ReP USP - Resultado da busca

Artigo de periodico
An evolutionary perspective on complex neuropsychiatric disease (2024)
McClellan, Jon M ; Zoghbi, Anthony W ; Buxbaum, Joseph D ; Cappi, Carolina ; Crowley, James J ; Flint, Jonathan ; Grice, Dorothy E ; Gulsuner, Suleyman ; Iyegbe, Conrad ; Jain, Sanjeev ; Kuo, Po-Hsiu ; Lattig, Maria Claudia ; Passos-Bueno, Maria Rita ; Purushottam, Meera ; Stein, Dan J ; Sunshine, Anna B ; Susser, Ezra S ; Walsh, Christopher A ; Wootton, Olivia ; King, Mary-Claire
Source: Neuron. Unidade: IB
Subjects: NEUROPSIQUIATRIA, MUTAÇÃO GENÉTICA, DERIVA GÊNICA, ALELOS, TRANSTORNO AUTÍSTICO, ESQUIZOFRENIA
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MCCLELLAN, Jon M et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron, v. 112, n. 1, p. 7-24, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.neuron.2023.10.037. Acesso em: 04 nov. 2024.
APA
McClellan, J. M., Zoghbi, A. W., Buxbaum, J. D., Cappi, C., Crowley, J. J., Flint, J., et al. (2024). An evolutionary perspective on complex neuropsychiatric disease. Neuron, 112( 1), 7-24. doi:10.1016/j.neuron.2023.10.037
NLM
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Vancouver
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Artigo de jornal-dep/entr
Passou da hora de rever o processo de contratação de professor doutor na USP [Depoimento] (2024)
Marques, Antonio Carlos ; Assis, Ana Paula A ; Navas, Carlos ; Floh, Eny Iochevet Segal ; Marques, Fernando ; Machado, Glauco ; Cesarino, Igor ; Visconti, Maria Aparecida ; Rossi, Magdalena ; Passos-Bueno, Maria Rita ; Sano, Paulo Takeo ; Grant, Taran
Source: Jornal da USP. Unidade: IB
Assunto: UNIVERSIDADE PÚBLICA
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MARQUES, Antonio Carlos et al. Passou da hora de rever o processo de contratação de professor doutor na USP [Depoimento]. Jornal da USP. São Paulo: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://jornal.usp.br/?p=728200. Acesso em: 04 nov. 2024. , 2024
APA
Marques, A. C., Assis, A. P. A., Navas, C., Floh, E. I. S., Marques, F., Machado, G., et al. (2024). Passou da hora de rever o processo de contratação de professor doutor na USP [Depoimento]. Jornal da USP. São Paulo: Instituto de Biociências, Universidade de São Paulo. Recuperado de https://jornal.usp.br/?p=728200
NLM
Marques AC, Assis APA, Navas C, Floh EIS, Marques F, Machado G, Cesarino I, Visconti MA, Rossi M, Passos-Bueno MR, Sano PT, Grant T. Passou da hora de rever o processo de contratação de professor doutor na USP [Depoimento] [Internet]. Jornal da USP. 2024 ;[citado 2024 nov. 04 ] Available from: https://jornal.usp.br/?p=728200
Vancouver
Marques AC, Assis APA, Navas C, Floh EIS, Marques F, Machado G, Cesarino I, Visconti MA, Rossi M, Passos-Bueno MR, Sano PT, Grant T. Passou da hora de rever o processo de contratação de professor doutor na USP [Depoimento] [Internet]. Jornal da USP. 2024 ;[citado 2024 nov. 04 ] Available from: https://jornal.usp.br/?p=728200
Artigo de periodico
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil (2024)
Migliavacca, Michele P ; Sobreira, Joselito ; Bermeo, Diana; Gomes, Mireille; Alencar, Dayse; Sussuchi, Luciane; Souza, Camila Alves; Silva, Juliana Santos; Kroll, José Eduardo; Burger, Matheus; Sousa, Rodrigo Guarischi ; Villela, Darine ; Yamamoto, Guilherme L ; Milanezi, Fernanda ; Horigoshi, Nelson; Cesar, Regina Grigolli; Carvalho, Werther Brunow de ; Honjo, Rachel Sayuri ; Bertola, Débora Romeo ; Kim, Chong Ae ; Souza, Lucian de; Procianoy, Renato S; Silveria, Rita C; Rosenberg, Carla ; Giugliani, Roberto ; Campana, Gustavo Aguiar; Scapulatempo-Neto, Cristovam ; Sobreira, Nara
Source: American Journal of Medical Genetics. Part A. Unidades: BIOINFORMÁTICA, FM, IB
Subjects: PEDIATRIA, SEQUENCIAMENTO GENÉTICO, DOENÇAS DO RECÉM-NASCIDO
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ABNT
MIGLIAVACCA, Michele P et al. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, n. ja, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63544. Acesso em: 04 nov. 2024.
APA
Migliavacca, M. P., Sobreira, J., Bermeo, D., Gomes, M., Alencar, D., Sussuchi, L., et al. (2024). Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, (ja). doi:10.1002/ajmg.a.63544
NLM
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Vancouver
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Artigo de periodico
The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics (2024)
Ferrari, Rafael Rodrigues; Ricardo, Paulo Cseri ; Dias, Felipe Cordeiro ; Araujo, Natalia de Souza; Soares, Dalliane Oliveira; Zhou, Qing-Song; Zhu, Chao-Dong; Coutinho, Luiz Lehmann ; Arias, Maria Cristina ; Batista, Thiago Mafra
Source: BMC Genomics. Unidades: ESALQ, IB
Subjects: ABELHAS-SEM-FERRÃO, FILOGENIA, GENOMAS, RNA, SEQUENCIAMENTO GENÉTICO
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ABNT
FERRARI, Rafael Rodrigues et al. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics. BMC Genomics, v. 25, p. 1-15, 2024Tradução . . Disponível em: https://doi.org/10.1186/s12864-024-10502-z. Acesso em: 04 nov. 2024.
APA
Ferrari, R. R., Ricardo, P. C., Dias, F. C., Araujo, N. de S., Soares, D. O., Zhou, Q. -S., et al. (2024). The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics. BMC Genomics, 25, 1-15. doi:10.1186/s12864-024-10502-z
NLM
Ferrari RR, Ricardo PC, Dias FC, Araujo N de S, Soares DO, Zhou Q-S, Zhu C-D, Coutinho LL, Arias MC, Batista TM. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics [Internet]. BMC Genomics. 2024 ; 25 1-15.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1186/s12864-024-10502-z
Vancouver
Ferrari RR, Ricardo PC, Dias FC, Araujo N de S, Soares DO, Zhou Q-S, Zhu C-D, Coutinho LL, Arias MC, Batista TM. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics [Internet]. BMC Genomics. 2024 ; 25 1-15.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1186/s12864-024-10502-z
Artigo de periodico
The role of co variation in shaping the response to selection in new world leaf-nosed bats (2024)
Rossoni, Daniela M ; Patterson, Bruce D ; Marroig, Gabriel ; Cheverud, James M ; Houle, David
Source: The American Naturalist. Unidade: IB
Subjects: EVOLUÇÃO, SELEÇÃO NATURAL, MORFOLOGIA ANIMAL, MORCEGOS
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ABNT
ROSSONI, Daniela M et al. The role of co variation in shaping the response to selection in new world leaf-nosed bats. The American Naturalist, v. 203, n. 4, 2024Tradução . . Disponível em: https://doi.org/10.1086/729219. Acesso em: 04 nov. 2024.
APA
Rossoni, D. M., Patterson, B. D., Marroig, G., Cheverud, J. M., & Houle, D. (2024). The role of co variation in shaping the response to selection in new world leaf-nosed bats. The American Naturalist, 203( 4). doi:10.1086/729219
NLM
Rossoni DM, Patterson BD, Marroig G, Cheverud JM, Houle D. The role of co variation in shaping the response to selection in new world leaf-nosed bats [Internet]. The American Naturalist. 2024 ; 203( 4):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1086/729219
Vancouver
Rossoni DM, Patterson BD, Marroig G, Cheverud JM, Houle D. The role of co variation in shaping the response to selection in new world leaf-nosed bats [Internet]. The American Naturalist. 2024 ; 203( 4):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1086/729219
Artigo de periodico
Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders (2024)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Scliar, Marília de Oliveira; Souza, Carolina Fischinger Moura de; Linden Jr, Hélio Van Der; Fernandes, Walter Luiz Magalhães; Otto, Paulo A ; Vianna-Morgante, Angela M ; Haddad, Luciana Amaral ; Honjo, Rachel Sayuri; Yamamoto, Guilherme Lopes; Kim, Chong Ae; Rosenberg, Carla ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino
Source: Molecular Neurobiology. Unidades: IB, BIOINFORMÁTICA, FM
Subjects: MICROCEFALIA, NEUROLOGIA, GENÉTICA
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TOLEZANO, Giovanna Cantini et al. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology, 2024Tradução . . Disponível em: https://doi.org/10.1007/s12035-023-03894-8. Acesso em: 04 nov. 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Scliar, M. de O., Souza, C. F. M. de, Linden Jr, H. V. D., et al. (2024). Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology. doi:10.1007/s12035-023-03894-8
NLM
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Artigo de periodico
Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function (2024)
Vasconcelos, Felipe Tadeu Galante Rocha de ; Ribeiro Junior, Antonio Fernando ; Souza, Brandow Willy ; Zogbi, Isabela de Aquino; Carvalho, Laura Machado Lara ; Feitosa, Letícia Nogueira ; Souza, Lucas Santos ; Saldys, Nathália Gagliardi ; Ferrari, Merari de Fátima Ramires ; Vainzof, Mariz
Source: Frontiers in Neurology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MÚSCULOS, DOENÇAS NEUROMUSCULARES, ENVELHECIMENTO
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VASCONCELOS, Felipe Tadeu Galante Rocha de et al. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function. Frontiers in Neurology, v. 15, 2024Tradução . . Disponível em: https://doi.org/10.3389/fneur.2024.1325222. Acesso em: 04 nov. 2024.
APA
Vasconcelos, F. T. G. R. de, Ribeiro Junior, A. F., Souza, B. W., Zogbi, I. de A., Carvalho, L. M. L., Feitosa, L. N., et al. (2024). Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function. Frontiers in Neurology, 15. doi:10.3389/fneur.2024.1325222
NLM
Vasconcelos FTGR de, Ribeiro Junior AF, Souza BW, Zogbi I de A, Carvalho LML, Feitosa LN, Souza LS, Saldys NG, Ferrari M de FR, Vainzof M. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function [Internet]. Frontiers in Neurology. 2024 ; 15[citado 2024 nov. 04 ] Available from: https://doi.org/10.3389/fneur.2024.1325222
Vancouver
Vasconcelos FTGR de, Ribeiro Junior AF, Souza BW, Zogbi I de A, Carvalho LML, Feitosa LN, Souza LS, Saldys NG, Ferrari M de FR, Vainzof M. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function [Internet]. Frontiers in Neurology. 2024 ; 15[citado 2024 nov. 04 ] Available from: https://doi.org/10.3389/fneur.2024.1325222
Artigo de periodico
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations (2024)
Costa, Silvia Souza da; Fishman, Veniamin ; Pinheiro, Mara; Rodrigueiro, Andre ; Sanseverino, Maria Teresa ; Zielinsky, Paulo ; Carvalho, Claudia M. B ; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino
Source: Chromosome Research: the international journal for all aspects of chromosome and nuclear biology. Unidade: IB
Subjects: ESTENOSE DA VALVA AÓRTICA, ARTÉRIA PULMONAR
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ABNT
COSTA, Silvia Souza da et al. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations. Chromosome Research: the international journal for all aspects of chromosome and nuclear biology, v. 32, n. 6, 2024Tradução . . Disponível em: https://doi.org/10.21203/rs.3.rs-3740005/v1. Acesso em: 04 nov. 2024.
APA
Costa, S. S. da, Fishman, V., Pinheiro, M., Rodrigueiro, A., Sanseverino, M. T., Zielinsky, P., et al. (2024). A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations. Chromosome Research: the international journal for all aspects of chromosome and nuclear biology, 32( 6). doi:10.21203/rs.3.rs-3740005/v1
NLM
Costa SS da, Fishman V, Pinheiro M, Rodrigueiro A, Sanseverino MT, Zielinsky P, Carvalho CMB, Rosenberg C, Krepischi ACV. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations [Internet]. Chromosome Research: the international journal for all aspects of chromosome and nuclear biology. 2024 ; 32( 6):[citado 2024 nov. 04 ] Available from: https://doi.org/10.21203/rs.3.rs-3740005/v1
Vancouver
Costa SS da, Fishman V, Pinheiro M, Rodrigueiro A, Sanseverino MT, Zielinsky P, Carvalho CMB, Rosenberg C, Krepischi ACV. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations [Internet]. Chromosome Research: the international journal for all aspects of chromosome and nuclear biology. 2024 ; 32( 6):[citado 2024 nov. 04 ] Available from: https://doi.org/10.21203/rs.3.rs-3740005/v1
Artigo de periodico
Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition (2024)
Leite, Jean Michel Rocha Sampaio ; Pereira, Jaqueline Lopes ; Souza, Camila Alves de ; Soler, Júlia Maria Pavan ; Netto, Regina Celia Mingroni ; Fisberg, Regina Mara ; Rogero, Marcelo Macedo ; Sarti, Flávia Mori
Source: Lipids in Health and Disease. Unidades: IME, IB, FSP, EACH
Assunto: DISLIPIDEMIAS
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LEITE, Jean Michel Rocha Sampaio et al. Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition. Lipids in Health and Disease, v. 23, n. 229, p. 01-10, 2024Tradução . . Disponível em: http://dx.doi.org/10.1186/s12944-024-02085-1. Acesso em: 04 nov. 2024.
APA
Leite, J. M. R. S., Pereira, J. L., Souza, C. A. de, Soler, J. M. P., Netto, R. C. M., Fisberg, R. M., et al. (2024). Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition. Lipids in Health and Disease, 23( 229), 01-10. doi:10.1186/s12944-024-02085-1
NLM
Leite JMRS, Pereira JL, Souza CA de, Soler JMP, Netto RCM, Fisberg RM, Rogero MM, Sarti FM. Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition [Internet]. Lipids in Health and Disease. 2024 ; 23( 229): 01-10.[citado 2024 nov. 04 ] Available from: http://dx.doi.org/10.1186/s12944-024-02085-1
Vancouver
Leite JMRS, Pereira JL, Souza CA de, Soler JMP, Netto RCM, Fisberg RM, Rogero MM, Sarti FM. Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition [Internet]. Lipids in Health and Disease. 2024 ; 23( 229): 01-10.[citado 2024 nov. 04 ] Available from: http://dx.doi.org/10.1186/s12944-024-02085-1
Artigo de periodico
Disentangling the contemporary and historical effects of landscape on the population genomic variation of two bird species restricted to the highland forest enclaves of northeastern Brazil (2024)
Batalha-Filho, Henrique ; Barreto, Silvia Britto ; Silveira, Mario Henrique Barros; Miyaki, Cristina Yumi ; Afonso, Sandra ; Ferrand, Nuno; Carneiro, Miguel
Source: Heredity. Unidade: IB
Subjects: PÁSSAROS, BIOGEOGRAFIA, ECOLOGIA
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ABNT
BATALHA-FILHO, Henrique et al. Disentangling the contemporary and historical effects of landscape on the population genomic variation of two bird species restricted to the highland forest enclaves of northeastern Brazil. Heredity, v. 132, p. 77–88, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41437-023-00662-1. Acesso em: 04 nov. 2024.
APA
Batalha-Filho, H., Barreto, S. B., Silveira, M. H. B., Miyaki, C. Y., Afonso, S., Ferrand, N., & Carneiro, M. (2024). Disentangling the contemporary and historical effects of landscape on the population genomic variation of two bird species restricted to the highland forest enclaves of northeastern Brazil. Heredity, 132, 77–88. doi:10.1038/s41437-023-00662-1
NLM
Batalha-Filho H, Barreto SB, Silveira MHB, Miyaki CY, Afonso S, Ferrand N, Carneiro M. Disentangling the contemporary and historical effects of landscape on the population genomic variation of two bird species restricted to the highland forest enclaves of northeastern Brazil [Internet]. Heredity. 2024 ; 132 77–88.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41437-023-00662-1
Vancouver
Batalha-Filho H, Barreto SB, Silveira MHB, Miyaki CY, Afonso S, Ferrand N, Carneiro M. Disentangling the contemporary and historical effects of landscape on the population genomic variation of two bird species restricted to the highland forest enclaves of northeastern Brazil [Internet]. Heredity. 2024 ; 132 77–88.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41437-023-00662-1
Artigo de periodico
A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC) (2024)
Nunes, Beatriz Azevedo ; Romano, Ana Karolina Ferreira Gonçalves ; Morgan, Mariana Aparecida Pasa ; Gonçalves, Alice Andrade ; Cardozo, Laís Faria Masulk ; Almeida, Luiz Gustavo Dufner de ; Haddad, Luciana Amaral ; Crippa, Ana Chrystina de Souza ; Antoniuk, Sergio Antonio ; Abagge, Kerstin Taniguchi
Source: Anais Brasileiros de Dermatologia. Unidade: IB
Assunto: DOENÇAS GENÉTICAS
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ABNT
NUNES, Beatriz Azevedo et al. A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC). Anais Brasileiros de Dermatologia, v. 99, n. 5, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.abd.2023.11.004. Acesso em: 04 nov. 2024.
APA
Nunes, B. A., Romano, A. K. F. G., Morgan, M. A. P., Gonçalves, A. A., Cardozo, L. F. M., Almeida, L. G. D. de, et al. (2024). A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC). Anais Brasileiros de Dermatologia, 99( 5). doi:10.1016/j.abd.2023.11.004
NLM
Nunes BA, Romano AKFG, Morgan MAP, Gonçalves AA, Cardozo LFM, Almeida LGD de, Haddad LA, Crippa AC de S, Antoniuk SA, Abagge KT. A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC) [Internet]. Anais Brasileiros de Dermatologia. 2024 ; 99( 5):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.abd.2023.11.004
Vancouver
Nunes BA, Romano AKFG, Morgan MAP, Gonçalves AA, Cardozo LFM, Almeida LGD de, Haddad LA, Crippa AC de S, Antoniuk SA, Abagge KT. A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC) [Internet]. Anais Brasileiros de Dermatologia. 2024 ; 99( 5):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.abd.2023.11.004
Artigo de periodico
A new record of ground sloth in the Ribeira de Iguape valley, southeastern Brazil (2024)
Chahud, Artur ; Pereira, Gabriella da Costa ; Costa, Paulo Ricardo de Oliveira ; Okumura, Mercedes
Source: Carnets de Geologie. Unidade: IB
Assunto: XENARTHRA
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ABNT
CHAHUD, Artur et al. A new record of ground sloth in the Ribeira de Iguape valley, southeastern Brazil. Carnets de Geologie, v. 24, n. 4, p. 83-89, 2024Tradução . . Disponível em: https://doi.org/10.2110/carnets.2024.2404. Acesso em: 04 nov. 2024.
APA
Chahud, A., Pereira, G. da C., Costa, P. R. de O., & Okumura, M. (2024). A new record of ground sloth in the Ribeira de Iguape valley, southeastern Brazil. Carnets de Geologie, 24( 4), 83-89. doi:10.2110/carnets.2024.2404
NLM
Chahud A, Pereira G da C, Costa PR de O, Okumura M. A new record of ground sloth in the Ribeira de Iguape valley, southeastern Brazil [Internet]. Carnets de Geologie. 2024 ; 24( 4): 83-89.[citado 2024 nov. 04 ] Available from: https://doi.org/10.2110/carnets.2024.2404
Vancouver
Chahud A, Pereira G da C, Costa PR de O, Okumura M. A new record of ground sloth in the Ribeira de Iguape valley, southeastern Brazil [Internet]. Carnets de Geologie. 2024 ; 24( 4): 83-89.[citado 2024 nov. 04 ] Available from: https://doi.org/10.2110/carnets.2024.2404
Artigo de periodico
A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis (2024)
Carvalho, Laura Machado Lara ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Current Obesity Reports. Unidades: FM, IB
Subjects: OBESIDADE, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Laura Machado Lara et al. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, n. 26 Ja 2024, 2024Tradução . . Disponível em: https://doi.org/10.1007/s13679-023-00543-y. Acesso em: 04 nov. 2024.
APA
Carvalho, L. M. L., Jorge, A. A. de L., Bertola, D. R., Krepischi, A. C. V., & Rosenberg, C. (2024). A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, (26 Ja 2024). doi:10.1007/s13679-023-00543-y
NLM
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s13679-023-00543-y
Vancouver
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s13679-023-00543-y
Artigo de periodico
Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors (2024)
Novaes, Gabriela Machado; Lima, Caroline; Longo, Carla; Machado, Pedro Henrique; Silva, Thais Peron; Olberg, Giovanna Gonçalves de Oliveira; Módolo, Diego Grando; Pereira, Márcia Cristina Leite; Santos , Tiago Goss; Zatz, Mayana ; Lagares, David; Franco, Marcelo de; Ho, Paulo Lee; Bulstrode, Harry; Okamoto, Oswaldo Keith ; Kaid, Carolini
Source: Molecular Therapy. Unidade: IB
Subjects: CÉLULAS-TRONCO, IMUNOTERAPIA, ZIKA VÍRUS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOVAES, Gabriela Machado et al. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors. Molecular Therapy, v. 32, n. 2, p. 440-456, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.ymthe.2024.01.006. Acesso em: 04 nov. 2024.
APA
Novaes, G. M., Lima, C., Longo, C., Machado, P. H., Silva, T. P., Olberg, G. G. de O., et al. (2024). Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors. Molecular Therapy, 32( 2), 440-456. doi:10.1016/j.ymthe.2024.01.006
NLM
Novaes GM, Lima C, Longo C, Machado PH, Silva TP, Olberg GG de O, Módolo DG, Pereira MCL, Santos TG, Zatz M, Lagares D, Franco M de, Ho PL, Bulstrode H, Okamoto OK, Kaid C. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors [Internet]. Molecular Therapy. 2024 ; 32( 2): 440-456.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ymthe.2024.01.006
Vancouver
Novaes GM, Lima C, Longo C, Machado PH, Silva TP, Olberg GG de O, Módolo DG, Pereira MCL, Santos TG, Zatz M, Lagares D, Franco M de, Ho PL, Bulstrode H, Okamoto OK, Kaid C. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors [Internet]. Molecular Therapy. 2024 ; 32( 2): 440-456.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ymthe.2024.01.006
Artigo de periodico
Liana attachment to supports leads to profound changes in xylem anatomy and transcriptional profile of cambium and differentiating xylem (2024)
Lima, André Carvalho ; Andrade, Sónia Cristina da Silva; Gerolamo, Caian Souza ; Souza, Diego Trindade de ; Coutinho, Luiz Lehmann ; Rossi, Magdalena ; Angyalossy, Veronica
Source: Plant Cell and Environment. Unidades: IB, ESALQ
Subjects: XILEMA, PLANTAS TREPADEIRAS, MADEIRA, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, André Carvalho et al. Liana attachment to supports leads to profound changes in xylem anatomy and transcriptional profile of cambium and differentiating xylem. Plant Cell and Environment, p. 1-17, 2024Tradução . . Disponível em: https://doi.org/10.1111/pce.15094. Acesso em: 04 nov. 2024.
APA
Lima, A. C., Andrade, S. C. da S., Gerolamo, C. S., Souza, D. T. de, Coutinho, L. L., Rossi, M., & Angyalossy, V. (2024). Liana attachment to supports leads to profound changes in xylem anatomy and transcriptional profile of cambium and differentiating xylem. Plant Cell and Environment, 1-17. doi:10.1111/pce.15094
NLM
Lima AC, Andrade SC da S, Gerolamo CS, Souza DT de, Coutinho LL, Rossi M, Angyalossy V. Liana attachment to supports leads to profound changes in xylem anatomy and transcriptional profile of cambium and differentiating xylem [Internet]. Plant Cell and Environment. 2024 ; 1-17.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/pce.15094
Vancouver
Lima AC, Andrade SC da S, Gerolamo CS, Souza DT de, Coutinho LL, Rossi M, Angyalossy V. Liana attachment to supports leads to profound changes in xylem anatomy and transcriptional profile of cambium and differentiating xylem [Internet]. Plant Cell and Environment. 2024 ; 1-17.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/pce.15094
Artigo de periodico
Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders (2024)
Rezende, Raissa Carneiro ; Andrade, Nathalia Liberatoscioli Menezes ; Dantas, Naiara Castelo Branco ; Cellin, Laurana de Polli ; Krepischi, Ana Cristina Victorino ; Lerario, Antonio Marcondes ; Jorge, Alexander Augusto de Lima
Source: JOURNAL OF PEDIATRICS. Unidades: IB, FM
Subjects: ANÁLISE DE SEQUÊNCIA DE DNA, TRANSTORNOS DO CRESCIMENTO, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REZENDE, Raissa Carneiro et al. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders. JOURNAL OF PEDIATRICS, v. 265, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58750. Acesso em: 04 nov. 2024.
APA
Rezende, R. C., Andrade, N. L. M., Dantas, N. C. B., Cellin, L. de P., Krepischi, A. C. V., Lerario, A. M., & Jorge, A. A. de L. (2024). Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders. JOURNAL OF PEDIATRICS, 265. doi:10.1016/j.jpeds.2023.113841
NLM
Rezende RC, Andrade NLM, Dantas NCB, Cellin L de P, Krepischi ACV, Lerario AM, Jorge AA de L. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders [Internet]. JOURNAL OF PEDIATRICS. 2024 ; 265[citado 2024 nov. 04 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58750
Vancouver
Rezende RC, Andrade NLM, Dantas NCB, Cellin L de P, Krepischi ACV, Lerario AM, Jorge AA de L. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders [Internet]. JOURNAL OF PEDIATRICS. 2024 ; 265[citado 2024 nov. 04 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58750
Artigo de periodico
Biogeographic perspectives on human genetic diversification (2024)
Hünemeier, Tábita
Source: Molecular Biology and Evolution. Unidade: IB
Subjects: GENÔMICA, BIOGEOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HÜNEMEIER, Tábita. Biogeographic perspectives on human genetic diversification. Molecular Biology and Evolution, v. 41, n. 3, 2024Tradução . . Disponível em: https://doi.org/10.1093/molbev/msae029. Acesso em: 04 nov. 2024.
APA
Hünemeier, T. (2024). Biogeographic perspectives on human genetic diversification. Molecular Biology and Evolution, 41( 3). doi:10.1093/molbev/msae029
NLM
Hünemeier T. Biogeographic perspectives on human genetic diversification [Internet]. Molecular Biology and Evolution. 2024 ; 41( 3):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1093/molbev/msae029
Vancouver
Hünemeier T. Biogeographic perspectives on human genetic diversification [Internet]. Molecular Biology and Evolution. 2024 ; 41( 3):[citado 2024 nov. 04 ] Available from: https://doi.org/10.1093/molbev/msae029
Artigo de periodico
Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies (2024)
Dangoni, Gustavo D; Teixeira, Anne Caroline B; Costa, Silvia S. da; Scliar, Marília O; Carvalho, Laura Machado Lara ; Silva, Luciana N; Novak, Estela M; Vince, Carolina S. C; Maschietto, Mariana C; Sugayama, Sofia M. M; Odone-filho, Vicente ; Krepischi, Ana Cristina Victorino
Source: Pediatric Research. Unidades: IB, FM
Subjects: NEOPLASIAS, NEUROBLASTOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DANGONI, Gustavo D et al. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies. Pediatric Research, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41390-023-03000-7. Acesso em: 04 nov. 2024.
APA
Dangoni, G. D., Teixeira, A. C. B., Costa, S. S. da, Scliar, M. O., Carvalho, L. M. L., Silva, L. N., et al. (2024). Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies. Pediatric Research. doi:10.1038/s41390-023-03000-7
NLM
Dangoni GD, Teixeira ACB, Costa SS da, Scliar MO, Carvalho LML, Silva LN, Novak EM, Vince CSC, Maschietto MC, Sugayama SMM, Odone-filho V, Krepischi ACV. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies [Internet]. Pediatric Research. 2024 ;[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41390-023-03000-7
Vancouver
Dangoni GD, Teixeira ACB, Costa SS da, Scliar MO, Carvalho LML, Silva LN, Novak EM, Vince CSC, Maschietto MC, Sugayama SMM, Odone-filho V, Krepischi ACV. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies [Internet]. Pediatric Research. 2024 ;[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41390-023-03000-7
Artigo de periodico
Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants (2024)
Torres, William Bertani ; Lezirovitz, Karina ; Coutinho, Danillo Alencar ; Pardono, Eliete; Costa, Silvia Souza da; Antunes, Larissa do Nascimento; Oliveira, Judite de; Otto, Paulo A ; Pingault, Véronique ; Mingroni Netto, Regina Celia
Source: Audiology Research. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, GENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, PIGMENTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TORRES, William Bertani et al. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, v. 14, n. 1, p. 9-25, 2024Tradução . . Disponível em: https://doi.org/10.3390/audiolres14010002. Acesso em: 04 nov. 2024.
APA
Torres, W. B., Lezirovitz, K., Coutinho, D. A., Pardono, E., Costa, S. S. da, Antunes, L. do N., et al. (2024). Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, 14( 1), 9-25. doi:10.3390/audiolres14010002
NLM
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/audiolres14010002
Vancouver
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/audiolres14010002
Artigo de periodico
Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population (2024)
Leite, Jean Michel Rocha Sampaio ; Ribeiro, Adele; Pereira, Jaqueline Lopes ; Souza, Camila Alves de ; Heider, Dominik ; Soler, Júlia Maria Pavan ; Mingroni Netto, Regina Celia ; Fisberg, Regina Mara ; Rogero, Marcelo Macedo ; Sarti, Flávia Mori
Source: Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. Unidades: IME, IB, FSP, EACH
Assunto: POPULAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEITE, Jean Michel Rocha Sampaio et al. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism, v. 63, p. 311-321, 2024Tradução . . Disponível em: http://dx.doi.org/10.1016/j.clnesp.2024.06.045. Acesso em: 04 nov. 2024.
APA
Leite, J. M. R. S., Ribeiro, A., Pereira, J. L., Souza, C. A. de, Heider, D., Soler, J. M. P., et al. (2024). Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism, 63, 311-321. doi:10.1016/j.clnesp.2024.06.045
NLM
Leite J M R S, Ribeiro A, Pereira JL, Souza CA de, Heider D, Soler JMP, Mingroni Netto RC, Fisberg RM, Rogero MM, Sarti FM. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population [Internet]. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. 2024 ; 63 311-321.[citado 2024 nov. 04 ] Available from: http://dx.doi.org/10.1016/j.clnesp.2024.06.045
Vancouver
Leite J M R S, Ribeiro A, Pereira JL, Souza CA de, Heider D, Soler JMP, Mingroni Netto RC, Fisberg RM, Rogero MM, Sarti FM. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population [Internet]. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. 2024 ; 63 311-321.[citado 2024 nov. 04 ] Available from: http://dx.doi.org/10.1016/j.clnesp.2024.06.045

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