Sandeep Aryal
Affiliations: | 2015-2021 | Harvard Medical School, Boston, MA, United States |
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"Sandeep Aryal"
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| Aryal S, Anand D, Huang H, et al. (2023) Proteomic profiling of retina and retinal pigment epithelium combined embryonic tissue to facilitate ocular disease gene discovery. Human Genetics |
| Siddam AD, Duot M, Coomson SY, et al. (2023) High-Throughput Transcriptomics of Conditional Knockout Lens Identifies Downstream Networks Linked to Cataract Pathology. Cells. 12 |
| Aryal S, Anand D, Huang H, et al. (2023) Proteomic profiling of retina and retinal pigment epithelium combined embryonic tissue to facilitate ocular disease gene discovery. Research Square |
| Parreno J, Emin G, Vu MP, et al. (2022) Methodologies to unlock the molecular expression and cellular structure of ocular lens epithelial cells. Frontiers in Cell and Developmental Biology. 10: 983178 |
| Rowan S, Jiang S, Francisco SG, et al. (2021) Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts. Investigative Ophthalmology & Visual Science. 62: 10 |
| Aryal S, Longo F, Klann E. (2021) Genetic removal of p70 S6K1 corrects coding sequence length-dependent alterations in mRNA translation in fragile X syndrome mice. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Rajan KS, Doniger T, Cohen-Chalamish S, et al. (2020) Developmentally Regulated Novel Non-coding Anti-sense Regulators of mRNA Translation in . Iscience. 23: 101780 |
| Aryal S, Viet J, Weatherbee BAT, et al. (2020) The cataract-linked RNA-binding protein Celf1 post-transcriptionally controls the spatiotemporal expression of the key homeodomain transcription factors Pax6 and Prox1 in lens development. Human Genetics |
| Alimadadi A, Aryal S, Manandhar I, et al. (2020) Identification of Upstream Transcriptional Regulators of Ischemic Cardiomyopathy Using Cardiac RNA-Seq Meta-Analysis. International Journal of Molecular Sciences. 21 |
| Aryal S, Anand D, Hernandez FG, et al. (2019) MS/MS in silico subtraction-based proteomic profiling as an approach to facilitate disease gene discovery: application to lens development and cataract. Human Genetics |