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swine UCHL3 (show Uchl3 ELISA Kits), RIT1 and CCND3 (show CCND3 ELISA Kits) genes were differentially expressed in tissues including small intestine, large intestine, liver, muscle, fat, lung, spleen and kidney
Biochemical Classification of Disease-associated Mutants of RAS-like Protein Expressed in Many Tissues (RIT1).
We report on a 2.5-year-old male patient with clinical signs of NS and hematologic abnormalities, in whom a novel heterozygous substitution in RIT1 with probable pathogenicity was detected.
Mutations in RIT1 cause Noonan syndrome. Mutations in RIT1 affect RAS-MAPK (show MAPK1 ELISA Kits)/MEK (show MAP2K1 ELISA Kits)-ERK (show EPHB2 ELISA Kits) signaling. The mutant RIT1 protein may possess reduced GTPase (show RACGAP1 ELISA Kits) activity or a diminished ability to interact with cellular GTPase (show RACGAP1 ELISA Kits) activating proteins.
elevated expression of RIT1 may contribute to the progression of endometrial cancer and thus may serve as a novel prognostic marker and a promising molecular target for the treatment of endometrial cancer.
Because of the relatively high frequency of mutations in RIT1 among patients with NS and its occurrence in different populations, we suggest that it should be added to the list of genes included in panels for the molecular diagnosis of NS.
A genotype-phenotype correlation analysis of available records indicated that germline RIT1 mutations cause a noonan syndrome phenotype characterized by a mild facial appearance.
four additional cases of Noonan syndrome with mutations in RIT1, were identified.
Data identify RIT1 as a driver oncogene (show RAB1A ELISA Kits) in a specific subset of lung adenocarcinomas.
we highlight recent studies using transgenic and knockout animal models which have begun to elucidate the physiological roles for the Rit subfamily, including emerging roles in the regulation of neuronal morphology and cellular survival signaling
ROC1 knockdown remarkably inhibited bladder cancer cell growth, arrested cells at the G2 phase of the cell cycle, and induced the p53 (show TP53 ELISA Kits)-dependent cell senescence.
the Rit-p38 (show CRK ELISA Kits)-MSK1 (show RPS6KA5 ELISA Kits)/2 signaling pathway may have an important role in the stress-dependent regulation of CREB (show CREB1 ELISA Kits)-dependent gene expression.
these data identify a new and unexpected role for Rit in injury-induced neurogenesis, functioning as a selective survival mechanism for immature hippocampal neurons within the subgranular zone of the dentate gyrus following TBI.
our studies establish the Rit GTPases as critical regulators of an evolutionarily conserved, p38 MAPK (show MAPK14 ELISA Kits)-dependent signaling cascade
Rin (show RIT2 ELISA Kits) and Rit Bind to PAR6 (show PARD6A ELISA Kits) GTP (show AK3 ELISA Kits)-dependently and regulate cell transformation
This gene encodes a member of a subfamily of Ras-related GTPases. The encoded protein is involved in regulating p38 MAPK-dependent signaling cascades related to cellular stress. This protein also cooperates with nerve growth factor to promote neuronal development and regeneration. Alternate splicing results in multiple transcript variants.
GTP-binding protein Rit1
, Ras-like without CAAX 1
, GTP-binding protein Roc1
, Ric-like, expressed in many tissues
, ras-like protein expressed in many tissues
, ras-like without CAAX protein 1
, RAS-like protein expressed in many tissues