Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis (2007)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: ISQUEMIA; RIM (PATOLOGIA;IRRIGAÇÃO SANGUÍNEA); CAMUNDONGOS; RESUMOS (SIMPÓSIOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio avanços em pesquisas médicas
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ABNT
BASTOS, A. et al. Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 dez. 2025. , 2007 -
APA
Bastos, A., Piontek, K., Silva, A., Martini, D., Menezes, L., Fonseca, I., et al. (2007). Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Bastos A, Piontek K, Silva A, Martini D, Menezes L, Fonseca I, Germino G, Onuchic LF. Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis. Clinics. 2007 ; 62 S78.[citado 2025 dez. 27 ] -
Vancouver
Bastos A, Piontek K, Silva A, Martini D, Menezes L, Fonseca I, Germino G, Onuchic LF. Pkd1 haploinsufficiency increases functional and morphological damage following renal ischemia /repersufion in mice: extend analysis. Clinics. 2007 ; 62 S78.[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
- 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
- Clinical aspects of autosomal recessive polycystic kidney disease
- Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1
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