(Q37419954)

20 August 2017

8 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

6 November 2020

The inheritance of pathogenic mitochondrial DNA mutations (English)

1 reference

20 August 2017

1 reference

20 September 2020

8 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

6 November 2020

mitochondrial disease

8 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

6 November 2020

1 reference

2 August 2019

1 reference

14 September 2019

1 reference

1 reference

6 November 2020

3

P F Chinnery

1 reference

20 August 2017

L M Cree

1

1 reference

20 August 2017

D C Samuels

series ordinal

2

1 reference

20 August 2017

language of work or name

English

0 references

publication date

19 March 2009

1 reference

Biochimica et Biophysica Acta

20 August 2017

1 December 2009

8 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

6 November 2020

9 references

20 August 2017

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

6 November 2020

1792

1 reference

20 August 2017

12

1 reference

20 August 2017

1097-1102

1 reference

Creative Commons Attribution 3.0 Unported

20 August 2017

8 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

20 September 2020

on focus list of Wikimedia project

6 November 2020

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

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Strong purifying selection in transmission of mammalian mitochondrial DNA

23 August 2017

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A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

23 August 2017

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Prevalence of mitochondrial DNA disease in adults

23 August 2017

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Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

23 August 2017

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Treatment for mitochondrial disorders

23 August 2017

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Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

23 August 2017

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The transmission of OXPHOS disease and methods to prevent this

23 August 2017

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Premature ageing in mice expressing defective mitochondrial DNA polymerase

23 August 2017

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Paternal inheritance of mitochondrial DNA

23 August 2017

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Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome

23 August 2017

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Leber hereditary optic neuropathy

23 August 2017

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Random genetic drift determines the level of mutant mtDNA in human primary oocytes

23 August 2017

1 reference

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Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study

23 August 2017

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Ubiquitin tag for sperm mitochondria

23 August 2017

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Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993

23 August 2017

1 reference

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A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle

23 August 2017

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Staging of gastrulating mouse embryos by morphological landmarks in the dissecting microscope.

23 August 2017

1 reference

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Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

23 August 2017

1 reference

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Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation

23 August 2017

1 reference

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Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

23 August 2017

1 reference

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Maternal inheritance of human mitochondrial DNA

23 August 2017

1 reference

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X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

23 August 2017

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Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome

23 August 2017

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23 August 2017

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Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation

14 September 2017

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Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes

28 September 2017

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A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy

26 June 2018

1 reference

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Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children

26 June 2018

1 reference

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The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Generation of stella-GFP transgenic mice: a novel tool to study germ cell development.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Molecular control of mitochondrial function in preimplantation mouse embryos.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785871

Nuclear transfer to prevent mitochondrial DNA diseases

2 September 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Genotypes from patients indicate no paternal mitochondrial DNA contribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Risk of developing a mitochondrial DNA deletion disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Homoplasmy, heteroplasmy, and mitochondrial dystonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

The epidemiology of pathogenic mitochondrial DNA mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19303927

12 December 2020

10.1016/J.BBADIS.2009.03.002

Identifiers

DOI

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

19303927

1 reference