Gene expression profile pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy (2010)
- Authors:
- USP affiliated authors: SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; DUARTE, GERALDO - FMRP ; MOLFETTA, GREICE ANDREOTTI DE - FMRP
- Unidade: FMRP
- Subjects: NEOPLASIAS; EXPRESSÃO GÊNICA; GRAVIDEZ
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Conference titles: Genes and Cancer Meeting 2010
-
ABNT
SILVA JÚNIOR, Wilson Araújo da et al. Gene expression profile pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy. 2010, Anais.. Warwick: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2010. . Acesso em: 23 abr. 2024. -
APA
Silva Júnior, W. A. da, Duarte, G., Molfetta, G. A. de, Zanette, D. L., Jungbluth, A., & Old, L. J. (2010). Gene expression profile pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy. In Abstracts. Warwick: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Silva Júnior WA da, Duarte G, Molfetta GA de, Zanette DL, Jungbluth A, Old LJ. Gene expression profile pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy. Abstracts. 2010 ;[citado 2024 abr. 23 ] -
Vancouver
Silva Júnior WA da, Duarte G, Molfetta GA de, Zanette DL, Jungbluth A, Old LJ. Gene expression profile pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy. Abstracts. 2010 ;[citado 2024 abr. 23 ] - Gene expression profile during pregnancy reveals similar genetic program in cancer and placenta development: identification of novel targets for cancer immunotherapy
- Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ?
- Idenficação de marcadores moleculares regulados pelo mecanismo de metilação em linhagens tumorais de cabeça e pescoço
- Análise mutacional dos genes Col1a1 e Col1a2 em pacientes com suspeita clínica de osteogênese imperfeita
- 1031-1034delTAAC (Leu125Stop): a novel familial UBE3A mutation causing Angelman syndrome in two siblings showing distinct phenotypes
- Biochemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine
- Inferring ancestry in the Ribeirão Preto population
- Analysis of expression and methylation regulation of th MGC16121 and CR596471 genes and neighbor microRNAs
- Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil
- Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
