Literature DB >> 17280874

Depletion of mtDNA: syndromes and genes.

Simona Alberio1, Rossana Mineri, Valeria Tiranti, Massimo Zeviani.   

Abstract

Maintenance of mitochondrial DNA (mtDNA) requires the concerted activity of several nuclear-encoded factors that participate in its replication, being part of the mitochondrial replisome or ensuring the balanced supply of dNTPs to mitochondria. In the past decade, a growing number of syndromes associated with dysfunction due to tissue-specific depletion of mtDNA (MDS) have been reported. This article reviews the current knowledge of the genes responsible for these disorders, the impact of different mutations in the epidemiology of MDS and their role in the pathogenic mechanisms underlying the different clinical presentations.

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Year:  2006        PMID: 17280874     DOI: 10.1016/j.mito.2006.11.010

Source DB:  PubMed          Journal:  Mitochondrion        ISSN: 1567-7249            Impact factor:   4.160


  30 in total

1.  Succinyl-CoA ligase deficiency: a mitochondrial hepatoencephalomyopathy.

Authors:  Johan L K Van Hove; Margarita S Saenz; Janet A Thomas; Renata C Gallagher; Mark A Lovell; Laura Z Fenton; Sarah Shanske; Sommer M Myers; Ronald J A Wanders; Jos Ruiter; Marjolein Turkenburg; Hans R Waterham
Journal:  Pediatr Res       Date:  2010-08       Impact factor: 3.756

Review 2.  Inherited mitochondrial diseases of DNA replication.

Authors:  William C Copeland
Journal:  Annu Rev Med       Date:  2008       Impact factor: 13.739

Review 3.  Mitochondrial DNA repair in aging and disease.

Authors:  Nadiya M Druzhyna; Glenn L Wilson; Susan P LeDoux
Journal:  Mech Ageing Dev       Date:  2008-03-13       Impact factor: 5.432

Review 4.  Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review.

Authors:  Ting-Yu Yen; Wuh-Liang Hwu; Yin-Hsiu Chien; Mei-Hwan Wu; Ming-Tai Lin; Lon-Yen Tsao; Wu-Shiun Hsieh; Ni-Chung Lee
Journal:  Eur J Pediatr       Date:  2007-09-11       Impact factor: 3.183

5.  Mitochondrial DNA 4977 bp deletion is a common phenomenon in hair and increases with age.

Authors:  Yijie Zheng; Xiaofeng Luo; Junfeng Zhu; Xuan Zhang; Yinting Zhu; Huihua Cheng; Zhiqiu Xia; Na Su; Nengpei Zhang; Junyi Zhou
Journal:  Bosn J Basic Med Sci       Date:  2012-08       Impact factor: 3.363

6.  Hematopoiesis in the thymidine kinase 2 deficient mouse model of mitochondrial DNA depletion syndrome.

Authors:  Xiaoshan Zhou; Magnus Johansson; Nicola Solaroli; Björn Rozell; Alf Grandien; Anna Karlsson
Journal:  J Inherit Metab Dis       Date:  2010-05-04       Impact factor: 4.982

7.  Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes.

Authors:  Tuomas Komulainen; Milla-Riikka Hautakangas; Reetta Hinttala; Salla Pakanen; Vesa Vähäsarja; Petri Lehenkari; Päivi Olsen; Päivi Vieira; Outi Saarenpää-Heikkilä; Johanna Palmio; Hannu Tuominen; Pietari Kinnunen; Kari Majamaa; Heikki Rantala; Johanna Uusimaa
Journal:  JIMD Rep       Date:  2015-05-05

Review 8.  Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options.

Authors:  Ayman W El-Hattab; Fernando Scaglia
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 9.  [Metabolic myopathies - an overview].

Authors:  M Lammens; B Schoser
Journal:  Pathologe       Date:  2009-09       Impact factor: 1.011

10.  Mutations in mitochondrial DNA polymerase-gamma promote breast tumorigenesis.

Authors:  Keshav K Singh; Vanniarajan Ayyasamy; Kjerstin M Owens; Manika Sapru Koul; Marija Vujcic
Journal:  J Hum Genet       Date:  2009-07-24       Impact factor: 3.172

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