Specific malignancies associated with neurofibromatosis 1 demonstrate loss of both alleles which supports the hypothesis that NF1 acts as a tumor suppressor in some tissue. The absence of LOH(loss of heterozygosity) in benign tumors of NF1 patients suggests that the second NF1 allele may be functional. Antibody and mRNA detection of the NF1 gene product is not sensitive enough to be convincing that absence of signal means loss of neurofibromin function. Identification of NF1 patients with large deletions that encompass the entire gene is the goal.

Project Start
1997-03-06
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
33
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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