ReP USP - Resultado da busca

Artigo de periodico
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) (2023)
Kobayashi, Gerson S ; Silva, Gleiciele A. Vieira; Branco, Elisa Varella ; Moreira, Danielle P; Kitajima, João Paulo F. W; Hemza, Claudia R.M.L; Mingroni Netto, Regina Celia ; Lojudice, Fernando H ; Oiticica, Jeanne ; Bento, Ricardo F ; Batissoco, Ana C ; Lezirovitz, Karina
Fonte: Stem Cell Research. Unidades: IB, FM
Assuntos: PERDA AUDITIVA, CÉLULAS-TRONCO
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ABNT
KOBAYASHI, Gerson S et al. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A). Stem Cell Research, v. 71, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2023.103181. Acesso em: 08 out. 2024.
APA
Kobayashi, G. S., Silva, G. A. V., Branco, E. V., Moreira, D. P., Kitajima, J. P. F. W., Hemza, C. R. M. L., et al. (2023). Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A). Stem Cell Research, 71. doi:10.1016/j.scr.2023.103181
NLM
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Vancouver
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Artigo de periodico
Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss (2022)
Silva, Rodrigo Salazar da ; Dantas, Vitor Lima Goes ; Alves, Leandro Ucela; Batissoco, Ana Carla ; Oiticica, Jeanne ; Lawrence, Elizabeth A ; Kawafi, Abdelwahab ; Yang, Yishi ; Nicastro, Fernanda Stávale; Novaes, Beatriz Caiuby ; Hammond, Chrissy ; Kague, Érika ; Mingroni Netto, Regina Celia
Fonte: Human Molecular Genetics. Unidades: IB, FM
Assuntos: SURDEZ, MUTAÇÃO GENÉTICA
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ABNT
SILVA, Rodrigo Salazar da et al. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, v. 31, n. Ja 2022, 2022Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddab325. Acesso em: 08 out. 2024.
APA
Silva, R. S. da, Dantas, V. L. G., Alves, L. U., Batissoco, A. C., Oiticica, J., Lawrence, E. A., et al. (2022). Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, 31( Ja 2022). doi:10.1093/hmg/ddab325
NLM
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2022 ; 31( Ja 2022):[citado 2024 out. 08 ] Available from: https://doi.org/10.1093/hmg/ddab325
Vancouver
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2022 ; 31( Ja 2022):[citado 2024 out. 08 ] Available from: https://doi.org/10.1093/hmg/ddab325
Artigo de periodico
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss (2020)
Silva, Rodrigo Salazar da ; Dantas, Vitor Lima Goes ; Alves, Leandro Ucela; Batissoco, Ana Carla ; Oiticica, Jeanne ; Lawrence, Elizabeth A ; Kawafi, Abdelwahab ; Yang, Yishi ; Nicastro, Fernanda Stávale; Novaes, Beatriz Caiuby ; Hammond, Chrissy ; Kague, Érika ; Mingroni Netto, Regina Celia
Fonte: Human Molecular Genetics. Unidades: IB, FM
Assuntos: AUDIÇÃO, SURDEZ, MUTAÇÃO GENÉTICA
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ABNT
SILVA, Rodrigo Salazar da et al. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, v. 29, n. 2, p. 3691–3705, 2020Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddaa240. Acesso em: 08 out. 2024.
APA
Silva, R. S. da, Dantas, V. L. G., Alves, L. U., Batissoco, A. C., Oiticica, J., Lawrence, E. A., et al. (2020). NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, 29( 2), 3691–3705. doi:10.1093/hmg/ddaa240
NLM
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2020 ;29( 2): 3691–3705.[citado 2024 out. 08 ] Available from: https://doi.org/10.1093/hmg/ddaa240
Vancouver
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2020 ;29( 2): 3691–3705.[citado 2024 out. 08 ] Available from: https://doi.org/10.1093/hmg/ddaa240
Artigo de periodico
P3 Cognitive Potential in Cochlear Implant Users (2018)
Grasel, Signe; Greters, Mario; Goffi-Gomez, Maria Valeria Schimidt; Bittar, Roseli; Weber, Raimar; Oiticica, Jeanne; Bento, Ricardo Ferreira
Fonte: International archives of otorhinolaryngology. Unidade: FM
Assuntos: POTENCIAIS EVOCADOS, IMPLANTE DA CÓCLEA, PERDA AUDITIVA, MENINGITE
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ABNT
GRASEL, Signe et al. P3 Cognitive Potential in Cochlear Implant Users. International archives of otorhinolaryngology, v. 22, n. 4, p. 408-414, 2018Tradução . . Disponível em: https://doi.org/10.1055/s-0037-1613687. Acesso em: 08 out. 2024.
APA
Grasel, S., Greters, M., Goffi-Gomez, M. V. S., Bittar, R., Weber, R., Oiticica, J., & Bento, R. F. (2018). P3 Cognitive Potential in Cochlear Implant Users. International archives of otorhinolaryngology, 22( 4), 408-414. doi:10.1055/s-0037-1613687
NLM
Grasel S, Greters M, Goffi-Gomez MVS, Bittar R, Weber R, Oiticica J, Bento RF. P3 Cognitive Potential in Cochlear Implant Users [Internet]. International archives of otorhinolaryngology. 2018 ; 22( 4): 408-414.[citado 2024 out. 08 ] Available from: https://doi.org/10.1055/s-0037-1613687
Vancouver
Grasel S, Greters M, Goffi-Gomez MVS, Bittar R, Weber R, Oiticica J, Bento RF. P3 Cognitive Potential in Cochlear Implant Users [Internet]. International archives of otorhinolaryngology. 2018 ; 22( 4): 408-414.[citado 2024 out. 08 ] Available from: https://doi.org/10.1055/s-0037-1613687
Artigo de periodico
A Cell Junctional Protein Network Associated with Connexin-26 (2018)
Batissoco, Ana C; Salazar-Silva, Rodrigo; Oiticica, Jeanne; Bento, Ricardo F; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral
Fonte: International Journal of Molecular Sciences. Unidades: FM, IB
Assuntos: PERDA AUDITIVA HEREDITÁRIA, CONEXINAS, MUTAÇÃO GENÉTICA, SURDEZ
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ABNT
BATISSOCO, Ana C et al. A Cell Junctional Protein Network Associated with Connexin-26. International Journal of Molecular Sciences, v. 19, n. 9, p. 1-20, 2018Tradução . . Disponível em: https://doi.org/10.3390/ijms19092535. Acesso em: 08 out. 2024.
APA
Batissoco, A. C., Salazar-Silva, R., Oiticica, J., Bento, R. F., Mingroni Netto, R. C., & Haddad, L. A. (2018). A Cell Junctional Protein Network Associated with Connexin-26. International Journal of Molecular Sciences, 19( 9), 1-20. doi:10.3390/ijms19092535
NLM
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni Netto RC, Haddad LA. A Cell Junctional Protein Network Associated with Connexin-26 [Internet]. International Journal of Molecular Sciences. 2018 ; 19( 9): 1-20.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/ijms19092535
Vancouver
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni Netto RC, Haddad LA. A Cell Junctional Protein Network Associated with Connexin-26 [Internet]. International Journal of Molecular Sciences. 2018 ; 19( 9): 1-20.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/ijms19092535
Artigo de periodico
Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2 (2017)
Massucci-Bissoli, Milene; Lezirovitz, Karina; Oiticica, Jeanne; Bento, Ricardo Ferreira
Fonte: Clinics. Unidade: FM
Assuntos: CÓCLEA, ORELHA INTERNA, HUMANOS, PROLIFERAÇÃO CELULAR, CÉLULAS-TRONCO, PERDA AUDITIVA, TRANSPORTE ATRAVÉS DA MEMBRANA
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ABNT
MASSUCCI-BISSOLI, Milene et al. Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2. Clinics, v. 72, n. 11, p. 714-717, 2017Tradução . . Disponível em: https://doi.org/10.6061/clinics/2017(11)11. Acesso em: 08 out. 2024.
APA
Massucci-Bissoli, M., Lezirovitz, K., Oiticica, J., & Bento, R. F. (2017). Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2. Clinics, 72( 11), 714-717. doi:10.6061/clinics/2017(11)11
NLM
Massucci-Bissoli M, Lezirovitz K, Oiticica J, Bento RF. Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2 [Internet]. Clinics. 2017 ; 72( 11): 714-717.[citado 2024 out. 08 ] Available from: https://doi.org/10.6061/clinics/2017(11)11
Vancouver
Massucci-Bissoli M, Lezirovitz K, Oiticica J, Bento RF. Evidence of progenitor cells in the adult human cochlea: sphere formation and identification of ABCG2 [Internet]. Clinics. 2017 ; 72( 11): 714-717.[citado 2024 out. 08 ] Available from: https://doi.org/10.6061/clinics/2017(11)11
Trabalho de evento-resumo
Investigating deafness genes as a cause of sudden sensorineural hearing loss (2013)
Bernardino-Cruz, D; Oiticica, Jeanne; Bittar, R. S. M; Auricchio, Maria Teresa Ballester de Melo; Mingroni Netto, Regina Celia
Fonte: Resumos. Nome do evento: Congresso Brasileiro de Genética. Unidade: IB
Assuntos: SURDEZ, PERDA AUDITIVA NEUROSSENSORIAL, MUTAÇÃO GENÉTICA
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ABNT
BERNARDINO-CRUZ, D et al. Investigating deafness genes as a cause of sudden sensorineural hearing loss. 2013, Anais.. Ribeirão Preto: Sociedade Brasileira de Genática - SBG, 2013. Disponível em: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf. Acesso em: 08 out. 2024.
APA
Bernardino-Cruz, D., Oiticica, J., Bittar, R. S. M., Auricchio, M. T. B. de M., & Mingroni Netto, R. C. (2013). Investigating deafness genes as a cause of sudden sensorineural hearing loss. In Resumos. Ribeirão Preto: Sociedade Brasileira de Genática - SBG. Recuperado de http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
NLM
Bernardino-Cruz D, Oiticica J, Bittar RSM, Auricchio MTB de M, Mingroni Netto RC. Investigating deafness genes as a cause of sudden sensorineural hearing loss [Internet]. Resumos. 2013 ;[citado 2024 out. 08 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
Vancouver
Bernardino-Cruz D, Oiticica J, Bittar RSM, Auricchio MTB de M, Mingroni Netto RC. Investigating deafness genes as a cause of sudden sensorineural hearing loss [Internet]. Resumos. 2013 ;[citado 2024 out. 08 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf
Trabalho de evento-resumo periodico
Otospheres obtained in vitro from mouse cochlea sensory epithelia express connexin 26 (2013)
Batissoco, Ana Carla; Calizaya, Boris Juniors López; Hemza, Cláudia R. de Marchi L.; Oiticica, Jeanne; Mingroni Netto, Regina Celia ; Bento, Ricardo Ferreira
Fonte: International Archives of Otorhinolaryngology. Nome do evento: Congress of the Otorhinolaryngology Foundation. Unidades: IB, FM
Assuntos: SURDEZ, MUTAÇÃO GENÉTICA, MODELOS ANIMAIS, RATOS, CÉLULAS-TRONCO, CÓCLEA
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ABNT
BATISSOCO, Ana Carla et al. Otospheres obtained in vitro from mouse cochlea sensory epithelia express connexin 26. International Archives of Otorhinolaryngology. São Paulo: Fundacao Otorrinolaringologia. Disponível em: http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1416. Acesso em: 08 out. 2024. , 2013
APA
Batissoco, A. C., Calizaya, B. J. L., Hemza, C. R. de M. L., Oiticica, J., Mingroni Netto, R. C., & Bento, R. F. (2013). Otospheres obtained in vitro from mouse cochlea sensory epithelia express connexin 26. International Archives of Otorhinolaryngology. São Paulo: Fundacao Otorrinolaringologia. Recuperado de http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1416
NLM
Batissoco AC, Calizaya BJL, Hemza CR de ML, Oiticica J, Mingroni Netto RC, Bento RF. Otospheres obtained in vitro from mouse cochlea sensory epithelia express connexin 26 [Internet]. International Archives of Otorhinolaryngology. 2013 ; 17 18.[citado 2024 out. 08 ] Available from: http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1416
Vancouver
Batissoco AC, Calizaya BJL, Hemza CR de ML, Oiticica J, Mingroni Netto RC, Bento RF. Otospheres obtained in vitro from mouse cochlea sensory epithelia express connexin 26 [Internet]. International Archives of Otorhinolaryngology. 2013 ; 17 18.[citado 2024 out. 08 ] Available from: http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1416
Artigo de periodico
Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family (2012)
Lezirovitz, Karina; Batissoco, Ana Carla; Lima, Fernanda T; Auricchio, Maria Teresa Ballester de Melo; Nonose, Renata Watanabe; Santos, Simone R.; Guilherme, Luiza; Oiticica, Jeanne; Mingroni Netto, Regina Celia
Fonte: Gene. Unidade: IB
Assuntos: PERDA AUDITIVA, LINHAGEM CELULAR
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ABNT
LEZIROVITZ, Karina et al. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family. Gene, v. 511, n. 2, p. 280-284, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2012.09.023. Acesso em: 08 out. 2024.
APA
Lezirovitz, K., Batissoco, A. C., Lima, F. T., Auricchio, M. T. B. de M., Nonose, R. W., Santos, S. R., et al. (2012). Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family. Gene, 511( 2), 280-284. doi:10.1016/j.gene.2012.09.023
NLM
Lezirovitz K, Batissoco AC, Lima FT, Auricchio MTB de M, Nonose RW, Santos SR, Guilherme L, Oiticica J, Mingroni Netto RC. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family [Internet]. Gene. 2012 ; 511( 2): 280-284.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.gene.2012.09.023
Vancouver
Lezirovitz K, Batissoco AC, Lima FT, Auricchio MTB de M, Nonose RW, Santos SR, Guilherme L, Oiticica J, Mingroni Netto RC. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family [Internet]. Gene. 2012 ; 511( 2): 280-284.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.gene.2012.09.023
Trabalho de evento-resumo periodico
Viable, proliferating progenitor cells (2011)
Oiticica, Jeanne; Batissoco, Ana Carla; Lezirovitz, Karina; Barboza Junior, Luiz C. M; Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Bento, Ricardo F
Fonte: Otolaryngology - Head and Neck Surgery. Nome do evento: Annual Meeting of the American Academy of Otolaryngology-Head and Neck Surgery Foundantion. Unidades: IB, FM
Assuntos: IMUNOFLUORESCÊNCIA, FIBROBLASTOS, OUVIDO
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ABNT
OITICICA, Jeanne et al. Viable, proliferating progenitor cells. Otolaryngology - Head and Neck Surgery. Alexandria: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1177/0194599811415823a320. Acesso em: 08 out. 2024. , 2011
APA
Oiticica, J., Batissoco, A. C., Lezirovitz, K., Barboza Junior, L. C. M., Haddad, L. A., Mingroni Netto, R. C., & Bento, R. F. (2011). Viable, proliferating progenitor cells. Otolaryngology - Head and Neck Surgery. Alexandria: Instituto de Biociências, Universidade de São Paulo. doi:10.1177/0194599811415823a320
NLM
Oiticica J, Batissoco AC, Lezirovitz K, Barboza Junior LCM, Haddad LA, Mingroni Netto RC, Bento RF. Viable, proliferating progenitor cells [Internet]. Otolaryngology - Head and Neck Surgery. 2011 ; 145( 2): P232-P233.[citado 2024 out. 08 ] Available from: https://doi.org/10.1177/0194599811415823a320
Vancouver
Oiticica J, Batissoco AC, Lezirovitz K, Barboza Junior LCM, Haddad LA, Mingroni Netto RC, Bento RF. Viable, proliferating progenitor cells [Internet]. Otolaryngology - Head and Neck Surgery. 2011 ; 145( 2): P232-P233.[citado 2024 out. 08 ] Available from: https://doi.org/10.1177/0194599811415823a320
Trabalho de evento-resumo
Comparable in vitro phenotypes for otospheres from guinea pig and mouse cochleas (2010)
Oiticica, Jeanne; Barboza Júnior, Luiz Carlos de Melo; Batissoco, Ana Carla; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Bento, Ricardo Ferreira
Nome do evento: Congresso Brasileiro de Células-Tronco e Terapia Celular. Unidades: IB, FM
Assuntos: RATOS, FENÓTIPOS, COBAIAS
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ABNT
OITICICA, Jeanne et al. Comparable in vitro phenotypes for otospheres from guinea pig and mouse cochleas. 2010, Anais.. Gramado: Instituto de Biociências, Universidade de São Paulo, 2010. . Acesso em: 08 out. 2024.
APA
Oiticica, J., Barboza Júnior, L. C. de M., Batissoco, A. C., Mingroni Netto, R. C., Haddad, L. A., & Bento, R. F. (2010). Comparable in vitro phenotypes for otospheres from guinea pig and mouse cochleas. In . Gramado: Instituto de Biociências, Universidade de São Paulo.
NLM
Oiticica J, Barboza Júnior LC de M, Batissoco AC, Mingroni Netto RC, Haddad LA, Bento RF. Comparable in vitro phenotypes for otospheres from guinea pig and mouse cochleas. 2010 ;[citado 2024 out. 08 ]
Vancouver
Oiticica J, Barboza Júnior LC de M, Batissoco AC, Mingroni Netto RC, Haddad LA, Bento RF. Comparable in vitro phenotypes for otospheres from guinea pig and mouse cochleas. 2010 ;[citado 2024 out. 08 ]
Artigo de periodico
Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea (2010)
Oiticica, Jeanne; Barboza Junior, Luiz Carlos M; Batissoco, Ana Carla; Lezirovitz, Karina; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Bento, Ricardo Ferreira
Fonte: Journal of Translational Medicine. Unidades: FM, IB
Assuntos: FENÓTIPOS, GENÉTICA
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ABNT
OITICICA, Jeanne et al. Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea. Journal of Translational Medicine, v. 8, 2010Tradução . . Disponível em: https://doi.org/10.1186/1479-5876-8-119. Acesso em: 08 out. 2024.
APA
Oiticica, J., Barboza Junior, L. C. M., Batissoco, A. C., Lezirovitz, K., Mingroni Netto, R. C., Haddad, L. A., & Bento, R. F. (2010). Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea. Journal of Translational Medicine, 8. doi:10.1186/1479-5876-8-119
NLM
Oiticica J, Barboza Junior LCM, Batissoco AC, Lezirovitz K, Mingroni Netto RC, Haddad LA, Bento RF. Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea [Internet]. Journal of Translational Medicine. 2010 ; 8[citado 2024 out. 08 ] Available from: https://doi.org/10.1186/1479-5876-8-119
Vancouver
Oiticica J, Barboza Junior LCM, Batissoco AC, Lezirovitz K, Mingroni Netto RC, Haddad LA, Bento RF. Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea [Internet]. Journal of Translational Medicine. 2010 ; 8[citado 2024 out. 08 ] Available from: https://doi.org/10.1186/1479-5876-8-119

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