Literature Search

Li(Y),Zhu(M),Lin(X),Li(J),Yuan(Z),Liu(Y),Xu(… Exp Ther Med 2021-11-00

...NF1) is an autosomal dominant genetic disease that is caused by mutations in the NF1 gene. Various studies have previous...

Jääsaari(P),Visnapuu(V),Nyström(M),Peltonen(… Eur J Oral Sci 2012-12-00

...NF1) is a common, hereditary, neurocutaneous skeletal condition with a variety of osseous manifestations. Although NF1 a...

Fortunato(JT),Reys(B),Singh(P),Pan(E) Anticancer Res 2018-08-00

...NF1). While research has proposed that larger germ-line mutations in NF1 may be the driving factor that predisposes pati...

Packer(RJ),Iavarone(A),Jones(DTW),Blakeley(J… Neuro Oncol 2020-00-09

...NF1-associated gliomas. A consensus panel consisting of experts in NF1 and gliomas was convened to review the current mo...

Tassabehji(M),Strachan(T),Sharland(M),Colley… Am J Hum Genet 1993-07-00

...NF1 locus and a deletion at the NF1 locus demonstrated in a WS patient. This suggests either that WS and NF1 are allelic...

Garrido(MB),Jagtap(R),Matesi(CD),Diaz(V),Har… J Korean Assoc Oral Maxillofa… 2024-02-29

...NF1 gene have been detected in NF1 patients with CGCGs, validating that they are NF1-associated lesions. Oral manifestat...

Ritter(A),Cuddapah(S),Degenhardt(K),Kaspersk… Am J Med Genet A 2019-00-00

...NF1 and review NF1-related left ventricular hypertrophy. NF1 should be considered in the differential diagnosis for fetu...

Goetsch Weisman(A),Haws(T),Lee(J),Lewis(AM),… Compr Child Adolesc Nurs 2020-09-24

...NF1-specific transition knowledge and skills (NF1-TRAQ) (r = 0.632). Participants self-report adequate knowledge of NF1 ...

Zhang(L),Jiang(L),Zeng(L),Jin(Z),Dong(X),Zha… J Transl Med 2023-00-05

...NF1 in NOZ and EH-GB1 cells via siRNA or lv-shRNA mediated knockdown. Direct interaction between NF1 and YAP1 was detect...

Pemov(A),Li(H),Patidar(R),Hansen(NF),Sindiri… Oncogene 2017-00-01

...NF1 mutations and found somatic NF1 inactivation in 74% of the PN. One individual with three PNs had different NF1 somat...