CERQUA, CRISTINA

CERQUA, CRISTINA  

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Risultati 1 - 11 di 11 (tempo di esecuzione: 0.023 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome. 2017 CASSINA, MATTEOCERQUA, CRISTINASALVIATI, LEONARDOMARTINI, ALESSANDROCLEMENTI, MAURIZIOTREVISSON, EVA + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Age-Associated Loss of OPA1 in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence 2017 TEZZE, CATERINAROMANELLO, VANINADESBATS, MARIA ANDREAFADINI, GIAN PAOLOALBIERO, MATTIAFAVARO, GIULIACICILIOT, STEFANOSORIANO GARCIA - CUERVA, MARIA EUGENIAMORBIDONI, VALERIACERQUA, CRISTINABLAAUW, BERTZAMPIERI, SANDRASALVIATI, LEONARDOSCORRANO, LUCASANDRI, MARCO + CELL METABOLISM - -
Ambra1 deficiency impairs mitophagy in skeletal muscle 2022 Gambarotto, LisaMetti, SamueleChrisam, MartinaCerqua, CristinaArmani, AndreaSpizzotin, MariannaCastagnaro, SilviaGrumati, PaoloCescon, MatildeBraghetta, PaolaTrevisson, EvaCecconi, FrancescoBonaldo, Paolo + JOURNAL OF CACHEXIA, SARCOPENIA AND MUSCLE - -
Analysis of the interaction of mitochondria and ER with the cytoskeleton : from cellular to animal models 2010 Cerqua, Cristina - - -
Coenzyme Q biosynthesis in health and disease 2016 DESBATS, MARIA ANDREACERQUA, CRISTINAZORDAN, ROBERTATREVISSON, EVASALVIATI, LEONARDO + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2 2018 Cerqua, CristinaMorbidoni, ValeriaDesbats, Maria AndreaDoimo, MaraFrasson, ChiaraBALDOIN, MARIA CRISTINASartori, GeppoBasso, GiuseppeSalviati, LeonardoTrevisson, Eva + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
In mammalian skeletal muscle, phosphorylation of TOMM22 by protein kinase CSNK2/CK2 controls mitophagy. 2017 Romanello VCerqua CSalviati LSandri M + AUTOPHAGY - -
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome 2017 Cerqua, CristinaSartori, GeppoForlino, AntonellaMattevi, AndreaSalviati, LeonardoZuffardi, Orsetta + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function 2018 Doimo, MaraCalderan, CristinaDesbats, Maria AndreaCerqua, CristinaCassina, MatteoSartori, GeppoTrevisson, EvaSalviati, Leonardo + HUMAN MUTATION - -
The Splicing of the Mitochondrial Calcium Uniporter Genuine Activator MICU1 Is Driven by RBFOX2 Splicing Factor during Myogenic Differentiation 2022 Denis Vecellio ReaneCristina CerquaLeonardo SalviatiEva TrevissonAnna Raffaello + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
Vitamin K2 cannot substitute Coenzyme Q(10) as electron carrier in the mitochondrial respiratory chain of mammalian cells 2019 Cerqua C.Viola G.Salviati L.Trevisson E. + SCIENTIFIC REPORTS - -