(Q28768152)

2

0 references

Brian Reguly

3

0 references

Gabriel D Dakubo

4

0 references

Andrea Aguirre

5

0 references

Roy Wittock

6

0 references

Kerry Robinson

7

0 references

John P Jakupciak

8

0 references

Robert E Thayer

Creative Commons Attribution 2.0 Generic

9

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language of work or name

English

0 references

publication date

21 July 2006

0 references

published in

BMC Genomics

0 references

volume

7

0 references

issue

1

0 references

page(s)

185

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copyright license

start time

21 July 2006

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

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A reappraisal of complete mtDNA variation in East Asian families with hearing impairment

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Mitochondrial DNA as a potential tool for early cancer detection

20 June 2018

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Mitochondrial DNA mutations in human neoplasia

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Mitochondrial DNA determines androgen dependence in prostate cancer cell lines.

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Mitochondrial DNA analysis in clinical laboratory diagnostics

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mtDNA mutations increase tumorigenicity in prostate cancer

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Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

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Effect of fixatives and tissue processing on the content and integrity of nucleic acids

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20 June 2018

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20 June 2018

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A high frequency of sequence alterations is due to formalin fixation of archival specimens

20 June 2018

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A novel mitochondrial DNA-like sequence in the human nuclear genome

20 June 2018

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Nuclear insertion sequences of mitochondrial DNA predominate in hair but not in blood of elephants

20 June 2018

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Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Evidence that two reports of mtDNA cytochrome c oxidase "mutations" in Alzheimer's disease are based on nDNA pseudogenes of recent evolutionary origin

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

The DNA revolution in population genetics

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

A quick, direct method that can differentiate expressed mitochondrial genes from their nuclear pseudogenes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Accurate detection and quantitation of heteroplasmic mitochondrial point mutations by pyrosequencing.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Phantom mutation hotspots in human mitochondrial DNA.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Problems in FBI mtDNA database.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Numt, a recent transfer and tandem amplification of mitochondrial DNA to the nuclear genome of the domestic cat.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Insertions and duplications of mtDNA in the nuclear genomes of Old World monkeys and hominoids

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1538596

Mitochondrial diabetes: investigation and identification of a novel mutation

27 November 2018

1 reference

12 December 2020

Extremely high levels of human mitochondrial DNA heteroplasmy in single hair roots

1 reference

12 December 2020

Analysis of mtDNA copy number and composition of single mitochondrial particles using flow cytometry and PCR

1 reference

12 December 2020

Diagnosis of mitochondrial disease: assessment of mitochondrial DNA heteroplasmy in blood

1 reference

12 December 2020

Mitochondrial genome instability and mtDNA depletion in human cancers

1 reference

12 December 2020

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy

1 reference

12 December 2020

A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

1 reference

12 December 2020