Year |
Citation |
Score |
2019 |
Uytingco CR, Williams CL, Xie C, Shively DT, Green WW, Ukhanov K, Zhang L, Nishimura DY, Sheffield VC, Martens JR. BBS4 is required for IFT coordination and basal body number in mammalian olfactory cilia. Journal of Cell Science. PMID 30665891 DOI: 10.1242/Jcs.222331 |
0.369 |
|
2018 |
Jensen VL, Lambacher NJ, Li C, Mohan S, Williams CL, Inglis PN, Yoder BK, Blacque OE, Leroux MR. Role for intraflagellar transport in building a functional transition zone. Embo Reports. PMID 30429209 DOI: 10.15252/Embr.201845862 |
0.69 |
|
2017 |
Williams CL, Uytingco CR, Green WW, McIntyre JC, Ukhanov K, Zimmerman AD, Shively DT, Zhang L, Nishimura DY, Sheffield VC, Martens JR. Gene Therapeutic Reversal of Peripheral Olfactory Impairment in Bardet-Biedl Syndrome. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 28237838 DOI: 10.1016/J.Ymthe.2017.02.006 |
0.377 |
|
2016 |
Masyukova SV, Landis DE, Henke SJ, Williams CL, Pieczynski JN, Roszczynialski KN, Covington JE, Malarkey EB, Yoder BK. A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4. Plos Genetics. 12: e1005841. PMID 26863025 DOI: 10.1371/Journal.Pgen.1005841 |
0.672 |
|
2014 |
Williams CL, McIntyre JC, Norris SR, Jenkins PM, Zhang L, Pei Q, Verhey K, Martens JR. Direct evidence for BBSome-associated intraflagellar transport reveals distinct properties of native mammalian cilia. Nature Communications. 5: 5813. PMID 25504142 DOI: 10.1038/Ncomms6813 |
0.407 |
|
2013 |
McIntyre JC, Williams CL, Martens JR. Smelling the roses and seeing the light: gene therapy for ciliopathies. Trends in Biotechnology. 31: 355-63. PMID 23601268 DOI: 10.1016/J.Tibtech.2013.03.005 |
0.336 |
|
2012 |
McIntyre JC, Davis EE, Joiner A, Williams CL, Tsai IC, Jenkins PM, McEwen DP, Zhang L, Escobado J, Thomas S, Szymanska K, Johnson CA, Beales PL, Green ED, Mullikin JC, et al. Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model. Nature Medicine. 18: 1423-8. PMID 22941275 DOI: 10.1038/Nm.2860 |
0.652 |
|
2011 |
Masyukova SV, Winkelbauer ME, Williams CL, Pieczynski JN, Yoder BK. Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans. Human Molecular Genetics. 20: 2942-54. PMID 21546380 DOI: 10.1093/Hmg/Ddr198 |
0.693 |
|
2011 |
Williams CL, Li C, Kida K, Inglis PN, Mohan S, Semenec L, Bialas NJ, Stupay RM, Chen N, Blacque OE, Yoder BK, Leroux MR. MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis. The Journal of Cell Biology. 192: 1023-41. PMID 21422230 DOI: 10.1083/Jcb.201012116 |
0.692 |
|
2010 |
Williams CL, Masyukova SV, Yoder BK. Normal ciliogenesis requires synergy between the cystic kidney disease genes MKS-3 and NPHP-4. Journal of the American Society of Nephrology : Jasn. 21: 782-93. PMID 20150540 DOI: 10.1681/Asn.2009060597 |
0.697 |
|
2010 |
Williams CL, Winkelbauer ME, Leroux MR, Yoder BK. Restriction of access into the ciliary membrane requires MKS, NPHP, and BBS proteins F1000research. 1. DOI: 10.7490/F1000Research.68.1 |
0.676 |
|
2008 |
Williams CL, Winkelbauer ME, Schafer JC, Michaud EJ, Yoder BK. Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis. Molecular Biology of the Cell. 19: 2154-68. PMID 18337471 DOI: 10.1091/Mbc.E07-10-1070 |
0.675 |
|
2006 |
Schafer JC, Winkelbauer ME, Williams CL, Haycraft CJ, Desmond RA, Yoder BK. IFTA-2 is a conserved cilia protein involved in pathways regulating longevity and dauer formation in Caenorhabditis elegans. Journal of Cell Science. 119: 4088-100. PMID 16968739 DOI: 10.1242/Jcs.03187 |
0.628 |
|
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