Expression of PKD1 and PKD2 transcripts in normal and ADPKD kidneys during development (1999)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Assunto: NEFROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the American Society of Nephrology
- Volume/Número/Paginação/Ano: v. 10, n. supl., p. 415 res. 2095, 1999
- Conference titles: Annual Meeting and 1999 Renal Week
-
ABNT
CHAUVET, V. et al. Expression of PKD1 and PKD2 transcripts in normal and ADPKD kidneys during development. Journal of the American Society of Nephrology. Florida: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 1999 -
APA
Chauvet, V., Qian, F., Boute, N., Onuchic, L. F., Germino, G. G., Devuyst, O., & Gubler, M. C. (1999). Expression of PKD1 and PKD2 transcripts in normal and ADPKD kidneys during development. Journal of the American Society of Nephrology. Florida: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Chauvet V, Qian F, Boute N, Onuchic LF, Germino GG, Devuyst O, Gubler MC. Expression of PKD1 and PKD2 transcripts in normal and ADPKD kidneys during development. Journal of the American Society of Nephrology. 1999 ; 10( supl.): 415 res. 2095.[citado 2024 abr. 24 ] -
Vancouver
Chauvet V, Qian F, Boute N, Onuchic LF, Germino GG, Devuyst O, Gubler MC. Expression of PKD1 and PKD2 transcripts in normal and ADPKD kidneys during development. Journal of the American Society of Nephrology. 1999 ; 10( supl.): 415 res. 2095.[citado 2024 abr. 24 ] - Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease
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- 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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