(Q35790038)

English

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease

scientific article published on November 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

mitochondrial DNA

0 references

mitochondrial disease

1 reference

based on heuristic

inferred from title

author name string

Ren-Kui Bai

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Lee-Jun C Wong

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

publication date

1 November 2005

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

The Journal of Molecular Diagnostics

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

613-622

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Molecular analysis for mitochondrial DNA disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Compensatory amplification of mtDNA in a patient with a novel deletion/duplication and high mutant load

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Molecular characterization of ribosomal gene variation within and among NORs segregating in specialized populations of chicken

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Diseases of the mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

12 July 2018

Extensive investigations of mitochondrial DNA genome in treated HIV-infected subjects: beyond mitochondrial DNA depletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Clinical features of A3243G mitochondrial tRNA mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Implications of using the ND1 gene as a control region for real-time PCR analysis of mitochondrial DNA deletions in human skin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Quantification of mitochondrial DNA deletion, depletion, and overreplication: application to diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Diagnostic criteria for respiratory chain disorders in adults and children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Comprehensive scanning of the entire mitochondrial genome for mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867556

25 September 2018

Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased mitochondrial DNA in blood vessels and ragged‐red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Yield of mtDNA mutation analysis in 2,000 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantification of human mitochondrial DNA in a real time PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct detection of multiple point mutations in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathies:gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: a single-step approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative, noninvasive tissues for quantitative screening of mutant mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16258160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S1525-1578(10)60595-8

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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