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Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme

Data up to Jan 2025

Published1989
Citations109
References29

Total Citations Per Year

Abstract

References (29)

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1984 • 4,899 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping

1987 • 1,683 citations

Amplification, enhanced expression and possible rearrangement of EGF receptor gene in primary human brain tumours of glial origin

1985 • 1,523 citations

Identification of an Amplified, Highly Expressed Gene in a Human Glioma

1987 • 671 citations

Clonal Analysis of Human Colorectal Tumors

1987 • 638 citations

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1984 • 586 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

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

1987 • 472 citations

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

1987 • 440 citations

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1987 • 423 citations

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

1984 • 411 citations

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

1987 • 396 citations

Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13.

1987 • 206 citations

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

1984 • 171 citations

Chromosomal evolution in malignant human gliomas starts with specific and usually numerical deviations

1986 • 139 citations

Chromosomal composition of a series of 22 human low-grade gliomas

1987 • 122 citations

Chromosomal patterns in human malignant astrocytomas

1987 • 122 citations

A primary genetic map of markers for human chromosome 10

1988 • 95 citations

Localization of the Gene Encoding the Human Interleukin-2 Receptor on Chromosome 10

1985 • 75 citations

Biology of gliomas: heterogeneity, oncogenes, growth factors.

1986 • 74 citations

Chromosomal Locations of Human Tissue Plasminogen Activator and Urokinase Genes

1985 • 72 citations

An extended genetic linkage map of markers for human chromosome 10

1988 • 57 citations

Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization

1987 • 40 citations

Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15]

1988 • 19 citations

A single copy sarbclone, P1–101, from cosmid 3–3B, defines three RFLPs on 10pter–q23[HGM9 no. D10S4]

1987 • 16 citations

Isolation and Characterization of Hp10: a Specific Human Hepatic Protein cDNA

1985 • 1 citations

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Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme (1989) – Genomics | Metascience Observatory Explorer