Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors (2007)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: NEOPLASIAS HEPÁTICAS (ETIOLOGIA); DUTOS (FISIOPATOLOGIA); CISTOS INFLAMATÓRIOS; HEPATOPATIAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Volume/Número/Paginação/Ano: p. 1, res. 15, 2007
- Conference titles: Annual Meeting United States and Canadian Academy of Pathology
-
ABNT
DORN, Livia et al. Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors. 2007, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2007. p. 1. . Acesso em: 19 abr. 2024. -
APA
Dorn, L., Onuchic, L. F., Menezes, L. F. C., & Sergi, C. (2007). Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors. In Abstracts (p. 1). San Diego: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Dorn L, Onuchic LF, Menezes LFC, Sergi C. Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors. Abstracts. 2007 ; 1.[citado 2024 abr. 19 ] -
Vancouver
Dorn L, Onuchic LF, Menezes LFC, Sergi C. Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors. Abstracts. 2007 ; 1.[citado 2024 abr. 19 ] - Regulação do volume celular no ramo ascendente fino da alça de Henle de ratos
- Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12
- Genomic structure and exclusion of two candidate genes for the PKHD1 locus and three new polymorphic markers within the critical interval
- Direct association of full-lenght PKD1 and PKD2 proteins in mammalian cells
- Aumento regulatório do volume celular em túbulos de malpighi
- Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene
- Expression of PKD1 and PKD2 transcripts and proteins in human embryo and during normal kidney development
- Contribuições dos Modelos Animais ao Entendimento da Patogênese das Doenças Renais Policísticas
- Recombinant and endogenous polyductin (PD1) is secreted from primary cilia
- PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
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