Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation (2003)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: NEFROLOGIA; GENES; AMINOÁCIDOS
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2003
- Source:
- Título do periódico: Journal of the American Society of Nephrology
- Volume/Número/Paginação/Ano: v. 14
- Conference titles: Accredited Sponsor: The American Society of Nephrology
-
ABNT
FURU, Laszlo et al. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology, v. 14, 2003Tradução . . Acesso em: 24 abr. 2024. -
APA
Furu, L., Senderek, J., Gharavi, A., Hou, X., Esquivel, E. L., Nagasawa, Y., et al. (2003). Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology, 14. -
NLM
Furu L, Senderek J, Gharavi A, Hou X, Esquivel EL, Nagasawa Y, Avner E, Germino G, Guay-Woodford L, Somlo S, Büttner R, Zerres K, Onuchic LF. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 abr. 24 ] -
Vancouver
Furu L, Senderek J, Gharavi A, Hou X, Esquivel EL, Nagasawa Y, Avner E, Germino G, Guay-Woodford L, Somlo S, Büttner R, Zerres K, Onuchic LF. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 abr. 24 ] - 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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