(Q40971362)

25 September 2017

title

Both the rate and spectrum of loss of heterozygosity differ between human lymphoblastoid cells derived from various donors (English)

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25 September 2017

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de Nooij-van Dalen AG

1

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25 September 2017

Giphart MJ

2

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25 September 2017

Lohman PH

3

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25 September 2017

Giphart-Gassler M

4

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25 September 2017

language of work or name

English

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publication date

1 January 1999

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25 September 2017

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25 September 2017

volume

423

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25 September 2017

issue

1-2

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25 September 2017

page(s)

1-10

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25 September 2017

cites work

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Human tumor suppressor genes

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro

7 January 2021

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Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells

7 January 2021

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Reduction to homozygosity is the predominant spontaneous mutational event in cultured human lymphoblastoid cells

7 January 2021

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Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro

7 January 2021

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Genomic position influences spontaneous mutagenesis of an integrated retroviral vector containing the hprt cDNA as target for mutagenesis

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Genetic instability on chromosome 16 in a human B lymphoblastoid cell line

7 January 2021

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Spectrum of X-ray-induced mutations in the human hprt gene

7 January 2021

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Isolation and molecular characterization of spontaneous mutants of lymphoblastoid cells with extended loss of heterozygosity

7 January 2021

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A table for the estimation of the spontaneous mutations rate of cells in culture

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

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Trinucleotide repeat polymorphism at the human met-tRNA-i gene 1 (TRMI).

7 January 2021

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Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique.

7 January 2021

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A comparison of mutation induction at the tk and hprt loci in human lymphoblastoid cells; quantitative differences are due to an additional class of mutations at the autosomal tk locus.

7 January 2021

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Different cytotoxic and mutagenic responses induced by X-rays in two human lymphoblastoid cell lines derived from a single donor

7 January 2021

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In vitro mutagenesis at a single residue introduces B and T cell epitopes into a class I HLA molecule

7 January 2021

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Localization and characterization of serologic epitopes on HLA-A2

7 January 2021

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Different capacities for recombination in closely related human lymphoblastoid cell lines with different mutational responses to X-irradiation

7 January 2021

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The tumor suppressor p53 modifies mutational processes in a human lymphoblastoid cell line

7 January 2021

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Mutations in human lymphocytes commonly involve gene duplication and resemble those seen in cancer cels

7 January 2021

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Constitutional DNA-level aberrations in chromosome 22 in a patient with multiple meningiomas.

7 January 2021

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The monosomy 7 clone in interphase and metaphase cell population: a combined chromosome and primed in situ labeling study.

7 January 2021

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Chromosomal numerical aberrations in gastric carcinoma: analysis of eighteen cases using in situ hybridization.

7 January 2021

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10.1016/S0027-5107(98)00204-8

7 January 2021

Identifiers

DOI

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25 September 2017

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