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Artigo de periodico
Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer's disease pathology: a population-based autopsy study in an admixed sample (2023)
Paradela, Regina Silva; Justo, Alberto Fernando Oliveira; Paes, Vitor Ribeiro; Leite, Renata E. P.; Pasqualucci, Carlos Augusto ; Grinberg, Lea T.; Naslavsky, Michel Satya; Zatz, Mayana; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: ACTA NEUROPATHOLOGICA COMMUNICATIONS. Unidade: FM
Subjects: ALELOS, GENES, DOENÇA DE ALZHEIMER, DEMÊNCIA
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ABNT
PARADELA, Regina Silva et al. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer's disease pathology: a population-based autopsy study in an admixed sample. ACTA NEUROPATHOLOGICA COMMUNICATIONS, v. 11, n. 1, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58031. Acesso em: 15 nov. 2024.
APA
Paradela, R. S., Justo, A. F. O., Paes, V. R., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., et al. (2023). Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer's disease pathology: a population-based autopsy study in an admixed sample. ACTA NEUROPATHOLOGICA COMMUNICATIONS, 11( 1). doi:10.1186/s40478-023-01681-z
NLM
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer's disease pathology: a population-based autopsy study in an admixed sample [Internet]. ACTA NEUROPATHOLOGICA COMMUNICATIONS. 2023 ; 11( 1):[citado 2024 nov. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58031
Vancouver
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer's disease pathology: a population-based autopsy study in an admixed sample [Internet]. ACTA NEUROPATHOLOGICA COMMUNICATIONS. 2023 ; 11( 1):[citado 2024 nov. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58031
Artigo de periodico
CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems (2021)
Alkhnbashi, Omer S ; Mitrofanov, Alexander; Bonidia, Robson Parmezan ; Raden, Martin ; Tran, Van Dinh ; Eggenhofer, Florian ; Shah, Shiraz A ; Ozturk, Ekrem; Padilha, Victor Alexandre ; Sanches, Danilo Sipoli ; Carvalho, André Carlos Ponce de Leon Ferreira de ; Backofen, Rolf
Source: Nucleic Acids Research. Unidade: ICMC
Subjects: APRENDIZADO COMPUTACIONAL, BIOINFORMÁTICA, GENES
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ABNT
ALKHNBASHI, Omer S et al. CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems. Nucleic Acids Research, v. 49, p. w125-w130, 2021Tradução . . Disponível em: https://doi.org/10.1093/nar/gkab456. Acesso em: 15 nov. 2024.
APA
Alkhnbashi, O. S., Mitrofanov, A., Bonidia, R. P., Raden, M., Tran, V. D., Eggenhofer, F., et al. (2021). CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems. Nucleic Acids Research, 49, w125-w130. doi:10.1093/nar/gkab456
NLM
Alkhnbashi OS, Mitrofanov A, Bonidia RP, Raden M, Tran VD, Eggenhofer F, Shah SA, Ozturk E, Padilha VA, Sanches DS, Carvalho ACP de LF de, Backofen R. CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems [Internet]. Nucleic Acids Research. 2021 ; 49 w125-w130.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/nar/gkab456
Vancouver
Alkhnbashi OS, Mitrofanov A, Bonidia RP, Raden M, Tran VD, Eggenhofer F, Shah SA, Ozturk E, Padilha VA, Sanches DS, Carvalho ACP de LF de, Backofen R. CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems [Internet]. Nucleic Acids Research. 2021 ; 49 w125-w130.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/nar/gkab456
Artigo de periodico
Casboundary: automated definition of integral Cas cassettes (2021)
Padilha, Victor Alexandre ; Alkhnbashi, Omer S ; Tran, Van Dinh ; Shah, Shiraz A ; Carvalho, André Carlos Ponce de Leon Ferreira de ; Backofen, Rolf
Source: Bioinformatics. Unidade: ICMC
Subjects: BIOINFORMÁTICA, APRENDIZADO COMPUTACIONAL, GENES
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ABNT
PADILHA, Victor Alexandre et al. Casboundary: automated definition of integral Cas cassettes. Bioinformatics, v. 37, n. 10, p. 1352-1359, 2021Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btaa984. Acesso em: 15 nov. 2024.
APA
Padilha, V. A., Alkhnbashi, O. S., Tran, V. D., Shah, S. A., Carvalho, A. C. P. de L. F. de, & Backofen, R. (2021). Casboundary: automated definition of integral Cas cassettes. Bioinformatics, 37( 10), 1352-1359. doi:10.1093/bioinformatics/btaa984
NLM
Padilha VA, Alkhnbashi OS, Tran VD, Shah SA, Carvalho ACP de LF de, Backofen R. Casboundary: automated definition of integral Cas cassettes [Internet]. Bioinformatics. 2021 ; 37( 10): 1352-1359.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/bioinformatics/btaa984
Vancouver
Padilha VA, Alkhnbashi OS, Tran VD, Shah SA, Carvalho ACP de LF de, Backofen R. Casboundary: automated definition of integral Cas cassettes [Internet]. Bioinformatics. 2021 ; 37( 10): 1352-1359.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/bioinformatics/btaa984
Artigo de periodico
Higher rate of rheumatic manifestations and delay in diagnosis in Brazilian Fabry disease patients (2020)
Rosa Neto, Nilton Salles; Bento, Judith Campos de Barros; Pereira, Rosa Maria Rodrigues
Source: Advances in rheumatology. Unidade: FM
Subjects: REUMATOLOGIA, FENÓTIPOS, GENES, MUTAÇÃO
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ABNT
ROSA NETO, Nilton Salles e BENTO, Judith Campos de Barros e PEREIRA, Rosa Maria Rodrigues. Higher rate of rheumatic manifestations and delay in diagnosis in Brazilian Fabry disease patients. Advances in rheumatology, v. 60, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1186/s42358-019-0111-7. Acesso em: 15 nov. 2024.
APA
Rosa Neto, N. S., Bento, J. C. de B., & Pereira, R. M. R. (2020). Higher rate of rheumatic manifestations and delay in diagnosis in Brazilian Fabry disease patients. Advances in rheumatology, 60( 1). doi:10.1186/s42358-019-0111-7
NLM
Rosa Neto NS, Bento JC de B, Pereira RMR. Higher rate of rheumatic manifestations and delay in diagnosis in Brazilian Fabry disease patients [Internet]. Advances in rheumatology. 2020 ; 60( 1):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s42358-019-0111-7
Vancouver
Rosa Neto NS, Bento JC de B, Pereira RMR. Higher rate of rheumatic manifestations and delay in diagnosis in Brazilian Fabry disease patients [Internet]. Advances in rheumatology. 2020 ; 60( 1):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s42358-019-0111-7
Artigo de periodico
The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohort (2020)
Fernandes, A. M; Rocha-Braz, M. G. M; Franca, M. M; Lerario, A. M; Simoes, V. R. F; Zanardo, E. A; Kulikowski, L. D; Martin, R. M; Mendonca, Berenice Bilharinho de ; Ferraz-de-Souza, B
Source: Osteoporosis international. Unidade: FM
Subjects: COLÁGENO, GENES, OSTEOGÊNESE IMPERFEITA, DIAGNÓSTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, A. M et al. The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohort. Osteoporosis international, v. 31, n. 7, p. 1341-1352, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00198-020-05366-4. Acesso em: 15 nov. 2024.
APA
Fernandes, A. M., Rocha-Braz, M. G. M., Franca, M. M., Lerario, A. M., Simoes, V. R. F., Zanardo, E. A., et al. (2020). The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohort. Osteoporosis international, 31( 7), 1341-1352. doi:10.1007/s00198-020-05366-4
NLM
Fernandes AM, Rocha-Braz MGM, Franca MM, Lerario AM, Simoes VRF, Zanardo EA, Kulikowski LD, Martin RM, Mendonca BB de, Ferraz-de-Souza B. The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohort [Internet]. Osteoporosis international. 2020 ; 31( 7): 1341-1352.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00198-020-05366-4
Vancouver
Fernandes AM, Rocha-Braz MGM, Franca MM, Lerario AM, Simoes VRF, Zanardo EA, Kulikowski LD, Martin RM, Mendonca BB de, Ferraz-de-Souza B. The molecular landscape of osteogenesis imperfecta in a Brazilian tertiary service cohort [Internet]. Osteoporosis international. 2020 ; 31( 7): 1341-1352.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00198-020-05366-4
Artigo de periodico
CRISPRcasIdentifier: machine learning for accurate identification and classification of CRISPR-Cas systems (2020)
Padilha, Victor Alexandre ; Alkhnbashi, Omer S ; Shah, Shiraz A ; Carvalho, André Carlos Ponce de Leon Ferreira de ; Backofen, Rolf
Source: GigaScience. Unidade: ICMC
Subjects: APRENDIZADO COMPUTACIONAL, BIOINFORMÁTICA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PADILHA, Victor Alexandre et al. CRISPRcasIdentifier: machine learning for accurate identification and classification of CRISPR-Cas systems. GigaScience, v. 9, n. 6, p. 1-12, 2020Tradução . . Disponível em: https://doi.org/10.1093/gigascience/giaa062. Acesso em: 15 nov. 2024.
APA
Padilha, V. A., Alkhnbashi, O. S., Shah, S. A., Carvalho, A. C. P. de L. F. de, & Backofen, R. (2020). CRISPRcasIdentifier: machine learning for accurate identification and classification of CRISPR-Cas systems. GigaScience, 9( 6), 1-12. doi:10.1093/gigascience/giaa062
NLM
Padilha VA, Alkhnbashi OS, Shah SA, Carvalho ACP de LF de, Backofen R. CRISPRcasIdentifier: machine learning for accurate identification and classification of CRISPR-Cas systems [Internet]. GigaScience. 2020 ; 9( 6): 1-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/gigascience/giaa062
Vancouver
Padilha VA, Alkhnbashi OS, Shah SA, Carvalho ACP de LF de, Backofen R. CRISPRcasIdentifier: machine learning for accurate identification and classification of CRISPR-Cas systems [Internet]. GigaScience. 2020 ; 9( 6): 1-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/gigascience/giaa062
Artigo de periodico
Molecular targeting of PD-1 signaling pathway as a novel therapeutic approach in HTLV-1 infection (2020)
Keikha, Masoud; Ghazvini, Kiarash; Eslami, Majid; Yousefi, Bahman; Casseb, Jorge Simão do Rosário ; Yousefi, Masoud; Karbalaei, Mohsen
Source: Microbial pathogenesis. Unidade: FM
Subjects: ARTRITE, DERMATITE, GENES, LINFOMA, SÍNDROME DE SJOGREN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KEIKHA, Masoud et al. Molecular targeting of PD-1 signaling pathway as a novel therapeutic approach in HTLV-1 infection. Microbial pathogenesis, v. 144, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2020.104198. Acesso em: 15 nov. 2024.
APA
Keikha, M., Ghazvini, K., Eslami, M., Yousefi, B., Casseb, J. S. do R., Yousefi, M., & Karbalaei, M. (2020). Molecular targeting of PD-1 signaling pathway as a novel therapeutic approach in HTLV-1 infection. Microbial pathogenesis, 144. doi:10.1016/j.micpath.2020.104198
NLM
Keikha M, Ghazvini K, Eslami M, Yousefi B, Casseb JS do R, Yousefi M, Karbalaei M. Molecular targeting of PD-1 signaling pathway as a novel therapeutic approach in HTLV-1 infection [Internet]. Microbial pathogenesis. 2020 ; 144[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.micpath.2020.104198
Vancouver
Keikha M, Ghazvini K, Eslami M, Yousefi B, Casseb JS do R, Yousefi M, Karbalaei M. Molecular targeting of PD-1 signaling pathway as a novel therapeutic approach in HTLV-1 infection [Internet]. Microbial pathogenesis. 2020 ; 144[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.micpath.2020.104198
Artigo de periodico
Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes (2020)
Araújo, Thaís Fenz; Friedrich, Corinna; Grangeiro, Carlos Henrique Paiva; Martelli, Lúcia Regina; Grzesiuk, Juliana Dourado; Emich, Jana; Wyrwoll, Margot Julia; Kliesch, Sabine; Simões, Aguinaldo Luiz; Tüttelmann, Frank
Source: Andrology. Unidade: FMRP
Subjects: INFERTILIDADE MASCULINA, GENES, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, GENÉTICA
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ABNT
ARAÚJO, Thaís Fenz et al. Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes. Andrology, v. 8, n. 2, p. 434-441, 2020Tradução . . Disponível em: https://doi.org/10.1111/andr.12704. Acesso em: 15 nov. 2024.
APA
Araújo, T. F., Friedrich, C., Grangeiro, C. H. P., Martelli, L. R., Grzesiuk, J. D., Emich, J., et al. (2020). Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes. Andrology, 8( 2), 434-441. doi:10.1111/andr.12704
NLM
Araújo TF, Friedrich C, Grangeiro CHP, Martelli LR, Grzesiuk JD, Emich J, Wyrwoll MJ, Kliesch S, Simões AL, Tüttelmann F. Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes [Internet]. Andrology. 2020 ; 8( 2): 434-441.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/andr.12704
Vancouver
Araújo TF, Friedrich C, Grangeiro CHP, Martelli LR, Grzesiuk JD, Emich J, Wyrwoll MJ, Kliesch S, Simões AL, Tüttelmann F. Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes [Internet]. Andrology. 2020 ; 8( 2): 434-441.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/andr.12704
Artigo de periodico
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 (2020)
Lezirovitz, Karina; Vieira-silva, Gleiciele A; Batissoco, Ana C; Levy, Debora; Kitajima, Joao P; Trouillet, Alix; Ouyang, Ellen; Zebarjadi, Navid; Sampaio-Silva, Juliana; Bento, Ricardo Ferreira
Source: Human molecular genetics. Unidade: FM
Subjects: GENES, PERDA AUDITIVA, SURDEZ, NEURÔNIOS
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ABNT
LEZIROVITZ, Karina et al. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, v. 29, n. 9, p. 1520-1536, 2020Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddaa075. Acesso em: 15 nov. 2024.
APA
Lezirovitz, K., Vieira-silva, G. A., Batissoco, A. C., Levy, D., Kitajima, J. P., Trouillet, A., et al. (2020). A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, 29( 9), 1520-1536. doi:10.1093/hmg/ddaa075
NLM
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/hmg/ddaa075
Vancouver
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/hmg/ddaa075
Artigo de periodico
Molecular phylogeny of subgenus (Diptera: Culicidae) based on nuclear and mitochondrial protein-coding genes (2018)
Torres-Gutierrez, Carolina; Oliveira, Tatiane M. P. de; Emerson, Kevin J; Bergo, Eduardo Sterlino; Sallum, Maria Anice Mureb
Source: Royal Society Open Science. Unidade: FSP
Subjects: DIPTERA, CULICIDAE, FILOGENIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TORRES-GUTIERREZ, Carolina et al. Molecular phylogeny of subgenus (Diptera: Culicidae) based on nuclear and mitochondrial protein-coding genes. Royal Society Open Science, v. 5, n. 5, p. [14], 2018Tradução . . Disponível em: https://doi.org/10.1098/rsos.171900. Acesso em: 15 nov. 2024.
APA
Torres-Gutierrez, C., Oliveira, T. M. P. de, Emerson, K. J., Bergo, E. S., & Sallum, M. A. M. (2018). Molecular phylogeny of subgenus (Diptera: Culicidae) based on nuclear and mitochondrial protein-coding genes. Royal Society Open Science, 5( 5), [14]. doi:10.1098/rsos.171900
NLM
Torres-Gutierrez C, Oliveira TMP de, Emerson KJ, Bergo ES, Sallum MAM. Molecular phylogeny of subgenus (Diptera: Culicidae) based on nuclear and mitochondrial protein-coding genes [Internet]. Royal Society Open Science. 2018 ;5( 5): [14].[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rsos.171900
Vancouver
Torres-Gutierrez C, Oliveira TMP de, Emerson KJ, Bergo ES, Sallum MAM. Molecular phylogeny of subgenus (Diptera: Culicidae) based on nuclear and mitochondrial protein-coding genes [Internet]. Royal Society Open Science. 2018 ;5( 5): [14].[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rsos.171900
Artigo de periodico
Unexpected links reflect the noise in networks (2016)
Iambartsev, Anatoli; Perlin, Michael A.; Kovchegov, Yevgeniy; Shulzhenko, Natalia; Mine, Karina L.; Dong, Xiaoxi; Morgun, Andrey
Source: Biology Direct. Unidade: IME
Subjects: GENES, VARIAÇÃO GENÉTICA, GENÉTICA ESTATÍSTICA
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ABNT
IAMBARTSEV, Anatoli et al. Unexpected links reflect the noise in networks. Biology Direct, v. 11, n. 1, p. 1-12, 2016Tradução . . Disponível em: https://doi.org/10.1186/s13062-016-0155-0. Acesso em: 15 nov. 2024.
APA
Iambartsev, A., Perlin, M. A., Kovchegov, Y., Shulzhenko, N., Mine, K. L., Dong, X., & Morgun, A. (2016). Unexpected links reflect the noise in networks. Biology Direct, 11( 1), 1-12. doi:10.1186/s13062-016-0155-0
NLM
Iambartsev A, Perlin MA, Kovchegov Y, Shulzhenko N, Mine KL, Dong X, Morgun A. Unexpected links reflect the noise in networks [Internet]. Biology Direct. 2016 ; 11( 1): 1-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s13062-016-0155-0
Vancouver
Iambartsev A, Perlin MA, Kovchegov Y, Shulzhenko N, Mine KL, Dong X, Morgun A. Unexpected links reflect the noise in networks [Internet]. Biology Direct. 2016 ; 11( 1): 1-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s13062-016-0155-0
Artigo de periodico
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect (2015)
Tavares, Vanessa Luiza Romanelli ; Gordon, Christopher T; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Voisin, Norine; Tan, Tiong Y; Heggie, Andrew A; Pittoli, Siulan Vendramini Paulovich ; Propst, Evan J; Papsin, Blake C; Torres, Tatiana Teixeira ; Buermans, Henk; Capelo, Luciane Portas; Den Dunnen, Johan T; Guion-Almeida, Maria Leine; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS, GENES
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ABNT
TAVARES, Vanessa Luiza Romanelli et al. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, v. 23, n. 4, p. 481-485, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.132. Acesso em: 15 nov. 2024.
APA
Tavares, V. L. R., Gordon, C. T., Zechi-Ceide, R. M., Nakata, N. M. K., Voisin, N., Tan, T. Y., et al. (2015). Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, 23( 4), 481-485. doi:10.1038/ejhg.2014.132
NLM
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Vancouver
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Artigo de periodico-carta/editorial
SLC2A4gene: a promising target for pharmacogenomics of insulin resistance [Editorial] (2013)
Corrêa-Giannella, Maria Lucia; Machado, Ubiratan Fabres
Source: Pharmacogenomics. Unidades: FM, ICB
Subjects: INSULINA (RESISTÊNCIA), DIABETES MELLITUS, FARMACOLOGIA CLÍNICA, GENES
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ABNT
CORRÊA-GIANNELLA, Maria Lucia e MACHADO, Ubiratan Fabres. SLC2A4gene: a promising target for pharmacogenomics of insulin resistance [Editorial]. Pharmacogenomics. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://www.futuremedicine.com/doi/pdf/10.2217/pgs.13.45. Acesso em: 15 nov. 2024. , 2013
APA
Corrêa-Giannella, M. L., & Machado, U. F. (2013). SLC2A4gene: a promising target for pharmacogenomics of insulin resistance [Editorial]. Pharmacogenomics. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.2217/pgs.10.93
NLM
Corrêa-Giannella ML, Machado UF. SLC2A4gene: a promising target for pharmacogenomics of insulin resistance [Editorial] [Internet]. Pharmacogenomics. 2013 ; 14( 8): 847-850.[citado 2024 nov. 15 ] Available from: http://www.futuremedicine.com/doi/pdf/10.2217/pgs.13.45
Vancouver
Corrêa-Giannella ML, Machado UF. SLC2A4gene: a promising target for pharmacogenomics of insulin resistance [Editorial] [Internet]. Pharmacogenomics. 2013 ; 14( 8): 847-850.[citado 2024 nov. 15 ] Available from: http://www.futuremedicine.com/doi/pdf/10.2217/pgs.13.45
Artigo de periodico
Expression of Clock Genes in Human Subcutaneous and Visceral Adipose Tissues (2012)
Zanquetta, Melissa Moreira; Correa-Giannella, Maria Lúcia; Giannella-Neto, Daniel; Alonso, Paulino Alberto; Guimarães, Ligia Maria Martins Vaz; Meyer, Alberto; Villares, Sandra Mara Ferreira
Source: Chronobiology International. Unidade: FM
Subjects: EXPRESSÃO GÊNICA, GENES, ÍNDICE DE MASSA CORPORAL, TECIDO ADIPOSO, VÍSCERAS, TECIDO CONJUNTIVO SUBCUTÂNEO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANQUETTA, Melissa Moreira et al. Expression of Clock Genes in Human Subcutaneous and Visceral Adipose Tissues. Chronobiology International, v. 29, n. 3, p. 252-260, 2012Tradução . . Disponível em: http://informahealthcare.com/doi/pdf/10.3109/07420528.2012.657319. Acesso em: 15 nov. 2024.
APA
Zanquetta, M. M., Correa-Giannella, M. L., Giannella-Neto, D., Alonso, P. A., Guimarães, L. M. M. V., Meyer, A., & Villares, S. M. F. (2012). Expression of Clock Genes in Human Subcutaneous and Visceral Adipose Tissues. Chronobiology International, 29( 3), 252-260. doi:10.3109/07420528.2012.657319
NLM
Zanquetta MM, Correa-Giannella ML, Giannella-Neto D, Alonso PA, Guimarães LMMV, Meyer A, Villares SMF. Expression of Clock Genes in Human Subcutaneous and Visceral Adipose Tissues [Internet]. Chronobiology International. 2012 ; 29( 3): 252-260.[citado 2024 nov. 15 ] Available from: http://informahealthcare.com/doi/pdf/10.3109/07420528.2012.657319
Vancouver
Zanquetta MM, Correa-Giannella ML, Giannella-Neto D, Alonso PA, Guimarães LMMV, Meyer A, Villares SMF. Expression of Clock Genes in Human Subcutaneous and Visceral Adipose Tissues [Internet]. Chronobiology International. 2012 ; 29( 3): 252-260.[citado 2024 nov. 15 ] Available from: http://informahealthcare.com/doi/pdf/10.3109/07420528.2012.657319
Artigo de periodico
Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study (2012)
Kawai, Sayo; Oba-Shinjo, Sueli M.; Ito, Lucy S.; Uno, Miyuki; Marie, Suely K. N.; Hamajima, Nobuyuki
Source: BMC Clinical Pathology. Unidade: FM
Subjects: CRIANÇAS (CRESCIMENTO E DESENVOLVIMENTO), POLIMORFISMO, BIOMARCADORES, GENÓTIPOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAWAI, Sayo et al. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study. BMC Clinical Pathology, v. 12, n. 23, p. (online), 2012Tradução . . Disponível em: https://doi.org/10.1186/1472-6890-12-23. Acesso em: 15 nov. 2024.
APA
Kawai, S., Oba-Shinjo, S. M., Ito, L. S., Uno, M., Marie, S. K. N., & Hamajima, N. (2012). Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study. BMC Clinical Pathology, 12( 23), (online). doi:10.1186/1472-6890-12-23
NLM
Kawai S, Oba-Shinjo SM, Ito LS, Uno M, Marie SKN, Hamajima N. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study [Internet]. BMC Clinical Pathology. 2012 ; 12( 23): (online).[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6890-12-23
Vancouver
Kawai S, Oba-Shinjo SM, Ito LS, Uno M, Marie SKN, Hamajima N. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study [Internet]. BMC Clinical Pathology. 2012 ; 12( 23): (online).[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6890-12-23
Artigo de periodico-carta/editorial
Survivin expression patterns could reflect different roles in hepatocarcinogenesis, especially in non-alcoholic fatty liver disease-related hepatocellular carcinoma [Carta] (2011)
Stefano, José T.; Oliveira, Claudia P.; Carrilho, Flair J.; Alves, Venâncio A. F.
Source: Liver International. Unidade: FM
Subjects: NEOPLASIAS HEPÁTICAS, FÍGADO GORDUROSO, GENES, CIRROSE HEPÁTICA, CARCINOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANO, José T. et al. Survivin expression patterns could reflect different roles in hepatocarcinogenesis, especially in non-alcoholic fatty liver disease-related hepatocellular carcinoma [Carta]. Liver International. Oxford: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/j.1478-3231.2011.02567.x/pdf. Acesso em: 15 nov. 2024. , 2011
APA
Stefano, J. T., Oliveira, C. P., Carrilho, F. J., & Alves, V. A. F. (2011). Survivin expression patterns could reflect different roles in hepatocarcinogenesis, especially in non-alcoholic fatty liver disease-related hepatocellular carcinoma [Carta]. Liver International. Oxford: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/j.1478-3231.2011.02567.x/pdf
NLM
Stefano JT, Oliveira CP, Carrilho FJ, Alves VAF. Survivin expression patterns could reflect different roles in hepatocarcinogenesis, especially in non-alcoholic fatty liver disease-related hepatocellular carcinoma [Carta] [Internet]. Liver International. 2011 ; 31( 9): 1417.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1478-3231.2011.02567.x/pdf
Vancouver
Stefano JT, Oliveira CP, Carrilho FJ, Alves VAF. Survivin expression patterns could reflect different roles in hepatocarcinogenesis, especially in non-alcoholic fatty liver disease-related hepatocellular carcinoma [Carta] [Internet]. Liver International. 2011 ; 31( 9): 1417.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1478-3231.2011.02567.x/pdf
Artigo de periodico
Polymorphisms in alcohol metabolizing genes and the risk of head and neck cancer in a brazilian population (2010)
Garcia, Silvia Marçal Nunes; Curion, Otávio A; Carvalho, Marcos Brasilino de; Gattás, Gilka Jorge Fígaro
Source: Alcohol and alcoholism. Unidade: FM
Subjects: POLIMORFISMO, ÁLCOOL (METABOLISMO), GENES, NEOPLASIAS DE CABEÇA E PESCOÇO (GENÉTICA), POPULAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARCIA, Silvia Marçal Nunes et al. Polymorphisms in alcohol metabolizing genes and the risk of head and neck cancer in a brazilian population. Alcohol and alcoholism, v. 45, n. 1, p. 6-12, 2010Tradução . . Disponível em: http://alcalc.oxfordjournals.org/cgi/reprint/45/1/6. Acesso em: 15 nov. 2024.
APA
Garcia, S. M. N., Curion, O. A., Carvalho, M. B. de, & Gattás, G. J. F. (2010). Polymorphisms in alcohol metabolizing genes and the risk of head and neck cancer in a brazilian population. Alcohol and alcoholism, 45( 1), 6-12. Recuperado de http://alcalc.oxfordjournals.org/cgi/reprint/45/1/6
NLM
Garcia SMN, Curion OA, Carvalho MB de, Gattás GJF. Polymorphisms in alcohol metabolizing genes and the risk of head and neck cancer in a brazilian population [Internet]. Alcohol and alcoholism. 2010 ; 45( 1): 6-12.[citado 2024 nov. 15 ] Available from: http://alcalc.oxfordjournals.org/cgi/reprint/45/1/6
Vancouver
Garcia SMN, Curion OA, Carvalho MB de, Gattás GJF. Polymorphisms in alcohol metabolizing genes and the risk of head and neck cancer in a brazilian population [Internet]. Alcohol and alcoholism. 2010 ; 45( 1): 6-12.[citado 2024 nov. 15 ] Available from: http://alcalc.oxfordjournals.org/cgi/reprint/45/1/6
Artigo de periodico
Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure (2009)
Freitas, S. R.; ; Floriano, M. S.; Mill, J. G.; Krieger, José Eduardo
Source: Journal of human hypertension. Unidade: FM
Subjects: POLIMORFISMO, PRESSÃO SANGUÍNEA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, S. R. et al. Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure. Journal of human hypertension, v. 23, n. 8, p. 553-555, 2009Tradução . . Disponível em: https://doi.org/10.1038/jhh.2009.23. Acesso em: 15 nov. 2024.
APA
Freitas, S. R., ,, Floriano, M. S., Mill, J. G., & Krieger, J. E. (2009). Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure. Journal of human hypertension, 23( 8), 553-555. doi:10.1038/jhh.2009.23
NLM
Freitas SR, , Floriano MS, Mill JG, Krieger JE. Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure [Internet]. Journal of human hypertension. 2009 ; 23( 8): 553-555.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/jhh.2009.23
Vancouver
Freitas SR, , Floriano MS, Mill JG, Krieger JE. Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure [Internet]. Journal of human hypertension. 2009 ; 23( 8): 553-555.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/jhh.2009.23
Artigo de periodico
Structural basis of GC-I selectivity for thyroid hormone receptor isoforms (2008)
Bleicher, Lucas; Aparicio, Ricardo; Nunes, Fábio M.; Martinez, Leandro; Dias, Sandra M. Gomes; Figueira, Ana Carolina Migliorini; Santos, Maria Auxiliadora Morim; Venturelli, Walter H.; Silva, Rosangela da; Donate, Paulo Marcos; Neves, Francisco A. R.; Simeoni, Luiz A.; Baxter, John D.; Webb, Paul; Skaf, Munir S.; Polikarpov, Igor
Source: BMC Structural Biology. Unidades: IFSC, FFCLRP
Subjects: MOLÉCULA (SIMULAÇÃO), DIFRAÇÃO POR RAIOS X, HORMÔNIOS TIREOIDIANOS, GENES, RECEPTORES HORMONAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BLEICHER, Lucas et al. Structural basis of GC-I selectivity for thyroid hormone receptor isoforms. BMC Structural Biology, v. 8, n. Ja 2008, p. 1-13, 2008Tradução . . Disponível em: https://doi.org/10.1186/1472-6807-8-8. Acesso em: 15 nov. 2024.
APA
Bleicher, L., Aparicio, R., Nunes, F. M., Martinez, L., Dias, S. M. G., Figueira, A. C. M., et al. (2008). Structural basis of GC-I selectivity for thyroid hormone receptor isoforms. BMC Structural Biology, 8( Ja 2008), 1-13. doi:10.1186/1472-6807-8-8
NLM
Bleicher L, Aparicio R, Nunes FM, Martinez L, Dias SMG, Figueira ACM, Santos MAM, Venturelli WH, Silva R da, Donate PM, Neves FAR, Simeoni LA, Baxter JD, Webb P, Skaf MS, Polikarpov I. Structural basis of GC-I selectivity for thyroid hormone receptor isoforms [Internet]. BMC Structural Biology. 2008 ; 8( Ja 2008): 1-13.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6807-8-8
Vancouver
Bleicher L, Aparicio R, Nunes FM, Martinez L, Dias SMG, Figueira ACM, Santos MAM, Venturelli WH, Silva R da, Donate PM, Neves FAR, Simeoni LA, Baxter JD, Webb P, Skaf MS, Polikarpov I. Structural basis of GC-I selectivity for thyroid hormone receptor isoforms [Internet]. BMC Structural Biology. 2008 ; 8( Ja 2008): 1-13.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6807-8-8
Artigo de periodico
Nitrogen use efficiency: 2. Amino acid metabolism (2007)
Lea, P. J.; Azevedo, Ricardo Antunes de
Source: Annals of Applied Biology. Unidade: ESALQ
Subjects: AMINOÁCIDOS, GENES, METABOLISMO VEGETAL, NITROGÊNIO, NUTRIÇÃO VEGETAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEA, P. J. e AZEVEDO, Ricardo Antunes de. Nitrogen use efficiency: 2. Amino acid metabolism. Annals of Applied Biology, v. 151, n. 3, p. 269-275, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1744-7348.2007.00200.x. Acesso em: 15 nov. 2024.
APA
Lea, P. J., & Azevedo, R. A. de. (2007). Nitrogen use efficiency: 2. Amino acid metabolism. Annals of Applied Biology, 151( 3), 269-275. doi:10.1111/j.1744-7348.2007.00200.x
NLM
Lea PJ, Azevedo RA de. Nitrogen use efficiency: 2. Amino acid metabolism [Internet]. Annals of Applied Biology. 2007 ; 151( 3): 269-275.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1744-7348.2007.00200.x
Vancouver
Lea PJ, Azevedo RA de. Nitrogen use efficiency: 2. Amino acid metabolism [Internet]. Annals of Applied Biology. 2007 ; 151( 3): 269-275.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1744-7348.2007.00200.x

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