scispace - formally typeset
M

Maria C. Marchetto

Researcher at Salk Institute for Biological Studies

Publications -  113
Citations -  15382

Maria C. Marchetto is an academic researcher from Salk Institute for Biological Studies. The author has contributed to research in topics: Induced pluripotent stem cell & Neural stem cell. The author has an hindex of 48, co-authored 102 publications receiving 13119 citations. Previous affiliations of Maria C. Marchetto include University of California, San Diego & University of São Paulo.

Papers
More filters
Journal ArticleDOI

Mechanisms underlying inflammation in neurodegeneration.

TL;DR: There is evidence for a remarkable convergence in the mechanisms responsible for the sensing, transduction, and amplification of inflammatory processes that result in the production of neurotoxic mediators in neurodegenerative diseases.
Journal ArticleDOI

A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells

TL;DR: The model recapitulates early stages of a human neurodevelopmental disease and represents a promising cellular tool for drug screening, diagnosis and personalized treatment and provides evidence of an unexplored developmental window, before disease onset, in RTT syndrome.
Journal ArticleDOI

Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition

TL;DR: It is shown that an engineered human LINE-1 element can retrotranspose in neuronal precursors derived from rat hippocampus neural stem cells, indicating that neuronal genomes might not be static, but some might be mosaic because of de novo L1 retrotransposition events.
Journal ArticleDOI

L1 retrotransposition in neurons is modulated by MeCP2

TL;DR: It is shown that L1 neuronal transcription and retrotransposition in rodents are increased in the absence of methyl-CpG-binding protein 2 (MeCP2), a protein involved in global DNA methylation and human neurodevelopmental diseases and which patients with Rett syndrome, carrying MeCP2 mutations, have increased susceptibility for L1 retrotransposons.