<i>HRAS</i> mutation analysis in Costello syndrome: Genotype and phenotype correlationKaren W. Gripp, Katia Sol‐Church, Cynthia A. Agresta et al.|American Journal of Medical Genetics Part A|2005Cited by 189
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPasesTaiki Abe, Yoko Aoki|Cell Death and Differentiation|2019Cited by 127
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Assel Rakhmetova, Hiroki Kudo et al.|Nature Communications|2018Cited by 126
New Noonan syndrome model mice with RIT1 mutation exhibit cardiac hypertrophy and susceptibility to β-adrenergic stimulation-induced cardiac fibrosisShingo Takahara, Yoko Aoki|EBioMedicine|2019Cited by 32
LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretionTaiki Abe, Yoko Aoki|Cell Death and Disease|2023Cited by 18