Cibely C Fontes-Oliveira
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Explore the profile of Cibely C Fontes-Oliveira including associated specialties, affiliations and a list of published articles.
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7
Citations
198
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Recent Articles
1.
Harandi V, Oliveira B, Allamand V, Friberg A, Fontes-Oliveira C, Durbeej M
Antioxidants (Basel)
. 2020 Mar;
9(3).
PMID: 32197453
Congenital muscular dystrophy with laminin α2 chain-deficiency (LAMA2-CMD) is a severe neuromuscular disorder without a cure. Using transcriptome and proteome profiling as well as functional assays, we previously demonstrated significant...
2.
Fontes-Oliveira C, M Soares Oliveira B, Korner Z, Harandi V, Durbeej M
Sci Rep
. 2018 Nov;
8(1):16302.
PMID: 30389963
Congenital muscular dystrophy with laminin α2 chain-deficiency (LAMA2-CMD) is a severe muscle disorder with complex underlying pathogenesis. We have previously employed profiling techniques to elucidate molecular patterns and demonstrated significant...
3.
Fontes-Oliveira C, Steinz M, Schneiderat P, Mulder H, Durbeej M
Sci Rep
. 2017 Apr;
7:45272.
PMID: 28367954
Skeletal muscle has high energy requirement and alterations in metabolism are associated with pathological conditions causing muscle wasting and impaired regeneration. Congenital muscular dystrophy type 1A (MDC1A) is a severe...
4.
Belizario J, Fontes-Oliveira C, Borges J, Kashiabara J, Vannier E
Springerplus
. 2016 Jun;
5:619.
PMID: 27330885
Adult skeletal tissue is composed of heterogeneous population of cells that constantly self-renew by means of a controlled process of activation and proliferation of tissue-resident stem cells named satellite cells....
5.
Bancovik J, Moreira D, Carrasco D, Yao J, Porter D, Moura R, et al.
BMC Cancer
. 2015 Apr;
15:70.
PMID: 25879571
Background: We previously identified dermicidin (DCD), which encodes a growth and survival factor, as a gene amplified and overexpressed in a subset of breast tumors. Patients with DCD-positive breast cancer...
6.
de Oliveira B, Matsumura C, Fontes-Oliveira C, Gawlik K, Acosta H, Wernhoff P, et al.
Mol Cell Proteomics
. 2014 Jul;
13(11):3001-13.
PMID: 24994560
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most severe forms of muscular disease and is characterized by severe muscle weakness and delayed motor milestones....
7.
Korner Z, Fontes-Oliveira C, Holmberg J, Carmignac V, Durbeej M
Am J Pathol
. 2014 Mar;
184(5):1518-28.
PMID: 24631023
Congenital muscular dystrophy, caused by mutations in LAMA2 (the gene encoding laminin α2 chain), is a severe and incapacitating disease for which no therapy is yet available. We have recently...