Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Eleonora Paradies"'
Autor:
Ruggiero Gorgoglione, Roberta Seccia, Amer Ahmed, Angelo Vozza, Loredana Capobianco, Alessia Lodi, Federica Marra, Eleonora Paradies, Luigi Palmieri, Vincenzo Coppola, Vincenza Dolce, Giuseppe Fiermonte
Publikováno v:
Biomolecules, Vol 13, Iss 5, p 808 (2023)
The human mitochondrial carrier family (MCF) consists of 53 members. Approximately one-fifth of them are still orphans of a function. Most mitochondrial transporters have been functionally characterized by reconstituting the bacterially expressed pro
Externí odkaz:
https://doaj.org/article/dbbce2b9f7c34c37bf9fdd955f3125d4
Autor:
Maria Antonietta Di Noia, Pasquale Scarcia, Gennaro Agrimi, Ohiemi Benjamin Ocheja, Ehtisham Wahid, Isabella Pisano, Eleonora Paradies, Luigi Palmieri, Cataldo Guaragnella, Nicoletta Guaragnella
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5320 (2023)
Mitochondrial RTG (an acronym for ReTroGrade) signaling plays a cytoprotective role under various intracellular or environmental stresses. We have previously shown its contribution to osmoadaptation and capacity to sustain mitochondrial respiration i
Externí odkaz:
https://doaj.org/article/48010e7a9c464daeac536a17bc482248
Autor:
Roberta Seccia, Silvia De Santis, Maria A. Di Noia, Ferdinando Palmieri, Daniela V. Miniero, Raffaele Marmo, Eleonora Paradies, Antonella Santoro, Ciro L. Pierri, Luigi Palmieri, Carlo M. T. Marobbio, Angelo Vozza
Publikováno v:
Journal of Fungi, Vol 8, Iss 8, p 795 (2022)
The yeast mitochondrial transport of GTP and GDP is mediated by Ggc1p, a member of the mitochondrial carrier family. The physiological role of Ggc1p in S. cerevisiae is probably to transport GTP into mitochondria in exchange for GDP generated in the
Externí odkaz:
https://doaj.org/article/aa35e0edf64c447faf9856528a37510b
Autor:
Laura E Newman, Cheng-jing Zhou, Samatha Mudigonda, Alexa L Mattheyses, Eleonora Paradies, Carlo Marya Thomas Marobbio, Richard A Kahn
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99270 (2014)
ARF-like 2 (ARL2) is a member of the ARF family and RAS superfamily of regulatory GTPases, predicted to be present in the last eukaryotic common ancestor, and essential in a number of model genetic systems. Though best studied as a regulator of tubul
Externí odkaz:
https://doaj.org/article/58021e1773014482a3ef7b3b4a51b884
Autor:
Roberta, Seccia, Silvia, De Santis, Maria A, Di Noia, Ferdinando, Palmieri, Daniela V, Miniero, Raffaele, Marmo, Eleonora, Paradies, Antonella, Santoro, Ciro L, Pierri, Luigi, Palmieri, Carlo M T, Marobbio, Angelo, Vozza
Publikováno v:
Journal of fungi (Basel, Switzerland). 8(8)
The yeast mitochondrial transport of GTP and GDP is mediated by Ggc1p, a member of the mitochondrial carrier family. The physiological role of Ggc1p in
Autor:
Sahar Al-Mahdawi, Mark A. Pook, Giuseppe Merla, Nunzio Denora, Franco Taroni, Valentina Loira Villalobos Coa, Carlo M.T. Marobbio, L. Palmieri, Vito Porcelli, Mara Perrone, Sara Anjomani Virmouni, Mee Khoo, Eleonora Paradies, Angelo Vozza, Antonella Santoro
Publikováno v:
Human molecular genetics online (2018). doi:10.1093/hmg/ddy016
info:cnr-pdr/source/autori:Santoro, Antonella; Anjomani Virmouni, Sara; Paradies, Eleonora; Villalobos Coa, Valentina L; Al-Mahdawi, Sahar; Khoo, Mee; Porcelli, Vito; Vozza, Angelo; Perrone, Mara; Denora, Nunzio; Taroni, Franco; Merla, Giuseppe; Palmieri, Luigi; Pook, Mark A; Marobbio, Carlo M T/titolo:Effect Of Diazoxide on Friedreich Ataxia Models./doi:10.1093%2Fhmg%2Fddy016/rivista:Human molecular genetics online/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Santoro, Antonella; Anjomani Virmouni, Sara; Paradies, Eleonora; Villalobos Coa, Valentina L; Al-Mahdawi, Sahar; Khoo, Mee; Porcelli, Vito; Vozza, Angelo; Perrone, Mara; Denora, Nunzio; Taroni, Franco; Merla, Giuseppe; Palmieri, Luigi; Pook, Mark A; Marobbio, Carlo M T/titolo:Effect Of Diazoxide on Friedreich Ataxia Models./doi:10.1093%2Fhmg%2Fddy016/rivista:Human molecular genetics online/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume
This is a pre-copyedited, author-produced version of an article accepted for publication in Human Molecular Genetics following peer review. The version of record Antonella Santoro, Sara Anjomani Virmouni, Eleonora Paradies, Valentina L Villalobos Coa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3013d2b2d959d8c034477682084ac4b7
http://bura.brunel.ac.uk/handle/2438/16912
http://bura.brunel.ac.uk/handle/2438/16912
Autor:
Renzo Guerrini, Luna Laera, Sergio Giannattasio, Eleonora Paradies, Carlo M.T. Marobbio, Maria Anna Donati, Luigi Palmieri, Vito Porcelli, Eleonora Lamantea, Alessandra Castegna, Faruk Hossain, Alessio Menga, Anna De Grassi, Ciro Leonardo Pierri, Pasquale Scarcia, Francesco M. Lasorsa, Ruggiero Gorgoglione, Daniele Ghezzi, Isabella Pisano, Valeria Tiranti, Giuseppe Punzi, Matteo Ruggiu, Ferdinando Palmieri
Publikováno v:
Human molecular genetics
27 (2018): 499–504. doi:10.1093/hmg/ddx419
info:cnr-pdr/source/autori:Punzi, Giuseppe; Porcelli, Vito; Ruggiu, Matteo; Hossain, Md F; Menga, Alessio; Scarcia, Pasquale; Castegna, Alessandra; Gorgoglione, Ruggiero; Pierri, Ciro L; Laera, Luna; Lasorsa, Francesco M; Paradies, Eleonora; Pisano, Isabella; Marobbio, Carlo M T; Lamantea, Eleonora; Ghezzi, Daniele; Tiranti, Valeria; Giannattasio, Sergio; Donati, Maria A; Guerrini, Renzo; Palmieri, Luigi; Palmieri, Ferdinando; De Grassi, Anna/titolo:SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency./doi:10.1093%2Fhmg%2Fddx419/rivista:Human molecular genetics (Print)/anno:2018/pagina_da:499/pagina_a:504/intervallo_pagine:499–504/volume:27
27 (2018): 499–504. doi:10.1093/hmg/ddx419
info:cnr-pdr/source/autori:Punzi, Giuseppe; Porcelli, Vito; Ruggiu, Matteo; Hossain, Md F; Menga, Alessio; Scarcia, Pasquale; Castegna, Alessandra; Gorgoglione, Ruggiero; Pierri, Ciro L; Laera, Luna; Lasorsa, Francesco M; Paradies, Eleonora; Pisano, Isabella; Marobbio, Carlo M T; Lamantea, Eleonora; Ghezzi, Daniele; Tiranti, Valeria; Giannattasio, Sergio; Donati, Maria A; Guerrini, Renzo; Palmieri, Luigi; Palmieri, Ferdinando; De Grassi, Anna/titolo:SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency./doi:10.1093%2Fhmg%2Fddx419/rivista:Human molecular genetics (Print)/anno:2018/pagina_da:499/pagina_a:504/intervallo_pagine:499–504/volume:27
Mitochondrial diseases are a plethora of inherited neuromuscular disorders sharing defects in mitochondrial respiration, but largely different from one another for genetic basis and pathogenic mechanism. Whole exome sequencing was performed in a fami
Autor:
Eleonora Paradies, Arupa Ganguly, Linda Steinkrauss, Diva D. De León, Jose Bernardo Quintos, Ferdinando Palmieri, Lisa Swartz Topor, Kara E. Boodhansingh, Charles A. Stanley, Fiermonte Giuseppe, Christine T. Ferrara
Publikováno v:
The Journal of clinical endocrinology and metabolism 102 (2017): 942–949. doi:10.1210/jc.2016-3164
info:cnr-pdr/source/autori:Ferrara C.T.; Boodhansingh K.E.; Paradies E.; Giuseppe F.; Steinkrauss L.J.; Topor L.S.; Quintos J.B.; Ganguly A.; De Leon D.D.; Palmieri F.; Stanley C.A./titolo:Novel hypoglycemia phenotype in congenital hyperinsulinism due to dominant mutations of uncoupling protein 2/doi:10.1210%2Fjc.2016-3164/rivista:The Journal of clinical endocrinology and metabolism/anno:2017/pagina_da:942/pagina_a:949/intervallo_pagine:942–949/volume:102
info:cnr-pdr/source/autori:Ferrara C.T.; Boodhansingh K.E.; Paradies E.; Giuseppe F.; Steinkrauss L.J.; Topor L.S.; Quintos J.B.; Ganguly A.; De Leon D.D.; Palmieri F.; Stanley C.A./titolo:Novel hypoglycemia phenotype in congenital hyperinsulinism due to dominant mutations of uncoupling protein 2/doi:10.1210%2Fjc.2016-3164/rivista:The Journal of clinical endocrinology and metabolism/anno:2017/pagina_da:942/pagina_a:949/intervallo_pagine:942–949/volume:102
Context The rarest genetic form of congenital hyperinsulinism (HI) has been associated with dominant inactivating mutations in uncoupling protein 2 (UCP2), a mitochondrial inner membrane carrier that modulates oxidation of glucose vs amino acids. Obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe310ad587cc954a2f797bd8dc28b125
http://www.cnr.it/prodotto/i/369774
http://www.cnr.it/prodotto/i/369774
Autor:
Pasquale Scarcia, Ferdinando Palmieri, Valeria Mariajolanda Calcagnile, Giuseppe Fiermonte, Luigi Palmieri, Francesco De Leonardis, Daniela Amorese, Daniel Ricquier, Alessandra Castegna, Giovanni Parisi, Eleonora Paradies, Raffaele Marmo, Frédéric Bouillaud, Francesco M. Lasorsa, Angelo Vozza
Publikováno v:
Proceedings of the National Academy of Sciences. 111:960-965
Uncoupling protein 2 (UCP2) is involved in various physiological and pathological processes such as insulin secretion, stem cell differentiation, cancer, and aging. However, its biochemical and physiological function is still under debate. Here we sh
Autor:
Susanna Raho, Giovanni Parisi, Eleonora Paradies, Angelo Vozza, Vincenza Dolce, Luigina Muto, Francesco M. Lasorsa, Anna De Grassi, Giuseppe Fiermonte, Carlo M.T. Marobbio, Loredana Capobianco, Ciro Leonardo Pierri, Francesco De Leonardis
Publikováno v:
Biochimica et biophysica acta. Bioenergetics. 1858(2)
CoA is an essential cofactor that holds a central role in cell metabolism. Although its biosynthetic pathway is conserved across the three domains of life, the subcellular localization of the eukaryotic biosynthetic enzymes and the mechanism behind t