About: Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

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About: Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 Goto Sponge NotDistinct Permalink

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scientific article published on 01 May 1980

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1980 (uk) im Mai 1980 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 1980 (ast) scientific article published on 01 May 1980 (en)
publication date	wds:Q71198008-F55AB3EA-C4D7-4B6A-A41D-239E1AC7555A
publication date	1980-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71198008-480BC431-6B2B-4363-B265-487628B5797C
language of work or name	English
author name string	wds:Q71198008-00753CA0-BE37-46D4-929A-A5A19CA2E186 wds:Q71198008-43C03851-77B7-4E53-8F02-60131E0135D4 wds:Q71198008-70125402-59C1-46E6-A66F-F20AE05FB17F wds:Q71198008-9B21733F-E9F3-4EF2-B22F-2037347D1702 wds:Q71198008-C056C9FD-8DC8-4F25-AFD4-CE35AA2AB830 wds:Q71198008-EA76BFD1-1AE7-4BE3-AFFA-6FBC14810827 wds:Q71198008-FF9F77CA-278A-4EA2-9070-188C9C85216B
author name string	R S Sparkes M G Wilson A L Murphree M C Sparkes J J Yunis W Benedict J W Towner
rdfs:label	Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (en) Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (nl)
skos:prefLabel	Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (en) Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (nl)
name	Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (en) Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (nl)
title	wds:Q71198008-AB670020-2D16-4574-9B0B-7904CD3CDAD0
title	Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (en)
page(s)	wds:Q71198008-1AB181F7-8105-454C-867C-DAFA22AA3157
page(s)	1042-1044
instance of	wds:Q71198008-555125BF-DE30-4D93-84EB-209D20E83783
instance of	scholarly article
main subject	wds:Q71198008-3B5762F8-71F2-40BA-987A-32A97665E5C4
main subject	retinoblastoma
PubMed ID	wds:Q71198008-EFE6FC6E-544B-4257-B4E4-2220EC3E6B17
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7375916
PubMed ID	7375916
published in	wds:Q71198008-3738DB25-E1C9-467E-BEFC-147CCAF3B610
published in	Science
issue	wds:Q71198008-1D5A1A83-59AC-4685-B4C7-842F2B03F33F
volume	wds:Q71198008-242E954E-F797-404B-A3DE-F839F4AE47E9
issue	4447
volume	208
DOI	wds:Q71198008-C2BD6210-9497-4017-8A40-3B0084EB5445
DOI	http://dx.doi.org/10.1126/SCIENCE.7375916
DOI	10.1126/SCIENCE.7375916
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71198008
is cites work of	Molecular pathways in bladder cancer Tumor suppressor genes and medulloblastoma Live imaging of primary ocular vasculature formation in zebrafish Genetic and epigenetic losses of heterozygosity in cancer predisposition and progression Window panes of eternity. Health, disease, and inherited risk Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma Lack of expression of aminoacylase-1 in small cell lung cancer. Evidence for inactivation of genes encoded by chromosome 3p Retinoblastoma: Clues to Human Oncogenesis The tumor phenotype and the human gene map Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. Genetics of retinoblastoma: a study Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene Expression of recessive alleles by chromosomal mechanisms in retinoblastoma Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma Purification, biochemical characterization, and biological function of human esterase D Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus. Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus A null allele of esterase D is a marker for genetic events in retinoblastoma formation Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines Hereditary cancer: two hits revisited Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity. Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma Eight closely linked loci place the Wilson disease locus within 13q14-q21. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma One hit, two hits, three hits, more? Genomic changes in the development of retinoblastoma. The ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells Retinoblastoma in transgenic mice: models of hereditary retinoblastoma Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients. Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3) Aniridia and mental retardation with deletion of the short arm of chromosome 11. Chromosome 13 homozygosity in osteosarcoma without retinoblastoma Model Hereditary Cancers of Man The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional Translocation Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom. Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom Deletions of the esterase D locus from a survey of 200 retinoblastoma patients The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation Retinoblastoma: a model of oncogenesis Significance of Retinoma and Phthisis Bulbi for Retinoblastoma Retinoblastoma gene mutations in primary human bladder cancer Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy

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