ReP USP - Resultado da busca

Artigo de periodico
Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? (2015)
Faria, Ágatha Cristhina; Rabbi-Bortolini, Eliete; Reboucas, Maria R. G. O; Pereira, Andreia L. A. de S. Thiago; Frasson, Milena G. Tonini; Atique, Rodrigo; Lourenço, Naila Cristina Vilaça; Rosenberg, Carla ; Kobayashi, Gerson Shigeru; Passos-Bueno, Maria Rita ; Errera, Flávia Imbroisi Valle
Source: American Journal of Medical Genetics Part A. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS, GENÉTICA MOLECULAR, DOENÇAS GENÉTICAS, CÉREBRO (DESENVOLVIMENTO), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FARIA, Ágatha Cristhina et al. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?. American Journal of Medical Genetics Part A, v. No 2015, p. 1-7, 2015Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.37448. Acesso em: 03 nov. 2024.
APA
Faria, Á. C., Rabbi-Bortolini, E., Reboucas, M. R. G. O., Pereira, A. L. A. de S. T., Frasson, M. G. T., Atique, R., et al. (2015). Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? American Journal of Medical Genetics Part A, No 2015, 1-7. doi:10.1002/ajmg.a.37448
NLM
Faria ÁC, Rabbi-Bortolini E, Reboucas MRGO, Pereira ALA de ST, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? [Internet]. American Journal of Medical Genetics Part A. 2015 ; No 2015 1-7.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.37448
Vancouver
Faria ÁC, Rabbi-Bortolini E, Reboucas MRGO, Pereira ALA de ST, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? [Internet]. American Journal of Medical Genetics Part A. 2015 ; No 2015 1-7.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.37448
Artigo de periodico
Functionally conserved cis-regulatory elements of COL18A1 identified through zebrafish transgenesis (2010)
Kague, Érika; Bessling, Seneca; Lee, Josephine; Hu, Gui; Passos-Bueno, Maria Rita ; Fisher, Shannon
Source: Developmental Biology. Unidade: IB
Assunto: SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAGUE, Érika et al. Functionally conserved cis-regulatory elements of COL18A1 identified through zebrafish transgenesis. Developmental Biology, v. 337, n. 2, p. 496-505, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ydbio.2009.10.028. Acesso em: 03 nov. 2024.
APA
Kague, É., Bessling, S., Lee, J., Hu, G., Passos-Bueno, M. R., & Fisher, S. (2010). Functionally conserved cis-regulatory elements of COL18A1 identified through zebrafish transgenesis. Developmental Biology, 337( 2), 496-505. doi:10.1016/j.ydbio.2009.10.028
NLM
Kague É, Bessling S, Lee J, Hu G, Passos-Bueno MR, Fisher S. Functionally conserved cis-regulatory elements of COL18A1 identified through zebrafish transgenesis [Internet]. Developmental Biology. 2010 ; 337( 2): 496-505.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ydbio.2009.10.028
Vancouver
Kague É, Bessling S, Lee J, Hu G, Passos-Bueno MR, Fisher S. Functionally conserved cis-regulatory elements of COL18A1 identified through zebrafish transgenesis [Internet]. Developmental Biology. 2010 ; 337( 2): 496-505.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ydbio.2009.10.028
Artigo de periodico
Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? (2009)
Guion-Almeida, Maria Leine; Vendramini-Pittoli, Siulan; Passos-Bueno, Maria Rita ; Zechi-Ceide, Roseli Maria
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, IB
Assunto: ANOMALIA CRANIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?. American Journal of Medical Genetics. Part A, v. 149A, p. 2762-2764, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32816. Acesso em: 03 nov. 2024.
APA
Guion-Almeida, M. L., Vendramini-Pittoli, S., Passos-Bueno, M. R., & Zechi-Ceide, R. M. (2009). Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? American Journal of Medical Genetics. Part A, 149A, 2762-2764. doi:10.1002/ajmg.a.32816
NLM
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Vancouver
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Artigo de periodico
Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients (2009)
Masotti, Cibele; Ornelas, Camila Camanzano; Splendore-Gordonos, Alessandra; Moura, Ricardo; Felix, Temis Maria; Alonso, Nivaldo; Camargo, Anamaria Aranha; Passos-Bueno, Maria Rita
Source: BMC Medical Genetics. Unidade: IB
Assunto: DISOSTOSE MANDIBULOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MASOTTI, Cibele et al. Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients. BMC Medical Genetics, v. 10, p. 136-142, 2009Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-10-136. Acesso em: 03 nov. 2024.
APA
Masotti, C., Ornelas, C. C., Splendore-Gordonos, A., Moura, R., Felix, T. M., Alonso, N., et al. (2009). Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients. BMC Medical Genetics, 10, 136-142. doi:10.1186/1471-2350-10-136
NLM
Masotti C, Ornelas CC, Splendore-Gordonos A, Moura R, Felix TM, Alonso N, Camargo AA, Passos-Bueno MR. Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients [Internet]. BMC Medical Genetics. 2009 ; 10 136-142.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/1471-2350-10-136
Vancouver
Masotti C, Ornelas CC, Splendore-Gordonos A, Moura R, Felix TM, Alonso N, Camargo AA, Passos-Bueno MR. Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients [Internet]. BMC Medical Genetics. 2009 ; 10 136-142.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/1471-2350-10-136
Artigo de periodico
Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells (2008)
Costa, André de Mendonça; Bueno, Daniela Franco; Martins, Marília T.; Kerkis, Irina; Kerkis, Alexandre; Fanganiello, Roberto Dalto; Cerruti, Humberto; Alonso, Nivaldo; Passos-Bueno, Maria Rita
Source: Journal of Craniofacial Surgery. Unidade: IB
Subjects: CRÂNIO (DEFEITO), POLPA DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, André de Mendonça et al. Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells. Journal of Craniofacial Surgery, v. 19, n. ja 2008, p. 204-210, 2008Tradução . . Acesso em: 03 nov. 2024.
APA
Costa, A. de M., Bueno, D. F., Martins, M. T., Kerkis, I., Kerkis, A., Fanganiello, R. D., et al. (2008). Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells. Journal of Craniofacial Surgery, 19( ja 2008), 204-210.
NLM
Costa A de M, Bueno DF, Martins MT, Kerkis I, Kerkis A, Fanganiello RD, Cerruti H, Alonso N, Passos-Bueno MR. Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells. Journal of Craniofacial Surgery. 2008 ; 19( ja 2008): 204-210.[citado 2024 nov. 03 ]
Vancouver
Costa A de M, Bueno DF, Martins MT, Kerkis I, Kerkis A, Fanganiello RD, Cerruti H, Alonso N, Passos-Bueno MR. Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells. Journal of Craniofacial Surgery. 2008 ; 19( ja 2008): 204-210.[citado 2024 nov. 03 ]
Artigo de periodico
Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients (2006)
Jehee, Fernanda Sarquis; Alonso, Luís Garcia; Cavalcanti, Denise Pontes; Kim, Chong A.; Wall, Steven A.; Plast, F. C. S.; Mulliken, John B.; Sun, Miao; Jabs, Ethylin Wang; Boyadjiev, Simeon A.; Wilkie, Andrew O. M.; Passos-Bueno, Maria Rita
Source: Cleft Palate-Craniofacial Journal. Unidade: IB
Subjects: MALFORMAÇÕES, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal, v. 43, n. 2, p. 148-151, 2006Tradução . . Acesso em: 03 nov. 2024.
APA
Jehee, F. S., Alonso, L. G., Cavalcanti, D. P., Kim, C. A., Wall, S. A., Plast, F. C. S., et al. (2006). Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal, 43( 2), 148-151.
NLM
Jehee FS, Alonso LG, Cavalcanti DP, Kim CA, Wall SA, Plast FCS, Mulliken JB, Sun M, Jabs EW, Boyadjiev SA, Wilkie AOM, Passos-Bueno MR. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal. 2006 ; 43( 2): 148-151.[citado 2024 nov. 03 ]
Vancouver
Jehee FS, Alonso LG, Cavalcanti DP, Kim CA, Wall SA, Plast FCS, Mulliken JB, Sun M, Jabs EW, Boyadjiev SA, Wilkie AOM, Passos-Bueno MR. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal. 2006 ; 43( 2): 148-151.[citado 2024 nov. 03 ]
Artigo de periodico
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) (2004)
Tonini, M. M. O.; Passos-Bueno, Maria Rita ; Cerqueira, A.; Matioli, Sergio Russo ; Pavanello, Rita de Cássia M.; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: BIOLOGIA, GENÉTICA MÉDICA, MALFORMAÇÕES, DOENÇAS MUSCULOSQUELÉTICAS, DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, M. M. O. et al. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders, v. 14, n. 1, p. 33-38, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2003.07.001. Acesso em: 03 nov. 2024.
APA
Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Matioli, S. R., Pavanello, R. de C. M., & Zatz, M. (2004). Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders, 14( 1), 33-38. doi:10.1016/j.nmd.2003.07.001
NLM
Tonini MMO, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R de CM, Zatz M. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) [Internet]. Neuromuscular Disorders. 2004 ; 14( 1): 33-38.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Vancouver
Tonini MMO, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R de CM, Zatz M. Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD) [Internet]. Neuromuscular Disorders. 2004 ; 14( 1): 33-38.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Artigo de periodico
A transcript finishing initiative for closing gaps in the human transcriptome (2004)
Bettoni, Fabiana; Carraro, Maria Dirce; Pires, Lilian Campos Pires; Parmigiani, Rafael B; Ferreira, Elisa N; Moreira, Eloísa de Sá; Latorre, Maria do Rosário Dias de Oliveira; Simpson, Andrew J. G; Camargo, Anamaria A; Cruz, Luciana Oliveira; Degaki, Theri Leica; Festa, Fernanda; Massirer, Katlin B; Sogayar, Mari Cleide ; Camargo Filho, Fernando; Camargo, Luiz Paulo; Cunha, Marco A. V; De Souza, Sandro J; Faria Júnior, Milton; Giuliatti, Silvana; Kopp, Leonardo; Oliveira, Paulo. S. L; Paiva, Paulo B; Pereira, Anderson A; Pinheiro, Daniel G; Puga, Renato D; Souza, Jorge Estefano S; Albuquerque, Dulcineia M; Andrade, Luís E. C; Baia, Gilson S; Cavaleiro-Luna, Ana M. S; Cerutti, Janete M; Costa, Fernando F; Costanzi-Strauss, Eugenia ; Espreafico, Enilza Maria; Ferrasi, Adriana C; Ferro, Emer Suavinho ; Fortes, Maria A. H. Z; Furchi, Joelma R. F; Gianella-Neto, Daniel; Goldman, Gustavo Henrique; Goldman, Maria Helena de Souza; Gruber, Arthur ; Guimarães, Gustavo S; Hackel, Christine; Henrique-Silva, Flávio; Kimura, Edna Teruko ; Leoni, Suzana G; Macedo, Cláudia; Malnic, Bettina ; Manzini B., Carina V; Marie, Suely Kazue Nagahashi; Martinez-Rossi, Nilce Maria; Menossi, Marcelo; Miracca, Elisabete C; Nagai, Maria Aparecida; Nobrega, Francisco Gorgonio da; Nobrega, Marina Pasetto; Oba-Shinjo, Sueli M; Oliveira, Márika K; Orabona, Guilherme M; Otsuka, Audrey Y; Paço-Larson, Maria Luiza; Paixão, Beatriz M. C; Pandolfi, José R. C; Pardini, Maria I. M. C; Passos-Bueno, Maria Rita ; Passos, Geraldo Aleixo Silva; Pesquero, João B; Pessoa, Juliana G; Rahal, Paula; Rainho, Cláudia A; Reis, Caroline P; Ricca, Tatiana I; Rodrigues, Vanderlei; Rogatto, Silvia R; Romano, Camila M; Romeiro, Janaína G; Rossi, Antonio; Sá, Renata G; Sales, Magaly M; Sant'Anna, Simone C; Santarosa, Patrícia L; Segato, Fernando; Silva Júnior, Wilson Araújo da; Silva, Ismael D. C. G; Silva, Neusa P; Soares-Costa, Andrea; Sonati, Maria F; Strauss, Brian E; Tajara, Eloiza H; Valentini, Sandro R; Villanova, Fabiola V; Ward, Laura S; Zanette, Dalila L
Source: Genome Research. Unidades: FSP, IQ, ICB, FMRP, FCFRP, FORP, FMVZ, FM, IB
Assunto: HISTOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BETTONI, Fabiana et al. A transcript finishing initiative for closing gaps in the human transcriptome. Genome Research, v. 14, p. 1413-1423, 2004Tradução . . Disponível em: https://doi.org/10.1101/gr.2111304. Acesso em: 03 nov. 2024.
APA
Bettoni, F., Carraro, M. D., Pires, L. C. P., Parmigiani, R. B., Ferreira, E. N., Moreira, E. de S., et al. (2004). A transcript finishing initiative for closing gaps in the human transcriptome. Genome Research, 14, 1413-1423. doi:10.1101/gr.2111304
NLM
Bettoni F, Carraro MD, Pires LCP, Parmigiani RB, Ferreira EN, Moreira E de S, Latorre M do RD de O, Simpson AJG, Camargo AA, Cruz LO, Degaki TL, Festa F, Massirer KB, Sogayar MC, Camargo Filho F, Camargo LP, Cunha MAV, De Souza SJ, Faria Júnior M, Giuliatti S, Kopp L, Oliveira PSL, Paiva PB, Pereira AA, Pinheiro DG, Puga RD, Souza JES, Albuquerque DM, Andrade LEC, Baia GS, Cavaleiro-Luna AMS, Cerutti JM, Costa FF, Costanzi-Strauss E, Espreafico EM, Ferrasi AC, Ferro ES, Fortes MAHZ, Furchi JRF, Gianella-Neto D, Goldman GH, Goldman MH de S, Gruber A, Guimarães GS, Hackel C, Henrique-Silva F, Kimura ET, Leoni SG, Macedo C, Malnic B, Manzini B. CV, Marie SKN, Martinez-Rossi NM, Menossi M, Miracca EC, Nagai MA, Nobrega FG da, Nobrega MP, Oba-Shinjo SM, Oliveira MK, Orabona GM, Otsuka AY, Paço-Larson ML, Paixão BMC, Pandolfi JRC, Pardini MIMC, Passos-Bueno MR, Passos GAS, Pesquero JB, Pessoa JG, Rahal P, Rainho CA, Reis CP, Ricca TI, Rodrigues V, Rogatto SR, Romano CM, Romeiro JG, Rossi A, Sá RG, Sales MM, Sant'Anna SC, Santarosa PL, Segato F, Silva Júnior WA da, Silva IDCG, Silva NP, Soares-Costa A, Sonati MF, Strauss BE, Tajara EH, Valentini SR, Villanova FV, Ward LS, Zanette DL. A transcript finishing initiative for closing gaps in the human transcriptome [Internet]. Genome Research. 2004 ; 14 1413-1423.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1101/gr.2111304
Vancouver
Bettoni F, Carraro MD, Pires LCP, Parmigiani RB, Ferreira EN, Moreira E de S, Latorre M do RD de O, Simpson AJG, Camargo AA, Cruz LO, Degaki TL, Festa F, Massirer KB, Sogayar MC, Camargo Filho F, Camargo LP, Cunha MAV, De Souza SJ, Faria Júnior M, Giuliatti S, Kopp L, Oliveira PSL, Paiva PB, Pereira AA, Pinheiro DG, Puga RD, Souza JES, Albuquerque DM, Andrade LEC, Baia GS, Cavaleiro-Luna AMS, Cerutti JM, Costa FF, Costanzi-Strauss E, Espreafico EM, Ferrasi AC, Ferro ES, Fortes MAHZ, Furchi JRF, Gianella-Neto D, Goldman GH, Goldman MH de S, Gruber A, Guimarães GS, Hackel C, Henrique-Silva F, Kimura ET, Leoni SG, Macedo C, Malnic B, Manzini B. CV, Marie SKN, Martinez-Rossi NM, Menossi M, Miracca EC, Nagai MA, Nobrega FG da, Nobrega MP, Oba-Shinjo SM, Oliveira MK, Orabona GM, Otsuka AY, Paço-Larson ML, Paixão BMC, Pandolfi JRC, Pardini MIMC, Passos-Bueno MR, Passos GAS, Pesquero JB, Pessoa JG, Rahal P, Rainho CA, Reis CP, Ricca TI, Rodrigues V, Rogatto SR, Romano CM, Romeiro JG, Rossi A, Sá RG, Sales MM, Sant'Anna SC, Santarosa PL, Segato F, Silva Júnior WA da, Silva IDCG, Silva NP, Soares-Costa A, Sonati MF, Strauss BE, Tajara EH, Valentini SR, Villanova FV, Ward LS, Zanette DL. A transcript finishing initiative for closing gaps in the human transcriptome [Internet]. Genome Research. 2004 ; 14 1413-1423.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1101/gr.2111304
Artigo de periodico
Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation? (2004)
Maranduba, Carlos Magno da Costa; Moreira, Eloísa de Sá; Orabona, Guilherme Müller; Pavanello, Rita de Cássia M.; Vianna-Morgante, Angela M ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: RETARDO MENTAL, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARANDUBA, Carlos Magno da Costa et al. Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation?. American Journal of Medical Genetics. Part A, v. 124A, n. 4, p. 413-415, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20401. Acesso em: 03 nov. 2024.
APA
Maranduba, C. M. da C., Moreira, E. de S., Orabona, G. M., Pavanello, R. de C. M., Vianna-Morgante, A. M., & Passos-Bueno, M. R. (2004). Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation? American Journal of Medical Genetics. Part A, 124A( 4), 413-415. doi:10.1002/ajmg.a.20401
NLM
Maranduba CM da C, Moreira E de S, Orabona GM, Pavanello R de CM, Vianna-Morgante AM, Passos-Bueno MR. Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation? [Internet]. American Journal of Medical Genetics. Part A. 2004 ; 124A( 4): 413-415.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.20401
Vancouver
Maranduba CM da C, Moreira E de S, Orabona GM, Pavanello R de CM, Vianna-Morgante AM, Passos-Bueno MR. Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation? [Internet]. American Journal of Medical Genetics. Part A. 2004 ; 124A( 4): 413-415.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.a.20401
Artigo de periodico
Telethonin protein expression in neuromuscular disorders (2002)
Vainzof, Mariz ; Moreira, Eloisa S.; Suzuki, Oscar T.; Faulkner, Georgine; Valle, Georgio; Beggs, Alan H.; Carpen, Olli; Ribeiro, Alberto de Freitas ; Zanoteli, Edmar; Gurgel-Gianneti, Juliana; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Biochimica et Biophysica Acta. Unidades: IB, FM
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, v. 1588, n. 1, p. 33-40, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0925-4439(02)00113-8. Acesso em: 03 nov. 2024.
APA
Vainzof, M., Moreira, E. S., Suzuki, O. T., Faulkner, G., Valle, G., Beggs, A. H., et al. (2002). Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, 1588( 1), 33-40. doi:10.1016/s0925-4439(02)00113-8
NLM
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Vancouver
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Artigo de periodico
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome (2002)
Suzuki, Oscar T.; Sertié, Andréa Laurato; Der Kaloustian, Vazken M.; Kok, Fernando; Carpenter, M.; Murray, J; Czeizel, A E; Kliemann, Susana E.; Rosemberg, Sérgio; Monteiro, M.; Olsen, Bjorn Reino; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Unidades: IB, FM
Subjects: DEGENERAÇÃO RETINIANA, DOENÇAS RETINIANAS, CEGUEIRA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUZUKI, Oscar T. et al. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, v. 71, p. 1320-1329, 2002Tradução . . Acesso em: 03 nov. 2024.
APA
Suzuki, O. T., Sertié, A. L., Der Kaloustian, V. M., Kok, F., Carpenter, M., Murray, J., et al. (2002). Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, 71, 1320-1329.
NLM
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 nov. 03 ]
Vancouver
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 nov. 03 ]
Artigo de periodico
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? (2002)
Tonini, M. M. O.; Passos-Bueno, Maria Rita ; Cerqueira, A.; Pavanello, Rita de Cássia M.; Vainzof, Mariz ; Dubowitz, Victor; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, M. M. O. et al. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?. Neuromuscular Disorders, v. 12, n. 6, p. 554-557, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(02)00014-7. Acesso em: 03 nov. 2024.
APA
Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Pavanello, R. de C. M., Vainzof, M., Dubowitz, V., & Zatz, M. (2002). Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders, 12( 6), 554-557. doi:10.1016/s0960-8966(02)00014-7
NLM
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7
Vancouver
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7
Artigo de periodico
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours (2001)
Zorick, Todd S.; Mustacchi, Zan; Bando, Sílvia Yumi; Zatz, Mayana ; Moreira-Filho, Carlos Alberto; Olsen, Björn; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidade: IB
Assunto: SÍNDROME DE DOWN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZORICK, Todd S. et al. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours. European Journal of Human Genetics, v. 9, p. 811-814, 2001Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5200721. Acesso em: 03 nov. 2024.
APA
Zorick, T. S., Mustacchi, Z., Bando, S. Y., Zatz, M., Moreira-Filho, C. A., Olsen, B., & Passos-Bueno, M. R. (2001). High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours. European Journal of Human Genetics, 9, 811-814. doi:10.1038/sj.ejhg.5200721
NLM
Zorick TS, Mustacchi Z, Bando SY, Zatz M, Moreira-Filho CA, Olsen B, Passos-Bueno MR. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours [Internet]. European Journal of Human Genetics. 2001 ; 9 811-814.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/sj.ejhg.5200721
Vancouver
Zorick TS, Mustacchi Z, Bando SY, Zatz M, Moreira-Filho CA, Olsen B, Passos-Bueno MR. High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours [Internet]. European Journal of Human Genetics. 2001 ; 9 811-814.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/sj.ejhg.5200721
Artigo de periodico
The genome sequence of the plant pathogen "Xylella fastidiosa" (2000)
Simpson, A. J. G.; Reinach, Fernando de Castro; Passos-Bueno, Maria Rita ; Camargo, L E A; Carrer, H; Coutinho, L L; El Dorry, Hamza Fahmi Ali ; Goldman, G H; Goldman, M H S; Gomes, Suely Lopes ; Gruber, Arthur ; Krieger, José Eduardo; Lambais, Marcio Rodrigues; Marques, Marilis do Valle ; Menck, Carlos Frederico Martins ; Miyaki, Cristina Yumi ; Nagai, Maria Aparecida; Netto, Luis Eduardo Soares ; Nóbrega , F G; Oliveira, M C de; Rodrigues, V; Santelli, Roberto Vicente; Silva, A C R; Da Silva, Aline Maria ; Tsai, Siu Mui ; Van Sluys, Marie-Anne ; Verjovski-Almeida, Sergio ; Zago, M A; Zatz, Mayana
Source: Nature. Unidades: IQ, IB, ESALQ, FCFRP, FFCLRP, FMVZ, FM, ICB, FMRP
Assunto: GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMPSON, A. J. G. et al. The genome sequence of the plant pathogen "Xylella fastidiosa". Nature, v. 406, p. 151-157, 2000Tradução . . Disponível em: https://doi.org/10.1038/35018003. Acesso em: 03 nov. 2024.
APA
Simpson, A. J. G., Reinach, F. de C., Passos-Bueno, M. R., Camargo, L. E. A., Carrer, H., Coutinho, L. L., et al. (2000). The genome sequence of the plant pathogen "Xylella fastidiosa". Nature, 406, 151-157. doi:10.1038/35018003
NLM
Simpson AJG, Reinach F de C, Passos-Bueno MR, Camargo LEA, Carrer H, Coutinho LL, El Dorry HFA, Goldman GH, Goldman MHS, Gomes SL, Gruber A, Krieger JE, Lambais MR, Marques M do V, Menck CFM, Miyaki CY, Nagai MA, Netto LES, Nóbrega FG, Oliveira MC de, Rodrigues V, Santelli RV, Silva ACR, Da Silva AM, Tsai SM, Van Sluys M-A, Verjovski-Almeida S, Zago MA, Zatz M. The genome sequence of the plant pathogen "Xylella fastidiosa" [Internet]. Nature. 2000 ; 406 151-157.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/35018003
Vancouver
Simpson AJG, Reinach F de C, Passos-Bueno MR, Camargo LEA, Carrer H, Coutinho LL, El Dorry HFA, Goldman GH, Goldman MHS, Gomes SL, Gruber A, Krieger JE, Lambais MR, Marques M do V, Menck CFM, Miyaki CY, Nagai MA, Netto LES, Nóbrega FG, Oliveira MC de, Rodrigues V, Santelli RV, Silva ACR, Da Silva AM, Tsai SM, Van Sluys M-A, Verjovski-Almeida S, Zago MA, Zatz M. The genome sequence of the plant pathogen "Xylella fastidiosa" [Internet]. Nature. 2000 ; 406 151-157.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/35018003

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Indexado em

Normalized affiliation

Non normalized affiliation