Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hercilio Martelli Junior"'
Autor:
Lays Martin Sobral, Michele Gassen Kellermann, Edgard Graner, Hercilio Martelli-Junior, Ricardo Della Coletta
Publikováno v:
Brazilian Oral Research, Vol 24, Iss 2, Pp 182-188 (2010)
Cyclosporin A (CyA) induces gingival overgrowth via its stimulatory effects on expression of transforming growth factor-beta1 (TGF-β1) and collagen. It is not known whether CyA has a direct effect on gingival fibroblasts or induces its effect indire
Externí odkaz:
https://doaj.org/article/b5b0fa45adde4a7fa3ca0fe147747899
Autor:
Renato Assis, Machado, Helenara Salvati Bertolossi, Moreira, Sibele Nascimento, de Aquino, Hercilio, Martelli-Junior, Silvia Regina, de Almeida Reis, Darlene Camati, Persuhn, Tao, Wu, Yuan, Yuan, Ricardo D, Coletta
Publikováno v:
American journal of medical genetics. Part A. (2)
Autor:
Pamella Kelly Farias, de Aguiar, Ricardo D, Coletta, Allane Maria Lacerda Ferreira, de Oliveira, Renato Assis, Machado, Paulo Germano Cavalcante, Furtado, Lindalva Alves, de Oliveira, Sibele Nascimento, de Aquino, Hercilio, Martelli-Junior, Silvia Regina, de Almeida Reis, Helenara Salvati Bertolossi, Moreira, Darlene Camati, Persuhn
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 103(4)
The MTHFR rs1801131AC and rs1801133CT variants have been analyzed as putative genetic risk factors for oral clefts within various populations worldwide.To test the role of these polymorphisms in nonsyndromic cleft lip with or without cleft palate (NS
Autor:
Leonardo de Jesus Araujo, Guilherme Braga Muniz, Edmilson Santos, Joao Paulo Versiani Ladeia, Hercilio Martelli Junior, Paulo Rogerio Ferreti Bonan
Publikováno v:
São Paulo Medical Journal, Vol 131, Iss 5, Pp 351-355
CONTEXT: Tuberous sclerosis complex (TSC) is a genetic disease in the group known as neurocutaneous syndromes, with dominant autosomal inheritance. It is characterized by skin and adnexal lesions and central and peripheral nervous system tumors, with
Externí odkaz:
https://doaj.org/article/edf6b8d5cfae447fae1557791a9a90a8
Autor:
Sibele Nascimento, de Aquino, Ryuichi, Hoshi, Elizabete, Bagordakis, Maria Giulia Rezende, Pucciarelli, Ana Camila, Messetti, Helenara, Moreira, Andreia, Bufalino, Andréa, Borges, Ana Lucia, Rangel, Luciano Abreu, Brito, Mario Sergio, Oliveira Swerts, Hercilio, Martelli-Junior, Sergio R, Line, Edgard, Graner, Sílvia R A, Reis, Maria Rita, Passos-Bueno, Ricardo D, Coletta
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 100(1)
Polymorphisms within the MTHFR (rs2274976) and MTHFD1 (rs2236225) genes were previously associated with maternal susceptibility for having an offspring with nonsyndromic cleft lip with or without cleft palate (NSCL/P) in the Brazilian population. How
Autor:
Hercilio Martelli Junior
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientador: Luciano Resende Ferreira Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba Resumo: Fibromatose Gengival Hereditária (FGH) representa uma condição oral incomum (1:750.000), caracterizad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9291e3853aed3ca7aa139990b4e9396c
Publikováno v:
Oral Diseases; Jul2022, Vol. 28 Issue 5, pi-i, 1p
Publikováno v:
Oral Diseases; Jul2022, Vol. 28 Issue 5, p1369-1386, 18p, 1 Diagram, 3 Charts, 2 Graphs
Publikováno v:
Oral Diseases; Nov2022 Supplement S1, Vol. 28, p2588-2590, 3p, 1 Chart
Autor:
Costa, Cláudio Rodrigues Rezende, Braz, Shélida Vasconcelos, Toledo, Isabela Porto, Martelli‐Júnior, Hercilio, Mazzeu, Juliana Forte, Guerra, Eliete Neves Silva, Coletta, Ricardo D., Acevedo, Ana Carolina
Publikováno v:
Oral Diseases; May2021, Vol. 27 Issue 4, p881-893, 13p, 1 Diagram, 1 Chart