Clinical aspects of autosomal recessive polycystic kidney disease (2007)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: RIM (FISIOLOGIA); CISTOS (DIAGNÓSTICO); MORTALIDADE
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Volume/Número/Paginação/Ano: p. 20, res. FC08, 2007
- Conference titles: World Congress of Nephrology/WCN'07 Satellite Symposium on Pediatric Nephro-Urological Diseases
-
ABNT
DIAS, N. F. et al. Clinical aspects of autosomal recessive polycystic kidney disease. 2007, Anais.. São Paulo: Faculdade de Medicina, Universidade de São Paulo, 2007. p. 20. . Acesso em: 27 dez. 2025. -
APA
Dias, N. F., Lanzarini, V., Onuchic, L. F., & Koch, V. (2007). Clinical aspects of autosomal recessive polycystic kidney disease. In Abstracts (p. 20). São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Dias NF, Lanzarini V, Onuchic LF, Koch V. Clinical aspects of autosomal recessive polycystic kidney disease. Abstracts. 2007 ; 20.[citado 2025 dez. 27 ] -
Vancouver
Dias NF, Lanzarini V, Onuchic LF, Koch V. Clinical aspects of autosomal recessive polycystic kidney disease. Abstracts. 2007 ; 20.[citado 2025 dez. 27 ] - Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease
- Policistina-1, o produto do gene PKD1, induz resistência a apoptose e tubulogênese espontânea em células MDCK
- Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells
- Initial characterization of polyductin, the PKHD1 gene product
- Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis
- Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types
- Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1
- Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene
- Bases moleculares e celulares da doença renal policística autossômica recessiva
- Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1
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