Zobrazeno 1 - 10 of 53 pro vyhledávání: '"Camila F. Almeida"'
1
Akademický článek
Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouse
Autor: Nicolas Wein, Tatyana A. Vetter, Adeline Vulin, Tabatha R. Simmons, Emma C. Frair, Adrienne J. Bradley, Liubov V. Gushchina, Camila F. Almeida, Nianyuan Huang, Daniel Lesman, Dhanarajan Rajakumar, Robert B. Weiss, Kevin M. Flanigan
Publikováno v: Molecular Therapy: Methods & Clinical Development, Vol 26, Iss , Pp 279-293 (2022)
Duchenne muscular dystrophy (DMD) is typically caused by mutations that disrupt the DMD reading frame, but nonsense mutations in the 5′ part of the gene induce utilization of an internal ribosomal entry site (IRES) in exon 5, driving expression of
Externí odkaz: https://doaj.org/article/937ffb28cf15459caaa9793b8cebec7b
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2
Akademický článek
Promising AAV.U7snRNAs vectors targeting DMPK improve DM1 hallmarks in patient-derived cell lines
Autor: Camila F. Almeida, Florence Robriquet, Tatyana A. Vetter, Nianyuan Huang, Reid Neinast, Lumariz Hernandez-Rosario, Dhanarajan Rajakumar, W. David Arnold, Kim L. McBride, Kevin M. Flanigan, Robert B. Weiss, Nicolas Wein
Publikováno v: Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Myotonic dystrophy type 1 (DM1) is the most common form of muscular dystrophy in adults and affects mainly the skeletal muscle, heart, and brain. DM1 is caused by a CTG repeat expansion in the 3′UTR region of the DMPK gene that sequesters musclebli
Externí odkaz: https://doaj.org/article/64f77f1950614b9e88620a368751f95d
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3
Akademický článek
Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy
Autor: Stephanie A. Fernandes, Camila F. Almeida, Lucas S. Souza, Monize Lazar, Paula Onofre-Oliveira, Guilherme L. Yamamoto, Letícia Nogueira, Letícia Y. Tasaki, Rafaela R. Cardoso, Rita C. M. Pavanello, Helga C. A. Silva, Merari F. R. Ferrari, Anne Bigot, Vincent Mouly, Mariz Vainzof, Annemieke Aartsma-Rus, James Dowling, Maaike van Putten
Publikováno v: Disease Models & Mechanisms, Vol 13, Iss 2 (2020)
X-linked myopathy with excessive autophagy (XMEA) is a genetic disease associated with weakness of the proximal muscles. It is caused by mutations in the VMA21 gene, coding for a chaperone that functions in the vacuolar ATPase (v-ATPase) assembly. Mu
Externí odkaz: https://doaj.org/article/b0cb6d4e3d1a46c39a87d324c172427c
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4
Akademický článek
Muscle Satellite Cells: Exploring the Basic Biology to Rule Them
Autor: Camila F. Almeida, Stephanie A. Fernandes, Antonio F. Ribeiro Junior, Oswaldo Keith Okamoto, Mariz Vainzof
Publikováno v: Stem Cells International, Vol 2016 (2016)
Adult skeletal muscle is a postmitotic tissue with an enormous capacity to regenerate upon injury. This is accomplished by resident stem cells, named satellite cells, which were identified more than 50 years ago. Since their discovery, many researche
Externí odkaz: https://doaj.org/article/f43c0589045943158d046a0f0f065af8
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5
Akademický článek
Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, Largemyd and mdx/Largemyd.
Autor: Aurea B Martins-Bach, Jackeline Malheiros, Béatrice Matot, Poliana C M Martins, Camila F Almeida, Waldir Caldeira, Alberto F Ribeiro, Paulo Loureiro de Sousa, Noura Azzabou, Alberto Tannús, Pierre G Carlier, Mariz Vainzof
Publikováno v: PLoS ONE, Vol 10, Iss 2, p e0117835 (2015)
Quantitative nuclear magnetic resonance imaging (MRI) has been considered a promising non-invasive tool for monitoring therapeutic essays in small size mouse models of muscular dystrophies. Here, we combined MRI (anatomical images and transverse rela
Externí odkaz: https://doaj.org/article/79f88b1f38d94442a785793864f42fe2
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7
Satellite cells deficiency and defective regeneration in dynamin 2-related centronuclear myopathy
Autor: Marc Bitoun, Camila F Almeida, Mariz Vainzof
Publikováno v: FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2021, 35 (4), pp.e21346. ⟨10.1096/fj.202001313rrr⟩
International audience; Dynamin 2 (DNM2) is a ubiquitously expressed protein involved in many functions related to trafficking and remodeling of membranes and cytoskeleton dynamics. Mutations in the DNM2 gene cause the autosomal dominant centronuclea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b607a267b94f82def5a1247632973ca4
https://pubmed.ncbi.nlm.nih.gov/33715228
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8
Skeletal Muscle Injury by Electroporation: A Model to Study Degeneration/Regeneration Pathways in Muscle
Autor: Camila F, Almeida, Mariz, Vainzof
Publikováno v: Methods in molecular biology (Clifton, N.J.). 2063
Skeletal muscle has a remarkable capacity to regenerate after injuries mainly due to a reservoir of precursor cells named satellite cells (SCs), which are responsible for after-birth growth and response to lesions, either by exercise or disease. Upon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7623a900543ff6c8424ad513e18d6152
https://pubmed.ncbi.nlm.nih.gov/31667769
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9
Skeletal Muscle Injury by Electroporation: A Model to Study Degeneration/Regeneration Pathways in Muscle
Autor: Camila F. Almeida, Mariz Vainzof
Publikováno v: Methods in Molecular Biology ISBN: 9781071601372
Skeletal muscle has a remarkable capacity to regenerate after injuries mainly due to a reservoir of precursor cells named satellite cells (SCs), which are responsible for after-birth growth and response to lesions, either by exercise or disease. Upon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd75ef4ab37a7da088971e1c1c323453
https://doi.org/10.1007/978-1-0716-0138-9_12
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10
Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies
Autor: Antonio Fernando Ribeiro, Stephanie A. Fernandes, Mariz Vainzof, A.L.F. Santos, Lucas Santos Souza, Camila F. Almeida, P.C.G. Onofre-Oliveira, Danielle A. Guerrieri, Renata Ishiba
Publikováno v: Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Satellite cells (SCs) are the main muscle stem cells responsible for its regenerative capacity. In muscular dystrophies, however, a failure of the regenerative process results in muscle degeneration and weakness. To analyze the effect of different de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d989faa696300a31b86749928bfae5ee
https://doi.org/10.1038/s41598-019-48156-7
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