Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Silvia Maria Gomes Massironi"'
Autor:
Fábio Daumas Nunes, Maria da Graça Silva Valenzuela, Camila Oliveira Rodini, Silvia Maria Gomes Massironi, Gui Mi Ko
Publikováno v:
Brazilian Oral Research, Vol 21, Iss 2, Pp 127-133 (2007)
A comparative nonisotopic in situ hybridization (ISH) analysis was carried out for the detection of Bmp-4, Shh and Wnt-5a transcripts during mice odontogenesis from initiation to cap stage. Bmp-4 was expressed early in the epithelium and then in the
Externí odkaz:
https://doaj.org/article/7072901fd5c64084aeb387dd0109bef5
Autor:
Bruna Cristina Garcia Orlando, Karina Eiko Kiataqui, Thiago Moirinho Reis -Silva, Claudia Madalena Cabrera Mori, CMC, Mariana Manes, Daniel Nascimento Lago-Santos, Silvia Maria Gomes Massironi, Eduardo Fernandes Bondan, Thiago Berti Kirsten, Maria Martha Martha Bernardi
Publikováno v:
SSRN Electronic Journal.
Autor:
Danilo Wadt, Cezar Guizzo, Dennis Albert Zanatto, Ana Tada Fonseca Brasil Antiorio, Jilma Alemán-Laporte, Mariana de Souza Aranha Garcia-Gomes, Guilherme Andrade Marson, Pedro Kenzo Yamamoto, Maria Martha Bernardi, Claudia Madalena Cabrera Mori, Silvia Maria Gomes Massironi, Sandra Regina Alexandre-Ribeiro
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Bio Protoc
Universidade de São Paulo (USP)
instacron:USP
Bio Protoc
Despite the great number of test batteries already known to assess the behavior of genetically modified and inbred strains of mice, only a few of them focus on basic neurological parameters. The purpose of the battery test proposed is to settle a spe
Autor:
Pedro Kenzo Yamamoto, Orfa Yineth Galvis-Alonso, Márcia Carolina Millán Olivato, Silvia Maria Gomes Massironi, Maria Lúcia Zaidan Dagli, Ivo Lebrun, Ana Tada Fonseca Brasil Antiorio, Jorge Camilo Flório, Thaísa Meira Sandini, Sandra Regina Alexandre-Ribeiro, Mariana de Souza Aranha Garcia-Gomes, Jorge Mejia, Maria Martha Bernardi, Susan Ienne, Tiago Antonio de Souza, Claudia Madalena Cabrera Mori, Dennis Albert Zanatto
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
The tremor mutant phenotype results from an autosomal recessive spontaneous mutation arisen in a Swiss–Webster mouse colony. The mutant mice displayed normal development until three weeks of age when they began to present motor impairment comprised
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48493981195adad7f9957a1862278f2e
Autor:
Silvia Maria Gomes Massironi, Mariana de Souza Aranha Garcia Gomes, Nicássia de Sousa Oliveira, Geissiane de Moraes Marcondes, Pedro Kenzo Yamamoto, Claudia Madalena Cabrera Mori, Marianna Manes, Maria Martha Bernardi, Tiago Antonio de Souza
Publikováno v:
Revista de Educação Continuada em Medicina Veterinária e Zootecnia do CRMV-SP. 16:8-14
O camundongo mutante recessivo bate-palmas (bapa) originou-se de mutagênese química induzida por ENU (N-ethyl-N-nitrosourea) e apresenta alterações posturais com movimentos anormais dos membros posteriores quando levantado pela cauda. No sequenci
Autor:
Joana Bom, Vanessa Yamamoto Tambellini, Ana Tada Fonseca Brasil Antiorio, Márcio Augusto Caldas Rocha Carvalho, Claudia Madalena Cabrera Mori, Rosália Regina de Luca, Juliana Bortolatto, Danilo Wadt, Silvia Maria Gomes Massironi
Publikováno v:
Brazilian Journal of Veterinary Research and Animal Science, Vol 56, Iss 1 (2019)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
The introduction of new strains of mice in specific pathogen-free (SPF) animal facilities should be performed carefully to avoid breaking sanitary barriers. To meet this need, animals should be rederived to reduce infection risk and thus avoid resear
Autor:
Sandra Regina Alexandre-Ribeiro, Maria Martha Bernardi, Julia Zaccarelli-Magalhães, Thaísa Meira Sandini, Marianna Manes, Claudia Madalena Cabrera Mori, Danilo Wadt, Mariana de Souza Aranha Garcia-Gomes, Jorge Camilo Flório, Silvia Maria Gomes Massironi
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
Otoconia are crucial for the correct processing of positional information and orientation. Mice lacking otoconia cannot sense the direction of the gravity vector and cannot swim properly. This study aims to characterize the behavior of mergulhador (m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bad73ae39518a2bf0367e0ee8af443b
Autor:
Carlos Frederico Martins Menck, Sandra Regina Alexandre-Ribeiro, Pedro Kenzo Yamamoto, Ana Tada Fonseca Brasil Antiorio, Claudia Madalena Cabrera Mori, Silvia Maria Gomes Massironi, Nicassia de Souza Oliveira, Mariana de Souza Aranha Garcia-Gomes, Tiago Antonio de Souza, Dennis Albert Zanatto, Maria Martha Bernardi
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
The recessive mutant mice bate palmas (bapa) - claps in Portuguese arose from N-ethyl-N-nitrosourea mutagenesis. A single nucleotide, T > C, change in exon 13, leading to a Thr1289 Ala substitution, was identified in the lysine (K)-specific methyltra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52d9b23632ed02d7398836aba85cf869
Autor:
Gui Mi Ko, Silvia Maria Gomes Massironi, Carlos Frederico Martins Menck, Carolina Batista Ariza, S.G. Ocanha, Marimelia Porcionatto, P.C. Mazzonetto, T.A. de Souza
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease. 1865(6)
Abnormalities in cerebellar structure and function may cause ataxia, a neurological dysfunction of motor coordination. In the course of the present study, we characterized a mutant mouse lineage with an ataxia-like phenotype. We localized the mutatio
Publikováno v:
Scientific Reports
Marfan syndrome (MFS) is an autosomal dominant disease of the connective tissue, affecting mostly the skeletal, ocular and cardiovascular systems, caused by mutations in the FBN1 gene. The existence of modifier genes has been postulated based on the