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GENETIC EPIDEMIOLOGY OF CANCER IN UTAH GENEALOGIES

GENETIC EPIDEMIOLOGY OF CANCER IN UTAH GENEALOGIES
犹他州谱系中癌症的遗传流行病学
批准号:
3168379
负责人:
MARK H SKOLNICK
金额:
$22.55万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1981
资助国家:
美国
项目状态:
已结题
起止时间:
1981-04-01 至 1989-11-30

项目摘要

项目成果

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中文摘要
翻译
这项研究旨在了解癌症的基本原因
英文摘要
This research seeks to understand fundamental causes of cancer in a defined population in which both genetic and environmental factors will be examined. The computerized genealogy of the 1.3 million Utah Mormons and the records of the Utah Cancer Registry provide the basis for analysis of cancer occurrence in relatives. This population is stable, cooperative, and genetically similar to other populations of Northern European origin. The continued development and refinement of the linking of records within the genealogy and between the genealogy, cancer registry and death certificates is essential for the use of these resources for population based analysis. Another goal of the research is the improvement of the database system for access to and analysis of records. Clusters of relatives with cancer will be identified from the genealogy and auxiliary records. All cancer clusters with three or more relatives affected at the same site will be examined for the types of cancers which occur together. Some pedigrees, in which a large number of related people are found to have had cancer, will be examined for linkage between a gene causing cancer and cellular oncogenes. If tight linkage to oncogenes is excluded, a general linkage study will be performed which will analyze genetic models and gene penetrance. Cases of cancer occurring within families will be compared to those with no family history, and environmental factors known to be associated with cancer will be compared. In the process of analysis, the tools for analysis of pedigrees, occurrence of diseases in relatives, and measurement of the large population database will continue to be developed. The results will allow an assessment of the importance of genes in causing and a model for the study of other diseases caused by both genetic and environmental factos.
期刊论文(39)
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会议论文
The power of identity-by-state methods for linkage analysis.
用于连锁分析的逐状态身份方法的强大功能。
DOI: --
发表时间: 1990
期刊: American journal of human genetics
影响因子: 9.8
作者: [Bishop,DT, Williamson,JA]
通讯作者: Williamson,JA
Chiasma-based models of multilocus recombination: increased power for exclusion mapping and gene ordering.
基于交叉的多位点重组模型:增强排除图谱和基因排序的能力。
DOI: 10.1016/0888-7543(89)90059-1
发表时间: 1989
期刊: Genomics
影响因子: 4.4
作者: [Goldgar,DE, Fain,PR, Kimberling,WJ]
通讯作者: Kimberling,WJ
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12).
CRYB1 基因座 (17q11.2----17q12) 上有一个罕见的 PvuII RFLP。
DOI: 10.1093/nar/17.2.826
发表时间: 1989
期刊: Nucleic acids research
影响因子: 14.9
作者: [Barker,DF, Fain,PR, Wright,EC, Nguyen,K, Tsui,LC]
通讯作者: Tsui,LC
A genomic search for linkage of neurofibromatosis to RFLPs.
神经纤维瘤病与 RFLP 关联的基因组搜索。
DOI: 10.1136/jmg.24.9.536
发表时间: 1987
期刊: Journal of medical genetics
影响因子: 4
作者: [Barker,D, Wright,E, Nguyen,K, Cannon,L, Fain,P, Goldgar,D, Bishop,DT, Carey,J, Kivlin,J, Willard,H]
通讯作者: Willard,H
共 28 条
    GENETIC EPIDEMIOLOGY OF CANCER IN UTAH GENEALOGIES
    • 批准号:
      6245899
    • 项目类别:
    • 资助金额:
      $2.15万
    • 财政年份:
      1997
    • 负责人:
      MARK H SKOLNICK
    • 依托单位:
    MAPPING COLORECTAL CANCER SUSCEPTIBILITY LOCI
    • 批准号:
      2105755
    • 项目类别:
    • 资助金额:
      $22.33万
    • 财政年份:
      1994
    • 负责人:
      MARK H SKOLNICK
    • 依托单位:
    MAPPING COLORECTAL CANCER SUSCEPTIBILITY LOCI
    • 批准号:
      2105754
    • 项目类别:
    • 资助金额:
      $21.08万
    • 财政年份:
      1994
    • 负责人:
      MARK H SKOLNICK
    • 依托单位:
    MAPPING AND CLONING THE 17Q-LINKED BREAST CANCER LOCUS
    • 批准号:
      2097008
    • 项目类别:
    • 资助金额:
      $26.27万
    • 财政年份:
      1993
    • 负责人:
      MARK H SKOLNICK
    • 依托单位:
    海外基金