| Year |
Citation |
Score |
| 2024 |
Wifvat K, Camacho ET, Kawski M, Léveillard T, Wirkus S. Optimal Control with RdCVFL for Degenerating Photoreceptors. Bulletin of Mathematical Biology. 86: 29. PMID 38345678 DOI: 10.1007/s11538-024-01256-6 |
0.383 |
|
| 2023 |
Clérin E, Aït-Ali N, Sahel JA, Léveillard T. Restoration of Rod-Derived Metabolic and Redox Signaling to Prevent Blindness. Cold Spring Harbor Perspectives in Medicine. PMID 37848252 DOI: 10.1101/cshperspect.a041284 |
0.454 |
|
| 2023 |
Teal CJ, Ho MT, Huo L, Harada H, Bahlmann LC, Léveillard T, Monnier PP, Ramachandran A, Shoichet MS. Affinity-controlled release of rod-derived cone viability factor enhances cone photoreceptor survival. Acta Biomaterialia. PMID 36898472 DOI: 10.1016/j.actbio.2023.03.003 |
0.313 |
|
| 2023 |
Zeitz C, Roger JE, Audo I, Michiels C, Sánchez-Farías N, Varin J, Frederiksen H, Wilmet B, Callebert J, Gimenez ML, Bouzidi N, Blond F, Guilllonneau X, Fouquet S, Léveillard T, et al. Shedding light on myopia by studying complete congenital stationary night blindness. Progress in Retinal and Eye Research. 101155. PMID 36669906 DOI: 10.1016/j.preteyeres.2022.101155 |
0.396 |
|
| 2022 |
Ren X, Léveillard T. Modulating antioxidant systems as a therapeutic approach to retinal degeneration. Redox Biology. 57: 102510. PMID 36274523 DOI: 10.1016/j.redox.2022.102510 |
0.344 |
|
| 2022 |
Aït-Ali N, Léveillard T. The Emergence of Rod-Cone Cellular Interaction. Frontiers in Genetics. 13: 900849. PMID 36017494 DOI: 10.3389/fgene.2022.900849 |
0.337 |
|
| 2021 |
Zeitz C, Méjécase C, Michiels C, Condroyer C, Wohlschlegel J, Foussard M, Antonio A, Démontant V, Emmenegger L, Schalk A, Neuillé M, Orhan E, Augustin S, Bonnet C, Estivalet A, et al. Mutated Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy. International Journal of Molecular Sciences. 22. PMID 34360642 DOI: 10.3390/ijms22157875 |
0.323 |
|
| 2021 |
Sahel JA, Grieve K, Pagot C, Authié C, Mohand-Said S, Paques M, Audo I, Becker K, Chaumet-Riffaud AE, Azoulay L, Gutman E, Léveillard T, Zeitz C, Picaud S, Dalkara D, et al. Assessing photoreceptor status in retinal dystrophies: from high resolution imaging to functional vision. American Journal of Ophthalmology. PMID 34000280 DOI: 10.1016/j.ajo.2021.04.013 |
0.328 |
|
| 2021 |
Millet-Puel G, Pinault M, Cordonnier M, Fontaine V, Sahel JA, Léveillard T. Cone-Enriched Cultures from the Retina of Chicken Embryos to Study Rod to Cone Cellular Interactions. Journal of Visualized Experiments : Jove. PMID 33818576 DOI: 10.3791/61998 |
0.482 |
|
| 2021 |
Wifvat K, Camacho ET, Wirkus S, Léveillard T. The Role of RdCVFL in a Mathematical Model of Photoreceptor Interactions. Journal of Theoretical Biology. 110642. PMID 33636201 DOI: 10.1016/j.jtbi.2021.110642 |
0.361 |
|
| 2021 |
Klipfel L, Cordonnier M, Thiébault L, Clérin E, Blond F, Millet-Puel G, Mohand-Saïd S, Goureau O, Sahel JA, Nandrot EF, Léveillard T. A Splice Variant in Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells. Cells. 10. PMID 33477551 DOI: 10.3390/cells10010179 |
0.372 |
|
| 2020 |
Conart JB, Blot G, Augustin S, Millet-Puel G, Roubeix C, Beguier F, Charles-Messance H, Touhami S, Sahel JA, Berrod JP, Léveillard T, Guillonneau X, Delarasse C, Sennlaub F. Insulin inhibits inflammation-induced cone death in retinal detachment. Journal of Neuroinflammation. 17: 358. PMID 33243251 DOI: 10.1186/s12974-020-02039-1 |
0.348 |
|
| 2020 |
Solaguren-Beascoa M, Bujakowska KM, Méjécase C, Emmenegger L, Orhan E, Neuillé M, Mohand-Saïd S, Condroyer C, Lancelot ME, Michiels C, Demontant V, Antonio A, Letexier M, Saraiva JP, Lonjou C, et al. WDR34, a candidate gene for non-syndromic rod-cone dystrophy. Clinical Genetics. PMID 33124039 DOI: 10.1111/cge.13872 |
0.331 |
|
| 2020 |
Beguier F, Housset M, Roubeix C, Augustin S, Zagar Y, Nous C, Mathis T, Eandi C, Benchaboune M, Drame-Maigné A, Carpentier W, Chardonnet S, Touhami S, Blot G, Conart JB, ... ... Leveillard T, et al. The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte Elimination. Immunity. 53: 429-441.e8. PMID 32814029 DOI: 10.1016/J.Immuni.2020.07.021 |
0.308 |
|
| 2020 |
Clérin E, Marussig M, Sahel JA, Léveillard T. Metabolic and Redox Signaling of the Nucleoredoxin-Like-1 Gene for the Treatment of Genetic Retinal Diseases. International Journal of Molecular Sciences. 21. PMID 32120883 DOI: 10.3390/Ijms21051625 |
0.502 |
|
| 2019 |
Blond F, Léveillard T. Functional Genomics of the Retina to Elucidate its Construction and Deconstruction. International Journal of Molecular Sciences. 20. PMID 31590277 DOI: 10.3390/Ijms20194922 |
0.507 |
|
| 2019 |
Camacho ET, Brager D, Elachouri G, Korneyeva T, Millet-Puel G, Sahel JA, Léveillard T. A Mathematical Analysis of Aerobic Glycolysis Triggered by Glucose Uptake in Cones. Scientific Reports. 9: 4162. PMID 30858444 DOI: 10.1038/S41598-019-39901-Z |
0.442 |
|
| 2019 |
Léveillard T, Philp NJ, Sennlaub F. Is Retinal Metabolic Dysfunction at the Center of the Pathogenesis of Age-related Macular Degeneration? International Journal of Molecular Sciences. 20. PMID 30754662 DOI: 10.3390/Ijms20030762 |
0.407 |
|
| 2019 |
Léveillard T, Klipfel L. Mechanisms Underlying the Visual Benefit of Cell Transplantation for the Treatment of Retinal Degenerations. International Journal of Molecular Sciences. 20. PMID 30696106 DOI: 10.3390/Ijms20030557 |
0.488 |
|
| 2018 |
Sahel JA, Léveillard T. Maintaining Cone Function in Rod-Cone Dystrophies. Advances in Experimental Medicine and Biology. 1074: 499-509. PMID 29721982 DOI: 10.1007/978-3-319-75402-4_62 |
0.496 |
|
| 2017 |
Léveillard T, Aït-Ali N. Cell Signaling with Extracellular Thioredoxin and Thioredoxin-Like Proteins: Insight into Their Mechanisms of Action. Oxidative Medicine and Cellular Longevity. 2017: 8475125. PMID 29138681 DOI: 10.1155/2017/8475125 |
0.363 |
|
| 2017 |
El Shamieh S, Méjécase C, Bertelli M, Terray A, Michiels C, Condroyer C, Fouquet S, Sadoun M, Clérin E, Liu B, Léveillard T, Goureau O, Sahel JA, Audo I, Zeitz C. Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy. Genes. 8. PMID 29057815 DOI: 10.3390/Genes8100277 |
0.414 |
|
| 2017 |
Kole C, Klipfel L, Yang Y, Ferracane V, Blond F, Reichman S, Millet-Puel G, Clérin E, Aït-Ali N, Pagan D, Camara H, Delyfer MN, Nandrot EF, Sahel JA, Goureau O, et al. Otx2-Genetically Modified Retinal Pigment Epithelial Cells Rescue Photoreceptors after Transplantation. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 28988713 DOI: 10.1016/J.Ymthe.2017.09.007 |
0.542 |
|
| 2016 |
Léveillard T, Sahel JA. Metabolic and redox signaling in the retina. Cellular and Molecular Life Sciences : Cmls. PMID 27543457 DOI: 10.1007/S00018-016-2318-7 |
0.371 |
|
| 2016 |
Camacho ET, Léveillard T, Sahel JA, Wirkus S. Mathematical Model of the Role of RdCVF in the Coexistence of Rods and Cones in a Healthy Eye. Bulletin of Mathematical Biology. PMID 27444436 DOI: 10.1007/S11538-016-0185-X |
0.425 |
|
| 2016 |
Mei X, Chaffiol A, Kole C, Yang Y, Millet-Puel G, Clérin E, Aït-Ali N, Bennett J, Dalkara D, Sahel JA, Duebel J, Leveillard T. The thioredoxin encoded by the Rod-derived Cone Viability Factor gene protects cone photoreceptors against oxidative stress. Antioxidants & Redox Signaling. PMID 27025156 DOI: 10.1089/ars.2015.6509 |
0.653 |
|
| 2016 |
Kole C, Berdugo N, Da Silva C, Aït-Ali N, Millet-Puel G, Pagan D, Blond F, Poidevin L, Ripp R, Fontaine V, Wincker P, Zack DJ, Sahel JA, Poch O, Léveillard T. Identification of an Alternative Splicing Product of the Otx2 Gene Expressed in the Neural Retina and Retinal Pigmented Epithelial Cells. Plos One. 11: e0150758. PMID 26985665 DOI: 10.1371/Journal.Pone.0150758 |
0.542 |
|
| 2016 |
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448 |
0.329 |
|
| 2015 |
Léveillard T. Cancer metabolism of cone photoreceptors. Oncotarget. 6: 32285-6. PMID 26450906 DOI: 10.18632/Oncotarget.5963 |
0.467 |
|
| 2015 |
Orhan E, Dalkara D, Neuillé M, Lechauve C, Michiels C, Picaud S, Léveillard T, Sahel JA, Naash MI, Lavail MM, Zeitz C, Audo I. Genotypic and phenotypic characterization of P23H line 1 rat model. Plos One. 10: e0127319. PMID 26009893 DOI: 10.1371/Journal.Pone.0127319 |
0.397 |
|
| 2015 |
Aït-Ali N, Fridlich R, Millet-Puel G, Clérin E, Delalande F, Jaillard C, Blond F, Perrocheau L, Reichman S, Byrne LC, Olivier-Bandini A, Bellalou J, Moyse E, Bouillaud F, Nicol X, et al. Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis. Cell. 161: 817-32. PMID 25957687 DOI: 10.1016/J.Cell.2015.03.023 |
0.416 |
|
| 2015 |
Elachouri G, Lee-Rivera I, Clérin E, Argentini M, Fridlich R, Blond F, Ferracane V, Yang Y, Raffelsberger W, Wan J, Bennett J, Sahel JA, Zack DJ, Léveillard T. Thioredoxin rod-derived cone viability factor protects against photooxidative retinal damage. Free Radical Biology & Medicine. 81: 22-9. PMID 25596499 DOI: 10.1016/J.Freeradbiomed.2015.01.003 |
0.459 |
|
| 2015 |
Byrne LC, Dalkara D, Luna G, Fisher SK, Clérin E, Sahel JA, Léveillard T, Flannery JG. Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration. The Journal of Clinical Investigation. 125: 105-16. PMID 25415434 DOI: 10.1172/Jci65654 |
0.499 |
|
| 2014 |
Clérin E, Yang Y, Forster V, Fontaine V, Sahel JA, Léveillard T. Vibratome sectioning mouse retina to prepare photoreceptor cultures. Journal of Visualized Experiments : Jove. PMID 25548881 DOI: 10.3791/51954 |
0.43 |
|
| 2014 |
Ratnapriya R, Zhan X, Fariss RN, Branham KE, Zipprer D, Chakarova CF, Sergeev YV, Campos MM, Othman M, Friedman JS, Maminishkis A, Waseem NH, Brooks M, Rajasimha HK, Edwards AO, et al. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human Molecular Genetics. 23: 5827-37. PMID 24899048 DOI: 10.1093/Hmg/Ddu276 |
0.413 |
|
| 2014 |
Léveillard T, Fridlich R, Clérin E, Aït-Ali N, Millet-Puel G, Jaillard C, Yang Y, Zack D, Van-Dorsselaer A, Sahel JA. Therapeutic strategy for handling inherited retinal degenerations in a gene-independent manner using rod-derived cone viability factors Comptes Rendus - Biologies. 337: 207-213. PMID 24702847 DOI: 10.1016/J.Crvi.2013.12.002 |
0.545 |
|
| 2014 |
Léveillard T. Spare the rod, spoil the degeneration. Journal of Pediatric Ophthalmology and Strabismus. 51: 74. PMID 24661369 DOI: 10.3928/01913913-20140220-06 |
0.458 |
|
| 2013 |
Delyfer MN, Aït-Ali N, Camara H, Clérin E, Korobelnik JF, Sahel JA, Léveillard T. Transcriptomic analysis of human retinal surgical specimens using jouRNAI. Journal of Visualized Experiments : Jove. PMID 23979175 DOI: 10.3791/50375 |
0.459 |
|
| 2013 |
Sahel JA, Léveillard T, Picaud S, Dalkara D, Marazova K, Safran A, Paques M, Duebel J, Roska B, Mohand-Said S. Functional rescue of cone photoreceptors in retinitis pigmentosa. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv FüR Klinische Und Experimentelle Ophthalmologie. 251: 1669-77. PMID 23575948 DOI: 10.1007/S00417-013-2314-7 |
0.544 |
|
| 2013 |
Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578 |
0.346 |
|
| 2012 |
Jaillard C, Mouret A, Niepon ML, Clérin E, Yang Y, Lee-Rivera I, Aït-Ali N, Millet-Puel G, Cronin T, Sedmak T, Raffelsberger W, Kinzel B, Trembleau A, Poch O, Bennett J, et al. Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity. Human Molecular Genetics. 21: 2298-311. PMID 22343139 DOI: 10.1093/Hmg/Dds050 |
0.431 |
|
| 2012 |
Audo I, Bujakowska K, Orhan E, Poloschek CM, Defoort-Dhellemmes S, Drumare I, Kohl S, Luu TD, Lecompte O, Zrenner E, Lancelot ME, Antonio A, Germain A, Michiels C, Audier C, et al. Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics. 90: 321-30. PMID 22325361 DOI: 10.1016/J.Ajhg.2011.12.007 |
0.424 |
|
| 2012 |
Audo I, Bujakowska KM, Léveillard T, Mohand-Saïd S, Lancelot ME, Germain A, Antonio A, Michiels C, Saraiva JP, Letexier M, Sahel JA, Bhattacharya SS, Zeitz C. Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet Journal of Rare Diseases. 7: 8. PMID 22277662 DOI: 10.1186/1750-1172-7-8 |
0.408 |
|
| 2012 |
Sofat R, Casas JP, Webster AR, Bird AC, Mann SS, Yates JR, Moore AT, Sepp T, Cipriani V, Bunce C, Khan JC, Shahid H, Swaroop A, Abecasis G, Branham KE, ... ... Leveillard T, et al. Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology. 41: 250-62. PMID 22253316 DOI: 10.1093/Ije/Dyr204 |
0.319 |
|
| 2012 |
Bujakowska K, Audo I, Mohand-Saïd S, Lancelot ME, Antonio A, Germain A, Léveillard T, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Sahel JA, Bhattacharya SS, Zeitz C. CRB1 mutations in inherited retinal dystrophies. Human Mutation. 33: 306-15. PMID 22065545 DOI: 10.1002/Humu.21653 |
0.483 |
|
| 2011 |
Clérin E, Wicker N, Mohand-Saïd S, Poch O, Sahel JA, Léveillard T. ℮-conome: an automated tissue counting platform of cone photoreceptors for rodent models of retinitis pigmentosa. Bmc Ophthalmology. 11: 38. PMID 22185426 DOI: 10.1186/1471-2415-11-38 |
0.533 |
|
| 2011 |
Delyfer MN, Raffelsberger W, Mercier D, Korobelnik JF, Gaudric A, Charteris DG, Tadayoni R, Metge F, Caputo G, Barale PO, Ripp R, Muller JD, Poch O, Sahel JA, Léveillard T. Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death. Plos One. 6: e28791. PMID 22174898 DOI: 10.1371/Journal.Pone.0028791 |
0.448 |
|
| 2011 |
Fradot M, Busskamp V, Forster V, Cronin T, Léveillard T, Bennett J, Sahel JA, Roska B, Picaud S. Gene therapy in ophthalmology: validation on cultured retinal cells and explants from postmortem human eyes. Human Gene Therapy. 22: 587-93. PMID 21142470 DOI: 10.1089/Hum.2010.157 |
0.429 |
|
| 2010 |
Yang Y, Mohand-Said S, Léveillard T, Fontaine V, Simonutti M, Sahel JA. Transplantation of photoreceptor and total neural retina preserves cone function in P23H rhodopsin transgenic rat. Plos One. 5: e13469. PMID 20976047 DOI: 10.1371/Journal.Pone.0013469 |
0.459 |
|
| 2010 |
Léveillard T, Sahel JA. Rod-derived cone viability factor for treating blinding diseases: from clinic to redox signaling. Science Translational Medicine. 2: 26ps16. PMID 20375363 DOI: 10.1126/Scitranslmed.3000866 |
0.504 |
|
| 2010 |
Wunderlich KA, Leveillard T, Penkowa M, Zrenner E, Perez MT. Altered expression of metallothionein-I and -II and their receptor megalin in inherited photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 51: 4809-20. PMID 20357188 DOI: 10.1167/Iovs.09-5073 |
0.362 |
|
| 2010 |
Cronin T, Raffelsberger W, Lee-Rivera I, Jaillard C, Niepon ML, Kinzel B, Clérin E, Petrosian A, Picaud S, Poch O, Sahel JA, Léveillard T. The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress. Cell Death and Differentiation. 17: 1199-210. PMID 20139892 DOI: 10.1038/Cdd.2010.2 |
0.506 |
|
| 2009 |
Audo I, Kohl S, Leroy BP, Munier FL, Guillonneau X, Mohand-Saïd S, Bujakowska K, Nandrot EF, Lorenz B, Preising M, Kellner U, Renner AB, Bernd A, Antonio A, Moskova-Doumanova V, et al. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics. 85: 720-9. PMID 19896113 DOI: 10.1016/J.Ajhg.2009.10.013 |
0.431 |
|
| 2009 |
Bujakowska K, Maubaret C, Chakarova CF, Tanimoto N, Beck SC, Fahl E, Humphries MM, Kenna PF, Makarov E, Makarova O, Paquet-Durand F, Ekström PA, van Veen T, Leveillard T, Humphries P, et al. Study of gene-targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP). Investigative Ophthalmology & Visual Science. 50: 5927-33. PMID 19578015 DOI: 10.1167/Iovs.08-3275 |
0.52 |
|
| 2009 |
Fridlich R, Delalande F, Jaillard C, Lu J, Poidevin L, Cronin T, Perrocheau L, Millet-Puel G, Niepon ML, Poch O, Holmgren A, Van Dorsselaer A, Sahel JA, Léveillard T. The thioredoxin-like protein rod-derived cone viability factor (RdCVFL) interacts with TAU and inhibits its phosphorylation in the retina. Molecular & Cellular Proteomics : McP. 8: 1206-18. PMID 19279044 DOI: 10.1074/Mcp.M800406-Mcp200 |
0.427 |
|
| 2009 |
Yang Y, Mohand-Said S, Danan A, Simonutti M, Fontaine V, Clerin E, Picaud S, Léveillard T, Sahel JA. Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa. Molecular Therapy : the Journal of the American Society of Gene Therapy. 17: 787-95. PMID 19277021 DOI: 10.1038/Mt.2009.28 |
0.53 |
|
| 2008 |
Kalathur RK, Gagniere N, Berthommier G, Poidevin L, Raffelsberger W, Ripp R, Léveillard T, Poch O. RETINOBASE: a web database, data mining and analysis platform for gene expression data on retina. Bmc Genomics. 9: 208. PMID 18457592 DOI: 10.1186/1471-2164-9-208 |
0.517 |
|
| 2007 |
Chalmel F, Léveillard T, Jaillard C, Lardenois A, Berdugo N, Morel E, Koehl P, Lambrou G, Holmgren A, Sahel JA, Poch O. Rod-derived Cone Viability Factor-2 is a novel bifunctional-thioredoxin-like protein with therapeutic potential. Bmc Molecular Biology. 8: 74. PMID 17764561 DOI: 10.1186/1471-2199-8-74 |
0.519 |
|
| 2007 |
Cronin T, Léveillard T, Sahel JA. Retinal degenerations: from cell signaling to cell therapy; pre-clinical and clinical issues. Current Gene Therapy. 7: 121-9. PMID 17430131 DOI: 10.2174/156652307780363143 |
0.491 |
|
| 2007 |
Léveillard T, Mohand-Saïd S, Sahel JA. [Retinal repair by transplantation of photoreceptor precursors]. Medecine Sciences : M/S. 23: 240-2. PMID 17349277 DOI: 10.1051/Medsci/2007233240 |
0.424 |
|
| 2007 |
Audo I, Leveillard T, Sahel J. Phenotype-Genotype correlations : more than identifying risks ? Acta Ophthalmologica Scandinavica. 85: 0-0. DOI: 10.1111/J.1600-0420.2007.01063_2990.X |
0.343 |
|
| 2006 |
Lorentz O, Sahel J, Mohand-Saïd S, Leveillard T. Cone survival: identification of RdCVF. Advances in Experimental Medicine and Biology. 572: 315-9. PMID 17249590 DOI: 10.1007/0-387-32442-9_44 |
0.518 |
|
| 2006 |
Hanein S, Perrault I, Gerber S, Dollfus H, Dufier JL, Feingold J, Munnich A, Bhattacharya S, Kaplan J, Sahel JA, Rozet JM, Leveillard T. Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA. Advances in Experimental Medicine and Biology. 572: 9-14. PMID 17249548 DOI: 10.1007/0-387-32442-9_2 |
0.466 |
|
| 2005 |
Delyfer MN, Forster V, Neveux N, Picaud S, Léveillard T, Sahel JA. Evidence for glutamate-mediated excitotoxic mechanisms during photoreceptor degeneration in the rd1 mouse retina. Molecular Vision. 11: 688-96. PMID 16163266 |
0.352 |
|
| 2005 |
Sahel JA, Mohand-Said S, Léveillard T. [Neuroprotection of photoreceptor cells in rod-cone dystrophies: from cell therapy to cell signalling]. Comptes Rendus Biologies. 328: 163-8. PMID 15771002 DOI: 10.1016/J.Crvi.2004.12.007 |
0.483 |
|
| 2004 |
Hackam AS, Strom R, Liu D, Qian J, Wang C, Otteson D, Gunatilaka T, Farkas RH, Chowers I, Kageyama M, Leveillard T, Sahel JA, Campochiaro PA, Parmigiani G, Zack DJ. Identification of gene expression changes associated with the progression of retinal degeneration in the rd1 mouse. Investigative Ophthalmology & Visual Science. 45: 2929-42. PMID 15326104 DOI: 10.1167/Iovs.03-1184 |
0.52 |
|
| 2004 |
Huart LMd, Lorentz O, Goureau O, Léveillard T, Sahel JA. DNA repair in the degenerating mouse retina. Molecular and Cellular Neuroscience. 26: 441-449. PMID 15234348 DOI: 10.1016/J.Mcn.2004.04.002 |
0.444 |
|
| 2004 |
Léveillard T, Mohand-Saïd S, Lorentz O, Hicks D, Fintz AC, Clérin E, Simonutti M, Forster V, Cavusoglu N, Chalmel F, Dollé P, Poch O, Lambrou G, Sahel JA. Identification and characterization of rod-derived cone viability factor. Nature Genetics. 36: 755-9. PMID 15220920 DOI: 10.1038/Ng1386 |
0.557 |
|
| 2004 |
Delyfer MN, Léveillard T, Mohand-Saïd S, Hicks D, Picaud S, Sahel JA. Inherited retinal degenerations: therapeutic prospects. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. 96: 261-9. PMID 15145530 DOI: 10.1016/J.Biolcel.2004.01.006 |
0.539 |
|
| 2004 |
Léveillard T, Mohand-Saïd S, Fintz AC, Lambrou G, Sahel JA. The search for rod-dependent cone viability factors, secreted factors promoting cone viability. Novartis Foundation Symposium. 255: 117-27; discussion 1. PMID 14750600 |
0.468 |
|
| 2004 |
Léveillard T, Mohand‐Saïd S, Fintz AC, Lambrou G, Sahel J. The search for rod-dependent cone viability factors, secreted factors promoting cone viability. Novartis Foundation Symposium. 255: 117-130. DOI: 10.1002/0470092645.Ch9 |
0.544 |
|
| 2003 |
Cavusoglu N, Thierse D, Mohand-Saïd S, Chalmel F, Poch O, Van-Dorsselaer A, Sahel JA, Léveillard T. Differential proteomic analysis of the mouse retina: the induction of crystallin proteins by retinal degeneration in the rd1 mouse. Molecular & Cellular Proteomics : McP. 2: 494-505. PMID 12832458 DOI: 10.1074/Mcp.M300029-Mcp200 |
0.412 |
|
| 2003 |
Fintz AC, Audo I, Hicks D, Mohand-Said S, Léveillard T, Sahel J. Partial characterization of retina-derived cone neuroprotection in two culture models of photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 44: 818-25. PMID 12556418 |
0.369 |
|
| 2001 |
Mohand-Said S, Hicks D, Léveillard T, Picaud S, Porto F, Sahel JA. Rod–Cone Interactions:: Developmental and Clinical Significance Progress in Retinal and Eye Research. 20: 451-467. PMID 11390256 DOI: 10.1016/S1350-9462(01)00006-4 |
0.502 |
|
| 1999 |
Fuhrmann V, Kinkl N, Leveillard T, Sahel J, Hicks D. Fibroblast growth factor receptor 4 (FGFR4) is expressed in adult rat and human retinal photoreceptors and neurons. Journal of Molecular Neuroscience. 13: 187-197. PMID 10691305 DOI: 10.1385/Jmn:13:1-2:187 |
0.399 |
|
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