FERNANDEZ-VIZARRA BAILEY, ERIKA MARIA

FERNANDEZ-VIZARRA BAILEY, ERIKA MARIA  

Dipartimento di Scienze Biomediche - DSB  

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Risultati 1 - 20 di 67 (tempo di esecuzione: 0.029 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly 2020 Fernandez-Vizarra, ErikaTrani, GiuliaZeviani, Massimo + NEUROBIOLOGY OF DISEASE - -
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS 2019 Cerutti, RaffaeleViscomi, CarloFernandez-Vizarra, ErikaZeviani, Massimo + EMBO MOLECULAR MEDICINE - -
Assembly of mammalian oxidative phosphorylation complexes I-V and supercomplexes 2018 Fernandez-Vizarra, Erika + ESSAYS IN BIOCHEMISTRY - -
Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects 2009 Fernández-Vizarra, ErikaZeviani, Massimo + BIOCHIMICA ET BIOPHYSICA ACTA - -
Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution 2020 Fernández-Vizarra, ErikaZeviani, Massimo + MOLECULAR GENETICS AND METABOLISM - -
Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET 2020 Szibor, MartenFernandez-Vizarra, ErikaViscomi, CarloMoore, Anthony L + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
Blue-Native Electrophoresis to Study the OXPHOS Complexes 2021 Fernandez-Vizarra, ErikaZeviani, Massimo - METHODS IN MOLECULAR BIOLOGY Mitochondrial Gene Expression. Methods and Protocols
Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian Boy 2018 Fernandez-Vizarra, ErikaZeviani, Massimo + JOURNAL OF CHILD NEUROLOGY - -
CEDAR, an online resource for the reporting and exploration of complexome profiling data 2021 Fernandez-Vizarra, Erika + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B 2022 Brischigliaro, MicheleSturlese, MattiaFrigo, ElenaFernandez-Vizarra, ErikaMoro, StefanoViscomi, CarloZeviani, Massimo + EMBO REPORTS - -
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency 2016 Fernandez-Vizarra, ErikaZeviani, Massimo + EJMG - -
Cooperative assembly of the mitochondrial respiratory chain 2022 Fernández-Vizarra, Erika + TRENDS IN BIOCHEMICAL SCIENCES - -
COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation 2016 Fernández-Vizarra, Erika + CELL REPORTS - -
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration 2016 Fernandez-Vizarra, ErikaCerutti, RaffaeleD'Amati, GiuliaViscomi, CarloZeviani, Massimo + EMBO MOLECULAR MEDICINE - -
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defects 2021 Zeviani, MassimoFernández-Vizarra, Erika + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice 2009 Viscomi, CarloFernandez-Vizarra, ErikaPagano, ClaudioVettor, RobertoZeviani, Massimo + HUMAN MOLECULAR GENETICS ONLINE - -
Editorial: Mitochondrial OXPHOS System: Emerging Concepts and Technologies and Role in Disease 2022 Fernández-Vizarra, Erika + FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY - -
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 2016 Fernandez-Vizarra, ErikaZeviani, MassimoMari, Francesca + MOLECULAR GENETICS AND METABOLISM - -
FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency 2008 Fernandez-Vizarra, ErikaZeviani, Massimo + AMERICAN JOURNAL OF HUMAN GENETICS - -
Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly 2010 Fernández-Vizarra, Erika + MOLECULAR AND CELLULAR BIOLOGY - -