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Page 1
A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration.
Ratnapriya R, Jacobson SG, Cideciyan AV, English MA, Roman AJ, Sumaroka A, Sheplock R, Swaroop A. Ratnapriya R, et al. Among authors: english ma. Front Cell Dev Biol. 2021 Aug 17;9:720782. doi: 10.3389/fcell.2021.720782. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34485303 Free PMC article.
Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects.
Veleri S, Bishop K, Dalle Nogare DE, English MA, Foskett TJ, Chitnis A, Sood R, Liu P, Swaroop A. Veleri S, et al. Among authors: english ma. PLoS One. 2012;7(3):e34389. doi: 10.1371/journal.pone.0034389. Epub 2012 Mar 29. PLoS One. 2012. PMID: 22479622 Free PMC article.
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations.
Shimada H, Lu Q, Insinna-Kettenhofen C, Nagashima K, English MA, Semler EM, Mahgerefteh J, Cideciyan AV, Li T, Brooks BP, Gunay-Aygun M, Jacobson SG, Cogliati T, Westlake CJ, Swaroop A. Shimada H, et al. Among authors: english ma. Cell Rep. 2017 Jul 11;20(2):384-396. doi: 10.1016/j.celrep.2017.06.045. Cell Rep. 2017. PMID: 28700940 Free PMC article.
Selective transcriptomic dysregulation of metabolic pathways in liver and retina by short- and long-term dietary hyperglycemia.
Mondal AK, Brock DC, Rowan S, Yang ZH, Rojulpote KV, Smith KM, Francisco SG, Bejarano E, English MA, Deik A, Jeanfavre S, Clish CB, Remaley AT, Taylor A, Swaroop A. Mondal AK, et al. Among authors: english ma. iScience. 2024 Jan 19;27(2):108979. doi: 10.1016/j.isci.2024.108979. eCollection 2024 Feb 16. iScience. 2024. PMID: 38333717 Free PMC article.
17 results