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Artigo de periodico
Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry (2015)
Oliveira-Junior, Edgar Borges de; Zurro, Nuria Bengala; Prando, Carolina; Cabral-Marques, Otavio; Pereira, Paulo Vitor Soeiro; Schimke, Lena-Friederick; Klaver, Stefanie; Buzolin, Marcia; Blancas-Galicia, Lizbeth; Santos-Argumedo, Leopoldo; Pietropaolo-Cienfuegos, Dino Roberto; Espinosa-Rosales, Francisco; King, Alejandra; Sorensen, Ricardo; Porras, Oscar; Roxo Junior, Persio; Forte, Wilma Carvalho Neves; Orellana, Julio Cesar; Lozano, Alejandro; Galicchio, Miguel; Regairaz, Lorena; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Bezrodnik, Liliana; Oleastro, Matias; Danielian, Silvia; Condino Neto, Antonio
Source: Pediatric Blood & Cancer. Unidades: FMRP, ICB
Subjects: GENÉTICA MÉDICA, MUTAÇÃO, INFECÇÕES BACTERIANAS
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, v. 62, n. 12, p. 2101-2107, 2015Tradução . . Disponível em: https://doi.org/10.1002/pbc.25674. Acesso em: 13 nov. 2024.
APA
Oliveira-Junior, E. B. de, Zurro, N. B., Prando, C., Cabral-Marques, O., Pereira, P. V. S., Schimke, L. -F., et al. (2015). Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, 62( 12), 2101-2107. doi:10.1002/pbc.25674
NLM
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/pbc.25674
Vancouver
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/pbc.25674
Artigo de periodico
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity (2008)
Jalali, Ali; Aldinger, Kimberly A.; Chary, Ajit; McLone, David G.; Bowman, Robin M.; Le, Luan Cong; Jardine, Phillip; Newbury-Ecob, Ruth; Mallick, Andrew; Jafari, Nadereh; Russell, Eric J.; Curran, John; Nguyen, Pam; Ouahchi, Karim; Lee, Charles; Dobyns, William B.; Millen, Kathleen J.; Pina Neto, João Monteiro; Kessler, John A.; Bassuk, Alexander G.
Source: Human Genetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
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JALALI, Ali et al. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, v. 123, n. 3, p. 237-245, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00439-008-0467-y. Acesso em: 13 nov. 2024.
APA
Jalali, A., Aldinger, K. A., Chary, A., McLone, D. G., Bowman, R. M., Le, L. C., et al. (2008). Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, 123( 3), 237-245. doi:10.1007/s00439-008-0467-y
NLM
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
Vancouver
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
Artigo de periodico
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil (2008)
Pinto, Giovanny Rebouças; Yoshioka, France Keiko Nascimento; Clara, Carlos Afonso; Santos, Marcelo José dos; Almeida, José Reynaldo Walther de; Burbano, Rommel Rodríguez; Rey, Juan A.; Casartelli, Cacilda
Source: Journal of Neuro-Oncology. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, PROGNÓSTICO, GENÉTICA MÉDICA
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ABNT
PINTO, Giovanny Rebouças et al. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, v. 90, n. 3, p. 253-258, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11060-008-9664-8. Acesso em: 13 nov. 2024.
APA
Pinto, G. R., Yoshioka, F. K. N., Clara, C. A., Santos, M. J. dos, Almeida, J. R. W. de, Burbano, R. R., et al. (2008). WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, 90( 3), 253-258. doi:10.1007/s11060-008-9664-8
NLM
Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Vancouver
Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Artigo de periodico
A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects (2008)
Santos, Silvana Cristina dos; Pardono, Eliete; Costa, Maria Ione Ferreira da; Melo, Áurea Nogueira de; Graciani, Zodja; Souza, Alessandra Cavalcante de Albuquerque e; Lezirovitz, Karina; Thiele-Aguiar, Renata Soares; Mingroni Netto, Regina Celia ; Opitz, John M.; Kok, Fernando; Otto, Paulo A
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
SANTOS, Silvana Cristina dos et al. A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects. American Journal of Medical Genetics. Part A, v. 146A, n. 24, p. 3126-3131, 2008Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32580. Acesso em: 13 nov. 2024.
APA
Santos, S. C. dos, Pardono, E., Costa, M. I. F. da, Melo, Á. N. de, Graciani, Z., Souza, A. C. de A. e, et al. (2008). A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects. American Journal of Medical Genetics. Part A, 146A( 24), 3126-3131. doi:10.1002/ajmg.a.32580
NLM
Santos SC dos, Pardono E, Costa MIF da, Melo ÁN de, Graciani Z, Souza AC de A e, Lezirovitz K, Thiele-Aguiar RS, Mingroni Netto RC, Opitz JM, Kok F, Otto PA. A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 24): 3126-3131.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.32580
Vancouver
Santos SC dos, Pardono E, Costa MIF da, Melo ÁN de, Graciani Z, Souza AC de A e, Lezirovitz K, Thiele-Aguiar RS, Mingroni Netto RC, Opitz JM, Kok F, Otto PA. A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 24): 3126-3131.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.32580
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
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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: 13 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. 13 ] 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. 13 ] Available from: https://doi.org/10.1097/mcd.0b013e3280fa81de
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
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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: 13 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. 13 ] 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. 13 ] 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
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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: 13 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. 13 ]
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. 13 ]
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
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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: 13 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. 13 ] 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. 13 ] Available from: https://doi.org/10.1016/j.leukres.2005.04.022
Artigo de periodico
H19DMR methylation analysis in patients with Beckwith-Wiedemann syndrome and isolated hemihyperplasia (2005)
Gomes, Marcus Vinícius de Matos; Santos, Silvio Avelino dos; Ramos, Ester Silveira
Source: Genetics and Molecular Biology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
GOMES, Marcus Vinícius de Matos e SANTOS, Silvio Avelino dos e RAMOS, Ester Silveira. H19DMR methylation analysis in patients with Beckwith-Wiedemann syndrome and isolated hemihyperplasia. Genetics and Molecular Biology, v. 28, n. 2, p. 210-213, 2005Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572005000200005. Acesso em: 13 nov. 2024.
APA
Gomes, M. V. de M., Santos, S. A. dos, & Ramos, E. S. (2005). H19DMR methylation analysis in patients with Beckwith-Wiedemann syndrome and isolated hemihyperplasia. Genetics and Molecular Biology, 28( 2), 210-213. doi:10.1590/s1415-47572005000200005
NLM
Gomes MV de M, Santos SA dos, Ramos ES. H19DMR methylation analysis in patients with Beckwith-Wiedemann syndrome and isolated hemihyperplasia [Internet]. Genetics and Molecular Biology. 2005 ; 28( 2): 210-213.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/s1415-47572005000200005
Vancouver
Gomes MV de M, Santos SA dos, Ramos ES. H19DMR methylation analysis in patients with Beckwith-Wiedemann syndrome and isolated hemihyperplasia [Internet]. Genetics and Molecular Biology. 2005 ; 28( 2): 210-213.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/s1415-47572005000200005
Artigo de periodico
Association between birth weight, body mass index and IGF2/ApaI polymorphism (2005)
Gomes, M. V. M.; Soares, M. R.; Pasqualim-Neto, Amadeu; Marcondes, C. R.; Lôbo, Raysildo Barbosa; Ramos, Ester Silveira
Source: Growth Hormone and IGF Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, POLIMORFISMO
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ABNT
GOMES, M. V. M. et al. Association between birth weight, body mass index and IGF2/ApaI polymorphism. Growth Hormone and IGF Research, v. 15, p. 360-362, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.ghir.2005.06.016. Acesso em: 13 nov. 2024.
APA
Gomes, M. V. M., Soares, M. R., Pasqualim-Neto, A., Marcondes, C. R., Lôbo, R. B., & Ramos, E. S. (2005). Association between birth weight, body mass index and IGF2/ApaI polymorphism. Growth Hormone and IGF Research, 15, 360-362. doi:10.1016/j.ghir.2005.06.016
NLM
Gomes MVM, Soares MR, Pasqualim-Neto A, Marcondes CR, Lôbo RB, Ramos ES. Association between birth weight, body mass index and IGF2/ApaI polymorphism [Internet]. Growth Hormone and IGF Research. 2005 ; 15 360-362.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ghir.2005.06.016
Vancouver
Gomes MVM, Soares MR, Pasqualim-Neto A, Marcondes CR, Lôbo RB, Ramos ES. Association between birth weight, body mass index and IGF2/ApaI polymorphism [Internet]. Growth Hormone and IGF Research. 2005 ; 15 360-362.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ghir.2005.06.016
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
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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: 13 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. 13 ] 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. 13 ] 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
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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: 13 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. 13 ] 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. 13 ] 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
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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: 13 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. 13 ]
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. 13 ]
Artigo de periodico
Splenopancreatic field abnormality is not unique to trisomy 13 (2004)
Peres, Luiz César; Barbosa, Gustavo Henrique T. de Sales; Careta, Renata Scarpat; Nassif, Cristiane Miziara; Pina Neto, João Monteiro de; Giuliani, Liane R.; Martinhago, Ciro Dresch; Gomy, Israel
Source: Pediatric and Developmental Pathology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERES, Luiz César et al. Splenopancreatic field abnormality is not unique to trisomy 13. Pediatric and Developmental Pathology, v. 7, p. 91-94, 2004Tradução . . Acesso em: 13 nov. 2024.
APA
Peres, L. C., Barbosa, G. H. T. de S., Careta, R. S., Nassif, C. M., Pina Neto, J. M. de, Giuliani, L. R., et al. (2004). Splenopancreatic field abnormality is not unique to trisomy 13. Pediatric and Developmental Pathology, 7, 91-94.
NLM
Peres LC, Barbosa GHT de S, Careta RS, Nassif CM, Pina Neto JM de, Giuliani LR, Martinhago CD, Gomy I. Splenopancreatic field abnormality is not unique to trisomy 13. Pediatric and Developmental Pathology. 2004 ; 7 91-94.[citado 2024 nov. 13 ]
Vancouver
Peres LC, Barbosa GHT de S, Careta RS, Nassif CM, Pina Neto JM de, Giuliani LR, Martinhago CD, Gomy I. Splenopancreatic field abnormality is not unique to trisomy 13. Pediatric and Developmental Pathology. 2004 ; 7 91-94.[citado 2024 nov. 13 ]
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: 13 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. 13 ] 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. 13 ] Available from: https://doi.org/10.1016/j.nmd.2003.07.001
Artigo de periodico
Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor (2004)
Lima, E. M.; Rissino, J. D.; Harada, M. L.; Assumpção, P. P.; Demachki, S.; Guimarães, A. C.; Casartelli, Cacilda; Smith, M. A. C.; Burbano, R. R.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, E. M. et al. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, v. 37, n. 12, p. 1831-1838, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001200008. Acesso em: 13 nov. 2024.
APA
Lima, E. M., Rissino, J. D., Harada, M. L., Assumpção, P. P., Demachki, S., Guimarães, A. C., et al. (2004). Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, 37( 12), 1831-1838. doi:10.1590/s0100-879x2004001200008
NLM
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Vancouver
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Artigo de periodico
Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients (2004)
Brassesco, M. S.; Camparoto, M. L.; Tone, Luiz Gonzaga; Sakamoto-Hojo, Elza Tiemi
Source: Cytogenetic and Genome Research. Unidades: FMRP, FFCLRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRASSESCO, M. S. et al. Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients. Cytogenetic and Genome Research, v. 104, p. 346-351, 2004Tradução . . Disponível em: https://doi.org/10.1159/000077514. Acesso em: 13 nov. 2024.
APA
Brassesco, M. S., Camparoto, M. L., Tone, L. G., & Sakamoto-Hojo, E. T. (2004). Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients. Cytogenetic and Genome Research, 104, 346-351. doi:10.1159/000077514
NLM
Brassesco MS, Camparoto ML, Tone LG, Sakamoto-Hojo ET. Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients [Internet]. Cytogenetic and Genome Research. 2004 ; 104 346-351.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1159/000077514
Vancouver
Brassesco MS, Camparoto ML, Tone LG, Sakamoto-Hojo ET. Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients [Internet]. Cytogenetic and Genome Research. 2004 ; 104 346-351.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1159/000077514
Artigo de periodico
High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC (2004)
Castro, Rosa Maria R. P. S.; Landemberger, Michele C.; Walz, Roger; Carlotti Júnior, Carlos Gilberto; Huang, Nancy; Cunha, Danielle Renzoni da; Moura, Ricardo; Caballero, Otávia L.; Sakamoto, Américo Ceiki; Nitrini, Ricardo; Brentani, Ricardo Renzo; Martins, Vilma Regina
Source: Journal of Neuroscience Methods. Unidades: FMRP, FM
Subjects: GENÉTICA MÉDICA, MUTAÇÃO GENÉTICA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Rosa Maria R. P. S. et al. High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC. Journal of Neuroscience Methods, v. 139, p. 263-269, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.jneumeth.2004.05.001. Acesso em: 13 nov. 2024.
APA
Castro, R. M. R. P. S., Landemberger, M. C., Walz, R., Carlotti Júnior, C. G., Huang, N., Cunha, D. R. da, et al. (2004). High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC. Journal of Neuroscience Methods, 139, 263-269. doi:10.1016/j.jneumeth.2004.05.001
NLM
Castro RMRPS, Landemberger MC, Walz R, Carlotti Júnior CG, Huang N, Cunha DR da, Moura R, Caballero OL, Sakamoto AC, Nitrini R, Brentani RR, Martins VR. High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC [Internet]. Journal of Neuroscience Methods. 2004 ; 139 263-269.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jneumeth.2004.05.001
Vancouver
Castro RMRPS, Landemberger MC, Walz R, Carlotti Júnior CG, Huang N, Cunha DR da, Moura R, Caballero OL, Sakamoto AC, Nitrini R, Brentani RR, Martins VR. High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC [Internet]. Journal of Neuroscience Methods. 2004 ; 139 263-269.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jneumeth.2004.05.001
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: 13 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. 13 ]
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. 13 ]
Artigo de periodico
Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes (2004)
Versiani, Beatriz Ribeiro; Gilbert-Barness, Enid; Giuliani, Liane Rosso; Peres, Luiz César; Pina Neto, João Monteiro de
Source: Clinical Dysmorphology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VERSIANI, Beatriz Ribeiro et al. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes. Clinical Dysmorphology, v. 13, p. 1-5, 2004Tradução . . Disponível em: https://doi.org/10.1097/00019605-200401000-00001. Acesso em: 13 nov. 2024.
APA
Versiani, B. R., Gilbert-Barness, E., Giuliani, L. R., Peres, L. C., & Pina Neto, J. M. de. (2004). Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes. Clinical Dysmorphology, 13, 1-5. doi:10.1097/00019605-200401000-00001
NLM
Versiani BR, Gilbert-Barness E, Giuliani LR, Peres LC, Pina Neto JM de. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes [Internet]. Clinical Dysmorphology. 2004 ; 13 1-5.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1097/00019605-200401000-00001
Vancouver
Versiani BR, Gilbert-Barness E, Giuliani LR, Peres LC, Pina Neto JM de. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes [Internet]. Clinical Dysmorphology. 2004 ; 13 1-5.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1097/00019605-200401000-00001

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