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Daniel Gibbs, Ph.D. - Publications

Affiliations: 
Neurosciences University of California, San Diego, La Jolla, CA 
Area:
cytoskeleton, visual system, retina, gene therapy, neural repair
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25 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
2022 Sinopoulou E, Rosenzweig ES, Conner JM, Gibbs D, Weinholtz CA, Weber JL, Brock JH, Nout-Lomas YS, Ovruchesky E, Takashima Y, Biane JS, Kumamaru H, Havton LA, Beattie MS, Bresnahan JC, et al. Rhesus macaque versus rat divergence in the corticospinal projectome. Neuron. PMID 35917818 DOI: 10.1016/j.neuron.2022.07.002  0.407
2018 Dulin JN, Adler AF, Kumamaru H, Poplawski GHD, Lee-Kubli C, Strobl H, Gibbs D, Kadoya K, Fawcett JW, Lu P, Tuszynski MH. Injured adult motor and sensory axons regenerate into appropriate organotypic domains of neural progenitor grafts. Nature Communications. 9: 84. PMID 29311559 DOI: 10.1038/S41467-017-02613-X  0.459
2017 Williams DS, Chadha A, Hazim R, Gibbs D. Gene therapy approaches for prevention of retinal degeneration in Usher syndrome. Gene Therapy. PMID 28054582 DOI: 10.1038/Gt.2016.81  0.452
2011 Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS. Retinal disease course in Usher syndrome 1B due to MYO7A mutations. Investigative Ophthalmology & Visual Science. 52: 7924-36. PMID 21873662 DOI: 10.1167/Iovs.11-8313  0.479
2011 Lopes VS, Gibbs D, Libby RT, Aleman TS, Welch DL, Lillo C, Jacobson SG, Radu RA, Steel KP, Williams DS. The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65. Human Molecular Genetics. 20: 2560-70. PMID 21493626 DOI: 10.1093/Hmg/Ddr155  0.49
2010 Yang Z, Tong Z, Chen Y, Zeng J, Lu F, Sun X, Zhao C, Wang K, Davey L, Chen H, London N, Muramatsu D, Salasar F, Carmona R, Kasuga D, ... ... Gibbs D, et al. Genetic and functional dissection of HTRA1 and LOC387715 in age-related macular degeneration. Plos Genetics. 6: e1000836. PMID 20140183 DOI: 10.1371/Journal.Pgen.1000836  0.348
2010 Gibbs D, Diemer T, Khanobdee K, Hu J, Bok D, Williams DS. Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B. Investigative Ophthalmology & Visual Science. 51: 1130-5. PMID 19643958 DOI: 10.1167/Iovs.09-4032  0.456
2009 Schwander M, Lopes V, Sczaniecka A, Gibbs D, Lillo C, Delano D, Tarantino LM, Wiltshire T, Williams DS, Müller U. A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15810-8. PMID 20016096 DOI: 10.1523/Jneurosci.4876-09.2009  0.468
2009 Gibbs D, Cideciyan AV, Jacobson SG, Williams DS. Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence. Investigative Ophthalmology & Visual Science. 50: 4386-93. PMID 19324852 DOI: 10.1167/Iovs.09-3471  0.499
2008 Yang Z, Stratton C, Francis PJ, Kleinman ME, Tan PL, Gibbs D, Tong Z, Chen H, Constantine R, Yang X, Chen Y, Zeng J, Davey L, Ma X, Hau VS, et al. Toll-like receptor 3 and geographic atrophy in age-related macular degeneration. The New England Journal of Medicine. 359: 1456-63. PMID 18753640 DOI: 10.1056/Nejmoa0802437  0.359
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  0.466
2008 Yang X, Zabriskie NA, Hau VS, Chen H, Tong Z, Gibbs D, Farhi P, Katz BJ, Luo L, Pearson E, Goldsmith J, Ma X, Kaminoh Y, Chen Y, Yu B, et al. Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort. Cell Cycle (Georgetown, Tex.). 7: 521-4. PMID 18287813 DOI: 10.4161/Cc.7.4.5388  0.309
2008 Diemer T, Gibbs D, Williams DS. Analysis of the rate of disk membrane digestion by cultured RPE cells. Advances in Experimental Medicine and Biology. 613: 321-6. PMID 18188960 DOI: 10.1007/978-0-387-74904-4_37  0.376
2007 Shukla D, Rajendran A, Gibbs D, Suganthalakshmi B, Zhang K, Sundaresan P. Unusual manifestations of x-linked retinoschisis: clinical profile and diagnostic evaluation. American Journal of Ophthalmology. 144: 419-423. PMID 17631851 DOI: 10.1016/J.Ajo.2007.05.016  0.31
2007 Cameron DJ, Yang Z, Gibbs D, Chen H, Kaminoh Y, Jorgensen A, Zeng J, Luo L, Brinton E, Brinton G, Brand JM, Bernstein PS, Zabriskie NA, Tang S, Constantine R, et al. HTRA1 variant confers similar risks to geographic atrophy and neovascular age-related macular degeneration. Cell Cycle (Georgetown, Tex.). 6: 1122-5. PMID 17426452 DOI: 10.4161/Cc.6.9.4157  0.307
2007 Hashimoto T, Gibbs D, Lillo C, Azarian SM, Legacki E, Zhang XM, Yang XJ, Williams DS. Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B. Gene Therapy. 14: 584-94. PMID 17268537 DOI: 10.1038/sj.gt.3302897  0.45
2007 Hashimoto T, Groisberg R, Zhang X, Gibbs D, Lillo C, Azarian S, Williams D, Yang X. Development of lentiviral vectors for gene therapy for Usher syndrome type 1B Acta Ophthalmologica Scandinavica. 85: 0-0. DOI: 10.1111/J.1600-0420.2007.01062_3343.X  0.369
2006 Yang Z, Camp NJ, Sun H, Tong Z, Gibbs D, Cameron DJ, Chen H, Zhao Y, Pearson E, Li X, Chien J, Dewan A, Harmon J, Bernstein PS, Shridhar V, et al. A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science (New York, N.Y.). 314: 992-3. PMID 17053109 DOI: 10.1126/Science.1133811  0.363
2006 Azarian SM, McLeod I, Lillo C, Gibbs D, Yates JR, Williams DS. Proteomic analysis of mature melanosomes from the retinal pigmented epithelium. Journal of Proteome Research. 5: 521-9. PMID 16512666 DOI: 10.1021/Pr0502323  0.446
2005 Kitamoto J, Libby RT, Gibbs D, Steel KP, Williams DS. Myosin VI is required for normal retinal function. Experimental Eye Research. 81: 116-20. PMID 15978262 DOI: 10.1016/J.Exer.2005.02.014  0.503
2004 Gibbs D, Azarian SM, Lillo C, Kitamoto J, Klomp AE, Steel KP, Libby RT, Williams DS. Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes. Journal of Cell Science. 117: 6473-83. PMID 15572405 DOI: 10.1242/Jcs.01580  0.473
2003 Gibbs D, Williams DS. Isolation and culture of primary mouse retinal pigmented epithelial cells. Advances in Experimental Medicine and Biology. 533: 347-52. PMID 15180284 DOI: 10.1007/978-1-4615-0067-4_44  0.4
2003 Gibbs D, Kitamoto J, Williams DS. Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein. Proceedings of the National Academy of Sciences of the United States of America. 100: 6481-6. PMID 12743369 DOI: 10.1073/Pnas.1130432100  0.5
2002 Udovichenko IP, Gibbs D, Williams DS. Actin-based motor properties of native myosin VIIa. Journal of Cell Science. 115: 445-50. PMID 11839794  0.33
2001 Liovic M, Stojan J, Bowden PE, Gibbs D, Vahlquist A, Lane EB, Komel R. A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes. The Journal of Investigative Dermatology. 116: 964-9. PMID 11407988 DOI: 10.1046/J.1523-1747.2001.01334.X  0.481
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