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Trabalho de evento-resumo periodico
Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2 (2004)
Gonzalez, Miguel A. Garcia; Piontek, Klaus; Lijuan, Liu; Menezes, Luis F.; Onuchie, Luiz; Lens, Xose M.; Germino, Gregory
Source: Journal of the American Society of Nephrology. Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN. Unidade: FM
Subjects: RIM (PATOLOGIA), CISTOS (GENÉTICA), MUTAÇÃO GENÉTICA, EXPERIMENTOS ANIMAIS, RATOS
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ABNT
GONZALEZ, Miguel A. Garcia et al. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 abr. 2026. , 2004
APA
Gonzalez, M. A. G., Piontek, K., Lijuan, L., Menezes, L. F., Onuchie, L., Lens, X. M., & Germino, G. (2004). Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gonzalez MAG, Piontek K, Lijuan L, Menezes LF, Onuchie L, Lens XM, Germino G. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. 2004 ; 15 219A.[citado 2026 abr. 30 ]
Vancouver
Gonzalez MAG, Piontek K, Lijuan L, Menezes LF, Onuchie L, Lens XM, Germino G. Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2. Journal of the American Society of Nephrology. 2004 ; 15 219A.[citado 2026 abr. 30 ]
Trabalho de evento-resumo periodico
Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin (2004)
Kaimori, Jun-Ya; Nagasawa, Yasuyuki; Gonzalez, Miguel A. Garcia; Menezes, Luis F.; Onuchie, Luiz; Woodford, Lisa Guay; Germino, Gregory; Somlo, Stefan
Source: Journal of the American Society of Nephrology. Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN. Unidade: FM
Subjects: RIM (PATOLOGIA), CISTOS (DIAGNÓSTICO;PATOLOGIA), NEFROPATIAS (DIAGNÓSTICO), GENES (ANÁLISE)
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ABNT
KAIMORI, Jun-Ya et al. Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 abr. 2026. , 2004
APA
Kaimori, J. -Y., Nagasawa, Y., Gonzalez, M. A. G., Menezes, L. F., Onuchie, L., Woodford, L. G., et al. (2004). Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Kaimori J-Y, Nagasawa Y, Gonzalez MAG, Menezes LF, Onuchie L, Woodford LG, Germino G, Somlo S. Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2026 abr. 30 ]
Vancouver
Kaimori J-Y, Nagasawa Y, Gonzalez MAG, Menezes LF, Onuchie L, Woodford LG, Germino G, Somlo S. Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2026 abr. 30 ]
Trabalho de evento-resumo periodico
Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD) (2004)
Gallagher, Rachel; Esquivel, Ernie; Tian, Xin; Samaroo, Tiffany; Jain, Dhanpat; Onuchie, Luiz; Woodford, Lisa Guay; Germino, Gregory; Somlo, Stefan
Source: Journal of the American Society of Nephrology. Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN. Unidade: FM
Subjects: RIM (PATOLOGIA), CISTOS (DIAGNÓSTICO;GENÉTICA), DOENÇAS BILIARES (DIAGNÓSTICO), GENÓTIPOS
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ABNT
GALLAGHER, Rachel et al. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 abr. 2026. , 2004
APA
Gallagher, R., Esquivel, E., Tian, X., Samaroo, T., Jain, D., Onuchie, L., et al. (2004). Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2026 abr. 30 ]
Vancouver
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2026 abr. 30 ]
Trabalho de evento-resumo periodico
Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts (2004)
Sharp, Angela M.; Messiaen, Ludwine M.; Page, Grier; Onuchie, Luiz; Woodford, Lisa Guay; Germino, Gregory; Somlo, Stefan
Source: Journal of the American Society of Nephrology. Conference titles: Abstracts issue journal of the american Society of Nephrology - JASN. Unidade: FM
Subjects: RIM (PATOLOGIA), CISTOS (DIAGNÓSTICO;GENÉTICA), GENOMAS (ANÁLISE), FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHARP, Angela M. et al. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 abr. 2026. , 2004
APA
Sharp, A. M., Messiaen, L. M., Page, G., Onuchie, L., Woodford, L. G., Germino, G., & Somlo, S. (2004). Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Sharp AM, Messiaen LM, Page G, Onuchie L, Woodford LG, Germino G, Somlo S. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2026 abr. 30 ]
Vancouver
Sharp AM, Messiaen LM, Page G, Onuchie L, Woodford LG, Germino G, Somlo S. Comprehensive genomic analysis for PKHD1 mutation in ARPKD cohorts. Journal of the American Society of Nephrology. 2004 ; 15 216A.[citado 2026 abr. 30 ]
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: 30 abr. 2026.
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 2026 abr. 30 ]
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 2026 abr. 30 ]
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: 30 abr. 2026.
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 2026 abr. 30 ]
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 2026 abr. 30 ]
Artigo de periodico
Identification of a novel cytokine, ML-1, and its expression in subjects with asthma (2001)
Kawaguchi, Mio; Onuchic, Luiz Fernando; Li, Xiao Dong; Essayan, David M.; Schroeder, John; Xiao, Hui Qing; Liu, Mark C.; Krishnaswamy, Guha; Germino, Gregory; Huang, Shau Ku
Source: Journal of Immunology. Unidade: FM
Assunto: CLÍNICA GERAL
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ABNT
KAWAGUCHI, Mio et al. Identification of a novel cytokine, ML-1, and its expression in subjects with asthma. Journal of Immunology, v. 167, n. 8, p. 4430-4435, 2001Tradução . . Acesso em: 30 abr. 2026.
APA
Kawaguchi, M., Onuchic, L. F., Li, X. D., Essayan, D. M., Schroeder, J., Xiao, H. Q., et al. (2001). Identification of a novel cytokine, ML-1, and its expression in subjects with asthma. Journal of Immunology, 167( 8), 4430-4435.
NLM
Kawaguchi M, Onuchic LF, Li XD, Essayan DM, Schroeder J, Xiao HQ, Liu MC, Krishnaswamy G, Germino G, Huang SK. Identification of a novel cytokine, ML-1, and its expression in subjects with asthma. Journal of Immunology. 2001 ; 167( 8): 4430-4435.[citado 2026 abr. 30 ]
Vancouver
Kawaguchi M, Onuchic LF, Li XD, Essayan DM, Schroeder J, Xiao HQ, Liu MC, Krishnaswamy G, Germino G, Huang SK. Identification of a novel cytokine, ML-1, and its expression in subjects with asthma. Journal of Immunology. 2001 ; 167( 8): 4430-4435.[citado 2026 abr. 30 ]

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