(Q39584736)

13 September 2017

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography (English)

1 reference

high-performance liquid chromatography

13 September 2017

1 reference

van Den Bosch BJ

1

1 reference

13 September 2017

de Coo RF

2

1 reference

13 September 2017

Scholte HR

3

1 reference

13 September 2017

Nijland JG

4

1 reference

13 September 2017

van Den Bogaard R

5

1 reference

13 September 2017

de Visser M

6

1 reference

13 September 2017

de Die-Smulders CE

7

1 reference

13 September 2017

Smeets HJ

8

1 reference

13 September 2017

language of work or name

English

0 references

publication date

1 October 2000

1 reference

13 September 2017

Nucleic Acids Research

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13 September 2017

28

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13 September 2017

E89

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13 September 2017

20

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Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations

13 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Mitochondrial myopathies: genetic mechanisms

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

A human mitochondrial DNA standard reference material for quality control in forensic identification, medical diagnosis, and mutation detection

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Identification by denaturing high-performance liquid chromatography of numerous polymorphisms in a candidate region for multiple sclerosis susceptibility

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=110805

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA

21 August 2018

1 reference

12 December 2020

Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene

1 reference

12 December 2020

Mutational scanning of mitochondrial DNA by two-dimensional electrophoresis

1 reference

12 December 2020

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

1 reference

12 December 2020

Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations

1 reference

12 December 2020

Mitochondrial encephalomyopathies: gene mutation. Vol. 10 No. 2, February 2000

1 reference

12 December 2020

An efficient salt-chloroform extraction of DNA from blood and tissues

1 reference

12 December 2020

Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA

1 reference

12 December 2020

Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism

1 reference

12 December 2020

Mitochondrial encephalomyopathies

1 reference

12 December 2020

A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis

1 reference

12 December 2020

Rapid and enhanced detection of mitochondrial DNA variation using single-strand conformation analysis of superposed restriction enzyme fragments from polymerase chain reaction-amplified products

1 reference

12 December 2020

Simultaneous detection of multiple point mutations using fluorescence-coupled competitive primer extension

1 reference

12 December 2020

Mitochondrial disorders

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12 December 2020

Direct detection of multiple point mutations in mitochondrial DNA

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/28.20.E89

1 reference

13 September 2017

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13 September 2017

1 reference