Literature DB >> 2375642

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

M Zeviani1, C Gellera, M Pannacci, G Uziel, A Prelle, S Servidei, S DiDonato.   

Abstract

By using a combination of Southern blot hybridization analysis, polymerase-chain reaction amplification, and direct nucleotide sequencing, we studied deletions of mitochondrial DNA (mtDNA) in several nonfamilial patients with progressive external ophthalmoplegia and Kearns-Sayre syndrome, and in some of their direct relatives. Results suggest that the heteroplasmic mtDNA populations are already present at a very early stage of development, and that there is no direct transmission of mtDNA heteroplasmy by maternal inheritance.

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Year:  1990        PMID: 2375642     DOI: 10.1002/ana.410280118

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  25 in total

Review 1.  Clinical mitochondrial genetics.

Authors:  P F Chinnery; N Howell; R M Andrews; D M Turnbull
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

2.  The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) were selectively amplified through generations.

Authors:  Y Kobayashi; K Ichihashi; S Ohta; K Nihei; Y Kagawa; M Yanagisawa; M Y Momoi
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

3.  Duplications of mitochondrial DNA: implications for pathogenesis.

Authors:  J Poulton
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Clinical, morphological, biochemical, and neuroradiological features of mitochondrial encephalomyopathies. Presentation of 19 patients.

Authors:  A Lindner; E Hofmann; M Naumann; G Becker; H Reichmann
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

5.  Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability.

Authors:  Dario Ronchi; Alessio Di Fonzo; Weiqiang Lin; Andreina Bordoni; Changwei Liu; Elisa Fassone; Serena Pagliarani; Mafalda Rizzuti; Li Zheng; Massimiliano Filosto; Maria Teresa Ferrò; Michela Ranieri; Francesca Magri; Lorenzo Peverelli; Hongzhi Li; Yate-Ching Yuan; Stefania Corti; Monica Sciacco; Maurizio Moggio; Nereo Bresolin; Binghui Shen; Giacomo Pietro Comi
Journal:  Am J Hum Genet       Date:  2013-01-24       Impact factor: 11.025

Review 6.  What cost mitochondria? The maintenance of functional mitochondrial DNA within and across generations.

Authors:  Duur K Aanen; Johannes N Spelbrink; Madeleine Beekman
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-07-05       Impact factor: 6.237

7.  A 7-year-old girl presenting with a Bartter-like phenotype: Answers.

Authors:  Yunsoo Choe; Eujin Park; Hye Sun Hyun; Jung Min Ko; Hee Gyung Kang; Jeong Hun Kim; Sung-Hye Park; Hae Il Cheong
Journal:  Pediatr Nephrol       Date:  2016-08-17       Impact factor: 3.714

8.  Clinical and laboratory findings in referrals for mitochondrial DNA analysis.

Authors:  P J Lamont; R Surtees; C E Woodward; J V Leonard; N W Wood; A E Harding
Journal:  Arch Dis Child       Date:  1998-07       Impact factor: 3.791

9.  Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder.

Authors:  S Nørby; P Lestienne; I Nelson; I M Nielsen; H Schmalbruch; O Sjö; M Warburg
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

10.  Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child.

Authors:  N G Larsson; H G Eiken; H Boman; E Holme; A Oldfors; M H Tulinius
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

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