ReP USP - Resultado da busca

Artigo de periodico
Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma (2023)
Assoni, Amanda Faria ; Mitsugi, Thiago Giove ; Wardenaar, René; Ferreira, Raiane Oliveira ; Jandrey, Elisa Helena Farias ; Novaes, Gabriela Machado ; Granha, Isabela Fonseca de Oliveira ; Bakker, Petra ; Kaid, Carolini ; Zatz, Mayana ; Foijer, Floris ; Okamoto, Oswaldo Keith
Fonte: Scientific Reports. Unidade: IB
Assuntos: MEDULOBLASTOMA, DEGENERAÇÃO NEURAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ASSONI, Amanda Faria et al. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma. Scientific Reports, v. 13, n. art. 19481, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41598-023-45319-5. Acesso em: 15 nov. 2024.
APA
Assoni, A. F., Mitsugi, T. G., Wardenaar, R., Ferreira, R. O., Jandrey, E. H. F., Novaes, G. M., et al. (2023). Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma. Scientific Reports, 13( art. 19481). doi:10.1038/s41598-023-45319-5
NLM
Assoni AF, Mitsugi TG, Wardenaar R, Ferreira RO, Jandrey EHF, Novaes GM, Granha IF de O, Bakker P, Kaid C, Zatz M, Foijer F, Okamoto OK. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma [Internet]. Scientific Reports. 2023 ; 13( art. 19481):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-023-45319-5
Vancouver
Assoni AF, Mitsugi TG, Wardenaar R, Ferreira RO, Jandrey EHF, Novaes GM, Granha IF de O, Bakker P, Kaid C, Zatz M, Foijer F, Okamoto OK. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma [Internet]. Scientific Reports. 2023 ; 13( art. 19481):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-023-45319-5
Artigo de periodico
IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis (2023)
Assoni, Amanda Faria; Guerrero, Erika N; Wardenaar, René; Oliveira, Danyllo; Bakker, Petra L; Alves, Luciana M; Carvalho, Valdemir M ; Okamoto, Oswaldo Keith ; Zatz, Mayana ; Foijer, Floris
Fonte: Brain Pathology. Unidade: IB
Assuntos: ESCLEROSE AMIOTRÓFICA LATERAL, MEDULOBLASTOMA, DEGENERAÇÃO NEURAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ASSONI, Amanda Faria et al. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis. Brain Pathology, 2023Tradução . . Disponível em: https://doi.org/10.1111/bpa.13206. Acesso em: 15 nov. 2024.
APA
Assoni, A. F., Guerrero, E. N., Wardenaar, R., Oliveira, D., Bakker, P. L., Alves, L. M., et al. (2023). IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis. Brain Pathology. doi:10.1111/bpa.13206
NLM
Assoni AF, Guerrero EN, Wardenaar R, Oliveira D, Bakker PL, Alves LM, Carvalho VM, Okamoto OK, Zatz M, Foijer F. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis [Internet]. Brain Pathology. 2023 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/bpa.13206
Vancouver
Assoni AF, Guerrero EN, Wardenaar R, Oliveira D, Bakker PL, Alves LM, Carvalho VM, Okamoto OK, Zatz M, Foijer F. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis [Internet]. Brain Pathology. 2023 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/bpa.13206
Artigo de periodico
Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Assuntos: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1831, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29575-z. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1831). doi:10.1038/s41467-022-29575-z
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome (2022)
Lima, Ariadne R.; Ferreira, Barbara M.; Zhang, Chaofan; Jolly, Angad; Du, Haowei ; White, Janson J.; Dawood, Moez; Lins, Tulio C.; Chiabai, Marcela A.; van Beusekom, Ellen; Cordoba, Mara S.; Rosa, Erica C. C. Caldas; Kayserili, Hulya; Kimonis, Virginia; Wu, Erica; Mellado, Cecilia; Aggarwal, Vineet; Richieri-Costa, Antonio ; Brunoni, Décio; Canó, Talyta M.; Jorge, Alexander A. L. ; Kim, Chong Ae ; Honjo, Rachel ; Bertola, Débora R. ; Dandalo-Girardi, Raissa M.; Bayram, Yavuz; Gezdirici, Alper; Yilmaz-Gulec, Elif; Gumus, Evren; Yilmaz, Gülay C.; Okamoto, Nobuhiko ; Ohashi, Hirofumi; Coban–Akdemir, Zeynep; Mitani, Tadahiro; Jhangiani, Shalini N.; Muzny, Donna M.; Regattieri, Neysa A. P. ; Pogue, Robert ; Pereira, Rinaldo W.; Otto, Paulo A ; Gibbs, Richard A.; Ali, Bassam R.; van Bokhoven, Hans; Brunner, Han G.; Sutton, V. Reid; Lupski, James R. ; Vianna-Morgante, Angela M ; Carvalho, Claudia M. B. ; Mazzeu, Juliana F.
Fonte: Human Mutation. Unidades: HRAC, FM, IB
Assuntos: FENÓTIPOS, MORFOLOGIA (ANATOMIA), SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Ariadne R. et al. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, v. 43, n. 7, p. 900-918, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24375. Acesso em: 15 nov. 2024.
APA
Lima, A. R., Ferreira, B. M., Zhang, C., Jolly, A., Du, H., White, J. J., et al. (2022). Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, 43( 7), 900-918. doi:10.1002/humu.24375
NLM
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/humu.24375
Vancouver
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/humu.24375
Artigo de periodico
Cultivando afetos: uma etnoarqueologia de plantas alimentícias entre os Asurini do Xingu (2022)
Cascon, Leandro Matthews ; Murrieta, Rui Sérgio Sereni ; Silva, Fabíola Andrea
Fonte: Habitus. Unidades: IB, MAE
Assuntos: PLANTAS CULTIVADAS, INDÍGENAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASCON, Leandro Matthews e MURRIETA, Rui Sérgio Sereni e SILVA, Fabíola Andrea. Cultivando afetos: uma etnoarqueologia de plantas alimentícias entre os Asurini do Xingu. Habitus, v. 20, n. 2, p. 511-535, 2022Tradução . . Disponível em: https://doi.org/10.18224/hab.v20i2.12730. Acesso em: 15 nov. 2024.
APA
Cascon, L. M., Murrieta, R. S. S., & Silva, F. A. (2022). Cultivando afetos: uma etnoarqueologia de plantas alimentícias entre os Asurini do Xingu. Habitus, 20( 2), 511-535. doi:10.18224/hab.v20i2.12730
NLM
Cascon LM, Murrieta RSS, Silva FA. Cultivando afetos: uma etnoarqueologia de plantas alimentícias entre os Asurini do Xingu [Internet]. Habitus. 2022 ; 20( 2): 511-535.[citado 2024 nov. 15 ] Available from: https://doi.org/10.18224/hab.v20i2.12730
Vancouver
Cascon LM, Murrieta RSS, Silva FA. Cultivando afetos: uma etnoarqueologia de plantas alimentícias entre os Asurini do Xingu [Internet]. Habitus. 2022 ; 20( 2): 511-535.[citado 2024 nov. 15 ] Available from: https://doi.org/10.18224/hab.v20i2.12730
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Assuntos: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1004, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-28648-3. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1004). doi:10.1038/s41467-022-28648-3
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Fonte: Human Mutation. Unidades: HRACF, HRAC, IB
Assuntos: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 15 nov. 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements (2021)
Tavares, Vanessa Luiza Romanelli ; Guimarães-Ramos, Sofia Ligia; Zhou, Yan; Masotti, Cibele; Ezquina, Suzana; Moreira, Danielle de Paula; Buermans, Henk; Freitas, Renato S; Dunnen, Johan T Den; Twigg, Stephen R F; Passos-Bueno, Maria Rita
Fonte: Journal of Medical Genetics. Unidades: IB, BIOINFORMÁTICA
Assuntos: GENÉTICA, DOENÇAS GENÉTICAS, FENÓTIPOS, MALFORMAÇÕES, VARIAÇÃO GENÉTICA, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Vanessa Luiza Romanelli et al. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2021-107825. Acesso em: 15 nov. 2024.
APA
Tavares, V. L. R., Guimarães-Ramos, S. L., Zhou, Y., Masotti, C., Ezquina, S., Moreira, D. de P., et al. (2021). New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics. doi:10.1136/jmedgenet-2021-107825
NLM
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Vancouver
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Artigo de periodico
Concurrent X chromosome inactivation and upregulation during non-human primate preimplantation development revealed by single-cell RNA-sequencing (2021)
Cidral, Ana Luíza; Mello, Joana C. Moreira de; Gribnau, Joost; Pereira, Lygia da Veiga
Fonte: Scientific Reports. Unidades: IB, BIOTECNOLOGIA
Assuntos: CROMOSSOMO X, SEQUENCIAMENTO GENÉTICO, EMBRIÃO, GENÉTICA MÉDICA, EPIGÊNESE GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CIDRAL, Ana Luíza et al. Concurrent X chromosome inactivation and upregulation during non-human primate preimplantation development revealed by single-cell RNA-sequencing. Scientific Reports, v. 11, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-89175-7. Acesso em: 15 nov. 2024.
APA
Cidral, A. L., Mello, J. C. M. de, Gribnau, J., & Pereira, L. da V. (2021). Concurrent X chromosome inactivation and upregulation during non-human primate preimplantation development revealed by single-cell RNA-sequencing. Scientific Reports, 11. doi:10.1038/s41598-021-89175-7
NLM
Cidral AL, Mello JCM de, Gribnau J, Pereira L da V. Concurrent X chromosome inactivation and upregulation during non-human primate preimplantation development revealed by single-cell RNA-sequencing [Internet]. Scientific Reports. 2021 ; 11[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-021-89175-7
Vancouver
Cidral AL, Mello JCM de, Gribnau J, Pereira L da V. Concurrent X chromosome inactivation and upregulation during non-human primate preimplantation development revealed by single-cell RNA-sequencing [Internet]. Scientific Reports. 2021 ; 11[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-021-89175-7
Artigo de periodico-carta/editorial
Author Correction: a global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection (2021)
Andreakos, Evangelos ; Abel, Laurent ; Vinh, Donald C. ; Kaja, Elzbieta ; Drolet, Beth A. ; Zhang, Qian ; O\2019Farrelly, Cliona ; Novelli, Giuseppe ; Gallego, Carlos Rodríguez ; Haerynck, Filomeen ; Prando, Carolina ; Pujol, Aurora ; Condino Neto, Antonio ; Su, Helen C. ; Casanova, Jean-Laurent ; Spaan, András N. ; Zatz, Mayana
Fonte: Nature Immunology. Unidades: ICB, IB
Assuntos: IMUNOLOGIA, INFECÇÕES POR CORONAVIRUS, CORONAVIRUS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDREAKOS, Evangelos et al. Author Correction: a global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection. Nature Immunology. New York: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/s41590-021-01096-9. Acesso em: 15 nov. 2024. , 2021
APA
Andreakos, E., Abel, L., Vinh, D. C., Kaja, E., Drolet, B. A., Zhang, Q., et al. (2021). Author Correction: a global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection. Nature Immunology. New York: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1038/s41590-021-01096-9
NLM
Andreakos E, Abel L, Vinh DC, Kaja E, Drolet BA, Zhang Q, O\2019Farrelly C, Novelli G, Gallego CR, Haerynck F, Prando C, Pujol A, Condino Neto A, Su HC, Casanova J-L, Spaan AN, Zatz M. Author Correction: a global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection [Internet]. Nature Immunology. 2021 ;1 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41590-021-01096-9
Vancouver
Andreakos E, Abel L, Vinh DC, Kaja E, Drolet BA, Zhang Q, O\2019Farrelly C, Novelli G, Gallego CR, Haerynck F, Prando C, Pujol A, Condino Neto A, Su HC, Casanova J-L, Spaan AN, Zatz M. Author Correction: a global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection [Internet]. Nature Immunology. 2021 ;1 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41590-021-01096-9
Artigo de periodico
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths (2021)
Bastard, Paul ; Gervais, Adrian ; Voyer, Tom Le ; Rosain, Jérémie ; Philippot, Quentin; Manry, Jérémy ; Michailidis, Eleftherios ; Hoffmann, Hans-Heinrich ; Eto, Shohei; Garcia-Prat, Marina; Bizien, Lucy; Parra-Martínez, Alba; Yang, Rui; Liis, Haljasmägi; Migaud, Mélanie; Särekannu, Karita; Maslovskaja, Julia; Prost, Nicolas de; Tandjaoui-Lambiotte, Yacine; Luyt , Charles-Edouard; Amador-Borrero, Blanca; Alexandre, Gaudet; Poissy, Julien; Morel, Pascal; Richard, Pascale; Cognasse, Fabrice; Troya, Jesus; Trouillet-Assant, Sophie; Belot, Alexandre; Saker, Kahina; Garçon, Pierre; Rivière, Jacques G; Lagier, Jean-Christophe; Gentile, Stéphanie; Rosen, Lindsey B; Shaw, Elana; Morio, Tomohiro; Tanaka, Junko; Dalmau, David; Tharaux, Pierre-Louis; Sene, Damien; Stepanian, Alain; Megarbane, Bruno; Triantafyllia, Vasiliki; Fekkar, Arnaud; Heath, James R; Franco, José Luis; Anaya, Juan-Manuel; Solé-Violán, Jordi; Imberti, Luisa; Biondi, Andrea; Bonfanti, Paolo; Castagnoli, Riccardo; Delmonte, Ottavia M; Zhang, Yu; Snow, Andrew L; Holland, Steven M; Biggs, Catherine M; Moncada-Vélez, Marcela; Arias, Andrés Augusto; Lorenzo, Lazaro; Boucherit, Soraya; Coulibaly, Boubacar; Anglicheau, Dany; Planas, Anna M; Haerynck, Filomeen; Duvlis, Sotirija; Nussbaum, Robert L; Ozcelik, Tayfun; Keles, Sevgi; Bousfiha, Ahmed A; ElBakkouri, Jalila; Ramirez-Santana, Carolina; Paul, Stéphane; Pan-Hammarström, Qiang; Hammarström, Lennart; Dupont, Annabelle; Kurolap, Alina; Metz, Christine N; Aiuti, Alessandro; Casari, Giorgio; Lampasona, Vito; Ciceri, Fabio; Barreiros, Lucila A; Dominguez-Garrido, Elena; Vidigal, Mateus; Zatz, Mayana ; Beek, Diederik van de; Sahanic, Sabina; Tancevski, Ivan; Stepanovskyy, Yurii; Boyarchuk, Oksana; Nukui, Yoko; Tsumura, Miyuki; Vidaur, Loreto; Tangye, Stuart G; Burrel, Sonia; Duffy, Darragh; Quintana-Murci, Lluis; Klocperk, Adam; Kann, Nelli Y; Shcherbina, Anna; Lau, Yu-Lung; Leung, Daniel; Coulongeat, Matthieu; Marlet, Julien; Koning, Rutger; Reyes, Luis Felipe; Chauvineau-Grenier, Angélique; Vene, Fabienne; Monneret, Guillaume; Nussenzweig, Michel C; Arrestier, Romain; Boudhabhay, Idris; Baris-Feldman, Hagit; Hagin, David; Wauters, Joost; Meyts, Isabelle; Dyer, Adam H; Kennelly, Sean P; Bourke, Nollaig M; Halwani, Rabih; Sharif-Askari, Narjes Saheb; Dorgham, Karim; Sallette, Jérome; Sedkaoui, Souad Mehlal; AlKhater, Suzan; Rigo-Bonnin, Raúl; Morandeira, Francisco; Roussel, Lucie; Vinh, Donald C; Ostrowski, Sisse Rye; Condino Neto, Antonio ; Prando, Carolina ; Bondarenko, Anastasiia; Spaan, András N; Gilardin, Laurent; Fellay, Jacques; Lyonnet, Stanislas; Bilguvar, Kaya; Lifton, Richard P; Mane, Shrikant; Anderson, Mark S; Boisson, Bertrand; Béziat, Vivien; Zhang, Shen-Ying; Andreakos, Evangelos; Hermine, Olivier; Pujol, Aurora; Peterson, Pärt; Mogensen, Trine; H Rowen, Lee; Mond, James; Debette, Stéphanie; Lamballerie, Xavier de; Duval, Xavier; Mentré, France; Zins, Marie; Soler-Palacin, Pere; Colobran, Roger; Gorochov, Guy; Solanich, Xavier; Susen, Sophie; Martinez-Picado, Javier; Raoult, Didier; Vasse, Marc; Gregersen, Peter K; Piemonti, Lorenzo; Rodríguez-Gallego, Carlos; Notarangelo, Luigi D; Su, Helen C; Kisand, Kai; Okada, Satoshi; Puel, Anne; Jouanguy, Emmanuelle; Rice, Charles M; Tiberghien, Pierre; Zhang, Qian; Cobat, Aurélie; Abel, Laurent; Casanova, Jean-Laurent
Fonte: Science Immunology. Unidades: IB, ICB
Assuntos: COVID-19, INFECÇÕES POR CORONAVIRUS, ANTICORPOS, IMUNOLOGIA, HOMENS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASTARD, Paul et al. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths. Science Immunology, v. 6, n. 62, p. 1-30, 2021Tradução . . Disponível em: https://doi.org/10.1126/sciimmunol.abl4340. Acesso em: 15 nov. 2024.
APA
Bastard, P., Gervais, A., Voyer, T. L., Rosain, J., Philippot, Q., Manry, J., et al. (2021). Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths. Science Immunology, 6( 62), 1-30. doi:10.1126/sciimmunol.abl4340
NLM
Bastard P, Gervais A, Voyer TL, Rosain J, Philippot Q, Manry J, Michailidis E, Hoffmann H-H, Eto S, Garcia-Prat M, Bizien L, Parra-Martínez A, Yang R, Liis H, Migaud M, Särekannu K, Maslovskaja J, Prost N de, Tandjaoui-Lambiotte Y, Luyt C-E, Amador-Borrero B, Alexandre G, Poissy J, Morel P, Richard P, Cognasse F, Troya J, Trouillet-Assant S, Belot A, Saker K, Garçon P, Rivière JG, Lagier J-C, Gentile S, Rosen LB, Shaw E, Morio T, Tanaka J, Dalmau D, Tharaux P-L, Sene D, Stepanian A, Megarbane B, Triantafyllia V, Fekkar A, Heath JR, Franco JL, Anaya J-M, Solé-Violán J, Imberti L, Biondi A, Bonfanti P, Castagnoli R, Delmonte OM, Zhang Y, Snow AL, Holland SM, Biggs CM, Moncada-Vélez M, Arias AA, Lorenzo L, Boucherit S, Coulibaly B, Anglicheau D, Planas AM, Haerynck F, Duvlis S, Nussbaum RL, Ozcelik T, Keles S, Bousfiha AA, ElBakkouri J, Ramirez-Santana C, Paul S, Pan-Hammarström Q, Hammarström L, Dupont A, Kurolap A, Metz CN, Aiuti A, Casari G, Lampasona V, Ciceri F, Barreiros LA, Dominguez-Garrido E, Vidigal M, Zatz M, Beek D van de, Sahanic S, Tancevski I, Stepanovskyy Y, Boyarchuk O, Nukui Y, Tsumura M, Vidaur L, Tangye SG, Burrel S, Duffy D, Quintana-Murci L, Klocperk A, Kann NY, Shcherbina A, Lau Y-L, Leung D, Coulongeat M, Marlet J, Koning R, Reyes LF, Chauvineau-Grenier A, Vene F, Monneret G, Nussenzweig MC, Arrestier R, Boudhabhay I, Baris-Feldman H, Hagin D, Wauters J, Meyts I, Dyer AH, Kennelly SP, Bourke NM, Halwani R, Sharif-Askari NS, Dorgham K, Sallette J, Sedkaoui SM, AlKhater S, Rigo-Bonnin R, Morandeira F, Roussel L, Vinh DC, Ostrowski SR, Condino Neto A, Prando C, Bondarenko A, Spaan AN, Gilardin L, Fellay J, Lyonnet S, Bilguvar K, Lifton RP, Mane S, Anderson MS, Boisson B, Béziat V, Zhang S-Y, Andreakos E, Hermine O, Pujol A, Peterson P, Mogensen T, H Rowen L, Mond J, Debette S, Lamballerie X de, Duval X, Mentré F, Zins M, Soler-Palacin P, Colobran R, Gorochov G, Solanich X, Susen S, Martinez-Picado J, Raoult D, Vasse M, Gregersen PK, Piemonti L, Rodríguez-Gallego C, Notarangelo LD, Su HC, Kisand K, Okada S, Puel A, Jouanguy E, Rice CM, Tiberghien P, Zhang Q, Cobat A, Abel L, Casanova J-L. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths [Internet]. Science Immunology. 2021 ; 6( 62): 1-30.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciimmunol.abl4340
Vancouver
Bastard P, Gervais A, Voyer TL, Rosain J, Philippot Q, Manry J, Michailidis E, Hoffmann H-H, Eto S, Garcia-Prat M, Bizien L, Parra-Martínez A, Yang R, Liis H, Migaud M, Särekannu K, Maslovskaja J, Prost N de, Tandjaoui-Lambiotte Y, Luyt C-E, Amador-Borrero B, Alexandre G, Poissy J, Morel P, Richard P, Cognasse F, Troya J, Trouillet-Assant S, Belot A, Saker K, Garçon P, Rivière JG, Lagier J-C, Gentile S, Rosen LB, Shaw E, Morio T, Tanaka J, Dalmau D, Tharaux P-L, Sene D, Stepanian A, Megarbane B, Triantafyllia V, Fekkar A, Heath JR, Franco JL, Anaya J-M, Solé-Violán J, Imberti L, Biondi A, Bonfanti P, Castagnoli R, Delmonte OM, Zhang Y, Snow AL, Holland SM, Biggs CM, Moncada-Vélez M, Arias AA, Lorenzo L, Boucherit S, Coulibaly B, Anglicheau D, Planas AM, Haerynck F, Duvlis S, Nussbaum RL, Ozcelik T, Keles S, Bousfiha AA, ElBakkouri J, Ramirez-Santana C, Paul S, Pan-Hammarström Q, Hammarström L, Dupont A, Kurolap A, Metz CN, Aiuti A, Casari G, Lampasona V, Ciceri F, Barreiros LA, Dominguez-Garrido E, Vidigal M, Zatz M, Beek D van de, Sahanic S, Tancevski I, Stepanovskyy Y, Boyarchuk O, Nukui Y, Tsumura M, Vidaur L, Tangye SG, Burrel S, Duffy D, Quintana-Murci L, Klocperk A, Kann NY, Shcherbina A, Lau Y-L, Leung D, Coulongeat M, Marlet J, Koning R, Reyes LF, Chauvineau-Grenier A, Vene F, Monneret G, Nussenzweig MC, Arrestier R, Boudhabhay I, Baris-Feldman H, Hagin D, Wauters J, Meyts I, Dyer AH, Kennelly SP, Bourke NM, Halwani R, Sharif-Askari NS, Dorgham K, Sallette J, Sedkaoui SM, AlKhater S, Rigo-Bonnin R, Morandeira F, Roussel L, Vinh DC, Ostrowski SR, Condino Neto A, Prando C, Bondarenko A, Spaan AN, Gilardin L, Fellay J, Lyonnet S, Bilguvar K, Lifton RP, Mane S, Anderson MS, Boisson B, Béziat V, Zhang S-Y, Andreakos E, Hermine O, Pujol A, Peterson P, Mogensen T, H Rowen L, Mond J, Debette S, Lamballerie X de, Duval X, Mentré F, Zins M, Soler-Palacin P, Colobran R, Gorochov G, Solanich X, Susen S, Martinez-Picado J, Raoult D, Vasse M, Gregersen PK, Piemonti L, Rodríguez-Gallego C, Notarangelo LD, Su HC, Kisand K, Okada S, Puel A, Jouanguy E, Rice CM, Tiberghien P, Zhang Q, Cobat A, Abel L, Casanova J-L. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths [Internet]. Science Immunology. 2021 ; 6( 62): 1-30.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciimmunol.abl4340
Artigo de periodico
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation (2021)
Bonfante, Betty; Faux, Pierr; Navarro, Nicolas; Mendoza-Revilla, Javier; Dubied, Morgane; Montillot, Charlotte; Wentworth, Emma; Poloni, Lauriane; Varón-González, Ceferino; Jones, Philip; Xiong, Ziyi; Fuentes-Guajardo, Macarena; Palmal, Sagnik; Chacón-Duque, Juan Camilo; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Jaramillo, Claudia; Arias, William; Barquera, Rodrigo; Everardo-Martínez, Paola; Sánchez-Quinto, Mirsha; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Cerqueira, Caio C. Silva de; Hünemeier, Tábita ; Ramallo, Virginia; Liu, Fan; Weinberg, Seth M; Shaffer, John R; Stergiakouli, Evie; Howe, Laurence J; Hysi, Pirro G; Spector, Timothy D; Gonzalez-José, Rolando; Schüler-Faccini, Lavinia; Bortolini, Maria-Cátira; Acuña-Alonzo, Victor; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Thauvin-Robinet, Christel; Faivre, Laurence; Costedoat, Caroline; Balding, David; Cox, Timothy; Kayser, Manfred; Duplomb, Laurence; Yalcin, Binnaz; Cotney, Justin; Adhikari, Kaustubh; Ruiz-Linares, Andrés
Fonte: Science Advances. Unidade: IB
Assuntos: PELE, GENOMAS, GENEALOGIA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONFANTE, Betty et al. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Science Advances, v. 7, n. 6, 2021Tradução . . Disponível em: https://doi.org/10.1126/sciadv.abc6160. Acesso em: 15 nov. 2024.
APA
Bonfante, B., Faux, P., Navarro, N., Mendoza-Revilla, J., Dubied, M., Montillot, C., et al. (2021). A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Science Advances, 7( 6). doi:10.1126/sciadv.abc6160
NLM
Bonfante B, Faux P, Navarro N, Mendoza-Revilla J, Dubied M, Montillot C, Wentworth E, Poloni L, Varón-González C, Jones P, Xiong Z, Fuentes-Guajardo M, Palmal S, Chacón-Duque JC, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Barquera R, Everardo-Martínez P, Sánchez-Quinto M, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Liu F, Weinberg SM, Shaffer JR, Stergiakouli E, Howe LJ, Hysi PG, Spector TD, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Thauvin-Robinet C, Faivre L, Costedoat C, Balding D, Cox T, Kayser M, Duplomb L, Yalcin B, Cotney J, Adhikari K, Ruiz-Linares A. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation [Internet]. Science Advances. 2021 ; 7( 6):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciadv.abc6160
Vancouver
Bonfante B, Faux P, Navarro N, Mendoza-Revilla J, Dubied M, Montillot C, Wentworth E, Poloni L, Varón-González C, Jones P, Xiong Z, Fuentes-Guajardo M, Palmal S, Chacón-Duque JC, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Barquera R, Everardo-Martínez P, Sánchez-Quinto M, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Liu F, Weinberg SM, Shaffer JR, Stergiakouli E, Howe LJ, Hysi PG, Spector TD, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Thauvin-Robinet C, Faivre L, Costedoat C, Balding D, Cox T, Kayser M, Duplomb L, Yalcin B, Cotney J, Adhikari K, Ruiz-Linares A. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation [Internet]. Science Advances. 2021 ; 7( 6):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciadv.abc6160
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) (2020)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly
Fonte: BioRxiv (The Preprint Server for Biology). Unidades: IB, BIOINFORMÁTICA
Assuntos: GENOMAS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), p. 1-29, 2020Tradução . . Disponível em: https://doi.org/10.1101/2020.09.15.298026. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., & Nunes, K. (2020). Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), 1-29. doi:10.1101/2020.09.15.298026
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Artigo de periodico
Development of a comprehensive noninvasive prenatal test (2018)
Malcher, Carolina; Yamamoto, Guilherme L; Burnham, Philip; Ezquina, Suzana A. M; Lourenço, Naila C. V; Balkassmi, Sahilla; Antonio, David S. Marco; Hsia, Gabriella S. P; Gollop, Thomaz; Pavanello, Rita C; Lopes, Marco Antônio; Bakker, Egbert; Zatz, Mayana ; Bertola, Débora; Vlaminck, Iwijn De; Passos-Bueno, Maria Rita
Fonte: Genetics and Molecular Biology. Unidades: IB, FM
Assuntos: DIAGNÓSTICO PRÉ-NATAL, SEQUENCIAMENTO GENÉTICO, ANORMALIDADES CROMOSSÔMICAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALCHER, Carolina et al. Development of a comprehensive noninvasive prenatal test. Genetics and Molecular Biology, v. 41, n. 3, p. 545-554, 2018Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-gmb-2017-0177. Acesso em: 15 nov. 2024.
APA
Malcher, C., Yamamoto, G. L., Burnham, P., Ezquina, S. A. M., Lourenço, N. C. V., Balkassmi, S., et al. (2018). Development of a comprehensive noninvasive prenatal test. Genetics and Molecular Biology, 41( 3), 545-554. doi:10.1590/1678-4685-gmb-2017-0177
NLM
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck ID, Passos-Bueno MR. Development of a comprehensive noninvasive prenatal test [Internet]. Genetics and Molecular Biology. 2018 ; 41( 3): 545-554.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0177
Vancouver
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck ID, Passos-Bueno MR. Development of a comprehensive noninvasive prenatal test [Internet]. Genetics and Molecular Biology. 2018 ; 41( 3): 545-554.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0177
Artigo de periodico
Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins (2017)
Jehee, Fernanda S; Oliveira, Valdirene T. de; Gurgel Giannetti, Juliana; Pietra, Rafaella X; Rubatino, Fernando V. M; Carobin, Natália V; Vianna, Gabrielle S; Freitas, Mariana L. de; Fernandes, Karla S; Ribeiro, Beatriz S. V; Brüggenwirth, Hennie T; Ali-Amin, Roza; White, Janson J; Akdemir, Zeynep C; Jhangiani, Shalini N; Gibbs, Richard A; Lupski, James R; Varela, Monica C; Koiffmann, Celia Priszkulnik ; Rosenberg, Carla ; Carvalho, Cláudia M. B
Fonte: American Journal of Medical Genetics. Part A. Unidade: IB
Assuntos: DOENÇAS GENÉTICAS, GENÉTICA MÉDICA, DELEÇÃO DE GENES, FENÓTIPOS, OBESIDADE, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda S et al. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins. American Journal of Medical Genetics. Part A, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38315. Acesso em: 15 nov. 2024.
APA
Jehee, F. S., Oliveira, V. T. de, Gurgel Giannetti, J., Pietra, R. X., Rubatino, F. V. M., Carobin, N. V., et al. (2017). Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins. American Journal of Medical Genetics. Part A, 1-5. doi:10.1002/ajmg.a.38315
NLM
Jehee FS, Oliveira VT de, Gurgel Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, Freitas ML de, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R, White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann CP, Rosenberg C, Carvalho CMB. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 1-5.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.38315
Vancouver
Jehee FS, Oliveira VT de, Gurgel Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, Freitas ML de, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R, White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann CP, Rosenberg C, Carvalho CMB. Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 1-5.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.38315
Artigo de periodico
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability (2016)
Figueiredo, T; Melo, US ; Pessoa, ALS; Nóbrega, P. R; Kitajima, JP; Rusch, H; Vaz, F; Lucato, LT; Zatz, Mayana ; Kok, F ; Santos, S
Fonte: Molecular Psychiatry. Unidades: IB, FM
Assuntos: PESSOAS COM DEFICIÊNCIA INTELECTUAL, MUTAÇÃO GENÉTICA, QUOCIENTE DE INTELIGÊNCIA, GENÉTICA, NEUROPSIQUIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIGUEIREDO, T et al. A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability. Molecular Psychiatry, v. 21, p. 1125-1129, 2016Tradução . . Disponível em: https://doi.org/10.1038/mp.2015.150. Acesso em: 15 nov. 2024.
APA
Figueiredo, T., Melo, U. S., Pessoa, A. L. S., Nóbrega, P. R., Kitajima, J. P., Rusch, H., et al. (2016). A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability. Molecular Psychiatry, 21, 1125-1129. doi:10.1038/mp.2015.150
NLM
Figueiredo T, Melo US, Pessoa ALS, Nóbrega PR, Kitajima JP, Rusch H, Vaz F, Lucato LT, Zatz M, Kok F, Santos S. A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability [Internet]. Molecular Psychiatry. 2016 ; 21 1125-1129.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/mp.2015.150
Vancouver
Figueiredo T, Melo US, Pessoa ALS, Nóbrega PR, Kitajima JP, Rusch H, Vaz F, Lucato LT, Zatz M, Kok F, Santos S. A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability [Internet]. Molecular Psychiatry. 2016 ; 21 1125-1129.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/mp.2015.150
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
Fonte: European Journal of Human Genetics. Unidades: HRAC, IB
Assuntos: ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy (2006)
Tonini, Maria Manuela O; Lemmers, Richard J.L.F; Pavanello, Rita C M; Cerqueira, Antonia M.P; Frants, Rune R; Maarel, Silvere M. van der ; Zatz, Mayana
Fonte: Human Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, BIOLOGIA CELULAR, MÚSCULOS, SANGUE, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, Maria Manuela O et al. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, v. 119, p. 23-28, 2006Tradução . . Disponível em: https://doi.org/10.1007/s00439-005-0100-2. Acesso em: 15 nov. 2024.
APA
Tonini, M. M. O., Lemmers, R. J. L. F., Pavanello, R. C. M., Cerqueira, A. M. P., Frants, R. R., Maarel, S. M. van der, & Zatz, M. (2006). Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, 119, 23-28. doi:10.1007/s00439-005-0100-2
NLM
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Vancouver
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Artigo de periodico
Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype (2004)
Tonini, M. M. O; Pavanello, R C M; Gurgel-Giannetti, J; Lemmers, R J; Maarel, S M van der; Frants, R R; Zatz, Mayana
Fonte: Journal of Medical Genetics. Unidade: IB
Assuntos: GENÉTICA MÉDICA, MALFORMAÇÕES, DOENÇAS MUSCULOSQUELÉTICAS, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, M. M. O et al. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Journal of Medical Genetics, v. 41, n. 2, 2004Tradução . . Disponível em: https://doi.org/10.1136/jmg.2003.010637. Acesso em: 15 nov. 2024.
APA
Tonini, M. M. O., Pavanello, R. C. M., Gurgel-Giannetti, J., Lemmers, R. J., Maarel, S. M. van der, Frants, R. R., & Zatz, M. (2004). Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Journal of Medical Genetics, 41( 2). doi:10.1136/jmg.2003.010637
NLM
Tonini MMO, Pavanello RCM, Gurgel-Giannetti J, Lemmers RJ, Maarel SM van der, Frants RR, Zatz M. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype [Internet]. Journal of Medical Genetics. 2004 ; 41( 2):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmg.2003.010637
Vancouver
Tonini MMO, Pavanello RCM, Gurgel-Giannetti J, Lemmers RJ, Maarel SM van der, Frants RR, Zatz M. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype [Internet]. Journal of Medical Genetics. 2004 ; 41( 2):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmg.2003.010637
Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Fonte: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 15 nov. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.10193

Unidades USP

ReP

Filtros

Unidades USP

Departamento

Autores

Autores USP

Ano de publicação

Assuntos

Título da fonte

Agência de fomento

Indexado em

Afiliação dos autores externos não normalizada

País das instituições de afiliação dos autores externos