Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene (2002)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- DOI: 10.1002/ajmg.10468
- Assunto: GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 110, p. 346-352, 2002
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ONUCHIC, Luiz F. et al. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. American Journal of Medical Genetics, v. 110, p. 346-352, 2002Tradução . . Disponível em: https://doi.org/10.1002/ajmg.10468. Acesso em: 14 maio 2024. -
APA
Onuchic, L. F., Mrug, M., Hou, X., Eggermann, T., Bergmann, C., Zerres, K., et al. (2002). Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. American Journal of Medical Genetics, 110, 346-352. doi:10.1002/ajmg.10468 -
NLM
Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo. Stefan, Nagasawa Y, Germino GG, Woodford LMG. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene [Internet]. American Journal of Medical Genetics. 2002 ; 110 346-352.[citado 2024 maio 14 ] Available from: https://doi.org/10.1002/ajmg.10468 -
Vancouver
Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo. Stefan, Nagasawa Y, Germino GG, Woodford LMG. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene [Internet]. American Journal of Medical Genetics. 2002 ; 110 346-352.[citado 2024 maio 14 ] Available from: https://doi.org/10.1002/ajmg.10468 - 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
Informações sobre o DOI: 10.1002/ajmg.10468 (Fonte: oaDOI API)
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