...NF1s. Interestingly, three isoforms of NF1-A (NF1-A1, A2, A4) have two NLSs and translocate completely to the nucleus. I...
...NF1) according to standard NIH criteria. Analysis of the NF1 gene revealed a recurrent mutation in exon 37 (C6792A or Y2...
...NF1 patient-derived fibroblasts can be successfully reprogrammed in NF1(+/-) iPSCs with active RAS signaling and that NF...
...NF1 and the development of breast cancer in women; however, due to the rarity of both NF1 and male breast cancer, the sa...
...NF1) neurogenetic condition. As such, individuals with NF1 are born with a germline mutation in the NF1 gene, but may de...
...NF1 gene in two sporadic cases with neurofibromatosis type 1 (NF1) and explore their molecular mechanisms. Clinical data...
...NF1) is monogenic neurodevelopmental disorder caused by mutation of NF1 gene, which leads to increased susceptibility to...
...NF1 and to report the interventions described to address the needs of pediatric patients with NF1. A literature review w...
...NF1) is encoded by the NF1 tumour suppressor gene. Mutations result in a disorder known as Neurofibromatosis Type 1 (NF-...
...NF1, the incidence of headache in NF1 patients is not low. We report an NF1 family in which the proband presented with p...
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