Weibin Zhou, Ph.D. - Publications

Affiliations: 
2006 University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Neuroscience

54 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
2017 Hosono Y, Niknafs YS, Prensner JR, Iyer MK, Dhanasekaran SM, Mehra R, Pitchiaya S, Tien J, Escara-Wilke J, Poliakov A, Chu SC, Saleh S, Sankar K, Su F, Guo S, ... ... Zhou W, et al. Oncogenic Role of THOR, a Conserved Cancer/Testis Long Non-coding RNA. Cell. 171: 1559-1572.e20. PMID 29245011 DOI: 10.1016/j.cell.2017.11.040  0.6
2016 Tao ZS, Zhou WS, He XW, Liu W, Bai BL, Zhou Q, Huang ZL, Tu KK, Li H, Sun T, Lv YX, Cui W, Yang L. A comparative study of zinc, magnesium, strontium-incorporated hydroxyapatite-coated titanium implants for osseointegration of osteopenic rats Materials Science and Engineering C. 62: 226-232. DOI: 10.1016/j.msec.2016.01.034  0.48
2016 Yang L, Zhou W, Ma Y, Li X, Liang Y, Cui W, Wu P. Effects of Ni addition on mechanical properties of Sn58Bi solder alloy during solid-state aging Materials Science and Engineering A. 667: 368-375. DOI: 10.1016/j.msea.2016.05.015  0.48
2015 Tao ZS, Zhou WS, Tu KK, Huang ZL, Zhou Q, Sun T, Lv YX, Cui W, Yang L. Treatment study of distal femur for parathyroid hormone (1-34) and β-tricalcium phosphate on bone formation in critical-sized defects in osteopenic rats. Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association For Cranio-Maxillo-Facial Surgery. PMID 26507646 DOI: 10.1016/j.jcms.2015.09.004  0.48
2015 Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Zhang XC, Shen XJ, Li Q, Deng LQ, Dong JH, Lin WQ, Huang P, Jiang WJ, Lv J, Han J, et al. The Features of Genetic Prion Diseases Based on Chinese Surveillance Program. Plos One. 10: e0139552. PMID 26488179 DOI: 10.1371/journal.pone.0139552  0.68
2015 Tao ZS, Zhou WS, Qiang Z, Tu KK, Huang ZL, Xu HM, Sun T, Lv YX, Cui W, Yang L. Intermittent administration of human parathyroid hormone (1-34) increases fixation of strontium-doped hydroxyapatite coating titanium implants via electrochemical deposition in ovariectomized rat femur. Journal of Biomaterials Applications. PMID 26482573 DOI: 10.1177/0885328215610898  0.48
2015 Zhao M, Wan X, Li Y, Zhou W, Peng L. Multiplexed 3D FRET imaging in deep tissue of live embryos. Scientific Reports. 5: 13991. PMID 26387920 DOI: 10.1038/srep13991  0.72
2015 Gee HY, Zhang F, Ashraf S, Kohl S, Sadowski CE, Vega-Warner V, Zhou W, Lovric S, Fang H, Nettleton M, Zhu JY, Hoefele J, Weber LT, Podracka L, Boor A, et al. KANK deficiency leads to podocyte dysfunction and nephrotic syndrome. The Journal of Clinical Investigation. 125: 2375-84. PMID 25961457 DOI: 10.1172/JCI79504  0.72
2015 Ogino K, Low SE, Yamada K, Saint-Amant L, Zhou W, Muto A, Asakawa K, Nakai J, Kawakami K, Kuwada JY, Hirata H. RING finger protein 121 facilitates the degradation and membrane localization of voltage-gated sodium channels. Proceedings of the National Academy of Sciences of the United States of America. 112: 2859-64. PMID 25691753 DOI: 10.1073/pnas.1414002112  0.72
2015 Schueler M, Braun DA, Chandrasekar G, Gee HY, Klasson TD, Halbritter J, Bieder A, Porath JD, Airik R, Zhou W, LoTurco JJ, Che A, Otto EA, Böckenhauer D, Sebire NJ, et al. DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. American Journal of Human Genetics. 96: 81-92. PMID 25557784 DOI: 10.1016/j.ajhg.2014.12.002  0.72
2014 Huang L, Xiao A, Wecker A, McBride DA, Choi SY, Zhou W, Lipschutz JH. A possible zebrafish model of polycystic kidney disease: knockdown of wnt5a causes cysts in zebrafish kidneys. Journal of Visualized Experiments : Jove. PMID 25489842 DOI: 10.3791/52156  0.72
2014 Huang L, Xiao A, Choi SY, Kan Q, Zhou W, Chacon-Heszele MF, Ryu YK, McKenna S, Zuo X, Kuruvilla R, Lipschutz JH. Wnt5a is necessary for normal kidney development in zebrafish and mice. Nephron. Experimental Nephrology. 128: 80-8. PMID 25412793 DOI: 10.1159/000368411  0.72
2014 Zhao M, Zhang H, Li Y, Ashok A, Liang R, Zhou W, Peng L. Cellular imaging of deep organ using two-photon Bessel light-sheet nonlinear structured illumination microscopy. Biomedical Optics Express. 5: 1296-308. PMID 24876996 DOI: 10.1364/BOE.5.001296  0.72
2014 Gee HY, Ashraf S, Wan X, Vega-Warner V, Esteve-Rudd J, Lovric S, Fang H, Hurd TW, Sadowski CE, Allen SJ, Otto EA, Korkmaz E, Washburn J, Levy S, Williams DS, ... ... Zhou W, et al. Mutations in EMP2 cause childhood-onset nephrotic syndrome. American Journal of Human Genetics. 94: 884-90. PMID 24814193 DOI: 10.1016/j.ajhg.2014.04.010  0.72
2014 Gee HY, Otto EA, Hurd TW, Ashraf S, Chaki M, Cluckey A, Vega-Warner V, Saisawat P, Diaz KA, Fang H, Kohl S, Allen SJ, Airik R, Zhou W, Ramaswami G, et al. Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies. Kidney International. 85: 880-7. PMID 24257694 DOI: 10.1038/ki.2013.450  0.72
2014 Boucher RC, Zhou W. Zebrafish models of podocytopathies Podocytopathy. 183: 224-234. DOI: 10.1159/000360119  0.72
2013 Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, ... ... Zhou W, et al. ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. American Journal of Human Genetics. 93: 336-45. PMID 23891469 DOI: 10.1016/j.ajhg.2013.06.007  0.72
2013 Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, et al. ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling. The Journal of Clinical Investigation. 123: 3243-53. PMID 23867502 DOI: 10.1172/JCI69134  0.72
2013 Miller DL, Zhou W. A system for investigation of biological effects of diagnostic ultrasound on development of zebrafish embryos. Zebrafish. 10: 459-65. PMID 23848997 DOI: 10.1089/zeb.2013.0883  0.72
2013 Horstick EJ, Linsley JW, Dowling JJ, Hauser MA, McDonald KK, Ashley-Koch A, Saint-Amant L, Satish A, Cui WW, Zhou W, Sprague SM, Stamm DS, Powell CM, Speer MC, Franzini-Armstrong C, et al. Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy. Nature Communications. 4: 1952. PMID 23736855 DOI: 10.1038/ncomms2952  0.72
2013 Arif E, Kumari B, Wagner MC, Zhou W, Holzman LB, Nihalani D. Myo1c is an unconventional myosin required for zebrafish glomerular development. Kidney International. 84: 1154-65. PMID 23715127 DOI: 10.1038/ki.2013.201  0.72
2013 Hurd TW, Otto EA, Mishima E, Gee HY, Inoue H, Inazu M, Yamada H, Halbritter J, Seki G, Konishi M, Zhou W, Yamane T, Murakami S, Caridi G, Ghiggeri G, et al. Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype. Journal of the American Society of Nephrology : Jasn. 24: 967-77. PMID 23661805 DOI: 10.1681/ASN.2012101034  0.72
2013 Zhao M, Zhou W, Peng L. Parallel multi-color fluorescence lifetime tomography in deep tissue Bio-Optics: Design and Application, Boda 2013. BM4A.4.  0.72
2012 Chaki M, Airik R, Ghosh AK, Giles RH, Chen R, Slaats GG, Wang H, Hurd TW, Zhou W, Cluckey A, Gee HY, Ramaswami G, Hong CJ, Hamilton BA, Cervenka I, et al. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell. 150: 533-48. PMID 22863007 DOI: 10.1016/j.cell.2012.06.028  0.72
2012 Zhou W, Otto EA, Cluckey A, Airik R, Hurd TW, Chaki M, Diaz K, Lach FP, Bennett GR, Gee HY, Ghosh AK, Natarajan S, Thongthip S, Veturi U, Allen SJ, et al. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair. Nature Genetics. 44: 910-5. PMID 22772369 DOI: 10.1038/ng.2347  0.72
2012 Zhou W, Hildebrandt F. Inducible podocyte injury and proteinuria in transgenic zebrafish. Journal of the American Society of Nephrology : Jasn. 23: 1039-47. PMID 22440901 DOI: 10.1681/ASN.2011080776  0.72
2012 Hirata H, Wen H, Kawakami Y, Naganawa Y, Ogino K, Yamada K, Saint-Amant L, Low SE, Cui WW, Zhou W, Sprague SM, Asakawa K, Muto A, Kawakami K, Kuwada JY. Connexin 39.9 protein is necessary for coordinated activation of slow-twitch muscle and normal behavior in zebrafish. The Journal of Biological Chemistry. 287: 1080-9. PMID 22075003 DOI: 10.1074/jbc.M111.308205  0.72
2012 Zhao M, Zhou W, Peng L. Multi-Color in vivo fluorescence lifetime tomography Biomedical Optics, Biomed 2012. JM3A.71.  0.72
2011 Low SE, Amburgey K, Horstick E, Linsley J, Sprague SM, Cui WW, Zhou W, Hirata H, Saint-Amant L, Hume RI, Kuwada JY. TRPM7 is required within zebrafish sensory neurons for the activation of touch-evoked escape behaviors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 11633-44. PMID 21832193 DOI: 10.1523/JNEUROSCI.4950-10.2011  0.72
2011 Otto EA, Ramaswami G, Janssen S, Chaki M, Allen SJ, Zhou W, Airik R, Hurd TW, Ghosh AK, Wolf MT, Hoppe B, Neuhaus TJ, Bockenhauer D, Milford DV, Soliman NA, et al. Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy. Journal of Medical Genetics. 48: 105-16. PMID 21068128 DOI: 10.1136/jmg.2010.082552  0.72
2010 Otto EA, Hurd TW, Airik R, Chaki M, Zhou W, Stoetzel C, Patil SB, Levy S, Ghosh AK, Murga-Zamalloa CA, van Reeuwijk J, Letteboer SJ, Sang L, Giles RH, Liu Q, et al. Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. Nature Genetics. 42: 840-50. PMID 20835237 DOI: 10.1038/ng.662  0.72
2010 Zhou W, Boucher RC, Bollig F, Englert C, Hildebrandt F. Characterization of mesonephric development and regeneration using transgenic zebrafish. American Journal of Physiology. Renal Physiology. 299: F1040-7. PMID 20810610 DOI: 10.1152/ajprenal.00394.2010  0.72
2010 Hurd T, Zhou W, Jenkins P, Liu CJ, Swaroop A, Khanna H, Martens J, Hildebrandt F, Margolis B. The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development. Human Molecular Genetics. 19: 4330-44. PMID 20729296 DOI: 10.1093/hmg/ddq355  0.72
2010 Low SE, Ryan J, Sprague SM, Hirata H, Cui WW, Zhou W, Hume RI, Kuwada JY, Saint-Amant L. touché Is required for touch-evoked generator potentials within vertebrate sensory neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 9359-67. PMID 20631165 DOI: 10.1523/JNEUROSCI.1639-10.2010  0.72
2010 Zhou W, Dai J, Attanasio M, Hildebrandt F. Nephrocystin-3 is required for ciliary function in zebrafish embryos. American Journal of Physiology. Renal Physiology. 299: F55-62. PMID 20462968 DOI: 10.1152/ajprenal.00043.2010  0.72
2010 Low SE, Zhou W, Choong I, Saint-Amant L, Sprague SM, Hirata H, Cui WW, Hume RI, Kuwada JY. Na(v)1.6a is required for normal activation of motor circuits normally excited by tactile stimulation. Developmental Neurobiology. 70: 508-22. PMID 20225246 DOI: 10.1002/dneu.20791  0.72
2010 O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA, Seelow D, Nurnberg G, Becker C, Nuutinen M, Kärppä M, Ignatius J, Uusimaa J, Pakanen S, Jaakkola E, ... ... Zhou W, et al. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy. The Journal of Clinical Investigation. 120: 791-802. PMID 20179356 DOI: 10.1172/JCI40076  0.72
2010 Harville HM, Held S, Diaz-Font A, Davis EE, Diplas BH, Lewis RA, Borochowitz ZU, Zhou W, Chaki M, MacDonald J, Kayserili H, Beales PL, Katsanis N, Otto E, Hildebrandt F. Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mapping. Journal of Medical Genetics. 47: 262-7. PMID 19797195 DOI: 10.1136/jmg.2009.071365  0.72
2010 O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA, Seelow D, Nurnberg G, Becker C, Nuutinen M, Kärppä M, Ignatius J, Uusimaa J, Pakanen S, Jaakkola E, ... ... Zhou W, et al. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076) Journal of Clinical Investigation. 120: 1362. DOI: 10.1172/JCI40076C1  0.72
2009 Otto EA, Tory K, Attanasio M, Zhou W, Chaki M, Paruchuri Y, Wise EL, Wolf MT, Utsch B, Becker C, Nürnberg G, Nürnberg P, Nayir A, Saunier S, Antignac C, et al. Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). Journal of Medical Genetics. 46: 663-70. PMID 19508969 DOI: 10.1136/jmg.2009.066613  0.72
2009 Zhou W, Hildebrandt F. Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish. Gene Expression Patterns : Gep. 9: 282-8. PMID 19332147 DOI: 10.1016/j.gep.2009.03.003  0.72
2009 He C, Bartholomew CR, Zhou W, Klionsky DJ. Assaying autophagic activity in transgenic GFP-Lc3 and GFP-Gabarap zebrafish embryos. Autophagy. 5: 520-6. PMID 19221467 DOI: 10.4161/auto.5.4.7768  0.72
2009 Hildebrandt F, Heeringa SF, Rüschendorf F, Attanasio M, Nürnberg G, Becker C, Seelow D, Huebner N, Chernin G, Vlangos CN, Zhou W, O'Toole JF, Hoskins BE, Wolf MT, Hinkes BG, et al. A systematic approach to mapping recessive disease genes in individuals from outbred populations. Plos Genetics. 5: e1000353. PMID 19165332 DOI: 10.1371/journal.pgen.1000353  0.72
2008 Zhou W, Horstick EJ, Hirata H, Kuwada JY. Identification and expression of voltage-gated calcium channel beta subunits in Zebrafish. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 3842-52. PMID 19035348 DOI: 10.1002/dvdy.21776  0.72
2008 Otto EA, Helou J, Allen SJ, O'Toole JF, Wise EL, Ashraf S, Attanasio M, Zhou W, Wolf MT, Hildebrandt F. Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing. Human Mutation. 29: 418-26. PMID 18076122 DOI: 10.1002/humu.20669  0.72
2008 Saint-Amant L, Sprague SM, Hirata H, Li Q, Cui WW, Zhou W, Poudou O, Hume RI, Kuwada JY. The zebrafish ennui behavioral mutation disrupts acetylcholine receptor localization and motor axon stability. Developmental Neurobiology. 68: 45-61. PMID 17918238 DOI: 10.1002/dneu.20569  0.72
2007 Hirata H, Watanabe T, Hatakeyama J, Sprague SM, Saint-Amant L, Nagashima A, Cui WW, Zhou W, Kuwada JY. Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease. Development (Cambridge, England). 134: 2771-81. PMID 17596281 DOI: 10.1242/dev.004531  0.72
2007 Hildebrandt F, Zhou W. Nephronophthisis-associated ciliopathies. Journal of the American Society of Nephrology : Jasn. 18: 1855-71. PMID 17513324 DOI: 10.1681/ASN.2006121344  0.72
2006 Zhou W, Shirabe K, Kuwada JY. Molecular cloning and expression of two small leucine-rich proteoglycan (SLRP) genes, dspg3l and optcl, in zebrafish. Gene Expression Patterns : Gep. 6: 482-8. PMID 16458084 DOI: 10.1016/j.modgep.2005.11.003  0.72
2006 Zhou W, Saint-Amant L, Hirata H, Cui WW, Sprague SM, Kuwada JY. Non-sense mutations in the dihydropyridine receptor beta1 gene, CACNB1, paralyze zebrafish relaxed mutants. Cell Calcium. 39: 227-36. PMID 16368137 DOI: 10.1016/j.ceca.2005.10.015  0.72
2005 Hirata H, Saint-Amant L, Downes GB, Cui WW, Zhou W, Granato M, Kuwada JY. Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor beta-subunit. Proceedings of the National Academy of Sciences of the United States of America. 102: 8345-50. PMID 15928085 DOI: 10.1073/pnas.0500862102  0.72
2004 Hirata H, Saint-Amant L, Waterbury J, Cui W, Zhou W, Li Q, Goldman D, Granato M, Kuwada JY. accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1. Development (Cambridge, England). 131: 5457-68. PMID 15469975 DOI: 10.1242/dev.01410  0.72
2003 Xiao T, Shoji W, Zhou W, Su F, Kuwada JY. Transmembrane sema4E guides branchiomotor axons to their targets in zebrafish. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4190-8. PMID 12764107  0.72
2003 Masumoto J, Zhou W, Chen FF, Su F, Kuwada JY, Hidaka E, Katsuyama T, Sagara J, Taniguchi S, Ngo-Hazelett P, Postlethwait JH, Núñez G, Inohara N. Caspy, a zebrafish caspase, activated by ASC oligomerization is required for pharyngeal arch development. The Journal of Biological Chemistry. 278: 4268-76. PMID 12464617 DOI: 10.1074/jbc.M203944200  0.72
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