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Polymorphism in the PBX1 gene is related to cystinuria in Brazilian families.
Reis, Sabrina T; Leite, Katia R M; Marchini, Giovanni S; Guimarães, Ronaldo M; Viana, Nayara I; Pimenta, Ruan C A; Torricelli, Fabio C; Danilovic, Alexandre; Vicentini, Fábio Carvalho; Nahas, William Carlos; Srougi, Miguel; Mazzucchi, Eduardo.
Afiliação
  • Reis ST; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Leite KRM; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Marchini GS; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Guimarães RM; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Viana NI; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Pimenta RCA; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Torricelli FC; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Danilovic A; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Vicentini FC; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Nahas WC; Endourology and Stone Disease Section, Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Srougi M; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
  • Mazzucchi E; Laboratory of Medical Investigation (LIM55), Division of Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
J Cell Mol Med ; 23(2): 1593-1597, 2019 02.
Article em En | MEDLINE | ID: mdl-30450686
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Cistinúria / Nefrolitíase / Fator de Transcrição 1 de Leucemia de Células Pré-B Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male País/Região como assunto: America do sul / Brasil Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Cistinúria / Nefrolitíase / Fator de Transcrição 1 de Leucemia de Células Pré-B Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male País/Região como assunto: America do sul / Brasil Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido