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Artigo de periodico
NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology (2017)
Kaimori, Jun-ya; Lin, Cheng-Chao; Outeda, Patricia; Garcia-Gonzalez, Miguel A.; Menezes, Luis F.; Hartung, Erum A.; Li, Ao; Wu, Guanqing; Fujita, Hideaki; Sato, Yasunori; Nakanuma, Yasuni; Yamamoto, Satoko; Ichimaru, Naotsugu; Takahara, Shiro; Isaka, Yoshitaka; Watnick, Terry; Onuchic, Luiz F.; Guay-Woodford, Lisa M.; Germino, Gregory G.
Source: Scientific Reports. Unidade: FM
Subjects: CRIANÇAS, RIM, CARCINOGÊNESE, NEFROPATIAS, SINAIS E SINTOMAS
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KAIMORI, Jun-ya et al. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports, v. 7, n. 7733, p. 1-16, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-08284-4. Acesso em: 21 out. 2025.
APA
Kaimori, J. -ya, Lin, C. -C., Outeda, P., Garcia-Gonzalez, M. A., Menezes, L. F., Hartung, E. A., et al. (2017). NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports, 7( 7733), 1-16. doi:10.1038/s41598-017-08284-4
NLM
Kaimori J-ya, Lin C-C, Outeda P, Garcia-Gonzalez MA, Menezes LF, Hartung EA, Li A, Wu G, Fujita H, Sato Y, Nakanuma Y, Yamamoto S, Ichimaru N, Takahara S, Isaka Y, Watnick T, Onuchic LF, Guay-Woodford LM, Germino GG. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-16.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41598-017-08284-4
Vancouver
Kaimori J-ya, Lin C-C, Outeda P, Garcia-Gonzalez MA, Menezes LF, Hartung EA, Li A, Wu G, Fujita H, Sato Y, Nakanuma Y, Yamamoto S, Ichimaru N, Takahara S, Isaka Y, Watnick T, Onuchic LF, Guay-Woodford LM, Germino GG. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-16.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41598-017-08284-4
Artigo de periodico
Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1 (2014)
Boddu, Ravindra; Yang, Chaozhe; O'Connor, Amber K. O.; Hendrickson, Robert Curtis; Boone, Braden; Cui, Xiagqin; Garcia-Gonzalez, Miguel; Igarashi, Peter; Onuchic, Luiz F.; Germino, Gregory G.; Guay-Woodford, Lisa M.
Source: Journal of Molecular Medicine. Unidade: FM
Subjects: NEFROPATIAS, HERANÇA GENÉTICA, EXAMES MÉDICOS, RNA
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BODDU, Ravindra et al. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. Journal of Molecular Medicine, v. 92, p. 1045-1056, 2014Tradução . . Disponível em: https://doi.org/10.1007/s00109-014-1185-7. Acesso em: 21 out. 2025.
APA
Boddu, R., Yang, C., O'Connor, A. K. O., Hendrickson, R. C., Boone, B., Cui, X., et al. (2014). Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. Journal of Molecular Medicine, 92, 1045-1056. doi:10.1007/s00109-014-1185-7
NLM
Boddu R, Yang C, O'Connor AKO, Hendrickson RC, Boone B, Cui X, Garcia-Gonzalez M, Igarashi P, Onuchic LF, Germino GG, Guay-Woodford LM. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1 [Internet]. Journal of Molecular Medicine. 2014 ; 92 1045-1056.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s00109-014-1185-7
Vancouver
Boddu R, Yang C, O'Connor AKO, Hendrickson RC, Boone B, Cui X, Garcia-Gonzalez M, Igarashi P, Onuchic LF, Germino GG, Guay-Woodford LM. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1 [Internet]. Journal of Molecular Medicine. 2014 ; 92 1045-1056.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s00109-014-1185-7
Artigo de periodico
Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain (2011)
Ferreira, Frederico M.; Oliveira, Leandro C.; Germino, Gregory G.; Onuchic, José Nelson ; Onuchic, Luiz F.
Source: Proceedings of the National Academy of Sciences of the United States of America. Unidade: FM
Subjects: MACROMOLÉCULA (ANÁLISE), GENES, CÁLCIO (DEFICIÊNCIA), BIOLOGIA MOLECULAR, RIM (PATOLOGIA;FISIOPATOLOGIA)
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FERREIRA, Frederico M. et al. Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain. Proceedings of the National Academy of Sciences of the United States of America, v. 108, n. 24, p. 9833-9838, 2011Tradução . . Disponível em: http://www.pnas.org/content/108/24/9833.full.pdf+html?sid=431f74d2-a133-4f2d-93f3-f97288e0a505. Acesso em: 21 out. 2025.
APA
Ferreira, F. M., Oliveira, L. C., Germino, G. G., Onuchic, J. N., & Onuchic, L. F. (2011). Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain. Proceedings of the National Academy of Sciences of the United States of America, 108( 24), 9833-9838. doi:10.1073/pnas.1106766108
NLM
Ferreira FM, Oliveira LC, Germino GG, Onuchic JN, Onuchic LF. Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain [Internet]. Proceedings of the National Academy of Sciences of the United States of America. 2011 ; 108( 24): 9833-9838.[citado 2025 out. 21 ] Available from: http://www.pnas.org/content/108/24/9833.full.pdf+html?sid=431f74d2-a133-4f2d-93f3-f97288e0a505
Vancouver
Ferreira FM, Oliveira LC, Germino GG, Onuchic JN, Onuchic LF. Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain [Internet]. Proceedings of the National Academy of Sciences of the United States of America. 2011 ; 108( 24): 9833-9838.[citado 2025 out. 21 ] Available from: http://www.pnas.org/content/108/24/9833.full.pdf+html?sid=431f74d2-a133-4f2d-93f3-f97288e0a505
Artigo de periodico
Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion (2009)
Bastos, Ana P.; Piontek, Klaus; Silva, Ana Maria Gonçalves da; Martini, Dino; Menezes, Luis F.; Fonseca, Jonathan M.; Fonseca, Ivone I.; Germino, Gregory G.; Onuchic, Luiz F.
Source: JASN : Journal of the American Society of Nephrology. Unidades: IMT, FM
Subjects: ISQUEMIA, CISTOS (FORMAÇÃO), APOPTOSE, SEGUIMENTOS
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BASTOS, Ana P. et al. Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion. JASN : Journal of the American Society of Nephrology, v. 20, n. 11, p. 2389-2402, 2009Tradução . . Disponível em: https://doi.org/10.1681/asn.2008040435. Acesso em: 21 out. 2025.
APA
Bastos, A. P., Piontek, K., Silva, A. M. G. da, Martini, D., Menezes, L. F., Fonseca, J. M., et al. (2009). Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion. JASN : Journal of the American Society of Nephrology, 20( 11), 2389-2402. doi:10.1681/asn.2008040435
NLM
Bastos AP, Piontek K, Silva AMG da, Martini D, Menezes LF, Fonseca JM, Fonseca II, Germino GG, Onuchic LF. Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion [Internet]. JASN : Journal of the American Society of Nephrology. 2009 ; 20( 11): 2389-2402.[citado 2025 out. 21 ] Available from: https://doi.org/10.1681/asn.2008040435
Vancouver
Bastos AP, Piontek K, Silva AMG da, Martini D, Menezes LF, Fonseca JM, Fonseca II, Germino GG, Onuchic LF. Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion [Internet]. JASN : Journal of the American Society of Nephrology. 2009 ; 20( 11): 2389-2402.[citado 2025 out. 21 ] Available from: https://doi.org/10.1681/asn.2008040435
Artigo de periodico
Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm (2004)
Menezes, Luís Fernando Carvalho de; Cai, Yiqiang; Nagasawa, Yasuyuki; Silva, Ana M. G.; Watkins, Mary L.; Da Silva, Aline Maria ; Somlo, Stefan; Guay-Woodford, Lisa M.; Germino, Gregory G.; Onuchic, Luiz Fernando
Source: Kidney International. Unidades: IQ, FM
Subjects: BIOQUÍMICA, IMUNOFLUORESCÊNCIA
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MENEZES, Luís Fernando Carvalho de et al. Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm. Kidney International, v. 66, n. 4, p. 1345-1355, 2004Tradução . . Disponível em: https://doi.org/10.1111/j.1523-1755.2004.00844.x. Acesso em: 21 out. 2025.
APA
Menezes, L. F. C. de, Cai, Y., Nagasawa, Y., Silva, A. M. G., Watkins, M. L., Da Silva, A. M., et al. (2004). Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm. Kidney International, 66( 4), 1345-1355. doi:10.1111/j.1523-1755.2004.00844.x
NLM
Menezes LFC de, Cai Y, Nagasawa Y, Silva AMG, Watkins ML, Da Silva AM, Somlo S, Guay-Woodford LM, Germino GG, Onuchic LF. Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm [Internet]. Kidney International. 2004 ; 66( 4): 1345-1355.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1523-1755.2004.00844.x
Vancouver
Menezes LFC de, Cai Y, Nagasawa Y, Silva AMG, Watkins ML, Da Silva AM, Somlo S, Guay-Woodford LM, Germino GG, Onuchic LF. Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm [Internet]. Kidney International. 2004 ; 66( 4): 1345-1355.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1523-1755.2004.00844.x
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
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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: 21 out. 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 out. 21 ] 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 out. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
Artigo de periodico
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats (2002)
Onuchic, Luiz F.; Furu, Laszlo; Nagasawa, Yasuyuki; Hou, Xiaoying; Eggermann, Thomas; Ren, Zhiyong; Bergmann, Carsten; Senderek, Jan; Esquivel, Ernie; Zeltner, Raoul; Schöneborn, Sabine Rudnik; Mrug, Michael; Sweeney, William; Avner, Ellis D.; Zerres. Klaus; Woodford, Lisa M. Guay; Somlo, Stefan; Germino, Gregory G.
Source: American Journal of Human Genetics. Unidade: FM
Assunto: IMUNOGLOBULINAS
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ABNT
ONUCHIC, Luiz F. et al. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. American Journal of Human Genetics, v. 70, p. 1305-1317, 2002Tradução . . Acesso em: 21 out. 2025.
APA
Onuchic, L. F., Furu, L., Nagasawa, Y., Hou, X., Eggermann, T., Ren, Z., et al. (2002). PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. American Journal of Human Genetics, 70, 1305-1317.
NLM
Onuchic LF, Furu L, Nagasawa Y, Hou X, Eggermann T, Ren Z, Bergmann C, Senderek J, Esquivel E, Zeltner R, Schöneborn SR, Mrug M, Sweeney W, Avner ED, Zerres. Klaus, Woodford LMG, Somlo S, Germino GG. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. American Journal of Human Genetics. 2002 ; 70 1305-1317.[citado 2025 out. 21 ]
Vancouver
Onuchic LF, Furu L, Nagasawa Y, Hou X, Eggermann T, Ren Z, Bergmann C, Senderek J, Esquivel E, Zeltner R, Schöneborn SR, Mrug M, Sweeney W, Avner ED, Zerres. Klaus, Woodford LMG, Somlo S, Germino GG. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. American Journal of Human Genetics. 2002 ; 70 1305-1317.[citado 2025 out. 21 ]
Artigo de periodico
Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene (2002)
Nagasawa, Yasuyuki; Matthiesen, Sonja; Onuchic, Luiz F.; Hou, Xiaoying; Bergmann, Carsten; Esquivel, Ernie; Senderek, Jan; Ren, Zhiyoung; Zeltner, Raoul; Furu, Laszlo; Avner, Ellis; Moser, Markus; Somlo, Stefan; Woodford, Lisa Guay; Büttner, Reinhard; Zerres, Klaus; Germino, Gregory G.
Source: Journal of the American Society of Nephrology. Unidade: FM
Assunto: NEFROLOGIA
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ABNT
NAGASAWA, Yasuyuki et al. Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology, v. 13, p. 2239-2245, 2002Tradução . . Acesso em: 21 out. 2025.
APA
Nagasawa, Y., Matthiesen, S., Onuchic, L. F., Hou, X., Bergmann, C., Esquivel, E., et al. (2002). Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology, 13, 2239-2245.
NLM
Nagasawa Y, Matthiesen S, Onuchic LF, Hou X, Bergmann C, Esquivel E, Senderek J, Ren Z, Zeltner R, Furu L, Avner E, Moser M, Somlo S, Woodford LG, Büttner R, Zerres K, Germino GG. Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology. 2002 ; 13 2239-2245.[citado 2025 out. 21 ]
Vancouver
Nagasawa Y, Matthiesen S, Onuchic LF, Hou X, Bergmann C, Esquivel E, Senderek J, Ren Z, Zeltner R, Furu L, Avner E, Moser M, Somlo S, Woodford LG, Büttner R, Zerres K, Germino GG. Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. Journal of the American Society of Nephrology. 2002 ; 13 2239-2245.[citado 2025 out. 21 ]
Artigo de periodico
Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene (2002)
Onuchic, Luiz F.; Mrug, Michael; Hou, Xiaoying; Eggermann, Thomass; Bergmann, Carsten; Zerres, Klaus; Avner, Ellis D.; Furu, Laszlo; Somlo. Stefan; Nagasawa, Yasuyuki; Germino, Gregory G.; Woodford, Lisa M. Guay
Source: American Journal of Medical Genetics. Unidade: FM
Assunto: GENÉTICA
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ABNT
ONUCHIC, Luiz F. et al. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. American Journal of Medical Genetics, v. 110, p. 346-352, 2002Tradução . . Disponível em: https://doi.org/10.1002/ajmg.10468. Acesso em: 21 out. 2025.
APA
Onuchic, L. F., Mrug, M., Hou, X., Eggermann, T., Bergmann, C., Zerres, K., et al. (2002). Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. American Journal of Medical Genetics, 110, 346-352. doi:10.1002/ajmg.10468
NLM
Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo. Stefan, Nagasawa Y, Germino GG, Woodford LMG. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene [Internet]. American Journal of Medical Genetics. 2002 ; 110 346-352.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/ajmg.10468
Vancouver
Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo. Stefan, Nagasawa Y, Germino GG, Woodford LMG. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene [Internet]. American Journal of Medical Genetics. 2002 ; 110 346-352.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/ajmg.10468
Artigo de periodico
Biochemical characterization of bona fide polycystin-1 in vitro and in vivo (2001)
Boletta, Alessanda; Qian, Feng; Onuchic, Luiz Fernando; Bragonzi, Alessandra; Cortese, Marina; Deen, Peter M.; Courtoy, Pierre J.; Soria, Marco R.; Devuyst, Olivier; Monaco, Lucia; Germino, Gregory G.
Source: American Journal of Kidney Diseases. Unidade: FM
Assunto: CLÍNICA GERAL
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ABNT
BOLETTA, Alessanda et al. Biochemical characterization of bona fide polycystin-1 in vitro and in vivo. American Journal of Kidney Diseases, v. 38, n. 6, p. 1421-1429, 2001Tradução . . Disponível em: https://doi.org/10.1053/ajkd.2001.29282. Acesso em: 21 out. 2025.
APA
Boletta, A., Qian, F., Onuchic, L. F., Bragonzi, A., Cortese, M., Deen, P. M., et al. (2001). Biochemical characterization of bona fide polycystin-1 in vitro and in vivo. American Journal of Kidney Diseases, 38( 6), 1421-1429. doi:10.1053/ajkd.2001.29282
NLM
Boletta A, Qian F, Onuchic LF, Bragonzi A, Cortese M, Deen PM, Courtoy PJ, Soria MR, Devuyst O, Monaco L, Germino GG. Biochemical characterization of bona fide polycystin-1 in vitro and in vivo [Internet]. American Journal of Kidney Diseases. 2001 ; 38( 6): 1421-1429.[citado 2025 out. 21 ] Available from: https://doi.org/10.1053/ajkd.2001.29282
Vancouver
Boletta A, Qian F, Onuchic LF, Bragonzi A, Cortese M, Deen PM, Courtoy PJ, Soria MR, Devuyst O, Monaco L, Germino GG. Biochemical characterization of bona fide polycystin-1 in vitro and in vivo [Internet]. American Journal of Kidney Diseases. 2001 ; 38( 6): 1421-1429.[citado 2025 out. 21 ] Available from: https://doi.org/10.1053/ajkd.2001.29282
Artigo de periodico
Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells (2000)
Boletta, Alessandra; Qian, Fang; Onuchic, Luiz Fernando; Bhunia, Anil K.; Phakdeekitcharoen, Bunyong; Hanaoka, Kazushige; Guggino, William; Monaco, Lucia; Germino, Gregory G.
Source: Molecular Cell. Unidade: FM
Assunto: GENÉTICA MÉDICA
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ABNT
BOLETTA, Alessandra et al. Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells. Molecular Cell, v. 6, p. 1267-1273, 2000Tradução . . Acesso em: 21 out. 2025.
APA
Boletta, A., Qian, F., Onuchic, L. F., Bhunia, A. K., Phakdeekitcharoen, B., Hanaoka, K., et al. (2000). Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells. Molecular Cell, 6, 1267-1273.
NLM
Boletta A, Qian F, Onuchic LF, Bhunia AK, Phakdeekitcharoen B, Hanaoka K, Guggino W, Monaco L, Germino GG. Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells. Molecular Cell. 2000 ; 6 1267-1273.[citado 2025 out. 21 ]
Vancouver
Boletta A, Qian F, Onuchic LF, Bhunia AK, Phakdeekitcharoen B, Hanaoka K, Guggino W, Monaco L, Germino GG. Polycystin-1, the gene product of PKD1, induces resistance to apoptosis and spontaneous tubulogenesis in MDCK cells. Molecular Cell. 2000 ; 6 1267-1273.[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Current status of the PKHDI region transcription map (2000)
Onuchic, Luiz Fernando; Furu, L.; Nagasawa, Y.; Lakings, Alicia; Mangasser Stephan, K.; Avner, Ellis D.; Zerres, Klaus; Guay Woodford, Lisa M.; Somlo, Stefan; Germino, Gregory G.
Source: Journal of the American Society of Nephrology. Conference titles: Annual Meeting of the American Society of Nephrology. Unidade: FM
Assunto: NEFROLOGIA
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ABNT
ONUCHIC, Luiz Fernando et al. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. Toronto: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 2000
APA
Onuchic, L. F., Furu, L., Nagasawa, Y., Lakings, A., Mangasser Stephan, K., Avner, E. D., et al. (2000). Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. Toronto: Faculdade de Medicina, Universidade de São Paulo.
NLM
Onuchic LF, Furu L, Nagasawa Y, Lakings A, Mangasser Stephan K, Avner ED, Zerres K, Guay Woodford LM, Somlo S, Germino GG. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2025 out. 21 ]
Vancouver
Onuchic LF, Furu L, Nagasawa Y, Lakings A, Mangasser Stephan K, Avner ED, Zerres K, Guay Woodford LM, Somlo S, Germino GG. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2025 out. 21 ]
Artigo de periodico
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease (2000)
Hofmann, Yvonne; Becker, Jutta; Wright, Felicia; Avner, Ellis D.; Mrug, Michal; Guay Woodford, Lisa M.; Somlo, Stefan; Zerres, Klaus; Germino, Gregory G.; Onuchic, Luiz Fernando
Source: European Journal of Human Genetics. Unidade: FM
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOFMANN, Yvonne et al. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease. European Journal of Human Genetics, n. 8, p. 163-6, 2000Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5200426. Acesso em: 21 out. 2025.
APA
Hofmann, Y., Becker, J., Wright, F., Avner, E. D., Mrug, M., Guay Woodford, L. M., et al. (2000). Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease. European Journal of Human Genetics, ( 8), 163-6. doi:10.1038/sj.ejhg.5200426
NLM
Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease [Internet]. European Journal of Human Genetics. 2000 ;( 8): 163-6.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/sj.ejhg.5200426
Vancouver
Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease [Internet]. European Journal of Human Genetics. 2000 ;( 8): 163-6.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/sj.ejhg.5200426
Trabalho de evento-resumo periodico
Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene (2000)
Onuchic, Luiz Fernando; Lakings, Alicia; Germino, Gregory G.; Guay Woodford, Lisa M.
Source: Journal of the American Society of Nephrology. Conference titles: Annual Meeting of the American Society of Nephrology. Unidade: FM
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ONUCHIC, Luiz Fernando et al. Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 2000
APA
Onuchic, L. F., Lakings, A., Germino, G. G., & Guay Woodford, L. M. (2000). Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene. Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Onuchic LF, Lakings A, Germino GG, Guay Woodford LM. Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2025 out. 21 ]
Vancouver
Onuchic LF, Lakings A, Germino GG, Guay Woodford LM. Genomic organization and expression of a calmodulin-related gene on chromossome 6p12 and its exclusion as a PKHD1 candidate gene. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2025 out. 21 ]
Artigo de periodico
Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominat polycystic kidney disease (1998)
Watnick, Terry J.; Torres, Vicente E.; Gandolph, Michael A.; Qian, Feng; Onuchic, Luiz Fernando; Klinger, Katherine W.; Landes, Gregory; Germino, Gregory G.
Source: Molecular Cell. Unidade: FM
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 21 out. 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 out. 21 ]
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 out. 21 ]
Artigo de periodico
The molecular basis of focal cyst formation in human autosomal dominant polycistic kidney disease type I (1996)
Qian, Feng; Waitnick, Terry J.; Onuchic, Luiz F.; Germino, Gregory G.
Source: Cell. Unidade: FM
Assunto: NEFROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QIAN, Feng et al. The molecular basis of focal cyst formation in human autosomal dominant polycistic kidney disease type I. Cell, v. 87, n. 6, p. 979-987, 1996Tradução . . Acesso em: 21 out. 2025.
APA
Qian, F., Waitnick, T. J., Onuchic, L. F., & Germino, G. G. (1996). The molecular basis of focal cyst formation in human autosomal dominant polycistic kidney disease type I. Cell, 87( 6), 979-987.
NLM
Qian F, Waitnick TJ, Onuchic LF, Germino GG. The molecular basis of focal cyst formation in human autosomal dominant polycistic kidney disease type I. Cell. 1996 ; 87( 6): 979-987.[citado 2025 out. 21 ]
Vancouver
Qian F, Waitnick TJ, Onuchic LF, Germino GG. The molecular basis of focal cyst formation in human autosomal dominant polycistic kidney disease type I. Cell. 1996 ; 87( 6): 979-987.[citado 2025 out. 21 ]

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