Is mouse mitochondrial DNA protected from alkylation damage by AAG? (2016)
- Authors:
- Autor USP: PINTO, NADJA CRISTHINA DE SOUZA - IQ
- Unidade: IQ
- Subjects: DANO AO DNA; GENOMAS
- Language: Inglês
- Imprenta:
- Publisher: Associação Brasileira de Mutagênese e Genômica Ambiental
- Publisher place: Ribeirão Preto
- Date published: 2016
- Source:
- Título do periódico: Abstracts
- Conference titles: Congresso da MutaGen-Brasil
-
ABNT
BERRA, Carolina Maria e MEIRA, L. B e SOUZA-PINTO, Nadja Cristhina de. Is mouse mitochondrial DNA protected from alkylation damage by AAG? 2016, Anais.. Ribeirão Preto: Associação Brasileira de Mutagênese e Genômica Ambiental, 2016. . Acesso em: 23 abr. 2024. -
APA
Berra, C. M., Meira, L. B., & Souza-Pinto, N. C. de. (2016). Is mouse mitochondrial DNA protected from alkylation damage by AAG? In Abstracts. Ribeirão Preto: Associação Brasileira de Mutagênese e Genômica Ambiental. -
NLM
Berra CM, Meira LB, Souza-Pinto NC de. Is mouse mitochondrial DNA protected from alkylation damage by AAG? Abstracts. 2016 ;[citado 2024 abr. 23 ] -
Vancouver
Berra CM, Meira LB, Souza-Pinto NC de. Is mouse mitochondrial DNA protected from alkylation damage by AAG? Abstracts. 2016 ;[citado 2024 abr. 23 ] - Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria
- Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane
- Characterization of oxidative guanine damage and repair in mammalian telomeres
- The role of mitochondrial DNA damage in the citotoxicity of reactive oxygen species
- Formation and repair of oxidative damage in the mitochondrial DNA
- Base excision repair activities differ in human lung cancer cells and corresponding normal controls
- ExoMeg1: a new exonuclease from metagenomic library
- Expressão recombinante da proteína Fator de Transcrição Mitocondrial A (TFAM) em Escherichia coli
- PPAR coregulators are essential mediators of mitochondrial function and redox homeostasis in skeletal muscle cells
- Opposing action of NCoR1 and PGC-1 alpha in mitochondrial redox homeostasis
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