Results: 3

Mutación genética RAB11B: retraso psicomotor, braquicefalia, hipoplasia de cuerpo calloso. Primer caso descrito en España

El complejo proteico RAB11B, miembro del complejo Rab GTPasa, codificado por el gen RAB11B, juega un papel importante en el desarrollo neuronal y en la formación de las funciones cognitivas. El gen RAB11B codifica un miembro de la subfamilia de las Rab11 GTPasas que se asocia con el reciclaje de las end...

A novel lncRNA-mRNA-miRNA signature predicts recurrence and disease-free survival in cervical cancer

Braz. j. med. biol. res; 54 (11), 2021
Cervical cancer (CC) patients have a poor prognosis due to the high recurrence rate. However, there are still no effective molecular signatures to predict the recurrence and survival rates for CC patients. Here, we aimed to identify a novel signature based on three types of RNAs [messenger RNA (mRNAs), m...

Effects of Rab7 gene up-regulation on renal fibrosis induced by unilateral ureteral obstruction

Braz. j. med. biol. res; 53 (4), 2020
Rab7, an important member of the Rab family, is closely related to autophagy, endocytosis, apoptosis, and tumor suppression but few studies have described its association with renal fibrosis. In the early stage, our group studied the effects of Rab7 on production and degradation of extracellular matrix i...