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Artigo de periodico
Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells (2022)
Araújo, Isaac Jordão de Souza; Guimarães, Gustavo Narvaes ; Machado, Renato Assis; Bertassoni, Luiz Eduardo; Davies, Robert Philip Wynn ; Puppin-Rontani, Regina Maria
Source: Journal of Dentistry. Unidade: HRAC
Subjects: BIOMINERALIZAÇÃO, ODONTOBLASTO, PEPTÍDEOS
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ABNT
ARAÚJO, Isaac Jordão de Souza et al. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells. Journal of Dentistry, v. 121, n. Ja 2022, p. 7 , 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jdent.2022.104111. Acesso em: 21 ago. 2024.
APA
Araújo, I. J. de S., Guimarães, G. N., Machado, R. A., Bertassoni, L. E., Davies, R. P. W., & Puppin-Rontani, R. M. (2022). Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells. Journal of Dentistry, 121( Ja 2022), 7 . doi:10.1016/j.jdent.2022.104111
NLM
Araújo IJ de S, Guimarães GN, Machado RA, Bertassoni LE, Davies RPW, Puppin-Rontani RM. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells [Internet]. Journal of Dentistry. 2022 ; 121( Ja 2022): 7 .[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.jdent.2022.104111
Vancouver
Araújo IJ de S, Guimarães GN, Machado RA, Bertassoni LE, Davies RPW, Puppin-Rontani RM. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells [Internet]. Journal of Dentistry. 2022 ; 121( Ja 2022): 7 .[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.jdent.2022.104111
Artigo de periodico
Insight into the ontogeny of GnRH neurons from patients born without a nose (2020)
Delaney, Angela; Volochayev, Rita; Meader, Brooke; Lee, Janice; Almpani, Konstantinia; Noukelak, Germaine Y.; Henkind, Jennifer; Chalmers, Laura; Law, Jennifer R.; Williamson, Kathleen A.; Jacobsen, Christina M.; Buitrago, Tatiana Pineda; Perez, Orlando; Cho, Chie-Hee; Kaindl, Angela; Rauch, Anita; Steindl, Katharina; Garcia, Jose Elias; Russell, Bianca E.; Prasad, Rameshwar; Mondal, Uttam K.; Reigstad, Hallvard M.; Clements, Scott; Kim, Susan; Inoue, Kaoru; Arora, Gazal; Salnikov, Kathryn B.; DiOrio, Nicole P.; Prada, Rolando; Capri, Yline; Morioka, Kosuke; Mizota, Michiyo; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Tonello, Cristiano ; Pittoli, Siulan Vendramini Paulovich ; Dalben, Gisele da Silva ; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Seminara, Stephanie B.; Crowley Júnior, William F.; Plummer, Lacey; Hall, Janet E.; Graham Júnior, John M.; Lin, Angela E.; Shaw, Natalie D.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: HRAC
Subjects: HORMÔNIO LIBERADOR DE GONADOTROFINAS, AGENESIA, NARIZ (ANATOMIA), MALFORMAÇÕES, FENÓTIPOS
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ABNT
DELANEY, Angela et al. Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, v. 105, n. 5, p. 1538-1551, 2020Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgaa065. Acesso em: 21 ago. 2024.
APA
Delaney, A., Volochayev, R., Meader, B., Lee, J., Almpani, K., Noukelak, G. Y., et al. (2020). Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, 105( 5), 1538-1551. doi:10.1210/clinem/dgaa065
NLM
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Vancouver
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education (2020)
Kantar, Rami S. ; Breugem, Corstiaan C. ; Keith, Kristen ; Kassam, Serena ; Vijayakumar, Charanya ; Bow, Mikaela; Alfonso, Allyson R. ; Chahine, Elsa M. ; Ghotmi, Lilian H.; Patel, Krishna G.; Shetye, Pradip R.; Santiago, Pedro E.; Losee, Joseph E. ; Steinbacher, Derek M. ; Rossell-Perry, Percy ; Garib, Daniela Gamba ; Alonso, Nivaldo ; Mann, Robert J.; Prada-Madrid, Jose Rolando; Esenlik, Elçin ; Pamplona, María del Carmen ; Collares, Marcus Vinícius Martins ; Bennun, Ricardo D.; Kummer, Ann W. ; Giugliano, Carlos; Padwa, Bonnie L.; Raposo-Amaral, Cassio Eduardo; Tse, Raymond W. ; Sommerlad, Brian ; Flores, Roberto L. ; Hamdan, Usama S.
Source: The Cleft Palate-Craniofacial Journal. Unidades: FOB, HRAC
Subjects: SAÚDE BUCAL, FISSURA LÁBIOPALATINA, SIMULAÇÃO (APRENDIZAGEM)
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ABNT
KANTAR, Rami S. et al. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education. The Cleft Palate-Craniofacial Journal, v. 57, n. 10, p. 1238-1246, 2020Tradução . . Disponível em: https://doi.org/10.1177/1055665620944781. Acesso em: 21 ago. 2024.
APA
Kantar, R. S., Breugem, C. C., Keith, K., Kassam, S., Vijayakumar, C., Bow, M., et al. (2020). Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education. The Cleft Palate-Craniofacial Journal, 57( 10), 1238-1246. doi:10.1177/1055665620944781
NLM
Kantar RS, Breugem CC, Keith K, Kassam S, Vijayakumar C, Bow M, Alfonso AR, Chahine EM, Ghotmi LH, Patel KG, Shetye PR, Santiago PE, Losee JE, Steinbacher DM, Rossell-Perry P, Garib DG, Alonso N, Mann RJ, Prada-Madrid JR, Esenlik E, Pamplona M del C, Collares MVM, Bennun RD, Kummer AW, Giugliano C, Padwa BL, Raposo-Amaral CE, Tse RW, Sommerlad B, Flores RL, Hamdan US. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education [Internet]. The Cleft Palate-Craniofacial Journal. 2020 ; 57( 10): 1238-1246.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1177/1055665620944781
Vancouver
Kantar RS, Breugem CC, Keith K, Kassam S, Vijayakumar C, Bow M, Alfonso AR, Chahine EM, Ghotmi LH, Patel KG, Shetye PR, Santiago PE, Losee JE, Steinbacher DM, Rossell-Perry P, Garib DG, Alonso N, Mann RJ, Prada-Madrid JR, Esenlik E, Pamplona M del C, Collares MVM, Bennun RD, Kummer AW, Giugliano C, Padwa BL, Raposo-Amaral CE, Tse RW, Sommerlad B, Flores RL, Hamdan US. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education [Internet]. The Cleft Palate-Craniofacial Journal. 2020 ; 57( 10): 1238-1246.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1177/1055665620944781
Artigo de periodico
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome (2018)
Kievit, Anneke; Tessadori, Federico; Douben, Hannie; Jordens, Ingrid; Maurice, Madelon; Hoogeboom, Jeannette; Hennekam, Raoul; Nampoothiri, Sheela; Kayserili, Hülya; Castori, Marco; Whiteford, Margo; Motter, Connie; Melver, Catherine; Cunningham, Michael; Hing, Anne; Nakata, Nancy Mizue Kokitsu; Pittoli, Siulan Vendramini Paulovich; Richieri-Costa, Antonio; Baas, Annette F.; Breugem, Corstiaan C. ; Duran, Karen; Massink, Maarten; Derksen, Patrick W. B.; IJcken, Wilfred F. J. van; Unen, Leontine van; Simarro, Fernando Santos; Lapunzina, Pablo; Lopes, Vera Lúcia Gil da Silva; Mendes, Elaine Lustosa; Krall, Max; Slavotinek, Anne; Victor Martinez-Glez; Bakkers, Jeroen; Gassen, Koen L. I. van; Klein, Annelies de; Boogaard, Marie-José H. van den; Haaften, Gijs van
Source: European Journal of Human Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, ANOMALIA DENTÁRIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
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ABNT
KIEVIT, Anneke et al. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, v. 26, n. 2, p. 210-219, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41431-017-0010-5. Acesso em: 21 ago. 2024.
APA
Kievit, A., Tessadori, F., Douben, H., Jordens, I., Maurice, M., Hoogeboom, J., et al. (2018). Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, 26( 2), 210-219. doi:10.1038/s41431-017-0010-5
NLM
Kievit A, Tessadori F, Douben H, Jordens I, Maurice M, Hoogeboom J, Hennekam R, Nampoothiri S, Kayserili H, Castori M, Whiteford M, Motter C, Melver C, Cunningham M, Hing A, Nakata NMK, Pittoli SVP, Richieri-Costa A, Baas AF, Breugem CC, Duran K, Massink M, Derksen PWB, IJcken WFJ van, Unen L van, Simarro FS, Lapunzina P, Lopes VLG da S, Mendes EL, Krall M, Slavotinek A, Victor Martinez-Glez, Bakkers J, Gassen KLI van, Klein A de, Boogaard M-JH van den, Haaften G van. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome [Internet]. European Journal of Human Genetics. 2018 ; 26( 2): 210-219.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1038/s41431-017-0010-5
Vancouver
Kievit A, Tessadori F, Douben H, Jordens I, Maurice M, Hoogeboom J, Hennekam R, Nampoothiri S, Kayserili H, Castori M, Whiteford M, Motter C, Melver C, Cunningham M, Hing A, Nakata NMK, Pittoli SVP, Richieri-Costa A, Baas AF, Breugem CC, Duran K, Massink M, Derksen PWB, IJcken WFJ van, Unen L van, Simarro FS, Lapunzina P, Lopes VLG da S, Mendes EL, Krall M, Slavotinek A, Victor Martinez-Glez, Bakkers J, Gassen KLI van, Klein A de, Boogaard M-JH van den, Haaften G van. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome [Internet]. European Journal of Human Genetics. 2018 ; 26( 2): 210-219.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1038/s41431-017-0010-5
Artigo de periodico
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome (2014)
Gordon, Christopher T.; Cunniff, Christopher M.; Green, Glenn E.; Zechi-Ceide, Roseli Maria ; Johnson, Jason M.; Henderson, Alex; Petit, Florence; Nakata, Nancy Mizue Kokitsu ; Guion-Almeida, Maria Leine; Munnich, Arnold; Cunningham, Michael L.; Lyonnet, Stanislas; Amiel, Jeanne
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: DESENVOLVIMENTO MAXILOFACIAL, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher T. et al. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, v. 164, n. 7, p. 1850-1853, 2014Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36505. Acesso em: 21 ago. 2024.
APA
Gordon, C. T., Cunniff, C. M., Green, G. E., Zechi-Ceide, R. M., Johnson, J. M., Henderson, A., et al. (2014). Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, 164( 7), 1850-1853. doi:10.1002/ajmg.a.36505
NLM
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Vancouver
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Artigo de periodico
TBX22 mutations are a frequent cause of cleft palate (2004)
Marçano, Ana Carolina Braga; Doudney, K.; Braybrook, C.; Squires, R.; Patton, M. A.; Lees, M. M.; Richieri-Costa, Antonio; Lidral, Andrew C.; Murray, Jeffrey C.; Moore, G.E.; Stanier, P.
Source: Journal of Medical Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARÇANO, Ana Carolina Braga et al. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, v. 41, n. Ja 2004, p. 68-74, 2004Tradução . . Acesso em: 21 ago. 2024.
APA
Marçano, A. C. B., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., et al. (2004). TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, 41( Ja 2004), 68-74.
NLM
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 ago. 21 ]
Vancouver
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 ago. 21 ]

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