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Fapesp-Cepid, CEGH-CEL
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ResearcherID: J-3613-2015
Other Names: HUG-CELL; Human Genoma; Centro de Pesquisa do Genoma Humano
URL: http://www.researcherid.com/rid/J-3613-2015
Subject: Cell Biology; Genetics & Heredity
Keywords: genetics, genomics, stem-cells
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Institute of Bioscience; Department of Genetics and Evolutionary Biology
Role:
Description:
My URLs: http://www.genoma.ib.usp.br
 
 

This list contains papers that I have authored.

publication(s)  
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1.  Title: Congenital Muscular Dystrophy 1D Causes Matrix Metalloproteinase Activation And Blood-Brain Barrier Impairment
 Author(s): Schactae, Aryadnne L.; Palmas, Daphne; Michels, Monique; et al.
 Source: Current Neurovascular Research Volume: 14 Issue: 1 Pages: 60-64 Published: 2017
 Times Cited: 0
 DOI: 10.2174/1567202613666161201204549
added
14-Mar-17
2.  Title: Different Donors Mesenchymal Stromal Cells Secretomes Reveal Heterogeneous Profile of Relevance for Therapeutic Use
 Author(s): Assoni, Amanda; Coatti, Giuliana; Valadares, Marcos C.; et al.
 Source: Stem Cells and Development Volume: 26 Issue: 3 Pages: 206-214 Published: FEB 1 2017
 Times Cited: 2
 DOI: 10.1089/scd.2016.0218
added
18-Aug-17
3.  Title: Exomic variants of an elderly cohort of Brazilians in the ABraOM database
 Author(s): Naslavsky, Michel Satya; Yamamoto, Guilherme Lopes; de Almeida, Tatiana Ferreira; et al.
 Source: Human Mutation Volume: 38 Issue: 7 Pages: 751-763 Published: JUL 2017
 Times Cited: 1
 DOI: 10.1002/humu.23220
added
18-Aug-17
4.  Title: Myocardial Fibrosis Progression in Duchenne and Becker Muscular Dystrophy A Randomized Clinical Trial
 Author(s): Silva, Marly Conceicao; Magalhaes, Tiago Augusto; Alves Meira, Zilda Maria; et al.
 Source: Jama Cardiology Volume: 2 Issue: 2 Pages: 190-199 Published: FEB 2017
 Times Cited: 4
 DOI: 10.1001/jamacardio.2016.4801
added
18-Aug-17
5.  Title: Neuropathological diagnoses and clinical correlates in older adults in Brazil: A cross-sectional study
 Author(s): Suemoto, Claudia K.; Ferretti-Rebustini, Renata E. L.; Rodriguez, Roberta D.; et al.
 Source: Plos Medicine Volume: 14 Issue: 3 Published: MAR 2017
 Times Cited: 0
 DOI: 10.1371/journal.pmed.1002267
added
18-Aug-17
6.  Title: Repression of phosphatidylinositol transfer protein a ameliorates the pathology of Duchenne muscular dystrophy
 Author(s): Vieira, Natassia M.; Spinazzola, Janelle M.; Alexander, Matthew S.; et al.
 Source: Proceedings of the National Academy of Sciences of the United States of America Volume: 114 Issue: 23 Pages: 6080-6085 Published: JUN 6 2017
 Times Cited: 0
 DOI: 10.1073/pnas.1703556114
added
18-Aug-17
7.  Title: Targeted Molecular Investigation in Patients within the Clinical Spectrum of Auriculocondylar Syndrome
 Author(s): Romanelli Tavares, Vanessa L.; Zechi-Ceide, Roseli M.; Bertola, Debora R.; et al.
 Source: American Journal of Medical Genetics Part a Volume: 173 Issue: 4 Pages: 938-945 Published: APR 2017
 Times Cited: 0
 DOI: 10.1002/ajmg.a.38101
added
18-Aug-17
8.  Title: A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability
 Author(s): Figueiredo, T.; Melo, U. S.; Pessoa, A. L. S.; et al.
 Source: Molecular Psychiatry Volume: 21 Issue: 8 Pages: 1125-1129 Published: AUG 2016
 Times Cited: 1
 DOI: 10.1038/mp.2015.150
added
14-Mar-17
9.  Title: A MILD PANCREATIC SUFFICIENT CF-PHENOTYPE ON TWO UNRELATED PATIENTS WITH THE I148N;5T MUTATION
 Author(s): Nunes, Luisa Mesquita; Niewiandonski, Vivian D. T.; Gaburo, Nelson; et al.
 Source: Pediatric Pulmonology Volume: 51 Pages: S48 Published: APR 2016
 Times Cited: 0
added
14-Mar-17
10.  Title: A novel GFAP mutation in a type II (late-onset) Alexander disease patient
 Author(s): Brandao de Paiva, Anderson Rodrigues; Freua, Fernando; Lucato, Leandro Tavares; et al.
 Source: Journal of Neurology Volume: 263 Issue: 4 Pages: 821-822 Published: APR 2016
 Times Cited: 0
 DOI: 10.1007/s00415-016-8065-8
added
14-Mar-17
publication(s)  
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