...RIT1-associated mirror syndrome and non-immune hydrops fetalis (NIHF) further supports the role of Rasopathies in the pa...
...RIT1, and SMAD6. Trio sequencing facilitated the identification of pathogenic variation (55.6% were de novo missense var...
...RIT1 alterations. In this study, we generated a murine model of RIT1M90I-mutant lung cancer. RIT1M90I expression induced...
RIT1 is a small GTPase of the RAS family, and RIT1 mutations have been identified in lung cancer, leukemia, and the deve...
...RIT1-mutant lung tumors to SHP2 or RAS tricomplex inhibitors. Collectively, these findings highlight the importance of R...
...RIT1, SHOC2, and SOS1. The most significant contributor among these variants was PTPN11 (43.7 %; 31/71), followed by RAF...
...RIT1 mutations by polymerase chain reaction-direct sequencing. MET amplification and ALK and ROS1 translocations were as...
...RIT1 mutation-positive patients, we further performed a RIT1 analysis in RASopathy patients and identified 7 RIT1 mutati...
...RIT1, one in SHOC2, two in HRAS, three in BRAF, two in MAP2K1 and two in the NF1 gene). Two of them (p.Gly392Glu in the ...
...RIT1 and assess the clinical significance of RIT1 expression in endometrial cancer patients. The mRNA and protein expres...
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