| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2025 |
Nguyen MN, Chakraborty D, Messinger J, Sherry DM, Fliesler SJ, Pittler SJ. Modeling Retinitis Pigmentosa 59: T206A and K42E knock-in mutant mice are phenotypically similar. Biorxiv : the Preprint Server For Biology. PMID 39868263 DOI: 10.1101/2025.01.13.632845 |
0.01 |
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| 2024 |
Monson E, Cideciyan AV, Roman AJ, Sumaroka A, Swider M, Wu V, Viarbitskaya I, Jacobson SG, Fliesler SJ, Pittler SJ. Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an Modifier Variant. International Journal of Molecular Sciences. 25. PMID 38256083 DOI: 10.3390/ijms25021004 |
0.01 |
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| 2023 |
Pittler SJ, Fliesler SJ. Cells Special Issue: "The Molecular and Cellular Basis of Retinal Diseases". Cells. 12. PMID 37566012 DOI: 10.3390/cells12151933 |
0.01 |
|
| 2023 |
Nguyen MN, Chakraborty D, Rao SR, Onysk A, Radkiewicz M, Surmacz L, Swiezewska E, Soubeyrand E, Akhtar TA, Kraft TW, Sherry DM, Fliesler SJ, Pittler SJ. A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmission. Cell Death & Disease. 14: 420. PMID 37443173 DOI: 10.1038/s41419-023-05936-4 |
0.01 |
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| 2023 |
Rao SR, Pittler SJ, Fliesler SJ. Perspectives on Retinal Dolichol Metabolism, and Visual Deficits in Dolichol Metabolism-Associated Inherited Disorders. Advances in Experimental Medicine and Biology. 1415: 449-456. PMID 37440071 DOI: 10.1007/978-3-031-27681-1_66 |
0.01 |
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| 2022 |
Fliesler SJ, Ramachandra Rao S, Nguyen MN, KhalafAllah MT, Pittler SJ. Vertebrate Animal Models of RP59: Current Status and Future Prospects. International Journal of Molecular Sciences. 23. PMID 36362109 DOI: 10.3390/ijms232113324 |
0.01 |
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| 2020 |
Ramachandra Rao S, Skelton LA, Wu F, Onysk A, Spolnik G, Danikiewicz W, Butler MC, Stacks DA, Surmacz L, Mu X, Swiezewska E, Pittler SJ, Fliesler SJ. Retinal Degeneration Caused by Rod-Specific Dhdds Ablation Occurs without Concomitant Inhibition of Protein N-Glycosylation. Iscience. 23: 101198. PMID 32526701 DOI: 10.1016/j.isci.2020.101198 |
0.01 |
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| 2020 |
Ramachandra Rao S, Fliesler SJ, Kotla P, Nguyen MN, Pittler SJ. Lack of Overt Retinal Degeneration in a K42E Knock-In Mouse Model of RP59. Cells. 9. PMID 32272552 DOI: 10.3390/cells9040896 |
0.01 |
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| 2020 |
DeRamus ML, Davis SJ, Rao SR, Nyankerh C, Stacks D, Kraft TW, Fliesler SJ, Pittler SJ. Selective Ablation of Dehydrodolichyl Diphosphate Synthase in Murine Retinal Pigment Epithelium (RPE) Causes RPE Atrophy and Retinal Degeneration. Cells. 9. PMID 32245241 DOI: 10.3390/Cells9030771 |
0.01 |
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| 2017 |
DeRamus ML, Stacks DA, Zhang Y, Huisingh CE, McGwin G, Pittler SJ. GARP2 accelerates retinal degeneration in rod cGMP-gated cation channel β-subunit knockout mice. Scientific Reports. 7: 42545. PMID 28198469 DOI: 10.1038/Srep42545 |
0.01 |
|
| 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 |
0.01 |
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| 2016 |
Ding XQ, Thapa A, Ma H, Xu J, Elliott MH, Rodgers KK, Smith ML, Wang JS, Pittler SJ, Kefalov VJ. The B3 subunit of the cone cyclic nucleotide-gated channel regulates the light responses of cones and contributes to the channel structural flexibility. The Journal of Biological Chemistry. PMID 26893377 DOI: 10.1074/Jbc.M115.696138 |
0.01 |
|
| 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 |
0.01 |
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| 2014 |
Sarfare S, McKeown AS, Messinger J, Rubin G, Wei H, Kraft TW, Pittler SJ. Overexpression of rod photoreceptor glutamic acid rich protein 2 (GARP2) increases gain and slows recovery in mouse retina. Cell Communication and Signaling : Ccs. 12: 67. PMID 25323447 DOI: 10.1186/S12964-014-0067-5 |
0.01 |
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| 2013 |
Lu R, Levy AM, Zhang Q, Pittler SJ, Yao X. Dynamic near-infrared imaging reveals transient phototropic change in retinal rod photoreceptors. Journal of Biomedical Optics. 18: 106013. PMID 24165739 DOI: 10.1117/1.Jbo.18.10.106013 |
0.01 |
|
| 2012 |
Gilliam JC, Chang JT, Sandoval IM, Zhang Y, Li T, Pittler SJ, Chiu W, Wensel TG. Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegeneration. Cell. 151: 1029-41. PMID 23178122 DOI: 10.1016/J.Cell.2012.10.038 |
0.01 |
|
| 2012 |
Lu RW, Curcio CA, Zhang Y, Zhang QX, Pittler SJ, Deretic D, Yao XC. Investigation of the hyper-reflective inner/outer segment band in optical coherence tomography of living frog retina. Journal of Biomedical Optics. 17: 060504. PMID 22734727 DOI: 10.1117/1.Jbo.17.6.060504 |
0.01 |
|
| 2012 |
Zhang QX, Zhang Y, Lu RW, Li YC, Pittler SJ, Kraft TW, Yao XC. Comparative intrinsic optical signal imaging of wild-type and mutant mouse retinas. Optics Express. 20: 7646-54. PMID 22453443 DOI: 10.1364/Oe.20.007646 |
0.01 |
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| 2012 |
Zhang Y, Rubin GR, Fineberg N, Huisingh C, McGwin G, Pittler SJ, Kraft TW. Age-related changes in Cngb1-X1 knockout mice: prolonged cone survival. Documenta Ophthalmologica. Advances in Ophthalmology. 124: 163-75. PMID 22367173 DOI: 10.1007/S10633-012-9317-2 |
0.01 |
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| 2010 |
Peshenko IV, Olshevskaya EV, Yao S, Ezzeldin HH, Pittler SJ, Dizhoor AM. Activation of retinal guanylyl cyclase RetGC1 by GCAP1: stoichiometry of binding and effect of new LCA-related mutations. Biochemistry. 49: 709-17. PMID 20050595 DOI: 10.1021/bi901495y |
0.01 |
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| 2009 |
Zhang Y, Molday LL, Molday RS, Sarfare SS, Woodruff ML, Fain GL, Kraft TW, Pittler SJ. Knockout of GARPs and the β-subunit of the rod cGMP-gated channel disrupts disk morphogenesis and rod outer segment structural integrity. Journal of Cell Science. 122: 1192-200. PMID 19339551 DOI: 10.1242/Jcs.042531 |
0.01 |
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| 2009 |
Tuntivanich N, Pittler SJ, Fischer AJ, Omar G, Kiupel M, Weber A, Yao S, Steibel JP, Khan NW, Petersen-Jones SM. Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation. Investigative Ophthalmology & Visual Science. 50: 801-13. PMID 18775863 DOI: 10.1167/Iovs.08-2562 |
0.01 |
|
| 2007 |
Sarfare S, Pittler SJ. Focus on molecules: rod photoreceptor cGMP-gated cation channel. Experimental Eye Research. 85: 173-4. PMID 16697368 DOI: 10.1016/J.Exer.2006.03.011 |
0.01 |
|
| 2007 |
Ionita MA, Pittler SJ. Focus on molecules: rod cGMP phosphodiesterase type 6. Experimental Eye Research. 84: 1-2. PMID 16563379 DOI: 10.1016/j.exer.2005.12.012 |
0.01 |
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| 2005 |
Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EA, Traboulsi EI, Heon E, Pittler SJ, Milam AH, Maguire AM, Palczewski K, Stone EM, Bennett J. Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success. Proceedings of the National Academy of Sciences of the United States of America. 102: 6177-82. PMID 15837919 DOI: 10.1073/Pnas.0500646102 |
0.01 |
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| 2004 |
White JB, Thompson WJ, Pittler SJ. Characterization of 3',5' cyclic nucleotide phosphodiesterase activity in Y79 retinoblastoma cells: absence of functional PDE6. Molecular Vision. 10: 738-49. PMID 15480303 |
0.01 |
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| 2004 |
Pittler SJ, Zhang Y, Chen S, Mears AJ, Zack DJ, Ren Z, Swain PK, Yao S, Swaroop A, White JB. Functional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activity. The Journal of Biological Chemistry. 279: 19800-7. PMID 15001570 DOI: 10.1074/Jbc.M401864200 |
0.01 |
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| 2002 |
Koenekoop RK, Fishman GA, Iannaccone A, Ezzeldin H, Ciccarelli ML, Baldi A, Sunness JS, Lotery AJ, Jablonski MM, Pittler SJ, Maumenee I. Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 1325-30. PMID 12365911 DOI: 10.1001/Archopht.120.10.1325 |
0.01 |
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| Hide low-probability matches. |