Integrating MAGE-ML and bioconductor (2003)
- Autores:
- Autores USP: HOJO, ELZA TIEMI SAKAMOTO - FFCLRP ; PASSOS JUNIOR, GERALDO ALEIXO DA SILVA - FORP
- Unidades: FFCLRP; FORP
- Assunto: EXPRESSÃO GÊNICA
- Idioma: Inglês
- Imprenta:
- Nome do evento: International Meeting of the Microarray Gene Expression Data Society
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ABNT
MELLO, Stephano Spanó e PASSOS, Geraldo Aleixo Silva e SAKAMOTO-HOJO, Elza Tiemi. Integrating MAGE-ML and bioconductor. 2003, Anais.. Marseille: MGED, 2003. . Acesso em: 16 abr. 2024. -
APA
Mello, S. S., Passos, G. A. S., & Sakamoto-Hojo, E. T. (2003). Integrating MAGE-ML and bioconductor. In . Marseille: MGED. -
NLM
Mello SS, Passos GAS, Sakamoto-Hojo ET. Integrating MAGE-ML and bioconductor. 2003 ;[citado 2024 abr. 16 ] -
Vancouver
Mello SS, Passos GAS, Sakamoto-Hojo ET. Integrating MAGE-ML and bioconductor. 2003 ;[citado 2024 abr. 16 ] - Effect of 'gama'-radiation on the expression of the Ha-ras oncogene in ras-transfected and non-transfected mouse balb/3T3 fibroblasts
- Interlocus TCR V-gamma and TCR J-beta-1 V-J recombination measures of genomic instability in human lymphocytes treated with eugenol or carbamide peroxide
- Cell cycle arrest and apoptosis in TP53 subtypes of bladder carcinoma cell lines treated with cisplatin and gemcitabine
- The transcriptional and post-transcriptional control pathway of promiscuos gene expression (PGE) in the thymus
- Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene
- Alterations in gene expression, cell cycle control and apoptosis induced by ionizing radiation in fibroblast cell lines
- Transformed AT (ataxia telangiectasia) fibroblasts are capable to form TCR (T-cell receptor) 'beta'/'gama' rearrangements under control of P53 gene
- Differential gene expression induced by ionizing radiation in normal and ataxia telangiectasia fibroblast cell lines
- Cellular response to DNA damage induced by cisplatin in normal and DNA repair deficient cell lines
- Detection of t-cell receptor BV8.1-BDJ2.1 C(D)J recombination in murine fetal thymus organ culture
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