NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology (2017)
- Authors:
- Kaimori, Jun-ya
- Lin, Cheng-Chao
- Outeda, Patricia
- Garcia-Gonzalez, Miguel A.
- Menezes, Luis F.
- Hartung, Erum A.
- Li, Ao
- Wu, Guanqing
- Fujita, Hideaki
- Sato, Yasunori
- Nakanuma, Yasuni
- Yamamoto, Satoko
- Ichimaru, Naotsugu
- Takahara, Shiro
- Isaka, Yoshitaka
- Watnick, Terry
- Onuchic, Luiz F.
- Guay-Woodford, Lisa M.
- Germino, Gregory G.
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- DOI: 10.1038/s41598-017-08284-4
- Subjects: CRIANÇAS; RIM; CARCINOGÊNESE; NEFROPATIAS; SINAIS E SINTOMAS
- Language: Inglês
- Imprenta:
- Publisher place: United Kingdom
- Date published: 2017
- Source:
- Título: Scientific Reports
- ISSN: 2045-2322
- Volume/Número/Paginação/Ano: v. 7, n. 7733, p. 1-16, 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
KAIMORI, Jun-ya et al. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports, v. 7, n. 7733, p. 1-16, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-08284-4. Acesso em: 23 jan. 2026. -
APA
Kaimori, J. -ya, Lin, C. -C., Outeda, P., Garcia-Gonzalez, M. A., Menezes, L. F., Hartung, E. A., et al. (2017). NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports, 7( 7733), 1-16. doi:10.1038/s41598-017-08284-4 -
NLM
Kaimori J-ya, Lin C-C, Outeda P, Garcia-Gonzalez MA, Menezes LF, Hartung EA, Li A, Wu G, Fujita H, Sato Y, Nakanuma Y, Yamamoto S, Ichimaru N, Takahara S, Isaka Y, Watnick T, Onuchic LF, Guay-Woodford LM, Germino GG. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-16.[citado 2026 jan. 23 ] Available from: https://doi.org/10.1038/s41598-017-08284-4 -
Vancouver
Kaimori J-ya, Lin C-C, Outeda P, Garcia-Gonzalez MA, Menezes LF, Hartung EA, Li A, Wu G, Fujita H, Sato Y, Nakanuma Y, Yamamoto S, Ichimaru N, Takahara S, Isaka Y, Watnick T, Onuchic LF, Guay-Woodford LM, Germino GG. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-16.[citado 2026 jan. 23 ] Available from: https://doi.org/10.1038/s41598-017-08284-4 - PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
- Doenças císticas renais em pediatria
- Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene
- Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
- Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene
- PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
- Ausência de redução da capacidade de concentração urinária em camundongo heterozigoto para mutação nula no gene
- Inbred PKD+/- male mice have lower GFRs but non-significant differences in renal concentrating capacity than age-matched wild type controls
- Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts
- Molecular cloning of a novel cytokine-like gene
Informações sobre o DOI: 10.1038/s41598-017-08284-4 (Fonte: oaDOI API)
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