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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2017 | 2 |
2020 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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Page 1
Development of a three-dimensional organoid model to explore early retinal phenotypes associated with Alzheimer's disease.
Sci Rep. 2023 Aug 24;13(1):13827. doi: 10.1038/s41598-023-40382-4.
Sci Rep. 2023.
PMID: 37620502
Free PMC article.
Autophagy disruption reduces mTORC1 activation leading to retinal ganglion cell neurodegeneration associated with glaucoma.
Huang KC, Gomes C, Shiga Y, Belforte N, VanderWall KB, Lavekar SS, Fligor CM, Harkin J, Di Polo A, Meyer JS.
Huang KC, et al. Among authors: harkin j.
bioRxiv [Preprint]. 2023 Jan 4:2023.01.04.522687. doi: 10.1101/2023.01.04.522687.
bioRxiv. 2023.
PMID: 36711831
Free PMC article.
Preprint.
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Astrocytes modulate neurodegenerative phenotypes associated with glaucoma in OPTN(E50K) human stem cell-derived retinal ganglion cells.
Gomes C, VanderWall KB, Pan Y, Lu X, Lavekar SS, Huang KC, Fligor CM, Harkin J, Zhang C, Cummins TR, Meyer JS.
Gomes C, et al. Among authors: harkin j.
Stem Cell Reports. 2022 Jul 12;17(7):1636-1649. doi: 10.1016/j.stemcr.2022.05.006. Epub 2022 Jun 16.
Stem Cell Reports. 2022.
PMID: 35714595
Free PMC article.
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Extension of retinofugal projections in an assembled model of human pluripotent stem cell-derived organoids.
Fligor CM, Lavekar SS, Harkin J, Shields PK, VanderWall KB, Huang KC, Gomes C, Meyer JS.
Fligor CM, et al. Among authors: harkin j.
Stem Cell Reports. 2021 Sep 14;16(9):2228-2241. doi: 10.1016/j.stemcr.2021.05.009. Epub 2021 Jun 10.
Stem Cell Reports. 2021.
PMID: 34115986
Free PMC article.
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Defective Hand1 phosphoregulation uncovers essential roles for Hand1 in limb morphogenesis.
Firulli BA, Milliar H, Toolan KP, Harkin J, Fuchs RK, Robling AG, Firulli AB.
Firulli BA, et al. Among authors: harkin j.
Development. 2017 Jul 1;144(13):2480-2489. doi: 10.1242/dev.149963. Epub 2017 Jun 2.
Development. 2017.
PMID: 28576769
Free PMC article.
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HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure.
Firulli BA, George RM, Harkin J, Toolan KP, Gao H, Liu Y, Zhang W, Field LJ, Liu Y, Shou W, Payne RM, Rubart-von der Lohe M, Firulli AB.
Firulli BA, et al. Among authors: harkin j.
Cardiovasc Res. 2020 Mar 1;116(3):605-618. doi: 10.1093/cvr/cvz182.
Cardiovasc Res. 2020.
PMID: 31286141
Free PMC article.
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The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice.
Firulli BA, Toolan KP, Harkin J, Millar H, Pineda S, Firulli AB.
Firulli BA, et al. Among authors: harkin j.
Cardiovasc Res. 2017 Dec 1;113(14):1732-1742. doi: 10.1093/cvr/cvx166.
Cardiovasc Res. 2017.
PMID: 29016838
Free PMC article.
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