Bradley K. Yoder

Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function (2005)

Courtney J. Haycraft, Boglarka Banizs, Yesim Aydin-Son, Qihong Zhang, Edward J. Michaud, Bradley K. Yoder

Intraflagellar transport (IFT) proteins are essential for cilia assembly and have recently been associated with a number of developmental processes, such as left–right axis specification and limb...

Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function (2005)

Courtney J Haycraft, Boglarka Banizs, Yesim Aydin-Son, Qihong Zhang, Ed J Michaud, Bradley K Yoder

Intraflagellar transport (IFT) proteins are essential for cilia assembly and have recently been associated with a number of developmental processes, such as left-right axis specification and limb and...

Polaris, a Protein Involved in Left-Right Axis Patterning, Localizes to Basal Bodies and Cilia

Taulman, Patrick D., Haycraft, Courtney J., Balkovetz, Daniel F., Yoder, Bradley K.

Mutations in Tg737 cause a wide spectrum of phenotypes, including random left-right axis specification, polycystic kidney disease, liver and pancreatic defects, hydrocephalus, and skeletal patterning...

Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

Hou, Xiaoying, Mrug, Michal, Yoder, Bradley K., Lefkowitz, Elliot J., Kremmidiotis, Gabriel, D’Eustachio, Peter, ...

The congenital polycystic kidney (cpk) mutation is the most extensively characterized mouse model of polycystic kidney disease (PKD). The renal cystic disease is fully expressed in homozygotes and is...

A Novel Dynein Light Intermediate Chain Colocalizes with the Retrograde Motor for Intraflagellar Transport at Sites of Axoneme Assembly in Chlamydomonas and Mammalian Cells

Perrone, Catherine A., Tritschler, Douglas, Taulman, Patrick, Bower, Raqual, Yoder, Bradley K., Porter, Mary E.

The assembly of cilia and flagella depends on bidirectional intraflagellar transport (IFT). Anterograde IFT is driven by kinesin II, whereas retrograde IFT requires cytoplasmic dynein 1b (cDHC1b)....

XBX-1 Encodes a Dynein Light Intermediate Chain Required for Retrograde Intraflagellar Transport and Cilia Assembly in Caenorhabditis elegansV⃞

Schafer, Jenny C., Haycraft, Courtney J., Thomas, James H., Yoder, Bradley K., Swoboda, Peter

Intraflagellar transport (IFT) is a process required for flagella and cilia assembly that describes the dynein and kinesin mediated movement of particles along axonemes that consists of an A and a B...

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

Haycraft, Courtney J, Banizs, Boglarka, Aydin-Son, Yesim, Zhang, Qihong, Michaud, Edward J, Yoder, Bradley K

Intraflagellar transport (IFT) proteins are essential for cilia assembly and have recently been associated with a number of developmental processes, such as left–right axis specification and limb...

Polaris, a Protein Involved in Left-Right Axis Patterning, Localizes to Basal Bodies and Cilia

Taulman, Patrick D., Haycraft, Courtney J., Balkovetz, Daniel F., Yoder, Bradley K.

Mutations in Tg737 cause a wide spectrum of phenotypes, including random left-right axis specification, polycystic kidney disease, liver and pancreatic defects, hydrocephalus, and skeletal patterning...

Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

Hou, Xiaoying, Mrug, Michal, Yoder, Bradley K., Lefkowitz, Elliot J., Kremmidiotis, Gabriel, D’Eustachio, Peter, ...

The congenital polycystic kidney (cpk) mutation is the most extensively characterized mouse model of polycystic kidney disease (PKD). The renal cystic disease is fully expressed in homozygotes and is...

A Novel Dynein Light Intermediate Chain Colocalizes with the Retrograde Motor for Intraflagellar Transport at Sites of Axoneme Assembly in Chlamydomonas and Mammalian Cells

Perrone, Catherine A., Tritschler, Douglas, Taulman, Patrick, Bower, Raqual, Yoder, Bradley K., Porter, Mary E.

The assembly of cilia and flagella depends on bidirectional intraflagellar transport (IFT). Anterograde IFT is driven by kinesin II, whereas retrograde IFT requires cytoplasmic dynein 1b (cDHC1b)....

XBX-1 Encodes a Dynein Light Intermediate Chain Required for Retrograde Intraflagellar Transport and Cilia Assembly in Caenorhabditis elegansV⃞

Schafer, Jenny C., Haycraft, Courtney J., Thomas, James H., Yoder, Bradley K., Swoboda, Peter

Intraflagellar transport (IFT) is a process required for flagella and cilia assembly that describes the dynein and kinesin mediated movement of particles along axonemes that consists of an A and a B...

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

Haycraft, Courtney J, Banizs, Boglarka, Aydin-Son, Yesim, Zhang, Qihong, Michaud, Edward J, Yoder, Bradley K

Intraflagellar transport (IFT) proteins are essential for cilia assembly and have recently been associated with a number of developmental processes, such as left–right axis specification and limb...

Caenorhabditis elegans DYF-2, an Orthologue of Human WDR19, Is a Component of the Intraflagellar Transport Machinery in Sensory Cilia

Efimenko, Evgeni, Blacque, Oliver E., Ou, Guangshuo, Haycraft, Courtney J., Yoder, Bradley K., Scholey, Jonathan M., ...

The intraflagellar transport (IFT) machinery required to build functional cilia consists of a multisubunit complex whose molecular composition, organization, and function are poorly understood. Here,...

Sensory Ciliogenesis in Caenorhabditis elegans: Assignment of IFT Components into Distinct Modules Based on Transport and Phenotypic Profiles

Ou, Guangshuo, Koga, Makato, Blacque, Oliver E., Murayama, Takashi, Ohshima, Yasumi, Schafer, Jenny C., ...

Sensory cilium biogenesis within Caenorhabditis elegans neurons depends on the kinesin-2–dependent intraflagellar transport (IFT) of ciliary precursors associated with IFT particles to the axoneme...

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

Hovater, Michael B., Olteanu, Dragos, Hanson, Elizabeth L., Cheng, Nai-Lin, Siroky, Brian, Fintha, Attila, ...

Renal epithelial cells release ATP constitutively under basal conditions and release higher quantities of purine nucleotide in response to stimuli. ATP filtered at the glomerulus, secreted by...

Functional Redundancy of the B9 Proteins and Nephrocystins in Caenorhabditis elegans Ciliogenesis

Williams, Corey L., Winkelbauer, Marlene E., Schafer, Jenny C., Michaud, Edward J., Yoder, Bradley K.

Meckel-Gruber syndrome (MKS), nephronophthisis (NPHP), and Joubert syndrome (JBTS) are a group of heterogeneous cystic kidney disorders with partially overlapping loci. Many of the proteins...