Year |
Citation |
Score |
2024 |
Aljammal R, Saravanan T, Guan T, Rhodes S, Robichaux MA, Ramamurthy V. Excessive tubulin glutamylation leads to progressive cone-rod dystrophy and loss of outer segment integrity. Human Molecular Genetics. PMID 38297980 DOI: 10.1093/hmg/ddae013 |
0.465 |
|
2023 |
Moakedi F, Aljammal R, Poria D, Saravanan T, Rhodes SB, Reid C, Guan T, Kefalov VJ, Ramamurthy V. Prenylation is essential for the enrichment of cone phosphodiesterase-6 (PDE6) in outer segments and efficient cone phototransduction. Human Molecular Genetics. PMID 37384398 DOI: 10.1093/hmg/ddad108 |
0.473 |
|
2023 |
Munezero D, Aliff H, Salido E, Saravanan T, Sanzhaeva U, Guan T, Ramamurthy V. HSP90α is needed for the survival of rod photoreceptors and regulates the expression of rod PDE6 subunits. The Journal of Biological Chemistry. 299: 104809. PMID 37172722 DOI: 10.1016/j.jbc.2023.104809 |
0.447 |
|
2022 |
Matalkah F, Jeong B, Sheridan M, Horstick E, Ramamurthy V, Stoilov P. The Musashi proteins direct post-transcriptional control of protein expression and alternate exon splicing in vertebrate photoreceptors. Communications Biology. 5: 1011. PMID 36153373 DOI: 10.1038/s42003-022-03990-w |
0.412 |
|
2020 |
Sundar J, Matalkah F, Jeong B, Stoilov P, Ramamurthy V. The Musashi proteins MSI1 and MSI2 are required for photoreceptor morphogenesis and vision in mice. The Journal of Biological Chemistry. 296: 100048. PMID 33429214 DOI: 10.1074/jbc.RA120.015714 |
0.469 |
|
2020 |
Sundar J, Matalkah F, Jeong B, Stoilov P, Ramamurthy V. The Musashi proteins MSI1 and MSI2 are required for photoreceptor morphogenesis and vision in mice. The Journal of Biological Chemistry. PMID 33168629 DOI: 10.1074/jbc.RA120.015714 |
0.466 |
|
2020 |
Salido EM, Ramamurthy V. Proteoglycan IMPG2 shapes the interphotoreceptor matrix and modulates vision. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32265257 DOI: 10.1523/Jneurosci.2994-19.2020 |
0.475 |
|
2020 |
Lukovic D, Artero Castro A, Kaya KD, Munezero D, Gieser L, Davó-Martínez C, Corton M, Cuenca N, Swaroop A, Ramamurthy V, Ayuso C, Erceg S. Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1. Scientific Reports. 10: 5426. PMID 32214115 DOI: 10.1038/S41598-020-62047-2 |
0.492 |
|
2019 |
Sundar JC, Munezero D, Bryan-Haring C, Saravanan T, Jacques A, Ramamurthy V. Rhodopsin signaling mediates light-induced photoreceptor cell death in rd10 mice through a transducin-independent mechanism. Human Molecular Genetics. PMID 31925423 DOI: 10.1093/Hmg/Ddz299 |
0.503 |
|
2019 |
Dilan T, Ramamurthy V. The Dynamic and Complex Role of the Joubert Syndrome-Associated Ciliary Protein, ADP-Ribosylation Factor-Like GTPase 13B (ARL13B) in Photoreceptor Development and Maintenance. Advances in Experimental Medicine and Biology. 1185: 501-505. PMID 31884661 DOI: 10.1007/978-3-030-27378-1_82 |
0.406 |
|
2019 |
Moye AR, Bedoni N, Cunningham JG, Sanzhaeva U, Tucker ES, Mathers P, Peter VG, Quinodoz M, Paris LP, Coutinho-Santos L, Camacho P, Purcell MG, Winkelmann AC, Foster JA, Pugacheva EN, ... ... Ramamurthy V, et al. Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. Plos Genetics. 15: e1008315. PMID 31425546 DOI: 10.1371/Journal.Pgen.1008315 |
0.428 |
|
2019 |
Grenell A, Wang Y, Yam M, Swarup A, Dilan TL, Hauer A, Linton JD, Philp NJ, Gregor E, Zhu S, Shi Q, Murphy J, Guan T, Lohner D, Kolandaivelu S, ... Ramamurthy V, et al. Loss of MPC1 reprograms retinal metabolism to impair visual function. Proceedings of the National Academy of Sciences of the United States of America. 116: 3530-3535. PMID 30808746 DOI: 10.1073/Pnas.1812941116 |
0.389 |
|
2018 |
Dilan TL, Moye AR, Salido EM, Saravanan T, Saravanan K, Goldberg AFX, Ramamurthy V. ARL13B, a Joubert Syndrome-associated protein, is critical for retinogenesis and elaboration of mouse photoreceptor outer segments. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 30573647 DOI: 10.1523/Jneurosci.1761-18.2018 |
0.554 |
|
2018 |
Wright ZC, Loskutov Y, Murphy D, Stoilov P, Pugacheva E, Goldberg AFX, Ramamurthy V. ADP-Ribosylation Factor-Like 2 (ARL2) regulates cilia stability and development of outer segments in rod photoreceptor neurons. Scientific Reports. 8: 16967. PMID 30446707 DOI: 10.1038/S41598-018-35395-3 |
0.534 |
|
2018 |
Deng WT, Kolandaivelu S, Dinculescu A, Li J, Zhu P, Chiodo VA, Ramamurthy V, Hauswirth WW. Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits. Frontiers in Molecular Neuroscience. 11: 233. PMID 30038560 DOI: 10.3389/Fnmol.2018.00233 |
0.493 |
|
2018 |
Moye AR, Singh R, Kimler VA, Dilan TL, Munezero D, Saravanan T, Goldberg AFX, Ramamurthy V. ARL2BP, a protein linked to Retinitis Pigmentosa, is needed for normal photoreceptor cilia doublets and outer segment structure. Molecular Biology of the Cell. mbcE18010040. PMID 29718757 DOI: 10.1091/Mbc.E18-01-0040 |
0.566 |
|
2017 |
Dilan TL, Singh RK, Saravanan T, Moye A, Goldberg AFX, Stoilov P, Ramamurthy V. Bardet-Biedl Syndrome -8 (BBS8) protein is crucial for the development of outer segments in photoreceptor neurons. Human Molecular Genetics. PMID 29126234 DOI: 10.1093/Hmg/Ddx399 |
0.558 |
|
2016 |
Murphy D, Cieply B, Carstens R, Ramamurthy V, Stoilov P. The Musashi 1 Controls the Splicing of Photoreceptor-Specific Exons in the Vertebrate Retina. Plos Genetics. 12: e1006256. PMID 27541351 DOI: 10.1371/Journal.Pgen.1006256 |
0.47 |
|
2016 |
Christiansen JR, Pendse ND, Kolandaivelu S, Bergo MO, Young SG, Ramamurthy V. Deficiency of Isoprenylcysteine Carboxyl Methyltransferase (ICMT) Leads to Progressive Loss of Photoreceptor Function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 5107-14. PMID 27147662 DOI: 10.1523/Jneurosci.0176-16.2016 |
0.731 |
|
2016 |
Murphy D, Kolandaivelu S, Ramamurthy V, Stoilov P. Analysis of Alternative Pre-RNA Splicing in the Mouse Retina Using a Fluorescent Reporter. Methods in Molecular Biology (Clifton, N.J.). 1421: 269-86. PMID 26965271 DOI: 10.1007/978-1-4939-3591-8_20 |
0.317 |
|
2016 |
Wright ZC, Singh RK, Alpino R, Goldberg AF, Sokolov M, Ramamurthy V. ARL3 regulates trafficking of prenylated phototransduction proteins to the rod outer segment. Human Molecular Genetics. PMID 26936825 DOI: 10.1093/Hmg/Ddw077 |
0.568 |
|
2015 |
Murphy D, Singh R, Kolandaivelu S, Ramamurthy V, Stoilov P. Alternative Splicing Shapes the Phenotype of a Mutation in BBS8 To Cause Nonsyndromic Retinitis Pigmentosa. Molecular and Cellular Biology. 35: 1860-70. PMID 25776555 DOI: 10.1128/Mcb.00040-15 |
0.371 |
|
2015 |
Kmoch S, Majewski J, Ramamurthy V, Cao S, Fahiminiya S, Ren H, MacDonald IM, Lopez I, Sun V, Keser V, Khan A, Stránecký V, Hartmannová H, P?istoupilová A, Hoda?ová K, et al. Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness. Nature Communications. 6: 5614. PMID 25574898 DOI: 10.1038/Ncomms6614 |
0.461 |
|
2015 |
Ku CA, Chiodo VA, Boye SL, Hayes A, Goldberg AF, Hauswirth WW, Ramamurthy V. Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model. Human Molecular Genetics. 24: 670-84. PMID 25274777 DOI: 10.1093/Hmg/Ddu487 |
0.71 |
|
2015 |
Gupta C, Hayes A, Distefano MD, Ramamurthy V, Mertz B. Structural Study of AIPL1: Molecular Basis of its Function and its Role in Blinding Diseases Biophysical Journal. 108: 222a. DOI: 10.1016/J.Bpj.2014.11.1225 |
0.416 |
|
2014 |
Ramamurthy V, Jolicoeur C, Koutroumbas D, Mühlhans J, Le YZ, Hauswirth WW, Giessl A, Cayouette M. Numb regulates the polarized delivery of cyclic nucleotide-gated ion channels in rod photoreceptor cilia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 13976-87. PMID 25319694 DOI: 10.1523/Jneurosci.1938-14.2014 |
0.485 |
|
2014 |
Singh RK, Kolandaivelu S, Ramamurthy V. Early alteration of retinal neurons in Aipl1-/- animals. Investigative Ophthalmology & Visual Science. 55: 3081-92. PMID 24736053 DOI: 10.1167/Iovs.13-13728 |
0.521 |
|
2014 |
Kolandaivelu S, Ramamurthy V. AIPL1 protein and its indispensable role in cone photoreceptor function and survival. Advances in Experimental Medicine and Biology. 801: 43-8. PMID 24664679 DOI: 10.1007/978-1-4614-3209-8_6 |
0.539 |
|
2014 |
Kolandaivelu S, Singh RK, Ramamurthy V. AIPL1, A protein linked to blindness, is essential for the stability of enzymes mediating cGMP metabolism in cone photoreceptor cells. Human Molecular Genetics. 23: 1002-12. PMID 24108108 DOI: 10.1093/Hmg/Ddt496 |
0.567 |
|
2013 |
Gao X, Sinha S, Belcastro M, Woodard C, Ramamurthy V, Stoilov P, Sokolov M. Splice isoforms of phosducin-like protein control the expression of heterotrimeric G proteins. The Journal of Biological Chemistry. 288: 25760-8. PMID 23888055 DOI: 10.1074/Jbc.M113.486258 |
0.444 |
|
2013 |
Deng WT, Sakurai K, Kolandaivelu S, Kolesnikov AV, Dinculescu A, Li J, Zhu P, Liu X, Pang J, Chiodo VA, Boye SL, Chang B, Ramamurthy V, Kefalov VJ, Hauswirth WW. Cone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 11745-53. PMID 23864662 DOI: 10.1523/Jneurosci.1536-13.2013 |
0.509 |
|
2013 |
Majumder A, Pahlberg J, Boyd KK, Kerov V, Kolandaivelu S, Ramamurthy V, Sampath AP, Artemyev NO. Transducin translocation contributes to rod survival and enhances synaptic transmission from rods to rod bipolar cells. Proceedings of the National Academy of Sciences of the United States of America. 110: 12468-73. PMID 23836670 DOI: 10.1073/Pnas.1222666110 |
0.442 |
|
2012 |
Christiansen JR, Ramamurthy V. Greasing the protein biosynthesis machinery of photoreceptor neurons: Role for postprenylation processing of proteins. Cellular Logistics. 2: 15-19. PMID 22645706 DOI: 10.4161/Cl.19804 |
0.704 |
|
2011 |
Ku CA, Chiodo VA, Boye SL, Goldberg AF, Li T, Hauswirth WW, Ramamurthy V. Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis. Human Molecular Genetics. 20: 4569-81. PMID 21880665 DOI: 10.1093/Hmg/Ddr391 |
0.71 |
|
2011 |
Kolandaivelu S, Chang B, Ramamurthy V. Rod phosphodiesterase-6 (PDE6) catalytic subunits restore cone function in a mouse model lacking cone PDE6 catalytic subunit. The Journal of Biological Chemistry. 286: 33252-9. PMID 21799013 DOI: 10.1074/Jbc.M111.259101 |
0.467 |
|
2011 |
Christiansen JR, Kolandaivelu S, Bergo MO, Ramamurthy V. RAS-converting enzyme 1-mediated endoproteolysis is required for trafficking of rod phosphodiesterase 6 to photoreceptor outer segments. Proceedings of the National Academy of Sciences of the United States of America. 108: 8862-6. PMID 21555557 DOI: 10.1073/Pnas.1103627108 |
0.715 |
|
2010 |
Kirschman LT, Kolandaivelu S, Frederick JM, Dang L, Goldberg AF, Baehr W, Ramamurthy V. The Leber congenital amaurosis protein, AIPL1, is needed for the viability and functioning of cone photoreceptor cells. Human Molecular Genetics. 19: 1076-87. PMID 20042464 DOI: 10.1093/Hmg/Ddp571 |
0.556 |
|
2009 |
Ramamurthy V, Cayouette M. Development and disease of the photoreceptor cilium. Clinical Genetics. 76: 137-45. PMID 19790290 DOI: 10.1111/J.1399-0004.2009.01240.X |
0.498 |
|
2009 |
Kolandaivelu S, Huang J, Hurley JB, Ramamurthy V. AIPL1, a protein associated with childhood blindness, interacts with alpha-subunit of rod phosphodiesterase (PDE6) and is essential for its proper assembly. The Journal of Biological Chemistry. 284: 30853-61. PMID 19758987 DOI: 10.1074/Jbc.M109.036780 |
0.423 |
|
2008 |
Elliott J, Jolicoeur C, Ramamurthy V, Cayouette M. Ikaros confers early temporal competence to mouse retinal progenitor cells. Neuron. 60: 26-39. PMID 18940586 DOI: 10.1016/J.Neuron.2008.08.008 |
0.432 |
|
2008 |
Hendrickson A, Bumsted-O'Brien K, Natoli R, Ramamurthy V, Possin D, Provis J. Rod photoreceptor differentiation in fetal and infant human retina. Experimental Eye Research. 87: 415-26. PMID 18778702 DOI: 10.1016/J.Exer.2008.07.016 |
0.5 |
|
2006 |
Schwartz ML, Hurley JB, Ramamurthy V. Biochemical function of the LCA linked protein, aryl hydrocarbon receptor interacting protein like-1 (AIPL1). Role of AIPL1 in retina. Advances in Experimental Medicine and Biology. 572: 89-94. PMID 17249560 DOI: 10.1007/0-387-32442-9_14 |
0.483 |
|
2005 |
Taylor MR, Kikkawa S, Diez-Juan A, Ramamurthy V, Kawakami K, Carmeliet P, Brockerhoff SE. The zebrafish pob gene encodes a novel protein required for survival of red cone photoreceptor cells. Genetics. 170: 263-73. PMID 15716502 DOI: 10.1534/Genetics.104.036434 |
0.518 |
|
2004 |
Ramamurthy V, Niemi GA, Reh TA, Hurley JB. Leber congenital amaurosis linked to AIPL1: a mouse model reveals destabilization of cGMP phosphodiesterase. Proceedings of the National Academy of Sciences of the United States of America. 101: 13897-902. PMID 15365178 DOI: 10.1073/Pnas.0404197101 |
0.58 |
|
2004 |
Kennedy BN, Stearns GW, Smyth VA, Ramamurthy V, van Eeden F, Ankoudinova I, Raible D, Hurley JB, Brockerhoff SE. Zebrafish rx3 and mab21l2 are required during eye morphogenesis. Developmental Biology. 270: 336-49. PMID 15183718 DOI: 10.1016/J.Ydbio.2004.02.026 |
0.329 |
|
2004 |
Tucker CL, Ramamurthy V, Pina AL, Loyer M, Dharmaraj S, Li Y, Maumenee IH, Hurley JB, Koenekoop RK. Functional analyses of mutant recessive GUCY2D alleles identified in Leber congenital amaurosis patients: protein domain comparisons and dominant negative effects. Molecular Vision. 10: 297-303. PMID 15123990 |
0.316 |
|
2003 |
Ramamurthy V, Roberts M, van den Akker F, Niemi G, Reh TA, Hurley JB. AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins. Proceedings of the National Academy of Sciences of the United States of America. 100: 12630-5. PMID 14555765 DOI: 10.1073/Pnas.2134194100 |
0.484 |
|
2001 |
Ramamurthy V, Tucker C, Wilkie SE, Daggett V, Hunt DM, Hurley JB. Interactions within the coiled-coil domain of RetGC-1 guanylyl cyclase are optimized for regulation rather than for high affinity. The Journal of Biological Chemistry. 276: 26218-29. PMID 11306565 DOI: 10.1074/Jbc.M010495200 |
0.434 |
|
2000 |
Wilkie SE, Newbold RJ, Deery E, Walker CE, Stinton I, Ramamurthy V, Hurley JB, Bhattacharya SS, Warren MJ, Hunt DM. Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy. Human Molecular Genetics. 9: 3065-73. PMID 11115851 DOI: 10.1093/Hmg/9.20.3065 |
0.382 |
|
2000 |
Schmidt M, Ding H, Ramamurthy V, Mukerji I, Oliver D. Nucleotide binding activity of SecA homodimer is conformationally regulated by temperature and altered by prlD and azi mutations Journal of Biological Chemistry. 275: 15440-15448. PMID 10747939 DOI: 10.1074/Jbc.M000605200 |
0.355 |
|
1999 |
Tucker CL, Woodcock SC, Kelsell RE, Ramamurthy V, Hunt PM, Hurley JB. Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophy Proceedings of the National Academy of Sciences of the United States of America. 96: 9039-9044. PMID 10430891 DOI: 10.1073/Pnas.96.16.9039 |
0.429 |
|
1998 |
Ramamurthy V, Dapíc V, Oliver D. secG and Temperature Modulate Expression of Azide-Resistant and Signal Sequence Suppressor Phenotypes of Escherichia coli secA Mutants Journal of Bacteriology. 180: 6419-6423. DOI: 10.1128/Jb.180.23.6419-6423.1998 |
0.373 |
|
1997 |
Ramamurthy V, Oliver D. Topology of the integral membrane form of Escherichia coli SecA protein reveals multiple periplasmically exposed regions and modulation by ATP binding Journal of Biological Chemistry. 272: 23239-23246. PMID 9287332 DOI: 10.1074/Jbc.272.37.23239 |
0.304 |
|
1997 |
Snyders S, Ramamurthy V, Oliver D. Identification of a region of interaction between Escherichia coli SecA and SecY proteins. The Journal of Biological Chemistry. 272: 11302-6. PMID 9111035 DOI: 10.1074/Jbc.272.17.11302 |
0.382 |
|
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