ReP USP - Resultado da busca

Artigo de periodico
Velocardiofacail syndrome with a rare t(2:22) (2007)
Huber, Jair; Rainho, Claudia A.; Gomes, Marcus V.; Santos, Silvio Avelino dos; Ramos, Ester Silveira
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: ANORMALIDADES MÚLTIPLAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HUBER, Jair et al. Velocardiofacail syndrome with a rare t(2:22). Clinical Dysmorphology, v. 16, n. 3, p. 181-183, 2007Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3280fa81de. Acesso em: 08 nov. 2024.
APA
Huber, J., Rainho, C. A., Gomes, M. V., Santos, S. A. dos, & Ramos, E. S. (2007). Velocardiofacail syndrome with a rare t(2:22). Clinical Dysmorphology, 16( 3), 181-183. doi:10.1097/mcd.0b013e3280fa81de
NLM
Huber J, Rainho CA, Gomes MV, Santos SA dos, Ramos ES. Velocardiofacail syndrome with a rare t(2:22) [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 181-183.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e3280fa81de
Vancouver
Huber J, Rainho CA, Gomes MV, Santos SA dos, Ramos ES. Velocardiofacail syndrome with a rare t(2:22) [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 181-183.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e3280fa81de
Artigo de periodico
Mutation analysis of gene PAX6 in human gliomas (2007)
Pinto, G. R.; Clara, C. A.; Santos, M. J.; Almeida, J. R. W.; Burbano, R. R.; Rey, J. A.; Casartelli, Cacilda
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: MUTAÇÃO, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, G. R. et al. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research, v. 6, n. 4, p. 1019-1025, 2007Tradução . . Acesso em: 08 nov. 2024.
APA
Pinto, G. R., Clara, C. A., Santos, M. J., Almeida, J. R. W., Burbano, R. R., Rey, J. A., & Casartelli, C. (2007). Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research, 6( 4), 1019-1025.
NLM
Pinto GR, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research. 2007 ; 6( 4): 1019-1025.[citado 2024 nov. 08 ]
Vancouver
Pinto GR, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research. 2007 ; 6( 4): 1019-1025.[citado 2024 nov. 08 ]
Artigo de periodico
Shuttle mutagenesis and targeted disruption of a telomere-located essential gene of Leishmania (2007)
Squina, F. M.; Pedrosa, A. L.; Nunes, V. S.; Cruz, Ângela Kaysel; Tosi, Luiz Ricardo Orsini
Source: Parasitology. Unidade: FMRP
Subjects: LEISHMANIA, GENÉTICA MÉDICA, BIOLOGIA CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SQUINA, F. M. et al. Shuttle mutagenesis and targeted disruption of a telomere-located essential gene of Leishmania. Parasitology, v. 134, n. 4, p. 511-522, 2007Tradução . . Disponível em: https://doi.org/10.1017/s0031182006001892. Acesso em: 08 nov. 2024.
APA
Squina, F. M., Pedrosa, A. L., Nunes, V. S., Cruz, Â. K., & Tosi, L. R. O. (2007). Shuttle mutagenesis and targeted disruption of a telomere-located essential gene of Leishmania. Parasitology, 134( 4), 511-522. doi:10.1017/s0031182006001892
NLM
Squina FM, Pedrosa AL, Nunes VS, Cruz ÂK, Tosi LRO. Shuttle mutagenesis and targeted disruption of a telomere-located essential gene of Leishmania [Internet]. Parasitology. 2007 ; 134( 4): 511-522.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1017/s0031182006001892
Vancouver
Squina FM, Pedrosa AL, Nunes VS, Cruz ÂK, Tosi LRO. Shuttle mutagenesis and targeted disruption of a telomere-located essential gene of Leishmania [Internet]. Parasitology. 2007 ; 134( 4): 511-522.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1017/s0031182006001892
Artigo de periodico
Methylation pattern at the KvDMR in a child with beckwith-wiedermann syndrome conceived by ICSI.[Carta] (2007)
Gomes, M. V.; Gomes, C. C.; Pinto Junior, W.; Ramos, Ester Silveira
Source: American Journal of Medical Genetics. Part A. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, M. V. et al. Methylation pattern at the KvDMR in a child with beckwith-wiedermann syndrome conceived by ICSI.[Carta]. American Journal of Medical Genetics. Part A, v. 143A, n. 6, p. 625-629, 2007Tradução . . Acesso em: 08 nov. 2024.
APA
Gomes, M. V., Gomes, C. C., Pinto Junior, W., & Ramos, E. S. (2007). Methylation pattern at the KvDMR in a child with beckwith-wiedermann syndrome conceived by ICSI.[Carta]. American Journal of Medical Genetics. Part A, 143A( 6), 625-629.
NLM
Gomes MV, Gomes CC, Pinto Junior W, Ramos ES. Methylation pattern at the KvDMR in a child with beckwith-wiedermann syndrome conceived by ICSI.[Carta]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 6): 625-629.[citado 2024 nov. 08 ]
Vancouver
Gomes MV, Gomes CC, Pinto Junior W, Ramos ES. Methylation pattern at the KvDMR in a child with beckwith-wiedermann syndrome conceived by ICSI.[Carta]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 6): 625-629.[citado 2024 nov. 08 ]
Artigo de periodico
miRNA path: a database of miRNAs, target genes and metabolic pathways (2007)
Chiromatzo, A. O.; Oliveira, T. Y. K.; Pereira, G.; Costa, A. Y.; Montesco, C. A. E.; Gras, D. E.; Yosetake, F.; Vilar, J. B.; Cervato, M.; Prado, Pedro Roberto Rodrigues; Cardenas, R. G. C. C. L.; Cerri, R.; Borges, R. L.; Lemos, R. N.; Alvarenga, S. M.; Perallis, V. R. C.; Pinheiro, D. G.; Silva, I. T.; Brandão, R. M.; Cunha, M. A. V.; Giuliatti, Silvana; Silva Júnior, Wilson Araújo da
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHIROMATZO, A. O. et al. miRNA path: a database of miRNAs, target genes and metabolic pathways. Genetics and Molecular Research, v. 6, n. 4, p. 859-865, 2007Tradução . . Acesso em: 08 nov. 2024.
APA
Chiromatzo, A. O., Oliveira, T. Y. K., Pereira, G., Costa, A. Y., Montesco, C. A. E., Gras, D. E., et al. (2007). miRNA path: a database of miRNAs, target genes and metabolic pathways. Genetics and Molecular Research, 6( 4), 859-865.
NLM
Chiromatzo AO, Oliveira TYK, Pereira G, Costa AY, Montesco CAE, Gras DE, Yosetake F, Vilar JB, Cervato M, Prado PRR, Cardenas RGCCL, Cerri R, Borges RL, Lemos RN, Alvarenga SM, Perallis VRC, Pinheiro DG, Silva IT, Brandão RM, Cunha MAV, Giuliatti S, Silva Júnior WA da. miRNA path: a database of miRNAs, target genes and metabolic pathways. Genetics and Molecular Research. 2007 ; 6( 4): 859-865.[citado 2024 nov. 08 ]
Vancouver
Chiromatzo AO, Oliveira TYK, Pereira G, Costa AY, Montesco CAE, Gras DE, Yosetake F, Vilar JB, Cervato M, Prado PRR, Cardenas RGCCL, Cerri R, Borges RL, Lemos RN, Alvarenga SM, Perallis VRC, Pinheiro DG, Silva IT, Brandão RM, Cunha MAV, Giuliatti S, Silva Júnior WA da. miRNA path: a database of miRNAs, target genes and metabolic pathways. Genetics and Molecular Research. 2007 ; 6( 4): 859-865.[citado 2024 nov. 08 ]
Artigo de periodico
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome (2007)
Mazzeu, Juliana Forte; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla ; Szuhai, Karoly; Knijnenburg, Jeroen; Weiss, Janneke M. M.; Kerkis, Irina E.; Mustacchi, Zan; Colin, Guilherme; Mombach, Rômulo; Pavanello, Rita de Cássia M.; Otto, Paulo A ; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: CROMOSSOMOS (ANOMALIAS), GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAZZEU, Juliana Forte et al. Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome. American Journal of Medical Genetics. Part A, v. 143A, n. 15, p. 1790-1795, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31661. Acesso em: 08 nov. 2024.
APA
Mazzeu, J. F., Krepischi, A. C. V., Rosenberg, C., Szuhai, K., Knijnenburg, J., Weiss, J. M. M., et al. (2007). Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome. American Journal of Medical Genetics. Part A, 143A( 15), 1790-1795. doi:10.1002/ajmg.a.31661
NLM
Mazzeu JF, Krepischi ACV, Rosenberg C, Szuhai K, Knijnenburg J, Weiss JMM, Kerkis IE, Mustacchi Z, Colin G, Mombach R, Pavanello R de CM, Otto PA, Vianna-Morgante AM. Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 15): 1790-1795.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.31661
Vancouver
Mazzeu JF, Krepischi ACV, Rosenberg C, Szuhai K, Knijnenburg J, Weiss JMM, Kerkis IE, Mustacchi Z, Colin G, Mombach R, Pavanello R de CM, Otto PA, Vianna-Morgante AM. Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 15): 1790-1795.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.31661
Artigo de periodico
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY (2005)
Scrideli, Carlos Alberto; Baruffi, Marcelo R.; Squire, Jeremy A.; Ramos, Ester Silveira; Karaskowa, Jana; Heck, Benjamin; Tone, Luiz Gonzaga
Source: Leukemia Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, PEDIATRIA, LEUCEMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCRIDELI, Carlos Alberto et al. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. Leukemia Research, v. 29, p. 1465-1467, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.leukres.2005.04.022. Acesso em: 08 nov. 2024.
APA
Scrideli, C. A., Baruffi, M. R., Squire, J. A., Ramos, E. S., Karaskowa, J., Heck, B., & Tone, L. G. (2005). Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. Leukemia Research, 29, 1465-1467. doi:10.1016/j.leukres.2005.04.022
NLM
Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskowa J, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY [Internet]. Leukemia Research. 2005 ; 29 1465-1467.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.leukres.2005.04.022
Vancouver
Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskowa J, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY [Internet]. Leukemia Research. 2005 ; 29 1465-1467.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.leukres.2005.04.022
Artigo de periodico
Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma (2005)
khayat, A. S.; Gatti, L. Lobo; Lima, E. Moura; Assumpção, P. P. de; Motta, F. J. Nascimento; Harada, M. L.; Casartelli, Cacilda; Payão, S. L. Marques; Smith, M. A. Cardoso; Burbano, R. R.
Source: Clinical and Experimental Medicine. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KHAYAT, A. S. et al. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and Experimental Medicine, v. 5, p. 161-168, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10238-005-0081-4. Acesso em: 08 nov. 2024.
APA
khayat, A. S., Gatti, L. L., Lima, E. M., Assumpção, P. P. de, Motta, F. J. N., Harada, M. L., et al. (2005). Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and Experimental Medicine, 5, 161-168. doi:10.1007/s10238-005-0081-4
NLM
khayat AS, Gatti LL, Lima EM, Assumpção PP de, Motta FJN, Harada ML, Casartelli C, Payão SLM, Smith MAC, Burbano RR. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma [Internet]. Clinical and Experimental Medicine. 2005 ; 5 161-168.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1007/s10238-005-0081-4
Vancouver
khayat AS, Gatti LL, Lima EM, Assumpção PP de, Motta FJN, Harada ML, Casartelli C, Payão SLM, Smith MAC, Burbano RR. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma [Internet]. Clinical and Experimental Medicine. 2005 ; 5 161-168.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1007/s10238-005-0081-4
Artigo de periodico
Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil (2005)
Lima, E. M.; Araújo, J. J.; Harada, M. L.; Assumpção, P. P.; Burbano, R. R.; Casartelli, Cacilda
Source: Clinical and Experimental Medicine. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, E. M. et al. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, v. 5, p. 129-132, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10238-005-0077-0. Acesso em: 08 nov. 2024.
APA
Lima, E. M., Araújo, J. J., Harada, M. L., Assumpção, P. P., Burbano, R. R., & Casartelli, C. (2005). Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, 5, 129-132. doi:10.1007/s10238-005-0077-0
NLM
Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
Vancouver
Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
Artigo de periodico
Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors (2004)
Bello, M. Josefa; Alonso, M. Eva; Amiñoso, Cinthia; Anselmo, Nilson P.; Arjona, Dolores; Gonzalez-Gomez, Pilar; Lopez-Marin, Isabel; Campos, José M. de; Gutierrez, Manuel; Isla, Alberto; Kusak, M. Elena; Lassaletta, Luis; Sarasa, José L.; Vaquero, Jesus; Casartelli, Cacilda
Source: Mutation Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, PROCESSOS NEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BELLO, M. Josefa et al. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, v. 554, p. 23-32, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.mrfmmm.2004.02.011. Acesso em: 08 nov. 2024.
APA
Bello, M. J., Alonso, M. E., Amiñoso, C., Anselmo, N. P., Arjona, D., Gonzalez-Gomez, P., et al. (2004). Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, 554, 23-32. doi:10.1016/j.mrfmmm.2004.02.011
NLM
Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
Vancouver
Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
Artigo de periodico
De novo complex chromosome rearrangement: a study of two patients (2004)
Melo, D. G.; Huber, J.; Giuliani, L. R.; Mazzucatto, L. F.; Riegel, M.; Pina Neto, João Monteiro de
Source: Genetic Counseling. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, D. G. et al. De novo complex chromosome rearrangement: a study of two patients. Genetic Counseling, v. 15, n. 3, p. 303-310, 2004Tradução . . Acesso em: 08 nov. 2024.
APA
Melo, D. G., Huber, J., Giuliani, L. R., Mazzucatto, L. F., Riegel, M., & Pina Neto, J. M. de. (2004). De novo complex chromosome rearrangement: a study of two patients. Genetic Counseling, 15( 3), 303-310.
NLM
Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina Neto JM de. De novo complex chromosome rearrangement: a study of two patients. Genetic Counseling. 2004 ; 15( 3): 303-310.[citado 2024 nov. 08 ]
Vancouver
Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina Neto JM de. De novo complex chromosome rearrangement: a study of two patients. Genetic Counseling. 2004 ; 15( 3): 303-310.[citado 2024 nov. 08 ]
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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Artigo de periodico
Enhanced TGF'alfa'-EGFR expression and P53 alterations contributes to gastric tumors aggressiveness (2004)
Espinoza, Luis A.; Tone, Luiz Gonzaga; Barbieri Neto, José; Costa, Roberto Silva; Wang, Qiming J.; Ballejo, Gustavo
Source: Cancer Letters. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPINOZA, Luis A. et al. Enhanced TGF'alfa'-EGFR expression and P53 alterations contributes to gastric tumors aggressiveness. Cancer Letters, v. 212, p. 33-41, 2004Tradução . . Acesso em: 08 nov. 2024.
APA
Espinoza, L. A., Tone, L. G., Barbieri Neto, J., Costa, R. S., Wang, Q. J., & Ballejo, G. (2004). Enhanced TGF'alfa'-EGFR expression and P53 alterations contributes to gastric tumors aggressiveness. Cancer Letters, 212, 33-41.
NLM
Espinoza LA, Tone LG, Barbieri Neto J, Costa RS, Wang QJ, Ballejo G. Enhanced TGF'alfa'-EGFR expression and P53 alterations contributes to gastric tumors aggressiveness. Cancer Letters. 2004 ; 212 33-41.[citado 2024 nov. 08 ]
Vancouver
Espinoza LA, Tone LG, Barbieri Neto J, Costa RS, Wang QJ, Ballejo G. Enhanced TGF'alfa'-EGFR expression and P53 alterations contributes to gastric tumors aggressiveness. Cancer Letters. 2004 ; 212 33-41.[citado 2024 nov. 08 ]
Artigo de periodico
Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies (2003)
Engracia, V.; Leite, M. M. B. S.; Pagotto, Rubiani de Cassia; Zucoloto, Sérgio; Barbosa, C. A. A.; Mestriner, Moacyr Antonio
Source: American Journal of Medical Genetics. Unidade: FMRP
Subjects: HEPATOPATIAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENGRACIA, V. et al. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies. American Journal of Medical Genetics, n. 123A, p. 257-260, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20364. Acesso em: 08 nov. 2024.
APA
Engracia, V., Leite, M. M. B. S., Pagotto, R. de C., Zucoloto, S., Barbosa, C. A. A., & Mestriner, M. A. (2003). Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies. American Journal of Medical Genetics, ( 123A), 257-260. doi:10.1002/ajmg.a.20364
NLM
Engracia V, Leite MMBS, Pagotto R de C, Zucoloto S, Barbosa CAA, Mestriner MA. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies [Internet]. American Journal of Medical Genetics. 2003 ;( 123A): 257-260.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.20364
Vancouver
Engracia V, Leite MMBS, Pagotto R de C, Zucoloto S, Barbosa CAA, Mestriner MA. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies [Internet]. American Journal of Medical Genetics. 2003 ;( 123A): 257-260.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.20364
Artigo de periodico
Mitochondrial genome diversity of native americans supports a single early entry of founder populations into america (2002)
Silva Júnior, Wilson Araújo da; Bonatto, Sandro Luíz; Holanda, Adriano de Jesus; Ribeiro-dos-Santos, Andrea K. C.; Paixão, Beatriz M.; Goldman, Gustavo Henrique; Abe-Sandes, Kiyoko; Rodriguez-Delfin, Luis A.; Barbosa, Marcela Savoldi; Paço-Larson, Maria Luísa; Petzl-Erler, Maria Luiza; Valente, Valéria; Santos, Sidney Emanuel Batista dos; Zago, Marco Antônio
Source: American Journal of Human Genetics. Unidades: FCFRP, FMRP
Subjects: GENÉTICA MÉDICA, POPULAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JÚNIOR, Wilson Araújo da et al. Mitochondrial genome diversity of native americans supports a single early entry of founder populations into america. American Journal of Human Genetics, v. 71, p. 187-192, 2002Tradução . . Acesso em: 08 nov. 2024.
APA
Silva Júnior, W. A. da, Bonatto, S. L., Holanda, A. de J., Ribeiro-dos-Santos, A. K. C., Paixão, B. M., Goldman, G. H., et al. (2002). Mitochondrial genome diversity of native americans supports a single early entry of founder populations into america. American Journal of Human Genetics, 71, 187-192.
NLM
Silva Júnior WA da, Bonatto SL, Holanda A de J, Ribeiro-dos-Santos AKC, Paixão BM, Goldman GH, Abe-Sandes K, Rodriguez-Delfin LA, Barbosa MS, Paço-Larson ML, Petzl-Erler ML, Valente V, Santos SEB dos, Zago MA. Mitochondrial genome diversity of native americans supports a single early entry of founder populations into america. American Journal of Human Genetics. 2002 ; 71 187-192.[citado 2024 nov. 08 ]
Vancouver
Silva Júnior WA da, Bonatto SL, Holanda A de J, Ribeiro-dos-Santos AKC, Paixão BM, Goldman GH, Abe-Sandes K, Rodriguez-Delfin LA, Barbosa MS, Paço-Larson ML, Petzl-Erler ML, Valente V, Santos SEB dos, Zago MA. Mitochondrial genome diversity of native americans supports a single early entry of founder populations into america. American Journal of Human Genetics. 2002 ; 71 187-192.[citado 2024 nov. 08 ]
Artigo de periodico
Sotos syndrome (cerebral gigantism): analysis of 8 cases (2002)
Melo, Débora Gusmão; Acosta, Angelina Xavier; Salles, Maria Aparecida de Almeida; Pina Neto, João Monteiro de; Castro, José Daniel Vieira de; Santos, Antônio Carlos dos
Source: Arquivos de Neuro-Psiquiatria. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, DOENÇAS CEREBRAIS, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Débora Gusmão et al. Sotos syndrome (cerebral gigantism): analysis of 8 cases. Arquivos de Neuro-Psiquiatria, v. 60, n. 2A, p. 234-238, 2002Tradução . . Disponível em: https://doi.org/10.1590/s0004-282x2002000200009. Acesso em: 08 nov. 2024.
APA
Melo, D. G., Acosta, A. X., Salles, M. A. de A., Pina Neto, J. M. de, Castro, J. D. V. de, & Santos, A. C. dos. (2002). Sotos syndrome (cerebral gigantism): analysis of 8 cases. Arquivos de Neuro-Psiquiatria, 60( 2A), 234-238. doi:10.1590/s0004-282x2002000200009
NLM
Melo DG, Acosta AX, Salles MA de A, Pina Neto JM de, Castro JDV de, Santos AC dos. Sotos syndrome (cerebral gigantism): analysis of 8 cases [Internet]. Arquivos de Neuro-Psiquiatria. 2002 ; 60( 2A): 234-238.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s0004-282x2002000200009
Vancouver
Melo DG, Acosta AX, Salles MA de A, Pina Neto JM de, Castro JDV de, Santos AC dos. Sotos syndrome (cerebral gigantism): analysis of 8 cases [Internet]. Arquivos de Neuro-Psiquiatria. 2002 ; 60( 2A): 234-238.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s0004-282x2002000200009
Artigo de periodico
Phenotypic and behavioral variability within Angelman syndrome group with UPD (2002)
Fridman, Cintia; Varela, Monica Castro; Valente, Kette Dualibi Ramos; Marques-Dias, Maria Joaquina; Koiffmann, Celia Priszkulnik
Source: Genetics and Molecular Biology. Unidades: FM, IB
Subjects: GENÉTICA MÉDICA, SÍNDROME DE ANGELMAN, FENÓTIPOS, COMPORTAMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRIDMAN, Cintia et al. Phenotypic and behavioral variability within Angelman syndrome group with UPD. Genetics and Molecular Biology, v. 25, n. 2, p. 127-130, 2002Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572002000200002. Acesso em: 08 nov. 2024.
APA
Fridman, C., Varela, M. C., Valente, K. D. R., Marques-Dias, M. J., & Koiffmann, C. P. (2002). Phenotypic and behavioral variability within Angelman syndrome group with UPD. Genetics and Molecular Biology, 25( 2), 127-130. doi:10.1590/s1415-47572002000200002
NLM
Fridman C, Varela MC, Valente KDR, Marques-Dias MJ, Koiffmann CP. Phenotypic and behavioral variability within Angelman syndrome group with UPD [Internet]. Genetics and Molecular Biology. 2002 ; 25( 2): 127-130.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s1415-47572002000200002
Vancouver
Fridman C, Varela MC, Valente KDR, Marques-Dias MJ, Koiffmann CP. Phenotypic and behavioral variability within Angelman syndrome group with UPD [Internet]. Genetics and Molecular Biology. 2002 ; 25( 2): 127-130.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s1415-47572002000200002
Artigo de periodico
A further case of a Prader-Willi syndrome phenotype in a patient with angelman syndrome molecular defect (2002)
Molfetta, Greice Andreotti de; Félix, Têmis Maria; Riegel, Mariluce; Ferraz, Victor Evangelista de Faria; Pina Neto, João Monteiro de
Source: Arquivos de Neuro-Psiquiatria. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEUROGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOLFETTA, Greice Andreotti de et al. A further case of a Prader-Willi syndrome phenotype in a patient with angelman syndrome molecular defect. Arquivos de Neuro-Psiquiatria, v. 60, n. 4, p. 1011-1014, 2002Tradução . . Disponível em: https://doi.org/10.1590/s0004-282x2002000600024. Acesso em: 08 nov. 2024.
APA
Molfetta, G. A. de, Félix, T. M., Riegel, M., Ferraz, V. E. de F., & Pina Neto, J. M. de. (2002). A further case of a Prader-Willi syndrome phenotype in a patient with angelman syndrome molecular defect. Arquivos de Neuro-Psiquiatria, 60( 4), 1011-1014. doi:10.1590/s0004-282x2002000600024
NLM
Molfetta GA de, Félix TM, Riegel M, Ferraz VE de F, Pina Neto JM de. A further case of a Prader-Willi syndrome phenotype in a patient with angelman syndrome molecular defect [Internet]. Arquivos de Neuro-Psiquiatria. 2002 ; 60( 4): 1011-1014.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s0004-282x2002000600024
Vancouver
Molfetta GA de, Félix TM, Riegel M, Ferraz VE de F, Pina Neto JM de. A further case of a Prader-Willi syndrome phenotype in a patient with angelman syndrome molecular defect [Internet]. Arquivos de Neuro-Psiquiatria. 2002 ; 60( 4): 1011-1014.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s0004-282x2002000600024
Artigo de periodico
Diagnosis of patients with Prader-Willi and Angelman syndromes: the importance of an overall investigation (2002)
Varela, Monica Castro; Fridman, Cintia; Koiffmann, Celia Priszkulnik
Source: Genetics and Molecular Biology. Unidade: IB
Subjects: GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR, SÍNDROME DE ANGELMAN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VARELA, Monica Castro e FRIDMAN, Cintia e KOIFFMANN, Celia Priszkulnik. Diagnosis of patients with Prader-Willi and Angelman syndromes: the importance of an overall investigation. Genetics and Molecular Biology, v. 25, n. 1, p. 7-12, 2002Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572002000100003. Acesso em: 08 nov. 2024.
APA
Varela, M. C., Fridman, C., & Koiffmann, C. P. (2002). Diagnosis of patients with Prader-Willi and Angelman syndromes: the importance of an overall investigation. Genetics and Molecular Biology, 25( 1), 7-12. doi:10.1590/s1415-47572002000100003
NLM
Varela MC, Fridman C, Koiffmann CP. Diagnosis of patients with Prader-Willi and Angelman syndromes: the importance of an overall investigation [Internet]. Genetics and Molecular Biology. 2002 ; 25( 1): 7-12.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s1415-47572002000100003
Vancouver
Varela MC, Fridman C, Koiffmann CP. Diagnosis of patients with Prader-Willi and Angelman syndromes: the importance of an overall investigation [Internet]. Genetics and Molecular Biology. 2002 ; 25( 1): 7-12.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s1415-47572002000100003
Artigo de periodico
Association of the HLA-DRB1*0301 and HLA-DQA1*0501 alleles with graves' disease in a population representing the gene contribution from several ethnic backgrounds (2001)
Maciel, Léa Maria Zanini; Rodrigues, S. S.; Dibbern, R. S.; Navarro, P. A. A.; Donadi, Eduardo Antônio
Source: Thyroid. Unidade: FMRP
Subjects: DOENÇAS DA TIREOIDE, DOENÇAS IMUNOLÓGICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACIEL, Léa Maria Zanini et al. Association of the HLA-DRB1*0301 and HLA-DQA1*0501 alleles with graves' disease in a population representing the gene contribution from several ethnic backgrounds. Thyroid, v. 11, n. 1, p. 31-35, 2001Tradução . . Acesso em: 08 nov. 2024.
APA
Maciel, L. M. Z., Rodrigues, S. S., Dibbern, R. S., Navarro, P. A. A., & Donadi, E. A. (2001). Association of the HLA-DRB1*0301 and HLA-DQA1*0501 alleles with graves' disease in a population representing the gene contribution from several ethnic backgrounds. Thyroid, 11( 1), 31-35.
NLM
Maciel LMZ, Rodrigues SS, Dibbern RS, Navarro PAA, Donadi EA. Association of the HLA-DRB1*0301 and HLA-DQA1*0501 alleles with graves' disease in a population representing the gene contribution from several ethnic backgrounds. Thyroid. 2001 ; 11( 1): 31-35.[citado 2024 nov. 08 ]
Vancouver
Maciel LMZ, Rodrigues SS, Dibbern RS, Navarro PAA, Donadi EA. Association of the HLA-DRB1*0301 and HLA-DQA1*0501 alleles with graves' disease in a population representing the gene contribution from several ethnic backgrounds. Thyroid. 2001 ; 11( 1): 31-35.[citado 2024 nov. 08 ]

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Countries/Territories

Indexado em

Normalized affiliation

Non normalized affiliation