Corey L. Williams, Ph.D. - Publications

2009 Cell Biology University of Alabama, Birmingham, Birmingham, AL, United States 
Molecular Biology, Genetics

10 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
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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