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Page 1
Causes of death in patients with Berardinelli-Seip congenital generalized lipodystrophy.
Lima JG, Nobrega LHC, Lima NN, Dos Santos MCF, Silva PHD, Baracho MFP, Lima DN, de Melo Campos JTA, Ferreira LC, Freire Neto FP, Mendes-Aguiar CO, Jeronimo SMB. Lima JG, et al. Among authors: de melo campos jta. PLoS One. 2018 Jun 8;13(6):e0199052. doi: 10.1371/journal.pone.0199052. eCollection 2018. PLoS One. 2018. PMID: 29883474 Free PMC article.
The worldwide mutational landscape of Berardinelli-Seip congenital lipodystrophy.
Craveiro Sarmento AS, Ferreira LC, Lima JG, de Azevedo Medeiros LB, Barbosa Cunha PT, Agnez-Lima LF, Galvão Ururahy MA, de Melo Campos JTA. Craveiro Sarmento AS, et al. Among authors: de melo campos jta. Mutat Res Rev Mutat Res. 2019 Jul-Sep;781:30-52. doi: 10.1016/j.mrrev.2019.03.005. Epub 2019 Mar 23. Mutat Res Rev Mutat Res. 2019. PMID: 31416577 Review.
Nurses' knowledge about Berardinelli-Seip Congenital Lipodystrophy.
Cândido Dantas VK, Soares JDS, de Azevedo Medeiros LB, Craveiro Sarmento AS, Xavier Nobre TT, de Andrade FB, Gomes de Lima J, de Melo Campos JTA. Cândido Dantas VK, et al. Among authors: de melo campos jta. PLoS One. 2018 Jun 4;13(6):e0197784. doi: 10.1371/journal.pone.0197784. eCollection 2018. PLoS One. 2018. PMID: 29864145 Free PMC article.
Exploring Seipin: From Biochemistry to Bioinformatics Predictions.
Craveiro Sarmento AS, de Azevedo Medeiros LB, Agnez-Lima LF, Lima JG, de Melo Campos JTA. Craveiro Sarmento AS, et al. Among authors: de melo campos jta. Int J Cell Biol. 2018 Sep 19;2018:5207608. doi: 10.1155/2018/5207608. eCollection 2018. Int J Cell Biol. 2018. PMID: 30402103 Free PMC article. Review.
A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.
Lima JG, Helena C Nobrega L, Moura Bandeira FT, Pires Sousa AG, Medeiros de Araujo Macedo TB, Cavalcante Nogueira AC, Fernandes de Oliveira Filho A, Alves RJ, Costa Gurgel Castelo MH, Silva Coelho FM, Maia RE, Lima DN, Timoteo ARS, de Melo Campos JTA. Lima JG, et al. Among authors: de melo campos jta. Atherosclerosis. 2021 Apr;322:31-38. doi: 10.1016/j.atherosclerosis.2021.02.020. Epub 2021 Feb 23. Atherosclerosis. 2021. PMID: 33706081
High prevalence of Berardinelli-Seip Congenital Lipodystrophy in Rio Grande do Norte State, Northeast Brazil.
de Azevedo Medeiros LB, Cândido Dantas VK, Craveiro Sarmento AS, Agnez-Lima LF, Meireles AL, Xavier Nobre TT, de Lima JG, de Melo Campos JTA. de Azevedo Medeiros LB, et al. Among authors: de melo campos jta. Diabetol Metab Syndr. 2017 Oct 13;9:80. doi: 10.1186/s13098-017-0280-7. eCollection 2017. Diabetol Metab Syndr. 2017. PMID: 29046728 Free PMC article.
XPA deficiency affects the ubiquitin-proteasome system function.
de Sousa Leal AM, de Azevedo Medeiros LB, Muñoz-Cadavid CO, de Paula Oliveira R, de Souza Timóteo AR, de Oliveira AHS, Luis Fonseca Faustino A, da Silva VL, de Souza SJ, Braz Petta Lajus T, de Melo Campos JTA, Agnez-Lima LF. de Sousa Leal AM, et al. Among authors: de melo campos jta. DNA Repair (Amst). 2020 Oct;94:102937. doi: 10.1016/j.dnarep.2020.102937. Epub 2020 Jul 16. DNA Repair (Amst). 2020. PMID: 32693352
Resveratrol decreases the expression of genes involved in inflammation through transcriptional regulation.
Pinheiro DML, de Oliveira AHS, Coutinho LG, Fontes FL, de Medeiros Oliveira RK, Oliveira TT, Faustino ALF, Lira da Silva V, de Melo Campos JTA, Lajus TBP, de Souza SJ, Agnez-Lima LF. Pinheiro DML, et al. Among authors: de melo campos jta. Free Radic Biol Med. 2019 Jan;130:8-22. doi: 10.1016/j.freeradbiomed.2018.10.432. Epub 2018 Oct 24. Free Radic Biol Med. 2019. PMID: 30366059 Free article.