(Q40830086)

English

DNA Enrichment by Allele-Specific Hybridization (DEASH): A Novel Method for Haplotyping and for Detecting Low-Frequency Base Substitutional Variants and Recombinant DNA Molecules

scientific article published on October 1, 2003

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

DNA enrichment by allele-specific hybridization (DEASH): a novel method for haplotyping and for detecting low-frequency base substitutional variants and recombinant DNA molecules (English)

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

DNA Enrichment by Allele-Specific Hybridization (DEASH): A Novel Method for Haplotyping and for Detecting Low-Frequency Base Substitutional Variants and Recombinant DNA Molecules (English)

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

2

object named as

Celia A. May

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

author name string

Alec J. Jeffreys

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14525930

17 March 2024

publication date

1 October 2003

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

full work available at URL

http://genome.cshlp.org/content/13/10/2316.full.pdf

Portable Document Format

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

https://europepmc.org/articles/PMC403713

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

https://europepmc.org/articles/PMC403713?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

https://doi.org/10.1101/gr.1214603

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14525930

17 March 2024

https://syndication.highwire.org/content/doi/10.1101/gr.1214603

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

Genome Research

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

13

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

10

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

2316-2324

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Mitochondrial DNA in aging and degenerative disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

The biochemistry of aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Estimate of the mutation rate per nucleotide in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Somatic mutations and aging: a re-evaluation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Spontaneous mutation in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Genotyping by mass spectrometric analysis of short DNA fragments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Repeat instability at human minisatellites arising from meiotic recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Raising the sensitivity of fetal RhD typing and sex determination from maternal blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Detection of oncogene mutations in sputum precedes diagnosis of lung cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Detection of c-Ki-ras mutations in faecal samples from sporadic colorectal cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Achondroplasia is defined by recurrent G380R mutations of FGFR3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Detection of single DNA base differences by competitive oligonucleotide priming

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Identification of p53 gene mutations in bladder cancers and urine samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Identification of ras oncogene mutations in the stool of patients with curable colorectal tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Rapid isolation of desired sequences from lone linker PCR amplified cDNA mixtures: application to identification and recovery of expressed sequences in cloned genomic DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

24 September 2017

Universal DNA microarray method for multiplex detection of low abundance point mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

25 September 2017

Amplification refractory mutation system linear extension: a novel, gel-free, enzyme-linked immunoassay method for DNA genotyping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

25 September 2017

Monoallelic mutation analysis (MAMA) for identifying germline mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

25 September 2017

Birth prevalence study of the Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

17 June 2018

Detection of ras gene mutations in pancreatic juice and peripheral blood of patients with pancreatic adenocarcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

19 August 2018

Birth prevalence study of the Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=403713

19 August 2018

Determination of fetal RhD status by maternal plasma DNA analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-invasive determination of the paternal HLA haplotype of a fetus using kinetic PCR to detect fetal microchimerism in maternal plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene amplification to detect fetal nucleated cells in pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal determination of fetal rhesus D status by DNA amplification of peripheral blood of rhesus-negative mothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene mutations in saliva as molecular markers for head and neck squamous cell carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of K-ras oncogene mutations in bronchoalveolar lavage fluid for lung cancer diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot

1 reference

https://pubmed.ncbi.nlm.nih.gov/14525930

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

15

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

Cancer Research

24

54

1634

publication date

1994

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

Cancer Research

35

53

2472

publication date

1993

1 reference

10.1101/GR.1214603

https://api.crossref.org/works/10.1101/GR.1214603

17 March 2024

Identifiers

10.1101/GR.1214603

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

24 September 2017

ResearchGate publication ID

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