Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD) (2004)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: RIM (PATOLOGIA); CISTOS (DIAGNÓSTICO;GENÉTICA); DOENÇAS BILIARES (DIAGNÓSTICO); GENÓTIPOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the American Society of Nephrology
- ISSN: 1046-6673
- Volume/Número/Paginação/Ano: v. 15, Abstracts issue, p. 56A res. SU-FC061, 2004
- Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN
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ABNT
GALLAGHER, Rachel et al. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 10 jan. 2026. , 2004 -
APA
Gallagher, R., Esquivel, E., Tian, X., Samaroo, T., Jain, D., Onuchie, L., et al. (2004). Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2026 jan. 10 ] -
Vancouver
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2026 jan. 10 ] - 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
- Polyductin undergoes notch-like processing and regulated release from primary cilia
- Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease
- Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2
- Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin
- Dendrogram Analyses of Relative Expression Between Bladder Cancers and Controls Identify PTEN-HIF1α Association as an Alteration Characteristic of Malignancy
- Infundibular stenosis in Bardet–Biedl syndrome
- Clinical aspects of autosomal recessive polycystic kidney disease
- Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1
- Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
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