Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Renata F. Fonseca"'
Autor:
Ariadne Letra, Walid Fakhouri, Renata F Fonseca, Renato Menezes, Inga Kempa, Joanne L Prasad, Toby G McHenry, Andrew C Lidral, Lina Moreno, Jeffrey C Murray, Sandra Daack-Hirsch, Mary L Marazita, Eduardo E Castilla, Baiba Lace, Ieda M Orioli, Jose M Granjeiro, Brian C Schutte, Alexandre R Vieira
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45441 (2012)
Previous evidence from tooth agenesis studies suggested IRF6 and TGFA interact. Since tooth agenesis is commonly found in individuals with cleft lip/palate (CL/P), we used four large cohorts to evaluate if IRF6 and TGFA interaction contributes to CL/
Externí odkaz:
https://doaj.org/article/d97b262852a745979450c8ab3e86add3
Autor:
Jose A. Puppim de Oliveira, Anselmo Teixeira, Gilda Alves, Siane Lopes Bittencourt Rosas, Maria da Gloria da Costa Carvalho, Renata F. Fonseca
Publikováno v:
São Paulo Medical Journal, Vol 133, Iss 1, Pp 51-54
CONTEXT AND OBJECTIVE: The Epstein-Barr virus (EBV) is the most common cause of infectious mononucleosis and is also associated with several human tumors, including Burkitt's lymphoma, Hodgkin's lymphoma, some cases of gastric carcinoma and nasophary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818f53402ebfc9c2fdf71e9f9b1f618e
https://doi.org/10.1590/1516-3180.2013.1912814
https://doi.org/10.1590/1516-3180.2013.1912814
Autor:
Renato Menezes, Sandra R. Imoehl, Manika Govil, Jacqueline T. Hecht, Renata F. Fonseca, Stephen Tropp, Brett T. Chiquet, Lian Ma, Iêda M. Orioli, Eduardo E. Castilla, Mary L. Marazita, Andrew E. Czeizel, Jeffrey C. Murray, M. Adela Mansilla, Alexandre R. Vieira, Margaret E. Cooper, José Mauro Granjeiro, Ariadne Letra
Publikováno v:
The Cleft Palate-Craniofacial Journal. 48:363-370
Objective To assess the association between nonsyndromic (NS) cleft lip with or without cleft palate (CL(P)) and single-nucleotide polymorphisms (SNPs) within the CRISPLD2 gene (cysteine-rich secretory protein LCCL domain containing 2). Design Four S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c41e61edb12f3a22519dcaa9f7beaa
https://doi.org/10.1597/09-227
https://doi.org/10.1597/09-227
Autor:
Ariadne Letra, José Mauro Granjeiro, Alexandre R. Vieira, Manika Govil, Eduardo E. Castilla, Renato Menezes, Toby Goldstein McHenry, Mary L. Marazita, Renata F. Fonseca, Iêda M. Orioli
Publikováno v:
American Journal of Medical Genetics Part A. :1701-1710
Cleft lip/palate comprises a large fraction of all human birth defects, and is notable for its significant lifelong morbidity and complex etiology. Several studies have shown that genetic factors appear to play a significant role in the etiology of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaa4e1e811100aba15271e30cb0c0e51
https://doi.org/10.1002/ajmg.a.33482
https://doi.org/10.1002/ajmg.a.33482
Autor:
Ariadne Letra, B.C. Bjork, Manika Govil, Jon D. Hennebold, Melinda J. Murphy, Iêda M. Orioli, Rick A. Martin, Alexandre R. Vieira, Renata F. Fonseca, E. E. Castilla, Mary L. Marazita, José Mauro Granjeiro, Renato Menezes, Toby Goldstein McHenry
Publikováno v:
Journal of Dental Research. 89:927-932
Cleft lip/palate is a defect of craniofacial development. In previous reports, chromosome 6q has been suggested as a candidate region for cleft lip/palate. A multipoint posterior probability of linkage analysis of multiplex families from the Philippi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9de2c560eaf5652a4e7c3fa316f128a1
https://doi.org/10.1177/0022034510370004
https://doi.org/10.1177/0022034510370004
Autor:
Isabel do Val, Fernanda Ribeiro Lattario, Filomena Aste Silveira, Kátia Silveira da Silva, Renata F. Fonseca, Maria da Gloria Carvalho, Yara Furtado, Gutemberg Almeida, Paula Maldonado
Publikováno v:
Diagnostic Molecular Pathology. 19:15-19
Methylation is a chemical modification in which a methyl group (CH3) is added to the cytosine in the promoter region of the gene. It involves a very frequent epigenetic event that is found in many human cancers. Currently, there is no consensus on wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd43e6f4e509fa145ab0cc537f7ca91c
https://doi.org/10.1097/pdm.0b013e3181aa8f64
https://doi.org/10.1097/pdm.0b013e3181aa8f64
Autor:
Sânia O. Dias, Miguel A. Moreira, Eduardo E. Castilla, Ana Maria Bolognese, Renata F. Fonseca, Márcia Gonçalves Ribeiro, Kênia B. El-Jaick, Iêda M. Orioli, Eliane T. Pereira
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 79:573-580
BACKGROUND: Single median maxillary central incisor (SMMCI) is a rare anomaly that may occur alone or associated with other conditions, frequently as part of the holoprosencephaly (HPE) spectrum. However, it has been suggested that SMMCI alone, or as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fdf94e9b4bf706865abf478be449eab
https://doi.org/10.1002/bdra.20380
https://doi.org/10.1002/bdra.20380
Autor:
Iêda M. Orioli, Eduardo E. Castilla, Joaquín Dopazo, Miguel A. M. Moreira, Héctor N. Seuánez, Renata F. Fonseca, Flávia M. de Carvalho, Alexandre R. Vieira, Juan C. Mereb, Fernando A. Poletta, David Montaner
Publikováno v:
EUROPEAN JOURNAL OF ORAL SCIENCES
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
The etiology of cleft lip with or without cleft palate (CL±P) is complex and heterogeneous, and multiple genetic and environmental factors are involved. Some candidate genes reported to be associated with oral clefts are located on the X chromosome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f280bbc6027881b035a0974cbfbc6210
https://pubmed.ncbi.nlm.nih.gov/26331285
https://pubmed.ncbi.nlm.nih.gov/26331285
Autor:
Gilda Alves, Renata F. Fonseca, Maria da Gloria da Costa Carvalho, Anselmo Teixeira, Jose A. Puppim de Oliveira, Marcia Tie Kawamura
Publikováno v:
Memórias do Instituto Oswaldo Cruz, Volume: 107, Issue: 7, Pages: 953-954, Published: NOV 2012
Memórias do Instituto Oswaldo Cruz., Vol 107, Iss 7, Pp 953-954 (2012)
Memórias do Instituto Oswaldo Cruz., Vol 107, Iss 7, Pp 953-954 (2012)
Members of the Herpesviridae family have been implicated in a number of tumours in humans. At least 75% of the human population has had contact with cytomegalovirus (HCMV). In this work, we screened 75 Brazilian glioma biopsies for the presence of HC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b83e33146b9e8763cc4723d25e616dd3
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000700020&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000700020&lng=en&tlng=en
Autor:
Renata F. Fonseca, Eduardo E. Castilla, Eliana Ternes Pereira, Marcelo Aguiar Costa-Lima, Iêda M. Orioli
Publikováno v:
Molecular medicine reports. 1(5)
Beare-Stevenson syndrome (BSS) (MIM#123790) is a rare disorder characterized by craniofacial anomalies and cutis gyrata associated with anogenital anomalies and prominent umbilical stump. There are few reports on the syndrome, and molecular analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa5930d9242b2542f64e52f82ad9205
https://pubmed.ncbi.nlm.nih.gov/21479481
https://pubmed.ncbi.nlm.nih.gov/21479481