| Year |
Citation |
Score |
| 2023 |
Clearman KR, Haycraft CJ, Croyle MJ, Collawn JF, Yoder BK. Functions of the primary cilium in the kidney and its connection with renal diseases. Current Topics in Developmental Biology. 155: 39-94. PMID 38043952 DOI: 10.1016/bs.ctdb.2023.07.001 |
0.71 |
|
| 2023 |
Clearman KR, Timpratoom N, Patel D, Rains AB, Haycraft CJ, Croyle MJ, Reiter JF, Yoder BK. Rab35 is required for embryonic development and kidney and ureter homeostasis through regulation of epithelial cell junctions. Biorxiv : the Preprint Server For Biology. PMID 37745459 DOI: 10.1101/2023.09.11.556924 |
0.702 |
|
| 2022 |
Li Z, Zimmerman KA, Cherakara S, Chumley P, Collawn JF, Wang J, Haycraft CJ, Song CJ, Chacana T, Andersen RS, Croyle MJ, Aloria EJ, Hombal RP, Thomas IN, Chweih H, et al. CD206+ resident macrophages are a candidate biomarker for renal cystic disease in preclinical models and patients with ADPKD. Disease Models & Mechanisms. PMID 36457161 DOI: 10.1242/dmm.049810 |
0.624 |
|
| 2021 |
Bentley-Ford MR, Andersen RS, Croyle MJ, Haycraft CJ, Clearman KR, Foote JB, Reiter JF, Yoder BK. ATXN10 Is Required for Embryonic Heart Development and Maintenance of Epithelial Cell Phenotypes in the Adult Kidney and Pancreas. Frontiers in Cell and Developmental Biology. 9: 705182. PMID 34970537 DOI: 10.3389/fcell.2021.705182 |
0.649 |
|
| 2021 |
Bentley-Ford MR, LaBonty M, Thomas HR, Haycraft CJ, Scott M, LaFayette C, Croyle MJ, Andersen RS, Parant JM, Yoder BK. Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes. Genetics. PMID 34850872 DOI: 10.1093/genetics/iyab209 |
0.65 |
|
| 2021 |
Rockwell DM, O'Connor AK, Bentley-Ford MR, Haycraft CJ, Croyle MJ, Brewer KM, Berbari NF, Kesterson RA, Yoder BK. A transgenic Alx4-CreER mouse to analyze anterior limb and nephric duct development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 33728725 DOI: 10.1002/dvdy.328 |
0.574 |
|
| 2021 |
Bentley-Ford MR, Engle SE, Clearman KR, Haycraft CJ, Andersen RS, Croyle MJ, Rains AB, Berbari NF, Yoder BK. A mouse model of BBS identifies developmental and homeostatic effects of BBS5 mutation and identifies novel pituitary abnormalities. Human Molecular Genetics. PMID 33560420 DOI: 10.1093/hmg/ddab039 |
0.669 |
|
| 2018 |
Burns TA, Deepe RN, Bullard J, Phelps AL, Toomer KA, Hiriart E, Norris RA, Haycraft CJ, Wessels A. A Novel Mouse Model for Cilia-Associated Cardiovascular Anomalies with a High Penetrance of Total Anomalous Pulmonary Venous Return. Anatomical Record (Hoboken, N.J. : 2007). PMID 30289203 DOI: 10.1002/Ar.23909 |
0.312 |
|
| 2015 |
Gudi R, Haycraft CJ, Bell PD, Li Z, Vasu C. Centrobin-mediated regulation of the centrosomal protein 4.1-associated protein (CPAP) level limits centriole length during elongation stage. The Journal of Biological Chemistry. 290: 6890-902. PMID 25616662 DOI: 10.1074/Jbc.M114.603423 |
0.523 |
|
| 2014 |
Gilley SK, Stenbit AE, Pasek RC, Sas KM, Steele SL, Amria M, Bunni MA, Estell KP, Schwiebert LM, Flume P, Gooz M, Haycraft CJ, Yoder BK, Miller C, Pavlik JA, et al. Deletion of airway cilia results in noninflammatory bronchiectasis and hyperreactive airways. American Journal of Physiology. Lung Cellular and Molecular Physiology. 306: L162-9. PMID 24213915 DOI: 10.1152/Ajplung.00095.2013 |
0.779 |
|
| 2013 |
O'Connor AK, Malarkey EB, Berbari NF, Croyle MJ, Haycraft CJ, Bell PD, Hohenstein P, Kesterson RA, Yoder BK. An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue. Cilia. 2: 8. PMID 23819925 DOI: 10.1186/2046-2530-2-8 |
0.657 |
|
| 2011 |
Kierszenbaum AL, Rivkin E, Tres LL, Yoder BK, Haycraft CJ, Bornens M, Rios RM. GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tail. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 723-36. PMID 21337470 DOI: 10.1002/Dvdy.22563 |
0.662 |
|
| 2010 |
Steele SL, Wu Y, Kolb RJ, Gooz M, Haycraft CJ, Keyser KT, Guay-Woodford L, Yao H, Bell PD. Telomerase immortalization of principal cells from mouse collecting duct. American Journal of Physiology. Renal Physiology. 299: F1507-14. PMID 20926633 DOI: 10.1152/Ajprenal.00183.2010 |
0.336 |
|
| 2009 |
Berbari NF, O'Connor AK, Haycraft CJ, Yoder BK. The primary cilium as a complex signaling center. Current Biology : Cb. 19: R526-35. PMID 19602418 DOI: 10.1016/J.Cub.2009.05.025 |
0.622 |
|
| 2009 |
Ohazama A, Haycraft CJ, Seppala M, Blackburn J, Ghafoor S, Cobourne M, Martinelli DC, Fan CM, Peterkova R, Lesot H, Yoder BK, Sharpe PT. Primary cilia regulate Shh activity in the control of molar tooth number. Development (Cambridge, England). 136: 897-903. PMID 19211681 DOI: 10.1242/Dev.027979 |
0.684 |
|
| 2008 |
Haycraft CJ, Serra R. Cilia involvement in patterning and maintenance of the skeleton. Current Topics in Developmental Biology. 85: 303-32. PMID 19147010 DOI: 10.1016/S0070-2153(08)00811-9 |
0.308 |
|
| 2008 |
Johnson ET, Nicola T, Roarty K, Yoder BK, Haycraft CJ, Serra R. Role for primary cilia in the regulation of mouse ovarian function. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 2053-60. PMID 18629867 DOI: 10.1002/Dvdy.21612 |
0.675 |
|
| 2008 |
Tran PV, Haycraft CJ, Besschetnova TY, Turbe-Doan A, Stottmann RW, Herron BJ, Chesebro AL, Qiu H, Scherz PJ, Shah JV, Yoder BK, Beier DR. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nature Genetics. 40: 403-10. PMID 18327258 DOI: 10.1038/Ng.105 |
0.713 |
|
| 2007 |
Song B, Haycraft CJ, Seo HS, Yoder BK, Serra R. Development of the post-natal growth plate requires intraflagellar transport proteins. Developmental Biology. 305: 202-16. PMID 17359961 DOI: 10.1016/J.Ydbio.2007.02.003 |
0.65 |
|
| 2007 |
McGlashan SR, Haycraft CJ, Jensen CG, Yoder BK, Poole CA. Articular cartilage and growth plate defects are associated with chondrocyte cytoskeletal abnormalities in Tg737orpk mice lacking the primary cilia protein polaris. Matrix Biology : Journal of the International Society For Matrix Biology. 26: 234-46. PMID 17289363 DOI: 10.1016/j.matbio.2006.12.003 |
0.621 |
|
| 2007 |
Haycraft CJ, Zhang Q, Song B, Jackson WS, Detloff PJ, Serra R, Yoder BK. Intraflagellar transport is essential for endochondral bone formation. Development (Cambridge, England). 134: 307-16. PMID 17166921 DOI: 10.1242/Dev.02732 |
0.706 |
|
| 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 |
0.76 |
|
| 2006 |
Efimenko E, Blacque OE, Ou G, Haycraft CJ, Yoder BK, Scholey JM, Leroux MR, Swoboda P. Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia Molecular Biology of the Cell. 17: 4801-4811. PMID 16957054 DOI: 10.1091/Mbc.E06-04-0260 |
0.727 |
|
| 2006 |
Haycraft CJ, Zhang Q, Song B, Serra R, Yoder BK. Cilia/IFT in mammalian limb patterning Developmental Biology. 295: 431-432. DOI: 10.1016/J.Ydbio.2006.04.328 |
0.554 |
|
| 2005 |
Winkelbauer ME, Schafer JC, Haycraft CJ, Swoboda P, Yoder BK. The C. elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception. Journal of Cell Science. 118: 5575-87. PMID 16291722 DOI: 10.1242/Jcs.02665 |
0.774 |
|
| 2005 |
Haycraft CJ, Banizs B, Aydin-Son Y, Zhang Q, Michaud EJ, Yoder BK. Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. Plos Genetics. 1: e53. PMID 16254602 DOI: 10.1371/Journal.Pgen.0010053 |
0.722 |
|
| 2005 |
Kramer-Zucker AG, Olale F, Haycraft CJ, Yoder BK, Schier AF, Drummond IA. Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis. Development (Cambridge, England). 132: 1907-21. PMID 15790966 DOI: 10.1242/Dev.01772 |
0.603 |
|
| 2005 |
Zhang Q, Davenport JR, Croyle MJ, Haycraft CJ, Yoder BK. Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737(orpk) mutant mice. Laboratory Investigation; a Journal of Technical Methods and Pathology. 85: 45-64. PMID 15580285 DOI: 10.1038/Labinvest.3700207 |
0.679 |
|
| 2004 |
Li JB, Gerdes JM, Haycraft CJ, Fan Y, Teslovich TM, May-Simera H, Li H, Blacque OE, Li L, Leitch CC, Lewis RA, Green JS, Parfrey PS, Leroux MR, Davidson WS, et al. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell. 117: 541-52. PMID 15137946 DOI: 10.1016/S0092-8674(04)00450-7 |
0.641 |
|
| 2003 |
Schafer JC, Haycraft CJ, Thomas JH, Yoder BK, Swoboda P. XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans. Molecular Biology of the Cell. 14: 2057-70. PMID 12802075 DOI: 10.1091/Mbc.E02-10-0677 |
0.824 |
|
| 2003 |
Haycraft CJ, Schafer JC, Zhang Q, Taulman PD, Yoder BK. Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation. Experimental Cell Research. 284: 251-63. PMID 12651157 DOI: 10.1016/S0014-4827(02)00089-7 |
0.769 |
|
| 2001 |
Haycraft CJ, Swoboda P, Taulman PD, Thomas JH, Yoder BK. The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms. Development (Cambridge, England). 128: 1493-505. PMID 11290289 |
0.814 |
|
| 2001 |
Taulman PD, Haycraft CJ, Balkovetz DF, Yoder BK. Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Molecular Biology of the Cell. 12: 589-99. PMID 11251073 DOI: 10.1091/Mbc.12.3.589 |
0.783 |
|
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