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Year Number of Results
2002 1
2004 3
2005 1
2006 1
2007 1
2008 1
2009 1
2011 1
2012 1
2014 2
2016 2
2017 2
2018 1
2020 2
2021 1
2022 2
2023 3
2024 1

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26 results

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Page 1
Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor.
Colombo S, Reddy HP, Petri S, Williams DJ, Shalomov B, Dhindsa RS, Gelfman S, Krizay D, Bera AK, Yang M, Peng Y, Makinson CD, Boland MJ, Frankel WN, Goldstein DB, Dascal N. Colombo S, et al. Among authors: boland mj. Front Cell Neurosci. 2023 May 18;17:1175895. doi: 10.3389/fncel.2023.1175895. eCollection 2023. Front Cell Neurosci. 2023. PMID: 37275776 Free PMC article.
Annotating pathogenic non-coding variants in genic regions.
Gelfman S, Wang Q, McSweeney KM, Ren Z, La Carpia F, Halvorsen M, Schoch K, Ratzon F, Heinzen EL, Boland MJ, Petrovski S, Goldstein DB. Gelfman S, et al. Among authors: boland mj. Nat Commun. 2017 Aug 9;8(1):236. doi: 10.1038/s41467-017-00141-2. Nat Commun. 2017. PMID: 28794409 Free PMC article.
Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice.
Amador A, Bostick CD, Olson H, Peters J, Camp CR, Krizay D, Chen W, Han W, Tang W, Kanber A, Kim S, Teoh J, Sah M, Petri S, Paek H, Kim A, Lutz CM, Yang M, Myers SJ, Bhattacharya S, Yuan H, Goldstein DB, Poduri A, Boland MJ, Traynelis SF, Frankel WN. Amador A, et al. Among authors: boland mj. Brain. 2020 Jul 1;143(7):2039-2057. doi: 10.1093/brain/awaa147. Brain. 2020. PMID: 32577763 Free PMC article.
Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency.
Dugger SA, Dhindsa RS, Sampaio GA, Ressler AK, Rafikian EE, Petri S, Letts VA, Teoh J, Ye J, Colombo S, Peng Y, Yang M, Boland MJ, Frankel WN, Goldstein DB. Dugger SA, et al. Among authors: boland mj. PLoS Genet. 2023 Oct 2;19(10):e1010952. doi: 10.1371/journal.pgen.1010952. eCollection 2023 Oct. PLoS Genet. 2023. PMID: 37782669 Free PMC article.
26 results