(Q35127771)

English

The Use of Denaturing High-Performance Liquid Chromatography (DHPLC) for the Analysis of Genetic Variations: Impact for Diagnostics and Pharmacogenetics

scientific article published on April 1, 2003

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scholarly article

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: impact for diagnostics and pharmacogenetics (English)

1 reference

Europe PubMed Central

6 August 2017

The Use of Denaturing High-Performance Liquid Chromatography (DHPLC) for the Analysis of Genetic Variations: Impact for Diagnostics and Pharmacogenetics (English)

1 reference

10.1515/CCLM.2003.068

https://api.crossref.org/works/10.1515/CCLM.2003.068

2 January 2024

high-performance liquid chromatography

1 reference

based on heuristic

inferred from title

author name string

Mario Noyer-Weidner

2

1 reference

Europe PubMed Central

6 August 2017

Felix W. Frueh

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12747586

2 January 2024

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12747586

2 January 2024

publication date

1 April 2003

1 reference

Europe PubMed Central

6 August 2017

full work available at URL

https://www.degruyter.com/document/doi/10.1515/CCLM.2003.068/pdf

1 reference

10.1515/CCLM.2003.068

https://api.crossref.org/works/10.1515/CCLM.2003.068

2 January 2024

Clinical Chemistry and Laboratory Medicine

1 reference

Europe PubMed Central

6 August 2017

41

1 reference

Europe PubMed Central

6 August 2017

452-461

1 reference

Europe PubMed Central

6 August 2017

4

1 reference

Europe PubMed Central

6 August 2017

A physical map of the human genome

1 reference

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21 January 2018

The Sequence of the Human Genome

1 reference

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Use of cDNA microarrays to analyze dioxin-induced changes in human liver gene expression

1 reference

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21 January 2018

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 reference

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21 January 2018

Accessing genetic variation: genotyping single nucleotide polymorphisms

1 reference

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21 January 2018

Tracking changes in HIV-1 envelope quasispecies using DNA heteroduplex analysis.

1 reference

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21 January 2018

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

1 reference

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21 January 2018

Denaturing high-performance liquid chromatography: A review

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Modeling and analysis of competitive RT-PCR.

1 reference

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21 January 2018

Quantitative analysis of gene expression by ion-pair high-performance liquid chromatography.

1 reference

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21 January 2018

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

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21 January 2018

Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography.

1 reference

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21 January 2018

Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing

1 reference

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21 January 2018

DHPLC screening of cystic fibrosis gene mutations.

1 reference

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21 January 2018

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

1 reference

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21 January 2018

DHPLC analysis of the MECP2 gene in Italian Rett patients.

1 reference

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21 January 2018

Identification of seven novel mutations of F8C by DHPLC.

1 reference

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21 January 2018

Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice

1 reference

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21 January 2018

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.

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21 January 2018

The genetic basis of variability in drug responses

1 reference

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21 January 2018

Pharmacogenomics: the promise of personalized medicine

1 reference

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21 January 2018

Pharmacogenomics: translating functional genomics into rational therapeutics

1 reference

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21 January 2018

Pharmacogenetics and adverse drug reactions

1 reference

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21 January 2018

The use of denaturing high-pressure liquid chromatography for the detection of mutations in thiopurine methyltransferase

1 reference

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21 January 2018

A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency

1 reference

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21 January 2018

Pharmacogenetics and drug-induced arrhythmias

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Genetics of ventricular tachycardia.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Novel mutations in domain I of SCN5A cause Brugada syndrome

1 reference

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21 January 2018

Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome

1 reference

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21 January 2018

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

1 reference

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21 January 2018

Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatography.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

A strategy for examining complex mixtures of deoxyoligonucleotides using ion-pair-reverse-phase high-performance liquid chromatography, matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and informatics

1 reference

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21 January 2018

Stool screening for colorectal cancer: evolution from occult blood to molecular markers

1 reference

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21 January 2018

Trends in biomarker research for cancer detection

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Mutations in APC, Kirsten-ras, and p53--alternative genetic pathways to colorectal cancer.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Mitochondrial diseases in man and mouse

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

The role of DNA methylation in mammalian epigenetics

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Methylation and colorectal cancer

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

DNA methylation analysis: a review of current methodologies

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

A rapid, quantitative, non-radioactive bisulfite-SNuPE- IP RP HPLC assay for methylation analysis at specific CpG sites

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Simultaneous detection of CpG methylation and single nucleotide polymorphism by denaturing high performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Rapid Identification of Wilson's Disease Carriers by Denaturing High-Performance Liquid Chromatography

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.068

21 January 2018

Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography

1 reference

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21 January 2018

Drug Metabolism and Disposition

3

29

586

author name string

Cronin MT

publication date

2001

1 reference

10.1515/CCLM.2003.068

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2 January 2024

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

15

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Mutation analysis of p53 in ovarian tumors by DHPLC

16

1 reference

10.1515/CCLM.2003.068

https://api.crossref.org/works/10.1515/CCLM.2003.068

2 January 2024

Denaturing high pressure liquid chromatography (DHPLC) for the analysis of somatic p53 mutations

17

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Identification of specific BRCA1 and BRCA2 variants by DHPLC

18

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

19

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling

26

1 reference

10.1515/CCLM.2003.068

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2 January 2024

MeCP2 mutations in children with and without the phenotype of Rett syndrome

29

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2

33

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort

34

1 reference

10.1515/CCLM.2003.068

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2 January 2024

Cytochrome P450 CYP2D6 gene polymorphism and lung cancer susceptibility in Caucasians.

40

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2 January 2024

The role of the autonomic nerves in the control of nasal circulation.

50

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2 January 2024

Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography

52

1 reference

10.1515/CCLM.2003.068

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Nihon Geka Gakkai zasshi

57

103

472

author name string

Takeda S

publication date

2002

1 reference

10.1515/CCLM.2003.068

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2 January 2024

High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)

60

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Rapid screening mitochondrial DNA mutation by using denaturing high-performance liquid chromatography

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Biochimica et Biophysica Acta

69

1552

15

author name string

Muyrers-Chen I

publication date

2001

1 reference

10.1515/CCLM.2003.068

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2 January 2024

DNA methylation and cancer

70

1 reference

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DNA methylation: a profile of methods and applications

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Analysis of the methylation status of imprinted genes based on methylation-specific polymerase chain reaction combined with denaturing high-performance liquid chromatography

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Identifiers

10.1515/CCLM.2003.068

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

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