| Year |
Citation |
Score |
| 2024 |
Sullivan JM, Bagnell AM, Alevy J, Avila EM, Mihaljević L, Saavedra-Rivera PC, Kong L, Huh JS, McCray BA, Aisenberg WH, Zuberi AR, Bogdanik L, Lutz CM, Qiu Z, Quinlan KA, et al. Gain-of-function mutations of TRPV4 acting in endothelial cells drive blood-CNS barrier breakdown and motor neuron degeneration in mice. Science Translational Medicine. 16: eadk1358. PMID 38776392 DOI: 10.1126/scitranslmed.adk1358 |
0.369 |
|
| 2022 |
Liang JH, Alevy J, Akhanov V, Seo R, Massey CA, Jiang D, Zhou J, Sillitoe RV, Noebels JL, Samuel MA. Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects. Disease Models & Mechanisms. PMID 35972048 DOI: 10.1242/dmm.049642 |
0.473 |
|
| 2020 |
Burger CA, Alevy J, Casasent AK, Jiang D, Albrecht NE, Liang JH, Hirano AA, Brecha N, Samuel MA. LKB1 coordinates neurite remodeling to drive synapse layer emergence in the outer retina. Elife. 9. PMID 32378514 DOI: 10.7554/Elife.56931 |
0.501 |
|
| 2019 |
Alevy J, Burger CA, Albrecht NE, Jiang D, Samuel MA. Progressive myoclonic epilepsy-associated gene Kctd7 regulates retinal neurovascular patterning and function. Neurochemistry International. 104486. PMID 31175897 DOI: 10.1016/j.neuint.2019.104486 |
0.559 |
|
| 2018 |
Albrecht NE, Alevy J, Jiang D, Burger CA, Liu BI, Li F, Wang J, Kim SY, Hsu CW, Kalaga S, Udensi U, Asomugha C, Bohat R, Gaspero A, Justice MJ, et al. Rapid and Integrative Discovery of Retina Regulatory Molecules. Cell Reports. 24: 2506-2519. PMID 30157441 DOI: 10.1016/J.Celrep.2018.07.090 |
0.546 |
|
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