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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: A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations
 Author(s): Munford, V.; Castro, L. P.; Souto, R.; et al.
 Source: British Journal of Dermatology Volume: 176 Issue: 5 Pages: 1270-1278 Published: MAY 2017
 Times Cited: 2
added
10-Oct-17
2.  Title: Aqueous extract of Pinus caribaea inhibits the damage induced by ultraviolet radiations, in plasmid DNA
 Author(s): Vernhes Tamayo, Marioly; Schuch, Andre Passaglia; Fuentes-Leon, Fabiana; et al.
 Source: Journal of Pharmacy & Pharmacognosy Research Volume: 5 Issue: 4 Pages: 262-269 Published: JUL-AUG 2017
 Times Cited: 0
added
10-Oct-17
3.  Title: Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype
 Author(s): Wade, Emma M.; Jenkins, Zandra A.; Daniel, Philip B.; et al.
 Source: American Journal of Medical Genetics Part a Volume: 173 Issue: 7 Pages: 1739-1746 Published: JUL 2017
 Times Cited: 0
 DOI: 10.1002/ajmg.a.38267
added
10-Oct-17
4.  Title: Chaperone-mediated autophagy prevents cellular transformation by regulating MYC proteasomal degradation
 Author(s): Gomes, Luciana R.; Menck, Carlos F. M.; Cuervo, Ana Maria
 Source: Autophagy Volume: 13 Issue: 5 Pages: 928-940 Published: 2017
 Times Cited: 0
 DOI: 10.1080/15548627.2017.1293767
added
10-Oct-17
5.  Title: Clinical and genetic characterization of leukoencephalopathies in adults
 Author(s): Lynch, David S.; Brandao de Paiva, Anderson Rodrigues; Zhang, Wei Jia; et al.
 Source: Brain Volume: 140 Pages: 1204-1211 Published: MAY 2017
 Times Cited: 0
 DOI: 10.1093/brain/awx045
added
10-Oct-17
6.  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
7.  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: 3
 DOI: 10.1089/scd.2016.0218
added
18-Aug-17
8.  Title: Direct participation of DNA in the formation of singlet oxygen and base damage under UVA irradiation
 Author(s): Yagura, Teiti; Schuch, Andre Passaglia; Machado Garcia, Camila Carriao; et al.
 Source: Free Radical Biology and Medicine Volume: 108 Pages: 86-93 Published: JUL 2017
 Times Cited: 0
 DOI: 10.1016/j.freeradbiomed.2017.03.018
added
10-Oct-17
9.  Title: Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins
 Author(s): Jehee, Fernanda S.; de Oliveira, Valdirene T.; Gurgel-Giannetti, Juliana; et al.
 Source: American Journal of Medical Genetics Part a Volume: 173 Issue: 9 Pages: 2451-2455 Published: SEP 2017
 Times Cited: 0
 DOI: 10.1002/ajmg.a.38315
added
10-Oct-17
10.  Title: EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome
 Author(s): Miller, Emily E.; Kobayashi, Gerson S.; Musso, Camila M.; et al.
 Source: Human Molecular Genetics Volume: 26 Issue: 12 Pages: 2177-2191 Published: JUN 15 2017
 Times Cited: 0
 DOI: 10.1093/hmg/ddx078
added
10-Oct-17
publication(s)  
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