Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts (2004)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: RIM (PATOLOGIA); CISTOS (DIAGNÓSTICO;GENÉTICA); GENOMAS (ANÁLISE); FENÓTIPOS
- 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. 216A, res. F-PO679, 2004
- Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN
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ABNT
SHARP, Angela M. et al. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 maio 2024. , 2004 -
APA
Sharp, A. M., Messiaen, L. M., Page, G., Onuchie, L., Woodford, L. G., Germino, G., & Somlo, S. (2004). Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Sharp AM, Messiaen LM, Page G, Onuchie L, Woodford LG, Germino G, Somlo S. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2024 maio 16 ] -
Vancouver
Sharp AM, Messiaen LM, Page G, Onuchie L, Woodford LG, Germino G, Somlo S. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2024 maio 16 ] - 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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