| 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 |
0.772 |
|
| 2023 |
Katheria A, Schmolzer G, Law B, Yoder B, Clark E, El-Naggar W, Morales A, Dorner R, Mooso B, Rich W, Vora F, Finer N. Parental Perspectives on a Trial Using Waived Informed Consent at Birth. Research Square. PMID 37961362 DOI: 10.21203/rs.3.rs-3487820/v1 |
0.345 |
|
| 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 |
0.756 |
|
| 2023 |
Wilk EJ, Howton TC, Fisher JL, Oza VH, Brownlee RT, McPherson KC, Cleary HL, Yoder BK, George JF, Mrug M, Lasseigne BN. Prioritized polycystic kidney disease drug targets and repurposing candidates from pre-cystic and cystic mouse Pkd2 model gene expression reversion. Molecular Medicine (Cambridge, Mass.). 29: 67. PMID 37217845 DOI: 10.1186/s10020-023-00664-z |
0.532 |
|
| 2022 |
Wang J, Thomas HR, Thompson RG, Waldrep SC, Fogerty J, Song P, Li Z, Ma Y, Santra P, Hoover JD, Yeo NC, Drummond IA, Yoder BK, Amack JD, Perkins B, et al. Variable phenotypes and penetrance between and within different zebrafish ciliary transition zone mutants. Disease Models & Mechanisms. 15. PMID 36533556 DOI: 10.1242/dmm.049568 |
0.337 |
|
| 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, ... ... Yoder BK, 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 |
0.726 |
|
| 2022 |
Song C, Li Z, Ahmed UKB, Bland S, Yashchenko A, Liu S, Aloria E, Lever J, Gonzalez N, Bickel M, Giles C, Georgescu C, Wren J, Lang M, Benveniste E, ... ... Yoder B, et al. A Comprehensive Immune Cell Atlas of Cystic Kidney Disease Reveals the Involvement of Adaptive Immune Cells in Injury-Mediated Cyst Progression in Mice. Journal of the American Society of Nephrology : Jasn. PMID 35110364 DOI: 10.1681/ASN.2021030278 |
0.505 |
|
| 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 |
0.735 |
|
| 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 |
0.737 |
|
| 2021 |
Aloria EJG, Song CJ, Li Z, Croyle MJ, Mrug M, Zimmerman KA, Yoder BK. Ly6c Infiltrating Macrophages Promote Cyst Progression in Injured Conditional Mice. Kidney360. 2: 989-995. PMID 34396149 DOI: 10.34067/KID.0000882021 |
0.421 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 2021 |
Zimmerman KA, Song CJ, Aloria EJG, Li Z, Zhou J, Bland SJ, Yashchenko A, Crossman DK, Mrug M, Yoder BK. Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 101: 1382-1393. PMID 34158590 DOI: 10.1038/s41374-021-00627-0 |
0.481 |
|
| 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 |
0.685 |
|
| 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 |
0.748 |
|
| 2020 |
Bales KL, Bentley MR, Croyle MJ, Kesterson RA, Yoder BK, Gross AK. BBSome Component BBS5 Is Required for Cone Photoreceptor Protein Trafficking and Outer Segment Maintenance. Investigative Ophthalmology & Visual Science. 61: 17. PMID 32776140 DOI: 10.1167/Iovs.61.10.17 |
0.739 |
|
| 2020 |
Zimmerman KA, Huang J, He L, Revell DZ, Li Z, Hsu J, Fitzgibbon WR, Hazard ES, Hardiman G, Mrug M, Bell PD, Yoder BK, Saigusa T. Interferon Regulatory Factor‐5 in Resident Macrophage Promotes Polycystic Kidney Disease Kidney360. 1: 179-190. DOI: 10.34067/Kid.0001052019 |
0.349 |
|
| 2019 |
Larson-Casey JL, Vaid M, Gu L, He C, Cai GQ, Ding Q, Davis D, Berryhill TF, Wilson LS, Barnes S, Neighbors JD, Hohl RJ, Zimmerman KA, Yoder BK, Longhini ALF, et al. Increased flux through the mevalonate pathway mediates fibrotic repair without injury. The Journal of Clinical Investigation. PMID 31609245 DOI: 10.1172/Jci127959 |
0.339 |
|
| 2019 |
Revell DZ, Yoder BK. Intravital visualization of the primary cilium, tubule flow, and innate immune cells in the kidney utilizing an abdominal window imaging approach. Methods in Cell Biology. 154: 67-83. PMID 31493822 DOI: 10.1016/Bs.Mcb.2019.04.012 |
0.388 |
|
| 2019 |
Zimmerman KA, Song CJ, Li Z, Lever JM, Crossman DK, Rains A, Aloria EJ, Gonzalez NM, Bassler JR, Zhou J, Crowley MR, Revell DZ, Yan Z, Shan D, Benveniste EN, ... Yoder BK, et al. Tissue-Resident Macrophages Promote Renal Cystic Disease. Journal of the American Society of Nephrology : Jasn. PMID 31337691 DOI: 10.1681/Asn.2018080810 |
0.58 |
|
| 2019 |
Zimmerman KA, Bentley MR, Lever JM, Li Z, Crossman DK, Song CJ, Liu S, Crowley MR, George JF, Mrug M, Yoder BK. Single-Cell RNA Sequencing Identifies Candidate Renal Resident Macrophage Gene Expression Signatures across Species. Journal of the American Society of Nephrology : Jasn. PMID 30948627 DOI: 10.1681/Asn.2018090931 |
0.785 |
|
| 2019 |
Lever JM, Hull TD, Boddu R, Pepin ME, Black LM, Adedoyin OO, Yang Z, Traylor AM, Jiang Y, Li Z, Peabody JE, Eckenrode HE, Crossman DK, Crowley MR, Bolisetty S, ... ... Yoder BK, et al. Resident macrophages reprogram toward a developmental state after acute kidney injury. Jci Insight. 4. PMID 30674729 DOI: 10.1172/Jci.Insight.125503 |
0.302 |
|
| 2019 |
Zimmerman KA, Gonzalez NM, Chumley P, Chacana T, Harrington LE, Yoder BK, Mrug M. Urinary T cells correlate with rate of renal function loss in autosomal dominant polycystic kidney disease. Physiological Reports. 7: e13951. PMID 30632307 DOI: 10.14814/Phy2.13951 |
0.327 |
|
| 2019 |
Shan D, Rezonzew G, Mullen S, Roye R, Zhou J, Chumley P, Revell DZ, Challa AK, Kim H, Lockhart ME, Schoeb TR, Croyle MJ, Kesterson RA, Yoder BK, Guay-Woodford LM, et al. Heterozygous Pkhd1 mice develop cystic liver disease and proximal tubule ectasia that mimics radiographic signs of medullary sponge kidney. American Journal of Physiology. Renal Physiology. PMID 30600684 DOI: 10.1152/Ajprenal.00181.2018 |
0.386 |
|
| 2018 |
Chumley P, Zhou J, Mrug S, Chacko BK, Parant JM, Challa AK, Wilson LS, Berryhill TF, Barnes S, Kesterson RA, Bell PD, Darley-Usmar VM, Yoder BK, Mrug M. Truncating PKHD1 and PKD2 mutations alter energy metabolism. American Journal of Physiology. Renal Physiology. PMID 30566001 DOI: 10.1152/Ajprenal.00167.2018 |
0.359 |
|
| 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 |
0.681 |
|
| 2018 |
Lewis WR, Bales KL, Revell DZ, Croyle MJ, Engle SE, Song CJ, Malarkey EB, Uytingco CR, Shan D, Antonellis PJ, Nagy TR, Kesterson RA, Mrug MM, Martens JR, Berbari NF, ... ... Yoder BK, et al. Mks6 mutations reveal tissue- and cell type-specific roles for the cilia transition zone. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201801149R. PMID 30133325 DOI: 10.1096/Fj.201801149R |
0.797 |
|
| 2018 |
Zimmerman KA, Song CJ, Gonzalez-Mize N, Li Z, Yoder BK. Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver. American Journal of Physiology. Gastrointestinal and Liver Physiology. PMID 29543508 DOI: 10.1152/Ajpgi.00381.2017 |
0.782 |
|
| 2017 |
Puri P, Schaefer CM, Bushnell D, Taglienti ME, Kreidberg JA, Yoder BK, Bates CM. Ectopic phosphorylated Creb marks dedifferentiated proximal tubules in cystic kidney disease. The American Journal of Pathology. PMID 29107072 DOI: 10.1016/J.Ajpath.2017.09.015 |
0.344 |
|
| 2017 |
Song CJ, Zimmerman KA, Henke SJ, Yoder BK. Inflammation and Fibrosis in Polycystic Kidney Disease. Results and Problems in Cell Differentiation. 60: 323-344. PMID 28409351 DOI: 10.1007/978-3-319-51436-9_12 |
0.765 |
|
| 2016 |
Lewis WR, Malarkey EB, Tritschler D, Bower R, Pasek RC, Porath JD, Birket SE, Saunier S, Antignac C, Knowles MR, Leigh MW, Zariwala MA, Challa AK, Kesterson RA, Rowe SM, ... Yoder BK, et al. Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. Plos Genetics. 12: e1006220. PMID 27472056 DOI: 10.1371/Journal.Pgen.1006220 |
0.815 |
|
| 2016 |
Pasek RC, Malarkey E, Berbari NF, Sharma N, Kesterson RA, Tres LL, Kierszenbaum AL, Yoder BK. Coiled-coil domain containing 42 (Ccdc42) is necessary for proper sperm development and male fertility in the mouse. Developmental Biology. PMID 26945718 DOI: 10.1016/J.Ydbio.2016.01.042 |
0.77 |
|
| 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 |
0.669 |
|
| 2016 |
Sugiyama Y, Shelley EJ, Yoder BK, Kozmik Z, May-Simera HL, Beales PL, Lovicu FJ, McAvoy JW. Non-essential role for cilia in coordinating precise alignment of lens fibres. Mechanisms of Development. PMID 26825015 DOI: 10.1016/J.Mod.2016.01.003 |
0.419 |
|
| 2015 |
Sanders AA, de Vrieze E, Alazami AM, Alzahrani F, Malarkey EB, Sorusch N, Tebbe L, Kuhns S, van Dam TJ, Alhashem A, Tabarki B, Lu Q, Lambacher NJ, Kennedy JE, Bowie RV, ... ... Yoder BK, et al. KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome. Genome Biology. 16: 293. PMID 26714646 DOI: 10.1186/S13059-015-0858-Z |
0.321 |
|
| 2015 |
Mrug M, Zhou J, Yang C, Aronow BJ, Cui X, Schoeb TR, Siegal GP, Yoder BK, Guay-Woodford LM. Genetic and Informatic Analyses Implicate Kif12 as a Candidate Gene within the Mpkd2 Locus That Modulates Renal Cystic Disease Severity in the Cys1cpk Mouse. Plos One. 10: e0135678. PMID 26295839 DOI: 10.1371/Journal.Pone.0135678 |
0.381 |
|
| 2015 |
Zimmerman K, Yoder BK. SnapShot: Sensing and Signaling by Cilia. Cell. 161: 692-2.e1. PMID 25910215 DOI: 10.1016/J.Cell.2015.04.015 |
0.368 |
|
| 2015 |
Jiang L, Wei Y, Ronquillo CC, Marc RE, Yoder BK, Frederick JM, Baehr W. Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors. The Journal of Biological Chemistry. 290: 12765-78. PMID 25825494 DOI: 10.1074/Jbc.M115.638437 |
0.344 |
|
| 2015 |
Sanders A, Kuhns S, Wijk EV, Malarkey E, Yoder B, Vrieze Ed, Alazami A, Alkuraya F, Blacque O. Dataset supporting publication entitled: KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome Genome Biology. DOI: 10.5281/Zenodo.33941 |
0.309 |
|
| 2014 |
Thomas HR, Percival SM, Yoder BK, Parant JM. High-throughput genome editing and phenotyping facilitated by high resolution melting curve analysis. Plos One. 9: e114632. PMID 25503746 DOI: 10.1371/Journal.Pone.0114632 |
0.348 |
|
| 2014 |
Mrug M, Zhou J, Mrug S, Guay-Woodford LM, Yoder BK, Szalai AJ. Complement C3 activation in cyst fluid and urine from autosomal dominant polycystic kidney disease patients. Journal of Internal Medicine. 276: 539-40. PMID 25205519 DOI: 10.1111/Joim.12307 |
0.319 |
|
| 2014 |
Berbari NF, Malarkey EB, Yazdi SM, McNair AD, Kippe JM, Croyle MJ, Kraft TW, Yoder BK. Hippocampal and cortical primary cilia are required for aversive memory in mice. Plos One. 9: e106576. PMID 25184295 DOI: 10.1371/Journal.Pone.0106576 |
0.358 |
|
| 2014 |
Vijayakumar S, Dang S, Marinkovich MP, Lazarova Z, Yoder B, Torres VE, Wallace DP. Aberrant expression of laminin-332 promotes cell proliferation and cyst growth in ARPKD. American Journal of Physiology. Renal Physiology. 306: F640-54. PMID 24370592 DOI: 10.1152/Ajprenal.00104.2013 |
0.339 |
|
| 2014 |
Tower-Gilchrist C, Styers ML, Yoder BK, Berbari NF, Sztul E. Monitoring endosomal trafficking of the g protein-coupled receptor somatostatin receptor 3. Methods in Enzymology. 534: 261-80. PMID 24359959 DOI: 10.1016/B978-0-12-397926-1.00015-9 |
0.325 |
|
| 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 |
0.798 |
|
| 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 |
0.753 |
|
| 2013 |
Berbari NF, Pasek RC, Malarkey EB, Yazdi SM, McNair AD, Lewis WR, Nagy TR, Kesterson RA, Yoder BK. Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice. Proceedings of the National Academy of Sciences of the United States of America. 110: 7796-801. PMID 23599282 DOI: 10.1073/Pnas.1210192110 |
0.766 |
|
| 2013 |
Berezniuk I, Sironi JJ, Wardman J, Pasek RC, Berbari NF, Yoder BK, Fricker LD. Quantitative peptidomics of Purkinje cell degeneration mice. Plos One. 8: e60981. PMID 23593366 DOI: 10.1371/Journal.Pone.0060981 |
0.735 |
|
| 2013 |
Sharma N, Malarkey EB, Berbari NF, O'Connor AK, Vanden Heuvel GB, Mrug M, Yoder BK. Proximal tubule proliferation is insufficient to induce rapid cyst formation after cilia disruption. Journal of the American Society of Nephrology : Jasn. 24: 456-64. PMID 23411784 DOI: 10.1681/Asn.2012020154 |
0.357 |
|
| 2013 |
Berbari NF, Sharma N, Malarkey EB, Pieczynski JN, Boddu R, Gaertig J, Guay-Woodford L, Yoder BK. Microtubule modifications and stability are altered by cilia perturbation and in cystic kidney disease. Cytoskeleton (Hoboken, N.J.). 70: 24-31. PMID 23124988 DOI: 10.1002/Cm.21088 |
0.43 |
|
| 2013 |
Berbari NF, Pasek RC, Yoder BK. Neuronal cilia and obesity Cilia and Nervous System Development and Function. 2147483647: 165-191. DOI: 10.1007/978-94-007-5808-7_6 |
0.719 |
|
| 2012 |
Pasek RC, Berbari NF, Lewis WR, Kesterson RA, Yoder BK. Mammalian Clusterin associated protein 1 is an evolutionarily conserved protein required for ciliogenesis. Cilia. 1: 20. PMID 23351563 DOI: 10.1186/2046-2530-1-20 |
0.823 |
|
| 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, ... ... Yoder BK, 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 |
0.665 |
|
| 2012 |
Zhou J, Ouyang X, Schoeb TR, Bolisetty S, Cui X, Mrug S, Yoder BK, Johnson MR, Szalai AJ, Mrug M. Kidney injury accelerates cystogenesis via pathways modulated by heme oxygenase and complement. Journal of the American Society of Nephrology : Jasn. 23: 1161-71. PMID 22518005 DOI: 10.1681/Asn.2011050442 |
0.368 |
|
| 2012 |
Olteanu D, Liu X, Liu W, Roper VC, Sharma N, Yoder BK, Satlin LM, Schwiebert EM, Bevensee MO. Increased Na+/H+ exchanger activity on the apical surface of a cilium-deficient cortical collecting duct principal cell model of polycystic kidney disease. American Journal of Physiology. Cell Physiology. 302: C1436-51. PMID 22301060 DOI: 10.1152/Ajpcell.00063.2011 |
0.39 |
|
| 2012 |
Yoder B. NPHP and MKS proteins and the ciliary transition zone Cilia. 1: 1-1. DOI: 10.1186/2046-2530-1-S1-O13 |
0.515 |
|
| 2011 |
Berbari NF, Kin NW, Sharma N, Michaud EJ, Kesterson RA, Yoder BK. Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation. Developmental Biology. 360: 66-76. PMID 21945076 DOI: 10.1016/J.Ydbio.2011.09.001 |
0.49 |
|
| 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 |
0.792 |
|
| 2011 |
Croyle MJ, Lehman JM, O'Connor AK, Wong SY, Malarkey EB, Iribarne D, Dowdle WE, Schoeb TR, Verney ZM, Athar M, Michaud EJ, Reiter JF, Yoder BK. Role of epidermal primary cilia in the homeostasis of skin and hair follicles. Development (Cambridge, England). 138: 1675-85. PMID 21429982 DOI: 10.1242/dev.060210 |
0.657 |
|
| 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 |
0.658 |
|
| 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 |
0.724 |
|
| 2011 |
Sharma N, Kosan ZA, Stallworth JE, Berbari NF, Yoder BK. Soluble levels of cytosolic tubulin regulate ciliary length control. Molecular Biology of the Cell. 22: 806-16. PMID 21270438 DOI: 10.1091/Mbc.E10-03-0269 |
0.419 |
|
| 2010 |
Beckervordersandforth R, Tripathi P, Ninkovic J, Bayam E, Lepier A, Stempfhuber B, Kirchhoff F, Hirrlinger J, Haslinger A, Lie DC, Beckers J, Yoder B, Irmler M, Götz M. In vivo fate mapping and expression analysis reveals molecular hallmarks of prospectively isolated adult neural stem cells. Cell Stem Cell. 7: 744-58. PMID 21112568 DOI: 10.1016/J.Stem.2010.11.017 |
0.353 |
|
| 2010 |
Hellman NE, Liu Y, Merkel E, Austin C, Le Corre S, Beier DR, Sun Z, Sharma N, Yoder BK, Drummond IA. The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch. Proceedings of the National Academy of Sciences of the United States of America. 107: 18499-504. PMID 20937855 DOI: 10.1073/Pnas.1005998107 |
0.355 |
|
| 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 |
0.681 |
|
| 2010 |
Schneider L, Cammer M, Lehman J, Nielsen SK, Guerra CF, Veland IR, Stock C, Hoffmann EK, Yoder BK, Schwab A, Satir P, Christensen ST. Directional cell migration and chemotaxis in wound healing response to PDGF-AA are coordinated by the primary cilium in fibroblasts. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 25: 279-92. PMID 20110689 DOI: 10.1159/000276562 |
0.617 |
|
| 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 |
0.767 |
|
| 2009 |
O'Connor AK, Kesterson RA, Yoder BK. Generating conditional mutants to analyze ciliary functions: the use of Cre-lox technology to disrupt cilia in specific organs. Methods in Cell Biology. 93: 305-30. PMID 20409823 DOI: 10.1016/S0091-679X(08)93015-6 |
0.432 |
|
| 2009 |
Kesterson RA, Berbari NF, Pasek RC, Yoder BK. Utilization of conditional alleles to study the role of the primary cilium in obesity. Methods in Cell Biology. 94: 163-79. PMID 20362090 DOI: 10.1016/S0091-679X(08)94008-5 |
0.773 |
|
| 2009 |
Clement CA, Kristensen SG, Møllgård K, Pazour GJ, Yoder BK, Larsen LA, Christensen ST. The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation. Journal of Cell Science. 122: 3070-82. PMID 19654211 DOI: 10.1242/Jcs.049676 |
0.394 |
|
| 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 |
0.725 |
|
| 2009 |
Veland IR, Awan A, Pedersen LB, Yoder BK, Christensen ST. Primary cilia and signaling pathways in mammalian development, health and disease. Nephron. Physiology. 111: p39-53. PMID 19276629 DOI: 10.1159/000208212 |
0.478 |
|
| 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 |
0.747 |
|
| 2009 |
Lehman JM, Laag E, Michaud EJ, Yoder BK. An essential role for dermal primary cilia in hair follicle morphogenesis. The Journal of Investigative Dermatology. 129: 438-48. PMID 18987668 DOI: 10.1038/Jid.2008.279 |
0.657 |
|
| 2008 |
Sharma N, Berbari NF, Yoder BK. Ciliary dysfunction in developmental abnormalities and diseases. Current Topics in Developmental Biology. 85: 371-427. PMID 19147012 DOI: 10.1016/S0070-2153(08)00813-2 |
0.461 |
|
| 2008 |
Yoder BK. Ciliary function in mammalian development. Preface. Current Topics in Developmental Biology. 85: xv-xix. PMID 19146999 DOI: 10.1016/S0070-2153(08)00817-X |
0.307 |
|
| 2008 |
Nielsen SK, Møllgård K, Clement CA, Veland IR, Awan A, Yoder BK, Novak I, Christensen ST. Characterization of primary cilia and Hedgehog signaling during development of the human pancreas and in human pancreatic duct cancer cell lines. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 2039-52. PMID 18629868 DOI: 10.1002/Dvdy.21610 |
0.336 |
|
| 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 |
0.741 |
|
| 2008 |
Hovater MB, Olteanu D, Hanson EL, Cheng NL, Siroky B, Fintha A, Komlosi P, Liu W, Satlin LM, Bell PD, Yoder BK, Schwiebert EM. Loss of apical monocilia on collecting duct principal cells impairs ATP secretion across the apical cell surface and ATP-dependent and flow-induced calcium signals. Purinergic Signalling. 4: 155-70. PMID 18368523 DOI: 10.1007/S11302-007-9072-0 |
0.387 |
|
| 2008 |
Lehman JM, Michaud EJ, Schoeb TR, Aydin-Son Y, Miller M, Yoder BK. The Oak Ridge Polycystic Kidney mouse: modeling ciliopathies of mice and men. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 1960-71. PMID 18366137 DOI: 10.1002/Dvdy.21515 |
0.66 |
|
| 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 |
0.798 |
|
| 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 |
0.771 |
|
| 2008 |
Jones C, Roper VC, Foucher I, Qian D, Banizs B, Petit C, Yoder BK, Chen P. Ciliary proteins link basal body polarization to planar cell polarity regulation. Nature Genetics. 40: 69-77. PMID 18066062 DOI: 10.1038/Ng.2007.54 |
0.395 |
|
| 2008 |
Davenport J, Kale A, Sharma N, Yoder B. Ciliary dysfunction in adult mice results in slowly progressing cystic kidney disease and disrupts energy homeostasis Microscopy and Microanalysis. 14: 1482-1483. DOI: 10.1017/S1431927608081634 |
0.313 |
|
| 2007 |
Davenport JR, Watts AJ, Roper VC, Croyle MJ, van Groen T, Wyss JM, Nagy TR, Kesterson RA, Yoder BK. Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease. Current Biology : Cb. 17: 1586-94. PMID 17825558 DOI: 10.1016/J.Cub.2007.08.034 |
0.466 |
|
| 2007 |
Chizhikov VV, Davenport J, Zhang Q, Shih EK, Cabello OA, Fuchs JL, Yoder BK, Millen KJ. Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 9780-9. PMID 17804638 DOI: 10.1523/Jneurosci.5586-06.2007 |
0.471 |
|
| 2007 |
Yoder BK. Role of primary cilia in the pathogenesis of polycystic kidney disease. Journal of the American Society of Nephrology : Jasn. 18: 1381-8. PMID 17429051 DOI: 10.1681/Asn.2006111215 |
0.479 |
|
| 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 |
0.718 |
|
| 2007 |
Ou G, Koga M, Blacque OE, Murayama T, Ohshima Y, Schafer JC, Li C, Yoder BK, Leroux MR, Scholey JM. Sensory ciliogenesis in Caenorhabditis elegans: Assignment of IFT components into distinct modules based on transport and phenotypic profiles Molecular Biology of the Cell. 18: 1554-1569. PMID 17314406 DOI: 10.1091/Mbc.E06-09-0805 |
0.756 |
|
| 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 |
0.71 |
|
| 2007 |
Banizs B, Komlosi P, Bevensee MO, Schwiebert EM, Bell PD, Yoder BK. Altered pH(i) regulation and Na(+)/HCO3(-) transporter activity in choroid plexus of cilia-defective Tg737(orpk) mutant mouse. American Journal of Physiology. Cell Physiology. 292: C1409-16. PMID 17182727 DOI: 10.1152/Ajpcell.00408.2006 |
0.399 |
|
| 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 |
0.753 |
|
| 2007 |
Olteanu DS, Yoder BK, Bevensee MO, Schwiebert EM. NHE Dysregulation in Cilium Deficient Mouse Renal Principal Cells from orpk Mice The Faseb Journal. 21. DOI: 10.1096/Fasebj.21.5.A504 |
0.338 |
|
| 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 |
0.805 |
|
| 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 |
0.761 |
|
| 2006 |
Michaud EJ, Yoder BK. The primary cilium in cell signaling and cancer. Cancer Research. 66: 6463-7. PMID 16818613 DOI: 10.1158/0008-5472.Can-06-0462 |
0.366 |
|
| 2006 |
Yoder BK. More than just the postal service: novel roles for IFT proteins in signal transduction. Developmental Cell. 10: 541-2. PMID 16678768 DOI: 10.1016/J.Devcel.2006.04.010 |
0.369 |
|
| 2006 |
Yoder BK, Mulroy S, Eustace H, Boucher C, Sandford R. Molecular pathogenesis of autosomal dominant polycystic kidney disease. Expert Reviews in Molecular Medicine. 8: 1-22. PMID 16515728 DOI: 10.1017/S1462399406010362 |
0.415 |
|
| 2006 |
Siroky BJ, Ferguson WB, Fuson AL, Xie Y, Fintha A, Komlosi P, Yoder BK, Schwiebert EM, Guay-Woodford LM, Bell PD. Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells. American Journal of Physiology. Renal Physiology. 290: F1320-8. PMID 16396941 DOI: 10.1152/Ajprenal.00463.2005 |
0.318 |
|
| 2006 |
Olteanu D, Yoder BK, Liu W, Croyle MJ, Welty EA, Rosborough K, Wyss JM, Bell PD, Guay-Woodford LM, Bevensee MO, Satlin LM, Schwiebert EM. Heightened epithelial Na+ channel-mediated Na+ absorption in a murine polycystic kidney disease model epithelium lacking apical monocilia. American Journal of Physiology. Cell Physiology. 290: C952-63. PMID 16207792 DOI: 10.1152/Ajpcell.00339.2005 |
0.447 |
|
| 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 |
0.659 |
|
| 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 |
0.817 |
|
| 2005 |
Banizs B, Pike MM, Millican CL, Ferguson WB, Komlosi P, Sheetz J, Bell PD, Schwiebert EM, Yoder BK. Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus. Development (Cambridge, England). 132: 5329-39. PMID 16284123 DOI: 10.1242/Dev.02153 |
0.46 |
|
| 2005 |
Davenport JR, Yoder BK. An incredible decade for the primary cilium: a look at a once-forgotten organelle. American Journal of Physiology. Renal Physiology. 289: F1159-69. PMID 16275743 DOI: 10.1152/Ajprenal.00118.2005 |
0.426 |
|
| 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 |
0.752 |
|
| 2005 |
Liu W, Murcia NS, Duan Y, Weinbaum S, Yoder BK, Schwiebert E, Satlin LM. Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk mice. American Journal of Physiology. Renal Physiology. 289: F978-88. PMID 15972389 DOI: 10.1152/Ajprenal.00260.2004 |
0.34 |
|
| 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 |
0.699 |
|
| 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 |
0.738 |
|
| 2004 |
Zhang Q, Taulman PD, Yoder BK. Cystic kidney diseases: all roads lead to the cilium. Physiology (Bethesda, Md.). 19: 225-30. PMID 15304637 DOI: 10.1152/Physiol.00003.2004 |
0.783 |
|
| 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, ... ... Yoder BK, 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 |
0.721 |
|
| 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 |
0.827 |
|
| 2003 |
Perrone CA, Tritschler D, Taulman P, Bower R, Yoder BK, Porter ME. A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells. Molecular Biology of the Cell. 14: 2041-56. PMID 12802074 DOI: 10.1091/Mbc.E02-10-0682 |
0.805 |
|
| 2003 |
Zhang Q, Murcia NS, Chittenden LR, Richards WG, Michaud EJ, Woychik RP, Yoder BK. Loss of the Tg737 protein results in skeletal patterning defects. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 227: 78-90. PMID 12701101 DOI: 10.1002/Dvdy.10289 |
0.424 |
|
| 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 |
0.806 |
|
| 2002 |
Yoder BK, Hou X, Guay-Woodford LM. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. Journal of the American Society of Nephrology : Jasn. 13: 2508-16. PMID 12239239 DOI: 10.1097/01.Asn.0000029587.47950.25 |
0.51 |
|
| 2002 |
Hou X, Mrug M, Yoder BK, Lefkowitz EJ, Kremmidiotis G, D'Eustachio P, Beier DR, Guay-Woodford LM. Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. The Journal of Clinical Investigation. 109: 533-40. PMID 11854326 DOI: 10.1172/Jci14099 |
0.475 |
|
| 2002 |
Yoder BK, Tousson A, Millican L, Wu JH, Bugg CE, Schafer JA, Balkovetz DF. Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium. American Journal of Physiology. Renal Physiology. 282: F541-52. PMID 11832437 DOI: 10.1152/Ajprenal.00273.2001 |
0.496 |
|
| 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 |
0.831 |
|
| 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 |
0.815 |
|
| 2000 |
Murcia NS, Richards WG, Yoder BK, Mucenski ML, Dunlap JR, Woychik RP. The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development (Cambridge, England). 127: 2347-55. PMID 10804177 |
0.302 |
|
| 1998 |
Richards WG, Sweeney WE, Yoder BK, Wilkinson JE, Woychik RP, Avner ED. Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease. The Journal of Clinical Investigation. 101: 935-9. PMID 9486961 DOI: 10.1172/Jci2071 |
0.318 |
|
| 1996 |
Richards WG, Yoder BK, Isfort RJ, Detilleux PG, Foster C, Neilsen N, Woychik RP, Wilkinson JE. Oval cell proliferation associated with the murine insertional mutation TgN737Rpw. The American Journal of Pathology. 149: 1919-30. PMID 8952527 |
0.324 |
|
| 1996 |
Yoder BK, Richards WG, Sommardahl C, Sweeney WE, Michaud EJ, Wilkinson JE, Avner ED, Woychik RP. Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA. Kidney International. 50: 1240-8. PMID 8887283 DOI: 10.1038/Ki.1996.433 |
0.446 |
|
| 1995 |
Yoder BK, Richards WG, Sweeney WE, Wilkinson JE, Avener ED, Woychik RP. Insertional mutagenesis and molecular analysis of a new gene associated with polycystic kidney disease. Proceedings of the Association of American Physicians. 107: 314-23. PMID 8608416 |
0.319 |
|
| 1994 |
Yoder BK, Mao J, Erdos GW, West CM, Blumberg DD. Identification of a new spore coat protein gene in the cellular slime mold Dictyostelium discoideum. Developmental Biology. 163: 49-65. PMID 8174787 DOI: 10.1006/Dbio.1994.1122 |
0.338 |
|
| 1994 |
Yoder BK, Blumberg DD. The promoter of a gene encoding a novel Dictyostelium spore coat protein. Developmental Biology. 163: 38-48. PMID 8174786 DOI: 10.1006/Dbio.1994.1121 |
0.334 |
|
| 1991 |
Blumberg DD, Agarwal AK, Sloger MS, Yoder BK. Gene expression and chromatin structure in the cellular slime mold, Dictyostelium discoideum. Developmental Genetics. 12: 65-77. PMID 1646696 DOI: 10.1002/Dvg.1020120113 |
0.308 |
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