...Nf1+/- ) mice. Synchronized A530 cell cultures expressing typical glial markers were injected at the beginning of the da...
...NF1 (2), SMARCB1 (1), NF2 (1), MSH6 (1), PMS2 (1), and a patient with 47,XXY Klinefelter syndrome. Our results demonstra...
...NF1 1.32%, and ROS1 0.66%. We identified 48 cases with double or triple driver gene mutations. Multiple mutations were m...
...NF1, ERBB2, and KRT17 genes. Mutations in the AKT1, PIK3CA, and BRIP genes were associated with tumor recurrence, with a...
...NF1 (15%), and TP53 (13%) mutations were found at a higher incidence than previously reported and TP53 mutations were as...
...NF1 with shunted hydrocephalus, chronic infantile neurological cutaneous and articular (CINCA) syndrome, nephrotic cysti...
...NF1-deficient PNF cell lines, TAK-733 was found to reduce PNF cell viability the most. We then cultured the TAK-733‒resi...
...NF1) were found to be normal after NGS according to single-sperm-based SNP haplotype analysis (13 SNP sites). Three and ...
...NF1, and STK11 were observed in one case each. No IDH1, KRAS, or PBRM1 mutations were found. iCCAs with DPM pattern have...
...NF1, CDKN2A, CCND2, EGFR, and MYCN. By paired analysis, 68 mRNA transcripts were differentially expressed in recurrent/p...
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