| Mutations in TRPM1 are a common cause of complete congenital stationary night blindness MM van Genderen, MMC Bijveld, YB Claassen, RJ Florijn, JN Pearring, ... The American Journal of Human Genetics 85 (5), 730-736, 2009 | 259 | 2009 |
| Protein sorting, targeting and trafficking in photoreceptor cells JN Pearring, RY Salinas, SA Baker, VY Arshavsky Progress in retinal and eye research 36, 24-51, 2013 | 197 | 2013 |
| GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness NS Peachey, TA Ray, R Florijn, LB Rowe, T Sjoerdsma, ... The American Journal of Human Genetics 90 (2), 331-339, 2012 | 161 | 2012 |
| Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release RY Salinas, JN Pearring, JD Ding, WJ Spencer, Y Hao, VY Arshavsky The Journal of cell biology 216 (5), 1489, 2017 | 135 | 2017 |
| A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites JN Pearring, P Bojang, Y Shen, C Koike, T Furukawa, S Nawy, RG Gregg Journal of Neuroscience 31 (27), 10060-10066, 2011 | 108 | 2011 |
| De novo GMNN mutations cause autosomal-dominant primordial dwarfism associated with Meier-Gorlin syndrome LC Burrage, WL Charng, MK Eldomery, JR Willer, EE Davis, ... The American Journal of Human Genetics 97 (6), 904-913, 2015 | 83 | 2015 |
| Photoreceptor discs: built like ectosomes WJ Spencer, TR Lewis, JN Pearring, VY Arshavsky Trends in cell biology 30 (11), 904-915, 2020 | 61 | 2020 |
| Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutants B Ploier, LN Caro, T Morizumi, K Pandey, JN Pearring, MA Goren, ... Nature communications 7 (1), 12832, 2016 | 58 | 2016 |
| PRCD is essential for high-fidelity photoreceptor disc formation WJ Spencer, JD Ding, TR Lewis, C Yu, S Phan, JN Pearring, KY Kim, ... Proceedings of the National Academy of Sciences 116 (26), 13087-13096, 2019 | 48 | 2019 |
| Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation NS Peachey, JN Pearring, P Bojang Jr, ME Hirschtritt, G Sturgill-Short, ... Journal of neurophysiology 108 (9), 2442-2451, 2012 | 47 | 2012 |
| Guanylate cyclase 1 relies on rhodopsin for intracellular stability and ciliary trafficking JN Pearring, WJ Spencer, EC Lieu, VY Arshavsky Elife 4, e12058, 2015 | 34 | 2015 |
| Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration JN Pearring, JT San Agustin, ES Lobanova, CJ Gabriel, EC Lieu, ... PLoS genetics 13 (4), e1006740, 2017 | 32 | 2017 |
| Progressive Rod–Cone degeneration (PRCD) protein requires N-terminal S-acylation and rhodopsin binding for photoreceptor outer segment localization and maintaining … WJ Spencer, JN Pearring, RY Salinas, DR Loiselle, NP Skiba, ... Biochemistry 55 (36), 5028-5037, 2016 | 28 | 2016 |
| R9AP targeting to rod outer segments is independent of rhodopsin and is guided by the SNARE homology domain JN Pearring, EC Lieu, JR Winter, SA Baker, VY Arshavsky Molecular biology of the cell 25 (17), 2644-2649, 2014 | 19 | 2014 |
| The GARP domain of the rod CNG channel's β1-subunit contains distinct sites for outer segment targeting and connecting to the photoreceptor disk rim JN Pearring, J Martínez-Márquez, JR Willer, EC Lieu, RY Salinas, ... Journal of Neuroscience 41 (14), 3094-3104, 2021 | 14 | 2021 |
| Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors GMH Abdel-Salam, S Hellmuth, E Gradhand, S Käseberg, J Winter, ... Jci Insight 8 (22), 2023 | 4 | 2023 |
| Disrupting the ciliary gradient of active Arl3 affects rod photoreceptor nuclear migration AM Travis, S Manocha, JR Willer, TS Wessler, NP Skiba, JN Pearring Elife 12, e80533, 2023 | 4 | 2023 |
| Nyctalopin interacts with transient receptor potential channels in yeast P Bojang Jr, JN Pearring, RG Gregg Investigative Ophthalmology & Visual Science 50 (13), 5176-5176, 2009 | 4 | 2009 |
| The tectonic complex regulates membrane protein composition in the photoreceptor cilium HM Truong, KO Cruz-Colón, JY Martínez-Márquez, JR Willer, AM Travis, ... Nature Communications 14 (1), 5671, 2023 | 2 | 2023 |
| CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis N Nuzhat, K Van Schil, S Liakopoulos, M Bauwens, AD Rey, S Käseberg, ... The Journal of Clinical Investigation 133 (8), 2023 | 2 | 2023 |
Vadim ArshavskyDuke University在 duke.edu 的电子邮件经过验证
