Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

Published:1988-12 Issue:1 Volume:81 Page:41-48
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Mannens M.,Slater R. M.,Heyting C.,Bliek J.,de Kraker J.,Coad N.,de Pagter-Holthuizen P.,Pearson P. L.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00283727.pdf

Reference79 articles.

1. Ali IU, Lidereau R, Theillet C, Callakan R (1987) Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia. Science 238:185?188

2. Antonarakis SE, Philips JA, Mallonee RL, Kazazian HH, Fearon ER, Waber PG, Kronenberg HM, Ulrich A, Meyers DA (1983) Beta-globin locus is linked to the parathyroid hormone (PTH) locus and lies between the insulin and PTH locus in man. Proc Natl Acad Sci USA 80:6616?6619

3. Baas F, Bikker H, Geurts van Kessel A, Melsert R, Pearson PL, Vijlder JJM de, Ommen GJB van (1985) The human thyroglobin gene: a polymorphic marker localized distal to c-myc on chromosome 8 band q24. Hum Genet 69:138?143

4. Barker D, Holm T, White R (1984) A locus on chromosome 11p with multiple restriction site polymorphisms. Am J Hum Genet 36:1159?1171

5. Baylin SB, Fearon ER, Vogelstein B, Bustros A de, Sharkis SJ, Burke PJ, Staal SP, Nelkin BD (1987) Hypermethylation of the calcitonin gene is a property of human lymphoid and acute myeloid malignancies. Blood 2:412?417

Cited by 179 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Tumor Suppressor Genes;Holland‐Frei Cancer Medicine;2017-02-26

2. Retrospective analysis of FFPE based Wilms' Tumor samples through copy number and somatic mutation related Molecular Inversion Probe Based Array;Gene;2015-07

3. Pediatrik cerrahide sık karşılaşılan konjenital anomalilere genetik yaklaşım;Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy;2013-09-15

4. Genomic Imprinting and Uniparental Disomy;The Principles of Clinical Cytogenetics;2012-08-30

5. Analysis of Wilms Tumors Using SNP Mapping Array-Based Comparative Genomic Hybridization;PLoS ONE;2011-04-22

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3