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Massimiliano Caiazzo

Researcher at École Polytechnique Fédérale de Lausanne

Publications -  25
Citations -  2180

Massimiliano Caiazzo is an academic researcher from École Polytechnique Fédérale de Lausanne. The author has contributed to research in topics: Dopaminergic & Reprogramming. The author has an hindex of 13, co-authored 19 publications receiving 1886 citations. Previous affiliations of Massimiliano Caiazzo include Utrecht University & Vita-Salute San Raffaele University.

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Direct generation of functional dopaminergic neurons from mouse and human fibroblasts

TL;DR: A minimal set of three transcription factors were able to elicit dopaminergic neuronal conversion in prenatal and adult fibroblasts from healthy donors and Parkinson’s disease patients and might have significant implications for understanding critical processes for neuronal development, in vitro disease modelling and cell replacement therapies.
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Defined three-dimensional microenvironments boost induction of pluripotency

TL;DR: It is found that the physical cell confinement imposed by the 3D microenvironment boosts reprogramming through an accelerated mesenchymal-to-epithelial transition and increased epigenetic remodelling and it is concluded that 3Dmicroenvironmental signals act synergistically with reprograming transcription factors to increase somatic plasticity.
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Direct Conversion of Fibroblasts into Functional Astrocytes by Defined Transcription Factors

TL;DR: Direct cell reprogramming enables direct conversion of fibroblasts into functional neurons and oligodendrocytes using a minimal set of cell-lineage-specific transcription factors and it is proved both by gene-expression profiling and functional tests that iAstrocytes are comparable to native brain astroCytes.
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Neural tube morphogenesis in synthetic 3D microenvironments

TL;DR: Modular synthetic 3D matrices are used to show that early neural morphogenesis can be precisely controlled by the extracellular microenvironment and demonstrate how key ECM parameters are involved in specifying cytoskeleton-mediated symmetry-breaking events that ultimately lead to neural tube-like patterning along the dorsal–ventral (DV) axis.