VDR regulation in HC11ras transformed cells (2003)
- Authors:
- USP affiliated authors: FOLGUEIRA, MARIA APARECIDA AZEVEDO KOIKE - FM ; BRENTANI, MARIA MITZI - FM
- Unidade: FM
- Subjects: VITAMINA D; NEOPLASIAS MAMÁRIAS
- Language: Inglês
- Imprenta:
- Publisher place: Maastricht
- Date published: 2003
- Source:
- Título do periódico: Resumos
- Conference titles: Workshop on Vitamin D
-
ABNT
ROZENCHAN, P. B. et al. VDR regulation in HC11ras transformed cells. 2003, Anais.. Maastricht: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 01 maio 2024. -
APA
Rozenchan, P. B., Folgueira, M. A. A. K., Katayama, M. L. H., Snitscovsky, I. M. L., & Brentani, M. M. (2003). VDR regulation in HC11ras transformed cells. In Resumos. Maastricht: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Rozenchan PB, Folgueira MAAK, Katayama MLH, Snitscovsky IML, Brentani MM. VDR regulation in HC11ras transformed cells. Resumos. 2003 ;[citado 2024 maio 01 ] -
Vancouver
Rozenchan PB, Folgueira MAAK, Katayama MLH, Snitscovsky IML, Brentani MM. VDR regulation in HC11ras transformed cells. Resumos. 2003 ;[citado 2024 maio 01 ] - Effects of 1,25 (OH)2D3 on molecules involved in cell cycle control in H-RAS transformed mammary cells
- Genes differentially expressed in breast cancer (BC) sample as compared to normal breast tissue from women without cancer
- Expression of vitamin D receptor mRNA in the hippocampal formation of rats submitted to a model of temporal lobe epilepsy induced by pilocarpine
- Correlação clínico-patológica de pacientes com câncer de mama pós-quimioterapia neoadjuvante
- Uninvolved lymph nodes commonly modulated by the presence of breast cancer cells
- Gene expression associated to response to doxorubicin based primary chemotherapy in breast cancer
- C-myc and c-max mRNA expression in HC11 mouse mammary cells exposed to 1,25 (OH)2D3 are events unrelated to growth arrest
- Regulação da expressão de RNAM de VDR em células HC11 parentais ou transformadas com HRAS
- Gene expression profile associated to advanced breast cancer
- Differential gene profiling of malignant cells and fibroblasts from the primary and metastatic sites from breast cancer patients upon stroma-epithelial cell interaction
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