ReP USP - Resultado da busca

Artigo de periodico
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) (2004)
Bergmann, Carsten; Senderek, Jan; Kupper, Fabian; Schneider, Frank; Dornia, Christian; Windelen, Ellen; Eggermann, Thomas; Rudnik-Schoneborn, Sabine; Kirfel, Jutta; Furu, Laszlo; Onuchic, Luiz F.; Rossetti, Sandro; Harris, Peter C.; Somlo, Stefan; Guay-Woodford, Lisa; Germino, Gregory G.; Moser, Markus; Buttner, Reinhard; Zerresm, Klaus
Source: Human mutation. Unidade: FM
Subjects: CISTOS, RIM (FISIOPATOLOGIA), GENÓTIPOS, MUTAÇÃO GENÉTICA, ANTICORPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERGMANN, Carsten et al. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human mutation, v. 23, n. 5, p. 453-463, 2004Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf. Acesso em: 08 jan. 2025.
APA
Bergmann, C., Senderek, J., Kupper, F., Schneider, F., Dornia, C., Windelen, E., et al. (2004). PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human mutation, 23( 5), 453-463. Recuperado de http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
NLM
Bergmann C, Senderek J, Kupper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schoneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Buttner R, Zerresm K. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) [Internet]. Human mutation. 2004 ; 23( 5): 453-463.[citado 2025 jan. 08 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
Vancouver
Bergmann C, Senderek J, Kupper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schoneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Buttner R, Zerresm K. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) [Internet]. Human mutation. 2004 ; 23( 5): 453-463.[citado 2025 jan. 08 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
Artigo de periodico
Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation (2003)
Furu, Laszlo; Senderek, Jan; Gharavi, Ali; Hou, Xiaoying; Esquivel, Ernie L.; Nagasawa, Yasuyuki; Avner, Ellis; Germino, Gregory; Guay-Woodford, Lisa; Somlo, Stefan; Büttner, Reinhard; Zerres, Klaus; Onuchic, Luiz Fernando
Source: Journal of the American Society of Nephrology. Conference titles: Accredited Sponsor: The American Society of Nephrology. Unidade: FM
Subjects: NEFROLOGIA, GENES, AMINOÁCIDOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 jan. 2025.
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 2025 jan. 08 ]
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 2025 jan. 08 ]
Artigo de periodico
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1) (2003)
Bergmann, Carsten; Senderek, Jan; Sedlacek, Beate; Pegiazoglou, Ioannis; Puglia, Patricia; Eggermann, Thomas; Rudnick-Schöneborn, Sabine; Furu, Laszlo; Baca, Monica de; Germino, Gregory; Guay-Woodford, Lisa; Somlo, Stefan; Moser, Markus; Büttner, Reinhard; Zerres, Klaus; Onuchic, Luiz Fernando
Source: Journal of the American Society of Nephrology. Conference titles: Accredited Sponsor: The American Society of Nephrology. Unidade: FM
Subjects: NEFROLOGIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERGMANN, Carsten et al. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology, v. 14, 2003Tradução . . Acesso em: 08 jan. 2025.
APA
Bergmann, C., Senderek, J., Sedlacek, B., Pegiazoglou, I., Puglia, P., Eggermann, T., et al. (2003). Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology, 14.
NLM
Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnick-Schöneborn S, Furu L, Baca M de, Germino G, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K, Onuchic LF. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology. 2003 ; 14[citado 2025 jan. 08 ]
Vancouver
Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnick-Schöneborn S, Furu L, Baca M de, Germino G, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K, Onuchic LF. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology. 2003 ; 14[citado 2025 jan. 08 ]
Artigo de periodico
A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6 (1999)
Park, Jong Hoon; Dixit, Mehul P.; Onuchic, Luiz Fernando; Wu, Guanqing; Goncharuk, Andrey N.; Kneitz, Susanne; Santarine, Lorenzo B.; Hayashi, Tomohito; Avner, Ellis D.; Guay-Woodford, Lisa; Zerres, Klaus; Germino, Gregory G.; Somlo, Stefan
Source: Genomics. Unidade: FM
Subjects: GENÉTICA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARK, Jong Hoon et al. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics, v. 57, p. 249-255, 1999Tradução . . Acesso em: 08 jan. 2025.
APA
Park, J. H., Dixit, M. P., Onuchic, L. F., Wu, G., Goncharuk, A. N., Kneitz, S., et al. (1999). A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics, 57, 249-255.
NLM
Park JH, Dixit MP, Onuchic LF, Wu G, Goncharuk AN, Kneitz S, Santarine LB, Hayashi T, Avner ED, Guay-Woodford L, Zerres K, Germino GG, Somlo S. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics. 1999 ; 57 249-255.[citado 2025 jan. 08 ]
Vancouver
Park JH, Dixit MP, Onuchic LF, Wu G, Goncharuk AN, Kneitz S, Santarine LB, Hayashi T, Avner ED, Guay-Woodford L, Zerres K, Germino GG, Somlo S. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics. 1999 ; 57 249-255.[citado 2025 jan. 08 ]
Artigo de periodico
Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12 (1998)
Mücher, Gabi; Becker, Jutta; Knapp, Michael; Büttner, Reinhard; Moser, Markus; Rudnik-Schöneborn, Sabine; Somlo, Stefan; Germino, Greg; Onuchic, Luiz Fernando; Avner, Ellis; Guay-Woodford, Lisa; Zerres, Klaus
Source: Genomics. Unidade: FM
Assunto: MEDICINA INTERNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MÜCHER, Gabi et al. Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12. Genomics, v. 48, p. 40-45, 1998Tradução . . Acesso em: 08 jan. 2025.
APA
Mücher, G., Becker, J., Knapp, M., Büttner, R., Moser, M., Rudnik-Schöneborn, S., et al. (1998). Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12. Genomics, 48, 40-45.
NLM
Mücher G, Becker J, Knapp M, Büttner R, Moser M, Rudnik-Schöneborn S, Somlo S, Germino G, Onuchic LF, Avner E, Guay-Woodford L, Zerres K. Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12. Genomics. 1998 ; 48 40-45.[citado 2025 jan. 08 ]
Vancouver
Mücher G, Becker J, Knapp M, Büttner R, Moser M, Rudnik-Schöneborn S, Somlo S, Germino G, Onuchic LF, Avner E, Guay-Woodford L, Zerres K. Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2(beta), and GSTA1 at 6p21.1-p12. Genomics. 1998 ; 48 40-45.[citado 2025 jan. 08 ]

USP Schools

ReP

Filtros

Authors

Subjects

Non normalized affiliation