Literature DB >> 11735374

Lessons from mitochondrial DNA mutations.

S DiMauro1.   

Abstract

The small, maternally inherited mitochondrial DNA (mtDNA) has turned out to be a hotbed of pathogenic mutations: 13 years into the era of "mitochondrial medicine", over 100 pathogenic point mutations and countless rearrangements have been associated with a variety of multisystemic or tissue-specific human diseases. MtDNA-related disorders can be divided into two major groups: those due to mutations in genes affecting mitochondrial protein synthesis in toto and those due to mutations in specific protein-coding genes. Pathogenesis is only partially explained by the rules of mitochondrial genetics and remains largely uncharted territory. Therapy is still woefully inadequate, but a number of promising approaches are being developed. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11735374     DOI: 10.1006/scdb.2001.0277

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  6 in total

1.  Single cell PCR from archival stained bone marrow slides: a method for molecular diagnosis and characterization.

Authors:  Stefanie Zanssen
Journal:  J Clin Lab Anal       Date:  2004       Impact factor: 2.352

2.  Bayesian network and mechanistic hierarchical structure modeling of increased likelihood of developing intractable childhood epilepsy from the combined effect of mtDNA variants, oxidative damage, and copy number.

Authors:  Brenda Luna; Sanjiv Bhatia; Changwon Yoo; Quentin Felty; David I Sandberg; Michael Duchowny; Ziad Khatib; Ian Miller; John Ragheb; Jayakar Prasanna; Deodutta Roy
Journal:  J Mol Neurosci       Date:  2014-07-16       Impact factor: 3.444

3.  hNOA1 interacts with complex I and DAP3 and regulates mitochondrial respiration and apoptosis.

Authors:  Tingdong Tang; Bin Zheng; Sheng-Hong Chen; Anne N Murphy; Krystyna Kudlicka; Huilin Zhou; Marilyn G Farquhar
Journal:  J Biol Chem       Date:  2008-12-22       Impact factor: 5.157

4.  Saturation of the human phenome.

Authors:  Mark E Samuels
Journal:  Curr Genomics       Date:  2010-11       Impact factor: 2.236

5.  Integrated analysis of the involvement of nitric oxide synthesis in mitochondrial proliferation, mitochondrial deficiency and apoptosis in skeletal muscle fibres.

Authors:  Gabriela Silva Rodrigues; Rosely Oliveira Godinho; Beatriz Hitomi Kiyomoto; Juliana Gamba; Acary Souza Bulle Oliveira; Beny Schmidt; Célia Harumi Tengan
Journal:  Sci Rep       Date:  2016-02-09       Impact factor: 4.379

6.  Large-scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype.

Authors:  Abdulaziz Alsemari; Hindi Nasser Al-Hindi
Journal:  Clin Case Rep       Date:  2015-11-23
  6 in total

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