Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls (2003)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: NEFROLOGIA; RATOS
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2003
- Source:
- Título: Journal of the American Society of Nephrology
- Volume/Número/Paginação/Ano: v. 14
- Conference titles: Accredited Sponsor: The American Society of Nephrology
-
ABNT
SOUSA, Mauri et al. Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls. Journal of the American Society of Nephrology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 jan. 2026. , 2003 -
APA
Sousa, M., Piontek, K., Menezes, L. F., Araujo, M., Germino, G. G., & Onuchic, L. F. (2003). Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls. Journal of the American Society of Nephrology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Sousa M, Piontek K, Menezes LF, Araujo M, Germino GG, Onuchic LF. Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls. Journal of the American Society of Nephrology. 2003 ; 14[citado 2026 jan. 23 ] -
Vancouver
Sousa M, Piontek K, Menezes LF, Araujo M, Germino GG, Onuchic LF. Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls. Journal of the American Society of Nephrology. 2003 ; 14[citado 2026 jan. 23 ] - PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
- NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology
- Doenças císticas renais em pediatria
- Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene
- Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
- Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene
- PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
- Ausência de redução da capacidade de concentração urinária em camundongo heterozigoto para mutação nula no gene
- Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts
- Molecular cloning of a novel cytokine-like gene
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