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Literature DB >> 8281018

Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.

I Nelson¹, S Gerasimov, C Marsac, P Lestienne, P Boursot.

Abstract

Entities: Species

Mesh：

Substances：
DNA, Mitochondrial

Year: 1993 PMID： 8281018 DOI： 10.1007/BF00360907

Source DB: PubMed Journal: Mamm Genome ISSN： 0938-8990 Impact factor: 2.957

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References

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21 in total

1. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Authors: J Hayashi; S Ohta; A Kikuchi; M Takemitsu; Y Goto; I Nonaka
Journal: Proc Natl Acad Sci U S A Date: 1991-12-01 Impact factor: 11.205

2. A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

Authors: E A Schon; R Rizzuto; C T Moraes; H Nakase; M Zeviani; S DiMauro
Journal: Science Date: 1989-04-21 Impact factor: 47.728

3. Listing of stocks and strains of mice in the genus Mus derived from the feral state.

Authors: M Potter
Journal: Curr Top Microbiol Immunol Date: 1986 Impact factor: 4.291

Review 4. Mitochondrial diseases: genotype versus phenotype.

Authors: D C Wallace
Journal: Trends Genet Date: 1993-04 Impact factor: 11.639

5. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Authors: J M Shoffner; M T Lott; A S Voljavec; S A Soueidan; D A Costigan; D C Wallace
Journal: Proc Natl Acad Sci U S A Date: 1989-10 Impact factor: 11.205

6. [Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].

Authors: I Nelson; L d'Auriol; F Galibert; G Ponsot; P Lestienne
Journal: C R Acad Sci III Date: 1989

Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.

1. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

2. A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

3. Listing of stocks and strains of mice in the genus Mus derived from the feral state.

Review 4. Mitochondrial diseases: genotype versus phenotype.

5. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

6. [Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].

Review 7. Mitochondrial DNA copy number and mitochondrial DNA deletion in adult and senescent rats.

8. Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

9. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

10. Heteroplasmy in mice with deletion of a large coding region of mitochondrial DNA.