...RIT1-associated mirror syndrome and non-immune hydrops fetalis (NIHF) further supports the role of Rasopathies in the pa...
...RIT1, SHOC2, and SOS1. The most significant contributor among these variants was PTPN11 (43.7 %; 31/71), followed by RAF...
...RIT1, MRAS, and KRAS, revealing interfaces that govern RAS isoform selectivity and nucleotide specificity. Biochemical a...
...RIT1 may act as a non-canonical driver oncogene in lung cancer. However, the lack of a RIT1-mutant lung cancer model has...
...RIT1 mutation-positive patients, we further performed a RIT1 analysis in RASopathy patients and identified 7 RIT1 mutati...
...RIT1 and assess the clinical significance of RIT1 expression in endometrial cancer patients. The mRNA and protein expres...
...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 mutations by polymerase chain reaction-direct sequencing. MET amplification and ALK and ROS1 translocations were as...
...RIT1 missense mutations. Thus, we confirm that RIT1 is responsible for approximately 10% of the patients negative for mu...
...RIT1 were also associated with these syndromes. Because of the genetic and clinical heterogeneity of NCFCS, it is challe...
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