| Year |
Citation |
Score |
| 2024 |
Wongchaisuwat N, Amato A, Yang P, Everett L, Pennesi ME, Huang D, Chen S. Optical Coherence Tomography Split-Spectrum Amplitude-Decorrelation Optoretinography Detects Early Central Cone Photoreceptor Dysfunction in Retinal Dystrophies. Translational Vision Science & Technology. 13: 5. PMID 39361318 DOI: 10.1167/tvst.13.10.5 |
0.381 |
|
| 2024 |
DeVine T, Elizondo G, Gaston G, Babcock SJ, Matern D, Shchepinov MS, Pennesi ME, Harding CO, Gillingham MB. iPSC-Derived LCHADD Retinal Pigment Epithelial Cells Are Susceptible to Lipid Peroxidation and Rescued by Transfection of a Wildtype AAV-HADHA Vector. Investigative Ophthalmology & Visual Science. 65: 22. PMID 39283617 DOI: 10.1167/iovs.65.11.22 |
0.307 |
|
| 2024 |
Pennesi ME, Wang YZ, Birch DG. Deep learning aided measurement of outer retinal layer metrics as biomarkers for inherited retinal degenerations: opportunities and challenges. Current Opinion in Ophthalmology. 35: 447-454. PMID 39259656 DOI: 10.1097/ICU.0000000000001088 |
0.347 |
|
| 2024 |
Kalaw FGP, Wagner NE, de Oliveira TB, Everett LA, Yang P, Pennesi ME, Borooah S. Using multi-modal imaging to refine the phenotype of PRPH2-associated retinal degeneration. Ophthalmology. Retina. PMID 39089460 DOI: 10.1016/j.oret.2024.07.016 |
0.35 |
|
| 2024 |
Igelman AD, White E, Tayyib A, Everett L, Vincent A, Heon E, Zeitz C, Michaelides M, Mahroo OA, Katta M, Webster A, Preising M, Lorenz B, Khateb S, Banin E, ... ... Pennesi ME, et al. Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study. The British Journal of Ophthalmology. PMID 39079892 DOI: 10.1136/bjo-2023-323747 |
0.348 |
|
| 2024 |
MacLaren RE, Audo I, Fischer MD, Huckfeldt R, Lam B, Pennesi ME, Sisk R, Gow JA, Li J, Zhu K, Tsang SF. An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study. Human Gene Therapy. PMID 38970425 DOI: 10.1089/hum.2024.017 |
0.454 |
|
| 2024 |
Pierce EA, Ashimatey BS, Jayasundera T, Hoyng C, Lam BL, Lorenz B, Kim K, Rashid A, Myers R, Pennesi ME. Twelve-month Natural History Study of Centrosomal Protein 290 (CEP290)-associated Inherited Retinal Degeneration. Ophthalmology Science. 4: 100483. PMID 38881603 DOI: 10.1016/j.xops.2024.100483 |
0.301 |
|
| 2024 |
Pierce EA, Aleman TS, Jayasundera KT, Ashimatey BS, Kim K, Rashid A, Jaskolka MC, Myers RL, Lam BL, Bailey ST, Comander JI, Lauer AK, Maguire AM, Pennesi ME. Gene Editing for -Associated Retinal Degeneration. The New England Journal of Medicine. PMID 38709228 DOI: 10.1056/NEJMoa2309915 |
0.335 |
|
| 2024 |
Lam BL, Pennesi ME, Kay CN, Panda S, Gow JA, Zhao G, MacLaren RE. Assessment of Visual Function With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study. Ophthalmology. PMID 38423215 DOI: 10.1016/j.ophtha.2024.02.023 |
0.311 |
|
| 2024 |
Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, ... Pennesi ME, et al. Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101106. PMID 38420906 DOI: 10.1016/j.gim.2024.101106 |
0.324 |
|
| 2023 |
Wongchaisuwat N, Amato A, Lamborn AE, Yang P, Everett L, Pennesi ME. Retinitis pigmentosa GTPase regulator-related retinopathy and gene therapy. Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society. 37: 276-286. PMID 38155670 DOI: 10.4103/sjopt.sjopt_168_23 |
0.316 |
|
| 2023 |
Duncan JL, Cheng P, Maguire MG, Ayala AA, Birch DG, Cheetham JK, Durham TA, Fahim AT, Hoyng CB, Ishikawa H, Michaelides M, Pennesi ME, Alain-Sahel J, Stingl K, Weng CY. Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment through Two Years. American Journal of Ophthalmology. PMID 36764426 DOI: 10.1016/j.ajo.2023.02.002 |
0.367 |
|
| 2022 |
Birch DG, Samarakoon L, Melia M, Duncan JL, Ayala AR, Audo I, Cheetham JK, Durham TA, Iannaccone A, Pennesi ME, Stingl K. The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene. Investigative Ophthalmology & Visual Science. 63: 17. PMID 35293952 DOI: 10.1167/iovs.63.3.17 |
0.32 |
|
| 2021 |
Patterson EJ, Langlo CS, Georgiou M, Kalitzeos A, Pennesi ME, Neitz J, Hardcastle AJ, Neitz M, Michaelides M, Carroll J. Comparing Retinal Structure in Patients with Achromatopsia and Blue Cone Monochromacy Using OCT. Ophthalmology Science. 1. PMID 36186895 DOI: 10.1016/j.xops.2021.100047 |
0.315 |
|
| 2021 |
Scruggs BA, Vasconcelos HM, Matioli da Palma M, Kogachi K, Pennesi ME, Yang P, Bailey ST, Lauer AK. Injection pressure levels for creating blebs during subretinal gene therapy. Gene Therapy. PMID 34580433 DOI: 10.1038/s41434-021-00294-2 |
0.314 |
|
| 2021 |
Georgiou M, Fujinami K, Vincent A, Nasser F, Khateb S, Vargas ME, Thiadens AAHJ, de Carvalho ER, Nguyen XT, De Guimarães TAC, Robson AG, Mahroo OA, Pontikos N, Arno G, Fujinami-Yokokawa Y, ... ... Pennesi ME, et al. KCNV2-associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints - KCNV2 Study Group Report 2. American Journal of Ophthalmology. PMID 33737031 DOI: 10.1016/j.ajo.2021.03.004 |
0.387 |
|
| 2020 |
Ryals RC, Patel S, Acosta C, McKinney M, Pennesi ME, Sahay G. The effects of PEGylation on LNP based mRNA delivery to the eye. Plos One. 15: e0241006. PMID 33119640 DOI: 10.1371/journal.pone.0241006 |
0.377 |
|
| 2020 |
Ryals RC, Huang SJ, Wafai D, Bernert C, Steele W, Six M, Bonthala S, Titus H, Yang P, Gillingham M, Pennesi ME. A Ketogenic & Low-Protein Diet Slows Retinal Degeneration in rd10 Mice. Translational Vision Science & Technology. 9: 18. PMID 33117609 DOI: 10.1167/tvst.9.11.18 |
0.343 |
|
| 2020 |
Yang P, Lockard R, Titus H, Hiblar J, Weller K, Wafai D, Weleber RG, Duvoisin RM, Morgans CW, Pennesi ME. Suppression of cGMP-Dependent Photoreceptor Cytotoxicity With Mycophenolate Is Neuroprotective in Murine Models of Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 61: 25. PMID 32785677 DOI: 10.1167/Iovs.61.10.25 |
0.443 |
|
| 2020 |
Hormel TT, Jia Y, Jian Y, Hwang TS, Bailey ST, Pennesi ME, Wilson DJ, Morrison JC, Huang D. Plexus-specific retinal vascular anatomy and pathologies as seen by projection-resolved optical coherence tomographic angiography. Progress in Retinal and Eye Research. 100878. PMID 32712135 DOI: 10.1016/J.Preteyeres.2020.100878 |
0.362 |
|
| 2019 |
Pennesi ME, Birch DG, Duncan JL, Bennett J, Girach A. CHOROIDEREMIA: Retinal Degeneration With an Unmet Need. Retina (Philadelphia, Pa.). PMID 31021898 DOI: 10.1097/Iae.0000000000002553 |
0.374 |
|
| 2019 |
Patel S, Ryals RC, Weller KK, Pennesi ME, Sahay G. Lipid nanoparticles for delivery of messenger RNA to the back of the eye. Journal of Controlled Release : Official Journal of the Controlled Release Society. PMID 30986436 DOI: 10.1016/J.Jconrel.2019.04.015 |
0.338 |
|
| 2019 |
Fahim AT, Bouzia Z, Branham KH, Kumaran N, Vargas ME, Feathers KL, Perera ND, Young K, Khan NW, Heckenlively JR, Webster AR, Pennesi ME, Ali RR, Thompson DA, Michaelides M. Detailed clinical characterisation, unique features and natural history of autosomal recessive -associated retinal degeneration. The British Journal of Ophthalmology. PMID 30979730 DOI: 10.1136/bjophthalmol-2018-313580 |
0.329 |
|
| 2019 |
Jiang D, Ryals RC, Huang SJ, Weller KK, Titus HE, Robb BM, Saad FW, Salam RA, Hammad H, Yang P, Marks DL, Pennesi ME. Monomethyl Fumarate Protects the Retina From Light-Induced Retinopathy. Investigative Ophthalmology & Visual Science. 60: 1275-1285. PMID 30924852 DOI: 10.1167/Iovs.18-24398 |
0.319 |
|
| 2019 |
Hagag AM, Wang J, Lu K, Harman G, Weleber RG, David Huang, Yang P, Pennesi ME, Jia Y. Projection-Resolved Optical Coherence Tomographic Angiography of Retinal Plexuses in Retinitis Pigmentosa. American Journal of Ophthalmology. PMID 30849344 DOI: 10.1016/J.Ajo.2019.02.034 |
0.364 |
|
| 2019 |
Alabduljalil T, Patel RC, Alqahtani AA, Gao SS, Gale MJ, Zhang M, Jia Y, Huang D, Chiang PW, Chen R, Wang J, Weleber RG, Pennesi ME, Yang P. Correlation of Outer Retinal Degeneration and Choriocapillaris Loss in Stargardt disease using en face OCT and OCT Angiography. American Journal of Ophthalmology. PMID 30771335 DOI: 10.1016/J.Ajo.2019.02.007 |
0.36 |
|
| 2019 |
Ong T, Pennesi ME, Birch DG, Lam BL, Tsang SH. Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease. Pharmaceutical Research. 36: 34. PMID 30617669 DOI: 10.1007/S11095-018-2564-5 |
0.404 |
|
| 2018 |
Pennesi ME, Weleber RG, Yang P, Whitebirch C, Thean B, Flotte TR, Humphries M, Chegarnov E, Beasley KN, Stout JT, Chulay JD. Results at 5 Years after Gene Therapy for RPE65-deficient Retinal Dystrophy. Human Gene Therapy. PMID 29869534 DOI: 10.1089/hum.2018.014 |
0.304 |
|
| 2018 |
Wang Z, Camino A, Hagag AM, Wang J, Weleber RG, Yang P, Pennesi ME, Huang D, Li D, Jia Y. Automated detection of preserved photoreceptor on optical coherence tomography in choroideremia based on machine learning. Journal of Biophotonics. PMID 29341445 DOI: 10.1002/Jbio.201700313 |
0.342 |
|
| 2017 |
Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW, Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE, ... ... Pennesi ME, et al. Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. Jama Ophthalmology. PMID 28542676 DOI: 10.1001/Jamaophthalmol.2017.1401 |
0.365 |
|
| 2017 |
Ryals RC, Andrews MD, Datta S, Coyner AS, Fischer CM, Wen Y, Pennesi ME, McGill TJ. Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence Tomography. Investigative Ophthalmology & Visual Science. 58: 1378-1386. PMID 28253400 DOI: 10.1167/Iovs.16-20363 |
0.339 |
|
| 2016 |
Patel RC, Gao SS, Zhang M, Alabduljalil T, Al-Qahtani A, Weleber RG, Yang P, Jia Y, Huang D, Pennesi ME. OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF CHOROIDAL NEOVASCULARIZATION IN FOUR INHERITED RETINAL DYSTROPHIES. Retina (Philadelphia, Pa.). PMID 27336230 DOI: 10.1097/Iae.0000000000001159 |
0.325 |
|
| 2016 |
Sun LW, Johnson RD, Langlo CS, Cooper RF, Razeen MM, Russillo MC, Dubra A, Connor TB, Han DP, Pennesi ME, Kay CN, Weinberg DV, Stepien KE, Carroll J. Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome. Investigative Ophthalmology & Visual Science. 57: 2428-2442. PMID 27145477 DOI: 10.1167/Iovs.15-18246 |
0.363 |
|
| 2016 |
Weleber RG, Pennesi ME, Wilson DJ, Kaushal S, Erker LR, Jensen L, McBride MT, Flotte TR, Humphries M, Calcedo R, Hauswirth WW, Chulay JD, Stout JT. Results at 2 Years after Gene Therapy for RPE65-Deficient Leber Congenital Amaurosis and Severe Early-Childhood-Onset Retinal Dystrophy. Ophthalmology. PMID 27102010 DOI: 10.1016/J.Ophtha.2016.03.003 |
0.312 |
|
| 2015 |
Xiong WH, Pang JJ, Pennesi ME, Duvoisin RM, Wu SM, Morgans CW. The Effect of PKCα on the Light Response of Rod Bipolar Cells in the Mouse Retina. Investigative Ophthalmology & Visual Science. 56: 4961-74. PMID 26230760 DOI: 10.1167/Iovs.15-16622 |
0.761 |
|
| 2015 |
Jia Y, Bailey ST, Hwang TS, McClintic SM, Gao SS, Pennesi ME, Flaxel CJ, Lauer AK, Wilson DJ, Hornegger J, Fujimoto JG, Huang D. Quantitative optical coherence tomography angiography of vascular abnormalities in the living human eye. Proceedings of the National Academy of Sciences of the United States of America. 112: E2395-402. PMID 25897021 DOI: 10.1073/Pnas.1500185112 |
0.365 |
|
| 2015 |
Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, et al. Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium. Investigative Ophthalmology & Visual Science. 56: 918-31. PMID 25667399 DOI: 10.1167/Iovs.14-16049 |
0.307 |
|
| 2015 |
Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Li D, Wu SM, Gross RL. Corrigendum to "Effects of elevated intraocular pressure on mouse retinal ganglion cells" [Vision Res. 45 (2004) 169-179] DOI: 10.1016/j.visres.2004.08.008 Vision Research. 117: 136. DOI: 10.1016/j.visres.2015.10.005 |
0.632 |
|
| 2014 |
Messenger WB, Yang P, Pennesi ME. Ophthalmic findings in an infant with phosphomannomutase deficiency. Documenta Ophthalmologica. Advances in Ophthalmology. 128: 149-53. PMID 24493206 DOI: 10.1007/s10633-014-9427-0 |
0.343 |
|
| 2013 |
Pennesi ME. A little algae a day keeps the retinal degeneration specialist away? Jama Ophthalmology. 131: 983-4. PMID 23700100 DOI: 10.1001/jamaophthalmol.2013.4468 |
0.357 |
|
| 2012 |
Pennesi ME, Michaels KV, Magee SS, Maricle A, Davin SP, Garg AK, Gale MJ, Tu DC, Wen Y, Erker LR, Francis PJ. Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomography. Investigative Ophthalmology & Visual Science. 53: 4644-56. PMID 22562504 DOI: 10.1167/Iovs.12-9611 |
0.345 |
|
| 2012 |
Courtney RJ, Pennesi ME. Inherited retinal degenerations with systemic manifestations. International Ophthalmology Clinics. 52: 119-47. PMID 22124242 DOI: 10.1097/IIO.0b013e31823bbe56 |
0.345 |
|
| 2012 |
Gregory-Evans K, Pennesi ME, Weleber RG. Retinitis Pigmentosa and Allied Disorders Retina Fifth Edition. 2: 761-835. DOI: 10.1016/B978-1-4557-0737-9.00040-0 |
0.308 |
|
| 2011 |
Courtney RJ, Pennesi ME. Retinal dystrophy in 2 brothers with α-Mannosidosis. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 799-802. PMID 21670350 DOI: 10.1001/archophthalmol.2011.134 |
0.427 |
|
| 2009 |
Abd-El-Barr MM, Pennesi ME, Saszik SM, Barrow AJ, Lem J, Bramblett DE, Paul DL, Frishman LJ, Wu SM. Genetic dissection of rod and cone pathways in the dark-adapted mouse retina. Journal of Neurophysiology. 102: 1945-55. PMID 19587322 DOI: 10.1152/Jn.00142.2009 |
0.701 |
|
| 2009 |
Hayashi A, Naseri A, Pennesi ME, de Juan E. Subretinal delivery of immunoglobulin G with gold nanoparticles in the rabbit eye. Japanese Journal of Ophthalmology. 53: 249-56. PMID 19484444 DOI: 10.1007/s10384-009-0655-x |
0.447 |
|
| 2008 |
Pennesi ME, Nishikawa S, Matthes MT, Yasumura D, LaVail MM. The relationship of photoreceptor degeneration to retinal vascular development and loss in mutant rhodopsin transgenic and RCS rats. Experimental Eye Research. 87: 561-70. PMID 18848932 DOI: 10.1016/j.exer.2008.09.004 |
0.333 |
|
| 2007 |
Abd-El-Barr MM, Sykoudis K, Andrabi S, Eichers ER, Pennesi ME, Tan PL, Wilson JH, Katsanis N, Lupski JR, Wu SM. Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome. Vision Research. 47: 3394-407. PMID 18022666 DOI: 10.1016/j.visres.2007.09.016 |
0.67 |
|
| 2007 |
Albini TA, Abd-El-Barr MM, Carvounis PE, Iyer MN, Lakhanpal RR, Pennesi ME, Chevez-Barrios P, Wu SM, Holz ER. Long-term retinal toxicity of intravitreal commercially available preserved triamcinolone acetonide (Kenalog) in rabbit eyes. Investigative Ophthalmology & Visual Science. 48: 390-5. PMID 17197559 DOI: 10.1167/iovs.06-0145 |
0.745 |
|
| 2006 |
Pennesi ME, Bramblett DE, Cho JH, Tsai MJ, Wu SM. A role for bHLH transcription factors in retinal degeneration and dysfunction. Advances in Experimental Medicine and Biology. 572: 155-61. PMID 17249569 DOI: 10.1007/0-387-32442-9_23 |
0.57 |
|
| 2006 |
Gao H, Pennesi ME, Qiao X, Iyer MN, Wu SM, Holz ER, Mieler WF. Intravitreal moxifloxacin: retinal safety study with electroretinography and histopathology in animal models. Investigative Ophthalmology & Visual Science. 47: 1606-11. PMID 16565399 DOI: 10.1167/iovs.05-0702 |
0.745 |
|
| 2005 |
Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Li D, Wu SM, Gross RL. Effects of elevated intraocular pressure on mouse retinal ganglion cells. Vision Research. 45: 169-79. PMID 15581918 DOI: 10.1016/j.visres.2004.08.008 |
0.721 |
|
| 2004 |
Gao H, Pennesi ME, Shah K, Qiao X, Hariprasad SM, Mieler WF, Wu SM, Holz ER. Intravitreal voriconazole: an electroretinographic and histopathologic study. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 1687-92. PMID 15534131 DOI: 10.1001/archopht.122.11.1687 |
0.777 |
|
| 2004 |
Bramblett DE, Pennesi ME, Wu SM, Tsai MJ. The transcription factor Bhlhb4 is required for rod bipolar cell maturation. Neuron. 43: 779-93. PMID 15363390 DOI: 10.1016/j.neuron.2004.08.032 |
0.586 |
|
| 2003 |
Gao H, Pennesi M, Shah K, Qiao X, Hariprasad SM, Mieler WF, Wu SM, Holz ER. Safety of intravitreal voriconazole: electroretinographic and histopathologic studies. Transactions of the American Ophthalmological Society. 101: 183-9; discussion 18. PMID 14971576 |
0.781 |
|
| 2003 |
Gross RL, Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Wu SM. A mouse model of elevated intraocular pressure: retina and optic nerve findings. Transactions of the American Ophthalmological Society. 101: 163-9; discussion 16. PMID 14971574 |
0.721 |
|
| 2003 |
Pennesi ME, Howes KA, Baehr W, Wu SM. Guanylate cyclase-activating protein (GCAP) 1 rescues cone recovery kinetics in GCAP1/GCAP2 knockout mice. Proceedings of the National Academy of Sciences of the United States of America. 100: 6783-8. PMID 12732716 DOI: 10.1073/Pnas.1130102100 |
0.541 |
|
| 2003 |
Qiao X, Pennesi M, Seong E, Gao H, Burmeister M, Wu SM. Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain. Vision Research. 43: 859-65. PMID 12668055 DOI: 10.1016/S0042-6989(02)00393-0 |
0.734 |
|
| 2003 |
Yoo SY, Pennesi ME, Weeber EJ, Xu B, Atkinson R, Chen S, Armstrong DL, Wu SM, Sweatt JD, Zoghbi HY. SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity. Neuron. 37: 383-401. PMID 12575948 DOI: 10.1016/S0896-6273(02)01190-X |
0.606 |
|
| 2003 |
Pennesi ME, Cho JH, Yang Z, Wu SH, Zhang J, Wu SM, Tsai MJ. BETA2/NeuroD1 null mice: a new model for transcription factor-dependent photoreceptor degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 453-61. PMID 12533605 DOI: 10.1523/Jneurosci.23-02-00453.2003 |
0.561 |
|
| 2003 |
Pennesi ME, Cho J, Yang Z, Wu SH, Zhang J, Wu SM, Tsai M. BETA2/NeuroD1 Null Mice: A New Model for Transcription Factor-Dependent Photoreceptor Degeneration The Journal of Neuroscience. 23: 453-461. DOI: 10.1523/JNEUROSCI.23-02-00453.2003 |
0.48 |
|
| 2002 |
Howes KA, Pennesi ME, Sokal I, Church-Kopish J, Schmidt B, Margolis D, Frederick JM, Rieke F, Palczewski K, Wu SM, Detwiler PB, Baehr W. GCAP1 rescues rod photoreceptor response in GCAP1/GCAP2 knockout mice. The Embo Journal. 21: 1545-54. PMID 11927539 DOI: 10.1093/Emboj/21.7.1545 |
0.548 |
|
| 1998 |
Pennesi ME, Lyubarsky AL, Pugh EN. Extreme responsiveness of the pupil of the dark-adapted mouse to steady retinal illumination. Investigative Ophthalmology & Visual Science. 39: 2148-56. PMID 9761294 |
0.412 |
|
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