| Year |
Citation |
Score |
| 2019 |
Lee MS, Philippe J, Katsanis N, Zhou W. Polyketide Synthase Plays a Conserved Role in Otolith Formation. Zebrafish. PMID 31188077 DOI: 10.1089/Zeb.2019.1734 |
0.409 |
|
| 2018 |
Reichold M, Klootwijk ED, Reinders J, Otto EA, Milani M, Broeker C, Laing C, Wiesner J, Devi S, Zhou W, Schmitt R, Tegtmeier I, Sterner C, Doellerer H, Renner K, et al. Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. Journal of the American Society of Nephrology : Jasn. PMID 29654216 DOI: 10.1681/Asn.2017111179 |
0.3 |
|
| 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 |
0.446 |
|
| 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 |
0.447 |
|
| 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 |
0.459 |
|
| 2015 |
Wan X, Chen Z, Choi WI, Gee HY, Hildebrandt F, Zhou W. Loss of Epithelial Membrane Protein 2 Aggravates Podocyte Injury via Upregulation of Caveolin-1. Journal of the American Society of Nephrology : Jasn. PMID 26264854 DOI: 10.1681/Asn.2014121197 |
0.318 |
|
| 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 |
0.35 |
|
| 2015 |
Lee MS, Hwang KS, Oh HW, Ji-Ae K, Kim HT, Cho HS, Lee JJ, Yeong Ko J, Choi JH, Jeong YM, You KH, Kim J, Park DS, Nam KH, Aizawa S, ... ... Zhou W, et al. IFT46 plays an essential role in cilia development. Developmental Biology. 400: 248-57. PMID 25722189 DOI: 10.1016/J.Ydbio.2015.02.009 |
0.336 |
|
| 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 |
0.754 |
|
| 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 |
0.326 |
|
| 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 |
0.32 |
|
| 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 |
0.375 |
|
| 2013 |
Ashraf S, Gee HY, Woerner S, Xie LX, Vega-Warner V, Lovric S, Fang H, Song X, Cattran DC, Avila-Casado C, Paterson AD, Nitschké P, Bole-Feysot C, Cochat P, Esteve-Rudd J, ... ... Zhou W, et al. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. The Journal of Clinical Investigation. 123: 5179-89. PMID 24270420 DOI: 10.1172/Jci69000 |
0.374 |
|
| 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 |
0.383 |
|
| 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 |
0.387 |
|
| 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 |
0.313 |
|
| 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 |
0.751 |
|
| 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 |
0.391 |
|
| 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 |
0.381 |
|
| 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 |
0.307 |
|
| 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 |
0.305 |
|
| 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 |
0.316 |
|
| 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 |
0.78 |
|
| 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 |
0.732 |
|
| 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 |
0.326 |
|
| 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 |
0.325 |
|
| 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 |
0.313 |
|
| 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 |
0.761 |
|
| 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 |
0.342 |
|
| 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 |
0.776 |
|
| 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 |
0.352 |
|
| 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 |
0.323 |
|
| 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 |
0.31 |
|
| 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 |
0.358 |
|
| 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 |
0.317 |
|
| 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 |
0.305 |
|
| 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 |
0.753 |
|
| 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 |
0.336 |
|
| 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 |
0.795 |
|
| 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 |
0.809 |
|
| 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 |
0.345 |
|
| 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 |
0.611 |
|
| 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 |
0.815 |
|
| 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 |
0.813 |
|
| 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 |
0.794 |
|
| 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 DOI: 10.1523/Jneurosci.23-10-04190.2003 |
0.755 |
|
| 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 |
0.608 |
|
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