Fetal gastroschisis: Maternal and fetal methylation profile

Autor: Sandra F Centofanti, Samar N. Chehimi, Amanda B Freitas, Rossana Pulcineli Vieira Francisco, J. G. Damasceno, Leslie Domenici Kulikowski, Maria de Lourdes Brizot, Gilmar de Souza Osmundo-Junior

Publikováno v: Prenatal Diagnosis. 41:449-456

Objective The purpose of this study was to describe the genomic deoxyribonucleic acid (DNA) methylation profile in fetuses with gastroschisis, determine whether the profile was inherited, and investigate any possible correlations with maternal risk f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c38dcee7777d86a12ad01acf5e0b216
https://doi.org/10.1002/pd.5881

Influence of creep feeder position on the behavior and performance of preweaning piglets and sows in a hot climate environment

Autor: Jamilly G. Damasceno, Héllen Krislen Souza Lima, Pedro Henrique Nascimento, Vitor de Oliveira Araújo, Jacqueline S. Neves, Allan P Schinckel, Natália C. Oliveira, Bruno M. Monteiro, Elaine L.L. Nascimento, Juliana Silva, Rafael Aquino de Oliveira, Maria de Fátima Araújo Vieira, Cesar Augusto Pospissil Garbossa, Ewerson S. Oliveira

Publikováno v: Anais da Academia Brasileira de Ciências, Volume: 93, Issue: 3, Article number: e20200248, Published: 10 MAY 2021
Anais da Academia Brasileira de Ciências, Vol 93, Iss 3 (2021)
Anais da Academia Brasileira de Ciências v.93 n.3 2021
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

The use of creep feeding for preweaning piglets is important to improve the performance of the piglets. The objective of this experiment was evaluate the effect of using or altering the position of piglet’s creep feeder during lactation on piglet�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086c8176b34c94feb88b7b72b2a66564
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652021000501306&lng=en&tlng=en

Breakpoint delineation in 5p‐ patients leads to new insights about microcephaly and the typical high‐pitched cry

Autor: Evelin Aline Zanardo, José Ricardo Magliocco Ceroni, J. G. Damasceno, F. A. R. Madia, Samar N. Chehimi, Gil Monteiro Novo Filho, Marília M. Montenegro, Leslie Domenici Kulikowski, Alexandre T. Dias, Yanca Gasparini, Thaís Virgínia Moura Machado Costa, Amom M. Nascimento, Chong Ae Kim

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine

Background Cri du chat syndrome (CdCS) is a rare syndrome caused by a partial or complete deletion of the short arm of chromosome 5 (5p‐). The main clinical features include a high‐pitched cry, facial asymmetry, microcephaly, round face at birth,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6276d6407ad604c6e62f5b7d74077dd5
https://doaj.org/article/efd42a79e0bf410cb0c3de2027bd665a

Caracterização e Classificação de Bots Utilizando a Rede de Comentários do Reddit

Autor: Daniel R. Figueiredo, Rafael G. Damasceno

Publikováno v: Anais do Workshop em Desempenho de Sistemas Computacionais e de Comunicação (WPerformance).

Redes sociais online desempenham um papel cada vez mais importante na sociedade, tendo em vista sua influência na formação de opinião de milhões de usuários. Contudo, a presença de bots (usuários com comportamento programado) surge como uma p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5772ac5462d4bbdd46d6f7e4528ef2af
https://doi.org/10.5753/wperformance.2019.6471

Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines

Autor: Amom M. Nascimento, Samar N. Chehimi, Rachel Sayuri Honjo, Thaís Virgínia Moura Machado Costa, José Ricardo Magliocco Ceroni, Gil M. Novo-Filho, Alexandre T. Dias, Yanca Gasparini, Chong Ae Kim, F. A. R. Madia, Evelin Aline Zanardo, Leslie Domenici Kulikowski, J. G. Damasceno, Marília M. Montenegro

Publikováno v: Cytogenetic and genome research. 157(3)

Mosaic trisomy 12 is a rare anomaly, and only 9 cases of live births with this condition have been reported in the literature. The clinical phenotype is variable, including neuropsychomotor developmental delay, congenital heart disease, microcephaly,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90629ea1954e00586a6624f3b7a63031
https://pubmed.ncbi.nlm.nih.gov/30933946