Samuele G Marro
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Explore the profile of Samuele G Marro including associated specialties, affiliations and a list of published articles.
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9
Citations
198
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Recent Articles
1.
Salemi S, Baljinnyam E, Liu N, Hu R, Marro S, Webb B
Stem Cell Res
. 2025 Jan;
83:103662.
PMID: 39874649
We have described a novel mitochondrial disorder caused by biallelic pathogenic variants in the methionyl-tRNA synthetase 2 gene (MARS2), now termed Combined oxidative phosphorylation deficiency 25 (COXPD25). This study focuses...
2.
Matera A, Compagnion A, Pedicone C, Kotah J, Ivanov A, Monsorno K, et al.
Immunity
. 2024 Dec;
58(1):197-217.e13.
PMID: 39657671
The gene inositol polyphosphate-5-phosphatase D (INPP5D), which encodes the lipid phosphatase SH2-containing inositol polyphosphate 5-phosphatase 1 (SHIP1), is associated with the risk of Alzheimer's disease (AD). How it influences microglial...
3.
Stewart A, Fulton S, Durand-de Cuttoli R, Thompson R, Chen P, Brindley E, et al.
bioRxiv
. 2024 Sep;
PMID: 39345578
Protein monoaminylation is a class of posttranslational modification (PTM) that contributes to transcription, physiology and behavior. While recent analyses have focused on histones as critical substrates of monoaminylation, the broader...
4.
Durens M, Baljinnyam E, Grisanti L, Hu R, Marro S
Stem Cell Res
. 2024 Jun;
79:103455.
PMID: 38896969
Calcium indicators are sensitive tools to image neural activity. However, their use in human induced pluripotent stem cells (iPSC)-derived neurons is limited by silencing of the transgene. We generated the...
5.
Min A, Javidfar B, Missall R, Doanman D, Durens M, Graziani M, et al.
J Virol
. 2023 Nov;
97(12):e0159523.
PMID: 38032195
Our mouse model is a powerful tool for investigating the genetic mechanisms governing central nervous system (CNS) human immunodeficiency virus type-1 (HIV-1) infection and latency in the CNS at a...
6.
Janas J, Zhang L, Luu J, Demeter J, Meng L, Marro S, et al.
Mol Cell
. 2022 Nov;
82(24):4627-4646.e14.
PMID: 36417913
Cell lineage specification is accomplished by a concerted action of chromatin remodeling and tissue-specific transcription factors. However, the mechanisms that induce and maintain appropriate lineage-specific gene expression remain elusive. Here,...
7.
Raj N, McEachin Z, Harousseau W, Zhou Y, Zhang F, Merritt-Garza M, et al.
Cell Rep
. 2021 Apr;
35(2):108991.
PMID: 33852833
Transcriptional silencing of the FMR1 gene in fragile X syndrome (FXS) leads to the loss of the RNA-binding protein FMRP. In addition to regulating mRNA translation and protein synthesis, emerging...
8.
Nobuta H, Yang N, Ng Y, Marro S, Sabeur K, Chavali M, et al.
Cell Stem Cell
. 2019 Oct;
25(4):531-541.e6.
PMID: 31585094
Pelizaeus-Merzbacher disease (PMD) is an X-linked leukodystrophy caused by mutations in Proteolipid Protein 1 (PLP1), encoding a major myelin protein, resulting in profound developmental delay and early lethality. Previous work...
9.
Marro S, Chanda S, Yang N, Janas J, Valperga G, Trotter J, et al.
Neuron
. 2019 Jul;
103(4):617-626.e6.
PMID: 31257103
The autism-associated synaptic-adhesion gene Neuroligin-4 (NLGN4) is poorly conserved evolutionarily, limiting conclusions from Nlgn4 mouse models for human cells. Here, we show that the cellular and subcellular expression of human...
10.
Zhang Z, Marro S, Zhang Y, Arendt K, Patzke C, Zhou B, et al.
Sci Transl Med
. 2018 Aug;
10(452).
PMID: 30068571
Fragile X syndrome (FXS) is an X chromosome-linked disease leading to severe intellectual disabilities. FXS is caused by inactivation of the fragile X mental retardation 1 () gene, but how...