Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease (1998)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Assunto: GENÉTICA
- Language: Inglês
- Source:
- Título: Molecular Cell
- Volume/Número/Paginação/Ano: v. 2, p. 247-251, 1998
-
ABNT
WATNICK, Terry J. et al. Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease. Molecular Cell, v. 2, p. 247-251, 1998Tradução . . Acesso em: 06 jan. 2025. -
APA
Watnick, T. J., Torres, V. E., Gandolph, M. A., Qian, F., Onuchic, L. F., Klinger, K. W., et al. (1998). Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease. Molecular Cell, 2, 247-251. -
NLM
Watnick TJ, Torres VE, Gandolph MA, Qian F, Onuchic LF, Klinger KW, Landes G, Germino GG. Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease. Molecular Cell. 1998 ; 2 247-251.[citado 2025 jan. 06 ] -
Vancouver
Watnick TJ, Torres VE, Gandolph MA, Qian F, Onuchic LF, Klinger KW, Landes G, Germino GG. Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease. Molecular Cell. 1998 ; 2 247-251.[citado 2025 jan. 06 ] - Regulação do volume celular no ramo ascendente fino da alça de Henle de ratos
- Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12
- Genomic structure and exclusion of two candidate genes for the PKHD1 locus and three new polymorphic markers within the critical interval
- Direct association of full-lenght PKD1 and PKD2 proteins in mammalian cells
- Aumento regulatório do volume celular em túbulos de malpighi
- Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene
- Expression of PKD1 and PKD2 transcripts and proteins in human embryo and during normal kidney development
- Contribuições dos Modelos Animais ao Entendimento da Patogênese das Doenças Renais Policísticas
- Recombinant and endogenous polyductin (PD1) is secreted from primary cilia
- PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
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