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Artigo de periodico
GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas (2010)
Custódio, Aline Cadurin; Almeida, Luciana Oliveira de; Pinto, Giovanny Rebouças; Santos, Marcelo José dos; Almeida, José Reynaldo Walther de; Clara, Carlos Afonso; Rey, Juan A; Casartelli, Cacilda
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: POLIMORFISMO, GENÉTICA
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ABNT
CUSTÓDIO, Aline Cadurin et al. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, v. 9, n. 4, p. 2328-2334, 2010Tradução . . Acesso em: 05 out. 2024.
APA
Custódio, A. C., Almeida, L. O. de, Pinto, G. R., Santos, M. J. dos, Almeida, J. R. W. de, Clara, C. A., et al. (2010). GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, 9( 4), 2328-2334.
NLM
Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 out. 05 ]
Vancouver
Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 out. 05 ]
Artigo de periodico
A splice variant of the Neurospora crassa hex-1 transcript, which encodes the major protein of the Woronin body, is modulated by extracellular phosphate and pH changes (2009)
Leal, Juliana; Squina, Fábio M.; Freitas, Janaína S.; Silva, Emiliana M.; Ono, Carlos J.; Martinez-Rossi, Nilce Maria; Rossi, Antônio
Source: FEBS Letters. Unidade: FMRP
Assunto: GENÉTICA BIOQUÍMICA
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LEAL, Juliana et al. A splice variant of the Neurospora crassa hex-1 transcript, which encodes the major protein of the Woronin body, is modulated by extracellular phosphate and pH changes. FEBS Letters, v. 583, n. 1, p. 180-184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.febslet.2008.11.050. Acesso em: 05 out. 2024.
APA
Leal, J., Squina, F. M., Freitas, J. S., Silva, E. M., Ono, C. J., Martinez-Rossi, N. M., & Rossi, A. (2009). A splice variant of the Neurospora crassa hex-1 transcript, which encodes the major protein of the Woronin body, is modulated by extracellular phosphate and pH changes. FEBS Letters, 583( 1), 180-184. doi:10.1016/j.febslet.2008.11.050
NLM
Leal J, Squina FM, Freitas JS, Silva EM, Ono CJ, Martinez-Rossi NM, Rossi A. A splice variant of the Neurospora crassa hex-1 transcript, which encodes the major protein of the Woronin body, is modulated by extracellular phosphate and pH changes [Internet]. FEBS Letters. 2009 ; 583( 1): 180-184.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.febslet.2008.11.050
Vancouver
Leal J, Squina FM, Freitas JS, Silva EM, Ono CJ, Martinez-Rossi NM, Rossi A. A splice variant of the Neurospora crassa hex-1 transcript, which encodes the major protein of the Woronin body, is modulated by extracellular phosphate and pH changes [Internet]. FEBS Letters. 2009 ; 583( 1): 180-184.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.febslet.2008.11.050
Artigo de periodico
HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus (2009)
Simões, Renata T.; Gonçalves, Maria Alice G.; Castelli, Erick C.; M. Júnior, Celso; Bettini, Jussara de Sousa Ribeiro; Discorde, Magali L.; Duarte, Geraldo; Quintana, Silvana Maria; Simões, Aguinaldo Luiz; Moreau, Philippe; Carosella, Edgardo D.; Soares, Edson Garcia; Donadi, Eduardo Antônio
Source: Modern Pathology. Unidade: FMRP
Subjects: PAPILLOMAVIRUS, NEOPLASIAS DO COLO UTERINO, POLIMORFISMO
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SIMÕES, Renata T. et al. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus. Modern Pathology, v. 22, n. 8, p. 1075-1082, 2009Tradução . . Disponível em: https://doi.org/10.1038/modpathol.2009.67. Acesso em: 05 out. 2024.
APA
Simões, R. T., Gonçalves, M. A. G., Castelli, E. C., M. Júnior, C., Bettini, J. de S. R., Discorde, M. L., et al. (2009). HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus. Modern Pathology, 22( 8), 1075-1082. doi:10.1038/modpathol.2009.67
NLM
Simões RT, Gonçalves MAG, Castelli EC, M. Júnior C, Bettini J de SR, Discorde ML, Duarte G, Quintana SM, Simões AL, Moreau P, Carosella ED, Soares EG, Donadi EA. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus [Internet]. Modern Pathology. 2009 ; 22( 8): 1075-1082.[citado 2024 out. 05 ] Available from: https://doi.org/10.1038/modpathol.2009.67
Vancouver
Simões RT, Gonçalves MAG, Castelli EC, M. Júnior C, Bettini J de SR, Discorde ML, Duarte G, Quintana SM, Simões AL, Moreau P, Carosella ED, Soares EG, Donadi EA. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus [Internet]. Modern Pathology. 2009 ; 22( 8): 1075-1082.[citado 2024 out. 05 ] Available from: https://doi.org/10.1038/modpathol.2009.67
Artigo de periodico
Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis (2009)
Meola, Juliana; Dentillo, Daniel Blassioli; Rosa e Silva, Júlio César; Ferriani, Rui Alberto; Veiga, Luciana Caricati da Silva; Paz, Cláudia Cristina Paro de; Giuliatti, Silvana; Martelli, Lúcia Regina
Source: Fertility and Sterility. Unidade: FMRP
Subjects: ENDOMETRIOSE, ENDOMÉTRIO, EXPRESSÃO GÊNICA
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MEOLA, Juliana et al. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis. Fertility and Sterility, v. 91, n. 5, p. 1676-1680, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.fertnstert.2008.02.158. Acesso em: 05 out. 2024.
APA
Meola, J., Dentillo, D. B., Rosa e Silva, J. C., Ferriani, R. A., Veiga, L. C. da S., Paz, C. C. P. de, et al. (2009). Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis. Fertility and Sterility, 91( 5), 1676-1680. doi:10.1016/j.fertnstert.2008.02.158
NLM
Meola J, Dentillo DB, Rosa e Silva JC, Ferriani RA, Veiga LC da S, Paz CCP de, Giuliatti S, Martelli LR. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis [Internet]. Fertility and Sterility. 2009 ; 91( 5): 1676-1680.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.fertnstert.2008.02.158
Vancouver
Meola J, Dentillo DB, Rosa e Silva JC, Ferriani RA, Veiga LC da S, Paz CCP de, Giuliatti S, Martelli LR. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis [Internet]. Fertility and Sterility. 2009 ; 91( 5): 1676-1680.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.fertnstert.2008.02.158
Artigo de periodico-carta/editorial
A importância dos estudos genéticos sobre câncer de pulmão.[Editorial] (2009)
Silva Júnior, Wilson Araújo da
Source: Jornal Brasileiro de Pneumologia. Unidade: FMRP
Subjects: NEOPLASIAS PULMONARES, GENÉTICA (ESTUDO)
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SILVA JÚNIOR, Wilson Araújo da. A importância dos estudos genéticos sobre câncer de pulmão.[Editorial]. Jornal Brasileiro de Pneumologia. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/eb996844-8b09-46c6-a4d3-3db497eea663/001782927.pdf. Acesso em: 05 out. 2024. , 2009
APA
Silva Júnior, W. A. da. (2009). A importância dos estudos genéticos sobre câncer de pulmão.[Editorial]. Jornal Brasileiro de Pneumologia. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/eb996844-8b09-46c6-a4d3-3db497eea663/001782927.pdf
NLM
Silva Júnior WA da. A importância dos estudos genéticos sobre câncer de pulmão.[Editorial] [Internet]. Jornal Brasileiro de Pneumologia. 2009 ; 35( 8): 721-722.[citado 2024 out. 05 ] Available from: https://repositorio.usp.br/directbitstream/eb996844-8b09-46c6-a4d3-3db497eea663/001782927.pdf
Vancouver
Silva Júnior WA da. A importância dos estudos genéticos sobre câncer de pulmão.[Editorial] [Internet]. Jornal Brasileiro de Pneumologia. 2009 ; 35( 8): 721-722.[citado 2024 out. 05 ] Available from: https://repositorio.usp.br/directbitstream/eb996844-8b09-46c6-a4d3-3db497eea663/001782927.pdf
Artigo de periodico
Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities (2009)
Rebelo, Camila Carvalho; Furtado, João Marcello Fortes; Honjo, Rachel Sayuri; Veiga, Kledione Falcão; Ramos, Ester Silveira; Ferraz, Victor Evangelista de Faria; Paula, Jayter Silva de
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: DOENÇAS DA CÓRNEA, CRIANÇAS
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ABNT
REBELO, Camila Carvalho et al. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities. Clinical Dysmorphology, v. 18, n. 3, p. 142-144, 2009Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e32831368ff. Acesso em: 05 out. 2024.
APA
Rebelo, C. C., Furtado, J. M. F., Honjo, R. S., Veiga, K. F., Ramos, E. S., Ferraz, V. E. de F., & Paula, J. S. de. (2009). Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities. Clinical Dysmorphology, 18( 3), 142-144. doi:10.1097/mcd.0b013e32831368ff
NLM
Rebelo CC, Furtado JMF, Honjo RS, Veiga KF, Ramos ES, Ferraz VE de F, Paula JS de. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 142-144.[citado 2024 out. 05 ] Available from: https://doi.org/10.1097/mcd.0b013e32831368ff
Vancouver
Rebelo CC, Furtado JMF, Honjo RS, Veiga KF, Ramos ES, Ferraz VE de F, Paula JS de. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 142-144.[citado 2024 out. 05 ] Available from: https://doi.org/10.1097/mcd.0b013e32831368ff
Artigo de periodico
Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies (2009)
Gomes, M. V.; Huber, J.; Ferriani, Rui Alberto; Amaral Neto, A. M.; Ramos, Ester Silveira
Source: Molecular Human Reproduction. Unidade: FMRP
Subjects: REPRODUÇÃO, CRIANÇAS, GENÉTICA
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ABNT
GOMES, M. V. et al. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies. Molecular Human Reproduction, v. 15, n. 8, p. 471-477, 2009Tradução . . Disponível em: https://doi.org/10.1093/molehr/gap038. Acesso em: 05 out. 2024.
APA
Gomes, M. V., Huber, J., Ferriani, R. A., Amaral Neto, A. M., & Ramos, E. S. (2009). Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies. Molecular Human Reproduction, 15( 8), 471-477. doi:10.1093/molehr/gap038
NLM
Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies [Internet]. Molecular Human Reproduction. 2009 ; 15( 8): 471-477.[citado 2024 out. 05 ] Available from: https://doi.org/10.1093/molehr/gap038
Vancouver
Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies [Internet]. Molecular Human Reproduction. 2009 ; 15( 8): 471-477.[citado 2024 out. 05 ] Available from: https://doi.org/10.1093/molehr/gap038
Artigo de periodico
Genomic ancestry in urban Afro-brazilians (2008)
Muniz, Yara Costa Netto; Ferreira, Luzitano Brandão; Mendes-Júnior, Celso Teixeira; Wiezel, Cláudia Emília Vieira; Simões, Aguinaldo Luiz
Source: Annals of Human Biology. Unidade: FMRP
Subjects: HEREDITARIEDADE, AFRODESCENDENTES
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ABNT
MUNIZ, Yara Costa Netto et al. Genomic ancestry in urban Afro-brazilians. Annals of Human Biology, v. 35, n. 1, p. 104-111, 2008Tradução . . Disponível em: https://doi.org/10.1080/03014460701782256. Acesso em: 05 out. 2024.
APA
Muniz, Y. C. N., Ferreira, L. B., Mendes-Júnior, C. T., Wiezel, C. E. V., & Simões, A. L. (2008). Genomic ancestry in urban Afro-brazilians. Annals of Human Biology, 35( 1), 104-111. doi:10.1080/03014460701782256
NLM
Muniz YCN, Ferreira LB, Mendes-Júnior CT, Wiezel CEV, Simões AL. Genomic ancestry in urban Afro-brazilians [Internet]. Annals of Human Biology. 2008 ; 35( 1): 104-111.[citado 2024 out. 05 ] Available from: https://doi.org/10.1080/03014460701782256
Vancouver
Muniz YCN, Ferreira LB, Mendes-Júnior CT, Wiezel CEV, Simões AL. Genomic ancestry in urban Afro-brazilians [Internet]. Annals of Human Biology. 2008 ; 35( 1): 104-111.[citado 2024 out. 05 ] Available from: https://doi.org/10.1080/03014460701782256
Artigo de periodico
Distribution of hemoglobin phenotypes in four different districts of Porto Velho, Rondônia, Brazil (2008)
Andrade-Casseb, A.; Krauze, A.; Lafontaine, R. M.; Tada, M. S.; Silva Júnior, Wilson Araújo da; Simões, Aguinaldo Luiz; Engracia, V.
Source: Human Biology(Detroit): the international journal of population biology. Unidade: FMRP
Subjects: MALÁRIA, FENÓTIPOS
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ANDRADE-CASSEB, A. et al. Distribution of hemoglobin phenotypes in four different districts of Porto Velho, Rondônia, Brazil. Human Biology(Detroit): the international journal of population biology, v. 80, n. 5, p. 573-579, 2008Tradução . . Acesso em: 05 out. 2024.
APA
Andrade-Casseb, A., Krauze, A., Lafontaine, R. M., Tada, M. S., Silva Júnior, W. A. da, Simões, A. L., & Engracia, V. (2008). Distribution of hemoglobin phenotypes in four different districts of Porto Velho, Rondônia, Brazil. Human Biology(Detroit): the international journal of population biology, 80( 5), 573-579.
NLM
Andrade-Casseb A, Krauze A, Lafontaine RM, Tada MS, Silva Júnior WA da, Simões AL, Engracia V. Distribution of hemoglobin phenotypes in four different districts of Porto Velho, Rondônia, Brazil. Human Biology(Detroit): the international journal of population biology. 2008 ; 80( 5): 573-579.[citado 2024 out. 05 ]
Vancouver
Andrade-Casseb A, Krauze A, Lafontaine RM, Tada MS, Silva Júnior WA da, Simões AL, Engracia V. Distribution of hemoglobin phenotypes in four different districts of Porto Velho, Rondônia, Brazil. Human Biology(Detroit): the international journal of population biology. 2008 ; 80( 5): 573-579.[citado 2024 out. 05 ]
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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ABNT
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
Artigo de periodico
Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil (2008)
Soares, Simone Cardoso; Abé-Sandes, Kiyoko; Nascimento Filho, V. B.; Nunes, F. M. F.; Silva Júnior, Wilson Araújo da
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: MALÁRIA, POLIMORFISMO
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ABNT
SOARES, Simone Cardoso et al. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil. Genetics and Molecular Research, v. 7, n. 4, p. 1011-1019, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-4gmr439. Acesso em: 05 out. 2024.
APA
Soares, S. C., Abé-Sandes, K., Nascimento Filho, V. B., Nunes, F. M. F., & Silva Júnior, W. A. da. (2008). Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil. Genetics and Molecular Research, 7( 4), 1011-1019. doi:10.4238/vol7-4gmr439
NLM
Soares SC, Abé-Sandes K, Nascimento Filho VB, Nunes FMF, Silva Júnior WA da. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil [Internet]. Genetics and Molecular Research. 2008 ; 7( 4): 1011-1019.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-4gmr439
Vancouver
Soares SC, Abé-Sandes K, Nascimento Filho VB, Nunes FMF, Silva Júnior WA da. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil [Internet]. Genetics and Molecular Research. 2008 ; 7( 4): 1011-1019.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-4gmr439
Artigo de periodico
Report of a chimeric origin of transposable elements in a bovine-coding gene (2008)
Almeida, L. M.; Amaral, M. E. J.; Silva, I. T.; Silva Júnior, W. A.; Riggs, P. K.; Carareto, C. M.
Source: Genetics and molecular research. Unidade: FMRP
Subjects: BOVINOS, GENOMAS
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ABNT
ALMEIDA, L. M. et al. Report of a chimeric origin of transposable elements in a bovine-coding gene. Genetics and molecular research, v. 7, n. 1, p. 107-116, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-1gmr371. Acesso em: 05 out. 2024.
APA
Almeida, L. M., Amaral, M. E. J., Silva, I. T., Silva Júnior, W. A., Riggs, P. K., & Carareto, C. M. (2008). Report of a chimeric origin of transposable elements in a bovine-coding gene. Genetics and molecular research, 7( 1), 107-116. doi:10.4238/vol7-1gmr371
NLM
Almeida LM, Amaral MEJ, Silva IT, Silva Júnior WA, Riggs PK, Carareto CM. Report of a chimeric origin of transposable elements in a bovine-coding gene [Internet]. Genetics and molecular research. 2008 ; 7( 1): 107-116.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-1gmr371
Vancouver
Almeida LM, Amaral MEJ, Silva IT, Silva Júnior WA, Riggs PK, Carareto CM. Report of a chimeric origin of transposable elements in a bovine-coding gene [Internet]. Genetics and molecular research. 2008 ; 7( 1): 107-116.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-1gmr371
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: 05 out. 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 out. 05 ] 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 out. 05 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Artigo de periodico
Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer (2008)
Lima, E. M.; Leal, M. F.; Burbano, R. R.; Khayat, A. S.; Assumpção, P. P.; Bello, M. J.; Rey, J. A.; Smith, M. A. C.; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, E. M. et al. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, v. 41, n. 6, p. 539-543, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000600017. Acesso em: 05 out. 2024.
APA
Lima, E. M., Leal, M. F., Burbano, R. R., Khayat, A. S., Assumpção, P. P., Bello, M. J., et al. (2008). Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, 41( 6), 539-543. doi:10.1590/s0100-879x2008000600017
NLM
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 out. 05 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Vancouver
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 out. 05 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Artigo de periodico
Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report (2008)
Queiroz, Alexandra Mussolino de; Raffaini, Maria Stella G. Gomes; Camargo, Laura Maria de; Pina Neto, João Monteiro de; Melo, Débora Gusmão; Silva, Raquel Assed Bezerra da
Source: Journal of Dentistry for Children. Unidades: FORP, FMRP
Subjects: ANORMALIDADES CROMOSSÔMICAS, ODONTOLOGIA (TRATAMENTO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUEIROZ, Alexandra Mussolino de et al. Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report. Journal of Dentistry for Children, v. 74, n. 1, p. 67-72, 2008Tradução . . Acesso em: 05 out. 2024.
APA
Queiroz, A. M. de, Raffaini, M. S. G. G., Camargo, L. M. de, Pina Neto, J. M. de, Melo, D. G., & Silva, R. A. B. da. (2008). Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report. Journal of Dentistry for Children, 74( 1), 67-72.
NLM
Queiroz AM de, Raffaini MSGG, Camargo LM de, Pina Neto JM de, Melo DG, Silva RAB da. Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report. Journal of Dentistry for Children. 2008 ; 74( 1): 67-72.[citado 2024 out. 05 ]
Vancouver
Queiroz AM de, Raffaini MSGG, Camargo LM de, Pina Neto JM de, Melo DG, Silva RAB da. Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report. Journal of Dentistry for Children. 2008 ; 74( 1): 67-72.[citado 2024 out. 05 ]
Artigo de periodico
Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects (2008)
Demacq, Caroline; Vasconcellos, Vivian B.; Marcaccini, Andrea M.; Gerlach, Raquel Fernanda; Silva Júnior, Wilson Araújo da; Tanus-Santos, José Eduardo
Source: Clinical Chemistry and Laboratory Medicine. Unidades: FORP, FMRP
Subjects: POLIMORFISMO, METALOPROTEINASES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEMACQ, Caroline et al. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, v. 46, n. 1, p. 57-63, 2008Tradução . . Disponível em: https://doi.org/10.1515/cclm.2008.014. Acesso em: 05 out. 2024.
APA
Demacq, C., Vasconcellos, V. B., Marcaccini, A. M., Gerlach, R. F., Silva Júnior, W. A. da, & Tanus-Santos, J. E. (2008). Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, 46( 1), 57-63. doi:10.1515/cclm.2008.014
NLM
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 out. 05 ] Available from: https://doi.org/10.1515/cclm.2008.014
Vancouver
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 out. 05 ] Available from: https://doi.org/10.1515/cclm.2008.014
Artigo de periodico
SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL (2008)
Proto-Siqueira, Rodrigo; Panepucci, Rodrigo A.; Careta, Francisco P.; Lee, Abigail; Clear, Andrew; Morris, Kelly; Owen, Carolyn; Rizzatti, Edgard G.; Silva Júnior, Wilson Araújo; Falcão, Roberto Passetto; Zago, Marco Antonio; Gribben, John G.
Source: Blood. Unidade: FMRP
Subjects: LEUCEMIA, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PROTO-SIQUEIRA, Rodrigo et al. SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL. Blood, v. 112, n. 2, p. 394-397, 2008Tradução . . Disponível em: https://doi.org/10.1182/blood-2007-11-124065. Acesso em: 05 out. 2024.
APA
Proto-Siqueira, R., Panepucci, R. A., Careta, F. P., Lee, A., Clear, A., Morris, K., et al. (2008). SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL. Blood, 112( 2), 394-397. doi:10.1182/blood-2007-11-124065
NLM
Proto-Siqueira R, Panepucci RA, Careta FP, Lee A, Clear A, Morris K, Owen C, Rizzatti EG, Silva Júnior WA, Falcão RP, Zago MA, Gribben JG. SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL [Internet]. Blood. 2008 ; 112( 2): 394-397.[citado 2024 out. 05 ] Available from: https://doi.org/10.1182/blood-2007-11-124065
Vancouver
Proto-Siqueira R, Panepucci RA, Careta FP, Lee A, Clear A, Morris K, Owen C, Rizzatti EG, Silva Júnior WA, Falcão RP, Zago MA, Gribben JG. SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL [Internet]. Blood. 2008 ; 112( 2): 394-397.[citado 2024 out. 05 ] Available from: https://doi.org/10.1182/blood-2007-11-124065
Artigo de periodico-carta/editorial
A selective clinical cytogenetic study in prenatal and pediatric pathology. [Carta]: a comparison with unselected studies (2008)
Pina Neto, João Monteiro de; Ortolan, Daniela; Bitar, Vanessa S.; Mazzucatto, Luis Fernando; Fernandez, Heloísa H. L.; Peres, Luis César
Source: American Journal of Medical Genetics. Part A. Unidade: FMRP
Subjects: CITOGENÉTICA, PATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINA NETO, João Monteiro de et al. A selective clinical cytogenetic study in prenatal and pediatric pathology. [Carta]: a comparison with unselected studies. American Journal of Medical Genetics. Part A. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 out. 2024. , 2008
APA
Pina Neto, J. M. de, Ortolan, D., Bitar, V. S., Mazzucatto, L. F., Fernandez, H. H. L., & Peres, L. C. (2008). A selective clinical cytogenetic study in prenatal and pediatric pathology. [Carta]: a comparison with unselected studies. American Journal of Medical Genetics. Part A. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Pina Neto JM de, Ortolan D, Bitar VS, Mazzucatto LF, Fernandez HHL, Peres LC. A selective clinical cytogenetic study in prenatal and pediatric pathology. [Carta]: a comparison with unselected studies. American Journal of Medical Genetics. Part A. 2008 ; 146A( 11): 1497-1501.[citado 2024 out. 05 ]
Vancouver
Pina Neto JM de, Ortolan D, Bitar VS, Mazzucatto LF, Fernandez HHL, Peres LC. A selective clinical cytogenetic study in prenatal and pediatric pathology. [Carta]: a comparison with unselected studies. American Journal of Medical Genetics. Part A. 2008 ; 146A( 11): 1497-1501.[citado 2024 out. 05 ]
Artigo de periodico
Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil (2008)
Pinto, G. R.; Yoshioka, F. K. N.; Silva, R. L. L.; Clara, C. A.; Santos, M. J.; Almeida, J. R. W.; Burbano, R. R.; Rey, J. A.; Casartelli, C.
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, G. R. et al. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil. Genetics and Molecular Research, v. 7, n. 1, p. 207-216, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-1gmr415. Acesso em: 05 out. 2024.
APA
Pinto, G. R., Yoshioka, F. K. N., Silva, R. L. L., Clara, C. A., Santos, M. J., Almeida, J. R. W., et al. (2008). Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil. Genetics and Molecular Research, 7( 1), 207-216. doi:10.4238/vol7-1gmr415
NLM
Pinto GR, Yoshioka FKN, Silva RLL, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil [Internet]. Genetics and Molecular Research. 2008 ; 7( 1): 207-216.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-1gmr415
Vancouver
Pinto GR, Yoshioka FKN, Silva RLL, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil [Internet]. Genetics and Molecular Research. 2008 ; 7( 1): 207-216.[citado 2024 out. 05 ] Available from: https://doi.org/10.4238/vol7-1gmr415
Artigo de periodico
eNOS haptolotypes associated with gestational hypertension on preeclampsia (2008)
Sandrim, Valéria C.; Palei, Ana C. T.; Cavalli, Ricardo Carvalho; Araújo, Francielle M.; Ramos, Ester Silveira; Duarte, Geraldo; Tanus-Santos, José Eduardo
Source: Pharmacogenomics. Unidade: FMRP
Subjects: POLIMORFISMO, HIPERTENSÃO NA GRAVIDEZ, PRÉ-ECLÂMPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIM, Valéria C. et al. eNOS haptolotypes associated with gestational hypertension on preeclampsia. Pharmacogenomics, v. 9, n. 10, p. 1467-1473, 2008Tradução . . Disponível em: https://doi.org/10.2217/14622416.9.10.1467. Acesso em: 05 out. 2024.
APA
Sandrim, V. C., Palei, A. C. T., Cavalli, R. C., Araújo, F. M., Ramos, E. S., Duarte, G., & Tanus-Santos, J. E. (2008). eNOS haptolotypes associated with gestational hypertension on preeclampsia. Pharmacogenomics, 9( 10), 1467-1473. doi:10.2217/14622416.9.10.1467
NLM
Sandrim VC, Palei ACT, Cavalli RC, Araújo FM, Ramos ES, Duarte G, Tanus-Santos JE. eNOS haptolotypes associated with gestational hypertension on preeclampsia [Internet]. Pharmacogenomics. 2008 ; 9( 10): 1467-1473.[citado 2024 out. 05 ] Available from: https://doi.org/10.2217/14622416.9.10.1467
Vancouver
Sandrim VC, Palei ACT, Cavalli RC, Araújo FM, Ramos ES, Duarte G, Tanus-Santos JE. eNOS haptolotypes associated with gestational hypertension on preeclampsia [Internet]. Pharmacogenomics. 2008 ; 9( 10): 1467-1473.[citado 2024 out. 05 ] Available from: https://doi.org/10.2217/14622416.9.10.1467

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