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Ziosi, Marcello
72
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Online (72)
Mediatypes
Articles (Online) (20)
OpenAccess-fulltext (52)
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1
The Drosophila TNF Eiger promotes Myc super-competition ind..:
Kodra, Albana L
;
Sharma Singh, Aditi
;
de la Cova, Claire
...
GENETICS. , 2024
Link:
https://doi.org/10.1093/..
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2
COVID-19 Causes Ferroptosis and Oxidative Stress in Human E..:
Jankauskas, Stanislovas S.
;
Kansakar, Urna
;
Sardu, Celestino
...
Antioxidants. 12 (2023) 2 - p. 326 , 2023
Link:
https://doi.org/10.3390/..
?
3
Discovery of target genes and pathways at GWAS loci by pool..:
Morris, John A.
;
Caragine, Christina
;
Daniloski, Zharko
...
Science. 380 (2023) 6646 - p. , 2023
Link:
https://doi.org/10.1126/..
?
4
An autoimmune disease risk variant: A trans master regulato..:
Brandt, Margot
;
Kim-Hellmuth, Sarah
;
Ziosi, Marcello
...
PLOS Genetics. 17 (2021) 7 - p. e1009684 , 2021
Link:
https://doi.org/10.1371/..
?
5
A polyclonal allelic expression assay for detecting regulat..:
Brandt, Margot
;
Gokden, Alper
;
Ziosi, Marcello
.
Genome Medicine. 12 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
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6
Coenzyme Q10 modulates sulfide metabolism and links the mit..:
González-García, Pilar
;
Hidalgo-Gutiérrez, Agustín
;
Mascaraque, Cristina
...
Human Molecular Genetics. 29 (2020) 19 - p. 3296-3311 , 2020
Link:
https://doi.org/10.1093/..
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7
Transcriptomic signatures across human tissues identify fun..:
Ferraro, Nicole M.
;
Strober, Benjamin J.
;
Einson, Jonah
...
Science. 369 (2020) 6509 - p. , 2020
Link:
https://doi.org/10.1126/..
?
8
USMG5 Ashkenazi Jewish founder mutation impairs mitochondri..:
Barca, Emanuele
;
Ganetzky, Rebecca D
;
Potluri, Prasanth
...
Human Molecular Genetics. 27 (2018) 19 - p. 3305-3312 , 2018
Link:
https://doi.org/10.1093/..
?
9
A splice-site mutation in USMG5 causes Leigh Syndrome due t..:
Barca, Emanuele
;
Falgarona, Marti Juanola
;
Emmanuele, Valentina
...
Neurology. 90 (2018) 15_supplement - p. , 2018
Link:
https://doi.org/10.1212/..
?
10
CoQ10 supplementation rescues nephrotic syndrome through no..:
Kleiner, Giulio
;
Barca, Emanuele
;
Ziosi, Marcello
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864 (2018) 11 - p. 3708-3722 , 2018
Link:
https://doi.org/10.1016/..
?
11
Metabolic studies of a patient harbouring a novel S487L mut..:
Arita, Juliana Harumi
;
Barros, Mário H.
;
Ravagnani, Felipe Gustavo
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864 (2018) 5 - p. 1896-1903 , 2018
Link:
https://doi.org/10.1016/..
?
12
Novel recessive mutations in COQ4 cause severe infantile ca..:
Sondheimer, Neal
;
Hewson, Stacy
;
Cameron, Jessie M.
...
Molecular Genetics and Metabolism Reports. 12 (2017) - p. 23-27 , 2017
Link:
https://doi.org/10.1016/..
?
13
Coenzyme Q deficiency causes impairment of the sulfide oxid..:
Ziosi, Marcello
;
Di Meo, Ivano
;
Kleiner, Giulio
...
Neurology. 88 (2017) 16_supplement - p. , 2017
Link:
https://doi.org/10.1212/..
?
14
The Role of Sulfide Oxidation Impairment in the Pathogenesi..:
Quinzii, Catarina M.
;
Luna-Sanchez, Marta
;
Ziosi, Marcello
...
Frontiers in Physiology. 8 (2017) - p. , 2017
Link:
https://doi.org/10.3389/..
?
15
Decreased Coenzyme Q10 Levels in Multiple System Atrophy Ce..:
Barca, Emanuele
;
Kleiner, Giulio
;
Tang, Guomei
...
Journal of Neuropathology & Experimental Neurology. 75 (2016) 7 - p. 663-672 , 2016
Link:
https://doi.org/10.1093/..
1-15