Literature Search

Mandal(AS),Shinohara(RT),Jung(B),Gardner(M),… medRxiv 2025-06-23

...NF1) and may be associated with other clinical manifestations of the genetic syndrome. NF1-specific growth charts that a...

Tak(E),Kim(M),Cho(Y),Choi(S),Kim(J),Han(B),K… Oncol Rep 2022-01-00

...NF1 transcript, NF1‑related pathway enrichment and NF1 mutation profile were measured and investigated using RNA sequenc...

Mandal(AS),Shinohara(RT),Jung(B),Gardner(M),… Neurology 2026-01-27

...NF1) and may be associated with other clinical manifestations of the genetic syndrome. NF1-specific growth charts that a...

Karvonen(SL),Koivunen(J),Nissinen(M),Ylä-Out… Br J Dermatol 2004-02-00

...NF1) protein (neurofibromin) accelerates the inactivation of Ras-GTP in various cell types. Somatic mutations of the NF1...

Kluwe(L),Nguyen(R),Vogt(J),Bengesser(K),Muss… Genes Chromosomes Cancer 2012-05-00

...NF1 patients have constitutional large NF1-deletions that are generally associated with more severe clinical manifestati...

Serra(E),Puig(S),Otero(D),Gaona(A),Kruyer(H)… Am J Hum Genet 1997-09-00

...NF1), one of the most common autosomal dominant disorders. The NF1 gene codes for a protein called "neurofibromin." It p...

Warrington(NM),Woerner(BM),Daginakatte(GC),D… Cancer Res 2007-09-15

...Nf1 optic glioma models suggest that this patterning results from cooperative effects of Nf1 loss in glial cells and the...

Tucker(T),Schnabel(C),Hartmann(M),Friedrich(… J Med Genet 2009-04-00

...NF1 patients. Eight of the 18 clinical biochemical measures of bone health had at least 10% of NF1 patients outside the ...

Thiel(C),Wilken(M),Zenker(M),Sticht(H),Fahso… Am J Med Genet A 2009-06-00

...NF1), was etiologically unresolved until recent reports demonstrated NF1 mutations in the majority of patients with NFNS...

Payne(JM),Barton(B),Shores(EA),North(KN) J Neurol 2013-01-00

...Nf1 (+/-) mice and children with NF1 using a well-validated measure of visuospatial learning. Children with NF1 (n = 71)...