Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA
Authors:
- Michio HiranoMHMichio Hirano
- Ramon MartiaRMRamon Martia
- Claudia Ferreiro-BarrosCFClaudia Ferreiro-Barros
- Maya R VilàMVMaya R Vilà
- Saba TadesseaSTSaba Tadessea
- Yutaka NishigakiaYNYutaka Nishigakia
- Ichizo NishinobINIchizo Nishinob
- Tuan H VuTVTuan H Vu
- 1 December 2001
- journal article
- review article
- Published by Elsevier in Seminars in Cell & Developmental Biology
- Vol. 12 (6) , 417-427
Abstract
No abstract availableKeywords
This publication has 87 references indexed in Scilit:
- Vertebrate Mitochondrial DNA—A Circle of SurprisesExperimental Cell Research, 2000
- Mitochondrial myopathy simulating spinal muscular atrophyPediatric Neurology, 1996
- Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemiaThe Journal of Pediatrics, 1996
- Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluationPediatric Neurology, 1996
- Ribonucleotide Reductase: Evidence for Specific Association with HeLa-Cell MitochondriaBiochemical and Biophysical Research Communications, 1994
- Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA DepletionBiochemical and Biophysical Research Communications, 1994
- Fatal infantile liver failure associated with mitochondrial DNA depletionThe Journal of Pediatrics, 1992
- Nucleus‐driven mutations of human mitochondrial DNAJournal of Inherited Metabolic Disease, 1992
- Mitochondrial Myopathy Caused by Long-Term Zidovudine TherapyNew England Journal of Medicine, 1990
- Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathyBiochemical and Biophysical Research Communications, 1990