Literature Search

Jeong(Seon-Yong),Park(Sang-Jin),Kim(Hyon J) J Korean Med Sci 2006-04-10

...NF1) is one of the most common autosomal dominant disorders in humans. NF1 is caused by mutations in the NF1 gene which ...

Upadhyaya(Meena) Expert Opin Med Diagn 2013-07-04

...NF1, genotype/phenotype studies, the RASopathies, NF1 tumorigenesis, mouse NF1 models and potential therapies. What read...

Yap(Yoon-Sim),McPherson(John R),Ong(Choon-Ki… Oncotarget 2015-11-20

...NF1 aberrations in various sporadic tumours. NF1 plays a critical role in a wide range of tumours. NF1 alterations appea...

Kuhrt(LD),Motta(E),Elmadany(N),Weidling(H),F… Dis Model Mech 2023-00-01

...NF1) is an autosomal dominant condition caused by germline mutations in the neurofibromin 1 (NF1) gene. Children with NF...

Ratner(Nancy),Miller(Shyra J) Nat Rev Cancer 2015-07-07

...NF1 mutations, we summarize current knowledge of NF1 disease, the NF1 gene and neurofibromin, neurofibromin signalling p...

Tong(Jiayuan),Hannan(Frances),Zhu(Yinghua),B… Nat Neurosci 2002-02-26

...NF1 mutations. Studies of neurofibromin, the protein encoded by NF1, have focused on its functions in tumorigenesis and ...

Legius(E),Marchuk(D A),Hall(B K),Andersen(L … Genomics 1992-09-22

...NF1)-related locus has been identified on chromosome 15. It contains a partial copy of the NF1 GAP-related domain, which...

Rutkowski(J L),Wu(K),Gutmann(D H),Boyer(P J)… Hum Mol Genet 2000-06-23

...NF1 allele and expressed both NF1 mRNA and protein, whereas the S100(+)cells typically lacked the NF1 transcript. Our fi...

Özdemir Zeydanlı(E),Özdek(Ş) Turk J Ophthalmol 2023-00-21

...NF1) has been reported in the aortic, cerebral, renal, celiac, and mesenteric vessels and is referred to as NF1 vasculop...

Kayes(LM),Schroeder(WT),Marchuk(DA),Collins(… Genomics 1992-10-00

...NF1). The pleomorphic cutaneous lesions of NF1 and the precedent for other genes being embedded within the NF1 gene prom...