ResearcherID.com
ResearcherID Thomson Reuters  

Fapesp-Cepid, CEGH-CEL
Create a ResearcherID badge for this researcher View publications analytics for this researcher
Close
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)  
First Page Previous Page Page   of  26  Go Next Page Last Page
  Sort by:    Results per page: 
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: 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
3. 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
4. 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
5. Title: ACTIVITY OF KREBS CYCLE ENZYMES IN mdx MICE
Author(s): Comim, Clarissa M.; Hoepers, Andreza; Ventura, Leticia; et al.
Source: Muscle & Nerve Volume: 53 Issue: 1 Pages: 91-95 Published: JAN 2016
Times Cited: 0
DOI: 10.1002/mus.24704
added
08-Aug-16
6. Title: An adverse immune-endocrine profile in patients with tuberculosis and type 2 diabetes
Author(s): Fernandez, R.; Diaz, A.; D'Attilio, L.; et al.
Source: Tuberculosis Volume: 101 Pages: 95-101 Published: DEC 2016
Times Cited: 0
DOI: 10.1016/j.tube.2016.09.001
added
14-Mar-17
7. Title: Analysis of the autophagic pathway during in vitro muscle differentiation in X-linked myopathy with excessive autophagy
Author(s): Fernandes, S.; Almeida, C.; Onofre-Oliveira, P.; et al.
Source: Neuromuscular Disorders Volume: 26 Pages: S194 Published: OCT 2016
Times Cited: 0
DOI: 10.1016/j.nmd.2016.06.390
added
14-Mar-17
8. Title: Apert and Crouzon Syndromes-Cognitive Development, Brain Abnormalities, and Molecular Aspects
Author(s): Fernandes, Marilyse B. L.; Maximino, Luciana P.; Perosa, Gimol B.; et al.
Source: American Journal of Medical Genetics Part a Volume: 170 Issue: 6 Pages: 1532-1537 Published: JUN 2016
Times Cited: 0
DOI: 10.1002/ajmg.a.37640
added
14-Mar-17
9. Title: Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D
Author(s): Comim, Clarissa M.; Schactae, Aryadnne L.; Soares, Jaime A.; et al.
Source: Molecular Neurobiology Volume: 53 Issue: 1 Pages: 402-407 Published: JAN 2016
Times Cited: 1
DOI: 10.1007/s12035-014-9024-y
added
12-Aug-16
10. Title: Cell Type-Dependent Nonspecific Fibroblast Growth Factor Signaling in Apert Syndrome
Author(s): Yeh, Erika; Atique, Rodrigo; Fanganiello, Roberto Dalto; et al.
Source: Stem Cells and Development Volume: 25 Issue: 16 Pages: 1249-1260 Published: AUG 2016
Times Cited: 0
DOI: 10.1089/scd.2016.0018
added
14-Mar-17
publication(s)  
First Page Previous Page Page   of  26  Go Next Page Last Page
  Sort by:    Results per page: