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