Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yanca Gasparini De Oliveira"'
Autor:
Gleyson Francisco da Silva Carvalho, Claudio Melo de Gusmão, Beatriz Martins Wolff, Lucas Liro Vieira, Yanca Gasparini de Oliveira, Mariana Ribeiro Costa, Rafaela da Silva Mendes, Matheus Augusto Araujo Castro, Mayara T. Sakuma, Fernando Kok, Bekim Sadikovic, Leslie Domenici Kulikowski
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-6 (2024)
Abstract Background/objectives KMT2B-related dystonia (DYT28, OMIM #617284) is a progressive neurological condition characterized by early onset movement disorders with autosomal dominant inheritance. In this study, we describe the use of a genome me
Externí odkaz:
https://doaj.org/article/e38394b069fe409d83aec71fa3b2331e
Autor:
Amanda Brasil de Freitas, Rossana Pulcineli Vieira Francisco, Mara Sandra Hoshida, Yanca Gasparini De Oliveira, Leslie Domenici Kulikowski, Maria de Lourdes Brizot
Publikováno v:
Birth Defects Research. 114:1291-1297
Autor:
Jullian Gabriel Damasceno, Gleyson Francisco da Silva Carvalho, Amom Mendes do Nascimento, Lucas Liro Vieira, Vanessa Tavares Almeida, Yanca Gasparini de Oliveira, Leslie Domenici Kulikowski
The diversity of techniques used in an academic research laboratory generates a range of raw data with different formats and information that can exceed 1 gigabyte or terabyte per processing performed. Thus, laboratories need to seek efficient soluti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33d3840cfb1bc0580750ba137453c190
https://doi.org/10.21203/rs.3.rs-2100001/v1
https://doi.org/10.21203/rs.3.rs-2100001/v1
Autor:
Samar Nasser Chehimi, Vanessa Tavares Almeida, Amom Mendes Nascimento, Évelin Aline Zanardo, Yanca Gasparini de Oliveira, Gleyson Francisco da Silva Carvalho, Beatriz Martins Wolff, Marilia Moreira Montenegro, Nilson Antônio de Assunção, Chong Ae Kim, Leslie Domenici Kulikowski
Publikováno v:
Clinics, Volume: 77, Article number: 100045, Published: 06 JUL 2022
Objectives Copy Number Variations (CNVs) in the human genome account for common populational variations but can also be responsible for genetic syndromes depending on the affected region. Although a deletion in 5p is responsible for a syndrome with h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82304336cd81347b17743a736c8439f0
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322022000100227&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322022000100227&lng=en&tlng=en
Autor:
Gleyson Francisco da Silva Carvalho, Thais Virginia Moura Machado Costa, Amom Mendes Nascimento, Beatriz Martins Wolff, Julian Gabriel Damasceno, Lucas Liro Vieira, Vanessa Tavares Almeida, Yanca Gasparini de Oliveira, Claudia Berlim de Mello, Mauro Muszkat, Leslie Domenici Kulikowski
Publikováno v:
Clinical Neurology and Neurosurgery. 228:107714