Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Danielle Ribeiro Lucon"'
Autor:
Felipe Luz Torres Silva, Mayara Ferreira Euzébio, Juliana Silveira Ruas, Mayra Troiani Franco, Alejandro Enzo Cassone, Thais Junqueira, Danielle Ribeiro Lucon, Izilda Aparecida Cardinalli, Luis Henrique Pereira, Priscila Pini Zenatti, Patricia Yoshioka Jotta, Mariana Maschietto
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Pediatric sarcomas present heterogeneous morphology, genetics and clinical behavior posing a challenge for an accurate diagnosis. DNA methylation is an epigenetic modification that coordinates chromatin structure and regulates gene expressio
Externí odkaz:
https://doaj.org/article/cccf1954e3c14402a2fad4dd095233ca
Autor:
Antonio Victor Campos Coelho, Bruna Mascaro-Cordeiro, Danielle Ribeiro Lucon, Maria Soares Nóbrega, Rodrigo de Souza Reis, Rodrigo Bertollo de Alexandre, Livia Maria Silva Moura, Gustavo Santos de Oliveira, Rafael Lucas Muniz Guedes, Marcel Pinheiro Caraciolo, Nuria Bengala Zurro, Murilo Castro Cervato, João Bosco Oliveira
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Rare diseases affect up to 13.2 million individuals in Brazil. The Brazilian Rare Genomes Project is envisioned to further the implementation of genomic medicine into the Brazilian public healthcare system. Here we report the validation results of a
Externí odkaz:
https://doaj.org/article/e5119c6c2b3948508f5dfa34f830ae7b
Autor:
Danielle Ribeiro Lucon, Cristiane eRocha, Rogério eCraveiro, Dagmar eDillo, Izilda A Cardinalli, Denise Pontes Cavalcanti, Simone dos Santos Aguiar, Claudia Vianna Maurer-Morelli, Jose Andres Yunes
Publikováno v:
Frontiers in Oncology, Vol 3 (2013)
Medulloblastoma (MB) is one of the most common pediatric cancers, likely originating from abnormal development of cerebellar progenitor neurons. MicroRNA (miRNA) has been shown to play an important role in the development of the central nervous syste
Externí odkaz:
https://doaj.org/article/9bd67ea7de8640e4a27d0816c22410dd
Autor:
Antonio Victor Campos Coelho, Bruna Mascaro-Cordeiro, Danielle Ribeiro Lucon, Maria Soares Nóbrega, Rodrigo de Souza Reis, Rodrigo Bertollo de Alexandre, Livia Maria Silva Moura, Gustavo Santos de Oliveira, Rafael Lucas Muniz Guedes, Marcel Pinheiro Caraciolo, Nuria Bengala Zurro, Murilo Castro Cervato, João Bosco Oliveira
Publikováno v:
Frontiers in molecular biosciences. 9
Rare diseases affect up to 13.2 million individuals in Brazil. The Brazilian Rare Genomes Project is envisioned to further the implementation of genomic medicine into the Brazilian public healthcare system. Here we report the validation results of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::663ba286249285140743c9a30fc49c72
https://pubmed.ncbi.nlm.nih.gov/35586190
https://pubmed.ncbi.nlm.nih.gov/35586190
Publikováno v:
Genetics and Molecular Biology v.29 n.1 2006
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 29, Issue: 1, Pages: 36-37, Published: 2006
Genetics and Molecular Biology, Vol 29, Iss 1, Pp 36-37 (2006)
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 29, Issue: 1, Pages: 36-37, Published: 2006
Genetics and Molecular Biology, Vol 29, Iss 1, Pp 36-37 (2006)
Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a984e42ad7006cd467b8663bd88e63a7
https://doi.org/10.1590/s1415-47572006000100006
https://doi.org/10.1590/s1415-47572006000100006