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Julliane Tamara Araújo de Melo Campos
Julliane Tamara Araújo de Melo Campos
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Cited by
Cited by
Year
DNA damage by singlet oxygen and cellular protective mechanisms
LF Agnez-Lima, JTA Melo, AE Silva, AHS Oliveira, ARS Timoteo, ...
Mutation Research/Reviews in Mutation Research 751 (1), 15-28, 2012
2392012
Causes of death in patients with Berardinelli-Seip congenital generalized lipodystrophy
JG Lima, LHC Nobrega, NN Lima, MCF Dos Santos, PHD Silva, ...
PLoS One 13 (6), e0199052, 2018
602018
Resveratrol decreases the expression of genes involved in inflammation through transcriptional regulation
DML Pinheiro, AHS de Oliveira, LG Coutinho, FL Fontes, ...
Free Radical Biology and Medicine 130, 8-22, 2019
482019
The worldwide mutational landscape of Berardinelli-Seip congenital lipodystrophy
ASC Sarmento, LC Ferreira, JG Lima, LB de Azevedo Medeiros, ...
Mutation Research/Reviews in Mutation Research 781, 30-52, 2019
352019
High prevalence of Berardinelli-Seip Congenital Lipodystrophy in Rio Grande do Norte State, Northeast Brazil
LB de Azevedo Medeiros, VK Cândido Dantas, AS Craveiro Sarmento, ...
Diabetology & Metabolic Syndrome 9, 1-6, 2017
302017
Mitochondrial maintenance under oxidative stress depends on mitochondrially localised α-OGG1
D Lia, A Reyes, JTA de Melo Campos, T Piolot, J Baijer, JP Radicella, ...
Journal of Cell Science 131 (12), jcs213538, 2018
252018
SNPs in DNA repair genes associated to meningitis and host immune response
TA da Silva, FL Fontes, LG Coutinho, FRS de Souza, JTA de Melo, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 713 (1 …, 2011
242011
Exploring seipin: From biochemistry to bioinformatics predictions
AS Craveiro Sarmento, LB de Azevedo Medeiros, LF Agnez-Lima, ...
International Journal of Cell Biology 2018, 2018
232018
XPC deficiency is related to APE1 and OGG1 expression and function
JTA de Melo, AR de Souza Timoteo, TBP Lajus, JA Brandão, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 784, 25-33, 2016
212016
A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases
JG Lima, LHC Nobrega, FTM Bandeira, AGP Sousa, ...
Atherosclerosis 322, 31-38, 2021
172021
Impairment of respiratory muscle strength in Berardinelli-Seip congenital lipodystrophy subjects
JL Dantas de Medeiros, B Carneiro Bezerra, TA Brito de Araújo, ...
Respiratory Research 19, 1-11, 2018
102018
Changes in redox and endoplasmic reticulum homeostasis are related to congenital generalized lipodystrophy type 2
ASC Sarmento, JG Lima, AR de Souza Timoteo, MAG Ururahy, ...
Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2020
82020
Nurses' knowledge about Berardinelli-Seip congenital lipodystrophy
VK Cândido Dantas, JS Soares, LB de Azevedo Medeiros, ...
Plos one 13 (6), e0197784, 2018
82018
Congenital generalized lipodystrophy
JG Lima, MCF dos Santos, JTA de Melo Campos
Journal of Rare Diseases Research & Treatment 3 (2), 2018
82018
XPA deficiency affects the ubiquitin-proteasome system function
AM de Sousa Leal, LB de Azevedo Medeiros, CO Muñoz-Cadavid, ...
DNA repair 94, 102937, 2020
62020
Endoplasmic reticulum stress and muscle dysfunction in congenital lipodystrophies
JTA de Melo Campos, JLD de Medeiros, MEC de Melo, MA da Silva, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1867 (6), 166120, 2021
52021
High prevalence of Berardinelli-Seip Congenital Lipodystrophy in Rio Grande do Norte State, Northeast Brazil. Diabetol Metab Syndr. 2017; 9: 80
LB de Azevedo Medeiros, VK Cândido Dantas, AS Craveiro Sarmento, ...
5
Síndrome de Berardinelli-Seip: aspectos genéticos e morfofisiológicos
JG Lima, JTAM Campos
EDUFRN, 2020
32020
O julgamento da mutação
GK da Silva, JTA de Melo, AHS de Oliveira, EC Silva, SRB de Medeiros, ...
Genética na Escola 8 (1), 42-57, 2013
22013
Metagenomic evaluation of indigenous microbial diversity in tropical mangrove and semi-arid soils from petroliferous basin
CAG Blaha, ILV de Lima Santos, MS Pereira, CM Carvalho, CLV da Silva, ...
Journal of Biotechnology 2 (131), S239, 2007
22007
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