(Q35853237)

English

Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22

scientific article published in August 1990

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22 (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ataxia telangiectasia

1 reference

based on heuristic

inferred from title

author name string

McConville CM

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Formstone CJ

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Hernandez D

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Thick J

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Taylor AM

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 August 1990

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

18

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

15

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

4335-4343

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Disorders of B cells and helper T cells in the pathogenesis of the immunoglobulin deficiency of patients with ataxia telangiectasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Abnormal response of ataxia-telangiectasia cells to agents that break the deoxyribose moiety of DNA via a targeted free radical mechanism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

The incidence and gene frequency of ataxia-telangiectasia in the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Ramped field inversion gel electrophoresis: a cautionary note

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Inhibition of mammalian cell DNA synthesis by ionizing radiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

The breakpoint of an inversion of chromosome 14 in a T-cell leukemia: sequences downstream of the immunoglobulin heavy chain locus are implicated in tumorigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Report of the committee on linkage and gene order

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Increased radiosensitivity and the basic defect in ataxia telangiectasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Isolation and mapping of a polymorphic DNA sequence (pCJ52.75M1) on chromosome 11 [D11S385]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Physical mapping of the human chromosome 11q23 region containing the ataxia-telangiectasia locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

A primary linkage map of the human chromosome 11q22-23 region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Restoration of radiation resistance in ataxia telangiectasia cells by the introduction of normal human chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Is chromatid-type damage in ataxia telangiectasia after irradiation at G0 a consequence of defective repair?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=331249

11 July 2018

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precise in situ localization of NCAM, ETS1, and D11S29 on human meiotic chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual features in the inheritance of ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telandiectasia (AT). Clinical and cytogenetic findings in 5 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal radiosensitivity of ataxia telangiectasia cells at different cell cycle stages

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous cytogenetic abnormalities in lymphocytes from thirteen patients with ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of integrating DNA vectors to analyse the molecular defects in ionising radiation-sensitive mutants of mammalian cells including ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the nature of a defect in cells from individuals with ataxia-telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia-telangiectasia: a human mutation giving high-frequency misrepair of DNA double-stranded scissions

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breakage of the T cell receptor alpha chain locus in non malignant clones from patients with ataxia telangiectasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1975092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/18.15.4335

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

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