Literature DB >> 8739945

Functional mtDNA replication defect in a fibroblast line from a patient with mtDNA depletion.

K J Morten1, C Freeman Emmerson, J Poulton.   

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Year:  1996        PMID： 8739945     DOI： 10.1007/bf01799409

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  8 in total

1.  Similarity of human mitochondrial transcription factor 1 to high mobility group proteins.

Authors:  M A Parisi; D A Clayton
Journal:  Science       Date:  1991-05-17       Impact factor: 47.728

2.  Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments.

Authors:  J M Erickson; C L Rushford; D J Dorney; G N Wilson; R D Schmickel
Journal:  Gene       Date:  1981-12       Impact factor: 3.688

3.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

4.  Activation of the human mitochondrial transcription factor A gene by nuclear respiratory factors: a potential regulatory link between nuclear and mitochondrial gene expression in organelle biogenesis.

Authors:  J V Virbasius; R C Scarpulla
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-15       Impact factor: 11.205

5.  NRF-1, an activator involved in nuclear-mitochondrial interactions, utilizes a new DNA-binding domain conserved in a family of developmental regulators.

Authors:  C A Virbasius; J V Virbasius; R C Scarpulla
Journal:  Genes Dev       Date:  1993-12       Impact factor: 11.361

6.  Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA.

Authors:  H J Tritschler; F Andreetta; C T Moraes; E Bonilla; E Arnaudo; M J Danon; S Glass; B M Zelaya; E Vamos; N Telerman-Toppet
Journal:  Neurology       Date:  1992-01       Impact factor: 9.910

7.  Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.

Authors:  J Poulton; K Morten; C Freeman-Emmerson; C Potter; C Sewry; V Dubowitz; H Kidd; J Stephenson; W Whitehouse; F J Hansen
Journal:  Hum Mol Genet       Date:  1994-10       Impact factor: 6.150

8.  mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.

Authors:  C T Moraes; S Shanske; H J Tritschler; J R Aprille; F Andreetta; E Bonilla; E A Schon; S DiMauro
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025
  8 in total
  1 in total

1.  Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion.

Authors:  P Hargreaves; S Rahman; P Guthrie; J W Taanman; J V Leonard; J M Land; S J R Heales
Journal:  J Inherit Metab Dis       Date:  2002-02       Impact factor: 4.982
  1 in total

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