-based therapeutics for traumatic brain injury

TL;DR: Results suggest that PBD CD133+ABCG2+CXCR4+ MSCs have the potential for development as an autologous treatment for TBI and neurodegenerative disorders and that MSC derived cell products produced immediately after transplantation may aid in reducing the immediate cognitive defects of TBI.
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Stereotypical alterations in cortical patterning are associated with maternal illness-induced placental dysfunction.

TL;DR: Maternal illness during this period selectively alters the abundance and laminar positioning of neuronal subtypes influenced by the Tbr1, Satb2, and Ctip2/Fezf2 patterning axis and is sufficient to cause changes in social behavior and cognition in the adult.
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Discrete somatic niches coordinate proliferation and migration of primordial germ cells via Wnt signaling

TL;DR: It is shown that somatic cell microenvironments modulate germ cell proliferation via canonical Wnt signaling, whereas noncanonical Wnt5a–Ror2 signaling reciprocally promotes migration.