Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome (Q24627875)

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

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instance of

scholarly article

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title

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

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author name string

R G Langlois

series ordinal

1

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W L Bigbee

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2

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R H Jensen

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3

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J German

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4

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language of work or name

English

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publication date

January 1989

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published in

Proceedings of the National Academy of Sciences of the United States of America

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volume

86

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issue

2

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page(s)

670-4

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cites work

Molecular cloning of a human glycophorin B cDNA: nucleotide sequence and genomic relationship to glycophorin A

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Hybrid glycophorins from human erythrocyte membranes. I. Isolation and complete structural analysis of the hybrid sialoglycoprotein from Dantu-positive red cells of the N.E. variety

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7 April 2017

Clonal analysis of human colorectal tumors

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7 April 2017

Elevated spontaneous mutation rate in Bloom syndrome fibroblasts

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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Mutation and cancer: a model for Wilms' tumor of the kidney

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27 September 2017

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

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PubMed Central

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27 September 2017

Structural alterations of DNA ligase I in Bloom syndrome

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PubMed Central

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27 September 2017

Bloom syndrome: a single complementation group defines patients of diverse ethnic origin.

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27 September 2017

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma

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27 September 2017

Bloom's syndrome. XII. Report from the Registry for 1987.

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PubMed Central

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27 September 2017

Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes

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PubMed Central

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27 September 2017

No increased chromosome breakage in three Bloom's syndrome heterozygotes

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27 September 2017

Leukemia in a black child with Bloom's syndrome. Somatic recombination as a possible mechanism for neoplasia

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27 September 2017

Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

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27 September 2017

Unequal mitotic sister chromatid exchange and different length of Y chromosomes.

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30 May 2018

Flow cytometric characterization of normal and variant cells with monoclonal antibodies specific for glycophorin A.

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30 May 2018

The use of monoclonal antibodies to quantify the levels of sialoglycoproteins alpha and delta and variant sialoglycoproteins in human erythrocyte membranes

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PubMed Central

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30 May 2018

Somatic recombination as possible prelude to malignant transformation

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PubMed Central

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30 May 2018

Structural comparison of glycophorins and immunochemical analysis of genetic variants

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PubMed Central

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30 May 2018

Altered DNA ligase I activity in Bloom's syndrome cells

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=286535

retrieved

28 July 2018

DNA ligase I deficiency in Bloom's syndrome

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=286535

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28 July 2018

CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=286535

retrieved

28 November 2018

Bloom's syndrome: evidence for an increased mutation frequency in vivo.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=286535

retrieved

28 November 2018

Effects of Bloom's syndrome fibroblasts on genetic recombination and mutagenesis of herpes simplex virus type 1.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=286535

retrieved

28 November 2018

Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological demonstration of mitotic crossing-over in man

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between sister chromatid exchanges and chromosome aberrations in Bloom's syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of X-irradiation in G1 and G2 on Bloom's Syndrome and normal chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diphtheria toxin resistance in human fibroblast cell strains from normal and cancer-prone individuals

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitotic recombination and segregation of satellites in Bloom's syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion mapping illustrated by the MNSs blood group

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous carriers for Bloom syndrome exhibit a spontaneously increased micronucleus formation in cultured fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Background allelic variants in normal hemopoietic cells and Bloom's syndrome erythrocytes and the possible implication of somatic crossingover

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for chromosome instability in vivo in bloom syndrome: Increased numbers of micronuclei in exfoliated cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of genes on the short arm of chromosome 11 in bladder cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wilms tumor in three patients with Bloom syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disparate effects of 5-bromodeoxyuridine on sister-chromatid exchanges and chromosomal aberrations in Bloom syndrome fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2911598

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.86.2.670

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1509312

ADS bibcode

1989PNAS...86..670L

0 references

OpenCitations bibliographic resource ID

1509312

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1509312

PMC publication ID

286535

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1509312

PubMed publication ID

2911598

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1509312

ResearchGate publication ID

20243857

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