Sabrina Dusi

Via Adamello 16
Milan, 20139, Italy

Last Updated: 09/26/2026

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Found 18 publications

Rad51-mediated replication of damaged templates relies on monoSUMOylated DDK kinase.

Rad51-mediated replication of damaged templates relies on monoSUMOylated DDK kinase.

Journal: Nature communications
Published: January 24, 2022

Parental histone deposition on the replicated strands promotes error-free DNA damage tolerance and regulates drug resistance.

Parental histone deposition on the replicated strands promotes error-free DNA damage tolerance and regulates drug resistance.

Journal: Genes & development
Published: November 15, 2021

Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene.

Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene.

Journal: Mitochondrion
Published: June 18, 2018

TiO2-coated luminescent porous silicon micro-particles as a promising system for nanomedicine.

TiO2-coated luminescent porous silicon micro-particles as a promising system for nanomedicine.

Journal: Journal of materials chemistry. B
Published: March 28, 2018

AND-1 fork protection function prevents fork resection and is essential for proliferation.

AND-1 fork protection function prevents fork resection and is essential for proliferation.

Journal: Nature communications
Published: January 15, 2018

Platinum-induced mitochondrial DNA mutations confer lower sensitivity to paclitaxel by impairing tubulin cytoskeletal organization.

Platinum-induced mitochondrial DNA mutations confer lower sensitivity to paclitaxel by impairing tubulin cytoskeletal organization.

Journal: Human molecular genetics
Published: February 28, 2017

Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration.

Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration.

Journal: EMBO molecular medicine
Published: August 13, 2016

Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts.

Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts.

Journal: Acta neuropathologica communications
Published: April 23, 2016

Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism.

Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism.

Journal: Microbial cell (Graz, Austria)
Published: April 06, 2015

Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients.

Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients.

Journal: Neurobiology of disease
Published: December 05, 2014

COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency.

COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency.

Journal: American journal of human genetics
Published: November 20, 2014

Orange and blue luminescence emission to track functionalized porous silicon microparticles inside the cells of the human immune system.

Orange and blue luminescence emission to track functionalized porous silicon microparticles inside the cells of the human immune system.

Journal: Journal of materials chemistry. B
Published: October 07, 2014
Showing 1-12 of 18

Last Updated: 09/26/2026