Centro de Biologia Molecular e Engenharia Genética (CBMEG) da Unicamp
+55 (19) 3521-1092
Email: atendimento@cbmeg.unicamp.br
CBMEG
Av. Cândido Rondon, 400 - Cidade Universitária, Campinas - SP, 13083-875
Em breve.
Ciamponi, F.E., Procópio, D.P., Murad, N.F., Franco, T.T., Basso, T.O., Brandão, M.M. Multi-omics network model reveals key genes associated with p-coumaric acid stress response in an industrial yeast strain. (2022) Scientific Reports, 12 (1), art. no. 22466. DOI: 10.1038/s41598-022-26843-2. OPEN ACCESS: All Open Access, Gold, Green
Béliveau, C., Gagné, P., Picq, S., Vernygora, O., Keeling, C.I., Pinkney, K., Doucet, D., Wen, F., Johnston, J.S., Maaroufi, H., Boyle, B., Laroche, J., Dewar, K., Juretic, N., Blackburn, G., Nisole, A., Brunet, B., Brandão, M., Lumley, L., Duan, J., Quan, G., Lucarotti, C.J., Roe, A.D., Sperling, F.A.H., Levesque, R.C., Cusson, M. The Spruce Budworm Genome: Reconstructing the Evolutionary History of Antifreeze Proteins. (2022) Genome Biology and Evolution, 14 (6), art. no. evac087. DOI: 10.1093/gbe/evac087. OPEN ACCESS: All Open Access, Gold, Green
Murad, N.F., Silva-Brandão, K.L., Brandão, M.M. Mechanisms behind polyphagia in a pest insect: Responses of Spodoptera frugiperda (J.E. Smith) strains to preferential and alternative larval host plants assessed with gene regulatory networks. (2021) Biochimica et Biophysica Acta - Gene Regulatory Mechanisms, 1864 (3), art. no. 194687. DOI: 10.1016/j.bbagrm.2021.194687.
Murad, N.F., Brandão, M.M. Probabilistic Graphical Models Applied to Biological Networks. (2021) Advances in Experimental Medicine and Biology, 1346, pp. 119-130. DOI: 10.1007/978-3-030-80352-0_7.
de Barros Dantas, L.L., Brandão, M.M. Interactomes: Experimental and In Silico Approaches. (2021) Advances in Experimental Medicine and Biology, 1346, pp. 107-117. DOI: 10.1007/978-3-030-80352-0_6.
Silva-Brandão, K.L., Murad, N.F., Peruchi, A., Martins, C.H.Z., Omoto, C., Figueira, A., Brandão, M.M., Trigo, J.R. Transcriptome differential co-expression reveals distinct molecular response of fall-armyworm strains to DIMBOA. (2021) Pest Management Science, 77 (1), pp. 518-526. DOI: 10.1002/ps.6051
Brandão, M.M., Dantas, L.L., Silva-Filho, M.C. AtPIN: Arabidopsis thaliana protein interaction network. (2009) BMC Bioinformatics, 10, art. no. 454. DOI: 10.1186/1471-2105-10-454. OPEN ACCESS: All Open Access, Gold, Green
DA CRUZ PRS, ANANINA G, SECOLIN R, DA-SILVA-LOPES VL, LIMA CSP, DE FRANÇA PHC, DONATTI A, LOURENÇO GJ, DE ARAUJO TK, SIMIONI M, LOPES-CENDES I, COSTA FF, DE MELO MB. Demographic history differences between Hispanics and Brazilians imprint haplotype features. G3 (Bethesda). 2022 Jul 6;12(7):jkac111. doi: 10.1093/g3journal/jkac111.
VITURINO MG, NETO JM, BAJANO FF, COSTA SM, ROQUE AB, BORGES GF, ANANINA G, RIM PH, MEDINA FM, COSTA FF, VASCONCELLOS JP, MELO MB. Evaluation of APOE polymorphisms and the risk for age-related macular degeneration in a Southeastern Brazilian population. Exp Biol Med (Maywood). 2021 May;246(10):1148-1155. doi: 10.1177/1535370220985466.
ITO MT, DA SILVA COSTA SM, BAPTISTA LC, CARVALHO-SIQUEIRA GQ, ALBUQUERQUE DM, RIOS VM, OSPINA-PRIETO S, SAEZ R, VIEIRA KP, CENDES F, OZELO MC, SAAD STO, COSTA FF, MELO MB. Angiogenesis-related genes in endothelial progenitor cells may be involved in sickle cell stroke. J Am Heart Assoc. 2020;9(3):e014143. doi: 10.1161/JAHA.119.014143.
BAPTISTA LC, COSTA ML, SURITA FG, ROCHA CS, LOPES-CENDES I, SOUZA BB, COSTA FF, MELO MB. Placental transcriptome profile of women with sickle cell disease reveals differentially expressed genes involved in migration, trophoblast differentiation and inflammation. Blood Cells Mol Dis. 2020 Sep;84:102458. doi: 10.1016/j.bcmd.2020.102458.
HAUSER MA, ALLINGHAM, RR, AUNG T, VAN DER HEIDE CJ, ROTTER JI, WANG SH, ... MELO MB, ... KHOR CC.APBB2 is a significant risk locus for primary open angle glaucoma in individuals of African ancestry. JAMA. 2019;322(17):1682-1691. doi: 10.1001/jama.2019.16161.
CRUZ PRS, ANANINA G, GIL-DA-SILVA-LOPES VS, SIMIONI M, MENAA F, BEZERRA MAC, DOMINGOS IF, ARAÚJO AS, PELLEGRINO R, HAKONARSON H, COSTA FF, MELO MB. Genetic comparison of sickle cell anaemia cohorts from Brazil and United States reveals high levels of divergence. Sci Rep. 2019;9(1):10896. doi: 10.1038/s41598-019-47313-2.
CARVALHO-SIQUEIRA GQ, ANANINA G, SOUZA BB, BORGES MG, ITO MT, SILVA-COSTA SM, DOMINGOS IF, FALCÃO DA, LOPES-CENDES I, BEZERRA MAC, ARAÚJO AS, LUCENA-ARAÚJO AR, GONÇALVES MS, SAAD STO, COSTA FF, MELO MB. Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients. Exp Biol Med. (Maywood) 2019; 244(11):932-39. doi: 10.1177/1535370219849592.
OLIVEIRA MB, VASCONCELLOS JPC, ANANINA G, COSTA VP, MELO MB. Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population. Exp Biol Med. (Maywood) 2018;243(13):1083-91. doi: 10.1177/1535370218809709.
MARQUES AM, ANANINA G, COSTA VP, VASCONCELLOS JPC, MELO MB. Estimating the age of the Cys433Arg mutation in the MYOC gene in patients with primary open angle glaucoma. PLoS One. 2018;13(11):e0207409. doi: 10.1371/journal.pone.0207409.
KHOR CC, DO T, JIA H, NAKANO M, GEORGE R, ABU-AMERO K, DUVESH R, CHEN LJ, LI Z, NONGPIUR ME, PERERA SA, QIAO C, WONG H, SAKAI H, MELO MB et al. Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Nature Genet. 2016; 48(5):556-62. doi: 10.1038/ng.3540.
• FABBRI-SCARLLET, H; WERNER, R; SANCHES-GUARAGNA M; ANDRADE JGR; MACIEL-GUERRA, A. T.; HORNIG, N; HIORT, O; GUERRA-JUNIOR, G.; DE MELLO, MP. Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development? Sexual Development, p. 1-9, 2022. DOI: 10.1159/000524956
• WATANABE, A*; GUARAGNA, MS*; BELANGERO, VMS; CASIMIRO, FMS; PESQUERO, JB; FELTRAN, LS; PALMA, LM; VARELA, P; NEVES, PDMM; LERARIO, AM; SOUZA, ML; DE MELLO, MP; LUTAIF, AC; FERRARI, CR; SAMPSON, MG; ONUCHIC, LF; NOGUEIRA, PCK. APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses. Pediatric Nephrology , v. 1, p. 1-0, 2021. (*1a autoria compartilhada) DOI: 10.1007/s00467-021-04960-w
• GUARAGNA, MS.; DE SOUZA, MARCELA L.; LUTAIF, ANNA CRISTINA G.B.; MACIEL-GUERRA, ANDRÉA T.; BELANGERO, V.M.S.; GUERRA-JUNIOR, GIL; MELLO, M.P. Promises and Pitfalls of Whole-Exome Sequencing Exemplified by a Nephrotic Syndrome Family. Mol. Genet Genomics 2020 Jan;295(1):135-142. DOI: 10.1007/s00438-019-01609-0
• KARLSSON, L.; MICHELATTO, D. P. ; LUSA, A. L. G.; SILVA, CDAM; ÖSTBERG L; PERSSON, B.; GUERRA-JÚNIOR, GIL; LEMOS-MARINI, S. H. V.; BALDAZZI, L; MENABÒ, S; BALSAMO, A.; GREGGIO, N. A.; DE MELLO, M.P.; BARBARO M; LAJIC S. Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia. Clinical Biochemistry v. 73, p. 50-56, 2019. DOI: 10.1016/j.clinbiochem.2019.07.009
• FABBRI-SCALLET, HELENA; SOUSA, LIZANDRA MAIA; MACIEL-GUERRA, ANDRÉA TREVAS; GUERRA-JÚNIOR, GIL; DE MELLO, MARICILDA PALANDI. Mutation update for the gene involved in DSD and infertility. Human Mutation 2019; 1-11. DOI: 10.1002/humu.23916
• FABBRI, H. C. ; DE MELLO, MARICILDA PALANDI ; GUERRA-JÚNIOR, GIL ; MACIEL-GUERRA, ANDRÉA TREVAS ; ANDRADE JGR ; MAIA COSTA DE QUEIROZ, C ; MONLLEO, I. L. ; STRUVE, D ; HIORT, O ; WERNER, R . Functional Characterization of Five NR5A1 Gene Mutations Found in Patients with 46,XY Disorders of Sex Development. HUMAN MUTATION, v. 39, p. 114-123, 2018. DOI: 10.1002/humu.23353
• GUARAGNA, MS.; ANNA CRISTINA G.B. LUTAIF; CRISTIANE S.C. PIVETA; MARCELA L. SOUZA; SUÉLLEN R. DE SOUZA; TACIANE B. HENRIQUES; ANDRÉA T. MACIEL-GUERRA; VERA M.S. BELANGERO; GIL GUERRA-JUNIOR; Maricilda P. De Mello. NPHS2 mutations account for only 15% of Nephrotic Syndrome cases. BMC Medical Genetics 2015 Sep 29;16:88. DOI: 10.1186/s12881-015-0231-9