High-performance multiplex SNP analysis of three hemochromatosis-related mutations with capillary array electrophoresis microplates (Q30982529)

20 September 2017

High-performance multiplex SNP analysis of three hemochromatosis-related mutations with capillary array electrophoresis microplates (English)

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20 September 2017

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I Medintz

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20 September 2017

W W Wong

2

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20 September 2017

L Berti

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20 September 2017

L Shiow

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20 September 2017

J Tom

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20 September 2017

J Scherer

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20 September 2017

G Sensabaugh

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20 September 2017

R A Mathies

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20 September 2017

language of work or name

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1 March 2001

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20 September 2017

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20 September 2017

11

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3

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20 September 2017

413-421

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Conversion of capillary electrophoresis microchip genotyping data for analysis with Genetic Profiler software.

20 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Loss of heterozygosity assay for molecular detection of cancer using energy-transfer primers and capillary array electrophoresis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

High speed single nucleotide polymorphism typing of a hereditary haemochromatosis mutation with capillary array electrophoresis microplates

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Radial capillary array electrophoresis microplate and scanner for high-performance nucleic acid analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Rapid diagnosis of herpes simplex encephalitis using microchip electrophoresis of PCR products

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Molecular diagnostics on microfabricated electrophoretic devices: from slab gel- to capillary- to microchip-based assays for T- and B-cell lymphoproliferative disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

A PCR-SSP method for detecting the His63Asp mutation in the HFE gene associated with hereditary haemochromatosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

A PCR-SSP method for detecting the Cys282Tyr mutation in the HFE gene associated with hereditary haemochromatosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

High-throughput genetic analysis using microfabricated 96-sample capillary array electrophoresis microplates

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

DNA typing in thirty seconds with a microfabricated device

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

High-speed DNA genotyping using microfabricated capillary array electrophoresis chips

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

DNA sequencing using a four-color confocal fluorescence capillary array scanner.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Mutation analysis in hereditary hemochromatosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Haemochromatosis and HLA-H.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

High and low annealing temperatures increase both specificity and yield in touchdown and stepdown PCR.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Cassette labeling for facile construction of energy transfer fluorescent primers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Ultra-high-speed DNA fragment separations using microfabricated capillary array electrophoresis chips

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Comparison of fluorescence energy transfer primers with different donor-acceptor dye combinations.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

Energy transfer primers: a new fluorescence labeling paradigm for DNA sequencing and analysis

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311034

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis

25 November 2018

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12 December 2020

A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH)

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12 December 2020

SNP mining. The rush is on

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12 December 2020

Rapid genetic screening for haemochromatosis using heteroduplex technology

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12 December 2020

Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutation

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12 December 2020

Towards fully automated genome-wide polymorphism screening

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12 December 2020

Efficient large-scale screening for the hemochromatosis susceptibility gene mutation

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12 December 2020

Phenotype-genotype correlation in haemochromatosis subjects

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12 December 2020

Reading bits of genetic information: methods for single-nucleotide polymorphism analysis

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12 December 2020

Capillary array electrophoresis DNA sequencing

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12 December 2020

Rapid genetic screening for hemochromatosis using automated SSCP-based capillary electrophoresis (SSCP-CE)

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12 December 2020

Identifiers

DOI

10.1101/GR.164701

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20 September 2017

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20 September 2017

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