Investigating roles of dual tyrosine in DNA damage responses (2009)
- Authors:
- Autor USP: FORTI, FÁBIO LUÍS - IQ
- Unidade: IQ
- Subjects: DANO AO DNA; BIOQUÍMICA; REPARAÇÃO DE DNA
- Language: Inglês
- Imprenta:
- Publisher: UFMG
- Publisher place: Belo Horizonte
- Date published: 2009
- Source:
- Título: Abstracts
- Conference titles: Meeting in Fundamental Aspects of DNA Repair and Mutagenesis
-
ABNT
TORRES, T. E. e NASCIMENTO, Monica Helena Monteiro do e FORTI, Fabio Luis. Investigating roles of dual tyrosine in DNA damage responses. 2009, Anais.. Belo Horizonte: UFMG, 2009. . Acesso em: 13 mar. 2026. -
APA
Torres, T. E., Nascimento, M. H. M. do, & Forti, F. L. (2009). Investigating roles of dual tyrosine in DNA damage responses. In Abstracts. Belo Horizonte: UFMG. -
NLM
Torres TE, Nascimento MHM do, Forti FL. Investigating roles of dual tyrosine in DNA damage responses. Abstracts. 2009 ;[citado 2026 mar. 13 ] -
Vancouver
Torres TE, Nascimento MHM do, Forti FL. Investigating roles of dual tyrosine in DNA damage responses. Abstracts. 2009 ;[citado 2026 mar. 13 ] - Investigação estrutural da via de transdução de sinal da proteína SRC: interação de CSK com caveolina-1 depende do estado redox do domínio SH2
- Measuring the contributions of the Rho pathway to the DNA damage response in tumor epithelial cells
- Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability
- The use of HeLa cells as a model for studying DNA damage and repair
- Revisiting the roles of VHR/DUSP3 phosphatase in human diseases
- The small GTPase RhoA signals to DNA damage repair in tumor cells
- DUSP3 Signals for proliferation and genomic stability in human cells
- DUSP3 maintains genomic stability and cell proliferation by modulating NER pathway and cell cycle regulatory proteins
- Non-canonical role of Cdc42 GTPase and its novel interaction partners in genomic instability conditions
- Overactivated Cdc42 acts through Cdc42EP3/Borg2 and NCK to trigger DNA damage response signaling and sensitize cells to DNA-damaging agents
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