Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2 (2004)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: RIM (PATOLOGIA); CISTOS (GENÉTICA); MUTAÇÃO GENÉTICA; EXPERIMENTOS ANIMAIS; RATOS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the American Society of Nephrology
- ISSN: 1046-6673
- Volume/Número/Paginação/Ano: v. 15, Abstracts issue, p. 219A, res. F-PO698, 2004
- Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN
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ABNT
GONZALEZ, Miguel A. Garcia et al. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 jun. 2024. , 2004 -
APA
Gonzalez, M. A. G., Piontek, K., Lijuan, L., Menezes, L. F., Onuchie, L., Lens, X. M., & Germino, G. (2004). Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Gonzalez MAG, Piontek K, Lijuan L, Menezes LF, Onuchie L, Lens XM, Germino G. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. 2004 ; 15 219A.[citado 2024 jun. 11 ] -
Vancouver
Gonzalez MAG, Piontek K, Lijuan L, Menezes LF, Onuchie L, Lens XM, Germino G. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. 2004 ; 15 219A.[citado 2024 jun. 11 ] - 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
- Clinical aspects of autosomal recessive polycystic kidney disease
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