Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Maria Antonietta Calvaruso"'
Autor:
Ivana Kurelac, Mariantonietta Capristo, Anna Ghelli, Carla De Giovanni, Anna Maria Porcelli, Maria Antonietta Calvaruso, Christian Bergamini, Giuseppe Gasparre, Romana Fato, Pier Luigi Lollini, Michela Rugolo, Luisa Iommarini, Valerio Carelli, Valentina Giorgio, Patrizia Nanni
Publikováno v:
Human Molecular Genetics. 23:1453-1466
Mitochondrial DNA mutations are currently investigated as modifying factors impinging on tumor growth and aggressiveness, having been found in virtually all cancer types and most commonly affecting genes encoding mitochondrial complex I subunits. How
Autor:
Barbara Cannon, Nils-Göran Larsson, Aleksandra Trifunovic, Jan Nedergaard, Maria Antonietta Calvaruso, Anna Wredenberg, Daniel Edgar, Yolanda Cámara, Irina G. Shabalina, Leo Nijtmans
Publikováno v:
Cell Metab
Cell Metabolism, 10, 131-8
Cell Metabolism, 10, 2, pp. 131-8
Cell Metabolism, 10, 131-8
Cell Metabolism, 10, 2, pp. 131-8
Contains fulltext : 81777.pdf (Publisher’s version ) (Closed access) The mtDNA mutator mice have high levels of point mutations and linear deletions of mtDNA causing a progressive respiratory chain dysfunction and a premature aging phenotype. We ha
Autor:
Michela Rugolo, Vera De Nardo, Giuseppe Gasparre, Ivana Kurelac, Anna Maria Porcelli, Flemming Wibrand, Claudia Zanna, John Vissing, Andrea Martinuzzi, Anna Ghelli, Maria Antonietta Calvaruso, Alessandra Marchesini, Nur Selamoglu, Fevzi Daldal, Concetta Valentina Tropeano, Luisa Iommarini
Cytochrome b is the only mtDNA-encoded subunit of the mitochondrial complex III (CIII), the functional bottleneck of the respiratory chain. Previously, the human cytochrome b missense mutation m.15579A>G, which substitutes the Tyr 278 with Cys (p.278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e289c7ab6ee8b2863c6d5dc087ab2bcc
http://hdl.handle.net/11585/133718
http://hdl.handle.net/11585/133718
Autor:
Ivana Kurelac, Maria Antonietta Calvaruso, Luisa Iommarini, Anna Maria Porcelli, Giuseppe Gasparre
Respiratory chain complex I (CI) dysfunctions have been recognized as one of the most frequent causes of mitochondrial neuro-muscular disorders. Moreover, latest reports reveal that CI impairment is a major contributing factor in many other pathologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37d53134670f97a152a0dcc641d7effa
http://hdl.handle.net/11585/116356
http://hdl.handle.net/11585/116356
Autor:
Clara Musicco, +*a Antonella Cormio, b Maria Antonietta Calvaruso, c Luisa Iommarini, c Giuseppe Gasparre, d Anna Maria Porcelli, ce Anna Maria Timperio, f Lello Zolla, f, Maria Nicola Gadaleta
Publikováno v:
Molecular bioSystems
info:cnr-pdr/source/autori:Clara Musicco,+*a Antonella Cormio,b Maria Antonietta Calvaruso,c Luisa Iommarini,c Giuseppe Gasparre,d Anna Maria Porcelli,ce Anna Maria Timperio,f Lello Zolla,f and Maria Nicola Gadaleta,ab/titolo:Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I./doi:10.1039%2FC3MB70542K/rivista:Molecular bioSystems (Print)/anno:2014/pagina_da:1313/pagina_a:1319/intervallo_pagine:1313–1319/volume:10
info:cnr-pdr/source/autori:Clara Musicco,+*a Antonella Cormio,b Maria Antonietta Calvaruso,c Luisa Iommarini,c Giuseppe Gasparre,d Anna Maria Porcelli,ce Anna Maria Timperio,f Lello Zolla,f and Maria Nicola Gadaleta,ab/titolo:Analysis of Mitochondrial Proteome of Cybrid Cells Harbouring a Truncative Mitochondrial DNA Mutation in Respiratory Complex I./doi:10.1039%2FC3MB70542K/rivista:Molecular bioSystems (Print)/anno:2014/pagina_da:1313/pagina_a:1319/intervallo_pagine:1313–1319/volume:10
Transmitochondrial cytoplasmic hybrids (cybrids) are well established model systems to reveal the effects of mitochondrial DNA (mtDNA) mutations on cell metabolism excluding the interferences of a different nuclear background. The m.3571insC mutation
Autor:
Jan A.M. Smeitink, Leo G.J. Nijtmans, Federica Valsecchi, Richard D. Palmiter, Peter H.G.M. Willems, Maria Antonietta Calvaruso, Shane E. Kruse, Mariël A.M. van den Brand
Publikováno v:
Human Molecular Genetics, 21, 115-20
Human Molecular Genetics, 21, 1, pp. 115-20
Human Molecular Genetics, 21, 1, pp. 115-20
Item does not contain fulltext Mitochondrial complex I (CI) is a multi-subunit enzyme that forms the major entry point of nicotinamide adenine dinucleotide (NADH) electrons into the respiratory chain. Mutations in the NDUFS4 gene, encoding an accesso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74405bc1f72fda60829f1de34d2edec
http://hdl.handle.net/2066/108687
http://hdl.handle.net/2066/108687
Autor:
Ivana Kurelac, Claudia Zanna, Michela Rugolo, Anna Ghelli, John Vissing, Maria Antonietta Calvaruso, Luisa Iommarini, Fevzi Daldal, V. De Nardo, Giuseppe Gasparre, Andrea Martinuzzi, Anna Maria Porcelli, Nur Selamoglu, Alessandra Marchesini, Concetta Valentina Tropeano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505625399ac795fc16a1a1bc6935646b
http://hdl.handle.net/11585/128968
http://hdl.handle.net/11585/128968
Publikováno v:
A Structural Perspective on Respiratory Complex I ISBN: 9789400741379
Human mitochondrial complex I is one of the biggest membrane bound enzymes found in man. Its assembly is a complicated process and requires the combination of 45 subunits, encoded by the nuclear and mitochondrial genomes. It has become clear that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c469b14eaaafd848fb4fff4c84debf41
https://doi.org/10.1007/978-94-007-4138-6_10
https://doi.org/10.1007/978-94-007-4138-6_10
Autor:
Richard J. Rodenburg, Maria Antonietta Calvaruso, Leo G.J. Nijtmans, Jan A.M. Smeitink, Michèl A.A.P. Willemsen, Mariël A.M. van den Brand
Publikováno v:
Mitochondrion, 11, 5, pp. 778-82
Mitochondrion, 11, 778-82
Mitochondrion, 11, 778-82
Contains fulltext : 97157.pdf (Publisher’s version ) (Closed access) We report a new mutation in m.12146 A>G in the mt-tRNA(His) in a family with a remarkable clinical history having different degrees of lactic acidosis and stroke-like episodes. Bi
Autor:
Fevzi Daldal, Leonardo Caporali, Anna Ghelli, Maria Antonietta Calvaruso, Michela Rugolo, Concetta Valentina Tropeano, Valerio Carelli
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837:e52-e53