Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types (2006)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: ISQUEMIA; CAMUNDONGOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the american society of nephrology
- ISSN: 1046-6673
- Volume/Número/Paginação/Ano: v. 17, p. 776A, res. SA-PO960, 2006
- Conference titles: Abstracts
-
ABNT
BASTOS, A. P et al. Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types. Journal of the american society of nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 dez. 2025. , 2006 -
APA
Bastos, A. P., Piontek, K., Menezes, L. F., Fonseca, I. I., Tovo, F. M., Castro, I., et al. (2006). Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types. Journal of the american society of nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Bastos AP, Piontek K, Menezes LF, Fonseca II, Tovo FM, Castro I, Germino GG, Onuchic LF. Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types. Journal of the american society of nephrology. 2006 ; 17 776A.[citado 2025 dez. 27 ] -
Vancouver
Bastos AP, Piontek K, Menezes LF, Fonseca II, Tovo FM, Castro I, Germino GG, Onuchic LF. Ischemia/reperfusion injury determines increased early tubular dysfunction in Pkd1 haploinsufficient mice compared to wil types. Journal of the american society of nephrology. 2006 ; 17 776A.[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
- 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
- Clinical aspects of autosomal recessive polycystic kidney disease
- Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1
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