Results 161 to 170 of about 25,840 (207)

Zebrafish neurofibromatosis type 1 mutants show disruption of sleep but not of circadian rhythms. [PDF]

Sleep
Lee DA, Oikonomou G, Chiu Y, Cho AD, Xu J, Cammidge T, Singh C, Prober DA.   +7 more
europepmc   +1 more source

Cognitive and autism-like abnormalities are associated with gut microbiome alterations in a mouse model of Neurofibromatosis type I

Hannan A, Reisinger S, de Garde Nv, Kong G, Muhammad A, Lu D, Senthilkumar P, Kiridena P, Gubert C, Dabscheck G, Payne J.   +10 more
europepmc   +1 more source

Current states in understanding oligodendroglia-mediated neurological issues in neurofibromatosis type 1 (NF1). [PDF]

Acta Neuropathol Commun
Aghoghovwia BE, Shen CE, Bano S, Shyamala N, Echeandia Marrero A, Irshad K, Sharafaldin S, Brossier NM, Pan Y.   +8 more
europepmc   +1 more source

Molecular Dynamics Simulations of the SPRED2^Leu100Pro EVH-1 Domain Complexed with the GAP-Related Domain of Neurofibromin. [PDF]

Int J Mol Sci
Terrusa M, Sangiovanni E, Motta M, Tartaglia M, Prandi IG, Chillemi G.   +5 more
europepmc   +1 more source

Pleomorphic Carcinoma With EGFR and Concomitant Mutations Transformed From Lung Adenocarcinoma: A Case Report. [PDF]

Cancer Rep (Hoboken)
Akazawa Y, Sato T, Yagami Y, Kesen Y, Furo T, Watanabe A, Endo J, Nakano M, Kurata H, Matsuo H, Nakahara Y, Sasaki J, Naoki K.   +12 more
europepmc   +1 more source

A transcriptomic, proteomic, and functional genetic atlas dissects neurofibromin function in the peripheral nervous system. [PDF]

Proc Natl Acad Sci U S A
Vasudevan HN, Arang N, Sacconi Nunez M, Kennedy P, Payne E, Mohabeer S, Chien J, Wright A, Sale MJ, Krogan NJ, Forget A, McCormick F.   +11 more
europepmc   +1 more source

A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1 [PDF]

Journal of Neurochemistry, 2015
AbstractNeurofibromatosis type 1 (NF1) is an autosomal dominant genetic condition caused by dominant loss‐of‐function mutations of the tumor suppressor gene NF1 that encodes neurofibromin, a negative regulator of RAS activity. Mutation analysis of NF1 located at 17q11.2 has been hampered by the large size of the gene, the high rate of new mutations ...
Teresa Esposito, Giulio Piluso, Dario Saracino   +2 more
exaly   +3 more sources