Rho GtPases signaling: from cytoskeleton regulation to nuclear DNA damage response and rapair (2016)
- Authors:
- Autor USP: FORTI, FÁBIO LUÍS - IQ
- Unidade: IQ
- Subjects: CITOESQUELETO; DANO NUCLEAR
- Language: Inglês
- Imprenta:
- Publisher: International Forum for Cell Biology
- Publisher place: Bethesda
- Date published: 2016
- Source:
- Título do periódico: Abstracts
- Conference titles: American Society for Cell Biology Annual Meeting/ASCB
-
ABNT
FORTI, Fabio Luis e MAGALHÃES, Yuli Thamires. Rho GtPases signaling: from cytoskeleton regulation to nuclear DNA damage response and rapair. 2016, Anais.. Bethesda: International Forum for Cell Biology, 2016. . Acesso em: 12 set. 2024. -
APA
Forti, F. L., & Magalhães, Y. T. (2016). Rho GtPases signaling: from cytoskeleton regulation to nuclear DNA damage response and rapair. In Abstracts. Bethesda: International Forum for Cell Biology. -
NLM
Forti FL, Magalhães YT. Rho GtPases signaling: from cytoskeleton regulation to nuclear DNA damage response and rapair. Abstracts. 2016 ;[citado 2024 set. 12 ] -
Vancouver
Forti FL, Magalhães YT. Rho GtPases signaling: from cytoskeleton regulation to nuclear DNA damage response and rapair. Abstracts. 2016 ;[citado 2024 set. 12 ] - Effects DUSP3 silencing on cell proliferation and cell cycle regulators of xeroderma pigmentosum deficient cell lineages
- The RhoA GTPase mediate the repair pathways triggered by UV-promoted DNA lesions in mewo cells
- The RhoA and RhoB small GTPases mediate the repair signaling pathways triggered by UV-promoted DNA lesions
- Investigação estrutural da via de transdução de sinal da proteína SRC interação de CSK com caveolina1 depende do estado redox do domínio SH2
- Measuring the contributions of the Rho pathway to the DNA damage response in tumor epithelial cells
- Rac1 GTPase-deficient HeLa cells present reduced DNA repair, proliferation, and survival under UV or gamma irradiation
- Revisiting the roles of VHR/DUSP3 phosphatase in human diseases
- DUSP3 Signals for proliferation and genomic stability in human cells
- Investigação estrutural da interação da quinase CSK com caveolina 1: dependência do estado redox do domínio SH2
- The endoplasmic reticulum chaperone protein disulfide isomerase (PDII) is required for PDGF-induced RhoGTPase activation and Nox1 NADPH oxidase-dependent vascular smooth muscle cell migration
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
