Loss of Heterozygosity

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Loss of Heterozygosity. / Schwarzenbach, Heidi.

Brenner´s Encyclopedia of Genetics. Hrsg. / Stanley Maloy; Kelly Hughes. Band 2e, 4 2. Aufl. Brenner, 2013. S. 271-273.

Publikationen: SCORING: Beitrag in Buch/SammelwerkSCORING: Beitrag in SammelwerkForschungBegutachtung

Harvard

Schwarzenbach, H 2013, Loss of Heterozygosity. in S Maloy & K Hughes (Hrsg.), Brenner´s Encyclopedia of Genetics. 2. Aufl., Bd. 2e, 4, Brenner, S. 271-273.

APA

Schwarzenbach, H. (2013). Loss of Heterozygosity. in S. Maloy, & K. Hughes (Hrsg.), Brenner´s Encyclopedia of Genetics (2. Aufl., Band 2e, 4, S. 271-273). Brenner.

Vancouver

Schwarzenbach H. Loss of Heterozygosity. in Maloy S, Hughes K, Hrsg., Brenner´s Encyclopedia of Genetics. 2. Aufl. Band 2e, 4. Brenner. 2013. S. 271-273

Bibtex

@inbook{2b338a91744c4be0a9e379c705c9db1d,
title = "Loss of Heterozygosity",
abstract = "Loss of heterozygosity (LOH) is a common form of allelic imbalance by which a heterozygous somatic cell becomes homozygous because one of the two alleles gets lost. This form of chromosome instability is sufficient to provide selective growth advantage and has been recognized as a major cause of tumorigenesis. In 1929, the genetic mechanism of LOH was explained for the first time by studying mutant spots induced by X-rays in Drosophila melanogaster. Later on, the detection of LOH has been used to identify genomic regions that harbor putative tumor suppressor genes and to characterize different tumor types, pathological stages, and progression. This identification has provided important insight into the molecular mechanisms of malignant transformation and may deliver the targets for future therapy. Screening for LOH can be performed at polymorphic markers in tumor tissue and {\textquoteleft}liquid biopsies{\textquoteright} and be a promising diagnostic and prognostic tool.",
author = "Heidi Schwarzenbach",
year = "2013",
language = "English",
isbn = "978-0-08-096156-9",
volume = "2e, 4",
pages = "271--273",
editor = "Stanley Maloy and Kelly Hughes",
booktitle = "Brenner´s Encyclopedia of Genetics",
publisher = "Brenner",
edition = "2.",

}

RIS

TY - CHAP

T1 - Loss of Heterozygosity

AU - Schwarzenbach, Heidi

PY - 2013

Y1 - 2013

N2 - Loss of heterozygosity (LOH) is a common form of allelic imbalance by which a heterozygous somatic cell becomes homozygous because one of the two alleles gets lost. This form of chromosome instability is sufficient to provide selective growth advantage and has been recognized as a major cause of tumorigenesis. In 1929, the genetic mechanism of LOH was explained for the first time by studying mutant spots induced by X-rays in Drosophila melanogaster. Later on, the detection of LOH has been used to identify genomic regions that harbor putative tumor suppressor genes and to characterize different tumor types, pathological stages, and progression. This identification has provided important insight into the molecular mechanisms of malignant transformation and may deliver the targets for future therapy. Screening for LOH can be performed at polymorphic markers in tumor tissue and ‘liquid biopsies’ and be a promising diagnostic and prognostic tool.

AB - Loss of heterozygosity (LOH) is a common form of allelic imbalance by which a heterozygous somatic cell becomes homozygous because one of the two alleles gets lost. This form of chromosome instability is sufficient to provide selective growth advantage and has been recognized as a major cause of tumorigenesis. In 1929, the genetic mechanism of LOH was explained for the first time by studying mutant spots induced by X-rays in Drosophila melanogaster. Later on, the detection of LOH has been used to identify genomic regions that harbor putative tumor suppressor genes and to characterize different tumor types, pathological stages, and progression. This identification has provided important insight into the molecular mechanisms of malignant transformation and may deliver the targets for future therapy. Screening for LOH can be performed at polymorphic markers in tumor tissue and ‘liquid biopsies’ and be a promising diagnostic and prognostic tool.

M3 - SCORING: Contribution to collected editions/anthologies

SN - 978-0-08-096156-9

VL - 2e, 4

SP - 271

EP - 273

BT - Brenner´s Encyclopedia of Genetics

A2 - Maloy, Stanley

A2 - Hughes, Kelly

PB - Brenner

ER -