Literature DB >> 17510790

Disorders of nuclear-mitochondrial intergenomic communication.

Antonella Spinazzola1, Massimo Zeviani.   

Abstract

In the course of evolution, mitochondria lost their independence, and mtDNA became "slave" of nDNA, depending on numerous nucleus-encoded factors for its integrity, replication and expression. Mutations in any of these factors may alter the cross-talk between the two genomes and cause diseases that affect mtDNA integrity or expression, being inherited as mendelian traits.

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Year:  2007        PMID: 17510790     DOI: 10.1007/s10540-007-9036-1

Source DB:  PubMed          Journal:  Biosci Rep        ISSN: 0144-8463            Impact factor:   3.840


  14 in total

Review 1.  A diagnostic algorithm for metabolic myopathies.

Authors:  Andres Berardo; Salvatore DiMauro; Michio Hirano
Journal:  Curr Neurol Neurosci Rep       Date:  2010-03       Impact factor: 5.081

Review 2.  Mitochondrial genome changes and neurodegenerative diseases.

Authors:  Milena Pinto; Carlos T Moraes
Journal:  Biochim Biophys Acta       Date:  2013-11-16

3.  Mitochondrial dysfunction in mut methylmalonic acidemia.

Authors:  Randy J Chandler; Patricia M Zerfas; Sara Shanske; Jennifer Sloan; Victoria Hoffmann; Salvatore DiMauro; Charles P Venditti
Journal:  FASEB J       Date:  2008-12-16       Impact factor: 5.191

4.  Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance.

Authors:  Hasan O Akman; Beatriz Dorado; Luis C López; Angeles García-Cazorla; Maya R Vilà; Lauren M Tanabe; William T Dauer; Eduardo Bonilla; Kurenai Tanji; Michio Hirano
Journal:  Hum Mol Genet       Date:  2008-05-08       Impact factor: 6.150

5.  Mitochondrial transcription factor B2 is essential for metabolic function in Drosophila melanogaster development.

Authors:  Cristina Adán; Yuichi Matsushima; Rosana Hernández-Sierra; Raquel Marco-Ferreres; Miguel Angel Fernández-Moreno; Emiliano González-Vioque; Manuel Calleja; Juan J Aragón; Laurie S Kaguni; Rafael Garesse
Journal:  J Biol Chem       Date:  2008-02-28       Impact factor: 5.157

6.  FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency.

Authors:  Daniele Ghezzi; Ann Saada; Pio D'Adamo; Erika Fernandez-Vizarra; Paolo Gasparini; Valeria Tiranti; Orly Elpeleg; Massimo Zeviani
Journal:  Am J Hum Genet       Date:  2008-09-04       Impact factor: 11.025

7.  A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization.

Authors:  Kieren T Lythgow; Gavin Hudson; Peter Andras; Patrick F Chinnery
Journal:  Mitochondrion       Date:  2010-12-31       Impact factor: 4.160

Review 8.  Cardiological manifestations of mitochondrial respiratory chain disorders.

Authors:  A Berardo; O Musumeci; A Toscano
Journal:  Acta Myol       Date:  2011-06

9.  Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice.

Authors:  Carlo Viscomi; Antonella Spinazzola; Marco Maggioni; Erika Fernandez-Vizarra; Valeria Massa; Claudio Pagano; Roberto Vettor; Marina Mora; Massimo Zeviani
Journal:  Hum Mol Genet       Date:  2008-09-24       Impact factor: 6.150

Review 10.  Mitochondrial genetics.

Authors:  Patrick Francis Chinnery; Gavin Hudson
Journal:  Br Med Bull       Date:  2013-05-22       Impact factor: 4.291

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