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

Data up to Jan 2025

Published1990
Citations83
References51

Total Citations Per Year

Abstract

References (51)

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

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

1985 • 555 citations

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1984 • 538 citations

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours

1984 • 426 citations

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.

1985 • 415 citations

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1984 • 411 citations

Loss of a Harvey ras allele in sporadic Wilms' tumour

1984 • 336 citations

Human lymphoblastoid lines from lymph node and spleen

1968 • 261 citations

Mutation assay at the thymidine kinase locus in diploid human lymphoblasts

1982 • 245 citations

Isolation of a human lymphoblastoid line heterozygous at the thymidine kinase locus: Possibility for a rapid human cell mutation assay

1978 • 206 citations

Human thymidine kinase gene: molecular cloning and nucleotide sequence of a cDNA expressible in mammalian cells.

1984 • 205 citations

Analysis of trifluorothymidine-resistant (TFTr) mutants of L5178Y/TK+/− mouse lymphoma cells

1985 • 158 citations

Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations

1986 • 150 citations

Deletion and amplification of the HGPRT locus in Chinese hamster cells.

1983 • 147 citations

In vivo somatic mutations in human lymphocytes frequently result from major gene alterations

1985 • 146 citations

Alterations of the hprt gene in human in vivo-derived 6-thioguanine-resistant T lymphocytes

1985 • 143 citations

A human c-erbA oncogene homologue is closely proximal to the chromosome 17 breakpoint in acute promyelocytic leukemia.

1984 • 122 citations

Locus specificity in the mutability of L5178Y mouse lymphoma cells: the role of multilocus lesions.

1986 • 122 citations

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma.

1986 • 106 citations

Chromosome 11 aberrations in small colony L5178Y TKPsu−/− mutants early in their clonal history

1985 • 103 citations

The molecular nature of mutations in cultured mammalian cells: A review

1985 • 95 citations

Structure of mutant alleles at the aprt locus of Chinese hamster ovary cells

1983 • 94 citations

Recessive mutant genes predisposing to human cancer.

1986 • 93 citations

High-frequency nonrandom mutational event at the adenine phosphoribosyltransferase (aprt) locus of sib-selected CHO variants heterozygous foraprt

1982 • 87 citations

Mutation and growth rates from Luria-Delbrück fluctuation tests

1982 • 84 citations

In situ analysis of trifluorothymidine-resistant (TFTr) mutants of L5178Y/TK+/− mouse lymphoma cells

1985 • 77 citations

SOUTHERN ANALYSIS OF GENOMIC ALTERATIONS IN GAMMA-RAY-INDUCED APRT- HAMSTER CELL MUTANTS

1986 • 77 citations

Chemically induced aneuploidy in mammalian cells in culture

1986 • 66 citations

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

1988 • 62 citations

High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells.

1983 • 56 citations

Loss of alleles at polymorphic loci on chromosome 2 in uveal melanoma

1986 • 55 citations

The utilization of trifluorothymidine (TFT) to select for thymidine kinase-deficient (TK−/−) mutants from L5178Y/TK+/− mouse lymphoma cells

1981 • 54 citations

Molecular characterization of 15 rearrangements among 90 human in vivo somatic mutants shows that deletions predominate.

1987 • 53 citations

High-frequency mutation at the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells due to deletion of the gene.

1983 • 52 citations

Model involving gene inactivation in the generation of autosomal recessive mutants in mammalian cells in culture.

1982 • 45 citations

Alterations of Gene Structure in Ethyl Methane Sulfonate-Induced Mutants of Mammalian Cells

1982 • 41 citations

Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer.

1988 • 40 citations

The aprt heterozygote/hemizygote system for screening mutagenic agents allows detection of large deletions

1988 • 36 citations

Localization of the oncogene c‐erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17

1985 • 36 citations

Mechanism of mutation at the aprt locus in Chinese hamster ovary cells: analysis of heterozygotes and hemizygotes.

1983 • 34 citations

High frequency ?switching? at the adenine phosphoribosyltransferase locus in multipotent mouse teratocarcinoma stem cells

1984 • 32 citations

Chromosome 14 marker appearance in a human B lymphoblastoid cell line of nonmalignant origin

1986 • 32 citations

Structural alterations of the aprt locus induced by deoxyribonucleoside triphosphate pool imbalances in Chinese hamster ovary cells.

1984 • 29 citations

Expression of recessiveAprt ? mutations in mouse CAK cells resulting from chromosome loss and duplication

1983 • 27 citations

DNA methylation and genetic inactivation at thymidine kinase locus: Two different mechanisms for silencing autosomal genes

1988 • 26 citations

Amplification versus mutation as a mechanism for reversion of anHGPRT mutation

1984 • 25 citations

Persistence of X-ray-induced chromosomal rearrangements in long-term cultures of human diploid fibroblasts.

1984 • 24 citations

High resolution chromosome analysis of constitutional and acquired t(15;17) maps c-erbA to Subband 17q11.2

1986 • 19 citations

Germ-line chromosomal localization of humanc-erb-A oncogene

1985 • 12 citations

Mutation assay in diploid human lymphoblasts: methodological aspects.

1977 • 6 citations

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Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in… (1990) – Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis | Metascience Observatory Explorer