...NF1 (7 patients [2.2%]), and CDKN2A (7 patients [2.2%]). Copy number alterations and fusions were infrequent. In 61.0% o...
...NF1 (ARID1A, 52.6%; ARID2, 48.5%; ARID1A/2, 63.6%; and ARID-WT, 13.3%; p < 0.0001) and KRAS (ARID1A, 3.5%; ARID2, 3.1%; ...
...NF1, PIN1, MIB1, PDS5A, MCM7, and MLH1, was significantly downregulated (all P<0.05), while PAX8 gene expression was sig...
...Nf1 and Gstp1) were identified as key candidate genes regulating epididymal sperm quality on the HPT axis, which may aff...
...NF1 in the other patients, she suggests that pathological activation of RAS-dependent pathways plays a central role in t...
...nf1(0-3) Rydberg states were found to be metastable and to have lifetimes of more than 5 micros beyond n=50. Members of ...
...NF1, NF2) and tuberous sclerosis complex (TSC) type 1 and 2 (TSC1, TSC2). Li Fraumeni Syndrome, Constitutional Mismatch ...
...NF1</i> (32.4%), <i>CDK12</i> (29.0%), <i>PIK3CA</i> (28.0%), <i>NOTCH3</i> (1...
...NF1 patients, peripheral neuropathy and plexopathy, predisposing conditions such as Li Fraumeni syndrome in paediatric c...
...NF1, NF2, and schwannomatosis) are hereditary tumor predisposition syndromes with a risk for poor quality of life (QOL) ...
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