| Muscle satellite cells: exploring the basic biology to rule them CF Almeida, SA Fernandes, AF Ribeiro Junior, O Keith Okamoto, ... Stem cells international 2016 (1), 1078686, 2016 | 73 | 2016 |
| Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies AF Ribeiro Jr, LS Souza, CF Almeida, R Ishiba, SA Fernandes, ... Scientific reports 9 (1), 11842, 2019 | 59 | 2019 |
| Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern A Cotta, JF Paim, AL da-Cunha-Junior, RX Neto, SV Nunes, MM Navarro, ... BMC Clinical Pathology 14, 1-5, 2014 | 27 | 2014 |
| Muscle phenotypic variability in limb girdle muscular dystrophy 2 G JF Paim, A Cotta, AP Vargas, MM Navarro, J Valicek, E Carvalho, ... Journal of Molecular Neuroscience 50, 339-344, 2013 | 26 | 2013 |
| Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy … AB Martins-Bach, J Malheiros, B Matot, PCM Martins, CF Almeida, ... PloS one 10 (2), e0117835, 2015 | 23 | 2015 |
| Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouse N Wein, TA Vetter, A Vulin, TR Simmons, EC Frair, AJ Bradley, ... Molecular Therapy-Methods & Clinical Development 26, 279-293, 2022 | 21 | 2022 |
| The mdx mutation in the 129/Sv background results in a milder phenotype: Transcriptome comparative analysis searching for the protective factors PC Calyjur, CF Almeida, D Ayub-Guerrieri, AF Ribeiro, SA Fernandes, ... PloS one 11 (3), e0150748, 2016 | 16 | 2016 |
| Comparative transcriptome analysis of muscular dystrophy models Largemyd, Dmdmdx/Largemyd and Dmdmdx: what makes them different? CF Almeida, P Martins, M Vainzof European Journal of Human Genetics 24 (9), 1301-1309, 2016 | 15 | 2016 |
| Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy SA Fernandes, CF Almeida, LS Souza, M Lazar, P Onofre-Oliveira, ... Disease Models & Mechanisms 13 (2), dmm041244, 2020 | 14 | 2020 |
| Skeletal muscle injury by electroporation: a model to study degeneration/regeneration pathways in muscle CF Almeida, M Vainzof Nucleic Acid Detection and Structural Investigations: Methods and Protocols …, 2020 | 8 | 2020 |
| GP 40 LGMD2G with clinical presentation of congenital muscular dystrophy: A rare phenotype CF Almeida, BL Lima, PCG Onofre-Oliveira, RCM Pavanello, M Zatz, ... Neuromuscular Disorders 22 (9), 831, 2012 | 8 | 2012 |
| Satellite cells deficiency and defective regeneration in dynamin 2‐related centronuclear myopathy CF Almeida, M Bitoun, M Vainzof FASEB Journal 35 (4), e21346, 2021 | 7 | 2021 |
| Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse R Ishiba, ALF Santos, CF Almeida, LC Caires, AF Ribeiro, ... Journal of Molecular Histology 50, 375-387, 2019 | 6 | 2019 |
| Satellite cell alteration in DNM2-related centronuclear myopathy C Almeida, M Bitoun, M Vainzof Neuromuscular Disorders 27, S174, 2017 | 2 | 2017 |
| Promising AAV.U7snRNAs vectors targeting DMPK improve DM1 hallmarks in patient-derived cell lines CF Almeida, F Robriquet, TA Vetter, N Huang, R Neinast, ... Frontiers in Cell and Developmental Biology 11, 1181040, 2023 | 1 | 2023 |
| Direct Reprogramming of Human Fibroblasts into Myoblasts to Investigate Therapies for Neuromuscular Disorders CF Almeida, EC Frair, N Huang, R Neinast, KL McBride, RB Weiss, ... JoVE (Journal of Visualized Experiments), e61991, 2021 | 1 | 2021 |
| AP 14: A new in/del in the critical splicing region of the VMA21 gene causing X-linked myopathy with excessive autophagy (XMEA) M Vainzof, M Lazar, GL Yamamoto, CF Almeida, P Onofre-Oliveira, ... Neuromuscular Disorders 24 (9), 834-835, 2014 | 1 | 2014 |
| P. 5.8 Why is LGMD2G rare? CF Almeida, PCG Onofre-Oliveira, M Zatz, L Negrao, M Vainzof Neuromuscular Disorders 23 (9), 766, 2013 | 1 | 2013 |
| Skeletal muscle regeneration in DNM2-related centronuclear myopathy CF Almeida Universidade de São Paulo, 2019 | | 2019 |
| CONGENITAL MYOPATHIES (CNM): P. 141High frequency of manifesting carriers in the recessive X-linked myotubular myopathy L Souza, C Almeida, L Silva, R Pavanello, J Gurgel-Gianneti, E Zanoteli, ... Neuromuscular Disorders 28, S71-S72, 2018 | | 2018 |
Mariz VainzofCentro de Estudos do Genoma Humano e Células Tronco, IBUSP在 usp.br 的电子邮件经过验证
