Yoder, Bradley K.

The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia

Yoder, B. K., Hou, X., & Guay-Woodford, L. M. (2002) · Journal of the American Society of Nephrology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 935

Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function

Haycraft, C. J., Banizs, B., Aydin-Son, Y., Zhang, Q., Michaud, E. J., & Yoder, B. K. (2005) · PLoS Genetics

Genetic and Kidney Cyst DiseasesHedgehog Signaling Pathway Studies

Cited by 902

The Primary Cilium as a Complex Signaling Center

Berbari, N. F., O'Connor, A. K., Haycraft, C. J., & Yoder, B. K. (2009) · Current Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 621

Disruption of Intraflagellar Transport in Adult Mice Leads to Obesity and Slow-Onset Cystic Kidney Disease

Davenport, J. R., Watts, A. J., Roper, V. C., Croyle, M. J., van Groen, T., Wyss, J. M., Nagy, T. R., Kesterson, R. A., & Yoder, B. K. (2007) · Current Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 482

Dysfunctional cilia lead to altered ependyma and choroid plexus function,and result in the formation of hydrocephalus

Banizs, B., Pike, M. M., Millican, C. L., Ferguson, W. B., Komlosi, P., Sheetz, J., Bell, P. D., Schwiebert, E. M., & Yoder, B. K. (2005) · Development

Genetic and Kidney Cyst DiseasesCerebrospinal fluid and hydrocephalus

Cited by 400

In Vivo Fate Mapping and Expression Analysis Reveals Molecular Hallmarks of Prospectively Isolated Adult Neural Stem Cells

Beckervordersandforth, R., Tripathi, P., Ninkovic, J., Bayam, E., Lepier, A., Stempfhuber, B., Kirchhoff, F., Hirrlinger, J., Haslinger, A., Lie, D. C., et al. (2010) · Cell Stem Cell

Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation

Cited by 335

Directional Cell Migration and Chemotaxis in Wound Healing Response to PDGF-AA are Coordinated by the Primary Cilium in Fibroblasts

Schneider, L., Cammer, M., Lehman, J., Nielsen, S., Guerra, C., Veland, I., Stock, C., Hoffmann, E., Yoder, B., Schwab, A., et al. (2010) · Cellular Physiology and Biochemistry

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 250

Lack of Primary Cilia Primes Shear-Induced Endothelial-to-Mesenchymal Transition

Egorova, A. D., Khedoe, P. P. S. J., Goumans, M.-J. T. H., Yoder, B. K., Nauli, S. M., ten Dijke, P., Poelmann, R. E., & Hierck, B. P. (2011) · Circulation Research

Genetic and Kidney Cyst DiseasesCongenital heart defects research

Cited by 195

Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice

Berbari, N. F., Pasek, R. C., Malarkey, E. B., Yazdi, S. M. Z., McNair, A. D., Lewis, W. R., Nagy, T. R., Kesterson, R. A., & Yoder, B. K. (2013) · Proceedings of the National Academy of Sciences

Genetic and Kidney Cyst DiseasesRegulation of Appetite and Obesity

Cited by 98

Hippocampal and Cortical Primary Cilia Are Required for Aversive Memory in Mice

Berbari, N. F., Malarkey, E. B., Yazdi, S. M. Z. R., McNair, A. D., Kippe, J. M., Croyle, M. J., Kraft, T. W., & Yoder, B. K. (2014) · PLoS ONE

Genetic and Kidney Cyst DiseasesMemory and Neural Mechanisms

Cited by 69