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One or more keywords matched the following items that are connected to Pazour, Gregory
Item TypeName
Academic Article The vertebrate primary cilium is a sensory organelle.
Academic Article Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization.
Academic Article Pericentrin forms a complex with intraflagellar transport proteins and polycystin-2 and is required for primary cilia assembly.
Academic Article Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference.
Academic Article Cooperative binding of Agrobacterium tumefaciens VirE2 protein to single-stranded DNA.
Academic Article Localization of transient receptor potential ion channels in primary and motile cilia of the female murine reproductive organs.
Academic Article The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly.
Academic Article Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella.
Academic Article Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease.
Concept Ion Channels
Concept Calcium Channels
Concept TRPV Cation Channels
Concept TRPP Cation Channels
Concept Potassium Channels
Academic Article Casein kinase 1d functions at the centrosome and Golgi to promote ciliogenesis.
Academic Article BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia.
Academic Article Cilia in cystic kidney and other diseases.
Academic Article E3 ubiquitin ligase Wwp1 regulates ciliary dynamics of the Hedgehog receptor Smoothened.
Academic Article c-Jun N-terminal kinase (JNK) signaling contributes to cystic burden in polycystic kidney disease.
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  • Hyperpolarization Activated Cyclic Nucleotide Gated Channels