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Adult mouse fibroblasts retain organ-specific transcriptomic identity.
Forte E, Ramialison M, Nim HT, Mara M, Li JY, Cohn R, Daigle SL, Boyd S, Stanley EG, Elefanty AG, Hinson JT, Costa MW, Rosenthal NA, Furtado MB. Forte E, et al. Among authors: ramialison m. Elife. 2022 Mar 16;11:e71008. doi: 10.7554/eLife.71008. Elife. 2022. PMID: 35293863 Free PMC article.
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets.
Bouveret R, Waardenberg AJ, Schonrock N, Ramialison M, Doan T, de Jong D, Bondue A, Kaur G, Mohamed S, Fonoudi H, Chen CM, Wouters MA, Bhattacharya S, Plachta N, Dunwoodie SL, Chapman G, Blanpain C, Harvey RP. Bouveret R, et al. Among authors: ramialison m. Elife. 2015 Jul 6;4:e06942. doi: 10.7554/eLife.06942. Elife. 2015. PMID: 26146939 Free PMC article.
A novel conditional mouse model for Nkx2-5 reveals transcriptional regulation of cardiac ion channels.
Furtado MB, Wilmanns JC, Chandran A, Tonta M, Biben C, Eichenlaub M, Coleman HA, Berger S, Bouveret R, Singh R, Harvey RP, Ramialison M, Pearson JT, Parkington HC, Rosenthal NA, Costa MW. Furtado MB, et al. Among authors: ramialison m. Differentiation. 2016 Jan-Mar;91(1-3):29-41. doi: 10.1016/j.diff.2015.12.003. Epub 2016 Feb 17. Differentiation. 2016. PMID: 26897459
Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling.
Furtado MB, Wilmanns JC, Chandran A, Perera J, Hon O, Biben C, Willow TJ, Nim HT, Kaur G, Simonds S, Wu Q, Willians D, Salimova E, Plachta N, Denegre JM, Murray SA, Fatkin D, Cowley M, Pearson JT, Kaye D, Ramialison M, Harvey RP, Rosenthal NA, Costa MW. Furtado MB, et al. Among authors: ramialison m. JCI Insight. 2017 Mar 23;2(6):e88271. doi: 10.1172/jci.insight.88271. JCI Insight. 2017. PMID: 28352650 Free PMC article.
TrawlerWeb: an online de novo motif discovery tool for next-generation sequencing datasets.
Dang LT, Tondl M, Chiu MHH, Revote J, Paten B, Tano V, Tokolyi A, Besse F, Quaife-Ryan G, Cumming H, Drvodelic MJ, Eichenlaub MP, Hallab JC, Stolper JS, Rossello FJ, Bogoyevitch MA, Jans DA, Nim HT, Porrello ER, Hudson JE, Ramialison M. Dang LT, et al. Among authors: ramialison m. BMC Genomics. 2018 Apr 5;19(1):238. doi: 10.1186/s12864-018-4630-0. BMC Genomics. 2018. PMID: 29621972 Free PMC article.
Metformin intervention prevents cardiac dysfunction in a murine model of adult congenital heart disease.
Wilmanns JC, Pandey R, Hon O, Chandran A, Schilling JM, Forte E, Wu Q, Cagnone G, Bais P, Philip V, Coleman D, Kocalis H, Archer SK, Pearson JT, Ramialison M, Heineke J, Patel HH, Rosenthal NA, Furtado MB, Costa MW. Wilmanns JC, et al. Among authors: ramialison m. Mol Metab. 2019 Feb;20:102-114. doi: 10.1016/j.molmet.2018.11.002. Epub 2018 Nov 15. Mol Metab. 2019. PMID: 30482476 Free PMC article.
Variable outcomes of human heart attack recapitulated in genetically diverse mice.
Salimova E, Nowak KJ, Estrada AC, Furtado MB, McNamara E, Nguyen Q, Balmer L, Preuss C, Holmes JW, Ramialison M, Morahan G, Rosenthal NA. Salimova E, et al. Among authors: ramialison m. NPJ Regen Med. 2019 Mar 4;4:5. doi: 10.1038/s41536-019-0067-6. eCollection 2019. NPJ Regen Med. 2019. PMID: 30854227 Free PMC article.
66 results