Genomics. 1990 Jan;6(1):174-7.

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.

Zhang FR, Delattre O, Rouleau G, Couturier J, Lefrançois, Thomas G, Aurias A.

Source

CNRS-URA 620, Institut Curie, Paris, France.

Abstract

The recurrent translocation breakpoint on chromosome 22 of neuroepithelioma has been localized between two probes, D22S1 and D22S15, by both in situ hybridization and somatic cell hybrids. These two probes have further been shown to be genetically linked at theta = 0.0 and a lod score of 5.3. The two probes were unaffected by a partial deletion of the chromosome 22 long arm of a meningioma, showing that the meningioma locus is distal to that of the neuroepithelioma.

PMID:: 2303258; [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms

Publication Types

Research Support, Non-U.S. Gov't

MeSH Terms

LinkOut - more resources

Medical

chromosome 22 - Genetics Home Reference

Supplemental Content

Save items

Related citations in PubMed

Review [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma]. [Verh K Acad Geneeskd Belg. 1995]
Review [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG. Verh K Acad Geneeskd Belg. 1995; 57(5):389-422.
Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes. [Cancer Genet Cytogenet. 1994]
Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes.
Desmaze C, Zucman J, Delattre O, Melot T, Thomas G, Aurias A. Cancer Genet Cytogenet. 1994 May; 74(1):13-8.
Translocation of c-sis protooncogene in peripheral neuroepithelioma. [Cancer Genet Cytogenet. 1987]
Translocation of c-sis protooncogene in peripheral neuroepithelioma.
Thiele CJ, Whang-Peng J, Kao-Shan CS, Miser J, Israel MA. Cancer Genet Cytogenet. 1987 Jan; 24(1):119-28.
Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers. [Oncogene. 1995]
Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N. Oncogene. 1995 Mar 16; 10(6):1087-93.
Review Analysis of chromosome 22 loci in meningioma. Alterations in the leukemia inhibitory factor (LIF) locus. [Mol Chem Neuropathol. 1994]
Review Analysis of chromosome 22 loci in meningioma. Alterations in the leukemia inhibitory factor (LIF) locus.
Pergolizzi RG, Erster SH. Mol Chem Neuropathol. 1994 Feb-Apr; 21(2-3):189-217.

See reviews... See all...

Cited by 5 PubMed Central articles

Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition. [Eur J Hum Genet. 2010]
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.
Rio M, Malan V, Boissel S, Toutain A, Royer G, Gobin S, Morichon-Delvallez N, Turleau C, Bonnefont JP, Munnich A, et al. Eur J Hum Genet. 2010 Mar; 18(3):285-90. Epub 2009 Oct 21.
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11. [Proc Natl Acad Sci U S A. 1990]
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11.
Cherif D, Julier C, Delattre O, Derré J, Lathrop GM, Berger R. Proc Natl Acad Sci U S A. 1990 Sep; 87(17):6639-43.
Streamlined approach to creating yeast artificial chromosome libraries from specialized cell sources. [Proc Natl Acad Sci U S A. 1990]
Streamlined approach to creating yeast artificial chromosome libraries from specialized cell sources.
Feingold JM, Ogden SD, Denny CT. Proc Natl Acad Sci U S A. 1990 Nov; 87(21):8637-41.

See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
UniSTS
Genetic, physical, and sequence mapping reagents in the UniSTS database associated with the current articles through references on sequence tagged site (STS) submissions as well as automated searching of PubMed abstracts and full-text PubMed Central articles for marker names.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma l...
The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.
Genomics. 1990 Jan ;6(1):174-7.

PubMed
The influence of local recurrence of extremity soft tissue sarcoma on metastasis...
The influence of local recurrence of extremity soft tissue sarcoma on metastasis and survival.
Cancer. 1990 Mar 1 ;65(5):1119-29.

PubMed
Motor learning in patients with cerebellar dysfunction.
Motor learning in patients with cerebellar dysfunction.
Brain. 1990 Feb ;113 ( Pt 1):103-20.

PubMed
cDNA cloning of a novel cell adhesion protein expressed in human squamous carcin...
cDNA cloning of a novel cell adhesion protein expressed in human squamous carcinoma cells.
Biochem Biophys Res Commun. 1990 Jan 30 ;166(2):984-92.

PubMed
Diagnostic ultrasound in breast cancer: analysis of retrotumorous echo patterns ...
Diagnostic ultrasound in breast cancer: analysis of retrotumorous echo patterns correlated with sonic attenuation by cancerous connective tissue.
J Clin Ultrasound. 1979 Dec ;7(6):471-9.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to: