ReP USP - Resultado da busca

Artigo de periodico
The complete mitochondrial genome of Trigonisca nataliae (Hymenoptera, Apidae) assemblage reveals heteroplasmy in the control region (2023)
Françoso, Elaine ; Zuntini, Alexandre Rizzo; Ricardo, Paulo Cseri ; Araujo, Natalia de Souza; Silva, João Paulo Naldi ; Brown, Mark J. F; Arias, Maria Cristina
Source: Gene. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, APIDAE, HYMENOPTERA, ABELHAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANÇOSO, Elaine et al. The complete mitochondrial genome of Trigonisca nataliae (Hymenoptera, Apidae) assemblage reveals heteroplasmy in the control region. Gene, v. 881, p. Se 2023, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147621. Acesso em: 04 jul. 2024.
APA
Françoso, E., Zuntini, A. R., Ricardo, P. C., Araujo, N. de S., Silva, J. P. N., Brown, M. J. F., & Arias, M. C. (2023). The complete mitochondrial genome of Trigonisca nataliae (Hymenoptera, Apidae) assemblage reveals heteroplasmy in the control region. Gene, 881, Se 2023. doi:10.1016/j.gene.2023.147621
NLM
Françoso E, Zuntini AR, Ricardo PC, Araujo N de S, Silva JPN, Brown MJF, Arias MC. The complete mitochondrial genome of Trigonisca nataliae (Hymenoptera, Apidae) assemblage reveals heteroplasmy in the control region [Internet]. Gene. 2023 ; 881 Se 2023.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.gene.2023.147621
Vancouver
Françoso E, Zuntini AR, Ricardo PC, Araujo N de S, Silva JPN, Brown MJF, Arias MC. The complete mitochondrial genome of Trigonisca nataliae (Hymenoptera, Apidae) assemblage reveals heteroplasmy in the control region [Internet]. Gene. 2023 ; 881 Se 2023.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.gene.2023.147621
Artigo de periodico
Health-related quality of life and associated factors: regional differences among oldest-old in Brazil (2022)
Freitas, Javanna L. G. da S; Silva, Jaíza M. M; Nóbrega, Júlia Cristina L; Simões, Raisa F. M; Medeiros, Juliana B; Alves, Ricardo O; Santos, Jair L. F; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Menezes, Tarciana N. de; Santos, Silvana
Source: Inquiry. Unidades: FMRP, EE, IB
Subjects: QUALIDADE DE VIDA, IDOSOS, LONGEVIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, Javanna L. G. da S et al. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil. Inquiry, v. 59, 2022Tradução . . Disponível em: https://doi.org/10.1177/00469580221086922. Acesso em: 04 jul. 2024.
APA
Freitas, J. L. G. da S., Silva, J. M. M., Nóbrega, J. C. L., Simões, R. F. M., Medeiros, J. B., Alves, R. O., et al. (2022). Health-related quality of life and associated factors: regional differences among oldest-old in Brazil. Inquiry, 59. doi:10.1177/00469580221086922
NLM
Freitas JLG da S, Silva JMM, Nóbrega JCL, Simões RFM, Medeiros JB, Alves RO, Santos JLF, Duarte YA de O, Zatz M, Matheson D, Menezes TN de, Santos S. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil [Internet]. Inquiry. 2022 ; 59[citado 2024 jul. 04 ] Available from: https://doi.org/10.1177/00469580221086922
Vancouver
Freitas JLG da S, Silva JMM, Nóbrega JCL, Simões RFM, Medeiros JB, Alves RO, Santos JLF, Duarte YA de O, Zatz M, Matheson D, Menezes TN de, Santos S. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil [Internet]. Inquiry. 2022 ; 59[citado 2024 jul. 04 ] Available from: https://doi.org/10.1177/00469580221086922
Artigo de periodico
Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study (2022)
Nóbrega, Júlia Cristina Leite; Medeiros, Juliana Barbosa; Freitas, Javanna Lacerda Gomes da Silva; Silva, Jaíza M. M; Simões, Raisa Fernandes Mariz; Olinda, Ricardo; Santos, Jair Licio Ferreira ; Menezes, Tarciana Nobre; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Santos, Silvana
Source: BMC Geriatrics. Unidades: FMRP, EE, IB
Subjects: IDOSOS, LONGEVIDADE, MORTALIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NÓBREGA, Júlia Cristina Leite et al. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study. BMC Geriatrics, v. 22, 2022Tradução . . Disponível em: https://doi.org/10.1186/s12877-022-02810-4. Acesso em: 04 jul. 2024.
APA
Nóbrega, J. C. L., Medeiros, J. B., Freitas, J. L. G. da S., Silva, J. M. M., Simões, R. F. M., Olinda, R., et al. (2022). Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study. BMC Geriatrics, 22. doi:10.1186/s12877-022-02810-4
NLM
Nóbrega JCL, Medeiros JB, Freitas JLG da S, Silva JMM, Simões RFM, Olinda R, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study [Internet]. BMC Geriatrics. 2022 ; 22[citado 2024 jul. 04 ] Available from: https://doi.org/10.1186/s12877-022-02810-4
Vancouver
Nóbrega JCL, Medeiros JB, Freitas JLG da S, Silva JMM, Simões RFM, Olinda R, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study [Internet]. BMC Geriatrics. 2022 ; 22[citado 2024 jul. 04 ] Available from: https://doi.org/10.1186/s12877-022-02810-4
Artigo de periodico
Disentangling Signatures of Selection Before and After European Colonization in Latin Americans (2022)
Mendoza-Revilla, Javier; Chacón-Duque, J. Camilo; Fuentes-Guajardo, Macarena; Ormond, Louise; Wang, Ke; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Acuña-Alonzo, Victor; Jaramillo, Claudia; Arias, William; Barquera, Rodrigo; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Cerqueira, Caio C. Silva de; Rivera, Keyla M. Badillo; Nieves-Colón, Maria A; Gignoux, Christopher R; Wojcik, Genevieve L; Moreno-Estrada, Andrés; Hünemeier, Tábita ; Ramallo, Virginia; Schuler-Faccini, Lavinia; Gonzalez-José, Rolando; Bortolini, Maria-Cátira; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Balding, David; Fumagalli, Matteo; Adhikari, Kaustubh; Ruiz-Linares, Andrés; Hellenthal, Garrett
Source: Molecular Biology and Evolution. Unidade: IB
Subjects: COLONIZAÇÃO, SELEÇÃO NATURAL, GENEALOGIA, DEMOGRAFIA, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDOZA-REVILLA, Javier et al. Disentangling Signatures of Selection Before and After European Colonization in Latin Americans. Molecular Biology and Evolution, v. 39, n. 4, 2022Tradução . . Disponível em: https://doi.org/10.1093/molbev/msac076. Acesso em: 04 jul. 2024.
APA
Mendoza-Revilla, J., Chacón-Duque, J. C., Fuentes-Guajardo, M., Ormond, L., Wang, K., Hurtado, M., et al. (2022). Disentangling Signatures of Selection Before and After European Colonization in Latin Americans. Molecular Biology and Evolution, 39( 4). doi:10.1093/molbev/msac076
NLM
Mendoza-Revilla J, Chacón-Duque JC, Fuentes-Guajardo M, Ormond L, Wang K, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Barquera R, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Rivera KMB, Nieves-Colón MA, Gignoux CR, Wojcik GL, Moreno-Estrada A, Hünemeier T, Ramallo V, Schuler-Faccini L, Gonzalez-José R, Bortolini M-C, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Fumagalli M, Adhikari K, Ruiz-Linares A, Hellenthal G. Disentangling Signatures of Selection Before and After European Colonization in Latin Americans [Internet]. Molecular Biology and Evolution. 2022 ; 39( 4):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1093/molbev/msac076
Vancouver
Mendoza-Revilla J, Chacón-Duque JC, Fuentes-Guajardo M, Ormond L, Wang K, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Barquera R, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Rivera KMB, Nieves-Colón MA, Gignoux CR, Wojcik GL, Moreno-Estrada A, Hünemeier T, Ramallo V, Schuler-Faccini L, Gonzalez-José R, Bortolini M-C, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Fumagalli M, Adhikari K, Ruiz-Linares A, Hellenthal G. Disentangling Signatures of Selection Before and After European Colonization in Latin Americans [Internet]. Molecular Biology and Evolution. 2022 ; 39( 4):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1093/molbev/msac076
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
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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
Challenging definitions and diagnostic approaches for ancient rare diseases: the case of poliomyelitis (2021)
Berner, Margit; Pany-Kucera, Doris; Doneus, Nives; Sladek, Vladimír; Gamble, Michelle; Eggers, Sabine
Source: International Journal of Paleopathology. Unidade: IB
Subjects: DOENÇAS RARAS, ANÁLISE MORFOLÓGICA, VÍRUS, ATROFIA MUSCULAR, BIOMECÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNER, Margit et al. Challenging definitions and diagnostic approaches for ancient rare diseases: the case of poliomyelitis. International Journal of Paleopathology, v. 33, n. Ju 2021, p. 113-127, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ijpp.2021.04.003. Acesso em: 04 jul. 2024.
APA
Berner, M., Pany-Kucera, D., Doneus, N., Sladek, V., Gamble, M., & Eggers, S. (2021). Challenging definitions and diagnostic approaches for ancient rare diseases: the case of poliomyelitis. International Journal of Paleopathology, 33( Ju 2021), 113-127. doi:10.1016/j.ijpp.2021.04.003
NLM
Berner M, Pany-Kucera D, Doneus N, Sladek V, Gamble M, Eggers S. Challenging definitions and diagnostic approaches for ancient rare diseases: the case of poliomyelitis [Internet]. International Journal of Paleopathology. 2021 ; 33( Ju 2021): 113-127.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.ijpp.2021.04.003
Vancouver
Berner M, Pany-Kucera D, Doneus N, Sladek V, Gamble M, Eggers S. Challenging definitions and diagnostic approaches for ancient rare diseases: the case of poliomyelitis [Internet]. International Journal of Paleopathology. 2021 ; 33( Ju 2021): 113-127.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.ijpp.2021.04.003
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1038/s41586-021-04008-x
Artigo de periodico
Insights from the genetic characterization of central precocious puberty associated with multiple anomalies (2021)
Canton, Ana Pinheiro Machado ; Krepischi, Ana Cristina Victorino ; Montenegro, Luciana Ribeiro; Costa, Silvia; Rosenberg, Carla ; Steunou, Virginie; Sobrier, Marie-Laure; Santana, Lucas ; Honjo, Rachel Sayuri ; Kim, Chong Ae ; Francis de Zegher; Idkowiak, Jan; Gilligan, Lorna C; Arlt, Wiebke; Funari, Mariana Ferreira de Assis ; Jorge, Alexander Augusto de Lima ; Mendonca, Berenice Bilharinho de ; Netchine, Irène; Brito, Vinicius Nahime ; Latronico, Ana Claudia
Source: Human Reproduction. Unidades: IB, FM
Subjects: PUBERDADE PRECOCE, GENÉTICA, DOENÇAS GENÉTICAS, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CANTON, Ana Pinheiro Machado et al. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, v. 36, n. 2, p. 506-518, 2021Tradução . . Disponível em: https://doi.org/10.1093/humrep/deaa306. Acesso em: 04 jul. 2024.
APA
Canton, A. P. M., Krepischi, A. C. V., Montenegro, L. R., Costa, S., Rosenberg, C., Steunou, V., et al. (2021). Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, 36( 2), 506-518. doi:10.1093/humrep/deaa306
NLM
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1093/humrep/deaa306
Vancouver
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1093/humrep/deaa306
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
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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Artigo de periodico
Prediction of eye, hair and skin colour in Latin Americans (2021)
Palmal, Sagnik; Adhikari, Kaustubh; Mendoza-Revilla, Javier; Fuentes-Guajardo, Macarena; Cerqueira, Caio Cesar Silva de; Bonfant, Betty; Chacón-Duque, Juan Camilo; Sohail, Anood; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Jaramillo, Claudia; Arias, William; Lozano, Rodrigo Barquera; Everardo-Martínez, Paola; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Hünemeier, Tábita ; Ramallo, Virginia; Parolin, Maria-Laura; Gonzalez-José, Rolando; Schüler-Faccini, Lavinia; Bortolini, Maria-Cátira; Acuña-Alonzo, Victor; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Balding, David; Faux, Pierre; Ruiz-Linares, Andrés
Source: Forensic Science International: Genetics. Unidade: IB
Subjects: MISCIGENAÇÃO, PELE, OLHO, CABELO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALMAL, Sagnik et al. Prediction of eye, hair and skin colour in Latin Americans. Forensic Science International: Genetics, v. 53, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.fsigen.2021.102517. Acesso em: 04 jul. 2024.
APA
Palmal, S., Adhikari, K., Mendoza-Revilla, J., Fuentes-Guajardo, M., Cerqueira, C. C. S. de, Bonfant, B., et al. (2021). Prediction of eye, hair and skin colour in Latin Americans. Forensic Science International: Genetics, 53. doi:10.1016/j.fsigen.2021.102517
NLM
Palmal S, Adhikari K, Mendoza-Revilla J, Fuentes-Guajardo M, Cerqueira CCS de, Bonfant B, Chacón-Duque JC, Sohail A, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Lozano RB, Everardo-Martínez P, Gómez-Valdés J, Villamil-Ramírez H, Hünemeier T, Ramallo V, Parolin M-L, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Faux P, Ruiz-Linares A. Prediction of eye, hair and skin colour in Latin Americans [Internet]. Forensic Science International: Genetics. 2021 ; 53[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102517
Vancouver
Palmal S, Adhikari K, Mendoza-Revilla J, Fuentes-Guajardo M, Cerqueira CCS de, Bonfant B, Chacón-Duque JC, Sohail A, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Lozano RB, Everardo-Martínez P, Gómez-Valdés J, Villamil-Ramírez H, Hünemeier T, Ramallo V, Parolin M-L, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Faux P, Ruiz-Linares A. Prediction of eye, hair and skin colour in Latin Americans [Internet]. Forensic Science International: Genetics. 2021 ; 53[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102517
Artigo de periodico
Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study (2021)
Nóbrega, Júlia Cristina Leite; Medeiros, Juliana Barbosa; Santos, Tácila Thamires de Melo; Alves, Saionara Açucena Vieira; Freitas, Javanna Lacerda Gomes da Silva; Silva , Jaíza M. M; Simões, Raisa Fernandes Mariz; Brito, Allisson de Lima ; Weller, Mathias; Santos, Jair Licio Ferreira ; Menezes, Tarciana Nobre; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Santos, Silvana
Source: Inquiry. Unidades: FMRP, EE, IB
Subjects: ENVELHECIMENTO, CAPACIDADE FUNCIONAL, SAÚDE DO IDOSO, DOENÇA CRÔNICA, DESIGUALDADES SOCIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NÓBREGA, Júlia Cristina Leite et al. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study. Inquiry, v. 58, 2021Tradução . . Disponível em: https://doi.org/10.1177/00469580211007264. Acesso em: 04 jul. 2024.
APA
Nóbrega, J. C. L., Medeiros, J. B., Santos, T. T. de M., Alves, S. A. V., Freitas, J. L. G. da S., Silva , J. M. M., et al. (2021). Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study. Inquiry, 58. doi:10.1177/00469580211007264
NLM
Nóbrega JCL, Medeiros JB, Santos TT de M, Alves SAV, Freitas JLG da S, Silva JMM, Simões RFM, Brito A de L, Weller M, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study [Internet]. Inquiry. 2021 ; 58[citado 2024 jul. 04 ] Available from: https://doi.org/10.1177/00469580211007264
Vancouver
Nóbrega JCL, Medeiros JB, Santos TT de M, Alves SAV, Freitas JLG da S, Silva JMM, Simões RFM, Brito A de L, Weller M, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study [Internet]. Inquiry. 2021 ; 58[citado 2024 jul. 04 ] Available from: https://doi.org/10.1177/00469580211007264
Artigo de periodico
HLA-G genetic diversity and evolutive aspects in worldwide populations (2021)
Castelli, Erick C ; Almeida, Bibiana S. de; Muniz , Yara C. N; Silva, Nayane S. B; Passos, Marília R. S; Souza, Andreia S; Page, Abigail E; Dyble, Mark; Smith, Daniel; Aguileta, Gabriela; Bertranpetit, Jaume; Migliano, Andrea B; Duarte, Yeda Aparecida de Oliveira ; Scliar, Marília O; Wang, Jaqueline; Passos-Bueno, Maria Rita ; Naslavsky, Michel ; Zatz, Mayana ; Mendes-Junior, Celso Teixeira; Donadi, Eduardo A
Source: Scientific Reports. Unidades: EE, BIOINFORMÁTICA, IB, FFCLRP, FMRP
Subjects: GENÉTICA DE POPULAÇÕES, VARIAÇÃO GENÉTICA, DIVERSIDADE GENÉTICA, ANTÍGENOS HLA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTELLI, Erick C et al. HLA-G genetic diversity and evolutive aspects in worldwide populations. Scientific Reports, v. 11, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-02106-4. Acesso em: 04 jul. 2024.
APA
Castelli, E. C., Almeida, B. S. de, Muniz , Y. C. N., Silva, N. S. B., Passos, M. R. S., Souza, A. S., et al. (2021). HLA-G genetic diversity and evolutive aspects in worldwide populations. Scientific Reports, 11. doi:10.1038/s41598-021-02106-4
NLM
Castelli EC, Almeida BS de, Muniz YCN, Silva NSB, Passos MRS, Souza AS, Page AE, Dyble M, Smith D, Aguileta G, Bertranpetit J, Migliano AB, Duarte YA de O, Scliar MO, Wang J, Passos-Bueno MR, Naslavsky M, Zatz M, Mendes-Junior CT, Donadi EA. HLA-G genetic diversity and evolutive aspects in worldwide populations [Internet]. Scientific Reports. 2021 ; 11[citado 2024 jul. 04 ] Available from: https://doi.org/10.1038/s41598-021-02106-4
Vancouver
Castelli EC, Almeida BS de, Muniz YCN, Silva NSB, Passos MRS, Souza AS, Page AE, Dyble M, Smith D, Aguileta G, Bertranpetit J, Migliano AB, Duarte YA de O, Scliar MO, Wang J, Passos-Bueno MR, Naslavsky M, Zatz M, Mendes-Junior CT, Donadi EA. HLA-G genetic diversity and evolutive aspects in worldwide populations [Internet]. Scientific Reports. 2021 ; 11[citado 2024 jul. 04 ] Available from: https://doi.org/10.1038/s41598-021-02106-4
Artigo de periodico
An in vitro stem cell model of human epiblast and yolk sac interaction (2021)
Mackinlay, Kirsty ML; Weatherbee, Bailey AT; Rosa, Viviane Souza; Handford, Charlotte E; Hudson, George; Coorens, Tim; Pereira, Lygia da Veiga ; Behjati, Sam; Vallier, Ludovic; Shahbazi, Marta N; Zernicka-Goetz, Magdalena
Source: eLife. Unidade: IB
Subjects: CÉLULAS-TRONCO, FERTILIZAÇÃO "IN VITRO", EMBRIOGÊNESE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACKINLAY, Kirsty ML et al. An in vitro stem cell model of human epiblast and yolk sac interaction. eLife, v. 10, 2021Tradução . . Disponível em: https://doi.org/10.7554/eLife.63930. Acesso em: 04 jul. 2024.
APA
Mackinlay, K. M. L., Weatherbee, B. A. T., Rosa, V. S., Handford, C. E., Hudson, G., Coorens, T., et al. (2021). An in vitro stem cell model of human epiblast and yolk sac interaction. eLife, 10. doi:10.7554/eLife.63930
NLM
Mackinlay KML, Weatherbee BAT, Rosa VS, Handford CE, Hudson G, Coorens T, Pereira L da V, Behjati S, Vallier L, Shahbazi MN, Zernicka-Goetz M. An in vitro stem cell model of human epiblast and yolk sac interaction [Internet]. eLife. 2021 ; 10[citado 2024 jul. 04 ] Available from: https://doi.org/10.7554/eLife.63930
Vancouver
Mackinlay KML, Weatherbee BAT, Rosa VS, Handford CE, Hudson G, Coorens T, Pereira L da V, Behjati S, Vallier L, Shahbazi MN, Zernicka-Goetz M. An in vitro stem cell model of human epiblast and yolk sac interaction [Internet]. eLife. 2021 ; 10[citado 2024 jul. 04 ] Available from: https://doi.org/10.7554/eLife.63930
Artigo de periodico
Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders (2021)
Calpena, Eduardo; Wurmser, Maud; McGowan, Simon J; Atique, Rodrigo; Bertola, Débora R; Cunningham , Michael L; Gustafson, Jonas A; Johnson, David; Morton, Jenny E. V; Passos-Bueno, Maria Rita ; Timberlake, Andre T; Lifton, Richa P; Wall, Steven A; Twigg, Stephen R. F; Maire, Pascal; Wilkie, Andrew O. M
Source: Journal of Medical Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS, DOENÇAS CONGÊNITAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALPENA, Eduardo et al. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2020-107459. Acesso em: 04 jul. 2024.
APA
Calpena, E., Wurmser, M., McGowan, S. J., Atique, R., Bertola, D. R., Cunningham , M. L., et al. (2021). Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of Medical Genetics. doi:10.1136/jmedgenet-2020-107459
NLM
Calpena E, Wurmser M, McGowan SJ, Atique R, Bertola DR, Cunningham ML, Gustafson JA, Johnson D, Morton JEV, Passos-Bueno MR, Timberlake AT, Lifton RP, Wall SA, Twigg SRF, Maire P, Wilkie AOM. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 jul. 04 ] Available from: https://doi.org/10.1136/jmedgenet-2020-107459
Vancouver
Calpena E, Wurmser M, McGowan SJ, Atique R, Bertola DR, Cunningham ML, Gustafson JA, Johnson D, Morton JEV, Passos-Bueno MR, Timberlake AT, Lifton RP, Wall SA, Twigg SRF, Maire P, Wilkie AOM. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 jul. 04 ] Available from: https://doi.org/10.1136/jmedgenet-2020-107459
Artigo de periodico
Evolutionary perspectives on bee mtDNA from mito-OMICS analyses of a solitary species (2020)
Françoso, Elaine; Araujo, Natalia de Souza; Ricardo, Paulo Cseri; Santos, Priscila Karla Ferreira; Zuntini, Alexandre Rizzo; Arias, Maria Cristina
Source: Apidologie. Unidade: IB
Subjects: GENOMAS, GENÉTICA DE POPULAÇÕES, ABELHAS, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANÇOSO, Elaine et al. Evolutionary perspectives on bee mtDNA from mito-OMICS analyses of a solitary species. Apidologie, v. 51, p. 531–544, 2020Tradução . . Disponível em: https://doi.org/10.1007/s13592-020-00740-x. Acesso em: 04 jul. 2024.
APA
Françoso, E., Araujo, N. de S., Ricardo, P. C., Santos, P. K. F., Zuntini, A. R., & Arias, M. C. (2020). Evolutionary perspectives on bee mtDNA from mito-OMICS analyses of a solitary species. Apidologie, 51, 531–544. doi:10.1007/s13592-020-00740-x
NLM
Françoso E, Araujo N de S, Ricardo PC, Santos PKF, Zuntini AR, Arias MC. Evolutionary perspectives on bee mtDNA from mito-OMICS analyses of a solitary species [Internet]. Apidologie. 2020 ; 51 531–544.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1007/s13592-020-00740-x
Vancouver
Françoso E, Araujo N de S, Ricardo PC, Santos PKF, Zuntini AR, Arias MC. Evolutionary perspectives on bee mtDNA from mito-OMICS analyses of a solitary species [Internet]. Apidologie. 2020 ; 51 531–544.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1007/s13592-020-00740-x
Artigo de periodico
Human auditory ossicles as an alternative optimal source of ancient DNA (2020)
Sirak, Kendra; Fernandes, Daniel; Cheronet, Olivia; Harney, Eadaoin; Mah, Matthew; Mallick , Swapan; Rohland , Nadin; Adamski , Nicole; Broomandkhoshbacht, Nasreen; Callan , Kimberly; Candilio , Francesca; Lawson, Ann Marie; Mandl, Kirsten; Oppenheimer, Jonas; Stewardson, Kristin; Zalzala, Fatma; Anders, Alexandra; Bartík, Juraj; Coppa, Alfredo; Dashtseveg, Tumen; Évinger, Sándor; Farkaš, Zdeněk; Hajdu, Tamás; Bayarsaikhan, Jamsranjav; McIntyre, Lauren; Moiseyev, Vyacheslav; Okumura, Mercedes ; Pap, Ildikó; Pietrusewsky, Michael; Raczky, Pál; Šefčáková, Alena; Soficaru, Andrei; Szeniczey, Tamás; Szőke, Béla Miklós; Gerven, Dennis Van; Vasilyev, Sergey; Bell, Lynne; Reich, David; Pinhasi, Ron
Source: Genome Research. Unidade: IB
Subjects: ARQUEOLOGIA, DNA, OSSOS FACIAIS, CRÂNIO, PALEONTOLOGIA HUMANA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIRAK, Kendra et al. Human auditory ossicles as an alternative optimal source of ancient DNA. Genome Research, v. 30, p. 427-436, 2020Tradução . . Disponível em: http://www.genome.org/cgi/doi/10.1101/gr.260141.119. Acesso em: 04 jul. 2024.
APA
Sirak, K., Fernandes, D., Cheronet, O., Harney, E., Mah, M., Mallick , S., et al. (2020). Human auditory ossicles as an alternative optimal source of ancient DNA. Genome Research, 30, 427-436. doi:10.1101/gr.260141.119
NLM
Sirak K, Fernandes D, Cheronet O, Harney E, Mah M, Mallick S, Rohland N, Adamski N, Broomandkhoshbacht N, Callan K, Candilio F, Lawson AM, Mandl K, Oppenheimer J, Stewardson K, Zalzala F, Anders A, Bartík J, Coppa A, Dashtseveg T, Évinger S, Farkaš Z, Hajdu T, Bayarsaikhan J, McIntyre L, Moiseyev V, Okumura M, Pap I, Pietrusewsky M, Raczky P, Šefčáková A, Soficaru A, Szeniczey T, Szőke BM, Gerven DV, Vasilyev S, Bell L, Reich D, Pinhasi R. Human auditory ossicles as an alternative optimal source of ancient DNA [Internet]. Genome Research. 2020 ; 30 427-436.[citado 2024 jul. 04 ] Available from: http://www.genome.org/cgi/doi/10.1101/gr.260141.119.
Vancouver
Sirak K, Fernandes D, Cheronet O, Harney E, Mah M, Mallick S, Rohland N, Adamski N, Broomandkhoshbacht N, Callan K, Candilio F, Lawson AM, Mandl K, Oppenheimer J, Stewardson K, Zalzala F, Anders A, Bartík J, Coppa A, Dashtseveg T, Évinger S, Farkaš Z, Hajdu T, Bayarsaikhan J, McIntyre L, Moiseyev V, Okumura M, Pap I, Pietrusewsky M, Raczky P, Šefčáková A, Soficaru A, Szeniczey T, Szőke BM, Gerven DV, Vasilyev S, Bell L, Reich D, Pinhasi R. Human auditory ossicles as an alternative optimal source of ancient DNA [Internet]. Genome Research. 2020 ; 30 427-436.[citado 2024 jul. 04 ] Available from: http://www.genome.org/cgi/doi/10.1101/gr.260141.119.
Artigo de periodico
Structural variation of the malaria-associated human glycophorin A-B-E region (2020)
Louzada, Sandra; Algady, Walid; Weyell, Eleanor; Zuccherato, Luciana W; Brajer, Paulina; Almalki, Faisal; Scliar, Marilia O; Naslavsky, Michel ; Yamamoto, Guilherme L; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana ; Yang, Fengtang; Hollox, Edward J
Source: BMC Genomics. Unidades: IB, EE
Subjects: VARIAÇÃO GENÉTICA, PLASMODIUM FALCIPARUM, MALÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOUZADA, Sandra et al. Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics, v. 21, n. artigo 446, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12864-020-06849-8. Acesso em: 04 jul. 2024.
APA
Louzada, S., Algady, W., Weyell, E., Zuccherato, L. W., Brajer, P., Almalki, F., et al. (2020). Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics, 21( artigo 446). doi:10.1186/s12864-020-06849-8
NLM
Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky M, Yamamoto GL, Duarte YA de O, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Structural variation of the malaria-associated human glycophorin A-B-E region [Internet]. BMC Genomics. 2020 ; 21( artigo 446):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1186/s12864-020-06849-8
Vancouver
Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky M, Yamamoto GL, Duarte YA de O, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Structural variation of the malaria-associated human glycophorin A-B-E region [Internet]. BMC Genomics. 2020 ; 21( artigo 446):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1186/s12864-020-06849-8
Artigo de periodico
A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia (2019)
Adhikari, Kaustubh; Mendoza-Revilla, Javier; Sohail, Anood; Fuentes-Guajardo, Macarena; Lampert, Jodie; Chacón-Duque, Juan-Camilo; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Acuña-Alonzo, Victor; Jaramillo, Claudia; Arias, William; Lozano, Rodrigo Barquera; Everardo, Paola; Gomez-Valdes, Jorge; Villamil-Ramírez, Hugo; Cerqueira, Caio C. Silva de; Hünemeier, Tábita ; Ramallo, Virginia; Schuler-Faccini, Lavinia; Salzano, Francisco M; González José, Rolando; Bortolini, Maria Cátira; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Tobin, Desmond J; Fumagalli, atteo; Balding, David; Ruiz-Linares, Andrés
Source: Nature Communicatios. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, PELE, PIGMENTOS, POLIMORFISMO, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ADHIKARI, Kaustubh et al. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Nature Communicatios, v. 10, n. Ja 2019, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41467-018-08147-0. Acesso em: 04 jul. 2024.
APA
Adhikari, K., Mendoza-Revilla, J., Sohail, A., Fuentes-Guajardo, M., Lampert, J., Chacón-Duque, J. -C., et al. (2019). A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Nature Communicatios, 10( Ja 2019). doi:10.1038/s41467-018-08147-0
NLM
Adhikari K, Mendoza-Revilla J, Sohail A, Fuentes-Guajardo M, Lampert J, Chacón-Duque J-C, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Lozano RB, Everardo P, Gomez-Valdes J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Schuler-Faccini L, Salzano FM, González José R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Tobin DJ, Fumagalli atteo, Balding D, Ruiz-Linares A. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia [Internet]. Nature Communicatios. 2019 ; 10( Ja 2019):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1038/s41467-018-08147-0
Vancouver
Adhikari K, Mendoza-Revilla J, Sohail A, Fuentes-Guajardo M, Lampert J, Chacón-Duque J-C, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Lozano RB, Everardo P, Gomez-Valdes J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Schuler-Faccini L, Salzano FM, González José R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Tobin DJ, Fumagalli atteo, Balding D, Ruiz-Linares A. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia [Internet]. Nature Communicatios. 2019 ; 10( Ja 2019):[citado 2024 jul. 04 ] Available from: https://doi.org/10.1038/s41467-018-08147-0
Artigo de periodico
Conserved numts mask a highly divergent mitochondrial-COI gene in a species complex of Australian stingless bees Tetragonula (Hymenoptera: Apidae) (2019)
Françoso, Elaine ; Zuntini, Alexandre Rizzo ; Ricardo, Paulo Cseri ; Silva, João Paulo Naldi ; Brito, Rute; Oldroyd, Benjamin P. ; Arias, Maria Cristina
Source: Mitochondrial DNA Part A. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, ABELHAS, APIDAE, HYMENOPTERA, FILOGENIA, BIOGEOGRAFIA, GENÔMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANÇOSO, Elaine et al. Conserved numts mask a highly divergent mitochondrial-COI gene in a species complex of Australian stingless bees Tetragonula (Hymenoptera: Apidae). Mitochondrial DNA Part A, v. 30, n. 7, p. 806-817, 2019Tradução . . Disponível em: https://doi.org/10.1080/24701394.2019.1665036. Acesso em: 04 jul. 2024.
APA
Françoso, E., Zuntini, A. R., Ricardo, P. C., Silva, J. P. N., Brito, R., Oldroyd, B. P., & Arias, M. C. (2019). Conserved numts mask a highly divergent mitochondrial-COI gene in a species complex of Australian stingless bees Tetragonula (Hymenoptera: Apidae). Mitochondrial DNA Part A, 30( 7), 806-817. doi:10.1080/24701394.2019.1665036
NLM
Françoso E, Zuntini AR, Ricardo PC, Silva JPN, Brito R, Oldroyd BP, Arias MC. Conserved numts mask a highly divergent mitochondrial-COI gene in a species complex of Australian stingless bees Tetragonula (Hymenoptera: Apidae) [Internet]. Mitochondrial DNA Part A. 2019 ; 30( 7): 806-817.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1080/24701394.2019.1665036
Vancouver
Françoso E, Zuntini AR, Ricardo PC, Silva JPN, Brito R, Oldroyd BP, Arias MC. Conserved numts mask a highly divergent mitochondrial-COI gene in a species complex of Australian stingless bees Tetragonula (Hymenoptera: Apidae) [Internet]. Mitochondrial DNA Part A. 2019 ; 30( 7): 806-817.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1080/24701394.2019.1665036
Artigo de periodico
233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 (2018)
Lostal, William ; Urtizberea, J. Andoni; Richard, Isabelle ; Alonso-Jiménez, Alicia ; Carlier, Robert-Yves; Carson, Vincent ; Diaz-Manera, Jordi ; Eymard, Bruno; Fardeau, Michel; Gourlay, Marie-Laurence; Guglieri, Michela ; Hogrel, Jean-Yves ; Kullmann, Bruno; Levy, Jennifer ; Ono, Yasuko ; Prigent, Hélène ; Saenz, Amets ; Semplicini, Claudio ; Vainzof, Mariz ; Vissing, John ; Maggie, Walter
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, ENZIMAS, AMINOÁCIDOS, ENSAIO CLÍNICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOSTAL, William et al. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, v. 28, p. 540-549, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2018.03.010. Acesso em: 04 jul. 2024.
APA
Lostal, W., Urtizberea, J. A., Richard, I., Alonso-Jiménez, A., Carlier, R. -Y., Carson, V., et al. (2018). 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, 28, 540-549. doi:10.1016/j.nmd.2018.03.010
NLM
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010
Vancouver
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2024 jul. 04 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Countries/Territories

Funding Agencies

Indexado em

Non normalized affiliation

Countries of institutions of collaboration