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Page 1
Treatment of adult MPSI mouse brains with IDUA-expressing mesenchymal stem cells decreases GAG deposition and improves exploratory behavior.
da Silva FH, Pereira VG, Yasumura EG, Tenório LZ, de Carvalho LP, Lisboa BC, Matsumoto PK, Stilhano RS, Samoto VY, Calegare BF, Brandão Lde C, D'Almeida V, Filippo TR, Porcionatto M, Toma L, Nader HB, Valero VB, Camassola M, Nardi NB, Han SW. da Silva FH, et al. Among authors: lisboa bc. Genet Vaccines Ther. 2012 Apr 20;10(1):2. doi: 10.1186/1479-0556-10-2. Genet Vaccines Ther. 2012. PMID: 22520214 Free PMC article.
Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders.
Tahira AC, Barbosa AR, Feltrin AS, Gastaldi VD, de Toledo VHC, de Carvalho Pereira JG, Lisboa BCG, de Souza Reis VN, Dos Santos ACF, Maschietto M, Brentani H. Tahira AC, et al. Among authors: lisboa bcg. Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):390-414. doi: 10.1002/ajmg.b.32704. Epub 2018 Dec 9. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30537354 Free PMC article.
Brain areas involved with obsessive-compulsive disorder present different DNA methylation modulation.
de Oliveira KC, Camilo C, Gastaldi VD, Sant'Anna Feltrin A, Lisboa BCG, de Jesus Rodrigues de Paula V, Moretto AC, Lafer B, Hoexter MQ, Miguel EC, Maschietto M; Biobank for Aging Studies Group; Brentani H. de Oliveira KC, et al. Among authors: lisboa bcg. BMC Genom Data. 2021 Oct 30;22(1):45. doi: 10.1186/s12863-021-00993-0. BMC Genom Data. 2021. PMID: 34717534 Free PMC article.
Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.
Reis VN, Kitajima JP, Tahira AC, Feio-Dos-Santos AC, Fock RA, Lisboa BC, Simões SN, Krepischi AC, Rosenberg C, Lourenço NC, Passos-Bueno MR, Brentani H. Reis VN, et al. Among authors: lisboa bc. PLoS One. 2017 Jan 24;12(1):e0170386. doi: 10.1371/journal.pone.0170386. eCollection 2017. PLoS One. 2017. PMID: 28118382 Free PMC article.
A novel mechanism of NPM1 cytoplasmic localization in acute myeloid leukemia: the recurrent gene fusion NPM1-HAUS1.
Campregher PV, de Oliveira Pereira W, Lisboa B, Puga R, Deolinda ER, Helman R, Marti LC, Guerra JC, Manola KN, Petroni RC, Bezerra AM, Costa FF, Hamerschlak N, de Souza Santos FP. Campregher PV, et al. Haematologica. 2016 Jul;101(7):e287-90. doi: 10.3324/haematol.2015.137364. Epub 2016 Apr 1. Haematologica. 2016. PMID: 27036161 Free PMC article. Clinical Trial. No abstract available.
Clinical features of JAK2V617F- or CALR-mutated essential thrombocythemia and primary myelofibrosis.
Monte-Mor Bda C, Ayres-Silva Jde P, Correia WD, Coelho AC, Solza C, Daumas AH, Bonamino MH, Santos FP, Datoguia TS, Pereira Wde O, Lisboa BC, Ramos CF, Machado-Neto JA, Hamerschlak N, Campregher PV, Traina F, Pagnano KB, Zalcberg I. Monte-Mor Bda C, et al. Among authors: lisboa bc. Blood Cells Mol Dis. 2016 Sep;60:74-7. doi: 10.1016/j.bcmd.2016.03.003. Epub 2016 Mar 8. Blood Cells Mol Dis. 2016. PMID: 26994960 Clinical Trial. No abstract available.
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