Studies of Neurofibromatosis-1 Modifier Genes

Abstract

This project aims to collect NF1 patient DNAs required to identify neurofibroma burden modifier genes, to perform an allele association study for three classes of potential modifiers, and to evaluate more global approaches. Over four years we aim to collect 1200 DNAs from adult NF1 patients that represent the top and bottom 20% of dermal neurofibroma burden in various age cohorts. We will use these DNAs in a case-control allele association study that will test whether neurofibroma numerical variability reflects (1) allelic differences in genes that maintain genome stability; (2) differences in the NF1 gene itself or in closely linked genes; or (3) differences in genes involved in signaling between neurofibroma constituent cells. In the second year of this project we have continued to make progress towards our patient recruitment goal, in part by enlisting additional clinical collaborators. Among other major progress, we have implemented a relational database of approximately 25% of human genes, and we have used this database to identify and prioritize approximately 1000 candidate neurofibroma burden modifiers. We have also begun the genotyping of selected high priority SNPs and have published three review papers describing our bioinformatics efforts.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2005
Accession Number
ADA437252

Entities

People

  • Andre Bernards

Organizations

  • Massachusetts General Hospital

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Abstracts
  • Carrier Proteins
  • Cell Membrane
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Data Analysis
  • Diseases And Disorders
  • Fungi
  • Genetics
  • Health Services
  • Hematologic Diseases
  • Institutional Review Board
  • Neoplasms
  • Neuromuscular Diseases
  • Proteins
  • Skin Diseases

Fields of Study

  • Biology
  • Medicine

Readers

  • Molecular and Cellular Biology
  • Molecular and genetic basis of cancer.