• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Effect of learning about the human genome on the development of pathology].

作者信息

Szentirmay Zoltán

机构信息

Molekuláris Pathologiai Osztály, Országos Onkológiai Intézet, Budapest.

出版信息

Orv Hetil. 2003 Dec 21;144(51):2499-508.

PMID:14974156
Abstract

On the basis of data of the Human Genome Project, it was embraced the newest information about the gene content of the human genome, the disease genes, the parasitic DNA, the single nucleotide polymorphisms, the repeat sequences, the cytoskeletons, the regulation of cell proliferation, and their medical consequences. The applicability of the acquaintance with the human genome in pathology is presented with a few examples of our own. The significance of the single nucleotide polymorphisms in susceptibility to, or protection from, a host of disease is illustrated by the example of the allele variation of Apo-E gene. The copy number of the N-myc gene in neuroblastomas and HER2/neu gene in breast carcinomas was determined with quantitative PCR techniques. The monoclonally increased abnormal p53 protein expression was found in small cell lung cancer (in 90% frequency), in oro-pharyngeal carcinomas (82%), in esophageal squamous cell carcinomas (59%) in stomach cancer (33%), in colon carcinomas (27%) and in soft tissue sarcomas (13%). These data advert to the fact that the mutation of the p53 gene is much more frequent in those tumors in which the basic tissue is directly exposed to with the environmental carcinogens. It is now known, that near the repetitive sequences, gene rearrangement can more easily be evolve. Finally, we have determined the conditions of the accomplishment of the molecular pathological diagnosis: (1) It is applicable, when the classic morphology does not eventuate a conclusive result. (2) Well known and validated gene alterations are admissible to diagnostic purpose. (3) Only standard methods are applicable along with positive and negative controls. (4) The result has to correlate with the morphological picture, the immunohistochemical profile and the clinical data. (5) It is necessary to be able to appropriately interpret the molecular biological result, which is then incorporated in the pathological report. (6) The ethical, legal and social consequences must be considered.

摘要

相似文献

1
[Effect of learning about the human genome on the development of pathology].
Orv Hetil. 2003 Dec 21;144(51):2499-508.
2
[Frontier of mycobacterium research--host vs. mycobacterium].[分枝杆菌研究前沿——宿主与分枝杆菌]
Kekkaku. 2005 Sep;80(9):613-29.
3
[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].[通过新型人类基因的电子克隆和实验验证对NCBI人类基因数据库中出现的模型参考序列的一些错误进行分析、鉴定和校正]
Yi Chuan Xue Bao. 2004 May;31(5):431-43.
4
Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes.转录调控区域的单核苷酸多态性与环境响应基因的表达
Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):84-90. doi: 10.1016/j.taap.2004.09.024.
5
Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.联合阵列比较基因组杂交和单核苷酸多态性杂合性缺失分析揭示了宫颈癌复杂的基因改变。
BMC Genomics. 2007 Feb 20;8:53. doi: 10.1186/1471-2164-8-53.
6
[The Human Genome Project, genetic viability and genetic epidemiology].[人类基因组计划、遗传生存能力与遗传流行病学]
Orv Hetil. 2005 Dec 18;146(51):2575-80.
7
Aberrant expression of novel and previously described cell membrane markers in human breast cancer cell lines and tumors.新型及先前描述的细胞膜标志物在人乳腺癌细胞系和肿瘤中的异常表达。
Clin Cancer Res. 2005 Jun 15;11(12):4357-64. doi: 10.1158/1078-0432.CCR-04-2107.
8
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.利用表达数据和CGEMS全基因组乳腺癌关联研究来鉴定可能改变BRCA1/2突变携带者风险的基因。
Breast Cancer Res Treat. 2008 Nov;112(2):229-36. doi: 10.1007/s10549-007-9848-5. Epub 2007 Dec 20.
9
Human genetic polymorphisms.
Dev Biol Stand. 1994;83:107-10.
10
Health-related disparities: influence of environmental factors.与健康相关的差异:环境因素的影响
Med Clin North Am. 2005 Jul;89(4):721-38. doi: 10.1016/j.mcna.2005.02.001.