| Year |
Citation |
Score |
| 2023 |
Lewis TR, Makia MS, Castillo CM, Hao Y, Al-Ubaidi MR, Skiba NP, Conley SM, Arshavsky VY, Naash MI. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Elife. 12. PMID 37991486 DOI: 10.7554/eLife.89444 |
0.664 |
|
| 2023 |
Crane R, Tebbe L, Mwoyosvi ML, Al-Ubaidi MR, Naash MI. Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization. Communications Biology. 6: 933. PMID 37700068 DOI: 10.1038/s42003-023-05296-x |
0.315 |
|
| 2023 |
Ikelle L, Makia M, Lewis T, Crane R, Kakakhel M, Conley SM, Birtley JR, Arshavsky VY, Al-Ubaidi MR, Naash MI. Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones. Cellular and Molecular Life Sciences : Cmls. 80: 290. PMID 37698644 DOI: 10.1007/s00018-023-04929-y |
0.619 |
|
| 2023 |
Lewis TR, Makia MS, Castillo CM, Hao Y, Al-Ubaidi MR, Skiba NP, Conley SM, Arshavsky VY, Naash MI. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Biorxiv : the Preprint Server For Biology. PMID 37693615 DOI: 10.1101/2023.07.02.547380 |
0.664 |
|
| 2023 |
Ikelle L, Makia M, Lewis T, Crane R, Kakakhel M, Conley SM, Birtley JR, Arshavsky VY, Al-Ubaidi MR, Naash MI. Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones. Cellular and Molecular Life Sciences : Cmls. 80: 214. PMID 37466729 DOI: 10.1007/s00018-023-04851-3 |
0.72 |
|
| 2023 |
Lewis TR, Al-Ubaidi MR, Naash MI, Arshavsky VY. The Role of Peripherin-2/ROM1 Complexes in Photoreceptor Outer Segment Disc Morphogenesis. Advances in Experimental Medicine and Biology. 1415: 277-281. PMID 37440045 DOI: 10.1007/978-3-031-27681-1_40 |
0.41 |
|
| 2023 |
Tebbe L, Mwoyosvi ML, Crane R, Makia MS, Kakakhel M, Cosgrove D, Al-Ubaidi MR, Naash MI. The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1. Nature Communications. 14: 972. PMID 36810733 DOI: 10.1038/s41467-023-36431-1 |
0.477 |
|
| 2022 |
Zhao X, Tebbe L, Naash MI, Al-Ubaidi MR. The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural Retina. Frontiers in Pharmacology. 13: 919667. PMID 35873559 DOI: 10.3389/fphar.2022.919667 |
0.409 |
|
| 2022 |
Sinha T, Ikelle L, Makia MS, Crane R, Zhao X, Kakakhel M, Al-Ubaidi MR, Naash MI. Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis. Redox Biology. 54: 102375. PMID 35738087 DOI: 10.1016/j.redox.2022.102375 |
0.346 |
|
| 2022 |
Tebbe L, Sakthivel H, Makia MS, Kakakhel M, Conley SM, Al-Ubaidi MR, Naash MI. Prph2 disease mutations lead to structural and functional defects in the RPE. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 36: e22284. PMID 35344225 DOI: 10.1096/fj.202101562RR |
0.693 |
|
| 2021 |
Ikelle L, Naash MI, Al-Ubaidi MR. Modulation of SOD3 Levels Is Detrimental to Retinal Homeostasis. Antioxidants (Basel, Switzerland). 10. PMID 34679728 DOI: 10.3390/antiox10101595 |
0.39 |
|
| 2021 |
Eblimit A, Makia MS, Strayve D, Crane R, Conley SM, Sinha T, Acharya G, Al-Ubaidi MR, Naash MI. Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal Injection. Pharmaceutics. 13. PMID 34575586 DOI: 10.3390/pharmaceutics13091510 |
0.705 |
|
| 2021 |
Crane R, Conley SM, Al-Ubaidi MR, Naash MI. Gene Therapy to the Retina and the Cochlea. Frontiers in Neuroscience. 15: 652215. PMID 33815052 DOI: 10.3389/fnins.2021.652215 |
0.662 |
|
| 2021 |
Lewis TR, Makia MS, Castillo CM, Al-Ubaidi MR, Naash MI, Arshavsky VY. Photoreceptor disc enclosure is tightly controlled by peripherin-2 oligomerization. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33707293 DOI: 10.1523/JNEUROSCI.0041-21.2021 |
0.374 |
|
| 2021 |
Sinha T, Du J, Makia MS, Hurley JB, Naash MI, Al-Ubaidi MR. Absence of retbindin blocks glycolytic flux, disrupts metabolic homeostasis, and leads to photoreceptor degeneration. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33526685 DOI: 10.1073/pnas.2018956118 |
0.317 |
|
| 2020 |
Genc AM, Makia MS, Sinha T, Conley SM, Al-Ubaidi MR, Naash MI. Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration. International Journal of Molecular Sciences. 21. PMID 33138244 DOI: 10.3390/ijms21218083 |
0.738 |
|
| 2020 |
Sinha T, Naash MI, Al-Ubaidi MR. Flavins Act as a Critical Liaison Between Metabolic Homeostasis and Oxidative Stress in the Retina. Frontiers in Cell and Developmental Biology. 8: 861. PMID 32984341 DOI: 10.3389/fcell.2020.00861 |
0.333 |
|
| 2020 |
Kakakhel M, Tebbe L, Makia MS, Conley SM, Sherry DM, Al-Ubaidi MR, Naash MI. Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival. Proceedings of the National Academy of Sciences of the United States of America. PMID 32778589 DOI: 10.1073/Pnas.2010751117 |
0.647 |
|
| 2020 |
Strayve D, Makia MM, Kakakhel M, Sakthivel H, Conley SM, Al-Ubaidi MR, Naash MI. ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal disease. Human Molecular Genetics. PMID 32716032 DOI: 10.1093/Hmg/Ddaa160 |
0.735 |
|
| 2020 |
Genc AM, Makia MS, Sinha T, Conley SM, Al-Ubaidi MR, Naash MI. Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy. Investigative Ophthalmology & Visual Science. 61: 17. PMID 32516403 DOI: 10.1167/Iovs.61.6.17 |
0.717 |
|
| 2020 |
Lewis TR, Makia MS, Kakakhel M, Al-Ubaidi MR, Arshavsky VY, Naash MI. Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds Oligomerization. Frontiers in Cellular Neuroscience. 14: 92. PMID 32410962 DOI: 10.3389/Fncel.2020.00092 |
0.431 |
|
| 2020 |
Sinha T, Naash MI, Al-Ubaidi MR. The Symbiotic Relationship between the Neural Retina and Retinal Pigment Epithelium Is Supported by Utilizing Differential Metabolic Pathways. Iscience. 23: 101004. PMID 32252018 DOI: 10.1016/j.isci.2020.101004 |
0.337 |
|
| 2020 |
Tebbe L, Kakakhel M, Makia MS, Al-Ubaidi MR, Naash MI. The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases. Cells. 9. PMID 32213850 DOI: 10.3390/cells9030784 |
0.491 |
|
| 2020 |
Sinha T, Ikelle L, Naash MI, Al-Ubaidi MR. The Intersection of Serine Metabolism and Cellular Dysfunction in Retinal Degeneration. Cells. 9. PMID 32164325 DOI: 10.3390/cells9030674 |
0.334 |
|
| 2020 |
Chakraborty D, Strayve DG, Makia MS, Conley SM, Kakahel M, Al-Ubaidi MR, Naash MI. Novel molecular mechanisms for Prph2-associated pattern dystrophy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 34: 1211-1230. PMID 31914632 DOI: 10.1096/Fj.201901888R |
0.692 |
|
| 2019 |
Conley SM, Al-Ubaidi MR, Naash MI. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis. Advances in Experimental Medicine and Biology. 1185: 495-499. PMID 31884660 DOI: 10.1007/978-3-030-27378-1_81 |
0.6 |
|
| 2018 |
Conley SM, Stuck MW, Watson JN, Zulliger R, Burnett JL, Naash MI. Prph2 initiates outer segment morphogenesis but maturation requires Prph2/Rom1 oligomerization. Human Molecular Genetics. PMID 30307502 DOI: 10.1093/Hmg/Ddy359 |
0.681 |
|
| 2018 |
Sinha T, Makia M, Du J, Naash MI, Al-Ubaidi MR. Flavin homeostasis in the mouse retina during aging and degeneration. The Journal of Nutritional Biochemistry. 62: 123-133. PMID 30290331 DOI: 10.1016/j.jnutbio.2018.09.003 |
0.402 |
|
| 2018 |
Agbaga MG, Merriman DK, Brush RS, Lydic TA, Conley SM, Naash MI, Jackson S, Woods AS, Reid GE, Busik JV, Anderson RE. Differential Composition of DHA and Very Long Chain PUFAs in Rod and Cone Photoreceptors. Journal of Lipid Research. PMID 29986998 DOI: 10.1194/Jlr.M082495 |
0.781 |
|
| 2018 |
Zulliger R, Conley SM, Mwoyosvi ML, Al-Ubaidi MR, Naash MI. Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation. Human Molecular Genetics. PMID 29961824 DOI: 10.1093/Hmg/Ddy240 |
0.687 |
|
| 2018 |
Ikelle L, Naash MI, Al-Ubaidi MR. Role of Fibulins 2 and 5 in Retinal Development and Maintenance. Advances in Experimental Medicine and Biology. 1074: 275-280. PMID 29721953 DOI: 10.1007/978-3-319-75402-4_33 |
0.412 |
|
| 2018 |
Kelley RA, Conley SM, Makkia R, Watson JN, Han Z, Cooper MJ, Naash MI. DNA nanoparticles are safe and nontoxic in non-human primate eyes. International Journal of Nanomedicine. 13: 1361-1379. PMID 29563793 DOI: 10.2147/Ijn.S157000 |
0.652 |
|
| 2017 |
LaVail MM, Nishikawa S, Steinberg RH, Naash MI, Duncan JL, Trautmann N, Matthes MT, Yasumura D, Lau-Villacorta C, Chen J, Peterson WM, Yang H, Flannery JG. Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration. Experimental Eye Research. PMID 29122605 DOI: 10.1016/J.Exer.2017.10.023 |
0.43 |
|
| 2017 |
Kelley RA, Al-Ubaidi MR, Sinha T, Genc AM, Makia MS, Ikelle L, Naash MI. Ablation of the riboflavin-binding protein retbindin reduces flavin levels and leads to progressive and dose-dependent degeneration of rods and cones. The Journal of Biological Chemistry. PMID 29079576 DOI: 10.1074/jbc.M117.785105 |
0.441 |
|
| 2017 |
Conley SM, Stuck MW, Watson JN, Naash MI. Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa. Human Molecular Genetics. PMID 28053051 DOI: 10.1093/Hmg/Ddw408 |
0.72 |
|
| 2016 |
Chakraborty D, Conley SM, Zulliger R, Naash MI. The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function. Human Molecular Genetics. PMID 27365499 DOI: 10.1093/Hmg/Ddw193 |
0.708 |
|
| 2016 |
Chakraborty D, Conley SM, Pittler SJ, Naash MI. Role of RDS and Rhodopsin in Cngb1-Related Retinal Degeneration. Investigative Ophthalmology & Visual Science. 57: 787-97. PMID 26934134 DOI: 10.1167/Iovs.15-18516 |
0.692 |
|
| 2016 |
Stuck MW, Conley SM, Naash MI. PRPH2/RDS and ROM-1: Historical context, current views and future considerations. Progress in Retinal and Eye Research. PMID 26773759 DOI: 10.1016/J.Preteyeres.2015.12.002 |
0.726 |
|
| 2016 |
Kelley RA, Al-Ubaidi MR, Naash MI. The Potential Role of Flavins and Retbindin in Retinal Function and Homeostasis. Advances in Experimental Medicine and Biology. 854: 643-8. PMID 26427470 DOI: 10.1007/978-3-319-17121-0_85 |
0.357 |
|
| 2016 |
Conley SM, Whalen P, Lewin AS, Naash MI. Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation. Advances in Experimental Medicine and Biology. 854: 509-15. PMID 26427453 DOI: 10.1007/978-3-319-17121-0_68 |
0.676 |
|
| 2016 |
Mitra RN, Conley SM, Naash MI. Therapeutic Approach of Nanotechnology for Oxidative Stress Induced Ocular Neurodegenerative Diseases. Advances in Experimental Medicine and Biology. 854: 463-9. PMID 26427447 DOI: 10.1007/978-3-319-17121-0_62 |
0.578 |
|
| 2016 |
Stuck MW, Conley SM, Naash MI. RDS Functional Domains and Dysfunction in Disease. Advances in Experimental Medicine and Biology. 854: 217-22. PMID 26427414 DOI: 10.1007/978-3-319-17121-0_29 |
0.708 |
|
| 2015 |
Chakraborty D, Conley SM, DeRamus ML, Pittler SJ, Naash MI. Varying the GARP2-to-RDS Ratio Leads to Defects in Rim Formation and Rod and Cone Function. Investigative Ophthalmology & Visual Science. 56: 8187-98. PMID 26720471 DOI: 10.1167/Iovs.15-17785 |
0.656 |
|
| 2015 |
Zulliger R, Conley SM, Naash MI. Non-viral therapeutic approaches to ocular diseases: An overview and future directions. Journal of Controlled Release : Official Journal of the Controlled Release Society. 219: 471-87. PMID 26439665 DOI: 10.1016/J.Jconrel.2015.10.007 |
0.66 |
|
| 2015 |
Stuck MW, Conley SM, Naash MI. Retinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation. The Journal of Biological Chemistry. 290: 27901-13. PMID 26420485 DOI: 10.1074/Jbc.M115.683698 |
0.72 |
|
| 2015 |
Zulliger R, Conley SM, Mwoyosvi ML, Stuck MW, Azadi S, Naash MI. SNAREs Interact with Retinal Degeneration Slow and Rod Outer Segment Membrane Protein-1 during Conventional and Unconventional Outer Segment Targeting. Plos One. 10: e0138508. PMID 26406599 DOI: 10.1371/Journal.Pone.0138508 |
0.658 |
|
| 2015 |
Han Z, Banworth MJ, Makkia R, Conley SM, Al-Ubaidi MR, Cooper MJ, Naash MI. Genomic DNA nanoparticles rescue rhodopsin-associated retinitis pigmentosa phenotype. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 29: 2535-44. PMID 25713057 DOI: 10.1096/Fj.15-270363 |
0.709 |
|
| 2015 |
Murray AR, Vuong L, Brobst D, Fliesler SJ, Peachey NS, Gorbatyuk MS, Naash MI, Al-Ubaidi MR. Glycosylation of rhodopsin is necessary for its stability and incorporation into photoreceptor outer segment discs. Human Molecular Genetics. 24: 2709-23. PMID 25637522 DOI: 10.1093/hmg/ddv031 |
0.467 |
|
| 2015 |
Adijanto J, Naash MI. Nanoparticle-based technologies for retinal gene therapy. European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft FüR Pharmazeutische Verfahrenstechnik E.V. 95: 353-67. PMID 25592325 DOI: 10.1016/j.ejpb.2014.12.028 |
0.408 |
|
| 2015 |
Kelley RA, Al-Ubaidi MR, Naash MI. Retbindin is an extracellular riboflavin-binding protein found at the photoreceptor/retinal pigment epithelium interface. The Journal of Biological Chemistry. 290: 5041-52. PMID 25542898 DOI: 10.1074/jbc.M114.624189 |
0.444 |
|
| 2015 |
Zulliger R, Naash MI, Rajala RV, Molday RS, Azadi S. Impaired association of retinal degeneration-3 with guanylate cyclase-1 and guanylate cyclase-activating protein-1 leads to leber congenital amaurosis-1. The Journal of Biological Chemistry. 290: 3488-99. PMID 25477517 DOI: 10.1074/Jbc.M114.616656 |
0.385 |
|
| 2014 |
Conley SM, Naash MI. Gene therapy for PRPH2-associated ocular disease: challenges and prospects. Cold Spring Harbor Perspectives in Medicine. 4: a017376. PMID 25167981 DOI: 10.1101/Cshperspect.A017376 |
0.728 |
|
| 2014 |
Mitra RN, Merwin MJ, Han Z, Conley SM, Al-Ubaidi MR, Naash MI. Yttrium oxide nanoparticles prevent photoreceptor death in a light-damage model of retinal degeneration. Free Radical Biology & Medicine. 75: 140-8. PMID 25066531 DOI: 10.1016/J.Freeradbiomed.2014.07.013 |
0.624 |
|
| 2014 |
Stuck MW, Conley SM, Naash MI. The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse. Human Molecular Genetics. 23: 6260-74. PMID 25001182 DOI: 10.1093/Hmg/Ddu345 |
0.725 |
|
| 2014 |
Chakraborty D, Conley SM, Al-Ubaidi MR, Naash MI. Initiation of rod outer segment disc formation requires RDS. Plos One. 9: e98939. PMID 24897172 DOI: 10.1371/Journal.Pone.0098939 |
0.707 |
|
| 2014 |
Conley SM, Al-Ubaidi MR, Han Z, Naash MI. Rim formation is not a prerequisite for distribution of cone photoreceptor outer segment proteins. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 3468-79. PMID 24736412 DOI: 10.1096/Fj.14-251397 |
0.668 |
|
| 2014 |
Kanan Y, Brobst D, Han Z, Naash MI, Al-Ubaidi MR. Fibulin 2, a tyrosine O-sulfated protein, is up-regulated following retinal detachment. The Journal of Biological Chemistry. 289: 13419-33. PMID 24692557 DOI: 10.1074/jbc.M114.562157 |
0.434 |
|
| 2014 |
Han Z, Conley SM, Naash MI. Gene therapy for Stargardt disease associated with ABCA4 gene. Advances in Experimental Medicine and Biology. 801: 719-24. PMID 24664763 DOI: 10.1007/978-1-4614-3209-8_90 |
0.706 |
|
| 2014 |
Koirala A, Conley SM, Naash MI. Episomal maintenance of S/MAR-containing non-viral vectors for RPE-based diseases. Advances in Experimental Medicine and Biology. 801: 703-9. PMID 24664761 DOI: 10.1007/978-1-4614-3209-8_88 |
0.799 |
|
| 2014 |
Stuck MW, Conley SM, Shaw RA, Wolf R, Naash MI. Electrophysiological characterization of rod and cone responses in the baboon nonhuman primate model. Advances in Experimental Medicine and Biology. 801: 67-73. PMID 24664682 DOI: 10.1007/978-1-4614-3209-8_9 |
0.615 |
|
| 2014 |
Conley SM, Stuck MW, Burnett JL, Chakraborty D, Azadi S, Fliesler SJ, Naash MI. Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS. Human Molecular Genetics. 23: 3102-14. PMID 24463884 DOI: 10.1093/Hmg/Ddu014 |
0.751 |
|
| 2014 |
Mitra RN, Han Z, Merwin M, Al Taai M, Conley SM, Naash MI. Synthesis and characterization of glycol chitosan DNA nanoparticles for retinal gene delivery. Chemmedchem. 9: 189-96. PMID 24203490 DOI: 10.1002/Cmdc.201300371 |
0.668 |
|
| 2013 |
Al-Ubaidi MR, Naash MI, Conley SM. A perspective on the role of the extracellular matrix in progressive retinal degenerative disorders. Investigative Ophthalmology & Visual Science. 54: 8119-24. PMID 24346621 DOI: 10.1167/Iovs.13-13536 |
0.693 |
|
| 2013 |
Koirala A, Conley SM, Makkia R, Liu Z, Cooper MJ, Sparrow JR, Naash MI. Persistence of non-viral vector mediated RPE65 expression: case for viability as a gene transfer therapy for RPE-based diseases. Journal of Controlled Release : Official Journal of the Controlled Release Society. 172: 745-52. PMID 24035979 DOI: 10.1016/J.Jconrel.2013.08.299 |
0.811 |
|
| 2013 |
Koirala A, Conley SM, Naash MI. A review of therapeutic prospects of non-viral gene therapy in the retinal pigment epithelium. Biomaterials. 34: 7158-67. PMID 23796578 DOI: 10.1016/J.Biomaterials.2013.06.002 |
0.813 |
|
| 2013 |
Chakraborty D, Conley SM, Naash MI. Overexpression of retinal degeneration slow (RDS) protein adversely affects rods in the rd7 model of enhanced S-cone syndrome. Plos One. 8: e63321. PMID 23650562 DOI: 10.1371/Journal.Pone.0063321 |
0.731 |
|
| 2013 |
Koirala A, Makkia RS, Conley SM, Cooper MJ, Naash MI. S/MAR-containing DNA nanoparticles promote persistent RPE gene expression and improvement in RPE65-associated LCA. Human Molecular Genetics. 22: 1632-42. PMID 23335596 DOI: 10.1093/Hmg/Ddt013 |
0.828 |
|
| 2013 |
Han Z, Guo J, Conley SM, Naash MI. Retinal angiogenesis in the Ins2(Akita) mouse model of diabetic retinopathy. Investigative Ophthalmology & Visual Science. 54: 574-84. PMID 23221078 DOI: 10.1167/Iovs.12-10959 |
0.61 |
|
| 2013 |
Chakraborty D, Rodgers KK, Conley SM, Naash MI. Structural characterization of the second intra-discal loop of the photoreceptor tetraspanin RDS. The Febs Journal. 280: 127-38. PMID 23121719 DOI: 10.1111/Febs.12055 |
0.655 |
|
| 2012 |
Han Z, Conley SM, Makkia R, Guo J, Cooper MJ, Naash MI. Comparative analysis of DNA nanoparticles and AAVs for ocular gene delivery. Plos One. 7: e52189. PMID 23272225 DOI: 10.1371/Journal.Pone.0052189 |
0.63 |
|
| 2012 |
Han Z, Conley SM, Makkia RS, Cooper MJ, Naash MI. DNA nanoparticle-mediated ABCA4 delivery rescues Stargardt dystrophy in mice. The Journal of Clinical Investigation. 122: 3221-6. PMID 22886305 DOI: 10.1172/Jci64833 |
0.678 |
|
| 2012 |
Sherry DM, Kanan Y, Hamilton R, Hoffhines A, Arbogast KL, Fliesler SJ, Naash MI, Moore KL, Al-Ubaidi MR. Differential developmental deficits in retinal function in the absence of either protein tyrosine sulfotransferase-1 or -2. Plos One. 7: e39702. PMID 22745813 DOI: 10.1371/journal.pone.0039702 |
0.384 |
|
| 2012 |
Stuck MW, Conley SM, Naash MI. Defects in the outer limiting membrane are associated with rosette development in the Nrl-/- retina. Plos One. 7: e32484. PMID 22427845 DOI: 10.1371/Journal.Pone.0032484 |
0.694 |
|
| 2012 |
Han Z, Koirala A, Makkia R, Cooper MJ, Naash MI. Direct gene transfer with compacted DNA nanoparticles in retinal pigment epithelial cells: expression, repeat delivery and lack of toxicity. Nanomedicine (London, England). 7: 521-39. PMID 22356602 DOI: 10.2217/Nnm.11.158 |
0.758 |
|
| 2012 |
Conley SM, Chakraborty D, Naash MI. Mislocalization of oligomerization-incompetent RDS is associated with mislocalization of cone opsins and cone transducin. Advances in Experimental Medicine and Biology. 723: 657-62. PMID 22183390 DOI: 10.1007/978-1-4614-0631-0_83 |
0.69 |
|
| 2012 |
Chakraborty D, Conley SM, Nash Z, Ding XQ, Naash MI. Overexpression of ROM-1 in the cone-dominant retina. Advances in Experimental Medicine and Biology. 723: 633-9. PMID 22183387 DOI: 10.1007/978-1-4614-0631-0_80 |
0.713 |
|
| 2012 |
Conley SM, Cai X, Makkia R, Wu Y, Sparrow JR, Naash MI. Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy. Biochimica Et Biophysica Acta. 1822: 1169-79. PMID 22033104 DOI: 10.1016/J.Bbadis.2011.10.007 |
0.678 |
|
| 2012 |
Conley SM, Stuck MW, Naash MI. Structural and functional relationships between photoreceptor tetraspanins and other superfamily members. Cellular and Molecular Life Sciences : Cmls. 69: 1035-47. PMID 21655915 DOI: 10.1007/S00018-011-0736-0 |
0.715 |
|
| 2011 |
Macdonald IM, Naash MI, Ayyagari R. Retinal degenerations: genetics, mechanisms, and therapies. Journal of Ophthalmology. 2011: 764873. PMID 22132314 DOI: 10.1155/2011/764873 |
0.312 |
|
| 2011 |
Koirala A, Makkia RS, Cooper MJ, Naash MI. Nanoparticle-mediated gene transfer specific to retinal pigment epithelial cells. Biomaterials. 32: 9483-93. PMID 21885113 DOI: 10.1016/J.Biomaterials.2011.08.062 |
0.753 |
|
| 2011 |
Han Z, Conley SM, Naash MI. AAV and compacted DNA nanoparticles for the treatment of retinal disorders: challenges and future prospects. Investigative Ophthalmology & Visual Science. 52: 3051-9. PMID 21558483 DOI: 10.1167/Iovs.10-6916 |
0.628 |
|
| 2010 |
Chakraborty D, Conley SM, Stuck MW, Naash MI. Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS. Human Molecular Genetics. 19: 4799-812. PMID 20858597 DOI: 10.1093/Hmg/Ddq410 |
0.689 |
|
| 2010 |
Conley SM, Naash MI. Nanoparticles for retinal gene therapy. Progress in Retinal and Eye Research. 29: 376-97. PMID 20452457 DOI: 10.1016/J.Preteyeres.2010.04.004 |
0.671 |
|
| 2010 |
Cai X, Conley SM, Cheng T, Al-Ubaidi MR, Naash MI. A 350 bp region of the proximal promoter of Rds drives cell-type specific gene expression. Experimental Eye Research. 91: 186-94. PMID 20447394 DOI: 10.1016/J.Exer.2010.04.017 |
0.659 |
|
| 2010 |
Cai X, Conley SM, Naash MI. Gene therapy in the Retinal Degeneration Slow model of retinitis pigmentosa. Advances in Experimental Medicine and Biology. 664: 611-9. PMID 20238065 DOI: 10.1007/978-1-4419-1399-9_70 |
0.749 |
|
| 2010 |
Conley SM, Ding XQ, Naash MI. RDS in cones does not interact with the beta subunit of the cyclic nucleotide gated channel. Advances in Experimental Medicine and Biology. 664: 63-70. PMID 20238003 DOI: 10.1007/978-1-4419-1399-9_8 |
0.683 |
|
| 2010 |
Chakraborty D, Conley SM, Fliesler SJ, Naash MI. The function of oligomerization-incompetent RDS in rods. Advances in Experimental Medicine and Biology. 664: 39-46. PMID 20238000 DOI: 10.1007/978-1-4419-1399-9_5 |
0.677 |
|
| 2010 |
Conley SM, Stricker HM, Naash MI. Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene. Biochemistry. 49: 905-11. PMID 20055437 DOI: 10.1021/Bi901622W |
0.825 |
|
| 2010 |
Cai X, Conley SM, Nash Z, Fliesler SJ, Cooper MJ, Naash MI. Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 1178-91. PMID 19952284 DOI: 10.1096/Fj.09-139147 |
0.688 |
|
| 2009 |
Ding XQ, Quiambao AB, Fitzgerald JB, Cooper MJ, Conley SM, Naash MI. Ocular delivery of compacted DNA-nanoparticles does not elicit toxicity in the mouse retina. Plos One. 4: e7410. PMID 19823583 DOI: 10.1371/Journal.Pone.0007410 |
0.63 |
|
| 2009 |
Cai X, Nash Z, Conley SM, Fliesler SJ, Cooper MJ, Naash MI. A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles. Plos One. 4: e5290. PMID 19390689 DOI: 10.1371/Journal.Pone.0005290 |
0.683 |
|
| 2009 |
Cai X, Conley SM, Naash MI. RPE65: role in the visual cycle, human retinal disease, and gene therapy. Ophthalmic Genetics. 30: 57-62. PMID 19373675 DOI: 10.1080/13816810802626399 |
0.723 |
|
| 2009 |
Conley SM, Naash MI. Focus on molecules: RDS. Experimental Eye Research. 89: 278-9. PMID 19366620 DOI: 10.1016/J.Exer.2009.03.023 |
0.523 |
|
| 2009 |
Chakraborty D, Ding XQ, Conley SM, Fliesler SJ, Naash MI. Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones. Human Molecular Genetics. 18: 797-808. PMID 19050038 DOI: 10.1093/Hmg/Ddn406 |
0.685 |
|
| 2008 |
Conley SM, Cai X, Naash MI. Nonviral ocular gene therapy: assessment and future directions. Current Opinion in Molecular Therapeutics. 10: 456-63. PMID 18830921 |
0.617 |
|
| 2008 |
Farjo R, Peterson WM, Naash MI. Expression profiling after retinal detachment and reattachment: a possible role for aquaporin-0. Investigative Ophthalmology & Visual Science. 49: 511-21. PMID 18234993 DOI: 10.1167/Iovs.07-1013 |
0.784 |
|
| 2008 |
Nour M, Fliesler SJ, Naash MI. Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa. Advances in Experimental Medicine and Biology. 613: 129-38. PMID 18188937 DOI: 10.1007/978-0-387-74904-4_14 |
0.619 |
|
| 2008 |
Chakraborty D, Whalen P, Lewin AS, Naash MI. In vitro analysis of ribozyme-mediated knockdown of an ADRP associated rhodopsin mutation. Advances in Experimental Medicine and Biology. 613: 97-106. PMID 18188933 DOI: 10.1007/978-0-387-74904-4_10 |
0.305 |
|
| 2008 |
Chakraborty D, Ding XQ, Fliesler SJ, Naash MI. Outer segment oligomerization of Rds: evidence from mouse models and subcellular fractionation. Biochemistry. 47: 1144-56. PMID 18171083 DOI: 10.1021/bi701807c |
0.428 |
|
| 2008 |
Cai X, Conley S, Naash M. Nanoparticle applications in ocular gene therapy. Vision Research. 48: 319-24. PMID 17825344 DOI: 10.1016/J.Visres.2007.07.012 |
0.645 |
|
| 2007 |
Conley S, Nour M, Fliesler SJ, Naash MI. Late-onset cone photoreceptor degeneration induced by R172W mutation in Rds and partial rescue by gene supplementation. Investigative Ophthalmology & Visual Science. 48: 5397-407. PMID 18055786 DOI: 10.1167/Iovs.07-0663 |
0.78 |
|
| 2007 |
Farjo R, Fliesler SJ, Naash MI. Effect of Rds abundance on cone outer segment morphogenesis, photoreceptor gene expression, and outer limiting membrane integrity. The Journal of Comparative Neurology. 504: 619-30. PMID 17722028 DOI: 10.1002/Cne.21476 |
0.804 |
|
| 2007 |
Canola K, Angénieux B, Tekaya M, Quiambao A, Naash MI, Munier FL, Schorderet DF, Arsenijevic Y. Retinal stem cells transplanted into models of late stages of retinitis pigmentosa preferentially adopt a glial or a retinal ganglion cell fate. Investigative Ophthalmology & Visual Science. 48: 446-54. PMID 17197566 DOI: 10.1167/iovs.06-0190 |
0.376 |
|
| 2006 |
Ding XQ, Naash MI. Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds. Advances in Experimental Medicine and Biology. 572: 141-6. PMID 17249567 DOI: 10.1007/0-387-32442-9_21 |
0.39 |
|
| 2006 |
Farjo R, Skaggs J, Quiambao AB, Cooper MJ, Naash MI. Efficient non-viral ocular gene transfer with compacted DNA nanoparticles. Plos One. 1: e38. PMID 17183666 DOI: 10.1371/Journal.Pone.0000038 |
0.728 |
|
| 2006 |
Farjo R, Naash MI. The role of Rds in outer segment morphogenesis and human retinal disease. Ophthalmic Genetics. 27: 117-22. PMID 17148038 DOI: 10.1080/13816810600976806 |
0.799 |
|
| 2006 |
Farjo R, Skaggs JS, Nagel BA, Quiambao AB, Nash ZA, Fliesler SJ, Naash MI. Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors. The Journal of Cell Biology. 173: 59-68. PMID 16585269 DOI: 10.1083/Jcb.200509036 |
0.778 |
|
| 2006 |
Samardzija M, Wenzel A, Naash M, Remé CE, Grimm C. Rpe65 as a modifier gene for inherited retinal degeneration European Journal of Neuroscience. 23: 1028-1034. PMID 16519667 DOI: 10.1111/J.1460-9568.2006.04639.X |
0.517 |
|
| 2006 |
Naash MI, Ballard RM, Skaggs J, Nash Z, Quiambao AB, Cooper MJ, Farjo R. 882. Non-Viral Ocular Gene Transfer for Hereditary Retinal Degeneration Molecular Therapy. 13: S340. DOI: 10.1016/J.Ymthe.2006.08.971 |
0.787 |
|
| 2005 |
Ding XQ, Stricker HM, Naash MI. Role of the second intradiscal loop of peripherin/rds in homo and hetero associations. Biochemistry. 44: 4897-904. PMID 15779916 DOI: 10.1021/Bi048414I |
0.795 |
|
| 2005 |
Stricker HM, Ding XQ, Quiambao A, Fliesler SJ, Naash MI. The Cys214-->Ser mutation in peripherin/rds causes a loss-of-function phenotype in transgenic mice. The Biochemical Journal. 388: 605-13. PMID 15656787 DOI: 10.1042/Bj20041960 |
0.821 |
|
| 2004 |
Naash MI, Wu TH, Chakraborty D, Fliesler SJ, Ding XQ, Nour M, Peachey NS, Lem J, Qtaishat N, Al-Ubaidi MR, Ripps H. Retinal abnormalities associated with the G90D mutation in opsin. The Journal of Comparative Neurology. 478: 149-63. PMID 15349976 DOI: 10.1002/Cne.20283 |
0.672 |
|
| 2004 |
Nour M, Ding XQ, Stricker H, Fliesler SJ, Naash MI. Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression. Investigative Ophthalmology & Visual Science. 45: 2514-21. PMID 15277471 DOI: 10.1167/Iovs.04-0065 |
0.836 |
|
| 2004 |
Ding XQ, Nour M, Ritter LM, Goldberg AF, Fliesler SJ, Naash MI. The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic mice. Human Molecular Genetics. 13: 2075-87. PMID 15254014 DOI: 10.1093/Hmg/Ddh211 |
0.68 |
|
| 2004 |
Grimm C, Wenzel A, Stanescu D, Samardzija M, Hotop S, Groszer M, Naash M, Gassmann M, Remé C. Constitutive overexpression of human erythropoietin protects the mouse retina against induced but not inherited retinal degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 5651-8. PMID 15215287 DOI: 10.1523/Jneurosci.1288-04.2004 |
0.415 |
|
| 2004 |
Tan E, Ding XQ, Saadi A, Agarwal N, Naash MI, Al-Ubaidi MR. Expression of cone-photoreceptor-specific antigens in a cell line derived from retinal tumors in transgenic mice. Investigative Ophthalmology & Visual Science. 45: 764-8. PMID 14985288 DOI: 10.1167/Iovs.03-1114 |
0.309 |
|
| 2004 |
Nour M, Quiambao AB, Al-Ubaidi MR, Naash MI. Absence of functional and structural abnormalities associated with expression of EGFP in the retina. Investigative Ophthalmology & Visual Science. 45: 15-22. PMID 14691148 DOI: 10.1167/Iovs.03-0663 |
0.663 |
|
| 2003 |
Nour M, Naash MI. Mouse models of human retinal disease caused by expression of mutant rhodopsin. A valuable tool for the assessment of novel gene therapies. Advances in Experimental Medicine and Biology. 533: 173-9. PMID 15180262 DOI: 10.1007/978-1-4615-0067-4_22 |
0.626 |
|
| 2003 |
Nour M, Quiambao AB, Peterson WM, Al-Ubaidi MR, Naash MI. P2Y(2) receptor agonist INS37217 enhances functional recovery after detachment caused by subretinal injection in normal and rds mice. Investigative Ophthalmology & Visual Science. 44: 4505-14. PMID 14507899 DOI: 10.1167/Iovs.03-0453 |
0.652 |
|
| 2003 |
Li C, Ding XQ, O'Brien J, Al-Ubaidi MR, Naash MI. Molecular characterization of the skate peripherin/rds gene: relationship to its orthologues and paralogues. Investigative Ophthalmology & Visual Science. 44: 2433-41. PMID 12766040 DOI: 10.1167/Iovs.02-1152 |
0.362 |
|
| 2001 |
Quiambao AB, Tan E, Chang S, Komori N, Naash MI, Peachey NS, Matsumoto H, Ucker DS, Al-Ubaidi MR. Transgenic Bcl-2 expressed in photoreceptor cells confers both death-sparing and death-inducing effects. Experimental Eye Research. 73: 711-21. PMID 11747371 DOI: 10.1006/Exer.2001.1083 |
0.328 |
|
| 2001 |
Li C, Cheng M, Yang H, Peachey NS, Naash MI. Age-related changes in the mouse outer retina. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 78: 425-30. PMID 11444632 DOI: 10.1097/00006324-200106000-00015 |
0.338 |
|
| 2001 |
Tan E, Wang Q, Quiambao AB, Xu X, Qtaishat NM, Peachey NS, Lem J, Fliesler SJ, Pepperberg DR, Naash MI, Al-Ubaidi MR. The relationship between opsin overexpression and photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 42: 589-600. PMID 11222515 |
0.359 |
|
| 2001 |
Ren JC, Stubbs EB, Matthes MT, Yasumura D, Naash MI, LaVail MM, Peachey NS. Retinal degeneration in the nervous mutant mouse. IV. Inner retinal changes. Experimental Eye Research. 72: 243-52. PMID 11180973 DOI: 10.1006/Exer.2000.0961 |
0.39 |
|
| 2000 |
Penn JS, Li S, Naash MI. Ambient hypoxia reverses retinal vascular attenuation in a transgenic mouse model of autosomal dominant retinitis pigmentosa Investigative Ophthalmology and Visual Science. 41: 4007-4013. PMID 11053306 |
0.393 |
|
| 1999 |
Qtaishat NM, Okajima TI, Li S, Naash MI, Pepperberg DR. Retinoid kinetics in eye tissues of VPP transgenic mice and their normal littermates. Investigative Ophthalmology & Visual Science. 40: 1040-9. PMID 10235537 |
0.344 |
|
| 1998 |
Wu TH, Ting TD, Okajima TI, Pepperberg DR, Ho YK, Ripps H, Naash MI. Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa. Neuroscience. 87: 709-17. PMID 9758235 DOI: 10.1016/S0306-4522(98)00173-0 |
0.388 |
|
| 1997 |
Liu X, Wu TH, Stowe S, Matsushita A, Arikawa K, Naash MI, Williams DS. Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain. Journal of Cell Science. 110: 2589-97. PMID 9372448 |
0.369 |
|
| 1997 |
Naash MI, Al-Ubaidi MR, Anderson RE. Light exposure induces ubiquitin conjugation and degradation activities in the rat retina. Investigative Ophthalmology & Visual Science. 38: 2344-54. PMID 9344358 |
0.43 |
|
| 1997 |
Cheng T, Peachey NS, Li S, Goto Y, Cao Y, Naash MI. The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 8118-28. PMID 9334387 DOI: 10.1523/Jneurosci.17-21-08118.1997 |
0.478 |
|
| 1997 |
Wang M, Lam TT, Tso MOM, Naash MI. Expression of a mutant opsin gene increases the susceptibility of the retina to light damage Visual Neuroscience. 14: 55-62. PMID 9057268 |
0.406 |
|
| 1997 |
Qtaishat NM, Li S, Naash MI, Pepperberg DR. Retinoid kinetics in the vpp mouse, a model of autosomal dominant retinitis pigmentosa (ADRP) Investigative Ophthalmology and Visual Science. 38: S303. |
0.394 |
|
| 1996 |
Naash MI, Ripps H, Li S, Goto Y, Peachey NS. Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 7853-8. PMID 8987813 DOI: 10.1523/Jneurosci.16-24-07853.1996 |
0.457 |
|
| 1996 |
Naash ML, Peachey NS, Li ZY, Gryczan CC, Goto Y, Blanks J, Milam AH, Ripps H. Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin. Investigative Ophthalmology & Visual Science. 37: 775-82. PMID 8603862 |
0.429 |
|
| 1996 |
Novak L, Kuszak JR, Naash MI. The structure of Posterior Subcapsular Cataracts (PSCs) in retinal degenerative disease models Investigative Ophthalmology and Visual Science. 37. |
0.357 |
|
| 1996 |
Peachey NS, Cheng T, Goto Y, Li S, Naash MI. Photoreceptor degeneration in rds/+ heterozygotes Investigative Ophthalmology and Visual Science. 37: S503. |
0.418 |
|
| 1996 |
Naash MI, Li S, Roveri L, Peachey NS, Wu T. Photoreceptor degeneration associated with the expression of a G90D mutation in the opsin gene Investigative Ophthalmology and Visual Science. 37: S698. |
0.36 |
|
| 1996 |
Wu T, Li S, Kogut P, Peachey NS, Naash MI. Expression of P23H mutation in transgenic mice as a model for one form of human autosomal dominant retinitis pigmentosa Investigative Ophthalmology and Visual Science. 37: S999. |
0.353 |
|
| 1996 |
Penn JS, Li S, Tolman BL, Roberto KA, Naash MI. Retinal vascular attenuation in a transgenic mouse model of ADRP Investigative Ophthalmology and Visual Science. 37. |
0.467 |
|
| 1996 |
Steinberg RH, Flannery JG, Naash M, Oh P, Matthes MT, Yasumura D, Lau-Villacorta C, Chen J, LaVail MM. Transgenic rat models of inherited retinal degeneration caused by mutant opsin genes Investigative Ophthalmology and Visual Science. 37: S698. |
0.398 |
|
| 1995 |
Goto Y, Peachey NS, Ripps H, Naash MI. Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene. Investigative Ophthalmology & Visual Science. 36: 62-71. PMID 7822160 |
0.361 |
|
| 1993 |
Naash MI, Hollyfield JG, al-Ubaidi MR, Baehr W. Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene. Proceedings of the National Academy of Sciences of the United States of America. 90: 5499-503. PMID 8516292 DOI: 10.1073/Pnas.90.12.5499 |
0.448 |
|
| 1991 |
Naash M, Izbicka E, Anderson RE. Rat retina has an active and stable ubiquitin–protein conjugating system Journal of Neuroscience Research. 30: 433-441. PMID 1665870 DOI: 10.1002/jnr.490300220 |
0.478 |
|
| 1989 |
Naash MI, Anderson RE. Glutathione-dependent enzymes in intact rod outer segments Experimental Eye Research. 48: 309-318. PMID 2924815 DOI: 10.1016/S0014-4835(89)80080-6 |
0.378 |
|
| 1989 |
Naash MI, LaVail MM, Anderson RE. Factors affecting the susceptibility of the retina to light damage. Progress in Clinical and Biological Research. 314: 513-22. PMID 2608676 |
0.411 |
|
| 1988 |
Nielsen JC, Naash MI, Anderson RE. The regional distribution of vitamins E and C in mature and premature human retinas Investigative Ophthalmology and Visual Science. 29: 22-26. PMID 3335430 |
0.333 |
|
| 1988 |
Naash MI, Nielsen JC, Anderson RE. Regional distribution of glutathione peroxidase and glutathione-S-transferase in adult and premature human retinas Investigative Ophthalmology and Visual Science. 29: 149-152. PMID 3335428 |
0.381 |
|
| 1987 |
Penn JS, Naash MI, Anderson RE. Effect of light history on retinal antioxidants and light damage susceptibility in the rat Experimental Eye Research. 44: 779-788. PMID 3653273 DOI: 10.1016/S0014-4835(87)80041-6 |
0.444 |
|
| 1984 |
Naash MI, Anderson RE. Characterization of glutathione peroxidase in frog retina Current Eye Research. 3: 1299-1304. PMID 6334591 DOI: 10.3109/02713688409007416 |
0.321 |
|
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