Skip to search formSkip to main contentSkip to account menu

NF1 wt Allele

Known as: Neurofibromin 1 (Neurofibromatosis, Von Recklinghausen Disease, Watson Disease) wt Allele, VRNF, WSS 
Human NF1 wild type allele is located in the vicinity of 17p11.2 and is approximately 279 kb in length. This allele, which encodes neurofibromin… 
National Institutes of Health

Related topics

Related topics

7 relations
17q11.2Homo sapiensMalignant Peripheral Nerve Sheath TumorMesenchymal Glioblastoma

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1989
1989
Transplacental induction of peripheral nervous tumor in the Syrian golden hamster by N-nitroso-N-ethylurea. A new animal model for von Recklinghausen's neurofibromatosis.
Multiple peripheral nervous tumors were induced in 45 of 60 (75.0%) Syrian golden hamsters by transplacental administration of N… 
1988
1988
Expression of selected growth factors and oncogenes in neurofibrosarcomas complicating von Recklinghausen disease.
One neurofibrosarcoma from each of three patients with von Recklinghausen neurofibromatosis (VRNF) was studied for the expression… 
Review
1988
Review
1988
[Multiple duodenal and ampullary carcinoids and von Recklinghausen's neurofibromatosis].
A clinical case of multiple duodenal carcinoid involving the ampulla in a woman with von Recklinghausen's neurofibromatosis (VRNF… 
1987
1987
An exclusion map for Von Recklinghausen neurofibromatosis.
By using all the genetic linkage data available between Von Recklinghausen neurofibromatosis (VRNF) and various loci on the… 
1987
1987
DNA linkage analysis in Von Recklinghausen neurofibromatosis.
We have used DNA linkage analysis in 11 families with Von Recklinghausen neurofibromatosis (VRNF) in order to search for the… 
1987
1987
Von Recklinghausen neurofibromatosis and genetic linkage studies: clinical considerations.
For genetic linkage purposes, a subject at risk for Von Recklinghausen neurofibromatosis (VRNF) is one who has a first degree… 
Review
1987
Review
1987
Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosis.
Neurofibromatosis (NF) is one of the most frequent and clinically important Mendelian disorders in man, with an incidence of 1 in… 
1987
1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.
Linkage analysis on a panel of 15 Von Recklinghausen neurofibromatosis (VRNF) families with 19 polymorphic markers was carried… 
1987
1987
Von Recklinghausen neurofibromatosis (VRNF) and pregnancy A single case study
1987
1987
Dyschondrosteosis (Madelung's Deformity) Associated with Von Recklinghausen Neurofibromatosis (VRNF): Extension of the Spectrum of Dysplastic Phenomena Associated with NF
Dyschondrosteosis (Madelung's Deformity) Associated with Von Recklinghausen Neurofibromatosis (VRNF): Extension of the Spectrum… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)