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Artigo de periodico
Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts (2023)
Carvalho, Patrícia Conceição Gonzalez Dias; Hirata, Thiago Dominguez Crespo ; Alves, Leandro Yukio Mano ; Moscardini, Isabelle Franco; Nascimento, Ana Paula Barbosa do; Martins, André Guilherme Costa ; Sorgi, Sara; Harandi, Ali M; Ferreira, Daniela M ; Vianello, Eleonora ; Haks, Marielle C ; Ottenhoff, Tom H. M; Santoro, Francesco ; Murillo, Paola Martinez; Huttner, Angela; Siegrist, Claire Anne ; Medaglini, Donata ; Nakaya, Helder Takashi Imoto
Source: Frontiers in Immunology. Unidade: FCF
Subjects: GENÉTICA, VACINAÇÃO
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ABNT
CARVALHO, Patrícia Conceição Gonzalez Dias et al. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts. Frontiers in Immunology, v. 14, p. 1-10 art. 1259197, 2023Tradução . . Disponível em: https://dx.doi.org/10.3389/fimmu.2023.1259197. Acesso em: 06 nov. 2024.
APA
Carvalho, P. C. G. D., Hirata, T. D. C., Alves, L. Y. M., Moscardini, I. F., Nascimento, A. P. B. do, Martins, A. G. C., et al. (2023). Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts. Frontiers in Immunology, 14, 1-10 art. 1259197. doi:10.3389/fimmu.2023.1259197
NLM
Carvalho PCGD, Hirata TDC, Alves LYM, Moscardini IF, Nascimento APB do, Martins AGC, Sorgi S, Harandi AM, Ferreira DM, Vianello E, Haks MC, Ottenhoff THM, Santoro F, Murillo PM, Huttner A, Siegrist CA, Medaglini D, Nakaya HTI. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts [Internet]. Frontiers in Immunology. 2023 ; 14 1-10 art. 1259197.[citado 2024 nov. 06 ] Available from: https://dx.doi.org/10.3389/fimmu.2023.1259197
Vancouver
Carvalho PCGD, Hirata TDC, Alves LYM, Moscardini IF, Nascimento APB do, Martins AGC, Sorgi S, Harandi AM, Ferreira DM, Vianello E, Haks MC, Ottenhoff THM, Santoro F, Murillo PM, Huttner A, Siegrist CA, Medaglini D, Nakaya HTI. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts [Internet]. Frontiers in Immunology. 2023 ; 14 1-10 art. 1259197.[citado 2024 nov. 06 ] Available from: https://dx.doi.org/10.3389/fimmu.2023.1259197
Artigo de periodico-carta/editorial
Editorial: DNA repair and immune response (2022)
Basso, Paulo José ; Rocha, Clarissa Ribeiro Reily ; Biessen, Erik A. L. ; Pluijm, Ingrid Van der ; Menck, Carlos Frederico Martins ; Câmara, Niels Olsen Saraiva
Source: Frontiers in Immunology. Unidade: ICB
Subjects: MICROBIOLOGIA, IMUNOLOGIA, REPARAÇÃO DE DNA, GENÉTICA
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ABNT
BASSO, Paulo José et al. Editorial: DNA repair and immune response. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.3389/fimmu.2022.1034689. Acesso em: 06 nov. 2024. , 2022
APA
Basso, P. J., Rocha, C. R. R., Biessen, E. A. L., Pluijm, I. V. der, Menck, C. F. M., & Câmara, N. O. S. (2022). Editorial: DNA repair and immune response. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.3389/fimmu.2022.1034689
NLM
Basso PJ, Rocha CRR, Biessen EAL, Pluijm IV der, Menck CFM, Câmara NOS. Editorial: DNA repair and immune response [Internet]. Frontiers in Immunology. 2022 ; 13 1-4.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3389/fimmu.2022.1034689
Vancouver
Basso PJ, Rocha CRR, Biessen EAL, Pluijm IV der, Menck CFM, Câmara NOS. Editorial: DNA repair and immune response [Internet]. Frontiers in Immunology. 2022 ; 13 1-4.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3389/fimmu.2022.1034689
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
Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
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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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
Ethics of DNA research on human remains: five globally applicable guidelines (2021)
Alpaslan-Roodenberg, Songül; Anthony, David; Babiker, Hiba; Bánffy, Eszter Bánffy; Booth, Thomas; Capone, Patricia; Deshpande-Mukherjee, Arati; Eisenmann, Stefanie; Fehren-Schmitz, Lars; Frachetti, Michael; Fujita, Ricardo; Frieman, Catherine J; Fu, Qiaomei; Gibbon, Victoria; Haak, Wolfgang; Hajdinjak, Mateja; Hofmann, Kerstin P; Holguin, Brian; Inomata, Takeshi; Kanzawa-Kiriyama, Hideaki; Keegan, William; Kelso, Janet; Krause, Johannes; Kumaresan, Ganesan; Kusimba, Chapurukha; Kusimba, Sibel; Lalueza-Fox, Carles; Llamas, Bastien; MacEachern, Scott; Mallick, Swapan; Matsumura, Hirofumi; Morales-Arce, Ana Y; Matuzeviciute, Giedre Motuzaite; Mushrif-Tripathy, Veena; Nakatsuka, Nathan; Nores, Rodrigo; Ogola, Christine; Okumura, Mercedes ; Patterson, Nick; Pinhasi, Ron; Prasad, Samayamantri P. R; Prendergast, Mary E; Punzo, Jose Luis; Reich, David; Sawafuji, Rikai; Sawchuk, Elizabeth; Schiffels, Stephan; Sedig, Jakob; Shnaider, Svetlana; Sirak, Kendra; Skoglund, Pontus; Slon, Viviane; Snow, Meradeth; Soressi, Marie; Spriggs, Matthew; Stockhammer, Philipp W; Szécsényi-Nagy, Anna; Thangaraj, Kumarasamy; Tiesler, Vera; Tobler, Ray; Wang, Chuan-Chao; Warinner, Christina; Yasawardene, Surangi; Zahir, Muhammad
Source: Nature. Unidade: IB
Subjects: CIÊNCIA, ANTROPOLOGIA BIOLÓGICA, ARQUEOLOGIA, GENÉTICA, DNA
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ABNT
ALPASLAN-ROODENBERG, Songül et al. Ethics of DNA research on human remains: five globally applicable guidelines. Nature, v. No 2021, p. 41-45, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41586-021-04008-x. Acesso em: 06 nov. 2024.
APA
Alpaslan-Roodenberg, S., Anthony, D., Babiker, H., Bánffy, E. B., Booth, T., Capone, P., et al. (2021). Ethics of DNA research on human remains: five globally applicable guidelines. Nature, No 2021, 41-45. doi:10.1038/s41586-021-04008-x
NLM
Alpaslan-Roodenberg S, Anthony D, Babiker H, Bánffy EB, Booth T, Capone P, Deshpande-Mukherjee A, Eisenmann S, Fehren-Schmitz L, Frachetti M, Fujita R, Frieman CJ, Fu Q, Gibbon V, Haak W, Hajdinjak M, Hofmann KP, Holguin B, Inomata T, Kanzawa-Kiriyama H, Keegan W, Kelso J, Krause J, Kumaresan G, Kusimba C, Kusimba S, Lalueza-Fox C, Llamas B, MacEachern S, Mallick S, Matsumura H, Morales-Arce AY, Matuzeviciute GM, Mushrif-Tripathy V, Nakatsuka N, Nores R, Ogola C, Okumura M, Patterson N, Pinhasi R, Prasad SPR, Prendergast ME, Punzo JL, Reich D, Sawafuji R, Sawchuk E, Schiffels S, Sedig J, Shnaider S, Sirak K, Skoglund P, Slon V, Snow M, Soressi M, Spriggs M, Stockhammer PW, Szécsényi-Nagy A, Thangaraj K, Tiesler V, Tobler R, Wang C-C, Warinner C, Yasawardene S, Zahir M. Ethics of DNA research on human remains: five globally applicable guidelines [Internet]. Nature. 2021 ; No 2021 41-45.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41586-021-04008-x
Vancouver
Alpaslan-Roodenberg S, Anthony D, Babiker H, Bánffy EB, Booth T, Capone P, Deshpande-Mukherjee A, Eisenmann S, Fehren-Schmitz L, Frachetti M, Fujita R, Frieman CJ, Fu Q, Gibbon V, Haak W, Hajdinjak M, Hofmann KP, Holguin B, Inomata T, Kanzawa-Kiriyama H, Keegan W, Kelso J, Krause J, Kumaresan G, Kusimba C, Kusimba S, Lalueza-Fox C, Llamas B, MacEachern S, Mallick S, Matsumura H, Morales-Arce AY, Matuzeviciute GM, Mushrif-Tripathy V, Nakatsuka N, Nores R, Ogola C, Okumura M, Patterson N, Pinhasi R, Prasad SPR, Prendergast ME, Punzo JL, Reich D, Sawafuji R, Sawchuk E, Schiffels S, Sedig J, Shnaider S, Sirak K, Skoglund P, Slon V, Snow M, Soressi M, Spriggs M, Stockhammer PW, Szécsényi-Nagy A, Thangaraj K, Tiesler V, Tobler R, Wang C-C, Warinner C, Yasawardene S, Zahir M. Ethics of DNA research on human remains: five globally applicable guidelines [Internet]. Nature. 2021 ; No 2021 41-45.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41586-021-04008-x
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
Source: Journal of Medical Genetics. Unidades: IB, BIOINFORMÁTICA
Subjects: GENÉTICA, DOENÇAS GENÉTICAS, FENÓTIPOS, MALFORMAÇÕES, VARIAÇÃO GENÉTICA, ANORMALIDADES CRANIOFACIAIS
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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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
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
Source: Science Advances. Unidade: IB
Subjects: PELE, GENOMAS, GENEALOGIA, GENÉTICA
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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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1126/sciadv.abc6160
Artigo de periodico
Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome (2019)
Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Souza, Rosana Maria Candido ; Monteiro, Rejane Alves de Carvalho; Tonello, Cristiano; Freitas, Mariana L. de; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Mazzeu, Juliana F; Overes, Madelief; Ali-Amin, Roza; van Slegtenhorst, Marjon; Hoefsloot, Lies H; Jehee, Fernanda S
Source: American Journal of Medical Genetics. Unidades: HRAC, HRACF
Subjects: GENÉTICA, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
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ABNT
RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 06 nov. 2024.
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305
NLM
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Trabalho de evento-resumo periodico
Investigation of ubiquitin-ligase huwe1 in the modulation of ras pathway in leukaemia models (2018)
Ruckert, Mariana Tannús; Brouwers-Vos, A.; Tone, Luiz Gonzaga; Schuringa, J. J.; Silveira, Vanessa da Silva
Source: ESMO Open. Conference titles: Biennial Congress of the European Association for Cancer Research. Unidade: FMRP
Subjects: GENÉTICA, LEUCEMIA
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ABNT
RUCKERT, Mariana Tannús et al. Investigation of ubiquitin-ligase huwe1 in the modulation of ras pathway in leukaemia models. ESMO Open. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1136/esmoopen-2018-eacr25.682. Acesso em: 06 nov. 2024. , 2018
APA
Ruckert, M. T., Brouwers-Vos, A., Tone, L. G., Schuringa, J. J., & Silveira, V. da S. (2018). Investigation of ubiquitin-ligase huwe1 in the modulation of ras pathway in leukaemia models. ESMO Open. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1136/esmoopen-2018-eacr25.682
NLM
Ruckert MT, Brouwers-Vos A, Tone LG, Schuringa JJ, Silveira V da S. Investigation of ubiquitin-ligase huwe1 in the modulation of ras pathway in leukaemia models [Internet]. ESMO Open. 2018 ; 3 A289.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1136/esmoopen-2018-eacr25.682
Vancouver
Ruckert MT, Brouwers-Vos A, Tone LG, Schuringa JJ, Silveira V da S. Investigation of ubiquitin-ligase huwe1 in the modulation of ras pathway in leukaemia models [Internet]. ESMO Open. 2018 ; 3 A289.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1136/esmoopen-2018-eacr25.682
Trabalho de evento-resumo periodico
Effects of ubiquitin ligase HUWE1 on metabolic imbalances in leukemic cells (2017)
Ruckert, M.; Brouwers-Vos, A.; Tone, Luiz Gonzaga; Schuringa, J. J.; Silveira, Vanessa da Silva
Source: Pediatric Blood and Cancer. Conference titles: Congress of the International Society of Paediatric Oncology (SIOP). Unidade: FMRP
Subjects: LEUCEMIA, CARCINOGÊNESE, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RUCKERT, M. et al. Effects of ubiquitin ligase HUWE1 on metabolic imbalances in leukemic cells. Pediatric Blood and Cancer. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/pbc.26772. Acesso em: 06 nov. 2024. , 2017
APA
Ruckert, M., Brouwers-Vos, A., Tone, L. G., Schuringa, J. J., & Silveira, V. da S. (2017). Effects of ubiquitin ligase HUWE1 on metabolic imbalances in leukemic cells. Pediatric Blood and Cancer. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1002/pbc.26772
NLM
Ruckert M, Brouwers-Vos A, Tone LG, Schuringa JJ, Silveira V da S. Effects of ubiquitin ligase HUWE1 on metabolic imbalances in leukemic cells [Internet]. Pediatric Blood and Cancer. 2017 ; 64 S187.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/pbc.26772
Vancouver
Ruckert M, Brouwers-Vos A, Tone LG, Schuringa JJ, Silveira V da S. Effects of ubiquitin ligase HUWE1 on metabolic imbalances in leukemic cells [Internet]. Pediatric Blood and Cancer. 2017 ; 64 S187.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/pbc.26772
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
Source: Molecular Psychiatry. Unidades: IB, FM
Subjects: 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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1038/mp.2015.150
Artigo de periodico
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery (2016)
Scott, Eric M.; Halees, A.; Itan, Y.; Spencer, E. G.; He,Y.; Azab, M. A.; Gabriel, S. B.; Belkadi, A.; Boisson, B.; Abel, L.; Clark, A. G.; Consortium, Greater Middle East Variome; Alkuraya, F. S.; Casanova, J. L.; Gleeson, J. G.; Rahim, S. A.; Abdel-Hadi, S.; Abdel-Salam, G.; Abdel-Salam, E.; Abdou, M.; Abhytankar, A.; Adimi, P.; Ahmad, J.; Akcakus, M.; Aksu, G.; Hajjar, S. A.; Juamaah, S. A.; Muhsen, S. A.; Sannaa, N. A.; Tameni, S. A.; Al-Aama, J.; Al-Allawi, N.; Al-Baradie, R.; Al-Gazali, L.; Al-Hashem, A.; Al-Herz, W.; Al-Jeaid, D.; Al-Tawari, A.; Alangari, A.; Alcais, A.; AlFawaz, T.; Alsum, Z.; Ammar-Khodja, A.; Amouian, S.; Ammar-Khodja, A.; Arikan, C.; Aryani, O.; Aslanger, A.; Aydogmus, C.; Aytekin, C.; Azam, M.; Bansagi, B.; Barbouche, M. R.; Bastaki, L.; Ben-Omran, T.; Bindu, P. S.; Blancas, L.; Boisson-Dupuis, S.; Bonnet, D.; Stambouli, O. B.; Bousfiha, A.; Boussafara, L.; Boutros, J.; Bustamante, J.; Caksen, H.; Camcioglu, Y.; Catherinot, E.; Celik, F. C.; Ciancanelli, M.; Cipe, F. E.; Clark, G.; Cobat, A.; Comu, S.; Condie, A.; Condino-Neto, A.; Desai, M.; Dobyns, W.; Dogu, F.; Domaia, M.; Egritas, O.; Azbaoui, S. E.; Baghdadi, J. E.; Ruby, M. E.; El-Harouni, A.; Elfeky,R. A.; Elghazali, G.; Faqeih, E.; Fenerci, E.; Fieschi, C.; Funda, C.; Gamal, I.; Gelik, U.; Genel, F.; Gezdirici, A.; Girisha, K. M.; Goldstein, A.; Grattan-Smith, P.; Gupta, N.; Hahn, J.; Hatipoglu, N.; Hennekam, R.; Houshmand, M.; Ichai, P.; Ikinciogullari, A.; Ismail, S.; Jalas, C.; Jouanguy, E.; Kabra, M.; Kalkan, G.; Kara, M.; Karaca, N.; Karaer, K.; Kariminejad, A.; Kayserili, H.; Keser-Emiroglu, M.; Kilic, S. S.; Kissani, N.; Kokron, C.; Koul, R.; Kutukculer, N.; Lanternier, F.; Mahdaviani, A.; Mahlaoui, N.; Mansour, L.; Mansouri, D.; Margari, L.; Valente, E. M.; Marzouki, N.; Masri, A.; Megahed, A.; Megahed, H.; Mekki, N.; Mesdaghi, M.; Mikati, M.; Mojahedi, F.; Mulley, J.; Nampoothiri, S.; Navarrete, C.; Omar, T.; Oraby, A.; Pandaluz, A.; Parvaneh, N.; Patiroglu, T.; Koc, Z. P.; Pellier, I.; Picard, C.; Puel, A.; Raas-Rothschild, A.; Rajab, A.; Raoult, D.; Reisli, I.; Rezaei, N.; Sabri, A.; Sahin, Y.; Saleem, L.; Salem, F.; AlSediq, N. S.; Sanal, O.; Sanger, T.; Shakankiry, H.; Shang, L.; Shehata, N.; Shembesh, N.; Shkalim, V.; Softah, A.; Sogaty, S.; Soliman, N.; Sonmez Aunaci, F.; Sztriha, L.; Taibi-Berrah, L.; Temtamy, S.; Tonekaboni, H.; Trauner, D.; Tuysuz, B.; Varan, A.; Vogt, G.; Walsh, C.; Woods, G.; Yesil, G.; Yildiran, A.; Yildiz, B.; Yuksel, A.; Zaki, M.; Zhang, S. Y.
Source: Nature Genetics. Unidade: ICB
Subjects: VARIAÇÃO GENÉTICA, GENÉTICA, GENÉTICA DE POPULAÇÕES, IMUNOLOGIA, ALELOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCOTT, Eric M. et al. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, v. 48, n. 9, p. 1071-1076, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3592. Acesso em: 06 nov. 2024.
APA
Scott, E. M., Halees, A., Itan, Y., Spencer, E. G., He, Y., Azab, M. A., et al. (2016). Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, 48( 9), 1071-1076. doi:10.1038/ng.3592
NLM
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/ng.3592
Vancouver
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/ng.3592

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