...NF1-GAP related domain (NF1-GRD) were investigated. The NF1-GRD was unable to stimulate the GTPase of Ras[Asn33], Ras[Se...
...NF1 germline and two somatic mutations. In a plexiform neurofibroma from an NF1 patient, mutations in both NF1 alleles h...
...NF1) is an autosomal dominant genetic disorder caused by mutations in the NF1 gene. Patients with NF1 have a higher risk...
...NF1 gene (Nf1-/-). LPA promoted F-actin polymerization and increased migration and survival of Nf1-/- SCs as compared to...
...NF1. The classical double-hit inactivation of the NF1 gene suggests that the NF1 genetic background promoted melanoma ge...
...NF1) results from mutations in the NF1 tumor suppressor gene, which encodes the protein neurofibromin. NF1 patients disp...
...NF1 patients have private loss-of-function mutations scattered along the NF1 gene. Here, we present an original NF1 inve...
...NF1; OMIM 162200). Genotype-phenotype correlations in patients with NF1 may help to determine the risk group for develop...
...NF1) and large deletions of the NF1 gene region. The study participants were 16 patients with large NF1 deletions and 16...
...NF1) is one of the most common autosomal dominant cancer syndromes worldwide. Individuals with NF1 have a wide variety o...
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