Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Leonardo Caires dos Santos"'
Autor:
Natalia Nunes, Beatriz Carvalho Nunes, Malú Zamariolli, Diogo Cordeiro de Queiroz Soares, Leonardo Caires dos Santos, Anelisa Gollo Dantas, Vera Ayres Meloni, Sintia Iole Belangero, Vera Lúcia Gil-Da-Silva-Lopes, Chong Ae Kim, Maria Isabel Melaragno
Publikováno v:
Genetics Research, Vol 2024 (2024)
22q11.2 deletion syndrome (22q11.2DS) is a microdeletion syndrome with a broad and heterogeneous phenotype, even though most of the deletions present similar sizes, involving ∼3 Mb of DNA. In a relatively large population of a Brazilian 22q11.2DS c
Externí odkaz:
https://doaj.org/article/3aec9cf7c8f64a16aa4b81645a566b72
Autor:
Malú Zamariolli, Mileny Colovati, Mariana Moysés‐Oliveira, Natália Nunes, Leonardo Caires dos Santos, Ana B. Alvarez Perez, Silvia Bragagnolo, Maria Isabel Melaragno
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Oculo‐auriculo‐vertebral spectrum (OAVS) is a craniofacial developmental disorder that affects structures derived from the first and second pharyngeal arches. The clinically heterogeneous phenotype involves mandibular, oral, a
Externí odkaz:
https://doaj.org/article/d9f301b2b2bd48bcbc58c74a89019c4b
Autor:
Mariana Ferreira Leal, Leonardo Caires Dos Santos, Adrielle Martins de Oliveira, Paulo Santoro Belangero, Eduardo Antônio Figueiredo, Carina Cohen, Felipe de Seixas Alves, Wânia Hiromi Yanaguizawa, Carlos Vicente Andreoli, Alberto de Castro Pochini, Benno Ejnisman, Marília Cardoso Smith, Maria Teresa de Seixas Alves, Moises Cohen
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184141 (2017)
Rotator cuff tear is a common orthopedic condition. Metalloproteinases (MMP) and their inhibitors (TIMP) seem to play a role in the development of joint injuries and in the failure of tissue healing. However, the mechanisms of regulation of gene expr
Externí odkaz:
https://doaj.org/article/bc4979bf998e4b3da22a055fc42cee91
Autor:
Leonardo Caires dos Santos, Juliana Corrêa da Costa Ribeiro, Neusa Pereira Silva, Janete Cerutti, Maria Regina Regis da Silva, Maria de Lourdes Lopes Ferrari Chauffaille
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 33, Iss 6, Pp 417-424 (2011)
BACKGROUND: The detection of molecular and cytogenetic alterations is important for the diagnosis, prognosis and classification of myeloproliferative neoplasms. OBJECTIVE: The aim of this study was to detect the following mutations: JAK2 V617F, JAK2
Externí odkaz:
https://doaj.org/article/12863d17323e43e186d1a300627ee78c
Autor:
Sócrates Bezerra de Matos, Leonardo Caires dos Santos, Ciro Silveira e Pereira, Kleiton Silva Borges
Publikováno v:
Revista Saúde.com, Vol 3, Iss 2, Pp 77-86 (2007)
The Down Syndrome (DS) is a chromosomal disease characterized by expression of gene’s copy presents in chromosome 21 in triplicate. Is estimable that the incidence of DS is in the order of 1 in each 600/800 newborn babies and an average with 8000 n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e6f53b0d3c66d132f9d3eebf5aa738c
http://www.uesb.br/revista/rsc/v3/v3n2a09.pdf
http://www.uesb.br/revista/rsc/v3/v3n2a09.pdf
Autor:
Wisnieski F; Fernanda Wisnieski, Danielle Queiroz Calcagno, Mariana Ferreira Leal, Leonardo Caires dos Santos, Carolina de Oliveira Gigek, Elizabeth Suchi Chen, Thaís Brilhante Pontes, Marília de Arruda Cardoso Smith, Disciplina de Genética, Departamento de Morfologia e Genética, Universidade Federal de São Paulo, São Paulo 04023900, Brazil., Calcagno DQ, Leal MF, dos Santos LC, Gigek Cde O, Chen ES, Pontes TB, Assumpção PP, de Assumpção MB, Demachki S, Burbano RR, Smith Mde A
Publikováno v:
World journal of gastroenterology [World J Gastroenterol] 2013 Nov 07; Vol. 19 (41), pp. 7121-8.