Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease (Q30453083)

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

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scholarly article

1 reference

Europe PubMed Central

14 September 2017

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

1 reference

Europe PubMed Central

14 September 2017

mitochondrial DNA

0 references

Alzheimer's disease

1 reference

based on heuristic

inferred from title

author name string

Fahy E

1

1 reference

Europe PubMed Central

14 September 2017

Nazarbaghi R

2

1 reference

Europe PubMed Central

14 September 2017

Zomorrodi M

3

1 reference

Europe PubMed Central

14 September 2017

Herrnstadt C

4

1 reference

Europe PubMed Central

14 September 2017

Parker WD

5

1 reference

Europe PubMed Central

14 September 2017

Davis RE

6

1 reference

Europe PubMed Central

14 September 2017

Ghosh SS

7

1 reference

Europe PubMed Central

14 September 2017

language of work or name

0 references

publication date

1 August 1997

1 reference

Europe PubMed Central

14 September 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

14 September 2017

25

1 reference

Europe PubMed Central

14 September 2017

15

1 reference

Europe PubMed Central

14 September 2017

3102-3109

1 reference

Europe PubMed Central

14 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Mitochondrial disorders. Methods and specimen selection for diagnostic molecular pathology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

The development of mitochondrial medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Mitochondrial DNA diseases: histological and cellular studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

A single residue in DNA polymerases of the Escherichia coli DNA polymerase I family is critical for distinguishing between deoxy- and dideoxyribonucleotides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Viral dynamics in human immunodeficiency virus type 1 infection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 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=146869

20 June 2018

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Normal oxidative damage to mitochondrial and nuclear DNA is extensive

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Differential termination of primer extension: a novel, quantifiable method for detection of point mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

A comparison of single nucleotide primer extension with mispairing PCR-RFLP in detecting a point mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

20 June 2018

Purification of all forms of HeLa cell mitochondrial DNA and assessment of damage to it caused by hydrogen peroxide treatment of mitochondria or cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146869

26 November 2018

Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel use of limited primer extension in detecting mutations in human iduronate 2-sulfatase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide primer extension: quantitative range, variability, and multiplex analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation detection by solid phase primer extension

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ROC curves, test accuracy, and the description of diagnostic tests

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulindependent diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of heterogeneous viral populations by direct DNA sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9224611

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/25.15.3102

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

ResearchGate publication ID

0 references

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