Identification of genes silenced by methylation on head and neck tumor cell lineages (2007)
- Autores:
- Autores USP: JUNIOR, WILSON ARAÚJO DA SILVA - FMRP ; MOLFETTA, GREICE ANDREOTTI DE - FMRP
- Unidade: FMRP
- Assuntos: GENÉTICA MOLECULAR; NEOPLASIAS
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Abstracts
- Nome do evento: Annual Meeting of The American Society of Human Genetics
-
ABNT
KANETO, C. et al. Identification of genes silenced by methylation on head and neck tumor cell lineages. 2007, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 19 set. 2024. -
APA
Kaneto, C., Molfetta, G. A. de, Calmon, M., Moura, R., Kaiano, J., Rodrigues, R., et al. (2007). Identification of genes silenced by methylation on head and neck tumor cell lineages. In Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Kaneto C, Molfetta GA de, Calmon M, Moura R, Kaiano J, Rodrigues R, Zanetti C, Brentani H, Camargo A, Tajara E, Carraro D, Rahal P, Valentini S, Silva Júnior WA da. Identification of genes silenced by methylation on head and neck tumor cell lineages. Abstracts. 2007 ;[citado 2024 set. 19 ] -
Vancouver
Kaneto C, Molfetta GA de, Calmon M, Moura R, Kaiano J, Rodrigues R, Zanetti C, Brentani H, Camargo A, Tajara E, Carraro D, Rahal P, Valentini S, Silva Júnior WA da. Identification of genes silenced by methylation on head and neck tumor cell lineages. Abstracts. 2007 ;[citado 2024 set. 19 ] - 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
- 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
- Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation
- Construção do primeiro SAGEmap de Apis mellifera
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
