| Year |
Citation |
Score |
| 2023 |
Landowski M, Bhute VJ, Grindel S, Haugstad Z, Gyening YK, Tytanic M, Brush RS, Moyer LJ, Nelson DW, Davis CR, Yen CE, Ikeda S, Agbaga MP, Ikeda A. Transmembrane protein 135 regulates lipid homeostasis through its role in peroxisomal DHA metabolism. Communications Biology. 6: 8. PMID 36599953 DOI: 10.1038/s42003-022-04404-7 |
0.711 |
|
| 2022 |
Landowski M, Bhute VJ, Takimoto T, Grindel S, Shahi PK, Pattnaik BR, Ikeda S, Ikeda A. A mutation in transmembrane protein 135 impairs lipid metabolism in mouse eyecups. Scientific Reports. 12: 756. PMID 35031662 DOI: 10.1038/s41598-021-04644-3 |
0.718 |
|
| 2020 |
Lee WH, Bhute VJ, Higuchi H, Ikeda S, Palecek SP, Ikeda A. Metabolic alterations caused by the mutation and overexpression of the gene. Experimental Biology and Medicine (Maywood, N.J.). 1535370220932856. PMID 32515224 DOI: 10.1177/1535370220932856 |
0.702 |
|
| 2019 |
Macke EL, Henningsen E, Jessen E, Zumwalde NA, Landowski M, Western DE, Lee WH, Liu C, Gruenke NP, Doebley AL, Miller S, Pattnaik B, Ikeda S, Gumperz JE, Ikeda A. Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in Mice. Genetics. PMID 31754016 DOI: 10.1534/Genetics.119.302834 |
0.436 |
|
| 2018 |
Lewis SA, Takimoto T, Mehrvar S, Higuchi H, Doebley AL, Stokes G, Sheibani N, Ikeda S, Ranji M, Ikeda A. The effect of Tmem135 overexpression on the mouse heart. Plos One. 13: e0201986. PMID 30102730 DOI: 10.1371/Journal.Pone.0201986 |
0.384 |
|
| 2017 |
Bhute VJ, Bao X, Dunn KK, Knutson KR, McCurry EC, Jin G, Lee WH, Lewis S, Ikeda A, Palecek SP. Metabolomics Identifies Metabolic Markers of Maturation in Human Pluripotent Stem Cell-Derived Cardiomyocytes. Theranostics. 7: 2078-2091. PMID 28656061 DOI: 10.7150/Thno.19390 |
0.684 |
|
| 2016 |
Lee WH, Higuchi H, Ikeda S, Macke EL, Takimoto T, Pattnaik BR, Liu C, Chu LF, Siepka SM, Krentz KJ, Rubinstein CD, Kalejta RF, Thomson JA, Mullins RF, Takahashi JS, ... ... Ikeda A, et al. Mouse Tmem135 mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies. Elife. 5. PMID 27863209 DOI: 10.7554/Elife.19264 |
0.372 |
|
| 2016 |
Hines EA, Verheyden JM, Lashua AJ, Larson SC, Branchfield K, Domyan ET, Gao J, Harvey JF, Herriges JC, Hu L, McCulley DJ, Throckmorton K, Yokoyama S, Ikeda A, Xu G, et al. Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 26813283 DOI: 10.1002/Dvdy.24389 |
0.384 |
|
| 2016 |
Lee W, Higuchi H, Ikeda S, Macke EL, Takimoto T, Pattnaik BR, Liu C, Chu L, Siepka SM, Krentz KJ, Rubinstein CD, Kalejta RF, Thomson JA, Mullins RF, Takahashi JS, ... ... Ikeda A, et al. Author response: Mouse Tmem135 mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies Elife. DOI: 10.7554/Elife.19264.020 |
0.362 |
|
| 2015 |
Maddox DM, Collin GB, Ikeda A, Pratt CH, Ikeda S, Johnson BA, Hurd RE, Shopland LS, Naggert JK, Chang B, Krebs MP, Nishina PM. A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia. Investigative Ophthalmology & Visual Science. 56: 3776-87. PMID 26066746 DOI: 10.1167/Iovs.14-16047 |
0.354 |
|
| 2015 |
Narayanan P, Chatterton P, Ikeda A, Ikeda S, Corey DP, Ervasti JM, Perrin BJ. Length regulation of mechanosensitive stereocilia depends on very slow actin dynamics and filament-severing proteins. Nature Communications. 6: 6855. PMID 25897778 DOI: 10.1038/Ncomms7855 |
0.334 |
|
| 2015 |
Higuchi H, Macke EL, Lee WH, Miller SA, Xu JC, Ikeda S, Ikeda A. Genetic basis of age-dependent synaptic abnormalities in the retina. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 26: 21-32. PMID 25273269 DOI: 10.1007/S00335-014-9546-7 |
0.354 |
|
| 2014 |
Kawakami-Schulz SV, Verdoni AM, Sattler SG, Jessen E, Kao WW, Ikeda A, Ikeda S. Serum response factor: positive and negative regulation of an epithelial gene expression network in the destrin mutant cornea. Physiological Genomics. 46: 277-89. PMID 24550211 DOI: 10.1152/Physiolgenomics.00126.2013 |
0.748 |
|
| 2013 |
Kawakami-Schulz SV, Sattler SG, Doebley AL, Ikeda A, Ikeda S. Genetic modification of corneal neovascularization in Dstn (corn1) mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 349-57. PMID 23929036 DOI: 10.1007/S00335-013-9468-9 |
0.387 |
|
| 2012 |
Kawakami-Schulz SV, Verdoni AM, Sattler SG, Ikeda A, Ikeda S. Differences in corneal phenotypes between destrin mutants are due to allelic difference and modified by genetic background. Molecular Vision. 18: 606-16. PMID 22419854 |
0.711 |
|
| 2012 |
Maddox DM, Ikeda S, Ikeda A, Zhang W, Krebs MP, Nishina PM, Naggert JK. An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice. Investigative Ophthalmology & Visual Science. 53: 1663-9. PMID 22323461 DOI: 10.1167/Iovs.11-8871 |
0.401 |
|
| 2011 |
Griep AE, John MC, Ikeda S, Ikeda A. Gene targeting in the mouse. Methods in Molecular Biology (Clifton, N.J.). 770: 293-312. PMID 21805269 DOI: 10.1007/978-1-61779-210-6_11 |
0.37 |
|
| 2010 |
Johnson BA, Cole BS, Geisert EE, Ikeda S, Ikeda A. Tyrosinase is the modifier of retinoschisis in mice. Genetics. 186: 1337-44. PMID 20876567 DOI: 10.1534/Genetics.110.120840 |
0.435 |
|
| 2010 |
Verdoni AM, Schuster KJ, Cole BS, Ikeda A, Kao WW, Ikeda S. A pathogenic relationship between a regulator of the actin cytoskeleton and serum response factor. Genetics. 186: 147-57. PMID 20610412 DOI: 10.1534/Genetics.110.117309 |
0.74 |
|
| 2010 |
Xu X, Kedlaya R, Higuchi H, Ikeda S, Justice MJ, Setaluri V, Ikeda A. Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration. Plos Genetics. 6: e1000956. PMID 20502676 DOI: 10.1371/Journal.Pgen.1000956 |
0.657 |
|
| 2010 |
Verdoni AM, Ikeda S, Ikeda A. Serum response factor is essential for the proper development of skin epithelium. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 64-76. PMID 20047077 DOI: 10.1007/S00335-009-9245-Y |
0.72 |
|
| 2008 |
Verdoni AM, Smith RS, Ikeda A, Ikeda S. Defects in actin dynamics lead to an autoinflammatory condition through the upregulation of CXCL5. Plos One. 3: e2701. PMID 18628996 DOI: 10.1371/Journal.Pone.0002701 |
0.736 |
|
| 2008 |
Verdoni AM, Aoyama N, Ikeda A, Ikeda S. Effect of destrin mutations on the gene expression profile in vivo. Physiological Genomics. 34: 9-21. PMID 18381839 DOI: 10.1152/Physiolgenomics.00285.2007 |
0.747 |
|
| 2008 |
Haider NB, Zhang W, Hurd R, Ikeda A, Nystuen AM, Naggert JK, Nishina PM. Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 145-54. PMID 18286335 DOI: 10.1007/S00335-008-9092-2 |
0.385 |
|
| 2008 |
Johnson BA, Aoyama N, Friedell NH, Ikeda S, Ikeda A. Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisis. Genetics. 178: 1785-94. PMID 18245825 DOI: 10.1534/Genetics.107.084905 |
0.358 |
|
| 2007 |
Hirasawa M, Xu X, Trask RB, Maddatu TP, Johnson BA, Naggert JK, Nishina PM, Ikeda A. Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum. Molecular and Cellular Neurosciences. 35: 161-70. PMID 17376701 DOI: 10.1016/J.Mcn.2007.02.013 |
0.604 |
|
| 2006 |
Johnson BA, Ikeda S, Pinto LH, Ikeda A. Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene. Visual Neuroscience. 23: 887-98. PMID 17266781 DOI: 10.1017/S0952523806230244 |
0.334 |
|
| 2006 |
Chang B, Heckenlively JR, Bayley PR, Brecha NC, Davisson MT, Hawes NL, Hirano AA, Hurd RE, Ikeda A, Johnson BA, McCall MA, Morgans CW, Nusinowitz S, Peachey NS, Rice DS, et al. The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Visual Neuroscience. 23: 11-24. PMID 16597347 DOI: 10.1017/S095252380623102X |
0.4 |
|
| 2005 |
Cursiefen C, Ikeda S, Nishina PM, Smith RS, Ikeda A, Jackson D, Mo JS, Chen L, Dana MR, Pytowski B, Kruse FE, Streilein JW. Spontaneous corneal hem- and lymphangiogenesis in mice with destrin-mutation depend on VEGFR3 signaling. The American Journal of Pathology. 166: 1367-77. PMID 15855638 DOI: 10.1016/S0002-9440(10)62355-3 |
0.375 |
|
| 2003 |
Ikeda S, Ikeda A, Naggert JK, Nishina PM. Towards understanding the function of the tubby gene family in the retina. Advances in Experimental Medicine and Biology. 533: 309-14. PMID 15180278 DOI: 10.1007/978-1-4615-0067-4_38 |
0.319 |
|
| 2002 |
Ikeda A, Naggert JK, Nishina PM. Genetic modification of retinal degeneration in tubby mice. Experimental Eye Research. 74: 455-61. PMID 12076089 DOI: 10.1006/Exer.2001.1139 |
0.374 |
|
| 2002 |
Haider NB, Ikeda A, Naggert JK, Nishina PM. Genetic modifiers of vision and hearing. Human Molecular Genetics. 11: 1195-206. PMID 12015279 DOI: 10.1093/Hmg/11.10.1195 |
0.405 |
|
| 2002 |
Collin GB, Marshall JD, Ikeda A, So WV, Russell-Eggitt I, Maffei P, Beck S, Boerkoel CF, Sicolo N, Martin M, Nishina PM, Naggert JK. Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome. Nature Genetics. 31: 74-8. PMID 11941369 DOI: 10.1038/Ng867 |
0.344 |
|
| 2002 |
Ikeda A, Zheng QY, Zuberi AR, Johnson KR, Naggert JK, Nishina PM. Microtubule-associated protein 1A is a modifier of tubby hearing (moth1). Nature Genetics. 30: 401-5. PMID 11925566 DOI: 10.1038/Ng838 |
0.386 |
|
| 2001 |
Ikeda A, Ikeda S, Gridley T, Nishina PM, Naggert JK. Neural tube defects and neuroepithelial cell death in Tulp3 knockout mice. Human Molecular Genetics. 10: 1325-34. PMID 11406614 DOI: 10.1093/Hmg/10.12.1325 |
0.391 |
|
| 2000 |
Ikeda S, Shiva N, Ikeda A, Smith RS, Nusinowitz S, Yan G, Lin TR, Chu S, Heckenlively JR, North MA, Naggert JK, Nishina PM, Duyao MP. Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene. Human Molecular Genetics. 9: 155-63. PMID 10607826 DOI: 10.1093/Hmg/9.2.155 |
0.417 |
|
| 1999 |
Kanda M, Shindo K, Xu X, Fujiwara N, Ikeda A, Nagamine T, Shibasaki H. Cortical mechanisms underlying point localization of pain spot as studied by event-related potentials following CO2 laser stimulation in man. Experimental Brain Research. 127: 131-40. PMID 10442404 |
0.553 |
|
| 1999 |
Ikeda A, Zheng QY, Rosenstiel P, Maddatu T, Zuberi AR, Roopenian DC, North MA, Naggert JK, Johnson KR, Nishina PM. Genetic modification of hearing in tubby mice: Evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss Human Molecular Genetics. 8: 1761-1767. PMID 10441341 DOI: 10.1093/Hmg/8.9.1761 |
0.41 |
|
| 1998 |
Nishina PM, North MA, Ikeda A, Yan Y, Naggert JK. Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans Genomics. 54: 215-220. PMID 9828123 DOI: 10.1006/Geno.1998.5567 |
0.311 |
|
| 1997 |
Lai C, Ikeda A, Terada K, Nagamine T, Honda M, Xu X, Yoshimura N, Howng S, Barrett G, Shibasaki H. Event-related potentials associated with judgment: comparison of S1- and S2-choice conditions in a contingent negative variation (CNV) paradigm. Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society. 14: 394-405. PMID 9415386 |
0.518 |
|
| 1996 |
Kanda M, Mima T, Xu X, Fujiwara N, Shindo K, Nagamine T, Ikeda A, Shibasaki H. Pain-related somatosensory evoked potentials can quantitatively evaluate hypalgesia in Wallenberg's syndrome. Acta Neurologica Scandinavica. 94: 131-6. PMID 8891059 |
0.55 |
|
| 1996 |
Kanda M, Fujiwara N, Xu X, Shindo K, Nagamine T, Ikeda A, Shibasaki H. Pain-related and cognitive components of somatosensory evoked potentials following CO2 laser stimulation in man. Electroencephalography and Clinical Neurophysiology. 100: 105-14. PMID 8617149 |
0.547 |
|
| 1995 |
Ikeda A, Shibasaki H, Nagamine T, Xu X, Terada K, Mima T, Kaji R, Kawai I, Tatsuoka Y, Kimura J. Peri-rolandic and fronto-parietal components of scalp-recorded giant SEPs in cortical myoclonus. Electroencephalography and Clinical Neurophysiology. 96: 300-9. PMID 7635075 DOI: 10.1016/0168-5597(95)00003-B |
0.528 |
|
| 1995 |
Xu X, Kanda M, Shindo K, Fujiwara N, Nagamine T, Ikeda A, Honda M, Tachibana N, Barrett G, Kaji R. Pain-related somatosensory evoked potentials following CO2 laser stimulation of foot in man. Electroencephalography and Clinical Neurophysiology. 96: 12-23. PMID 7530185 |
0.542 |
|
| 1994 |
Miyazaki M, Shibasaki H, Kanda M, Xu X, Shindo K, Honda M, Ikeda A, Nagamine T, Kaji R, Kimura J. Generator mechanism of pain-related evoked potentials following CO2 laser stimulation of the hand: scalp topography and effect of predictive warning signal. Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society. 11: 242-54. PMID 8051309 DOI: 10.1097/00004691-199403000-00010 |
0.561 |
|
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