...nf1, the murine counterpart of the human gene mutated in neurofibromatosis type 1 (NF1). Here, we show that GDNF-induced...
...NF1) is a common autosomal dominant genetic disorder caused by mutations in the NF1 gene. In this paper we report our ex...
Neurofibromatosis 1 (NF1) is a common genetic disorder with an autosomal dominant mode of inheritance, an increased morb...
...NF1 or AP1 recognition sequences. In transient transfections of COS cells, the NF1YY1TATA and NF1RYY1TATA promoters exhi...
...NF1)] or schwannomas [neurofibromatosis type 2 (NF2), schwannomatosis and Carney complex type 1] has greatly advanced ou...
Neurofibromatosis type 1 (NF1), the most common genetic disorder affecting the human nervous system, is characterized by...
To determine the frequency and nature of MRI lesions in children with neurofibromatosis type I (NF1), 50 patients aged 8...
...NF1) gene is frequently abnormal in another neural disorder, neurofibromatosis type 1; in addition, a potential mutation...
...NF1) reverse v-Ras-induced malignant phenotype. Since there is no homology in primary structures of RGL, Raf-1, and NF1,...
...NF1) gene, in two of three exons of the neurofibromatosis type 2 (NF2) gene, and in one of three exons of the tuberous s...
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