Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Simone Gomes Ferreira"'
Autor:
Vitor G.L. Dantas, Karina Lezirovitz, Guilherme L. Yamamoto, Carolina Fischinger Moura de Souza, Simone Gomes Ferreira, Regina C. Mingroni-Netto
Publikováno v:
Genetics and Molecular Biology, Vol 37, Iss 4, Pp 616-621 (2014)
We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals affected by high frequency hearing loss. Genomic scanning using the 50k Affymetrix microarray technology yielded a Lod Scor
Externí odkaz:
https://doaj.org/article/c364bfd91c294499bab93aaae51f8e5e
Autor:
Gerson Shigeru Kobayashi, Lucas Alvizi, Daniele Yumi Sunaga, Philippa Francis-West, Anna Kuta, Bruno Vinícius Pimenta Almada, Simone Gomes Ferreira, Leonardo Carmo de Andrade-Lima, Daniela Franco Bueno, Cássio Eduardo Raposo-Amaral, Carlos Frederico Menck, Maria Rita Passos-Bueno
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65677 (2013)
Non-syndromic cleft lip/palate (NSCL/P) is a complex, frequent congenital malformation, determined by the interplay between genetic and environmental factors during embryonic development. Previous findings have appointed an aetiological overlap betwe
Externí odkaz:
https://doaj.org/article/23e8af9151744110956a3f30e31a5654
Autor:
Simone Gomes Ferreira
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
Este estudo investigou o efeito protetor da melatonina sobre os danos ao DNA induzidos pela ciclofosfamida (20 e 50mg/kg) sobre as aberrações cromossômicas, fragmentação do DNA, ciclo celular e os sítios sensíveis a Fpg pelo Ensaio Cometa. Os
Autor:
Alejandra Filippo Gonzalez Neves dos Santos, Nathalia da Silva Lucarevschi, Eshefison Rodrigues Batista, Simone Gomes Ferreira
Publikováno v:
The IX Iberian Congress of Ichthyology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecda0d631c4fcb9f38366eee026bf45e
https://doi.org/10.3390/blsf2022013130
https://doi.org/10.3390/blsf2022013130
Autor:
Simone Gomes Ferreira, Rubens Spin-Neto, Simone Peixe Friedrichsdorf, Gladys Cristina Domingue, Victor E. Arana-Chavez
Publikováno v:
Acta Scientific Dental Scienecs. 4:48-53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94e5b88d2c6f89b0bb579ba9a68266b9
https://doi.org/10.31080/asds.2020.04.0848
https://doi.org/10.31080/asds.2020.04.0848
Autor:
Siulan Vendramini-Pittoli, Vanessa Luiza Romanelli Tavares, Renato da Silva Freitas, Simone Gomes Ferreira, Maria Leine Guion-Almeida, Gabriella Shih Ping Hsia, Christopher T. Gordon, Débora Romeo Bertola, Guilherme L. Yamamoto, Nancy Mizue Kokitsu-Nakata, Suzana A. M. Ezquina, Mayana Zatz, Jeanne Amiel, Roseli Maria Zechi-Ceide, Cesar Augusto Raposo-Amaral, Josiane Souza, Maria Rita Passos-Bueno
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Auriculocondylar syndrome, mainly characterized by micrognathia, small mandibular condyle, and question mark ears, is a rare disease segregating in an autosomal dominant pattern in the majority of the families reported in the literature. So far, path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be342c326bb1de53168eef0c9e4f26fd
https://doi.org/10.1002/ajmg.a.38101
https://doi.org/10.1002/ajmg.a.38101
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Marine calcareous algae are widespread in oceans of the world and known for their calcified cell walls and the generation of rhodolith beds that turn sandy bottoms into a complex structured ecosystem with high biodiversity. Rhodoliths are unattached,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1743a9eec9bf5cb77bf70b8d7ed73c5
https://doi.org/10.1016/j.micron.2015.02.004
https://doi.org/10.1016/j.micron.2015.02.004
Autor:
Eduardo Massaharu Aoki, Emiko Saito Arita, Reinaldo Abdala-Júnior, João Gualberto de Cerqueira Luz, Jefferson Xavier de Oliveira, Simone Gomes Ferreira, Arthur Rodriguez Gonzalez Cortes
Publikováno v:
Journal of Oral and Maxillofacial Surgery. 76:955.e1-955.e5
Temporomandibular disorders lead to parafunctional activity that may alter bone remodeling of mandibular components. This animal study aimed to assess the impact of temporomandibular joint discectomy on condylar bone microarchitecture.A total of 30 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e5c8b7efe165bb0c2f9b624d2185100
https://doi.org/10.1016/j.joms.2017.12.019
https://doi.org/10.1016/j.joms.2017.12.019
Autor:
Raquel Seruca, Têmis Maria Félix, Mayana Zatz, Luciano Abreu Brito, Carolina Malcher, Soraia Melo, Lucas Alvizi, Gerson Shigeru Kobayashi, Guilherme L. Yamamoto, Simone Gomes Ferreira, Joana Figueiredo, Michel S Naslavsky, Maria Rita Passos-Bueno, Nivaldo Alonso
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Nonsyndromic orofacial cleft (NSOFC) is a complex disease of still unclear genetic etiology. To investigate the contribution of rare epithelial cadherin (CDH1) gene variants to NSOFC, we target sequenced 221 probands. Candidate variants were evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdd75afc6420b946ca01bd3be50ee3ed
Autor:
Carolina Fischinger Moura de Souza, Karina Lezirovitz, Regina Célia Mingroni-Netto, Guilherme L. Yamamoto, Vitor G. L. Dantas, Simone Gomes Ferreira
Publikováno v:
Genetics and Molecular Biology, Volume: 37, Issue: 4, Pages: 616-621, Published: 14 NOV 2014
Genetics and Molecular Biology
Genetics and Molecular Biology, Vol 37, Iss 4, Pp 616-621 (2014)
Genetics and Molecular Biology v.37 n.4 2014
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology
Genetics and Molecular Biology, Vol 37, Iss 4, Pp 616-621 (2014)
Genetics and Molecular Biology v.37 n.4 2014
Sociedade Brasileira de Genética (SBG)
instacron:SBG
We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals affected by high frequency hearing loss. Genomic scanning using the 50k Affymetrix microarray technology yielded a Lod Scor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cd65e0da8c79df96637ebddfadc5d74
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572014000500002&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572014000500002&lng=en&tlng=en