Bertola(Débora R),Yamamoto(Guilherme L),Alme… Am J Med Genet A 2016-05-16

...RIT1 missense mutations. Thus, we confirm that RIT1 is responsible for approximately 10% of the patients negative for mu...

Codina-Solà(Marta),Rodríguez-Santiago(Benjam… Mol Autism 2015-05-13

...RIT1, ALG9). The analysis of rare inherited variants showed enrichment in relevant pathways such as the PI3K-Akt signali...

Berger(A H),Imielinski(M),Duke(F),Wala(J),Ka… Oncogene 2015-04-14

...RIT1 in ∼2% of lung adenocarcinoma cases that cluster in a hotspot near the switch II domain of the protein. RIT1 switch...

Justino(Ana),Dias(Patrícia),João Pina(Maria)… Eur J Hum Genet 2015-10-22

...RIT1 were also associated with these syndromes. Because of the genetic and clinical heterogeneity of NCFCS, it is challe...

Chen(Peng-Chieh),Yin(Jiani),Yu(Hui-Wen),Yuan… Proc Natl Acad Sci U S A 2014-10-03

...RIT1) and mitogen-activated protein kinase kinase 1 (MAP2K1) and previously unseen loss-of-function variants in RAS p21 ...

Nature 2014-09-16

...RIT1 activating mutations and newly described loss-of-function MGA mutations which are mutually exclusive with focal MYC...

Aoki(Yoko),Niihori(Tetsuya),Banjo(Toshihiro)… Am J Hum Genet 2013-09-16

...RIT1, encoding a member of the RAS subfamily, in 17 of 180 individuals (9%) with Noonan syndrome or a related condition ...

Kabir(Ahmad H),Paltridge(Nicholas G),Able(Am… Planta 2012-09-24

...RIT1 were upregulated in Fe-deficient roots of Santi. Expression of HA1 (proton extrusion) was also significantly higher...

Liu(G Y) Mol Biol Rep 2009-05-12

...RIT1 gene encodes a protein of 219 amino acids and has high homology with the GTP-binding protein Rit1 (RIT1) of two spe...

Garbett(Krassimira),Ebert(Philip J),Mitchell… Neurobiol Dis 2008-11-07

...RIT1, SFN, GADD45B, HSPA6, HSPB8 and SERPINH1). Overall, these expression patterns appear to be more associated with the...