Jean Bennett, MD PhD - Publications

Affiliations: 
Ophthalmology University of Pennsylvania, Philadelphia, PA, United States 
Area:
Ocular Gene Therapy
Website:
http://www.med.upenn.edu/apps/faculty/index.php/g327/p11214

140 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Yang U, Gentleman S, Gai X, Gorin MB, Borchert MS, Lee TC, Villanueva A, Koenekoop R, Maguire AM, Bennett J, Redmond TM, Nagiel A. Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy. Jama Ophthalmology. 1-9. PMID 31580392 DOI: 10.1001/jamaophthalmol.2019.3914  0.4
2019 Maguire AM, Russell S, Wellman JA, Chung DC, Yu ZF, Tillman A, Wittes J, Pappas J, Elci O, Marshall KA, McCague S, Reichert H, Davis M, Simonelli F, Leroy BP, ... ... Bennett J, et al. Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials. Ophthalmology. 126: 1273-1285. PMID 31443789 DOI: 10.1016/j.ophtha.2019.06.017  0.48
2019 Tuten WS, Vergilio GK, Young GJ, Bennett J, Maguire AM, Aleman TS, Brainard DH, Morgan JIW. Visual Function at the Atrophic Border in Choroideremia Assessed with Adaptive Optics Microperimetry. Ophthalmology. Retina. PMID 31235310 DOI: 10.1016/j.oret.2019.05.002  0.4
2018 Aleman TS, Uyhazi KE, Serrano LW, Vasireddy V, Bowman SJ, Ammar MJ, Pearson DJ, Maguire AM, Bennett J. RDH12 Mutations Cause a Severe Retinal Degeneration With Relatively Spared Rod Function. Investigative Ophthalmology & Visual Science. 59: 5225-5236. PMID 30372751 DOI: 10.1167/iovs.18-24708  0.4
2018 Bryant L, Lozynska O, Marsh A, Papp TE, van Gorder L, Serrano LW, Gai X, Maguire AM, Aleman TS, Bennett J. Identification of a novel pathogenic missense mutation in using whole exome sequencing: a case report. The British Journal of Ophthalmology. PMID 30030392 DOI: 10.1136/bjophthalmol-2017-311405  0.4
2018 Silson EH, Aleman TS, Willett A, Serrano LW, Pearson DJ, Rauschecker AM, Maguire AM, Baker CI, Bennett J, Ashtari M. Comparing Clinical Perimetry and Population Receptive Field Measures in Patients with Choroideremia. Investigative Ophthalmology & Visual Science. 59: 3249-3258. PMID 29971442 DOI: 10.1167/iovs.18-23929  0.4
2018 Song JY, Aravand P, Nikonov S, Leo L, Lyubarsky A, Bennicelli JL, Pan J, Wei Z, Shpylchak I, Herrera P, Bennett DJ, Commins N, Maguire AM, Pham J, den Hollander AI, ... ... Bennett J, et al. Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 29673930 DOI: 10.1016/j.ymthe.2018.03.015  0.4
2018 Bryant L, Lozynska O, Maguire AM, Aleman TS, Bennett J. Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration. Clinical Ophthalmology (Auckland, N.Z.). 12: 49-63. PMID 29343940 DOI: 10.2147/OPTH.S147684  0.4
2017 Carvalho LS, Turunen HT, Wassmer SJ, Luna-Velez MV, Xiao R, Bennett J, Vandenberghe LH. Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting. Frontiers in Neuroscience. 11: 503. PMID 28943836 DOI: 10.3389/fnins.2017.00503  0.72
2017 Bryant L, Lozynska O, Han G, Morgan JIW, Gai X, Maguire AM, Aleman T, Bennett J. On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness. Ophthalmic Genetics. 1-3. PMID 28805479 DOI: 10.1080/13816810.2017.1354384  0.4
2017 Russell S, Bennett J, Wellman JA, Chung DC, Yu ZF, Tillman A, Wittes J, Pappas J, Elci O, McCague S, Cross D, Marshall KA, Walshire J, Kehoe TL, Reichert H, et al. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial. Lancet (London, England). PMID 28712537 DOI: 10.1016/S0140-6736(17)31868-8  0.48
2017 Chung DC, McCague S, Yu ZF, Thill S, DiStefano-Pappas J, Bennett J, Cross D, Marshall K, Wellman J, High KA. Novel mobility test to assess functional vision in patients with inherited retinal dystrophies. Clinical & Experimental Ophthalmology. PMID 28697537 DOI: 10.1111/ceo.13022  0.48
2017 Ashtari M, Nikonova ES, Marshall KA, Young GJ, Aravand P, Pan W, Ying GS, Willett AE, Mahmoudian M, Maguire AM, Bennett J. The Role of the Human Visual Cortex in Assessment of the Long-Term Durability of Retinal Gene Therapy in Follow-on RPE65 Clinical Trial Patients. Ophthalmology. PMID 28237426 DOI: 10.1016/j.ophtha.2017.01.029  0.4
2016 Aleman TS, Han G, Serrano LW, Fuerst NM, Charlson ES, Pearson DJ, Chung DC, Traband A, Pan W, Ying GS, Bennett J, Maguire AM, Morgan JI. Natural History of the Central Structural Abnormalities in Choroideremia: A Prospective Cross-Sectional Study. Ophthalmology. PMID 27986385 DOI: 10.1016/j.ophtha.2016.10.022  0.48
2016 Ramachandran P, Lee V, Wei Z, Song JY, Casal G, Cronin T, Willett K, Huckfeldt R, Morgan JI, Aleman TS, Maguire AM, Bennett J. Evaluation of dose and safety of AAV7m8 and AAV8BP2 in the non-human primate retina. Human Gene Therapy. PMID 27750461 DOI: 10.1089/hum.2016.111  0.4
2016 Bennett J, Wellman J, Marshall KA, McCague S, Ashtari M, DiStefano-Pappas J, Elci OU, Chung DC, Sun J, Wright JF, Cross DR, Aravand P, Cyckowski LL, Bennicelli JL, Mingozzi F, et al. Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial. Lancet (London, England). PMID 27375040 DOI: 10.1016/S0140-6736(16)30371-3  0.56
2016 Garanto A, Chung DC, Duijkers L, Corral-Serrano JC, Messchaert M, Xiao R, Bennett J, Vandenberghe LH, Collin RW. In vitro and in vivo rescue of aberrant splicing in CEP290-associated LCA by antisense oligonucleotide delivery. Human Molecular Genetics. PMID 27106101 DOI: 10.1093/hmg/ddw118  0.72
2016 Shah N, Damani MR, Zhu XS, Bedoukian EC, Bennett J, Maguire AM, Leroy BP. Isolated maculopathy associated with biallelic CRB1 mutations. Ophthalmic Genetics. 1-4. PMID 27096895 DOI: 10.3109/13816810.2016.1155225  0.56
2016 Testa F, Maguire AM, Rossi S, Marshall K, Auricchio A, Melillo P, Bennett J, Simonelli F. Evaluation of Ocular Gene Therapy in an Italian Patient Affected by Congenital Leber Amaurosis Type 2 Treated in Both Eyes. Advances in Experimental Medicine and Biology. 854: 533-9. PMID 26427456 DOI: 10.1007/978-3-319-17121-0_71  0.56
2015 Sochor MA, Vasireddy V, Drivas TG, Wojno A, Doung T, Shpylchak I, Bennicelli J, Chung D, Bennett J, Lewis M. An Autogenously Regulated Expression System for Gene Therapeutic Ocular Applications. Scientific Reports. 5: 17105. PMID 26597678 DOI: 10.1038/srep17105  0.56
2015 Ablikim M, Achasov MN, Ai XC, Albayrak O, Albrecht M, Ambrose DJ, Amoroso A, An FF, An Q, Bai JZ, Ferroli RB, Ban Y, Bennett DW, Bennett JV, Bertani M, et al. Observation and Spin-Parity Determination of the X(1835) in J/ψ→γK_{S}^{0}K_{S}^{0}η. Physical Review Letters. 115: 091803. PMID 26371642 DOI: 10.1103/PhysRevLett.115.091803  0.4
2015 Ashtari M, Zhang H, Cook PA, Cyckowski LL, Shindler KS, Marshall KA, Aravand P, Vossough A, Gee JC, Maguire AM, Baker CI, Bennett J. Plasticity of the human visual system after retinal gene therapy in patients with Leber's congenital amaurosis. Science Translational Medicine. 7: 296ra110. PMID 26180100 DOI: 10.1126/scitranslmed.aaa8791  0.4
2015 Vasireddy V, Mills JA, Gaddameedi R, Basner-Tschakarjan E, Kohnke M, Black AD, Alexandrov K, Zhou S, Maguire AM, Chung DC, Mac H, Sullivan L, Gadue P, Bennicelli JL, French DL, ... Bennett J, et al. Correction: AAV-Mediated Gene Therapy for Choroideremia: Preclinical Studies in Personalized Models. Plos One. 10: e0129982. PMID 26090960 DOI: 10.1371/journal.pone.0129982  0.48
2015 Drivas TG, Wojno AP, Tucker BA, Stone EM, Bennett J. Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis. Science Translational Medicine. 7: 291ra97. PMID 26062849 DOI: 10.1126/scitranslmed.aaa5370  0.56
2015 Ramachandran PS, Song JY, Bennett J. Exploiting metabolic and antioxidant pathways to maintain vision in blinding disease. The Journal of Clinical Investigation. 125: 1390-2. PMID 25798615 DOI: 10.1172/JCI80821  0.56
2015 Pierce EA, Bennett J. The Status of RPE65 Gene Therapy Trials: Safety and Efficacy. Cold Spring Harbor Perspectives in Medicine. PMID 25635059 DOI: 10.1101/cshperspect.a017285  0.56
2015 Ashtari M, Zhang H, Cook PA, Cyckowski LL, Shindler KS, Marshall KA, Aravand P, Vossough A, Gee JC, Maguire AM, Baker CI, Bennett J. Plasticity of the human visual system after retinal gene therapy in patients with Leber's congenital amaurosis Science Translational Medicine. 7. DOI: 10.1126/scitranslmed.aaa8791  0.56
2014 Morgan JI, Han G, Klinman E, Maguire WM, Chung DC, Maguire AM, Bennett J. High-resolution adaptive optics retinal imaging of cellular structure in choroideremia. Investigative Ophthalmology & Visual Science. 55: 6381-97. PMID 25190651 DOI: 10.1167/iovs.13-13454  0.56
2014 Bennett J. My career path for developing gene therapy for blinding diseases: the importance of mentors, collaborators, and opportunities. Human Gene Therapy. 25: 663-70. PMID 25136912 DOI: 10.1089/hum.2014.2529  0.56
2014 Cronin T, Vandenberghe LH, Hantz P, Juttner J, Reimann A, Kacsó AE, Huckfeldt RM, Busskamp V, Kohler H, Lagali PS, Roska B, Bennett J. Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno-associated virus capsid and promoter. Embo Molecular Medicine. 6: 1175-90. PMID 25092770 DOI: 10.15252/emmm.201404077  0.56
2014 Black A, Vasireddy V, Chung DC, Maguire AM, Gaddameedi R, Tolmachova T, Seabra M, Bennett J. Adeno-associated virus 8-mediated gene therapy for choroideremia: preclinical studies in in vitro and in vivo models. The Journal of Gene Medicine. 16: 122-30. PMID 24962736 DOI: 10.1002/jgm.2768  0.56
2014 Drivas TG, Bennett J. CEP290 and the primary cilium. Advances in Experimental Medicine and Biology. 801: 519-25. PMID 24664739 DOI: 10.1007/978-1-4614-3209-8_66  0.56
2014 Hiebler S, Masuda T, Hacia JG, Moser AB, Faust PL, Liu A, Chowdhury N, Huang N, Lauer A, Bennett J, Watkins PA, Zack DJ, Braverman NE, Raymond GV, Steinberg SJ. The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder. Molecular Genetics and Metabolism. 111: 522-32. PMID 24503136 DOI: 10.1016/j.ymgme.2014.01.008  0.56
2014 Huckfeldt RM, Bennett J. Promising first steps in gene therapy for choroideremia. Human Gene Therapy. 25: 96-7. PMID 24502407 DOI: 10.1089/hum.2014.2503  0.56
2014 Ashtari M, Cyckowski L, Yazdi A, Viands A, Marshall K, Bókkon I, Maguire A, Bennett J. fMRI of retina-originated phosphenes experienced by patients with Leber congenital amaurosis. Plos One. 9: e86068. PMID 24465873 DOI: 10.1371/journal.pone.0086068  0.56
2014 Canver MC, Canver AC, Revere KE, Amado D, Bennett J, Chung DC. Novel mathematical algorithm for pupillometric data analysis. Computer Methods and Programs in Biomedicine. 113: 221-5. PMID 24129048 DOI: 10.1016/j.cmpb.2013.08.008  0.56
2014 Mackay DS, Borman AD, Sui R, van den Born LI, Berson EL, Ocaka LA, Davidson AE, Heckenlively JR, Branham K, Ren H, Lopez I, Maria M, Azam M, Henkes A, Blokland E, ... ... Bennett J, et al. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations. [34, 11, 1537-1546, 10.1002/humu.22398] Human Mutation. 35: 150-150. DOI: 10.1002/humu.22467  0.56
2013 Drivas TG, Holzbaur EL, Bennett J. Disruption of CEP290 microtubule/membrane-binding domains causes retinal degeneration. The Journal of Clinical Investigation. 123: 4525-39. PMID 24051377 DOI: 10.1172/JCI69448  0.56
2013 Willett K, Bennett J. Immunology of AAV-Mediated Gene Transfer in the Eye. Frontiers in Immunology. 4: 261. PMID 24009613 DOI: 10.3389/fimmu.2013.00261  0.56
2013 Bennicelli JL, Bennett J. Stem cells set their sights on retinitis pigmentosa. Elife. 2: e01291. PMID 23991287 DOI: 10.7554/eLife.01291  0.56
2013 Mackay DS, Borman AD, Sui R, van den Born LI, Berson EL, Ocaka LA, Davidson AE, Heckenlively JR, Branham K, Ren H, Lopez I, Maria M, Azam M, Henkes A, Blokland E, ... ... Bennett J, et al. Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations. Human Mutation. 34: 1537-46. PMID 23946133 DOI: 10.1002/humu.22398  0.56
2013 Vasireddy V, Mills JA, Gaddameedi R, Basner-Tschakarjan E, Kohnke M, Black AD, Alexandrov K, Zhou S, Maguire AM, Chung DC, Mac H, Sullivan L, Gadue P, Bennicelli JL, French DL, ... Bennett J, et al. AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models. Plos One. 8: e61396. PMID 23667438 DOI: 10.1371/journal.pone.0061396  0.56
2013 Simonato M, Bennett J, Boulis NM, Castro MG, Fink DJ, Goins WF, Gray SJ, Lowenstein PR, Vandenberghe LH, Wilson TJ, Wolfe JH, Glorioso JC. Progress in gene therapy for neurological disorders. Nature Reviews. Neurology. 9: 277-91. PMID 23609618 DOI: 10.1038/nrneurol.2013.56  0.56
2013 Testa F, Maguire AM, Rossi S, Pierce EA, Melillo P, Marshall K, Banfi S, Surace EM, Sun J, Acerra C, Wright JF, Wellman J, High KA, Auricchio A, Bennett J, et al. Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2. Ophthalmology. 120: 1283-91. PMID 23474247 DOI: 10.1016/j.ophtha.2012.11.048  0.56
2013 Wojno AP, Pierce EA, Bennett J. Seeing the light. Science Translational Medicine. 5: 175fs8. PMID 23467559 DOI: 10.1126/scitranslmed.3005798  0.56
2013 Vandenberghe LH, Bell P, Maguire AM, Xiao R, Hopkins TB, Grant R, Bennett J, Wilson JM. AAV9 targets cone photoreceptors in the nonhuman primate retina. Plos One. 8: e53463. PMID 23382846 DOI: 10.1371/journal.pone.0053463  0.56
2012 Cronin T, Chung DC, Yang Y, Nandrot EF, Bennett J. The Signalling Role of the avβ5-Integrin Can Impact the Efficacy of AAV in Retinal Gene Therapy. Pharmaceuticals (Basel, Switzerland). 5: 447-59. PMID 24281556 DOI: 10.3390/ph5050447  0.56
2012 Collin RW, den Hollander AI, van der Velde-Visser SD, Bennicelli J, Bennett J, Cremers FP. Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290. Molecular Therapy. Nucleic Acids. 1: e14. PMID 23343883 DOI: 10.1038/mtna.2012.3  0.56
2012 Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, ... Bennett J, et al. Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 8232-7. PMID 23150612 DOI: 10.1167/iovs.12-11025  0.56
2012 Drivas TG, Bennett J. The bionic retina: a small molecule with big potential for visual restoration. Neuron. 75: 185-7. PMID 22841303 DOI: 10.1016/j.neuron.2012.06.010  0.56
2012 Melillo P, Pecchia L, Testa F, Rossi S, Bennett J, Simonelli F. Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients Biomedical Engineering Online. 11. PMID 22812667 DOI: 10.1186/1475-925X-11-40  0.56
2012 Bennett J, Chung DC, Maguire A. Gene delivery to the retina: from mouse to man. Methods in Enzymology. 507: 255-74. PMID 22365778 DOI: 10.1016/B978-0-12-386509-0.00013-2  0.56
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  0.56
2012 Bennett J, Ashtari M, Wellman J, Marshall KA, Cyckowski LL, Chung DC, McCague S, Pierce EA, Chen Y, Bennicelli JL, Zhu X, Ying GS, Sun J, Wright JF, Auricchio A, et al. AAV2 gene therapy readministration in three adults with congenital blindness. Science Translational Medicine. 4: 120ra15. PMID 22323828 DOI: 10.1126/scitranslmed.3002865  0.56
2012 Cronin T, Lyubarsky A, Bennett J. Dark-rearing the rd10 mouse: implications for therapy. Advances in Experimental Medicine and Biology. 723: 129-36. PMID 22183325 DOI: 10.1007/978-1-4614-0631-0_18  0.56
2012 Bennett J, Maguire AM. Gene Therapy for Retinal Disease Retina Fifth Edition. 1: 652-668. DOI: 10.1016/B978-1-4557-0737-9.00034-5  0.56
2011 Chung DC, Fogelgren B, Park KM, Heidenberg J, Zuo X, Huang L, Bennett J, Lipschutz JH. Adeno-Associated Virus-Mediated Gene Transfer to Renal Tubule Cells via a Retrograde Ureteral Approach. Nephron Extra. 1: 217-23. PMID 22470395 DOI: 10.1159/000333071  0.48
2011 Stieger K, Cronin T, Bennett J, Rolling F. Adeno-associated virus mediated gene therapy for retinal degenerative diseases. Methods in Molecular Biology (Clifton, N.J.). 807: 179-218. PMID 22034031 DOI: 10.1007/978-1-61779-370-7_8  0.56
2011 Cronin T, Bennett J. Switching on the lights: the use of optogenetics to advance retinal gene therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 1190-2. PMID 21720380 DOI: 10.1038/mt.2011.115  0.56
2011 Vandenberghe LH, Bell P, Maguire AM, Cearley CN, Xiao R, Calcedo R, Wang L, Castle MJ, Maguire AC, Grant R, Wolfe JH, Wilson JM, Bennett J. Dosage thresholds for AAV2 and AAV8 photoreceptor gene therapy in monkey. Science Translational Medicine. 3: 88ra54. PMID 21697530 DOI: 10.1126/scitranslmed.3002103  0.56
2011 Ashtari M, Cyckowski LL, Monroe JF, Marshall KA, Chung DC, Auricchio A, Simonelli F, Leroy BP, Maguire AM, Shindler KS, Bennett J. The human visual cortex responds to gene therapy-mediated recovery of retinal function. The Journal of Clinical Investigation. 121: 2160-8. PMID 21606598 DOI: 10.1172/JCI57377  0.56
2011 Boldt K, Mans DA, Won J, van Reeuwijk J, Vogt A, Kinkl N, Letteboer SJ, Hicks WL, Hurd RE, Naggert JK, Texier Y, den Hollander AI, Koenekoop RK, Bennett J, Cremers FP, et al. Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. The Journal of Clinical Investigation. 121: 2169-80. PMID 21606596 DOI: 10.1172/JCI45627  0.56
2011 Millington-Ward S, Chadderton N, O'Reilly M, Palfi A, Goldmann T, Kilty C, Humphries M, Wolfrum U, Bennett J, Humphries P, Kenna PF, Farrar GJ. Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosa. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 642-9. PMID 21224835 DOI: 10.1038/mt.2010.293  0.56
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  0.56
2011 Ashtari M, Cyckowski LL, Monroe JF, Marshall KA, Chung DC, Auricchio A, Simonelli F, Leroy BP, Maguire AM, Shindler KS, Bennett J. The human visual cortex responds to gene therapy-mediated recovery of retinal function (The Journal of Clinical Investigation (2011) 121, 6, (2160-2168) DOI: 10.1172/JCI57377) Journal of Clinical Investigation. 121: 2945. DOI: 10.1172/JCI59208  0.56
2011 Bennett J, Maguire AM. The evolution of retinal gene therapy: From DNA to FDA Retina Today. 55-58.  0.56
2011 Den Hollander AI, Black A, Bennett J, Cremers FPM. Lighting a candle in the dark: Advances in genetics and gene therapy of recessive retinal dystrophies (Journal of Clinical Investigation (2010) 120, 9 (3042-3053) DOI: 10.1172/JCI42258) Journal of Clinical Investigation. 121: 456.  0.56
2010 den Hollander AI, Black A, Bennett J, Cremers FP. Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. The Journal of Clinical Investigation. 120: 3042-53. PMID 20811160 DOI: 10.1172/JCI42258  0.56
2010 Amado D, Mingozzi F, Hui D, Bennicelli JL, Wei Z, Chen Y, Bote E, Grant RL, Golden JA, Narfstrom K, Syed NA, Orlin SE, High KA, Maguire AM, Bennett J. Safety and efficacy of subretinal readministration of a viral vector in large animals to treat congenital blindness. Science Translational Medicine. 2: 21ra16. PMID 20374996 DOI: 10.1126/scitranslmed.3000659  0.56
2010 Simonelli F, Maguire AM, Testa F, Pierce EA, Mingozzi F, Bennicelli JL, Rossi S, Marshall K, Banfi S, Surace EM, Sun J, Redmond TM, Zhu X, Shindler KS, Ying GS, ... ... Bennett J, et al. Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration. Molecular Therapy : the Journal of the American Society of Gene Therapy. 18: 643-50. PMID 19953081 DOI: 10.1038/mt.2009.277  0.56
2010 Canver MC, Canver AC, Revere KE, Amado D, Bennett J, Chung DC. Algorithm for pupillometric data analysis Proceedings of the 2010 Ieee 36th Annual Northeast Bioengineering Conference, Nebec 2010. DOI: 10.1109/NEBC.2010.5458283  0.56
2009 Bennett J. Gene therapy for color blindness. The New England Journal of Medicine. 361: 2483-4. PMID 20018970 DOI: 10.1056/NEJMcibr0908643  0.56
2009 Maguire AM, High KA, Auricchio A, Wright JF, Pierce EA, Testa F, Mingozzi F, Bennicelli JL, Ying GS, Rossi S, Fulton A, Marshall KA, Banfi S, Chung DC, Morgan JI, ... ... Bennett J, et al. Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial. Lancet. 374: 1597-605. PMID 19854499 DOI: 10.1016/S0140-6736(09)61836-5  0.56
2009 Jacobs JB, Dell'Osso LF, Wang ZI, Acland GM, Bennett J. Using the NAFX to measure the effectiveness over time of gene therapy in canine LCA. Investigative Ophthalmology & Visual Science. 50: 4685-92. PMID 19458334 DOI: 10.1167/iovs.09-3387  0.56
2009 Zhang Y, Singh MK, Degenhardt KR, Lu MM, Bennett J, Yoshida Y, Epstein JA. Tie2Cre-mediated inactivation of plexinD1 results in congenital heart, vascular and skeletal defects. Developmental Biology. 325: 82-93. PMID 18992737 DOI: 10.1016/j.ydbio.2008.09.031  0.56
2008 Falk T, Xie JY, Zhang S, Kennedy J, Bennett J, Yool AJ, Sherman SJ. Over-expression of the potassium channel Kir2.3 using the dopamine-1 receptor promoter selectively inhibits striatal neurons. Neuroscience. 155: 114-27. PMID 18571331 DOI: 10.1016/j.neuroscience.2008.04.075  0.56
2008 Maguire AM, Simonelli F, Pierce EA, Pugh EN, Mingozzi F, Bennicelli J, Banfi S, Marshall KA, Testa F, Surace EM, Rossi S, Lyubarsky A, Arruda VR, Konkle B, Stone E, ... ... Bennett J, et al. Safety and efficacy of gene transfer for Leber's congenital amaurosis. The New England Journal of Medicine. 358: 2240-8. PMID 18441370 DOI: 10.1056/NEJMoa0802315  0.56
2008 Allocca M, Doria M, Petrillo M, Colella P, Garcia-Hoyos M, Gibbs D, Kim SR, Maguire A, Rex TS, Di Vicino U, Cutillo L, Sparrow JR, Williams DS, Bennett J, Auricchio A. Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice. The Journal of Clinical Investigation. 118: 1955-64. PMID 18414684 DOI: 10.1172/JCI34316  0.56
2008 Lebherz C, Maguire A, Tang W, Bennett J, Wilson JM. Novel AAV serotypes for improved ocular gene transfer. The Journal of Gene Medicine. 10: 375-82. PMID 18278824 DOI: 10.1002/jgm.1126  0.56
2008 Bennicelli J, Wright JF, Komaromy A, Jacobs JB, Hauck B, Zelenaia O, Mingozzi F, Hui D, Chung D, Rex TS, Wei Z, Qu G, Zhou S, Zeiss C, Arruda VR, ... ... Bennett J, et al. Reversal of blindness in animal models of leber congenital amaurosis using optimized AAV2-mediated gene transfer. Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 458-65. PMID 18209734 DOI: 10.1038/sj.mt.6300389  0.56
2008 Liu X, Rasmussen CA, Bennett J, Brandt CR, Gabelt BT, Kaufman PL. Progress and Prospects in Ocular Gene Therapy Ocular Therapeutics. 393-420. DOI: 10.1016/B978-012370585-3.50020-0  0.56
2007 Bennett J. Retinal progenitor cells--timing is everything. The New England Journal of Medicine. 356: 1577-9. PMID 17429090 DOI: 10.1056/NEJMcibr070209  0.56
2007 Zhang Z, Tang W, Zhou R, Shen X, Wei Z, Patel AM, Povlishock JT, Bennett J, Strauss JF. Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteins. Cell Motility and the Cytoskeleton. 64: 360-76. PMID 17323374 DOI: 10.1002/cm.20189  0.56
2007 Endo M, Zoltick PW, Chung DC, Bennett J, Radu A, Muvarak N, Flake AW. Gene transfer to ocular stem cells by early gestational intraamniotic injection of lentiviral vector. Molecular Therapy : the Journal of the American Society of Gene Therapy. 15: 579-87. PMID 17245352 DOI: 10.1038/sj.mt.6300092  0.56
2006 Shindler KS, Guan Y, Ventura E, Bennett J, Rostami A. Retinal ganglion cell loss induced by acute optic neuritis in a relapsing model of multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 12: 526-32. PMID 17086896 DOI: 10.1177/1352458506070629  0.56
2006 Wilson DF, Vinogradov SA, Grosul P, Sund N, Vacarezza MN, Bennett J. Imaging oxygen pressure in the rodent retina by phosphorescence lifetime. Advances in Experimental Medicine and Biology. 578: 119-24. PMID 16927680 DOI: 10.1007/0-387-29540-2_19  0.56
2006 Jacobs JB, Dell'Osso LF, Hertle RW, Acland GM, Bennett J. Eye movement recordings as an effectiveness indicator of gene therapy in RPE65-deficient canines: implications for the ocular motor system. Investigative Ophthalmology & Visual Science. 47: 2865-75. PMID 16799026 DOI: 10.1167/iovs.05-1233  0.56
2006 Bedrosian JC, Gratton MA, Brigande JV, Tang W, Landau J, Bennett J. In vivo delivery of recombinant viruses to the fetal murine cochlea: transduction characteristics and long-term effects on auditory function. Molecular Therapy : the Journal of the American Society of Gene Therapy. 14: 328-35. PMID 16765094 DOI: 10.1016/j.ymthe.2006.04.003  0.56
2006 Jacobson SG, Acland GM, Aguirre GD, Aleman TS, Schwartz SB, Cideciyan AV, Zeiss CJ, Komaromy AM, Kaushal S, Roman AJ, Windsor EA, Sumaroka A, Pearce-Kelling SE, Conlon TJ, Chiodo VA, ... ... Bennett J, et al. Safety of recombinant adeno-associated virus type 2-RPE65 vector delivered by ocular subretinal injection. Molecular Therapy : the Journal of the American Society of Gene Therapy. 13: 1074-84. PMID 16644289 DOI: 10.1016/j.ymthe.2006.03.005  0.56
2006 Bennett J. Commentary: an aye for eye gene therapy. Human Gene Therapy. 17: 177-9. PMID 16454651 DOI: 10.1089/hum.2006.17.177  0.56
2006 Zhang Z, Kostetskii I, Tang W, Haig-Ladewig L, Sapiro R, Wei Z, Patel AM, Bennett J, Gerton GL, Moss SB, Radice GL, Strauss JF. Deficiency of SPAG16L causes male infertility associated with impaired sperm motility. Biology of Reproduction. 74: 751-9. PMID 16382026 DOI: 10.1095/biolreprod.105.049254  0.56
2005 Wilson DF, Vinogradov SA, Grosul P, Kuroki A, Bennett J. Imaging oxygen pressure in the retina of the mouse eye. Advances in Experimental Medicine and Biology. 566: 159-65. PMID 16594148 DOI: 10.1007/0-387-26206-7_22  0.56
2005 Rex TS, Peet JA, Surace EM, Calvert PD, Nikonov SS, Lyubarsky AL, Bendo E, Hughes T, Pugh EN, Bennett J. The distribution, concentration, and toxicity of enhanced green fluorescent protein in retinal cells after genomic or somatic (virus-mediated) gene transfer. Molecular Vision. 11: 1236-45. PMID 16402024  0.56
2005 Bennett J. Strategies for delivery of rod-derived cone viability factor. Retina (Philadelphia, Pa.). 25: S47. PMID 16374333  0.56
2005 Keiser NW, Tang W, Wei Z, Bennett J. Spatial and temporal expression patterns of the choroideremia gene in the mouse retina. Molecular Vision. 11: 1052-60. PMID 16357828  0.56
2005 Cideciyan AV, Swider M, Aleman TS, Sumaroka A, Schwartz SB, Roman MI, Milam AH, Bennett J, Stone EM, Jacobson SG. ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina. Investigative Ophthalmology & Visual Science. 46: 4739-46. PMID 16303974 DOI: 10.1167/iovs.05-0805  0.56
2005 Wang F, Tang W, McGraw HM, Bennett J, Enquist LW, Friedman HM. Herpes simplex virus type 1 glycoprotein e is required for axonal localization of capsid, tegument, and membrane glycoproteins. Journal of Virology. 79: 13362-72. PMID 16227258 DOI: 10.1128/JVI.79.21.13362-13372.2005  0.56
2005 Acland GM, Aguirre GD, Bennett J, Aleman TS, Cideciyan AV, Bennicelli J, Dejneka NS, Pearce-Kelling SE, Maguire AM, Palczewski K, Hauswirth WW, Jacobson SG. Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness. Molecular Therapy : the Journal of the American Society of Gene Therapy. 12: 1072-82. PMID 16226919 DOI: 10.1016/j.ymthe.2005.08.008  0.56
2005 Wilson DF, Vinogradov SA, Grosul P, Vaccarezza MN, Kuroki A, Bennett J. Oxygen distribution and vascular injury in the mouse eye measured by phosphorescence-lifetime imaging. Applied Optics. 44: 5239-48. PMID 16149347 DOI: 10.1364/AO.44.005239  0.56
2005 Hahn P, Lindsten T, Tolentino M, Thompson CB, Bennett J, Dunaief JL. Persistent fetal ocular vasculature in mice deficient in bax and bak. Archives of Ophthalmology (Chicago, Ill. : 1960). 123: 797-802. PMID 15955981 DOI: 10.1001/archopht.123.6.797  0.56
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  0.56
2005 Zhang Z, Jones BH, Tang W, Moss SB, Wei Z, Ho C, Pollack M, Horowitz E, Bennett J, Baker ME, Strauss JF. Dissecting the axoneme interactome: the mammalian orthologue of Chlamydomonas PF6 interacts with sperm-associated antigen 6, the mammalian orthologue of Chlamydomonas PF16. Molecular & Cellular Proteomics : McP. 4: 914-23. PMID 15827353 DOI: 10.1074/mcp.M400177-MCP200  0.56
2005 Lebherz C, Maguire AM, Auricchio A, Tang W, Aleman TS, Wei Z, Grant R, Cideciyan AV, Jacobson SG, Wilson JM, Bennett J. Nonhuman primate models for diabetic ocular neovascularization using AAV2-mediated overexpression of vascular endothelial growth factor. Diabetes. 54: 1141-9. PMID 15793254 DOI: 10.2337/diabetes.54.4.1141  0.56
2005 Lebherz C, Auricchio A, Maguire AM, Rivera VM, Tang W, Grant RL, Clackson T, Bennett J, Wilson JM. Long-term inducible gene expression in the eye via adeno-associated virus gene transfer in nonhuman primates. Human Gene Therapy. 16: 178-86. PMID 15761258 DOI: 10.1089/hum.2005.16.178  0.56
2005 Schwartz SB, Aleman TS, Cideciyan AV, Windsor EA, Sumaroka A, Roman AJ, Rane T, Smilko EE, Bennett J, Stone EM, Kimberling WJ, Liu XZ, Jacobson SG. Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype. Investigative Ophthalmology & Visual Science. 46: 734-43. PMID 15671307 DOI: 10.1167/iovs.04-1136  0.56
2004 Schuettauf F, Vorwerk C, Naskar R, Orlin A, Quinto K, Zurakowski D, Dejneka NS, Klein RL, Meyer EM, Bennett J. Adeno-associated viruses containing bFGF or BDNF are neuroprotective against excitotoxicity. Current Eye Research. 29: 379-86. PMID 15764082 DOI: 10.1080/02713680490517872  0.56
2004 Dejneka NS, Kuroki AM, Fosnot J, Tang W, Tolentino MJ, Bennett J. Systemic rapamycin inhibits retinal and choroidal neovascularization in mice. Molecular Vision. 10: 964-72. PMID 15623986  0.56
2004 Rex TS, Tsui I, Hahn P, Maguire AM, Duan D, Bennett J, Dunaief JL. Adenovirus-mediated delivery of catalase to retinal pigment epithelial cells protects neighboring photoreceptors from photo-oxidative stress. Human Gene Therapy. 15: 960-7. PMID 15585111 DOI: 10.1089/hum.2004.15.960  0.56
2004 Wong WT, Rex TS, Auricchio A, Maguire AM, Chung D, Tang W, Bennett J. Effect of over-expression of pigment epithelium derived factor (PEDF) on developing retinal vasculature in the mouse. Molecular Vision. 10: 837-44. PMID 15547489  0.56
2004 Rex TS, Allocca M, Domenici L, Surace EM, Maguire AM, Lyubarsky A, Cellerino A, Bennett J, Auricchio A. Systemic but not intraocular Epo gene transfer protects the retina from light-and genetic-induced degeneration. Molecular Therapy : the Journal of the American Society of Gene Therapy. 10: 855-61. PMID 15509503 DOI: 10.1016/j.ymthe.2004.07.027  0.56
2004 Chen L, Wu W, Dentchev T, Zeng Y, Wang J, Tsui I, Tobias JW, Bennett J, Baldwin D, Dunaief JL. Light damage induced changes in mouse retinal gene expression. Experimental Eye Research. 79: 239-47. PMID 15325571 DOI: 10.1016/j.exer.2004.05.002  0.56
2004 Aleman TS, Jacobson SG, Chico JD, Scott ML, Cheung AY, Windsor EA, Furushima M, Redmond TM, Bennett J, Palczewski K, Cideciyan AV. Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosis. Investigative Ophthalmology & Visual Science. 45: 1259-71. PMID 15037595 DOI: 10.1167/iovs.03-1230  0.56
2004 Dejneka NS, Surace EM, Aleman TS, Cideciyan AV, Lyubarsky A, Savchenko A, Redmond TM, Tang W, Wei Z, Rex TS, Glover E, Maguire AM, Pugh EN, Jacobson SG, Bennett J. In utero gene therapy rescues vision in a murine model of congenital blindness. Molecular Therapy : the Journal of the American Society of Gene Therapy. 9: 182-8. PMID 14759802 DOI: 10.1016/j.ymthe.2003.11.013  0.56
2004 Bennett J. Gene therapy for Leber congenital amaurosis. Novartis Foundation Symposium. 255: 195-202; discussion . PMID 14750605  0.56
2004 Cideciyan AV, Aleman TS, Swider M, Schwartz SB, Steinberg JD, Brucker AJ, Maguire AM, Bennett J, Stone EM, Jacobson SG. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. Human Molecular Genetics. 13: 525-34. PMID 14709597 DOI: 10.1093/hmg/ddh048  0.56
2003 Liang FQ, Surace E, Dejneka NS, Maguire AM, Bennett J. Müller cell transduction by AAV2 in normal and degenerative retinas. Advances in Experimental Medicine and Biology. 533: 439-45. PMID 15180296  0.56
2003 Dejneka NS, Surace EM, Bennett J. Gene therapy for Leber congenital amaurosis. Advances in Experimental Medicine and Biology. 533: 415-22. PMID 15180293  0.56
2003 Hahn P, Lindsten T, Ying GS, Bennett J, Milam AH, Thompson CB, Dunaief JL. Proapoptotic bcl-2 family members, Bax and Bak, are essential for developmental photoreceptor apoptosis. Investigative Ophthalmology & Visual Science. 44: 3598-605. PMID 12882813 DOI: 10.1167/iovs.02-1113  0.56
2003 Dejneka NS, Rex TS, Bennett J. Gene therapy and animal models for retinal disease. Developments in Ophthalmology. 37: 188-98. PMID 12876838  0.56
2003 Surace EM, Auricchio A, Reich SJ, Rex T, Glover E, Pineles S, Tang W, O'Connor E, Lyubarsky A, Savchenko A, Pugh EN, Maguire AM, Wilson JM, Bennett J. Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transduction. Journal of Virology. 77: 7957-63. PMID 12829835 DOI: 10.1128/JVI.77.14.7957-7963.2003  0.56
2003 Reich SJ, Fosnot J, Kuroki A, Tang W, Yang X, Maguire AM, Bennett J, Tolentino MJ. Small interfering RNA (siRNA) targeting VEGF effectively inhibits ocular neovascularization in a mouse model. Molecular Vision. 9: 210-6. PMID 12789138  0.4
2003 Chen L, Dentchev T, Wong R, Hahn P, Wen R, Bennett J, Dunaief JL. Increased expression of ceruloplasmin in the retina following photic injury. Molecular Vision. 9: 151-8. PMID 12724641  0.56
2003 Anand V, Barral DC, Zeng Y, Brunsmann F, Maguire AM, Seabra MC, Bennett J. Gene therapy for choroideremia: in vitro rescue mediated by recombinant adenovirus. Vision Research. 43: 919-26. PMID 12668061  0.4
2003 Hansen KA, Sugino IK, Yagi F, Wang H, Tsukahara I, Gullapalli V, Bennett J, Zarbin MA. Adeno-associated virus encoding green fluorescent protein as a label for retinal pigment epithelium. Investigative Ophthalmology & Visual Science. 44: 772-80. PMID 12556413 DOI: 10.1167/iovs.02-0091  0.56
2002 Behling KC, Surace EM, Bennett J. Pigment epithelium-derived factor expression in the developing mouse eye. Molecular Vision. 8: 449-54. PMID 12447163  0.56
2002 Stettler DD, Das A, Bennett J, Gilbert CD. Lateral connectivity and contextual interactions in macaque primary visual cortex. Neuron. 36: 739-50. PMID 12441061 DOI: 10.1016/S0896-6273(02)01029-2  0.56
2002 Ho TT, Maguire AM, Aguirre GD, Surace EM, Anand V, Zeng Y, Salvetti A, Hopwood JJ, Haskins ME, Bennett J. Phenotypic rescue after adeno-associated virus-mediated delivery of 4-sulfatase to the retinal pigment epithelium of feline mucopolysaccharidosis VI. The Journal of Gene Medicine. 4: 613-21. PMID 12439853 DOI: 10.1002/jgm.302  0.56
2002 Auricchio A, Behling KC, Maguire AM, O'Connor EM, Bennett J, Wilson JM, Tolentino MJ. Inhibition of retinal neovascularization by intraocular viral-mediated delivery of anti-angiogenic agents. Molecular Therapy : the Journal of the American Society of Gene Therapy. 6: 490-4. PMID 12377190 DOI: 10.1006/mthe.2002.0702  0.56
2002 Auricchio A, Rivera VM, Clackson T, O'Connor EE, Maguire AM, Tolentino MJ, Bennett J, Wilson JM. Pharmacological regulation of protein expression from adeno-associated viral vectors in the eye. Molecular Therapy : the Journal of the American Society of Gene Therapy. 6: 238-42. PMID 12161190  0.48
2002 Duncan JL, Aleman TS, Gardner LM, De Castro E, Marks DA, Emmons JM, Bieber ML, Steinberg JD, Bennett J, Stone EM, MacDonald IM, Cideciyan AV, Maguire MG, Jacobson SG. Macular pigment and lutein supplementation in choroideremia. Experimental Eye Research. 74: 371-81. PMID 12014918 DOI: 10.1006/exer.2001.1126  0.56
2002 Jacobson SG, Cideciyan AV, Bennett J, Kingsley RM, Sheffield VC, Stone EM. Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 376-9. PMID 11879143  0.56
2002 Anand V, Duffy B, Yang Z, Dejneka NS, Maguire AM, Bennett J. A deviant immune response to viral proteins and transgene product is generated on subretinal administration of adenovirus and adeno-associated virus. Molecular Therapy : the Journal of the American Society of Gene Therapy. 5: 125-32. PMID 11829519 DOI: 10.1006/mthe.2002.0525  0.52
2001 Gupta AR, Dejneka NS, Maguire AM, Bennett J. Generation of transgenic mice for studies of ocular development and disease. Methods in Molecular Medicine. 47: 191-214. PMID 21394586 DOI: 10.1385/1-59259-085-3:191  0.52
2001 Karakousis PC, John SK, Behling KC, Surace EM, Smith JE, Hendrickson A, Tang WX, Bennett J, Milam AH. Localization of pigment epithelium derived factor (PEDF) in developing and adult human ocular tissues. Molecular Vision. 7: 154-63. PMID 11438800  0.56
2001 Gupta AR, Dejneka NS, D'Amato RJ, Yang Z, Syed N, Maguire AM, Bennett J. Strain-dependent anterior segment neovascularization following intravitreal gene transfer of basic fibroblast growth factor (bFGF). The Journal of Gene Medicine. 3: 252-9. PMID 11437330 DOI: 10.1002/1521-2254(200105/06)3:3<252::AID-JGM185>3.0.CO;2-S  0.52
2000 Bennett J, Zeng Y, Gupta AR, Maguire AM. Application of adenoviral vectors. Analysis of eye development. Methods in Molecular Biology (Clifton, N.J.). 135: 525-35. PMID 10791347  0.4
1999 Nesbit M, Nesbit HK, Bennett J, Andl T, Hsu MY, Dejesus E, McBrian M, Gupta AR, Eck SL, Herlyn M. Basic fibroblast growth factor induces a transformed phenotype in normal human melanocytes. Oncogene. 18: 6469-76. PMID 10597249 DOI: 10.1038/sj.onc.1203066  0.4
1999 Bennett J, Maguire AM, Cideciyan AV, Schnell M, Glover E, Anand V, Aleman TS, Chirmule N, Gupta AR, Huang Y, Gao GP, Nyberg WC, Tazelaar J, Hughes J, Wilson JM, et al. Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina. Proceedings of the National Academy of Sciences of the United States of America. 96: 9920-5. PMID 10449795  0.48
1998 Zeng Y, Rosborough RC, Li Y, Gupta AR, Bennett J. Temporal and spatial regulation of gene expression mediated by the promoter for the human tissue inhibitor of metalloproteinases-3 (TIMP-3)-encoding gene. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 211: 228-37. PMID 9520110 DOI: 10.1002/(SICI)1097-0177(199803)211:3<228::AID-AJA4>3.0.CO;2-J  0.4
1984 Bennett J, Pedersen RA. Early mouse embryos exhibit strain variation in radiation-induced sister-chromatid exchange: relationship with DNA repair. Mutation Research. 126: 153-7. PMID 6538931  0.92
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