Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype. (Q54856855)

From Wikidata

Jump to navigation Jump to search

scientific article published in May 2005

Language	Label	Description	Also known as
English	Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.	scientific article published in May 2005

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

based on heuristic

inferred from title

Stephen G Grant

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Viktoria N Evdokimova

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Reagan K McLoughlin

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Sharon L Wenger

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

language of work or name

0 references

publication date

1 May 2005

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

American Journal of Medical Genetics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

135

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

59-65

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Molecular epidemiology of human cancer: biomarkers of genotoxic exposure and susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Evidence for increased somatic cell mutations in patients with hepatocellular carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

MNSs and major glycophorins of human erythrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Simultaneous measurement of two cellular antigens and DNA using fluorescein-isothiocyanate, R-phycoerythrin, and propidium iodide on a standard FACScan.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

In vivo somatic mutation and segregation at the human glycophorin A (GPA) locus: phenotypic variation encompassing both gene-specific and chromosomal mechanisms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Somatic cell mutation frequency at the HPRT, T-cell antigen receptor and glycophorin A loci in Cockayne syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

The identification of fanconi anemia genotypes by clastogenic stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Segregation analysis with uncertain ascertainment: application to Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Fanconi's anemia--chromosome breakage studies in homozygotes and heterozygotes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Screening test for ataxia telangiectasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

The effect of chemotherapy on the in vivo frequency of glycophorin A 'null' variant erythrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Fanconi anemia: a pleotropic mutation with multiple cellular and developmental abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

The assessment of in vivo somatic mutations in survivors of childhood malignancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

8 June 2018

Fanconi anemia: prenatal diagnosis in 30 fetuses at risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

16 June 2018

A 20-year perspective on the International Fanconi Anemia Registry (IFAR).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

13 August 2018

Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

13 August 2018

Intercorrelations and sources of variability in three mutagenicity assays: a population-based study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849896

13 August 2018

Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitivity of somatic mutations in human umbilical cord blood to maternal environments

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequencies of HPRT- lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation frequency in human blood cells increases with age

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo somatic mutations in Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic cell genotoxicity at the glycophorin A locus in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of somatic mutations at the glycophorin A locus in erythrocytes of atomic bomb survivors using a single beam flow sorter

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic differentiation of Fanconi anemia, "idiopathic" aplastic anemia, and Fanconi anemia heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human in vivo somatic mutation measured at two loci: individuals with stably elevated background erythrocyte glycophorin A (gpa) variant frequencies exhibit normal T-lymphocyte hprt mutant frequencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome Abnormalities in Constitutional Aplastic Anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for increased somatic cell mutations at the glycophorin A locus in atomic bomb survivors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The GPA in vivo somatic mutation assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15822129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.30687

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15822129%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q54856855&oldid=1528503140"